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Egyptian Journal of Medical Human Genetics

中文名称：埃及医学人类遗传学杂志》上

ISSN：1110-8630
出版周期：-

发文量：597

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1.Can microRNA become next-generation tools in molecular diagnostics and therapeutics? A systematic review

机译：MicroRNA可以成为分子诊断和治疗方法的下一代工具吗？系统评价
- 作者：Saini Vandana;Dawar Rajni;Suneja Shilpa;Gangopadhyay Sukanya;Kaur Charanjeet
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Gene regulationmiRNA gene silencingmiRNA expression profilingmiRNA antagonistsmiRNA mimics;
2.Differential expression of viral pathogen-associated molecular pattern receptors mRNA in Egyptian chronic hepatitis C virus patients

机译：埃及慢性丙型肝炎病毒患者病毒病原菌相关分子模式受体mRNA的差异表达
- 作者：Suef Reda A.;Mohamed Ezz Elden M.;Mansour Mohamed T. M.;Weigand Kilian;Farag Mohamed M. S.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Hepatitis C virusTLR3 and TLR7 signalingIFN-α transcription;
3.Study of HOTAIR LncRNA in AML patients in context to FLT3-ITD and NPM1 mutations status

机译：在FLT3-ITD和NPM1突变状态下，AML患者Hotair LNCrNA研究
- 作者：Salah Mona;Zawam Hamdy;Fouad Neven Bahaa;Soliman Nohair;Maksoud Fatma Abdel Wahab Abdel
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- HOTAIRLncRNAAMLNPM1FLT3-ITD;
4.Susceptibility role of soluble HLA-G and HLA-G 14-bp insertion/deletion polymorphism in inflammatory bowel disease

机译：可溶性HLA-G和HLA-G14-BP插入/缺失多态性在炎性肠病中的易感性作用
- 作者：Abdul-Hussein Sarah S.;Ali Ekhlass N.;Alkhalidi Nawal M. F.;Zaki Neihaya H.;Adhiah Ali H.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Inflammatory bowel diseaseUlcerative colitisCrohn’s diseaseSoluble HLA-G14-bp Ins/Del polymorphism;
5.Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse

机译：CNTNAP2在自闭症表现中的作用概述了突触神经元之间信号传导的调节
- 作者：Agarwala Swati;Ramachandra Nallur B.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- WESCNTNAP2VariantsAutismSusceptibility;
6.HLA-A gene knockout using CRISPR/Cas9 system toward overcoming transplantation concerns

机译：HLA-A基因敲除使用CRISPR / CAS9系统延长移植问题
- 作者：Amiri Farshid;Ranjbar Maryam;Pirouzfar Mohammad;Nourigorji Marjan;Dianatpour Mehdi
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- HLA-AHSCTCRISPR/Cas9;
7.Computer-assisted evaluation of plant-derived β-secretase inhibitors in Alzheimer's disease

机译：在阿尔茨海默病中植物衍生的β-分泌酶抑制剂的计算机辅助评价
- 作者：Ullah Md. Asad;Johora Fatema Tuz;Sarkar Bishajit;Araf Yusha;Ahmed Nafisa;Nahar Abida Nurun;Akter Tanzina
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Alzheimer’s diseaseAmentoflavoneBilobetinβ-secretaseDockingEllagic acidInhibitors;
8.Screening of NKX2.5 gene in Moroccan Tetralogy of Fallot (TOF) patients: worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype

机译：筛查摩洛哥乳房的NKX2.5基因（TOF）患者：全球突变率比较显示R25C变异和TOF表型之间的重要关联
- 作者：EL Bouchikhi Ihssane;Belhassan Khadija;Moufid Fatima Zohra;Bouguenouch Laila;Samri Imane;Iraqui Houssani Mohammed;Ouldim Karim;Atmani Samir
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Tetralogy of Fallot (TOF)NKX2.5R25C mutationGenetic screeningMoroccan populationMutation rate;
9.Association between genetic polymorphism of XRCC7 (G6721T) and risk of acute lymphoblastic leukemia

机译：XRCC7（G6721T）遗传多态性与急性淋巴细胞风险与急性淋巴细胞白血病的关系
- 作者：Farokhian Farnoush;Beyzaei Zahra;Ramzi Mani;Geramizadeh Bita
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- XRCC7PolymorphismAcute lymphoblastic leukemiaSusceptibilityParents smoking statues;
10.Hematological and demographic profile of Pakistani children with isolated ventricular septal defects (VSDs)

机译：Pakistani儿童患有孤立的心室间隔缺损（VSDS）的血液学和人口统计学概况
- 作者：Sarwar Sumbal;Shabana;Ehsan Farah;Tahir Amna;Jamil Mahrukh;Shahid Saleem Ullah;Hasnain Shahida;Khan Asim;Hyder Syed Najam
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Ventricular septal defects (VSDs)Blood group distributionRed blood cell countWhite blood cell countPlatelet countLiver functionsChemical pathological tests;
11.Spinal muscular atrophy in Venezuela: quantitative analysis of SMN1 and SMN2 genes

机译：委内瑞拉脊柱肌萎缩：SMN1和SMN2基因的定量分析
- 作者：Yépez Yuri;Paradisi Irene;Arias Sergio
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Spinal muscular atrophySMN1SMN2Copy number variationsGenetic epidemiology;
12.Phenotypic and genetic evaluation of human monocyte-derived dendritic cells generated from whole blood for immunotherapy

机译：从全血中产生的人单核细胞衍生的树枝状细胞进行免疫疗法的表型和遗传评价
- 作者：Hussein Yousri M.;Hendawy Doaa M.;Alghamdy Abdalrahman N.;Raafat Nermin
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- AdherenceMonocyte-derivedCell separationDendritic cellPhenotype;
13.TNF-α -308 G>A and IL10 -1082A>G polymorphisms as potential risk factors for lymphoproliferative disorders in autoimmune rheumatic diseases

机译：TNF-α-308g> A和IL10 -1082A> G多态性作为自身免疫性风湿病淋巴抑制性疾病的潜在危险因素
- 作者：Tayel Manal Y.;Nazir Aida;Abdelhamid Ibtessam M.;Helmy Myriam A. S.;Zaki Nadia E.;Elsharkawy Nehad S.;Fayad Amira I.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Autoimmune rheumatic disease (ARD)CytokinesLymphoproliferative diseases (LPD)Single nucleotide polymorphisms (SNPs)PCR-sequence-specific primer (PCR-SSP);
14.Association of genetic variants with prostate cancer in Africa: a concise review

机译：非洲前列腺癌的遗传变异协会：简明审查
- 作者：Acheampong Emmanuel;Adu Evans Asamoah;Obirikorang Christian;Amoah George;Afriyie Osei Owusu;Yorke Joseph;Anto Enoch Odame;Gyamfi Michael Adu;Acheampong Emmanuella Nsenbah;Gyasi-Sarpong Christian Kofi;Yeboah Francis Agyemang
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Genetic variantsRisk allelesProstate cancer;
15.Combined markers for predicting cognitive deficit in patients with Alzheimer's disease

机译：用于预测阿尔茨海默病患者认知缺陷的组合标志物
- 作者：Hussen Dalia Farouk;Hussein Ayat Allah Farouk;Monzer Mahmoud Abdel Moety;Hammad Saida Ali
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Alzheimer’s disease (AD)Mild cognitive declineMini-Mental State Examination (MMSE)Cytokinesis-block micronucleus assay (CBMN)Micronuclei (MNi)Electroencephalogram (EEG)Neurophysiological markerCell cycle;
16.Mutational analysis of p53 gene in cervical cancer and useful polymorphic variants in exons 3 and 4

机译：宫颈癌P53基因的突变分析及外显子3和4中有用的多态性变体
- 作者：Gbadegesin Michael A.;Omotoso Olabode E.;Oluwasola Timothy A. O.;Okolo Clement A.;Soremekun Opeyemi;Ogun Gabriel O.;Oluwasola Abideen O.;Odunola Oyeronke A.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Genomic DNACervical carcinomaGene mutationPolymorphic variation;
17.Analysis of the androgen receptor (AR) gene in a cohort of Indonesian undermasculinized 46, XY DSD patients

机译：XY DSD患者群体下印度尼西亚队列雄激素受体（AR）基因的分析
- 作者：Listyasari Nurin Aisyiyah;Juniarto Achmad Zulfa;Robevska Gorjana;Ayers Katie L.;Sinclair Andrew H.;Faradz Sultana M. H.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Androgen receptorAndrogen insensitivity syndromeDisorders of sex development (DSD)Molecular geneticsSanger sequencingUndermasculinization;
18.Undescribed GJB2 c.35dupG homozygous prelingual distinguished from c.35delG homozygous/compound heterozygous deafs, dwelling a German ancestry Venezuelan isolate

机译：未描述的GJB2 C.35Dupg纯合子纯合并与C.35Delg纯合/化合物的杂合耳聋，居住德国血统委内瑞拉孤立
- 作者：Arias Sergio;Paradisi Irene;Hernández Alba;Kanzler Daniela
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Nonsyndromic deafnessGJB2 haplotypesConnexin 26DFNB1Diagnostic audiograms;
19.Development of a simple method for the analysis of phenylalanine in dried blood spot using tandem mass spectrometry

机译：利用串联质谱法促进干血斑苯丙氨酸分析的简单方法
- 作者：Gouda Amr S.;Nazim Walaa S.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- PhenylalanineMass spectrometryDried blood spotExternal standards;
20.Expression of miR-146a and miR-155 in Egyptian patients with Behet's disease: clinical significance and relationship with disease activity

机译：MIR-146A和MIR-155在埃及患者塞（Beget）疾病患者的表达：临床意义与疾病活动关系
- 作者：El Khateeb Engy;Nassef Ayatallah;Gheith Rasha;Erfan Aya;Abdelfattah Walaa
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Beh?et’s diseaseBeh?et’s Disease Current Activity FormMicroRNA-146aMicroRNA-155Quantitative reverse transcription real-time polymerase chain reaction;
21.Dysregulation of CCAAT/enhancer binding protein-alpha (CEBPA) expression in the bone marrow of acute myeloid leukemia patients

机译：CCAAT /增强剂结合蛋白-α（CEBPA）表达的骨髓骨髓骨髓表达的缺点
- 作者：Hassan Naglaa M.;Said Fadwa;Shafik Roxan E.;Abdellateif Mona S.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- AMLCEBPAFLT3Survival;
22.HOTAIR expression and prognostic impact in acute myeloid leukemia patients

机译：急性髓性白血病患者的热门表达和预后影响
- 作者：Eldin Rawda Ahmed Alaa;Osman Amany Ahmed;Hassan Mona Fathey Abdel Fattah;Ibrahim Shereen Abdel Monem;El-Sakhawy Yasmin Nabil
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- AMLEpigeneticslncRNAHOTAIR;
23.Lack of association between three common genetic variations of XPC and susceptibility to age-related macular degeneration, a preliminary study

机译：XPC的三种常见遗传变异与年龄相关性黄斑变性的易感性之间缺乏关联，初步研究
- 作者：Kalteh Sharareh;Saadat Mostafa
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- DNA repairLinkage disequilibriumMacular degenerationPolymorphismXPCRisk;
24.Effect of folic acid on animal models, cell cultures, and human oral clefts: a literature review

机译：叶酸对动物模型，细胞培养和人口口谱的影响：文献综述
- 作者：Bendahan Zita C.;Escobar Lina M.;Castellanos Jaime E.;González-Carrera Mara C.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Folic acidVitamin B complexCleft palateCleft lipCraniofacial abnormalitiesCell proliferation;
25.Evaluating of the association between ABO blood groups and coronavirus disease 2019 (COVID-19) in Iraqi patients

机译：评估伊拉克患者2019（Covid-19）的Abo血基和冠状病毒疾病之间的关联
- 作者：Adhiah Ali H.;Allami Risala H.;Mohsin Raghdan H.;Abdullah Maha H.;AL-Saady Ali J. R.;Alsudani Mustafa Y.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- COVID-19ABO blood groupAgeGender;
26.Case report: Pitt-Hopkins like syndrome with CNTNAP2 mutation

机译：病例报告：Pitt-Hopkins与CNTNAP2突变一样综合征
- 作者：AlBaazi Sawsan;Shareef Hula
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Pitt-Hopkins syndromePHSPitt-Hopkins-like syndrome intellectual deficitEpilepsyFacial dysmorphismCupid bowEsotropiaCNTNAP2TCF4NRXN1CASPR2Angelman syndromeRett’s syndromeJoubert syndrome1q43q44 microdeletion syndromeGene microarray studyWESCase report;
27.Recent advances in pharmacological diversification of Src family kinase inhibitors

机译：SRC系列激酶抑制剂的药理多样化的最新进展
- 作者：Negi Preeya;Cheke Rameshwar S.;Patil Vaishali M.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Src family kinaseSrc kinase inhibitorsAnticancer agentsAntidiabetic agentsAntituberculosis agents;
28.Association between genetic polymorphism of XRCC6 T-991C and risk of varicocele

机译：XRCC6 T-991C遗传多态性与毒素风险的关系
- 作者：Namvaran Mohammad Reza;Beyzaei Zahra;Mokhtari Mohammad Javad;Geramizadeh Bita
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- X-ray repair cross-complementing group 6 gene (XRCC6)VaricocelePolymorphismDNA repairNon-homologous end-joiningGenotype;
29.The association of manganese superoxide dismutase gene polymorphism (Rs4880) with diabetic macular edema in a cohort of type 2 diabetic Egyptian patients

机译：锰超氧化物歧化酶基因多态性（RS4880）与2型糖尿病埃及患者队列糖尿病黄斑水肿
- 作者：Abdou Doaa M.;Mohammed Nesrine S.;El Fouli Marwa;Medaney Hanan A.;El Kateb Sarah M.;El-Gabrty Safaa A.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Diabetic retinopathyMitochondrial targeting sequenceDiabetic macular edemaMn-SOD geneAla16Val (rs 4880);
30.Impact of Cytochromes P450 3A4 and 2B6 gene polymorphisms on predisposition and prognosis of acute myeloid leukemia: an Egyptian case-control study

机译：细胞色素P450 3A4和2B6基因多态性对急性髓性白血病易感性和预后的影响：埃及案例对照研究
- 作者：Botros Shahira Kamal Anis;El Gharbawi Nesrine;Shahin Gehan;Al Lithy Hend;El Sherbiny Mahmoud
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- AMLCYPGene polymorphism;
31.Role of swimming on muscle PGC-1α, FNDC5 mRNA, and assessment of serum omentin, adropin, and irisin in high carbohydrate high fat (HCHF) diet induced obesity in rats

机译：游泳在肌肉PGC-1α，FNDC5 mRNA和血清概念，Adropin和Irisin的评估高碳水化合物高脂肪（HCHF）饮食诱导大鼠肥胖症的作用
- 作者：Badawy Ehsan;El-laithy Nabila A.;Morsy Safaa M.;Ashour Magdi N.;Elias Tahany R.;Masoud Mahmoud M.;Aly Omnia
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- HCHF-dietIrisinAdropinOmentinPGC-1αFNDC5;
32.Structure-based design of some quinazoline derivatives as epidermal growth factor receptor inhibitors

机译：基于结构的一些喹唑啉衍生物作为表皮生长因子受体抑制剂的设计
- 作者：Ibrahim Muhammad Tukur;Uzairu Adamu;Shallangwa Gideon Adamu;Uba Sani
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Structure-basedDesignEGFRInhibitorsPharmacokineticPrediction;
33.Tumor necrosis factor induced protein 3 gene polymorphism and the susceptibility to chronic primary immune thrombocytopenia in Egyptian children: a case-control study

机译：肿瘤坏死因子诱导蛋白质3基因多态性及对埃及儿童慢性原发性免疫血小板减少症的敏感性：案例对照研究
- 作者：El-hady Marwa Abd;Mosallam Dalia S.;Anis Shahira K.;Mansour Basma S.;Yassa Marianne E.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Primary immune thrombocytopenia (PIT)Tumor necrosis factor associated induced protein 3 (TNFAIP3)(rs5029939 C G)PolymorphismPCR-RFLP and Egyptian children;
34.Novel mutation in perforin gene causing familial hemophagocytic lymphohistiocytosis type 2 in an Egyptian infant: case report

机译：穿孔基因的新突变，导致埃及婴儿的家族血糖淋巴管肾小球菌症2型2型：案例报告
- 作者：Almalky Mohamed;Saleh Safaa H. A.;Baz Eman Gamal;Fakhr Ahmed Elsadek
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Perforin (PRF1)Familial hemophagocytic lymphohistiocytosis 2 (FHL 2)Case reportNovel mutation;
35.Integrative analysis of mRNA and miRNA sequencing data for gliomas of various grades

机译：各种等级胶质瘤mRNA和miRNA测序数据的整合分析
- 作者：Gvaldin Dmitry Y.;Pushkin Anton A.;Timoshkina Nataliya N.;Rostorguev Eduard E.;Nalgiev Arbi M.;Kit Oleg I.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Gliomasthe Cancer Genome AtlasExpression patternsmRNA-miRNA interactionsSurvival prognosis;
36.A case of spastic paraplegia type 11 with a variation in the SPG11 gene

机译：一种痉挛性截瘫型11型具有SPG11基因变异的案例
- 作者：Elmas Muhsin;Gogus Basak;De?irmenci Banu;Solak Mustafa;Gleeson J. G.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Spastic ParaplegiaHereditaryCorpus callosum dysgenesisIntellectual disability;
37.Late-onset multiple acyl-CoA dehydrogenase deficiency with breast cancer

机译：晚期发病多种酰基 - CoA脱氢酶缺乏乳腺癌
- 作者：Pavithran Keechilat;Pachat Divya;Vijaykumar Dehannathparambil Kottarathil
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Multiple acyl-CoA dehydrogenase deficiencyMADDGlutaric aciduria type IIFatty acid metabolism;
38.Telomeric repeat-containing ribonucleic acid (TERRA) expression in patients with idiopathic pulmonary fibrosis

机译：特发性肺纤维化患者含有端粒重复的核糖核酸（Terra）表达
- 作者：El-Desoky Manal M.;Hewidy Asem A.;Fouda Ahmed M.;Hisham Fatma Azzahraa
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Gene expressionIdiopathic pulmonary fibrosisLong noncoding ribonucleic acidTelomeric repeat-containing ribonucleic acidUnusual interstitial pattern;
39.Identification of the most potent acetylcholinesterase inhibitors from plants for possible treatment of Alzheimer's disease: a computational approach

机译：鉴定来自植物的最有效的乙酰胆碱酯酶抑制剂，以治疗阿尔茨海默病：计算方法
- 作者：Sarkar Bishajit;Alam Sayka;Rajib Tiluttoma Khan;Islam Syed Sajidul;Araf Yusha;Ullah Md. Asad
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Alzheimer’s diseaseAcetylcholinesteraseMolecular dockingPhytochemicalsDruglikeness propertiesADMETPASS predictionNaringenin;
40.Prediction and in silico validation of MYH7 gene missense variants in the Iranian population: a bioinformatics analysis based on Iranome database

机译：伊朗人群中MyH7基因畸形变种的预测和硅验证：基于Iranome数据库的生物信息学分析
- 作者：Shahbazi Shirin
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- MYH7Iranian populationBioinformaticsInherited cardiomyopathy;
41.Understanding the genetic determinant of severity in viral diseases: a case of SARS-Cov-2 infection

机译：了解病毒疾病严重程度的遗传决定因素：SARS-COV-2感染的情况
- 作者：Oladejo Babayemi Olawale;Adeboboye Covenant Femi;Adebolu Tinuola Tokunbo
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- CoronavirusCOVID-19SARS-CoV-2Human leucocyte antigen (HLA) alleleToll-like receptor (TLR)Angiotensin-converting enzyme 2 (ACE2) gene;
42.Classic Cornelia de Lange syndrome with variant of unknown significance detected in NIPBL gene mutation: a case report

机译：尼皮布基因突变中检测到未知意义的变体的经典玉米塞曲综合征：案例报告
- 作者：Desai Jay J.;Nair Sreelata B.;Pappachan S.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Cornelia de Lange syndromeDevelopmental delayDysmorphismNIPBLMissense mutation;
43.Identification of primary copy number variations reveal enrichment of Calcium, and MAPK pathways sensitizing secondary sites for autism

机译：鉴定初级拷贝数变异揭示钙的富集，以及映射致敏次要地点的自闭症
- 作者：Agarwala Swati;Veerappa Avinash M.;Ramachandra Nallur B.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Autism subgenomeCNVsAutism-IPAAutism pathway analysisPrimary-hit;
44.Dysregulation in growth arrest-specific 5 and metastasis-associated lung adenocarcinoma transcript 1 gene expression predicts diagnosis and renal fibrosis in systemic lupus erythematosus patients

机译：生长逮捕特异性5和转移相关的肺腺癌转录物1基因表达中的失调预测系统性红斑狼疮患者的诊断和肾纤维化
- 作者：El-Desoky Manal M.;Shemies Rasha S.;El-Bahnasawy Amany S.;Mostafa Nora;Elhelaly Mona
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Growth arrest-specific 5Long non-coding RNAMetastasis-associated lung adenocarcinoma transcript 1Systemic lupus erythematosus;
45.Lysinuric protein intolerance: an overlooked diagnosis

机译：溶尿素蛋白质不耐受：忽略的诊断
- 作者：Olgac Asburce;Yenicesu Idil;Ozgul R?za K?ksal;Bibero?lu Gürsel;Tümer Leyla
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Lysinuric protein intoleranceShort statureHemophagocytic lymphohistiocytosis;
46.In silico prediction of HBD gene variants in the Iranian population

机译：在伊朗人群中HBD基因变异的硅预测中
- 作者：Moradi Keivan;Mohammadi Aboozar;Kazeminia Mohsen
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Hemoglobin Asub2/subδ-globin geneVariantThalassemiaIran;
47.Update on the genetic and epigenetic etiology of gestational diabetes mellitus: a review

机译：妊娠期糖尿病遗传和表观遗传病因的更新：综述
- 作者：Yahaya Tajudeen O.;Salisu Titilola;Abdulrahman Yusuf B.;Umar Abdulrazak K.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- AdiposityBeta-cell dysfunctionEpigeneticsInsulin resistanceObesity;
48.An in silico epitope-based peptide vaccine design against the 2019-nCoV

机译：在二氧化硅基肽疫苗设计中对2019年 - NCOV的疫苗设计
- 作者：Durojaye Olanrewaju Ayodeji;Mushiana Talifhani;Cosmas Samuel;Ibiang Glory Omini;Ibiang Mercy Omini
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
49.Protein secondary structure prediction (PSSP) using different machine algorithms

机译：使用不同机器算法的蛋白二级结构预测（PSSP）
- 作者：Afify Heba M.;Abdelhalim Mohamed B.;Mabrouk Mai S.;Sayed Ahmed Y.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Support vector machineProtein structure predictionDecision tree;
50.Assessment of vitamin D-binding protein (DBP) gene polymorphisms and their correlation with multiple sclerosis: a case-control study in a sample of the Syrian population

机译：维生素D型蛋白（DBP）基因多态性评估及其与多发性硬化的相关性：叙利亚人群样本中的病例对照研究
- 作者：Alhomsi Bushra;Aboualchamat Ghalia;Alkadi Imad
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Multiple sclerosisVitamin D deficiencyPolymorphismVitamin D-binding protein gene DBP;
51.Evaluation of glutathione S-transferase polymorphism in Iranian patients with type 2 diabetic microangiopathy

机译：伊朗患者患者谷胱甘肽S转移酶多态性评价2型糖尿病微肺病
- 作者：Hashemi-Soteh Mohammad Bagher;Ahmadzadeh Amiri Amir;Sheikh Rezaee Majid Reza;Ahmadzadeh Amiri Ali;Ahrari Rohodin;Ahmadzadeh Amiri Ahmad;Daneshvar Fatemeh
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Glutathione S-transferasesGene polymorphismsDiabetic retinopathyDiabetic nephropathyDiabetic neuropathy;
52.RUNX1 gene expression in Egyptian acute myeloid leukemia patients: may it have therapeutic implications?

机译：埃及急性髓性白血病患者的Runx1基因表达：愿它有治疗意义吗？
- 作者：Said Fadwa;Shafik Roxan E.;Hassan Naglaa M.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Acute myeloid leukemiaRUNX1Gene expressionEgypt;
53.Potential role of vitamin D receptor-related polymorphisms in bronchopulmonary dysplasia

机译：维生素D受体相关多态性在支气管扩张中的潜在作用
- 作者：Abuelhamd Walaa Alsharany;Gomaa Nancy Abdel Salam;Gad Alaa;El-Wakeel Rehab
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Bronchopulmonary dysplasiaPolymorphismPremature neonatesVitamin D receptor;
54.Inherited thrombophilia and recurrent pregnancy loss: a single-center case-control study in North-Western Algeria

机译：遗传性血栓性妊娠损失：阿尔及利亚西北部的单中心案例对照研究
- 作者：Nassour-Mokhtari Ilhem;Loukidi Bouchra;Moussouni Abdellatif;Bettioui Reda;Benhabib Riad;Merzouk Hafida;Aouar Amaria;Allal-Taouli Katia
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Recurrent pregnancy lossThrombophiliaFVLAPCR;
55.Role of engulfment and cell motility 1 (ELMO1) gene polymorphism in development of diabetic kidney disease

机译：吞噬和细胞运动1（ELMO1）基因多态性在糖尿病肾病发育中的作用
- 作者：Omar Thoria A.;Zewain Shimaa K.;Ghonaim Mohamed M.;Refaat Khadija A.;Abou-Elela Dalia H.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Type 2 diabetes mellitusDiabetic kidney diseaseSingle-nucleotide polymorphismELMO1Real-time PCR;
56.Association study between asthma and single nucleotide polymorphisms of ORMDL3, GSDMB, and IL1RL1 genes in an Algerian population

机译：阿尔及利亚人群中哮喘和单核苷酸多态性的哮喘和单核苷酸多态性研究
- 作者：Ziani Mouna;Henry Amanda P.;Hall Ian P.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Algerian populationAsthmaGSDMBIL1RL1ORMDL3Polymorphism;
57.Genetic polymorphism of HLA-G gene (G*01:03, G*01:04, and G*01:05N) in Iraqi patients with inflammatory bowel disease (ulcerative colitis and Crohn's disease)

机译：HLA-G基因的遗传多态性（G * 01：03，G * 01：04，和G * 01：05N）炎症性肠病（溃疡性结肠炎和克罗恩病）
- 作者：Abdul-Hussein Sarah S.;Ali Ekhlass N.;Zaki Neihaya H.;Adhiah Ali H.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Inflammatory bowel diseaseUlcerative colitisCrohn’s diseaseHLA-GNull allele;
58.Effect of Ag nanoparticles on viability of MCF-7 and Vero cell lines and gene expression of apoptotic genes

机译：Ag纳米粒子对MCF-7和VERO细胞系和凋亡基因基因表达的效果
- 作者：Sangour Maryam Hassan;Ali Iftikhar M.;Atwan Zeenah Weheed;Al Ali Ali Abd Al Lateef A.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- AgNPsZnS-Ag NPsApoptosisP53 PTEN;
59.Purinergic signalling pathway: therapeutic target in ovarian cancer

机译：嘌呤能信号通路：卵巢癌中的治疗靶标
- 作者：Chandran Nisha;Iyer Mahalaxmi;Siama Zothan;Vellingiri Balachandar;Narayanasamy Arul
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- AdenosineEctonucleotidasesChemoresistancePlateletsPurinergic signallingOvarian cancer (OC);
60.Angiotensin-converting enzyme insertion/deletion (I/D) gene polymorphism in Iraqi type 2 diabetic patients: association with the risk of cardiac autonomic neuropathy

机译：血管紧张素转换酶插入/缺失（I / D）伊拉克2型糖尿病患者的基因多态性：与心脏自主神经病变的风险联系
- 作者：Dhumad Muhanad M.;Hamdan Farqad B.;Al-Mayah Qasim S.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- DMCardiac autonomic neuropathyACE gene polymorphism;
61.Genotype association of IP6K3 gene with Hashimoto's thyroiditis in Algerian population (Aures region)

机译：IP6K3基因与阿尔及利亚人群甲状腺炎的基因型协会（AURE区域）
- 作者：Kherrour Warda;Kalicanin Dean;Bri Luka;Hambaba Leila;Yahia Mouloud;Benbia Souheyla;Perica Vesna Boraska
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Hashimoto’s thyroiditisIP6K3 geners791903 variantReal-time PCRGenetic association studyAlgerian population;
62.Insulin-like growth factor binding protein 1 DNA methylation in type 2 diabetes

机译：胰岛素样生长因子结合蛋白1 2型糖尿病中的DNA甲基化
- 作者：Hafez Sally M.;Abou-youssef Hazem. El-Sayed;Awad Mona Abdel-Kader;Kamel Solaf Ahmed;Youssef Rasha N.;Elshiekh Suzan Mahrous;Raslan Hala;Salah Nehal
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- EpigeneticsIGFBP1DNA methylationType 2 diabetes mellitus;
63.An in silico LLPS perturbation approach in the design of a novel SARS-CoV-2 spike receptor-binding domain inhibitor

机译：在硅LLPS扰动方法中的设计中的一种新型SARS-COV-2穗受体结合结构域抑制剂
- 作者：Durojaye Olanrewaju Ayodeji;Sedzro Divine Mensah;Mushiana Talifhani;Uzoeto Henrietta Onyinye;Cosmas Samuel;Ajima Judith Nnedimkpa;Ibiang Glory Omini
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
64.Characterization of the major human STAG3 variants using some proteomics and bioinformatics assays

机译：使用一些蛋白质组学和生物信息学测定的主要人体静脉3变体的表征
- 作者：Lafta Inam J.;Kudhair Bassam K.;Alabid Noralhuda N.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- STAG3 geneVariantsImmunoblottingImmunoprecipitationBioinformatics;
65.Contributory role of SARS-CoV-2 genomic variations and life expectancy in COVID-19 transmission and low fatality rate in Africa

机译：SARS-COV-2基因组变异和预期寿命在Covid-19传播中的贡献作用和非洲低死亡率
- 作者：Omotoso Olabode E.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- CoronavirusMutationsLow fatalityAgeSARS-CoV-2Africa;
66.Evaluation of the impact of adaptation of Klebsiella pneumoniae clinical isolates to benzalkonium chloride on biofilm formation

机译：基于苯并氯化物对生物膜形成对苯并氯化物的影响评价
- 作者：Elekhnawy Engy A.;Sonbol Fatma I.;Elbanna Tarek E.;Abdelaziz Ahmed A.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- AdaptationBenzalkonium chlorideBiofilmCell surface hydrophobicityKlebsiella pneumoniae;
67.Vitamin D receptor (VDR) gene FokI, BsmI, ApaI, and TaqI polymorphisms and osteoporosis risk: a meta-analysis

机译：维生素D受体（VDR）基因Foki，BSMI，Apai和Taqi多态性和骨质疏松症风险：Meta分析
- 作者：Yadav Upendra;Kumar Pradeep;Rai Vandana
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- OsteoporosisVitamin D receptorBsmIApaIFokITaqI;
68.In silico investigations on curcuminoids from Curcuma longa as positive regulators of the Wnt/β-catenin signaling pathway in wound healing

机译：在姜黄对姜黄素的研究中的姜黄素调查，作为Wnt /β-catenin信号传导途径的阳性调节剂在伤口愈合中
- 作者：Reshad Riyan Al Islam;Alam Sayka;Raihan Humaira Binte;Meem Kamrun Nahar;Rahman Fatima;Zahid Fardin;Rafid Md. Ikram;Rahman S. M. Obaydur;Omit Sadman;Ali Md. Hazrat
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Curcuminoids (curcumin Icurcumin II and curcumin III)Curcuma longaCasein kinase-1 (CK1)Glycogen synthase kinase-3β (GSK3B)Wnt/β-catenin;
69.The associations among RARRES2 rs17173608 gene polymorphism, serum chemerin, and non-traditional lipid profile in patients with metabolic syndrome

机译：RARRES2 RS17173608基因多态性，血清校长和代谢综合征患者的非传统脂质谱之间的关联
- 作者：Dahpy Marwa A.;Khairallah Marwa K.;Azoz Nashwa Mostafa A.;Ezzat Ghada M.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- ChemerinRARRES2 rs17173608Metabolic syndromeT-ARMS-PCRDiabetes mellitusObesity;
70.In vitro characterization of human bone marrow mesenchymal stem cell-derived motor neurons induced by epigenetic modifiers

机译：人骨髓间充质干细胞衍生的运动神经元的体外表征，由表观遗传改性剂诱导
- 作者：Sanooghi Davood;Vahdani Parham;Bagher Zohreh;Faghihi Faezeh;Lotfi Abolfazl
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Motor neuronBone marrowMesenchymal stem cellEpigeneticP300EZH-2;
71.Analysis of human aldehyde dehydrogenases (ALDH) gene expression pattern in breast cancer tissue samples: rutin-copper complex inhibit the breast cancer cell proliferation

机译：乳腺癌组织样品中的人醛脱氢酶（ALDH）基因表达模式分析：芦丁 - 铜复合物抑制乳腺癌细胞增殖
- 作者：Pattar Shridhar V.;Mirjankar Manisha R.;Kulkarni Suyamindra;Gai Pramod B.;Pujar Namadev K.;Premakshi H. G.;Mulla Sikandar I.;Babu R. L.;Kamanavalli Chandrappa M.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Aldehyde dehydrogenasesBreast cancerMolecular dockingRutin;
72.Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways

机译：先天性心脏病：遗传学，非遗传危险因素和信号通路
- 作者：Suluba Emmanuel;Shuwei Liu;Xia Qing;Mwanga Ally
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Congenital heart diseasesLong non-coding RNAsMicroRNAsCardiac transcription factor genesCopy number variantsSignaling pathways;
73.COVID-19 susceptibility: potential of ACE2 polymorphisms

机译：Covid-19易感性：ACE2多态性的潜力
- 作者：Chaudhary Mayank
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Single-nucleotide polymorphism (SNP)ACE2Severe acute respiratory syndrome (SARS)COVID-19SARS-CoV-2Coronavirus;
74.Potential treatment for chronic myeloid leukemia using microRNA: in silico comparison between plants and human microRNAs in targeting BCR-ABL1 gene

机译：使用Microrna的慢性髓性白血病的潜在治疗：在靶向BCR-ABL1基因植物和人微小植物中的硅比较中
- 作者：Mohamad Syarifah Faezah Syed;Elias Marjanu Hikmah
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- BCR-ABL1Chronic myeloid leukemiaCross-kingdomIn silicoMicroRNA3′ untranslated region;
75.The expression profile of circANKRD36 and ANKRD36 as diagnostic biomarkers of chronic kidney disease in patients with type 2 diabetes mellitus

机译：CircAnkRD36和ANKRD36作为2型糖尿病患者慢性肾病诊断生物标志物的表达谱
- 作者：Rashad Nearmeen M.;Sherif Mohamed H.;El-Shal Amal S.;Abdelsamad Mona A. E.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- CKDUACRCircANKRD36Gene expressioneGFRRT-PCR;
76.Molecular and environmental characterization of Noonan syndrome in Morocco reveals a significant association with consanguinity and advanced parental age

机译：摩洛哥中非南综合征的分子和环境表征揭示了与血缘和高级父母年龄的重要关联
- 作者：El Bouchikhi Ihssane;Bouguenouch Laila;Moufid Fatima Zohra;Samri Imane;Abdouss Fatima;Melhouf Moulay Abdelilah;Iraqui Houssaini Mohammed;Belhassan Khadija;Atmani Samir;Ouldim Karim
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Noonan syndrome (NS)PTPN11 mutationsPathogenic effect predictionMutation rateConsanguinityPaternal ageMoroccan populationMaternal age;
77.Prenatal presentation of Walker-Warburg syndrome with a POMT2 mutation: an extended fetal phenotype

机译：POMT2突变的Walker-Warburg综合征的产前呈现：延长的胎儿表型
- 作者：El-Dessouky Sara H.;Hosny Heba;Elarab Ahmed Ezz;Issa Mahmoud Y.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Walker–Warburg syndromeOcular abnormalitiesClenched hands and talipesCystic kidneysPOMT2 gene;
78.In silico studies of bioactive compounds from selected African plants with inhibitory activity against nitric oxide synthase and arginase implicated in asthma

机译：在含有抑制活性的来自氧化氮合酶的抑制活性的生物活性化合物和患有哮喘的氨基酶的基石
- 作者：Umar Haruna Isiyaku;Saliu Tolulope Peter;Josiah Sunday Solomon;Ajayi Adeola;Danjuma Jamilu Bala
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- ADMETArginaseAsthmaAzadirachta indicaCrinum glaucumIn silicoMangifera indicaNitric oxide synthase;
79.A novel mutation in MTM1 gene in newborn, resulting in centronuclear myopathy phenotype: a case report

机译：新生儿MTM1基因的一种新型突变，导致Centronuleclecat病变表型：案例报告
- 作者：Dudzik Aleksandra;Nedza Weronika;Koska Katarzyna;Starzec Katarzyna;Tomasik Tomasz;Grudzie Andrzej;Jaga Mateusz;Durlak Wojciech;Kwinta Przemko
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- X-linked myotubular myopathyCentronuclear myopathyHypotoniaRespiratory failureFeeding disorder;
80.Further observation of Hemoglobin Fontainebleau (a21(B2) Ala-Pro) in a Turkish family

机译：在土耳其家族中进一步观察血红蛋白氟丹白露（A21（B2）ALA-PRO）
- 作者：Akar Nejat;Ceylaner Serdar;Akisin Yasemin Ardicoglu;Tastan Gokce Su
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
81.Potential therapeutic target identification in the novel 2019 coronavirus: insight from homology modeling and blind docking study

机译：新型2019年冠状病毒的潜在治疗目标鉴定：来自同源性建模和盲人对接研究的洞察力
- 作者：Durojaye Olanrewaju Ayodeji;Mushiana Talifhani;Uzoeto Henrietta Onyinye;Cosmas Samuel;Udowo Victor Malachy;Osotuyi Abayomi Gaius;Ibiang Glory Omini;Gonlepa Miapeh Kous
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- CoronavirusProteinaseReplicationLigandInhibitors;
82.Strategies to target long non-coding RNAs in cancer treatment: progress and challenges

机译：在癌症治疗中靶向长期非编码RNA的策略：进步与挑战
- 作者：Fathi Dizaji Behdokht
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Long non-coding RNATherapeutic targetSystematic deliveryCancer treatment;
83.Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

机译：全末端测序和纯合性测定鉴定Ncor1和与非综合征先天性心脏缺陷相关的MAP2K3中的变体
- 作者：Gholipoorfeshkecheh Rahim;Agarwala Swati;G Kavya;Krishnappa Santhosh;Savitha Mysore R.;Ramachandra Nallur B.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Homozygous regionsMitogen-Activated Protein Kinase 3Nuclear CorepressorVentricular septal defectWhole-exome sequencingIn silico validation;
84.SHOX2 gene methylation in Egyptians having lung cancer

机译：埃及人患有肺癌的Shox2基因甲基化
- 作者：Rizk Mohamed Mostafa Mohamed Ahmed;Helal Suzan Mohamed Farouk;Gad Ahmed Youssef Shaaban;Younan Doreen Nazeih Assaad
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- SHOX2Lung cancerEgyptiansMethylation;
85.Identification of satellited markers by microdissection and fluorescence in situ hybridization: a clinical case of isodicentric chromosome 22

机译：通过微小杂交和荧光鉴定卫星标志物的透明标记：异教染色体22的临床案例
- 作者：Lemskaya Natalya A.;Romanenko Svetlana A.;Maksimova Yulia V.;Shorina Asia R.;Yudkin Dmitry V.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Bisatellite isodicentricMicrodissectionTetrasomySupernumerary marker chromosomeCongenital atresiaCryptorchidismMosaicismAcrocentricChromosome 22Repeats;
86.The role of glutathione S-transferase omega gene polymorphisms in childhood acute lymphoblastic leukemia: a case-control study

机译：谷胱甘肽S转移酶Omega基因多态性在儿童急性淋巴细胞白血病中的作用：一种案例对照研究
- 作者：Yassa Marianne E.;Arnaout Hanaa H.;Botros Shahira K.;Obaid Emad N.;Mahmoud Wael M.;Morgan Dalia S.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Acute lymphoblastic leukemia (ALL)GSTO1*A140D (rs4925) polymorphismGSTO2*N142D (rs156697) polymorphismPCR-RFLPEgyptian children;
87.Evaluation of the clinical value of circulating miR-101, miR-187 and miR-21 in neonatal sepsis diagnosis and prognosis

机译：评价新生脓毒症诊断和预后循环miR-101，miR-187和miR-21临床价值
- 作者：Salim Rabab F.;Sobeih Ahmed A.;Abd El Kareem Heba M.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Neonatal sepsismicroRNABiomarkersDiagnosisPrognosis;
88.SCGB3A1 gene DNA methylation status is associated with breast cancer in Egyptian female patients

机译：SCGB3A1基因DNA甲基化状态与埃及女性患者的乳腺癌有关
- 作者：Nomair Azhar Mohamed;Ahmed Sanaa Shawky;Mohammed Ayman Farouk;El Mansy Hazem;Nomeir Hanan Mohamed
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Breast cancerDNA methylationPyrosequencingSCGB3A1ATM;
89.The morbidity and mortality of COVID-19 are correlated with the Ile105Val glutathione S-transferase P1 polymorphism

机译：Covid-19的发病率和死亡率与ILE105VAL谷胱甘肽S-转移酶P1多态性相关
- 作者：Saadat Mostafa
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Ecologic studyEpidemiologic measuresPandemic;
90.Prognostic value of CIP2A gene expression in adult Egyptian acute myeloid leukemia patients

机译：CIP2A基因表达在成人埃及急性髓性白血病患者中的预后价值
- 作者：Shafik Roxan E.;Ibrahim Azza M.;Said Fadwa;Hassan Naglaa M.;Shafik Hanan E.;Shokralla Hala A.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- AMLCIP2ART-qPCR;
91.Association between ABO blood groups and susceptibility to COVID-19: profile of age and gender in Iraqi patients

机译：ABO血液团体与Covid-19的易感性 - 19：伊拉克患者的年龄和性别概况
- 作者：Adhiah Ali H.;Abdullah Maha H.;Alsudani Mustafa Y.;Shnawa Rasool M. S.;Al-Saady Ali J. R.;Allami Risala H.;Mishaal Khawla I.;Jassim Iftikhar A.;Taqi Estabraq A.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- COVID-19ABO blood groupsAgeGenderLogistic regression analysis;
92.rs2253310 and rs4946936 common variants of FOXO3 gene in octogenarians and cancer: a pilot study in north India

机译：RS2253310和RS4946936八十型雌雄生物和癌症的常见变体：印度北方的试点研究
- 作者：Tia Neelam;Lal Moti;Gambhir I. S.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- FOXO3Human longevityOctogenariansGastrointestinal tract cancerSingle nucleotide variants;
93.Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature

机译：使用MLPA和MIRNA表达分析在一群埃及儿童中筛选抗SHOX / PAR1区，具有非综合征短地
- 作者：Eid Ola M.;Eid Maha M.;Abdelrahman Amany H.;Abdel kader Rania M. A.;Farid Marwa;Mahrous Rana;Mekkawy Mona K.;Kamel Alaa K.;Mazen Inas;El-Bassyouni Hala T.
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2020年第1期
- Short statureCopy number variations (CNVs)Multiplex ligation-dependent probe amplification (MLPA)SHOXASMTmiRNAmiR-140;
94.Computer-aided design of some quinazoline analogues as epidermal growth factor receptor inhibitors

机译：一些喹唑啉类似物作为表皮生长因子受体抑制剂的计算机辅助设计
- 作者：Ibrahim Muhammad Tukur;Uzairu Adamu;Shallangwa Gideon Adamu;Uba Sani
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Computer-aidedDesignQuinazolineEGFRNSCLC;
95.Susceptibility to the novel coronavirus disease (COVID-19) is associated with ABO and Rh blood groups: a case-control study from Afghanistan

机译：对新型冠状病毒病（Covid-19）的易感性与ABO和RH血液组有关：来自阿富汗的病例对照研究
- 作者：Saify Khyber;Alborz Mohammad Sarwar;Saadat Mostafa
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- COVID-19SusceptibilityABORhBlood groups;
96.A genetic variant of the NAMPT gene rs4730153 as a risk factor for the metabolic syndrome in younger age: a single-centre pilot study in Yogyakarta, Indonesia

机译：命名基因RS4730153的遗传变异作为较年轻的代谢综合征的危险因素：印度尼西亚日惹的单中心试验研究
- 作者：Puspasari Anggelia;Hastuti Pramudji;Sadewa Ahmad Hamim;Mus Rosdiana;Maharani Citra;Setyawati Ika
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Genetic variantMetabolic syndromers4730153NAMPT;
97.N- and O-glycan analysis for the detection of glycosylation disorders

机译：用于检测糖基化疾病的N-和O-聚糖分析
- 作者：Gouda Amr Sobhi;Elbaz Azza Fahmy;Dupré Thierry;Ali Ola Sayed Mohamed;Zaki Maha Saad;Fateen Ekram Maher
- 期刊名称：《Egyptian Journal of Medical Human Genetics》 | 2021年第1期
- Congenital disorders of glycosylationInborn errors of metabolismGlycansWestern blottingLiquid chromatography-tandem mass spectrometryT-antigen;

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