机译:Nesp55 DMR的靶向缺失定义了另一个Gnas印迹控制区域,并提供了常染色体显性PHP-lb的小鼠模型
Endocrine Unit, Department of Medicine,Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114 Institute of Pathophysiology,University of Veterinary Medicine, 1210 Vienna, Austria Institute of Pathology, Medical University of Graz, 8036 Graz, Austria;
rnInstitute of Pathophysiology,University of Veterinary Medicine, 1210 Vienna, Austria;
rnVetOMICS Center, University of Veterinary Medicine, 1210 Vienna, Austria;
rnEndocrine Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114 Department of Bioengineering, University of Tokyo Graduate Schools of Engineering and Medicine, Tokyo 113-0033, Japan;
rnEndocrine Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114;
rnEndocrine Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114 Pediatric Nephrology Unit, Department of Pediatrics, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114;
genomic imprinting; Gsa; pseudohypoparathyroidism; parathyroid hormone; hormonal resistance;
机译:NESP55的新缺失导致A / B GNAS的母体烙印和常染色体显性假性甲状旁腺功能减退的Ib型丢失
机译:NESP55差异甲基化区域的缺失导致母体GNAS印记丢失和假性甲状旁腺功能减退症Ib型
机译:常染色体显性伪性甲状旁腺功能减退症Ib型:新型的遗传性缺失消融STX16导致A / B DMR烙印的丢失
机译:基于模型的多燃志式控制爆震区域的虚拟燃烧阶段目标校正
机译:KvDMR1的功能研究,KvDMR1是小鼠远端染色体7的印迹控制区域。
机译:Nesp55 DMR的靶向缺失定义了另一个Gnas印迹控制区域并提供了常染色体显性PHP-Ib的小鼠模型
机译:Nesp55 DMR的靶向缺失定义了另一个Gnas印迹控制区域,并提供了常染色体显性PHP-Ib的小鼠模型
机译:在常染色体显性多囊肾病小鼠模型中体内诱导体细胞pkd1突变。