Zobrazeno 1 - 10
of 322
pro vyhledávání: '"J Demaille"'
Autor:
M. Dupont, A. Goldsborough, T. Levayer, J. Savare, J.M. Rey, J.F. Rossi, J. Demaille, T. Lavabre-Bertrand
Publikováno v:
BioTechniques, Vol 33, Iss 1, Pp 158-164 (2002)
The detection of chimeric transcripts derived from aberrant chromosomal fusion events provides an exceptionally valuable tool for the diagnosis of leukemia. We have developed a simple, inexpensive, reproducible, and automated method to quantify RT-PC
Externí odkaz:
https://doaj.org/article/ff74b4025902406a8d1d7b94b62b9eb8
Autor:
Anne Girardet, Tal Anahory, Hervé Dechaud, Samir Hamamah, B. Hédon, Christine Coubes, M Claustres, J. Demaille
Publikováno v:
Molecular Human Reproduction. 9:421-427
We have developed a preimplantation genetic diagnosis (PGD) strategy for Duchenne muscular dystrophy (DMD) allowing the simultaneous amplification of four exons (6, 8, 28 and 32) of the dystrophin gene together with ZFX/ZFY genes for gender determina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e47d0f8d20195745f03909426fd67416
https://doi.org/10.1093/molehr/gag050
https://doi.org/10.1093/molehr/gag050
Publikováno v:
American Journal of Medical Genetics Part A. :115-118
We have conducted a segregation analysis in order to characterise the transmission of Behcet Disease (BD), a multifactorial condition with a strong genetic component. Complete information about BD status and pedigree was obtained on 104 probands from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d23981b76a1273ff57087f9864b7904
https://doi.org/10.1002/ajmg.a.20136
https://doi.org/10.1002/ajmg.a.20136
Autor:
T. Lavabre-Bertrand, J. Demaille, J F Rossi, M. Dupont, T. Levayer, J M Rey, Andrew S. Goldsborough, J. Savare
Publikováno v:
BioTechniques. 33:158-164
The detection of chimeric transcripts derived from aberrant chromosomal fusion events provides an exceptionally valuable tool for the diagnosis of leukemia. We have developed a simple, inexpensive, reproducible, and automated method to quantify RT-PC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9940423cbee5a39f8b84094c732777f9
https://doi.org/10.2144/02331md04
https://doi.org/10.2144/02331md04
Publikováno v:
Cytogenetic and Genome Research. 89:85-88
In this report we present the analysis of two overlapping mouse cosmid clones that contain the entire Kcnk6, Map3k11 and Pcnxl3 genes, as well as part of the Sipa1 gene. The sequence and genomic organisation of the Kcnk6 and Map3k11 genes are describ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09bcedb245304d6d65e0af5095048307
https://doi.org/10.1159/000015569
https://doi.org/10.1159/000015569
Autor:
J. Demaille
Publikováno v:
Fundamental & Clinical Pharmacology. 4:15s-20s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::070d8f3637b3ed5c95287fd70266d19e
https://doi.org/10.1111/j.1472-8206.1990.tb00056.x
https://doi.org/10.1111/j.1472-8206.1990.tb00056.x
Autor:
B, Khadaroo, S, Robbens, C, Ferraz, E, Derelle, S, Eychenié, R, Cooke, G, Peaucellier, M, Delseny, J, Demaille, Y, Van de Peer, A, Picard, H, Moreau
Publikováno v:
Cell cycle (Georgetown, Tex.). 3(4)
The Cdc25 protein phosphatase is a key enzyme involved in the regulation of the G(2)/M transition in metazoans and yeast. However, no Cdc25 ortholog has so far been identified in plants, although functional studies have shown that an activating depho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb97928d21003e44e9280feebaa01c7c
https://pubmed.ncbi.nlm.nih.gov/15004533
https://pubmed.ncbi.nlm.nih.gov/15004533
Autor:
J. Demaille, Franck Pellestor, Brigitte Andréo, G. Régnier‐Vigouroux, J.P. Soulie, M. Baudouin, Tal Anahory
Publikováno v:
Molecular human reproduction. 9(10)
The incidence of chromosomal aneuploidy was analysed in 104 unfertilized human oocytes and 56 first polar bodies using a double-label fluorescence in-situ hybridization (FISH) procedure. Combinations of centromeric (or locus-specific) DNA probes and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdaf86004dc5173a58ad091eafb41080
https://pubmed.ncbi.nlm.nih.gov/12970395
https://pubmed.ncbi.nlm.nih.gov/12970395
Publikováno v:
American journal of medical genetics. Part A. (2)
We have conducted a segregation analysis in order to characterise the transmission of Behçet Disease (BD), a multifactorial condition with a strong genetic component. Complete information about BD status and pedigree was obtained on 104 probands fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::af88cca3a638d3855ee7f5b0549bcb4f
https://pubmed.ncbi.nlm.nih.gov/12955762
https://pubmed.ncbi.nlm.nih.gov/12955762
Autor:
Pierre Sarda, Anne Girardet, Hervé Dechaud, Tal Anahory, J. Demaille, M Claustres, B. Hédon, Samir Hamamah
Publikováno v:
Molecular human reproduction. 9(2)
Retinoblastoma is a malignant intra-ocular tumour of developing retina initiated by inactivation of both alleles of the retinoblastoma susceptibility (RB1) gene. This paper reports the first clinical experience of preimplantation genetic diagnosis (P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61a65e13765669def6471bca304a5688
https://pubmed.ncbi.nlm.nih.gov/12569181
https://pubmed.ncbi.nlm.nih.gov/12569181