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pro vyhledávání: '"R Perrichot"'
Akademický článek
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Autor:
B. Whebe, Isabelle Quéré, A. Carre, R Perrichot, Claude Férec, B. Mercier, J. Cledes, P.M. Simon
Publikováno v:
European Journal of Human Genetics. 8:353-359
Autosomal dominant polycystic kidney disease (ADPKD) exhibits a genetically heterogeneous transmission involving at least three different genes. PKD1 gene linked mutations are responsible for the disease in about 85% of ADPKD cases. The search for mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8eebff429c8b0edf5c1402f784738c04
https://doi.org/10.1038/sj.ejhg.5200459
https://doi.org/10.1038/sj.ejhg.5200459
Publikováno v:
Nephron. 87(4)
Autosomal/dominant polycystic kidney disease (ADPKD) exhibits a high inter- and intrafamilial heterogeneity partly explained by the involvement of at least 3 different genes in the disorder transmission. PKD1, the major locus, is located on chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::393328325990f4865c60b42cf26fa8d0
https://pubmed.ncbi.nlm.nih.gov/11287778
https://pubmed.ncbi.nlm.nih.gov/11287778
Publikováno v:
Human genetics. 105(3)
Autosomal dominant polycystic kidney disease (ADPKD) is one of the most commonly inherited renal diseases. ADPKD is a genetically heterogeneous disorder involving at least three different genes. PKD1, the major locus mapped to chromosome 16p13.3 acco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::325f190b65df0317b04881c18dbc6fe2
https://pubmed.ncbi.nlm.nih.gov/10987650
https://pubmed.ncbi.nlm.nih.gov/10987650
Publikováno v:
Human mutation. 15(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fe01c447e422c15dfcf0ef90f643df17
https://pubmed.ncbi.nlm.nih.gov/10862097
https://pubmed.ncbi.nlm.nih.gov/10862097
Publikováno v:
Presse medicale (Paris, France : 1983). 29(8)
OBJECTIVES OF SYMPTOMATIC TREATMENT: The goal is to maintain quality of life, prevent immediate complications (thromboembolic events, infection, drug reactions), prevent late complications related to atherosclerosis, and limit the progression of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7b0840bc1de7c6897210f5398338e603
https://pubmed.ncbi.nlm.nih.gov/10738512
https://pubmed.ncbi.nlm.nih.gov/10738512
Autor:
Dominique Latinne, J. Y. Muller, R. Perrichot, Magali Giral, P. Coville, Dominique Chevrier, Jean-Denis Bignon, J. P. Soulillou
Publikováno v:
Tissue antigens. 50(2)
In a previous study on the effects of TAP1 and TAP2 gene polymorphism in kidney allograft recipients, we found no association between graft outcome and recipient/donor TAP1 and TAP2 allele polymorphism or compatibility, but we observed a surprising i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a47422629e5054fc86ffea3d7f5417c7
https://pubmed.ncbi.nlm.nih.gov/9271826
https://pubmed.ncbi.nlm.nih.gov/9271826
Publikováno v:
The Biochemical journal. 312
The involvement of dopamine (DA) receptor subtypes in regulation of renal phosphate transport by DA, either exogenous or locally synthesized from L-dihydroxyphenylalanine (L-dopa) was evaluated in opossum kidney (OK) cells with proximal tubular pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a8e8478a2abe7f178bc8204c9ecaed7
https://pubmed.ncbi.nlm.nih.gov/8526852
https://pubmed.ncbi.nlm.nih.gov/8526852
Publikováno v:
Nephrologie. 15(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::967cf24eb87130937c65df9a6443d0d8
https://pubmed.ncbi.nlm.nih.gov/8047206
https://pubmed.ncbi.nlm.nih.gov/8047206
Akademický článek
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