Prati
Xavier JEUNEMAITRE
Xavier JEUNEMAITRE
Université Paris Descartes
Potvrđena adresa e-pošte na inserm.fr
Naslov
Citirano
Citirano
Godina
Molecular basis of human hypertension: role of angiotensinogen
X Jeunemaitre, F Soubrier, YV Kotelevtsev, RP Lifton, CS Williams, ...
Cell 71 (1), 169-180, 1992
25941992
The 2017 international classification of the Ehlers–Danlos syndromes
F Malfait, C Francomano, P Byers, J Belmont, B Berglund, J Black, ...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2017
17692017
Human hypertension caused by mutations in WNK kinases
FH Wilson, S Disse-Nicodeme, KA Choate, K Ishikawa, ...
Science 293 (5532), 1107-1112, 2001
16932001
Angiotensin II type 1 receptor gene polymorphisms in human essential hypertension.
A Bonnardeaux, E Davies, X Jeunemaitre, I Fery, A Charru, E Clauser, ...
Hypertension 24 (1), 63-69, 1994
12271994
Links between dietary salt intake, renal salt handling, blood pressure, and cardiovascular diseases
P Meneton, X Jeunemaitre, HE de Wardener, GA Macgregor
Physiological reviews 85 (2), 679-715, 2005
10072005
Genetic testing in pheochromocytoma or functional paraganglioma
L Amar, J Bertherat, E Baudin, C Ajzenberg, B Bressac-de Paillerets, ...
Journal of Clinical Oncology 23 (34), 8812-8818, 2005
8002005
SDHA is a tumor suppressor gene causing paraganglioma
N Burnichon, JJ Brière, R Libé, L Vescovo, J Rivière, F Tissier, E Jouanno, ...
Human molecular genetics 19 (15), 3011-3020, 2010
7832010
A nucleotide substitution in the promoter of human angiotensinogen is associated with essential hypertension and affects basal transcription in vitro.
I Inoue, T Nakajima, CS Williams, J Quackenbush, R Puryear, M Powers, ...
The Journal of clinical investigation 99 (7), 1786-1797, 1997
7331997
Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus
L Zhu, R Vranckx, PK Van Kien, A Lalande, N Boisset, F Mathieu, ...
Nature genetics 38 (3), 343-349, 2006
7152006
Clinical presentation and penetrance of pheochromocytoma/paraganglioma syndromes
DE Benn, AP Gimenez-Roqueplo, JR Reilly, J Bertherat, J Burgess, ...
The Journal of Clinical Endocrinology & Metabolism 91 (3), 827-836, 2006
7132006
Mutations in the SDHB Gene Are Associated with Extra-adrenal and/or Malignant Phaeochromocytomas
AP Gimenez-Roqueplo, J Favier, P Rustin, C Rieubland, M Crespin, ...
Cancer research 63 (17), 5615-5621, 2003
6752003
A molecular variant of angiotensinogen associated with preeclampsia
K Ward, A Hata, X Jeunemaitre, C Helin, L Nelson, C Namikawa, ...
Nature genetics 4 (1), 59-61, 1993
6591993
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension
F Beuschlein, S Boulkroun, A Osswald, T Wieland, HN Nielsen, ...
Nature genetics 45 (4), 440-444, 2013
5802013
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension
X Jeunemaitre, RP Lifton, SC Hunt, RR Williams, JM Lalouel
Nature genetics 1 (1), 72-75, 1992
5701992
Succinate dehydrogenase B gene mutations predict survival in patients with malignant pheochromocytomas or paragangliomas
L Amar, E Baudin, N Burnichon, S Peyrard, S Silvera, J Bertherat, ...
The Journal of Clinical Endocrinology & Metabolism 92 (10), 3822-3828, 2007
5212007
Contribution of genetic polymorphism in the renin-angiotensin system to the development of renal complications in insulin-dependent diabetes: Genetique de la Nephropathie …
M Marre, X Jeunemaitre, Y Gallois, M Rodier, G Chatellier, C Sert, ...
The Journal of clinical investigation 99 (7), 1585-1595, 1997
4641997
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas
N Burnichon, V Rohmer, L Amar, P Herman, S Leboulleux, V Darrouzet, ...
The Journal of Clinical Endocrinology & Metabolism 94 (8), 2817-2827, 2009
4322009
The R22X mutation of the SDHD gene in hereditary paraganglioma abolishes the enzymatic activity of complex II in the mitochondrial respiratory chain and activates the hypoxia …
AP Gimenez-Roqueplo, J Favier, P Rustin, JJ Mourad, PF Plouin, ...
The American Journal of Human Genetics 69 (6), 1186-1197, 2001
4322001
First international consensus on the diagnosis and management of fibromuscular dysplasia
HL Gornik, A Persu, D Adlam, LS Aparicio, M Azizi, M Boulanger, ...
Vascular Medicine 24 (2), 164-189, 2019
4212019
Haplotypes of angiotensinogen in essential hypertension
X Jeunemaitre, I Inoue, C Williams, A Charru, J Tichet, M Powers, ...
The American Journal of Human Genetics 60 (6), 1448-1460, 1997
4201997
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