-
1
-
-
0027243501
-
Finding genes that cause human hypertension
-
Lifton, R.P & Jeunemaitre, X. Finding genes that cause human hypertension J. Hypertens. 11, 231-236 (1993).
-
(1993)
J. Hypertens.
, vol.11
, pp. 231-236
-
-
Lifton, R.P.1
Jeunemaitre, X.2
-
2
-
-
0015811064
-
Hereditary brachydactyly associated with hypertension
-
Bilginturan, N., Zileli, S., Karacadag, S. & Pirnar, T. Hereditary brachydactyly associated with hypertension J. Med Genet. 10, 253-259 (1973)
-
(1973)
J. Med Genet.
, vol.10
, pp. 253-259
-
-
Bilginturan, N.1
Zileli, S.2
Karacadag, S.3
Pirnar, T.4
-
3
-
-
0025006193
-
Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism
-
Ulick, S. et al. Defective fasciculata zone function as the mechanism of glucocorticoid-remediable aldosteronism. J Clin. Endocrinol Metab. 71, 1151-1157 (1990).
-
(1990)
J Clin. Endocrinol Metab.
, vol.71
, pp. 1151-1157
-
-
Ulick, S.1
-
4
-
-
0027052962
-
Glucocorticoid-remediable aldosteronism in a large kindred clinical spectrum and diagnosis using a characteristic biochemical phenotype
-
Rich, G M. et al Glucocorticoid-remediable aldosteronism in a large kindred clinical spectrum and diagnosis using a characteristic biochemical phenotype. Ann. Intern Med 116, 813-820 (1992).
-
(1992)
Ann. Intern Med
, vol.116
, pp. 813-820
-
-
Rich, G.M.1
-
5
-
-
0026580019
-
A chimaeric 11β-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton, R.P. et al. A chimaeric 11β-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature 355, 262-265 (1992)
-
(1992)
Nature
, vol.355
, pp. 262-265
-
-
Lifton, R.P.1
-
6
-
-
0027946089
-
Liddle's syndrome Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel
-
Shimkets, R A. et al. Liddle's syndrome Heritable human hypertension caused by mutations in the β subunit of the epithelial sodium channel Cell 79, 407-414 (1994).
-
(1994)
Cell
, vol.79
, pp. 407-414
-
-
Shimkets, R.A.1
-
7
-
-
0029092801
-
Hypertension caused by a truncated epithelial sodium channel γ subunit: Genetic heterogeneity of Liddle syndrom
-
Hansson, J.H. et al. Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndrom Nature Genet. 11,76-82 (1995).
-
(1995)
Nature Genet.
, vol.11
, pp. 76-82
-
-
Hansson, J.H.1
-
8
-
-
0002046250
-
Pseudohypoparathyroidism
-
(eds Scriver, C.R., Beaudet, A L , Sly, W.S. 6, Valle, D.) McGraw-Hill, New York
-
Spiegel, A.M. Pseudohypoparathyroidism. in The Metabolic Basis Of Inherited Disease. (eds Scriver, C.R., Beaudet, A L , Sly, W.S. 6, Valle, D.) 2013-2027 (McGraw-Hill, New York, 1989)
-
(1989)
The Metabolic Basis of Inherited Disease
, pp. 2013-2027
-
-
Spiegel, A.M.1
-
9
-
-
0028813978
-
Brachydactyly and mental retardation. An Albright hereditary osteodystrophy-like syndrome localized to 2q37
-
Wilson, L C. et al. Brachydactyly and mental retardation. an Albright hereditary osteodystrophy-like syndrome localized to 2q37. Am. J. Hum. Genet 56, 400-407 (1995).
-
(1995)
Am. J. Hum. Genet
, vol.56
, pp. 400-407
-
-
Wilson, L.C.1
-
10
-
-
0028963216
-
Differentiation of vascular smooth muscle cells and the regulation of protein kinase C-α
-
Haller, H , Lindschau, C., Quass, P., Distler, A. & Luft, F.C. Differentiation of vascular smooth muscle cells and the regulation of protein kinase C-α. Circ. Res 76, 21-29 (1995).
-
(1995)
Circ. Res
, vol.76
, pp. 21-29
-
-
Haller, H.1
Lindschau, C.2
Quass, P.3
Distler, A.4
Luft, F.C.5
-
11
-
-
0028923038
-
Parathyroid hormone-related peptide as a locally produced vasorelaxant: Regulation of its mRNA by hypertension in rats
-
Takahashi, K. et al. Parathyroid hormone-related peptide as a locally produced vasorelaxant: regulation of its mRNA by hypertension in rats. Biochem. Biophys. Res. Comm. 208, 447-455 (1995).
-
(1995)
Biochem. Biophys. Res. Comm.
, vol.208
, pp. 447-455
-
-
Takahashi, K.1
-
12
-
-
0028057743
-
Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene
-
Karaplis, A C. et al. Lethal skeletal dysplasia from targeted disruption of the parathyroid hormone-related peptide gene. Genes Dev. 8, 277-289 (1994).
-
(1994)
Genes Dev.
, vol.8
, pp. 277-289
-
-
Karaplis, A.C.1
-
13
-
-
0028231090
-
Genethon human genetic linkage map
-
Gyapay, G et al. Genethon human genetic linkage map Nature Genet 7, 246-339 (1994).
-
(1994)
Nature Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
-
14
-
-
0027080297
-
Application of automated DNA sizing technology for genotyping microsatellite loci
-
Ziegle, J. Application of automated DNA sizing technology for genotyping microsatellite loci. Genomics 14, 1026-1031 (1992)
-
(1992)
Genomics
, vol.14
, pp. 1026-1031
-
-
Ziegle, J.1
-
15
-
-
0000801438
-
A general simulation program for linkage analysis
-
abstr.
-
Weeks, D E , Ott, J & Lathrop, G.M A general simulation program for linkage analysis. Am. J. Hum Genet 47, A204 (abstr.) (1990)
-
(1990)
Am. J. Hum Genet
, vol.47
-
-
Weeks, D.E.1
Ott, J.2
Lathrop, G.M.3
-
16
-
-
0342499587
-
Strategies for multilocus linkage analysis in humans
-
Lathrop, G.M , Lalouel, J M , Julier, C & Ott, J. Strategies for multilocus linkage analysis in humans. Proc. Natl. Acad. Sci. USA 81, 3443-3446 (1984)
-
(1984)
Proc. Natl. Acad. Sci. USA
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
17
-
-
0027366195
-
Faster sequential genetic linkage computations
-
Cottingham, R.W Jr., Idury, R.M. & Schaffer, AA Faster sequential genetic linkage computations Am. J. Hum. Genet. 53, 252-263 (1993).
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 252-263
-
-
Cottingham Jr., R.W.1
Idury, R.M.2
Schaffer, A.A.3
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