Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Christine E, Boumah"'
Autor:
Nick Beaumont, Christine E. Boumah, Manickavasagam Sundaram, Carol E. Cass, Sylvia Y.M. Yao, Imogen Coe, Francis Y. P. Kwong, Anthony Davies, Mark Griffiths, Stephen A. Baldwin, James D. Young
Publikováno v:
Nature Medicine. 3:89-93
In most mammalian cells nucleoside uptake occurs primarily via broad-specificity, es (e, equilibrative; 5, sensitive to NBMPR inhibition) transporters that are potently inhibited by nitrobenzylthioinosine (NBMPR). These transporters are essential for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d7e2cbbc2f6fcd0755ffbfa1140e257
https://doi.org/10.1038/nm0197-89
https://doi.org/10.1038/nm0197-89
PTH regulates transcription of a number of genes involved in bone remodeling and calcium homeostasis. We have previously shown that the matrix metalloproteinase-13 (MMP-13) gene is induced by PTH in osteoblastic cells as a secondary response through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aaa5787e5d55d3f073ad3b068dcb51d
https://europepmc.org/articles/PMC2718752/
https://europepmc.org/articles/PMC2718752/
Autor:
Safia El-Samadi, Abdullah Alfadley, Christer Ullbro, Salma M. Wakil, Christine E. Boumah, Nujoud Al-Yousef, Kristian Thestrup-Pedersen, Brian F. Meyer, Svante Twetman
Publikováno v:
Acta dermato-venereologica. 86(1)
Papillon-Lefevre syndrome is an autosomal recessive disorder characterized by palmoplantar hyperkeratosis and aggressive periodontitis. The aim of the study was to identify underlying cathepsin C mutations in 39 subjects with Papillon-Lefevre syndrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3208863db3a0e0d34bf7357c40adda79
https://pubmed.ncbi.nlm.nih.gov/16585980
https://pubmed.ncbi.nlm.nih.gov/16585980
Publikováno v:
Progress in nucleic acid research and molecular biology. 80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89ed0df5dd01bcf294da559d266ba997
https://pubmed.ncbi.nlm.nih.gov/16164977
https://pubmed.ncbi.nlm.nih.gov/16164977
Publisher Summary Osteoblast activities are regulated, in a stage‐specific manner, by hormones including parathyroid hormone (PTH), (OH) 2 vitamin D 3 , estrogen, and glucocorticoids. Osteoblast differentiation is also regulated by cytokines and va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1ffc8717afb9c17e1d162c75ab5eaf7
https://doi.org/10.1016/s0079-6603(05)80007-8
https://doi.org/10.1016/s0079-6603(05)80007-8
Autor:
Oonagh Dowling, John A. Martignetti, Juliette Harris, Marc J. Glucksman, S. Bahabri, Kirtikant V. Sheth, Robert J. Desnick, S. Al Mayouf, Brian F. Meyer, Wafaa Al Sewairi, Christine E. Boumah, Marios Kambouris, W. Al Eid, Aida I. Al Aqeel
Publikováno v:
Nature genetics. 28(3)
The inherited osteolyses or 'vanishing bone' syndromes are a group of rare disorders of unknown etiology characterized by destruction and resorption of affected bones. The multicentric osteolyses are notable for interphalangeal joint erosions that mi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca37969d7627711afbde93c9982e4aba
https://pubmed.ncbi.nlm.nih.gov/11431682
https://pubmed.ncbi.nlm.nih.gov/11431682