Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Mathis Soubeyrand"'
Autor:
Frank Griscelli, Hélène Ezanno, Mathis Soubeyrand, Olivier Feraud, Noufissa Oudrhiri, Amélie Bonnefond, Ali G. Turhan, Philippe Froguel, Annelise Bennaceur-Griscelli
Publikováno v:
Stem Cell Research, Vol 29, Iss , Pp 56-59 (2018)
Heterozygous non-synonymous (p.S142F) mutation in HNF1A leads to maturity-onset diabetes of the young (MODY) type 3, which is a subtype of dominant inherited young-onset non-autoimmune diabetes due to the defect of insulin secretion from pancreatic b
Externí odkaz:
https://doaj.org/article/cb20890f6439468ba22478abf4a04ff4
Autor:
Cédric Aumont, Annelise Bennaceur-Griscelli, Mathis Soubeyrand, Jamila Faivre, Patricia Hugues, Claire Borie, Ali G. Turhan, Xavier Fund, Safa Sanekli, Estelle Balducci, Christophe Desterke
Publikováno v:
Leukemia & Lymphoma. 61:209-212
Chronic myeloid leukemia (CML) is characterized by the specific cytogenetic translocation t(9;22)(q34;q11), generating the Philadelphia (Ph) chromosome and its molecular counterpart BCR-ABL1. In 5%...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bd1f6aa2edc2801ccf73e1aa97965ed
https://doi.org/10.1080/10428194.2019.1658101
https://doi.org/10.1080/10428194.2019.1658101
Autor:
Philippe Froguel, Olivier Feraud, Noufissa Oudrhiri, Hélène Ezanno, Mathis Soubeyrand, Ali G. Turhan, Frank Griscelli, Annelise Bennaceur-Griscelli, Amélie Bonnefond
Publikováno v:
Stem Cell Research, Vol 29, Iss, Pp 56-59 (2018)
Heterozygous non-synonymous (p.S142F) mutation in HNF1A leads to maturity-onset diabetes of the young (MODY) type 3, which is a subtype of dominant inherited young-onset non-autoimmune diabetes due to the defect of insulin secretion from pancreatic b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1255e14d99a221bdd29d2f4fd9c13eab
https://doi.org/10.1016/j.scr.2018.02.017
https://doi.org/10.1016/j.scr.2018.02.017