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Results:
1-13
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Results: 13
Authors:
Roussanne, MC
Lieberherr, M
Souberbielle, JC
Sarfati, E
Drueke, T
Bourdeau, A
Citation: Mc. Roussanne et al., Human parathyroid cell proliferation in response to calcium, NPS R-467, calcitriol and phosphate, EUR J CL IN, 31(7), 2001, pp. 610-616
Authors:
Cho, SK
Bourdeau, A
Letarte, M
Zuniga-Pflucker, JC
Citation: Sk. Cho et al., Expression and function of CD105 during the onset of hematopoiesis from Flk1(+) precursors, BLOOD, 98(13), 2001, pp. 3635-3642
Authors:
Bourdeau, A
Faughnan, ME
McDonald, ML
Paterson, AD
Wanless, IR
Letarte, M
Citation: A. Bourdeau et al., Potential role of modifier genes influencing transforming growth factor-beta 1 levels in the development of vascular defects in endoglin heterozygousmice with hereditary hemorrhagic telangiectasia, AM J PATH, 158(6), 2001, pp. 2011-2020
Authors:
Bourdeau, A
Faughnan, ME
Letarte, M
Citation: A. Bourdeau et al., Endoglin-deficient mice, a unique model to study hereditary hemorrhagic telangiectasia, TREND CARD, 10(7), 2000, pp. 279-285
Authors:
Bourdeau, A
Letarte, M
Citation: A. Bourdeau et M. Letarte, Endoglin in the vascular and cardiovascular system, M S-MED SCI, 16(8-9), 2000, pp. 968-973
Authors:
Hory, BG
Roussanne, MC
Rostand, S
Bourdeau, A
Drueke, TB
Gogusev, J
Citation: Bg. Hory et al., Absence of response to human parathyroid hormone in athymic mice grafted with human parathyroid adenoma, hyperplasia or parathyroid cells maintained in culture, J ENDOC INV, 23(5), 2000, pp. 273-279
Apoptosis in parathyroid hyperplasia of patients with primary or secondaryuremic hyperparathyroidism
Authors:
Zhang, P
Duchambon, P
Gogusev, J
Nabarra, B
Sarfati, E
Bourdeau, A
Drueke, TB
Citation: P. Zhang et al., Apoptosis in parathyroid hyperplasia of patients with primary or secondaryuremic hyperparathyroidism, KIDNEY INT, 57(2), 2000, pp. 437-445
Authors:
Matsubara, S
Bourdeau, A
terBrugge, KG
Wallace, C
Letarte, M
Citation: S. Matsubara et al., Analysis of endoglin expression in normal brain tissue and in cerebral arteriovenous malformations, STROKE, 31(11), 2000, pp. 2653-2660
Authors:
Cymerman, U
Vera, S
Pece-Barbara, N
Bourdeau, A
White, RI
Dunn, J
Letarte, M
Citation: U. Cymerman et al., Identification of hereditary hemorrhagic telangiectasia type 1 in newbornsby protein expression and mutation analysis of endoglin, PEDIAT RES, 47(1), 2000, pp. 24-35
Authors:
Bourdeau, A
Cymerman, U
Paquet, ME
Meschino, W
McKinnon, WC
Guttmacher, AE
Becker, L
Letarte, M
Citation: A. Bourdeau et al., Endoglin expression is reduced in normal vessels but still detectable in arteriovenous malformations of patients with hereditary hemorrhagic telangiectasia type 1, AM J PATH, 156(3), 2000, pp. 911-923
Authors:
LeBel, C
Bourdeau, A
Lau, D
Hunt, P
Citation: C. Lebel et al., Biologic response to peripheral and central administration of recombinant human leptin in dogs, OBES RES, 7(6), 1999, pp. 577-585
Authors:
Roussanne, MC
Duchambon, P
Gogusev, J
Sarfati, E
Bourdeau, A
Drueke, TB
Citation: Mc. Roussanne et al., Parathyroid hyperplasia in chronic renal failure: role of calcium, phosphate, and calcitriol, NEPH DIAL T, 14, 1999, pp. 68-69
Authors:
Bourdeau, A
Dumont, DJ
Letarte, M
Citation: A. Bourdeau et al., A murine model of hereditary hemorrhagic telangiectasia, J CLIN INV, 104(10), 1999, pp. 1343-1351
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