Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Anne-Marie Houot"'
Autor:
Anne-Marie Houot, Pierre Corvol, Sandra Disse-Nicodeme, Jean-Marie Gasc, Céline Delaloy, Xavier Jeunemaitre, Jingyu Lu
Publikováno v:
Molecular and Cellular Biology. 23:9208-9221
WNK1 is a serine-threonine kinase, the expression of which is affected in pseudohypoaldosteronism type II, a Mendelian form of arterial hypertension. We characterized human WNK1 transcripts to determine the molecular mechanisms governing WNK1 express
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d71d2150df850b66ceac806c1e83c02
https://doi.org/10.1128/mcb.23.24.9208-9221.2003
https://doi.org/10.1128/mcb.23.24.9208-9221.2003
Autor:
M. B. Barrault, Florence Pinet, Anne-Marie Houot, R. Della Bruna, Florent Soubrier, Bruno Corman, Jean-Baptiste Michel, C. Klingler
Publikováno v:
Mechanisms of Ageing and Development. 84:1-13
The activity of the renin-angiotensin system as well as the ability of the kidney to retain sodium following salt restriction are reduced with age. The relationship between these age-related changes in renal function and the renin gene expression was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7e4c26355e67f58a411f46c24ce77c2
https://doi.org/10.1016/0047-6374(95)01630-i
https://doi.org/10.1016/0047-6374(95)01630-i
Autor:
F. H. M. Derkx, Anne-Marie Houot, I. S. Van Hooft, Florence Pinet, Florent Soubrier, E. Villard, Pierre Corvol, J.-D. Lalau
Publikováno v:
Journal of Biological Chemistry. 269:30307-30312
A case of familial elevation of plasma prorenin levels was discovered during an epidemiological survey of a Dutch population. Trypsin-activated prorenin was elevated in the 58-year-old father, his son, and one of his sisters. All family members were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0c492a42c96b2fb30d1e35404174fc0
https://doi.org/10.1016/s0021-9258(18)43813-6
https://doi.org/10.1016/s0021-9258(18)43813-6
Publikováno v:
Biochemical and Biophysical Research Communications. 189:134-140
Polymerase chain amplification experiments indicate that the germinal specific promoter of the angiotensin I-converting enzyme (ACE) is completely extinguished in somatic tissues. Despite this very strict specificity of expression, the gerimnal ACE p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8fdbbd2d76c6a70707e78d11bcb44b6
https://doi.org/10.1016/0006-291x(92)91535-x
https://doi.org/10.1016/0006-291x(92)91535-x
Autor:
Anne-Marie Houot, Céline Delaloy, Maud Clemessy, Martine Imbert-Teboul, Xavier Jeunemaitre, Juliette Hadchouel
Publikováno v:
The American journal of pathology. 169(1)
Large deletions in WNK1 are associated with inherited arterial hypertension. WNK1 encodes two types of protein: a kidney-specific isoform (KS-WNK1) lacking kinase activity and a ubiquitously expressed full-length isoform (L-WNK1) with serine threonin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1a0fbce31f498cf262deb16538f78e8
https://pubmed.ncbi.nlm.nih.gov/16816365
https://pubmed.ncbi.nlm.nih.gov/16816365
Autor:
Béatrice Fiquet-Kempf, Jacky Potier, Isabelle Desitter, Michel Delahousse, Nora Stern, Jean-Louis Ader, Anne-Marie Houot, Sandra Disse-Nicodeme, Xavier Jeunemaitre
Publikováno v:
Journal of hypertension. 19(11)
Background Familial hyperkalaemic hypertension (FHH) is a Mendelian form of low-renin hypertension characterized by hyperkalaemia and hyperchloraemic acidosis despite a normal glomerular filtration rate. To date, three different loci have been identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0efd85401c024a23d8a5d6417f8c713c
https://pubmed.ncbi.nlm.nih.gov/11677360
https://pubmed.ncbi.nlm.nih.gov/11677360
Autor:
Jean-Yves Le Heuzey, Pierre Corvol, Alain Carpentier, Benoit Diebold, Alain Berrebi, Sandra Disse, Louis Guize, Xavier Jeunemaitre, Eric Abergel, Anne-Marie Houot
Publikováno v:
American journal of human genetics. 65(5)
Myxomatous mitral-valve prolapse (MMVP), also called Barlow disease, is a common cardiac abnormality and affects up to 5% of the population. It is characterized by an excess of tissue that leads to billowing of the mitral leaflets, sometimes complica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b74d9a21a0662dedac5e4883253292ce
https://pubmed.ncbi.nlm.nih.gov/10521288
https://pubmed.ncbi.nlm.nih.gov/10521288
Publikováno v:
Human genetics. 88(3)
Although essential arterial hypertension is believed to have a strong genetic predisposition, the gene(s) responsible are unknown. The mechanisms underlying the regulation of blood pressure and experimental studies place the renin gene among the main
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8269e3ac7a8f8a24f97d40fde16c2e7
https://pubmed.ncbi.nlm.nih.gov/1346386
https://pubmed.ncbi.nlm.nih.gov/1346386
Publikováno v:
The Journal of biological chemistry. 266(23)
Overlapping genomic clones containing the entire sequence of the human angiotensin I-converting enzyme (ACE) gene were isolated from a lamda phage human DNA library. This gene spans 21 kilobases (kb) and comprises 26 exons, ranging in size from 88 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b36fc25b9f297ecc14e246a67635b73
https://pubmed.ncbi.nlm.nih.gov/1651327
https://pubmed.ncbi.nlm.nih.gov/1651327
Autor:
François Cambien, Florent Soubrier, Pierre Corvol, B Rigat, Xavier Jeunemaitre, Anne-Marie Houot
Publikováno v:
Hypertension (Dallas, Tex. : 1979). 16(6)
A prospective study was conducted to compare the frequency of renin gene polymorphisms in normotensive and hypertensive subjects. Hypertensive (n = 102, blood pressure 168 +/- 17/103 +/- 9 mm Hg) and normotensive (n = 120, blood pressure 122 +/- 10/7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a00d2fd9ce910afc02fb4ced1d4f7ed
https://pubmed.ncbi.nlm.nih.gov/1978831
https://pubmed.ncbi.nlm.nih.gov/1978831