机译:LRRC56中的双晶均突变,编码与肠有交通的蛋白质,引起粘液间隙和横向缺陷
Trypanosome Cell Biology Unit &
INSERM U1201 Institut Pasteur;
Yorkshire Regional Genetics Service St. James’s University Hospital;
Children’s Hospital of Eastern Ontario Research Institute University of Ottawa;
Trypanosome Cell Biology Unit &
INSERM U1201 Institut Pasteur;
Trypanosome Cell Biology Unit &
INSERM U1201 Institut Pasteur;
School of Medicine University of Leeds St. James’s University Hospital;
Yorkshire Regional Genetics Service St. James’s University Hospital;
Yorkshire Regional Genetics Service St. James’s University Hospital;
Yorkshire Regional Genetics Service St. James’s University Hospital;
Centre for PCD Diagnosis and Research Department of Infection Immunity and Inflammation RKCSB;
Centre for PCD Diagnosis and Research Department of Infection Immunity and Inflammation RKCSB;
Centre for PCD Diagnosis and Research Department of Infection Immunity and Inflammation RKCSB;
Centre for PCD Diagnosis and Research Department of Infection Immunity and Inflammation RKCSB;
Children’s Hospital of Eastern Ontario Research Institute University of Ottawa;
Children’s Hospital of Eastern Ontario Research Institute University of Ottawa;
Department of Pathology Children’s Hospital of Eastern Ontario;
Bradford Royal Infirmary;
Department of Molecular Biology and Biochemistry and Centre for Cell Biology Development and;
School of Medicine University of Leeds St. James’s University Hospital;
Yorkshire Regional Genetics Service St. James’s University Hospital;
Department of Molecular Biology and Biochemistry and Centre for Cell Biology Development and;
Children’s Hospital of Eastern Ontario Research Institute University of Ottawa;
Trypanosome Cell Biology Unit &
INSERM U1201 Institut Pasteur;
Yorkshire Regional Genetics Service St. James’s University Hospital;
ciliopathies; left-right asymmetry; cilia; flagella; dynein arms; trypanosome; intraflagellar transport; leucine-rich repeat protein;
机译:LRRC56中的双晶均突变,编码与肠有交通的蛋白质,引起粘液间隙和横向缺陷
机译:编码鞭毛内转运成分IFT144的WDR19中的突变引起广泛的纤毛病
机译:YRB1基因编码酵母Ran结合蛋白1的突变,损害核细胞质运输并抑制酵母交配缺陷。
机译:鉴定Cu,Zn-超氧化物歧化酶(Cu,Zn-SOD)基因的三种突变与家族性肌肌疏远硬化剂:HIV-1 TAT蛋白碱性结构域的转导,Zn-SOD进入PC12细胞
机译:pBR322编码的四环素抗性蛋白跨膜片段中随机突变的膜插入和蛋白活性影响
机译:LRRC56中的双等位基因突变编码与鞭毛内运输相关的蛋白质导致粘膜纤毛间隙和侧向缺陷。
机译:LRRC56中的双胞胎突变编码与肠有交通尿道转运相关的蛋白质,导致粘液间隙和横向缺陷