نتایج جستجو برای: numb chin syndrome

تعداد نتایج: 625728  

Journal: :Molecular and cellular biology 2001
T Imai A Tokunaga T Yoshida M Hashimoto K Mikoshiba G Weinmaster M Nakafuku H Okano

Musashi1 (Msi1) is an RNA-binding protein that is highly expressed in neural progenitor cells, including neural stem cells. In this study, the RNA-binding sequences for Msi1 were determined by in vitro selection using a pool of degenerate 50-mer sequences. All of the selected RNA species contained repeats of (G/A)U(n)AGU (n = 1 to 3) sequences which were essential for Msi1 binding. These consen...

Journal: :Mechanisms of Development 2009
Alexandre Baffet Beatrice Benoit Vanessa Gourhand Claire Heichette Denis Chretien Antoine Guichet

hypothesis, we used the Cre-loxP system to conditionally inactivate Numb and its homolog Numblike in RPCs at different stages of retinogenesis. We used retroviral vectors expressing Cre recombinase and a reporter to infect Numb/Numblike floxed mouse retinas at early (E13) and late (P0) stages of retinal development. Analysis of cell composition of the resulting knockout clones showed that Numb ...

Journal: :Mechanisms of Development 2009
Thorsten Boroviak Pen Rashbass

hypothesis, we used the Cre-loxP system to conditionally inactivate Numb and its homolog Numblike in RPCs at different stages of retinogenesis. We used retroviral vectors expressing Cre recombinase and a reporter to infect Numb/Numblike floxed mouse retinas at early (E13) and late (P0) stages of retinal development. Analysis of cell composition of the resulting knockout clones showed that Numb ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
W Zhong M M Jiang M D Schonemann J J Meneses R A Pedersen L Y Jan Y N Jan

During neurogenesis of the mammalian neocortex, neural progenitor cells divide to generate daughter cells that either become neurons or remain as progenitor cells. The mouse numb (m-numb) gene encodes a membrane-associated protein that is asymmetrically localized to the apical cell membrane of dividing cortical progenitor cells and may be segregated to only the apical daughter cell that has bee...

Journal: :Journal of Nervous & Mental Disease 2017

Journal: :Current Biology 2005
Sheetal Bhalerao Daniela Berdnik Tibor Török Juergen A. Knoblich

During asymmetric cell division, protein determinants are segregated into one of the two daughter cells. The Numb protein acts as a segregating determinant during both mouse and Drosophila development. In flies, Numb localizes asymmetrically and is required for cell-fate specification in the central and peripheral nervous systems, as well as during muscle and heart development. Whether its asym...

Journal: :Molecular biology of the cell 2004
Christian A Smith Sascha E Dho Julie Donaldson Ulrich Tepass C Jane McGlade

The adaptor protein Numb is necessary for the cell fate specification of progenitor cells in the Drosophila nervous system. Numb is evolutionarily conserved and previous studies have provided evidence for a similar functional role during mammalian development. The Numb protein has multiple protein-protein interaction regions including a phosphotyrosine binding (PTB) domain and a carboxy-termina...

Journal: :Neuron 2003
Hua-Shun Li Denan Wang Qin Shen Marcus D. Schonemann Jessica A. Gorski Kevin R. Jones Sally Temple Lily Yeh Jan Yuh Nung Jan

Numb and Numblike, conserved homologs of Drosophila Numb, have been implicated in cortical neurogenesis; however, analysis of their involvement in later stages of cortical development has been hampered by early lethality of double mutants in previous studies. Using Emx1(IREScre) to induce more restricted inactivation of Numb in the dorsal forebrain of numblike null mice beginning at E9.5, we ha...

Journal: :Cultural and Pedagogical Inquiry 1969

Journal: :American journal of medical genetics. Part A 2012
Filiz Hazan Pia Ostergaard Taylan Ozturk Esin Kantekin Fusun Atlihan Steve Jeffery Ferda Ozkinay

Microcephaly-lymphedema-chorioretinal dysplasia (MLCRD) syndrome is a rare syndrome that was first described in 1992. Characteristic craniofacial features include severe microcephaly, upslanting palpebral fissures, prominent ears, a broad nose, and a long philtrum with a pointed chin. Recently, mutations in KIF11 have been demonstrated to cause dominantly inherited MLCRD syndrome. Herein, we pr...

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