Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Christine Bellané-Chantelot"'
Autor:
Emmanuelle Motte-Signoret, Cécile Saint-Martin, Christine Bellané-Chantelot, Bernard Portha, Pascal Boileau
Publikováno v:
Metabolites, Vol 12, Iss 9, p 847 (2022)
Glucose homeostasis is a real challenge for extremely preterm infants (EPIs) who have both limited substrate availability and immature glucose metabolism regulation. In the first days of life, EPIs frequently develop transient glucose intolerance, wh
Externí odkaz:
https://doaj.org/article/0facc28b6e8d4250beb35e4431c4f240
Autor:
Sophie Lebon, Agnès Rötig, Béatrice Mougenot, Laure-Hélène Noël, Dominique Chauveau, Christine Bellané-Chantelot, Pierre Clavel, Pierre Rustin, Jean-Pierre Grünfeld, Bruno Guéry, Gabriel Choukroun
Publikováno v:
ResearcherID
The A3243G mutation of the mitochondrial tRNA(Leu) gene has been recently reported in rare patients with focal and segmental glomerulosclerosis (FSGS). However, the full spectrum of systemic and kidney manifestations in adults presenting with this mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86fb4bfe2a381fd4332b080425f2c113
https://doi.org/10.1097/01.asn.0000080180.51098.02
https://doi.org/10.1097/01.asn.0000080180.51098.02
Autor:
Philippe Mangin, Eric Drelon, Antoine Valeri, Pierre Teillac, Annick Cohen-Akenine, Georges Fournier, Imène Mellah, Rosette Lidereau, Christine Bellané-Chantelot, Hélène Blanché, Philippe Berthon, Olivier Cussenot, Robert de Petriconi, Philippe Millasseau, Alain Latil, Florence Demenais, Lucien Bachner, Norman J. Maitland, Gudrun Wöhr, Nadine Cohen, Ilya Chumakov, Richard E. Hautmann, Daniel Cohen, Alain Le Duc, Thomas Paiss, Walther Vogel
Publikováno v:
The American Journal of Human Genetics. 62:1416-1424
SummaryThere is genetic predisposition associated with ⩾10% of all cancer of the prostate (CaP). By means of a genomewide search on a selection of 47 French and German families, parametric and nonparametric linkage (NPL) analysis allowed identifica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::478768cd35b8a3eb00d0dc9a4096806d
https://doi.org/10.1086/301879
https://doi.org/10.1086/301879
Autor:
Christine Bellané-Chantelot, Christophe Vincent, Eric Haan, Rima Slim, Annie Nivelon, Fatima Graia, Didier Lacombe, Jean Weissenbach, Maria de Lurdes Pereira, David F. Callen, Denis Le Paslier, Sylvie Compain, Jocelyne Hélias, Christine Petit, Marie-France Croquette, Jacqueline Vigneron, Bruno Lacroix, Vasiliki Kalatzis, Michel Broyer, Jacqueline Levilliers, Daniel Cohen
Publikováno v:
Scopus-Elsevier
The analysis of a de novo 8q12.2-q21.2 deletion led to the identification of a proposed previously undescribed contiguous gene syndrome consisting of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, hydrocephalus and trapeze aplasia. This is the fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::800c51a2e73cf8abebad7b31d8f87ed7
https://pubmed.ncbi.nlm.nih.gov/7849713
https://pubmed.ncbi.nlm.nih.gov/7849713