-
1
-
-
0020673352
-
Plasma catecholamines and essential hypertension: An analytical review
-
Goldstein DSK. Plasma catecholamines and essential hypertension: an analytical review. Hypertension. 1983;5:86-99.
-
(1983)
Hypertension
, vol.5
, pp. 86-99
-
-
Goldstein, D.S.K.1
-
2
-
-
0022369972
-
Urinary calecholamines in essential hypertension: Results of 24-hour urine catecholamine analyses from patients in the Medical Research Council Trial for mild hypertension and from matched controls
-
Brown MJ, Causon RC, Barnes VF, Brennan P, Barnes G, Greenberg G. Urinary calecholamines in essential hypertension: results of 24-hour urine catecholamine analyses from patients in the Medical Research Council Trial for mild hypertension and from matched controls. Q J Med. 1985; 57:637-651.
-
(1985)
Q J Med
, vol.57
, pp. 637-651
-
-
Brown, M.J.1
Causon, R.C.2
Barnes, V.F.3
Brennan, P.4
Barnes, G.5
Greenberg, G.6
-
3
-
-
0023490535
-
Isolation and characterization of the human tyrosine hydroxylase gene: Identification of 5′ alternative splice sites responsible for multiple mRNAs
-
O'Malley KL, Anhalt MJ, Martin BM, Kelsoe JR, Winfield SL, Ginns EI. Isolation and characterization of the human tyrosine hydroxylase gene: identification of 5′ alternative splice sites responsible for multiple mRNAs. Biochemistry. 1987;26:6910-6914.
-
(1987)
Biochemistry
, vol.26
, pp. 6910-6914
-
-
O'Malley, K.L.1
Anhalt, M.J.2
Martin, B.M.3
Kelsoe, J.R.4
Winfield, S.L.5
Ginns, E.I.6
-
4
-
-
0023265418
-
A single human gene encoding multiple tyrosine hydroxylases with different predicted functional characteristics
-
Grima B, Lamouroux A, Boni C, Julien J, Javoy AF, Mallet J. A single human gene encoding multiple tyrosine hydroxylases with different predicted functional characteristics. Nature. 1987;326:707-711.
-
(1987)
Nature
, vol.326
, pp. 707-711
-
-
Grima, B.1
Lamouroux, A.2
Boni, C.3
Julien, J.4
Javoy, A.F.5
Mallet, J.6
-
5
-
-
0028912476
-
Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development
-
Zhou Q, Qualfe CJ, Palmiter RD. Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development. Nature. 1995;374:640-643.
-
(1995)
Nature
, vol.374
, pp. 640-643
-
-
Zhou, Q.1
Qualfe, C.J.2
Palmiter, R.D.3
-
6
-
-
0025872852
-
Tissue-specific and high-level expression of the human tyrosine hydroxylase gene in transgenic mice
-
Kaneda N, Sasaoka T, Kobayashi K, Kiuchi K, Nagatsu I, Kurosawa Y, Fujita K, Yokoyama M, Nomura T, Katsuki M, Nagatsu T. Tissue-specific and high-level expression of the human tyrosine hydroxylase gene in transgenic mice. Neuron. 1991;6:583-594.
-
(1991)
Neuron
, vol.6
, pp. 583-594
-
-
Kaneda, N.1
Sasaoka, T.2
Kobayashi, K.3
Kiuchi, K.4
Nagatsu, I.5
Kurosawa, Y.6
Fujita, K.7
Yokoyama, M.8
Nomura, T.9
Katsuki, M.10
Nagatsu, T.11
-
7
-
-
0025821074
-
Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene
-
Abstract
-
Polymeropoulos MH, Xiao H, Rath DS, Merril CR. Tetranucleotide repeat polymorphism at the human tyrosine hydroxylase gene. Nucleic Acids Res. 1991;19:3753. Abstract.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 3753
-
-
Polymeropoulos, M.H.1
Xiao, H.2
Rath, D.S.3
Merril, C.R.4
-
8
-
-
0028938495
-
Association of manic-depressive illness with tyrosine hydroxylase microsatellite marker
-
Letter
-
Meloni R, Leboyer M, Bellivier F, Barbe B, Samolyk D, Allilaire JF, Mallet J. Association of manic-depressive illness with tyrosine hydroxylase microsatellite marker. Lancet. 1995;345:932. Letter.
-
(1995)
Lancet
, vol.345
, pp. 932
-
-
Meloni, R.1
Leboyer, M.2
Bellivier, F.3
Barbe, B.4
Samolyk, D.5
Allilaire, J.F.6
Mallet, J.7
-
9
-
-
0029062529
-
Frequent sequence variant in the human tyrosine hydroxylase gene
-
Ludecke B, Bartholome K. Frequent sequence variant in the human tyrosine hydroxylase gene. Hum Genet. 1995;95:716.
-
(1995)
Hum Genet
, vol.95
, pp. 716
-
-
Ludecke, B.1
Bartholome, K.2
-
10
-
-
0026080111
-
A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies
-
Lahiri DK, Nurnberger JI. A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies. Nucleic Acids Res. 1991;19:5444.
-
(1991)
Nucleic Acids Res
, vol.19
, pp. 5444
-
-
Lahiri, D.K.1
Nurnberger, J.I.2
-
11
-
-
0019835136
-
Determination of a-methyldopa, a-methylnoradrenaline, noradrenaline and adrenaline in plasma high performance liquid chromatography with electrochemical detection
-
Jenner DA, Brown MJ, Lhoute FJM. Determination of a-methyldopa, a-methylnoradrenaline, noradrenaline and adrenaline in plasma high performance liquid chromatography with electrochemical detection. J Chromatogr. 1981;224:507-512.
-
(1981)
J Chromatogr
, vol.224
, pp. 507-512
-
-
Jenner, D.A.1
Brown, M.J.2
Lhoute, F.J.M.3
-
12
-
-
0020555508
-
Estimating genotype relative risk
-
Lathrop GM. Estimating genotype relative risk. Tissue Antigens. 1983; 22:160-166.
-
(1983)
Tissue Antigens
, vol.22
, pp. 160-166
-
-
Lathrop, G.M.1
-
13
-
-
0028832203
-
Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers
-
Holmans P, Clayton D. Efficiency of typing unaffected relatives in an affected-sib-pair linkage study with single-locus and multiple tightly linked markers. Am J Hum Genet. 1995;57:1221-1232.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1221-1232
-
-
Holmans, P.1
Clayton, D.2
-
14
-
-
0027946089
-
Liddle's syndrome: Heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel
-
Shimkets RA, Warnock DG, Bositis CM, Nelson-Williams C, Hansson JH, Schambelan M, Gill JR, Ulick S, Milora RV, Findling JW, Canessa CM, Rossier BC, Lifton RP. Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel. Cell. 1994;79:407-414.
-
(1994)
Cell
, vol.79
, pp. 407-414
-
-
Shimkets, R.A.1
Warnock, D.G.2
Bositis, C.M.3
Nelson-Williams, C.4
Hansson, J.H.5
Schambelan, M.6
Gill, J.R.7
Ulick, S.8
Milora, R.V.9
Findling, J.W.10
Canessa, C.M.11
Rossier, B.C.12
Lifton, R.P.13
-
15
-
-
0029092801
-
Hypertension caused by a truncated epithelial sodium channel gamma subunit: Genetic heterogeneity of Liddle syndrome
-
Hansson JH, Nelson-Williams C, Suzuki H, Schild L, Shimkets R, Lu Y, Canessa C, Iwasaki T, Rossier B, Lifton RP. Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome. Nat Genet. 1995;11:76-82.
-
(1995)
Nat Genet
, vol.11
, pp. 76-82
-
-
Hansson, J.H.1
Nelson-Williams, C.2
Suzuki, H.3
Schild, L.4
Shimkets, R.5
Lu, Y.6
Canessa, C.7
Iwasaki, T.8
Rossier, B.9
Lifton, R.P.10
-
16
-
-
0026580019
-
A chimaeric 11b-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton RP, Dluhy RG, Powers M, Rich GM, Cook S, Ulick S. Lalouel J. A chimaeric 11b-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature. 1992;355:262-265.
-
(1992)
Nature
, vol.355
, pp. 262-265
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, G.M.4
Cook, S.5
Ulick, S.6
Lalouel, J.7
-
17
-
-
0029160972
-
Human hypertension caused by mutations in the kidney isozyme of 11b-hydroxysteroid dehydrogenase
-
Mune T, Rogerson FM, Nikkila H, Agarwal AK, White PC. Human hypertension caused by mutations in the kidney isozyme of 11b-hydroxysteroid dehydrogenase. Nat Genet. 1995;10:394-399.
-
(1995)
Nat Genet
, vol.10
, pp. 394-399
-
-
Mune, T.1
Rogerson, F.M.2
Nikkila, H.3
Agarwal, A.K.4
White, P.C.5
-
18
-
-
0028999853
-
Insulin gene region-encoded susceptibility to IDDM maps upstream of the insulin gene
-
Undlien DE, Bennett ST, Todd JA, Akselsen HE, Ikaheimo I, Reijonen H, Knip M, Thorsby E, Ronningen KS. Insulin gene region-encoded susceptibility to IDDM maps upstream of the insulin gene. Diabetes. 1995;44: 620-625.
-
(1995)
Diabetes
, vol.44
, pp. 620-625
-
-
Undlien, D.E.1
Bennett, S.T.2
Todd, J.A.3
Akselsen, H.E.4
Ikaheimo, I.5
Reijonen, H.6
Knip, M.7
Thorsby, E.8
Ronningen, K.S.9
-
19
-
-
0029124966
-
The angiotensin converting enzyme gene in cardiovascular disease
-
Caulfield M, Newell-Price J. The angiotensin converting enzyme gene in cardiovascular disease. Br Heart J. 1995;74:207-208.
-
(1995)
Br Heart J
, vol.74
, pp. 207-208
-
-
Caulfield, M.1
Newell-Price, J.2
-
20
-
-
0029919236
-
Genes for ischaemic stroke: Strategies for their detection
-
Sharma P. Genes for ischaemic stroke: strategies for their detection. J Hypertens. 1996;14:277-285.
-
(1996)
J Hypertens
, vol.14
, pp. 277-285
-
-
Sharma, P.1
-
22
-
-
0018899616
-
Genetic influences on plasma and urinary norepinephrine after volume expansion and contraction in normal men
-
Miller JZ, Luft FC, Grim CE. Genetic influences on plasma and urinary norepinephrine after volume expansion and contraction in normal men. J Clin Endocrinol Metab. 1980;50:219-222.
-
(1980)
J Clin Endocrinol Metab
, vol.50
, pp. 219-222
-
-
Miller, J.Z.1
Luft, F.C.2
Grim, C.E.3
-
23
-
-
0028871202
-
Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisalellite locus
-
Bennett ST, Lucassen AM, Gough SCL, Powell EE, Undlien DE, Pritchard LE, Merriman ME, Kawaguchi Y, Dronsfield MJ, Pociot F, Nerup J, Bouzekri N, Cambon-Thomsen A, Ronningen KS, Barnett AH, Bain SC, Todd JA. Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisalellite locus. Nat Genet. 1995;9:284-292.
-
(1995)
Nat Genet
, vol.9
, pp. 284-292
-
-
Bennett, S.T.1
Lucassen, A.M.2
Gough, S.C.L.3
Powell, E.E.4
Undlien, D.E.5
Pritchard, L.E.6
Merriman, M.E.7
Kawaguchi, Y.8
Dronsfield, M.J.9
Pociot, F.10
Nerup, J.11
Bouzekri, N.12
Cambon-Thomsen, A.13
Ronningen, K.S.14
Barnett, A.H.15
Bain, S.C.16
Todd, J.A.17
-
24
-
-
0029908532
-
The causes of essential hypertension
-
Brown MJ. The causes of essential hypertension. Br J Clin Pharmacol. 1996;42:21-27.
-
(1996)
Br J Clin Pharmacol
, vol.42
, pp. 21-27
-
-
Brown, M.J.1
-
25
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K. The future of genetic studies of complex human diseases. Science. 1996;273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
26
-
-
0031058841
-
Genetic analysis of complex diseases
-
Risch N, Merikangas K. Genetic analysis of complex diseases. Science. 1997;275:1329-1330.
-
(1997)
Science
, vol.275
, pp. 1329-1330
-
-
Risch, N.1
Merikangas, K.2
|