EXPANDING THE PHENOTYPE OF NEURAL CREST CELL dISORDERS: HIRSCHSPRUNG DISEASE IN BRANCHIO-OCULO-FACIAL SYNDROME

Haldeman-Englert Chad R.; Berry Margaret N.; Stamper Tara H.; Jewett Tamison; Argenta Louis C.; Milunsky Aubrey

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EXPANDING THE PHENOTYPE OF NEURAL CREST CELL dISORDERS: HIRSCHSPRUNG DISEASE IN BRANCHIO-OCULO-FACIAL SYNDROME

机译：扩大神经C细胞表型的表型：分支-眼-眼综合征的Hirschsprung疾病

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来源
《American journal of medical genetics, Part A》 |2015年第8期|共2页
作者
Haldeman-Englert Chad R.; Berry Margaret N.; Stamper Tara H.; Jewett Tamison; Argenta Louis C.; Milunsky Aubrey;
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正文语种 eng
中图分类医学遗传学;
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1. EXPANDING THE PHENOTYPE OF NEURAL CREST CELL dISORDERS: HIRSCHSPRUNG DISEASE IN BRANCHIO-OCULO-FACIAL SYNDROME [J] . Haldeman-Englert Chad R., Berry Margaret N., Stamper Tara H., American journal of medical genetics, Part A . 2015,第8期

机译：扩大神经C细胞表型的表型：分支-眼-眼综合征的Hirschsprung疾病
2. Lack of beta1 integrins in enteric neural crest cells leads to a Hirschsprung-like phenotype. [J] . Breau MA, Pietri T, Eder O, Development . 2006,第9期

机译：肠神经c细胞中缺乏beta1整合素会导致Hirschsprung样表型。
3. MRI detection and histological localization of transplanted neural crest derived stem cells (NCSCs) labelled with superparamagnetic nanoparticles in future perspectives for cell therapy of Hirschsprung's disease [J] . Clasohm J., Merscher C., Mueller A., Neurogastroenterology and motility . 2017,第Suppla2期

机译：移植的神经嵴衍生干细胞（NCSCs）的MRI检测和组织学定位，用超顺磁性纳米粒子标记为Hirschsprung病的细胞疗法的视角下
4. Exploring the Myelinogenic Potential of Human Keratinocytes Derived Neural Crest Cells: Implications for Demyelinating Diseases [C] . Vivek K. Bajpai, Xiaoyan Wang, Ryan Zeiger AIChE Annual Meeting . 2015

机译：探索人角蛋白细胞衍生神经嵴细胞的近脉苷潜力：对脱髓鞘疾病的影响
5. A Characterization of Orofacial Phenotypes Resulting from the Tissue Specific Deletion of Pbx Genes within the Cranial Neural Crest Cell Population or the Cephalic Epithelium of the Developing Murine Embryo [D] . Hart, James C. 2018

机译：颅面神经rest细胞群或发育中的鼠胚胎的头皮上皮细胞组织特异性缺失导致的口面表型表征。
6. Mice Lacking Zfhx1b the Gene That Codes for Smad-Interacting Protein-1 Reveal a Role for Multiple Neural Crest Cell Defects in the Etiology of Hirschsprung Disease–Mental Retardation Syndrome [O] . Tom Van de Putte, Mitsuji Maruhashi, Annick Francis, 2003

机译：缺少Zfhx1b（编码Smad相互作用蛋白1的基因）的小鼠揭示了多发性神经C细胞缺损在Hirschsprung病-精神发育迟缓综合征的病因中的作用
7. Mice Lacking Zfhx1b, the Gene That Codes for Smad-Interacting Protein-1, Reveal a Role for Multiple Neural Crest Cell Defects in the Etiology of Hirschsprung Disease–Mental Retardation Syndrome [O] . Van de Putte Tom, Maruhashi Mitsuji, Francis Annick, 2003

机译：缺少Zfhx1b（编码Smad相互作用蛋白1的基因）的小鼠揭示了多发性神经rest细胞缺陷在Hirschsprung疾病-精神发育迟缓综合征的病因中的作用

EXPANDING THE PHENOTYPE OF NEURAL CREST CELL dISORDERS: HIRSCHSPRUNG DISEASE IN BRANCHIO-OCULO-FACIAL SYNDROME

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