Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Fernando Gibson"'
Autor:
François-Noël Gilly, Fernando Gibson, Martin Figeac, Françoise Galateau-Sallé, Julien Péron, Denis Maillet, Marie Brevet, Frédéric Leprêtre, Laurent Villeneuve, Sylvie Isaac, Olivier Glehen, Pierre Chirac
Publikováno v:
Human Pathology. 55:72-82
Malignant peritoneal mesotheliomas (MPM) are rare, accounting for approximately 8% of cases of mesothelioma in France. We performed comparative genomic hybridization (CGH) on frozen MPM samples using the Agilent Human Genome CGH 180 K array. Samples
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac8ecbf17badd06d8ae8b3db46cf5ffe
https://doi.org/10.1016/j.humpath.2016.04.015
https://doi.org/10.1016/j.humpath.2016.04.015
Autor:
Bengt Gustavsson, David MacHover, Kjell Magne Tveit, Göran Carlsson, Hans J. Schmoll, Fernando Gibson, Nicholas J. Petrelli, Arnaud Roth
Publikováno v:
Clinical Colorectal Cancer. 14:1-10
Herein we present a historical review of the development of systemic chemotherapy for colorectal cancer (CRC) in the metastatic and adjuvant treatment settings. We describe the discovery of 5-fluorouracil (5-FU) by Heidelberger and colleagues in 1957
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcd1e10ffabf02a86da2b78f346c7e6e
https://doi.org/10.1016/j.clcc.2014.11.002
https://doi.org/10.1016/j.clcc.2014.11.002
Publikováno v:
Diabetes. 54:2477-2481
α2-Heremans-Schmid glycoprotein (AHSG) is an abundant plasma protein synthesized predominantly in the liver. The AHSG gene, consisting of seven exons and spanning 8.2 kb of genomic DNA, is located at chromosome 3q27, a susceptibility locus for type
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ed597074798cf55364b3435ce0645e7
https://doi.org/10.2337/diabetes.54.8.2477
https://doi.org/10.2337/diabetes.54.8.2477
Autor:
Philippe Froguel, Fernando Gibson
Publikováno v:
Diabetes. 53:2977-2983
We have carried out a detailed reexamination of the genetics of the APM1 locus and its contribution to the genetic basis of type 2 diabetes susceptibility in the French Caucasian population. The G allele of single nucleotide polymorphism −11426 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7a846e3e78a704951616e8f8a1d2724
https://doi.org/10.2337/diabetes.53.11.2977
https://doi.org/10.2337/diabetes.53.11.2977
Autor:
Dennis Saw, Steve D.M. Brown, Philomena Mburu, Fernando Gibson, M. Cope, John Kendrick-Jones, Karen M. Steel, James Walsh, Xue Zhong Liu
Publikováno v:
Genes and Function. 1:191-203
The shaker-1 (Myo7a) mouse deafness locus is encoded by an unconventional myosin gene: myosin VIIA [Gibson, Walsh, Mburu, Varela, Brown, Antonio, Biesel, Steel and Brown (1995) Nature (London) 374, 62-64]. The myosin VIIA gene is expressed in hair ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::936ad394652c7359c59c935bcdd45130
https://doi.org/10.1046/j.1365-4624.1997.00020.x
https://doi.org/10.1046/j.1365-4624.1997.00020.x
Autor:
Michel Marre, Serge Hercberg, Konsta Duesing, Philippe Froguel, Guillaume Charpentier, Jean Tichet, Beverley Balkau, Ghazaleh Fatemifar, Fernando Gibson
Publikováno v:
Diabetes
OBJECTIVE—We performed a comprehensive genetic association study of common variation spanning the IGF2BP2 locus in order to replicate the association of the “confirmed” type 2 diabetes susceptibility variants rs4402960 and rs1470579 in the Fren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b13c4baf330ae8477a6b33f957ff08b
https://pubmed.ncbi.nlm.nih.gov/18430866
https://pubmed.ncbi.nlm.nih.gov/18430866
Autor:
Jean Tichet, Philippe Froguel, Guillaume Charpentier, Fernando Gibson, Serge Hercberg, Michel Marre, Konsta Duesing, Beverley Balkau, Ghazaleh Fatemifar
Publikováno v:
Diabetologia. 51(5)
Genome-wide association studies (GWASs) recently identified common variants in the CDKN2A/CDKN2B region on chromosome 9p as being strongly associated with type 2 diabetes. Since these association signals were not picked up by the French-Canadian GWAS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::769b55385b6e1ea9a1afdec6acbd8205
https://pubmed.ncbi.nlm.nih.gov/18368387
https://pubmed.ncbi.nlm.nih.gov/18368387
Autor:
Guillaume Charpentier, Fernando Gibson, Michel Marre, Philippe Froguel, Konsta Duesing, Beverley Balkau, Serge Hercberg, Jean Tichet
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 9, Iss 1, p 14 (2008)
BMC Medical Genetics, Vol 9, Iss 1, p 14 (2008)
Background PBX1 is a biological candidate gene for type 2 diabetes at the 1q21-q24 susceptibility locus. The aim of this study was to evaluate the association of common PBX1 variants with type 2 diabetes in French Caucasian subjects. Methods Employin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b835b2f3feba66f1c413cf85689e5f6e
https://pubmed.ncbi.nlm.nih.gov/18312624
https://pubmed.ncbi.nlm.nih.gov/18312624
Publikováno v:
Gastroenterology. 148:S-620
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::027ca68322072d5997ea9d01328d8c17
https://doi.org/10.1016/s0016-5085(15)32093-x
https://doi.org/10.1016/s0016-5085(15)32093-x
Publikováno v:
Diabetes
Diabetes, American Diabetes Association, 2005, 54 (10), pp.3040-2
Diabetes, American Diabetes Association, 2005, 54 (10), pp.3040-2
Upstream transcription factor 1 (USF1) is a ubiquitously expressed transcription factor of the basic helix-loop-helix leucine zipper family that has been shown to regulate the expression of a raft of key genes involved in glucose and lipid metabolism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::470fb67b74df586d99c64237b8d71edf
https://hal.archives-ouvertes.fr/hal-00174470
https://hal.archives-ouvertes.fr/hal-00174470
