نتایج جستجو برای: myh9 gene

تعداد نتایج: 1141526  

2014
Vitor G.L. Dantas Karina Lezirovitz Guilherme L. Yamamoto Carolina Fischinger Moura de Souza Simone Gomes Ferreira Regina C. Mingroni-Netto

We studied a family presenting 10 individuals affected by autosomal dominant deafness in all frequencies and three individuals affected by high frequency hearing loss. Genomic scanning using the 50k Affymetrix microarray technology yielded a Lod Score of 2.1 in chromosome 14 and a Lod Score of 1.9 in chromosome 22. Mapping refinement using microsatellites placed the chromosome 14 candidate regi...

1980
PAUL ERDŐS

The sequence A of nonnegative integers is an asymptotic basis of order h if every sufficiently large integer can be written as the sum of h elements of A . Let MhA denote the set of elements that have more than one representation as a sum of h elements of A . It is proved that there exists an asymptotic basis A such that MhA (x) = O(x1-1 11 +E) for every e > 0. An asymptotic basis A of order h ...

Journal: :Nefrología (English Edition) 2019

Journal: :Journal of cell science 2014
Cristina Casalou Cecília Seixas Ana Portelinha Petra Pintado Mafalda Barros José S Ramalho Susana S Lopes Duarte C Barral

The Arf-like protein Arl13b has been implicated in ciliogenesis and Sonic hedgehog signaling. Furthermore, we have previously shown that it regulates endocytic recycling traffic and interacts with actin. Herein, we report that the non-muscle myosin heavy chain IIA, also known as Myh9, is an Arl13b effector. Moreover, we found that both proteins localized to circular dorsal ruffles (CDRs) induce...

Journal: :Blood 2014
Fabien Pertuy Anita Eckly Josiane Weber Fabienne Proamer Jean-Yves Rinckel François Lanza Christian Gachet Catherine Léon

During proplatelet formation, a relatively homogeneous content of organelles is transported from the megakaryocyte (MK) to the nascent platelets along microtubule tracks. We found that platelets from Myh9(-/-) mice and a MYH9-RD patient were heterogeneous in their organelle content (granules and mitochondria). In addition, Myh9(-/-) MKs have an abnormal cytoplasmic clustering of organelles, sug...

Journal: :Mayo Clinic Proceedings 2017

2015
Blair R. Anderson David N. Howell Karen Soldano Melanie E. Garrett Nicholas Katsanis Marilyn J. Telen Erica E. Davis Allison E. Ashley-Koch Gregory S. Barsh

African Americans have a disproportionate risk for developing nephropathy. This disparity has been attributed to coding variants (G1 and G2) in apolipoprotein L1 (APOL1); however, there is little functional evidence supporting the role of this protein in renal function. Here, we combined genetics and in vivo modeling to examine the role of apol1 in glomerular development and pronephric filtrati...

Journal: :Journal of immunology 2006
Keira Reville John K Crean Sharon Vivers Ian Dransfield Catherine Godson

Lipoxins (LXs) are endogenously produced anti-inflammatory agents that modulate leukocyte trafficking and stimulate nonphlogistic macrophage phagocytosis of apoptotic neutrophils, thereby promoting the resolution of inflammation. Previous data suggest a role for altered protein phosphorylation and cytoskeletal rearrangement in LX-stimulated phagocytosis but the exact mechanisms remain unclear. ...

Journal: :Blood 2005
Josef D Franke Fan Dong Wayne L Rickoll Michael J Kelley Daniel P Kiehart

MYH9-related disorders are autosomal dominant syndromes, variably affecting platelet formation, hearing, and kidney function, and result from mutations in the human nonmuscle myosin-IIA heavy chain gene. To understand the mechanisms by which mutations in the rod region disrupt nonmuscle myosin-IIA function, we examined the in vitro behavior of 4 common mutant forms of the rod (R1165C, D1424N, E...

2004
Josef D. Franke Fan Dong Wayne L. Rickoll Michael J. Kelley Daniel P. Kiehart

MYH9-related disorders are autosomal dominant syndromes, variably affecting platelet formation, hearing, and kidney function, and result from mutations in the human nonmuscle myosin-IIA heavy chain gene. To understand the mechanisms by which mutations in the rod region disrupt nonmuscle myosin-IIA function, we examined the in vitro behavior of 4 common mutant forms of the rod (R1165C, D1424N, E...

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