نتایج جستجو برای: link recessive

تعداد نتایج: 212740  

Journal: :iranian journal of public health 0
p ghandil dd farhud s zeinali a ghadiri

hemophilia b is factor ix deficiency and is inherited as x-linked recessive disorder. the subject of carrier detection in hemophilias has received new impetus in the last several years. analysis of factor ix gene polymorphisms is considered the best approach for prenatal diagnosis and hemophilia b carrier detection, if the identification of the gene mutation is possible. allele frequencies of t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Matthew B Toomey Ricardo J Lopes Pedro M Araújo James D Johnson Małgorzata A Gazda Sandra Afonso Paulo G Mota Rebecca E Koch Geoffrey E Hill Joseph C Corbo Miguel Carneiro

Yellow, orange, and red coloration is a fundamental aspect of avian diversity and serves as an important signal in mate choice and aggressive interactions. This coloration is often produced through the deposition of diet-derived carotenoid pigments, yet the mechanisms of carotenoid uptake and transport are not well-understood. The white recessive breed of the common canary (Serinus canaria), wh...

Journal: :international journal of molecular and cellular medicine 0
saeid morovvati research center for human genetics, baqiyatallah university of medical sciences, mollasadra st, tehran (postal box: 19395-5487), iran sara amirpour amaraii tehran medical branch, islamic azad university, khaghani st, shariati ave, tehran, iran hosna zahed shekarabi tehran medical branch, islamic azad university, khaghani st, shariati ave, tehran, iran nastaran shahbazi tehran medical branch, islamic azad university, khaghani st, shariati ave, tehran, iran

in the rare hereditary bone disorder of osteopetrosis, reduced bone resorption function leads to both the development of densely sclerotic fragile bones and progressive obliteration of the marrow spaces and cranial foramina. marrow obliteration, typically associated with extramedullary hemopoiesis and hepatosplenomegaly, results in anemia and thrombocytopenia and nerve entrapment accounts for p...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2014
Rachael M Ivatt Alvaro Sanchez-Martinez Vinay K Godena Stephen Brown Elena Ziviani Alexander J Whitworth

Genetic analysis of Parkinson disease (PD) has identified several genes whose mutation causes inherited parkinsonism, as well as risk loci for sporadic PD. PTEN-induced kinase 1 (PINK1) and parkin, linked to autosomal recessive PD, act in a common genetic pathway regulating the autophagic degradation of mitochondria, termed mitophagy. We undertook a genome-wide RNAi screen as an unbiased approa...

Journal: :Journal of the American Society of Nephrology : JASN 2009
Patricia L Weng Simone Sanna-Cherchi Terry Hensle Ellen Shapiro Alan Werzberger Gianluca Caridi Claudia Izzi Anita Konka Adam C Reese Rong Cheng Samuel Werzberger Richard N Schlussel Robert D Burk Joseph H Lee Roberto Ravazzolo Francesco Scolari Gian Marco Ghiggeri Kenneth Glassberg Ali G Gharavi

Primary vesicoureteral reflux (pVUR) is one of the most common causes of pediatric kidney failure. Linkage scans suggest that pVUR is genetically heterogeneous with two loci on chromosomes 1p13 and 2q37 under autosomal dominant inheritance. Absence of pVUR in parents of affected individuals raises the possibility of a recessive contribution to pVUR. We performed a genome-wide linkage scan in 12...

Journal: :iranian journal of public health 0
r sasanfar a tolouei a hoseinipour dd farhud m dolati l hoghooghi rad

the 35delg mutation in the connexin 26 gene (cx26), at the dnfb1 locus is the most common mutation in the patients with autosomal recessive non-syndromic hearing loss (arnshl). we have studied a total of 224 deaf cases from 189 families in two populations of iran (sistan va bluchestan and hormozgan provinces) by prescreening nested pcr, polyacrylamide gel electrophoresis and consequent direct s...

Journal: :journal of family and reproductive health 0
ilana naghi department of obstetrics and gynecology, shahid beheshti university of medical sciences, tehran, iran. babak behnam department of medical genetics, tehran university of medical sciences.

a 39-year-old pregnant woman at 38 weeks of gestation was referred with labor pain to a hospital. she had consanguinity with her husband. a female newborn had multiple craniofacial anomalies and phocomelia in right upper limb. the disease locus was assigned to chromosome17q21. four days later, infant died of cardiopulmonary arrest.

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