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201. No evidence for the involvement of CAG/CTG repeats from within 18q21.33–q23 in bipolar disorder

203. The rat genetic and cytogenetic maps

204. Assignment of rat Jun family genes to chromosome 19 (Junb), chromosome 5q31-33 (Jun), and chromosome 16 (Jund)

205. Assignment of rat Jun family genes to chromosome 19 (Junb), chromosome 5q31-33 (Jun), and chromosome 16 (Jund)

207. Antagonistic Functions of Dishevelleds Regulate Frizzled3 Endocytosis via Filopodia Tips in Wnt-Mediated Growth Cone Guidance.

208. A Sequence-Ready BAC/PAC Contig and Partial Transcript Map of Approximately 1.5 Mb in Human Chromosome 17q25 Comprising Multiple Disease Genes

210. A Role for Atypical Cadherin Celsr3 in Hippocampal Maturation and Connectivity.

211. Atypical Cadherins Celsr1-3 Differentially Regulate Migration of Facial Branchiomotor Neurons in Mice.

212. Maturation of "Neocortex Isolé" In Vivo in Mice.

215. KIF2A deficiency causes early-onset neurodegeneration.

216. Inactivating Celsr2 promotes motor axon fasciculation and regeneration in mouse and human.

217. Identification of a novel brain-specific and reelin-regulated gene that encodes a protein colocalized with synapsin.

218. DIAPH3 deficiency links microtubules to mitotic errors, defective neurogenesis, and brain dysfunction.

219. Early loss of Scribble affects cortical development, interhemispheric connectivity and psychomotor activity.

220. Vsx1 and Chx10 paralogs sequentially secure V2 interneuron identity during spinal cord development.

221. Cajal‐Retzius neurons are required for the development of the human hippocampal fissure.

222. Celsr1 coordinates the planar polarity of vestibular hair cells during inner ear development.

223. Gut microbiota, biological and psychological alterations in alcohol use disorder

224. Planar cell polarity protein Celsr2 maintains structural and functional integrity of adult cortical synapses.

225. Reallocation of Olfactory Cajal-Retzius Cells Shapes Neocortex Architecture.

226. TRPV4 is associated with central rather than nephrogenic osmoregulation.

227. The atypical cadherin Celsr1 functions non-cell autonomously to block rostral migration of facial branchiomotor neurons in mice.

228. Hexameric β-amyloid as a key assembly in Alzheimer's disease : cellular formation and seeding effects

229. Mechanisms of stretch-mediated skin expansion at single-cell resolution

230. Etude du rôle des facteurs de transcription Dmrt3 et Dmrt5 dans le développement cortical: Dmrt3 et Dmrt5 maintiennent l'identité corticale dans les progéniteurs du télencéphale dorsal au cours du développement

231. Planar cell polarity genes control the connectivity of enteric neurons.

232. The Celsr3-Kif2a axis directs neuronal migration in the postnatal brain.

233. Early Forebrain Wiring: Genetic Dissection Using Conditional CeIsr3 Mutant Mice.

234. Author Correction: Onecut-dependent Nkx6.2 transcription factor expression is required for proper formation and activity of spinal locomotor circuits.

235. The development of cortical connections.

236. Molecular determinants regulating dimerization, processing and signaling of the amyloid precursor protein

237. Progress in the role of TRPV4 as an osmo- and mechanosensor in systemic osmoregulation and renal functions

238. Role of the TRPC1 Channel in Hippocampal Long-Term Depression and in Spatial Memory Extinction.

239. Role of transmembrane GXXXG motifs in APP dimerization and β-amyloid peptide oligomerization in Alzheimer’s disease

240. Planar cell polarity genes in motor axon guidance in the limb

241. Role of planar polarity proteins Celsr1-3 in neuronal migration and ciliogenesis

242. Transdifferentiation of pancreatic duct cells to β-cells in absence of the transcription factor HNF6

243. Rôle de la signalisation de la polarité cellulaire planaire dans les processus mnésiques

244. Aberrant generation of dentate gyrus granule cells is associated with epileptic susceptibility in p53 conditional knockout mice.

245. Auts2 enhances neurogenesis and promotes expansion of the cerebral cortex.

246. Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice.

247. DIAPH3 predicts survival of patients with MGMT -methylated glioblastoma.

248. Connecting neurodevelopment to neurodegeneration: a spotlight on the role of kinesin superfamily protein 2A (KIF2A).

249. Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice.

250. Celsr2-mediated morphological polarization and functional phenotype of reactive astrocytes in neural repair.

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