نتایج جستجو برای: protein family

تعداد نتایج: 1570166  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2005
Jana Hackbusch Klaus Richter Judith Müller Francesco Salamini Joachim F Uhrig

The organization of living cells is based on networks of interacting molecules. Systematic analysis of protein interactions of 3-aa loop extension (TALE) homeodomain proteins, fundamental regulators of plant meristem function and leaf development, revealed a highly connected, complex network. The network includes nine members of Arabidopsis thaliana ovate family proteins (AtOFPs), a plant-speci...

2016
T.B. Stanishneva-Konovalova N.I. Derkacheva S.V. Polevova O.S. Sokolova

Many cellular processes are associated with membrane remodeling. The BAR domain protein family plays a key role in the formation and detection of local membrane curvatures and in attracting other proteins, including the regulators of actin dynamics. Based on their structural and phylogenetic properties, BAR domains are divided into several groups which affect membrane in various ways and perfor...

2015
Tanmay Bhuin Jagat Kumar Roy

Membrane/protein trafficking in the secretory/biosynthetic and endocytic pathways is mediated by vesicles. Vesicle trafficking in eukaryotes is regulated by a class of small monomeric GTPases: the Rab protein family. Rab proteins represent the largest branch of the Ras superfamily GTPases, and have been concerned in a variety of intracellular vesicle trafficking and different intracellular sign...

Journal: :Nucleic acids research 1987
B. Dworniczak M. E. Mirault

In all eukaryotes examined so far, hsp70 gene families include cognate genes (hsc70) encoding proteins of about 70 Kd which are expressed constitutively during normal growth and development. We have investigated the structural relationship of heat-inducible and cognate members of the human hsp70 gene family. Among several human genomic clones isolated using Drosophila hsp/hsc70 probes, one cont...

Journal: :iranian journal of medical sciences 0
mohammad miryounesi genomic research center, shahid beheshti university of medical sciences, tehran, iran; soudeh ghafouri-fard department of medical genetics, shahid beheshti university of medical sciences, tehran, iran; majid fardaei department of medical genetics, shiraz university of medical sciences, shiraz, iran

congenital recessive myotonia is a rare genetic disorder caused by mutations in clcn1, which codes for the main skeletal muscle chloride channel clc-1. more than 120 mutations have been found in this gene. the main feature of this disorder is muscle membrane hyperexcitability. here, we report a 59-year male patient suffering from congenital myotonia. he had transient generalized myotonia, which...

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