User profiles for P. Ravassard
Pascal RavassardIINS Verified email at u-bordeaux.fr Cited by 1426 |
[HTML][HTML] The ectopic expression of Pax4 in the mouse pancreas converts progenitor cells into α and subsequently β cells
P Collombat, X Xu, P Ravassard, B Sosa-Pineda… - Cell, 2009 - cell.com
We have previously reported that the loss of Arx and/or Pax4 gene activity leads to a shift in
the fate of the different endocrine cell subtypes in the mouse pancreas, without affecting the …
the fate of the different endocrine cell subtypes in the mouse pancreas, without affecting the …
[HTML][HTML] A genetically engineered human pancreatic β cell line exhibiting glucose-inducible insulin secretion
P Ravassard, Y Hazhouz, S Pechberty… - The Journal of …, 2011 - Am Soc Clin Investig
… In this issue of the JCI, Ravassard and colleagues report that this has finally been achieved
successfully with a multistep process that led to the generation of cells, which they termed …
successfully with a multistep process that led to the generation of cells, which they termed …
A third vesicular glutamate transporter expressed by cholinergic and serotoninergic neurons
…, GC Bellenchi, V Bernard, P Ravassard… - Journal of …, 2002 - Soc Neuroscience
Two proteins previously known as Na + -dependent phosphate transporters have been
identified recently as vesicular glutamate transporters (VGLUT1 and VGLUT2). Together, …
identified recently as vesicular glutamate transporters (VGLUT1 and VGLUT2). Together, …
[PDF][PDF] The existence of a second vesicular glutamate transporter specifies subpopulations of glutamatergic neurons
…, C Gras, V Bernard, P Ravassard… - The Journal of …, 2001 - Soc Neuroscience
… Etienne Herzog,1 Gian Carlo Bellenchi,2 Christelle Gras,1 Veronique Bernard,3 Philippe
Ravassard… Grattier for technical support on electronic microscopy, P. Dreyfus for his patient and …
Ravassard… Grattier for technical support on electronic microscopy, P. Dreyfus for his patient and …
[PDF][PDF] Human β cell transcriptome analysis uncovers lncRNAs that are tissue-specific, dynamically regulated, and abnormally expressed in type 2 diabetes
… and antisense lncRNAs were more often islet-specific than the entire collection of annotated
genes (p < 10 À10 ), up to >3-fold when considering only islet-specific lncRNAs (p < 2$10 …
genes (p < 10 À10 ), up to >3-fold when considering only islet-specific lncRNAs (p < 2$10 …
Insulin storage and glucose homeostasis in mice null for the granule zinc transporter ZnT8 and studies of the type 2 diabetes–associated variants
…, P Froguel, R Scharfmann, V Stetsyuk, P Ravassard… - Diabetes, 2009 - Am Diabetes Assoc
OBJECTIVE Zinc ions are essential for the formation of hexameric insulin and hormone
crystallization. A nonsynonymous single nucleotide polymorphism rs13266634 in the SLC30A8 …
crystallization. A nonsynonymous single nucleotide polymorphism rs13266634 in the SLC30A8 …
Pancreatic islet enhancer clusters enriched in type 2 diabetes risk-associated variants
… significant enrichment relative to the null distribution of permuted counts for T2D and fasting
glycemia association P values of <0.001 (P values for these analyses are given in the text). …
glycemia association P values of <0.001 (P values for these analyses are given in the text). …
Multisensory control of hippocampal spatiotemporal selectivity
P Ravassard, A Kees, B Willers, D Ho, D Aharoni… - Science, 2013 - science.org
… The position code index is significantly greater in RW than VR (P < 10 −7 ) whereas disto-code
index is significantly greater in VR (P < 10 −6 ). (D) Similarity of the population of 91 …
index is significantly greater in VR (P < 10 −6 ). (D) Similarity of the population of 91 …
Localization of VGLUT3, the vesicular glutamate transporter type 3, in the rat brain
We have recently identified a third subtype of glutamate vesicular transporter (VGLUT) named
VGLUT3. In the present study, we provide a detailed account of the regional and cellular …
VGLUT3. In the present study, we provide a detailed account of the regional and cellular …
Intravenous scAAV9 delivery of a codon-optimized SMN1 sequence rescues SMA mice
…, S Duque, P Ravassard… - Human molecular …, 2011 - academic.oup.com
Spinal muscular atrophy (SMA) is the most common genetic disease leading to infant mortality.
This neuromuscular disorder is caused by the loss or mutation of the telomeric copy of …
This neuromuscular disorder is caused by the loss or mutation of the telomeric copy of …