Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Christine Guidal-Giroux"'
Autor:
Cécile Acquaviva, Delphine Mirebeau, Etienne Vilmer, Christine Guidal-Giroux, Raphaëlle Bertin, Hélène Cavé
Publikováno v:
Genes, Chromosomes and Cancer. 37:44-57
Deletion of the 9p21 chromosomal region is frequently found in childhood acute lymphoblastic leukemia (ALL). The target of these deletions is CDKN2A, a gene encoding both p16(INK4a) and p14(ARF). However, contiguous genes such as CDKN2B, encoding p15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75a7c4f7a13e1e9d670f6ae3acc06d46
https://doi.org/10.1002/gcc.10188
https://doi.org/10.1002/gcc.10188
Autor:
Raphaëlle, Bertin, Cécile, Acquaviva, Delphine, Mirebeau, Christine, Guidal-Giroux, Etienne, Vilmer, Hélène, Cavé
Publikováno v:
Genes, chromosomescancer. 37(1)
Deletion of the 9p21 chromosomal region is frequently found in childhood acute lymphoblastic leukemia (ALL). The target of these deletions is CDKN2A, a gene encoding both p16(INK4a) and p14(ARF). However, contiguous genes such as CDKN2B, encoding p15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e8b38b74ff6a7f489a00c6b9eb99da89
https://pubmed.ncbi.nlm.nih.gov/12661005
https://pubmed.ncbi.nlm.nih.gov/12661005
Autor:
C Chambon-Pautas, Michel Duval, Hélène Cavé, Bénédicte Gérard, Bernard Grandchamp, Christine Guidal-Giroux, Etienne Vilmer
Publikováno v:
Leukemia. 12(7)
Knowledge of the patterns of allelic loss has been useful in identifying tumor suppressor genes in many solid tumors. Although the loss of genetic material in acute lymphoblastic leukemias has been documented by cytogenetic studies and microsatellite
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b9b78076c9f9fcbde99f21731b88dfa
https://pubmed.ncbi.nlm.nih.gov/9665197
https://pubmed.ncbi.nlm.nih.gov/9665197
Autor:
Sophie Raynaud, Valère Cacheux, C Guo, Peter Marynen, Christian Bastard, Mathijs Baens, Bernard Grandchamp, Christine Guidal-Giroux, J. Grosgeorge, Hélène Cavé, Etienne Vilmer
Publikováno v:
Europe PubMed Central
A recurrent t(12;21)(p13;q22) has recently been described in human acute lymphoblastic leukemias (ALLs). This translocation fuses TEL and AML1, two genes previously cloned from translocation breakpoints in myeloid leukemias. In addition, allelic loss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3c82348d3f0257ccfd0a79b51471209
https://pubmed.ncbi.nlm.nih.gov/8639909
https://pubmed.ncbi.nlm.nih.gov/8639909