Výsledky vyhledávání - "Nathalie Burri"

Akademický článek

Complex Methylation Patterns Analyzed by Single-Strand Conformation Polymorphism

Autor: Nathalie Burri, Pascal Chaubert

Publikováno v: BioTechniques, Vol 26, Iss 2, Pp 232-234 (1999)

Externí odkaz: https://doaj.org/article/ca7d6dc2c8634bb197483a355063b6f7

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Frequent Methylation Silencing of p15INK4b(MTS2) and p16INK4a (MTS1) in B-Cell and T-Cell Lymphomas

Autor: Audrey S. Baur, Pascal Chaubert, Phil Shaw, Fred T. Bosman, Françoise Delacrétaz, Nathalie Burri

Publikováno v: Blood. 94:1773-1781

The methylation status of p15INK4b(MTS2), p16INK4a (MTS1) andp14ARF (p16β) was analyzed in 56 lymphomas by restriction-enzyme related polymerase chain reaction (PCR) (REP), methylation-specific PCR (MSP), and bisulfite genomic sequencing (BGS). Meth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68e8136944a4354cfe9ce7b8d26571b8
https://doi.org/10.1182/blood.v94.5.1773

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Consequences of Seven Novel Mutations on the Expression and Structure of Keratinocyte Transglutaminase

Autor: Amy S. Paller, Vivien C. Yee, Nathalie Burri, Marcel Huber, Adriana P.M. Lavrijsen, Eva Vikerfors, Daniel Hohl

Publikováno v: Journal of Biological Chemistry. 272:21018-21026

We report the molecular characterization of seven new keratinocyte transglutaminase mutations (R315C, S358R, V379L, G473S, R687C, deletion Delta679-696, R127Stop) found in lamellar ichthyosis patients. Arg-315, Ser-358, Val-379, and Gly-473 are highl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a9ca350ba55281f9b160d8c3da3c3b7
https://doi.org/10.1074/jbc.272.34.21018

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Methylation silencing and mutations of the p14ARF and p16INK4a genes in colon cancer

Autor: Michel Gillet, Pascal Chaubert, Bernard Sordat, Hanifa Bouzourene, Fred T. Bosman, Phillip Shaw, Nathalie Burri, Daniel F. Schorderet, Isabelle Sordat

Publikováno v: Laboratory investigation; a journal of technical methods and pathology. 81(2)

The INK4a-ARF locus encodes two tumor suppressor proteins involved in cell-cycle regulation, p16INK4a and p14ARF, whose functions are inactivated in many human cancers. The aim of this study was to evaluate p14ARF and p16INK4a gene inactivation and i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2aee373cb4af9edbb3d609aaa8253fe6
https://pubmed.ncbi.nlm.nih.gov/11232644

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