Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Nerve Tissue Proteins/genetics/metabolism"'
Publikováno v:
PLoS ONE, Vol 12, Iss 1, p e0169452 (2017)
PLoS ONE
PLOS ONE, Vol. 12, No 1 (2017) P. e0169452
PLoS ONE
PLOS ONE, Vol. 12, No 1 (2017) P. e0169452
Lrig1 is known to repress the epidermal growth through its inhibitory activity on EGFR, while CD44 promotes it. We analyzed the expression of these molecules in senescent atrophic human epidermis and in the epidermis of CD44KO mice. In normal human e
Autor:
Camilla Bellone, Jonathan Moss, Nicolas Toni, Denis Jabaudon, Christian Lüscher, Ilaria Vitali, Bruno Golding, Andres De la Rossa
Publikováno v:
Nature neuroscience
Nature Neuroscience
Nature Neuroscience, Vol. 16, No 2 (2013) pp. 193-200
Nature Neuroscience
Nature Neuroscience, Vol. 16, No 2 (2013) pp. 193-200
The molecular mechanisms that control how progenitors generate distinct subtypes of neurons, and how undifferentiated neurons acquire their specific identity during corticogenesis, are increasingly understood. However, whether postmitotic neurons can
Autor:
Junzheng Peng, Patricia B. Munroe, Guy Cloutier, Ekatherina Stoyanova, Zhao Qin, Jian-Zhong Shen, Tao Wu, W. Edward C. Bradley, Yujia Wang, Hongyu Luo, Shen-Jiang Hu, Georg Ehret, John Verner Raelson, Jiangping Wu, Zenghui Wu
Publikováno v:
Scientific Reports, Vol. 6 (2016) P. 38976
Scientific Reports
Scientific Reports
Several erythropoietin-producing hepatocellular receptor B family (EPHB) and their ligands, ephrinBs (EFNBs), are involved in blood pressure regulation in animal models. We selected 528 single nucleotide polymorphisms (SNPs) within the genes of EPHB6
Publikováno v:
Molecular and Cellular Proteomics, Vol. 11, No 8 (2012) pp. 244-54
Insulin secretory granules are β-cell vesicles dedicated to insulin processing, storage, and release. The secretion of insulin secretory granule content in response to an acute increase of glucose concentration is a highly regulated process allowing
Autor:
Cécile Lebrand, Jozsef Zoltan Kiss, O Riccio, Sahana Murthy, Alexandre Dayer, Gábor Szabó, Laszlo Vutskits, Tania Vitalis
Publikováno v:
Cerebral cortex (New York N.Y. : 1991)
Cerebral Cortex
Cerebral Cortex, vol. 22, no. 1, pp. 86-98
Cerebral Cortex, Vol. 22, No 1 (2012) pp. 86-98
Cerebral Cortex
Cerebral Cortex, vol. 22, no. 1, pp. 86-98
Cerebral Cortex, Vol. 22, No 1 (2012) pp. 86-98
The migration of cortical γ-aminobutyric acidergic interneurons has been extensively studied in rodent embryos, whereas few studies have documented their postnatal migration. Combining in vivo analysis together with time-lapse imaging on cortical sl
Autor:
Yoni E. Gutkovich, Rachel Ofir, Charna Dibner, Dale Frank, Yaniv M. Elkouby, Aharon Gefen, Sarah Elias
Publikováno v:
Developmental Biology, Vol. 338, No 1 (2010) pp. 50-62
In Xenopus embryos, XMeis3 protein activity is required for normal hindbrain formation. Our results show that XMeis3 protein knock down also causes a loss of primary neuron and neural crest cell lineages, without altering expression of Zic, Sox or Pa
Publikováno v:
Neurobiology of Disease, Vol 17, Iss 2, Pp 283-289 (2004)
Viral delivery of glial cell line-derived neurotrophic factor (GDNF) currently represents one of the most promising neuroprotective strategies for Parkinson's Disease (PD). However, the effect of this neurotrophic factor has never been tested in the
Autor:
Fred Bernard, J.F Ferveur, R. Cossard, J Silber, M Gullaud, A Lalouette, A Zider, A.Y Jeantet
Publikováno v:
Developmental Biology
Developmental Biology, Elsevier, 2003, 260 (2), pp.391-403
Developmental Biology, Elsevier, 2003, 260 (2), pp.391-403
0012-1606 (Print) Journal Article Research Support, Non-U.S. Gov't; Drosophila thoracic muscles are comprised of both direct flight muscles (DFMs) and indirect flight muscles (IFMs). The IFMs can be further subdivided into dorsolongitudinal muscles (
Autor:
Yann Grattau, Gilbert Di Paolo, Clémentine Ripoll, Charles Duyckaerts, Jack-Christophe Cossec, Isabelle Rivals, Samantha Stora, Fabrice de Chaumont, Diego E. Berman, Joris A. Veltman, Magalie Lecourtois, Jean M. Delabar, Marie-Claude Potier, Jérémie Lavaur, Stylianos E. Antonarakis, Jean-Christophe Olivo-Marin, Clotilde Mircher, Alexander Hoischen
Publikováno v:
Human Molecular Genetics, 21, 14, pp. 3156-72
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (14), pp.3156-3172. ⟨10.1093/hmg/dds142⟩
Human Molecular Genetics, 21, 3156-72
Human Molecular Genetics, Vol. 21, No 14 (2012) pp. 3156-72
Human Molecular Genetics, 2012, 21 (14), pp.3156-3172. ⟨10.1093/hmg/dds142⟩
Human Molecular Genetics
Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (14), pp.3156-3172. ⟨10.1093/hmg/dds142⟩
Human Molecular Genetics, 21, 3156-72
Human Molecular Genetics, Vol. 21, No 14 (2012) pp. 3156-72
Human Molecular Genetics, 2012, 21 (14), pp.3156-3172. ⟨10.1093/hmg/dds142⟩
Item does not contain fulltext Enlarged early endosomes have been observed in neurons and fibroblasts in Down syndrome (DS). These endosome abnormalities have been implicated in the early development of Alzheimer's disease (AD) pathology in these sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abc37d22c2eb99c7eb9ec061b8a9fb27
https://hdl.handle.net/2066/110063
https://hdl.handle.net/2066/110063
Autor:
Vincent Procaccio, Guillaume Nicolas, Arnaud Chevrollier, Dominique Bonneau, Frédéric Dubas, Naïg Gueguen, Valérie Desquiret, Pascal Reynier, Patrizia Amati-Bonneau, Julien Cassereau, Christophe Verny
Publikováno v:
Experimental Neurology
Experimental Neurology, 2011, 227 (1), pp.31-41. ⟨10.1016/j.expneurol.2010.09.006⟩
Experimental Neurology, 2011, 227 (1), pp.31-41. ⟨10.1016/j.expneurol.2010.09.006⟩
International audience; Charcot-Marie-Tooth (CMT) disease represents a large group of clinically and genetically heterogeneous disorders leading to inherited peripheral neuropathies affecting motor and sensory neurons. Mutations in the ganglioside-in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::157dbbccc0bb4c884a34b6f350fd8d7b
https://hal.univ-angers.fr/hal-03408479
https://hal.univ-angers.fr/hal-03408479