Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Protein Phosphatase 2/genetics"'
Autor:
de Jager, Vincent D, de Visscher, Sebastiaan A H J, Schuuring, Ed, Doff, Jan J, van Kempen, Léon C
Publikováno v:
GENES CHROMOSOMES & CANCER, 62(5), 297-300. Wiley
Cribriform adenocarcinoma of salivary gland (CASG) is a rare, salivary gland tumor. In this report, we describe a case of CASG harboring a novel PPP2R2A::PRKD1 fusion. A 58-year-old female presented with an intraoral mass adjacent to the lower left t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26590d6d052d3cc9b94522764f07397e
https://doi.org/10.1002/gcc.23122
https://doi.org/10.1002/gcc.23122
Autor:
Joost van den Oord, Dirk Schadendorf, Kathleen Oros Klein, Alan Spatz, Per Henrik Edqvist, Léon C van Kempen, Mounib Elchebly, Anne Helbling-Leclerc, Anke A.F. Van Rijk, Fredrik Pontén, Marguerite Stass, Stefan Michiels, Celia M. T. Greenwood, James S. Wilmott, Margaret Redpath, Andreas I. Papadakis, Richard A. Scolyer, Anne Dumay, Jasper Wouters, Jean Feunteun, Philippe Dessen, Ghanem Elias Ghanem
Publikováno v:
Science Translational Medicine, 8(369):369ra177. AMER ASSOC ADVANCEMENT SCIENCE
Male gender is independently and significantly associated with poor prognosis in melanoma of all clinical stages. The biological underpinnings of this sex difference remain largely unknown, but we hypothesized that gene expression from gonosomes (sex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::616f4d3e202c258a02e0658aa4de24d1
https://research.rug.nl/en/publications/d2bc7fba-e07b-4524-b202-f741086ee033
https://research.rug.nl/en/publications/d2bc7fba-e07b-4524-b202-f741086ee033
ADA (alteration/deficiency in activation) 3 is a conserved component of several transcriptional adaptor and HAT (histone acetyltransferase) complexes that regulate RNA polymerase IImediated gene expression. Within the HAT complexes ADA3 is associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8880c89712d950450528cfd7b4f95cf
Publikováno v:
European journal of medical genetics. 53(5)
Intellectual disability (ID) comprises a vast collection of clinically diverse and genetically heterogeneous disorders characterized primarily by central nervous system defects of varying severity with or without additional dysmorphic, metabolic, neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e45a4b9b4b1c3b35b6d73273b922bb59
https://pubmed.ncbi.nlm.nih.gov/20601260
https://pubmed.ncbi.nlm.nih.gov/20601260