نتایج جستجو برای: microdeletion

تعداد نتایج: 1516  

2014
Vladimir Camarena Lei Cao Clemer Abad Alexander Abrams Yaima Toledo Kimi Araki Masatake Araki Katherina Walz Juan I Young

2q23.1 microdeletion syndrome is characterized by intellectual disability, motor delay, autistic-like behaviors, and a distinctive craniofacial phenotype. All patients carry a partial or total deletion of methyl-CpG-binding domain protein 5 (MBD5), suggesting that haploinsufficiency of this gene is responsible for the phenotype. To confirm this hypothesis and to examine the role of MBD5 in vivo...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Ioana Carcea Shekhar B Patil Alfred J Robison Roxana Mesias Molly M Huntsman Robert C Froemke Joseph D Buxbaum George W Huntley Deanna L Benson

Abnormal cortical circuits underlie some cognitive and psychiatric disorders, yet the molecular signals that generate normal cortical networks remain poorly understood. Semaphorin 7A (Sema7A) is an atypical member of the semaphorin family that is GPI-linked, expressed principally postnatally, and enriched in sensory cortex. Significantly, SEMA7A is deleted in individuals with 15q24 microdeletio...

Journal: :Journal of medical genetics 2002
V Gatta L Stuppia G Calabrese E Morizio P Guanciali-Franchi G Palka

During the last few years, microdeletions of the long arm of the Y chromosome, involving loci AZFa, AZFb, and AZFc, have been identified as a major cause of infertility, leading to the disruption of genes involved in spermatogenesis. These microdeletions are usually de novo mutations, but in six cases transmission from fertile fathers to infertile sons has been reported. In four cases, the tran...

Journal: :Microscopy and Microanalysis 2009

Journal: :Taiwanese Journal of Obstetrics and Gynecology 2021

Journal: :Central European Journal of Immunology 2013

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