Výsledky vyhledávání - "Mansour Alemi"

Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcript

Autor: Alice Wong, Alessandro Prigione, Gino A Cortopassi, Robert Schoenfeld, Franco Taroni, Mansour Alemi, Salvatore DiMauro, Michio Hirano

Publikováno v: Free Radical Biology and Medicine. 42:32-43

Deletions within the mitochondrial DNA (mtDNA) cause Kearns Sayre syndrome (KSS) and chronic progressive external opthalmoplegia (CPEO). The clinical signs of KSS include muscle weakness, heart block, pigmentary retinopathy, ataxia, deafness, short s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87ea1c3dc350e904e6198445e2eb5b4c
https://doi.org/10.1016/j.freeradbiomed.2006.09.014

Zobrazit plný text záznamu

Rapid Test for Identification of a Human Papillomavirus 16 E6 L83V Variant

Autor: Erik Wilander, Mansour Alemi, Sonja Andersson, Jan Sällström

Publikováno v: Diagnostic Molecular Pathology. 8:97-100

A variant of human papillomavirus (HPV) 16 has been shown recently to be more prevalent in invasive cervical carcinoma than in preinvasive lesions. This HPV 16 variant possesses a common mutation (T to G) in nucleotide 350 (codon 83) of the E6 gene,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4aff75c4656489ae62c0a4e1855e6bc8
https://doi.org/10.1097/00019606-199906000-00006

Zobrazit plný text záznamu

Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts

Autor: Sangot Marzuki, Mansour Alemi, Steven R. Danielson, Warren Tong, Valerio Carelli, Alice Wong, Kari Majamaa, Andrea Martinuzzi, Gino A Cortopassi, Shan Shan Zhan

Publikováno v: Mitochondrion. 6(4)

Mutations in gene products expressed in the mitochondrion cause a nuclear transcriptional response that leads to neurological disease. To examine the extent to which the transcriptional profile was shared among 5 mitochondrial diseases (LHON, FRDA, M

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f24b357083e6634a7ca762ef5163b988
https://pubmed.ncbi.nlm.nih.gov/16815102

Zobrazit plný text záznamu

A complex nine base pair deletion in RET exon 11 common in sporadic medullary thyroid carcinoma

Autor: Steven D. Lucas, Göran Åkerström, J. Sällström, Mansour Alemi, Ulla Bergholm, Erik Wilander

Publikováno v: Oncogene. 14(17)

Genetic alteration of the RET proto-oncogene is associated with multiple endocrine neoplasia type 2A and 2B (MEN 2A and MEN 2B), familial medullary thyroid carcinoma (FMTC) and Hirschprung's disease. Oncogenically activated RET has also been demonstr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03c02a3aa8c8406b7871cf2a8ea61b81
https://pubmed.ncbi.nlm.nih.gov/9160884

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání