-
1
-
-
0027243501
-
Finding genes that cause human hypertension
-
Lifton, R. P. & Jeunemaitre, X. Finding genes that cause human hypertension. J. Hypertension 11, 231-236 (1993).
-
(1993)
J. Hypertension
, vol.11
, pp. 231-236
-
-
Lifton, R.P.1
Jeunemaitre, X.2
-
2
-
-
0026608764
-
Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus
-
Froguel, P. et al. Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus. Nature 356, 162-164 (1992).
-
(1992)
Nature
, vol.356
, pp. 162-164
-
-
Froguel, P.1
-
3
-
-
0027472126
-
Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus
-
Froguel, P. et al. Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus. New Engl. J. Med. 328, 697-701 (1993).
-
(1993)
New Engl. J. Med
, vol.328
, pp. 697-701
-
-
Froguel, P.1
-
4
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki, Y. et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 266, 66-71 (1994).
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
-
5
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
Fishel, R. et al. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell 75, 1027-1038 (1993).
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.1
-
6
-
-
0027145633
-
Mutations of a MutS homolog in hereditary nonpolyposis colorectal cancer
-
Leach, F. S. et al. Mutations of a MutS homolog in hereditary nonpolyposis colorectal cancer. Cell 75, 1215-1225 (1993).
-
(1993)
Cell
, vol.75
, pp. 1215-1225
-
-
Leach, F.S.1
-
7
-
-
0028350601
-
Mutation of a mutL homolog in hereditary colon cancer
-
Papadopoulos, N. et al. Mutation of a mutL homolog in hereditary colon cancer. Science 263, 1625-1629 (1994).
-
(1994)
Science
, vol.263
, pp. 1625-1629
-
-
Papadopoulos, N.1
-
8
-
-
0026919361
-
Hereditary hypertension caused by chimeric gene duplications and ectopic expression of aldosterone synthase
-
Lifton, R. P. et al. Hereditary hypertension caused by chimeric gene duplications and ectopic expression of aldosterone synthase. Nature Genet. 2, 66-74 (1992).
-
(1992)
Nature Genet
, vol.2
, pp. 66-74
-
-
Lifton, R.P.1
-
9
-
-
0026580019
-
A chimaeric 11b-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton, R. P. et al. A chimaeric 11b-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
-
10
-
-
0027946089
-
Liddle's syndrome: Heritable human hypertension caused by mutations in the subunit of the epithelial sodium channel
-
Shimkets, R. A. et al. Liddle's syndrome: heritable human hypertension caused by mutations in the subunit of the epithelial sodium channel. Cell. 79, 407-414 (1994).
-
(1994)
Cell
, vol.79
, pp. 407-414
-
-
Shimkets, R.A.1
-
11
-
-
0001182641
-
A familial renal disorder simulating primary aldosteronism but with negligible aldosterone secretion
-
Liddle, G. W., Bledsoe, T. & Coppage, W. S. A familial renal disorder simulating primary aldosteronism but with negligible aldosterone secretion. Trans. Amer. Assoc. Phys. 76, 199-213 (1963).
-
(1963)
Trans. Amer. Assoc. Phys
, vol.76
, pp. 199-213
-
-
Liddle, G.W.1
Bledsoe, T.2
Coppage, W.S.3
-
12
-
-
0027483065
-
Epithelial sodium channel related to proteins involved in neurodegeneration
-
Canessa, C. M., Horisberger, J.-D. & Rossier, B. C. Epithelial sodium channel related to proteins involved in neurodegeneration. Nature 361, 467-470 (1993).
-
(1993)
Nature
, vol.361
, pp. 467-470
-
-
Canessa, C.M.1
Horisberger, J.-D.2
Rossier, B.C.3
-
13
-
-
0027958441
-
Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits
-
Canessa, C. M. et al. Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits. Nature 367, 463-467 (1994).
-
(1994)
Nature
, vol.367
, pp. 463-467
-
-
Canessa, C.M.1
-
14
-
-
0028252575
-
Membrane topology of the epithelial sodium channel in intact cell
-
Canessa, C. M., Merillat, A.-M. & Rossier, B. C. Membrane topology of the epithelial sodium channel in intact cell. Amer. J. Physiol. 267, C1682-C1690 (1994).
-
(1994)
Amer. J. Physiol
, vol.267
, pp. C1682-C1690
-
-
Canessa, C.M.1
Merillat, A.-M.2
Rossier, B.C.3
-
15
-
-
0028332337
-
Biochemical analysis of the membrane topology of the amiloride-sensitive Na+ channel
-
Renard, S., Lingueglia, E., Voilley, N., Lazdunski, M. & Barbry, P. Biochemical analysis of the membrane topology of the amiloride-sensitive Na+ channel. J. biol. Chem. 269, 12981-12986 (1994).
-
(1994)
J. biol. Chem
, vol.269
, pp. 12981-12986
-
-
Renard, S.1
Lingueglia, E.2
Voilley, N.3
Lazdunski, M.4
Barbry, P.5
-
16
-
-
0029046975
-
A mutation in the epithelial sodium channel causing Liddle's disease increases channel activity in the Xenopus laevis ooocyte expression system
-
Schild, L. et al. A mutation in the epithelial sodium channel causing Liddle's disease increases channel activity in the Xenopus laevis ooocyte expression system. Proc. natn. Acad. Sci. U. S. A. 92, 5699-5703 (1995).
-
(1995)
Proc. natn. Acad. Sci. U.S.A
, vol.92
, pp. 5699-5703
-
-
Schild, L.1
-
17
-
-
0023976822
-
A case of Liddle's syndrome with familial occurrence. Nippon Naika Gakkai Zasshi
-
(Published in Japanese)
-
Fukutake, N. et al. A case of Liddle's syndrome with familial occurrence. Nippon Naika Gakkai Zasshi-J. Jap. Soc. Int. Med. 77, 441-442 (1988) (Published in Japanese).
-
(1988)
J. Jap. Soc. Int. Med
, vol.77
, pp. 441-442
-
-
Fukutake, N.1
-
18
-
-
0038611639
-
Inherited forms of mineralocorticoid hypertension: Glucocorticoid-remediable aldosteronism and the syndrome of apparent mineralocorticoid excess
-
Laragh, J. & Brenner, B.M.) (Raven Press, New York
-
Lifton, R. P. & Dluhy, R. G. Inherited forms of mineralocorticoid hypertension: Glucocorticoid-remediable aldosteronism and the syndrome of apparent mineralocorticoid excess. in Hypertension: Pathophysiology, Diagnosis and Management (eds Laragh, J. & Brenner, B. M.) 2163-2176 (Raven Press, New York, 1995).
-
(1995)
Hypertension: Pathophysiology, Diagnosis and Management
, pp. 2163-2176
-
-
Lifton, R.P.1
Dluhy, R.G.2
-
19
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms
-
Orita, M., Iwahana, H., Kanazawa, H., Hayashi, K. & Sekiya, T. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms. Proc. natn. Acad. Sci. U. S. A. 86, 2766-2770 (1989).
-
(1989)
Proc. natn. Acad. Sci. U.S.A
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
20
-
-
0027723477
-
A first-generation physical map of the human genome
-
Cohen, D., Chumakov, I. & Weissenbach, J. A first-generation physical map of the human genome. Nature 366, 698-701 (1993).
-
(1993)
Nature
, vol.366
, pp. 698-701
-
-
Cohen, D.1
Chumakov, I.2
Weissenbach, J.3
-
21
-
-
0029160972
-
Human hypertension caused by mutations in the kidney isozyme of 11-hydroxysteroid dehydrogenase
-
Mune, T., Regerson, F. M., Nikkila, H., Agarwal, A. K. & White, P. C. Human hypertension caused by mutations in the kidney isozyme of 11-hydroxysteroid dehydrogenase. Nature Genet. 10, 394-399 (1995).
-
(1995)
Nature Genet
, vol.10
, pp. 394-399
-
-
Mune, T.1
Regerson, F.M.2
Nikkila, H.3
Agarwal, A.K.4
White, P.C.5
-
22
-
-
0026669336
-
Molecular basis of human hypertension: Role of Angiotensinogen
-
Jeunemaitre, X. et al. Molecular basis of human hypertension: Role of Angiotensinogen. Cell 71, 169-180 (1992).
-
(1992)
Cell
, vol.71
, pp. 169-180
-
-
Jeunemaitre, X.1
-
23
-
-
0000023099
-
Attachment of a 40-base-pair G+C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single base changes
-
Sheffield, V., Cox, D. R., Lerman, L. S. & Myers, R. M. Attachment of a 40-base-pair G+C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single base changes. Proc. natn. Acad. Sci. U. S. A. 86, 232-236 (1989).
-
(1989)
Proc. natn. Acad. Sci. U.S.A
, vol.86
, pp. 232-236
-
-
Sheffield, V.1
Cox, D.R.2
Lerman, L.S.3
Myers, R.M.4
-
24
-
-
0019287863
-
The molecular genetics of human hemoglobins
-
Maniatis, T., Fritsch, E. F., Lauer, J. & Lawn, R. M. The molecular genetics of human hemoglobins. A. Rev. Genet. 14, 145-178 (1980).
-
(1980)
A. Rev. Genet
, vol.14
, pp. 145-178
-
-
Maniatis, T.1
Fritsch, E.F.2
Lauer, J.3
Lawn, R.M.4
-
25
-
-
0344267589
-
Pigments and inherited variation in human vision
-
Nathans, J., Sung, C.-H., Weitz, C. J. & Davenport, C. M. Pigments and inherited variation in human vision. J. gen. Physiol. 47, 110-131 (1992).
-
(1992)
J. gen. Physiol
, vol.47
, pp. 110-131
-
-
Nathans, J.1
Sung, C.-H.2
Weitz, C.J.3
Davenport, C.M.4
-
26
-
-
0027249921
-
A gene differentially expressed in the kidney of the spontaneously hypertensive rat cosegregates with increased blood pressure
-
Samani, N. J. et al. A gene differentially expressed in the kidney of the spontaneously hypertensive rat cosegregates with increased blood pressure. J. clin. Invest. 92, 1099-1103 (1993).
-
(1993)
J. clin. Invest
, vol.92
, pp. 1099-1103
-
-
Samani, N.J.1
-
27
-
-
0027336532
-
SA gene and blood pressure cosegregation using Dahl salt-sensitive rats
-
Harris, E. L., Dene, H. & Rapp, J. P. SA gene and blood pressure cosegregation using Dahl salt-sensitive rats. J. Hypertension 6, 330-334 (1993).
-
(1993)
J. Hypertension
, vol.6
, pp. 330-334
-
-
Harris, E.L.1
Dene, H.2
Rapp, J.P.3
-
28
-
-
0027336444
-
Molecular genetics of the SA-gene: Cosegregation with hypertension and mapping to rat chromsome 1
-
Lindpaintner, K. et al. Molecular genetics of the SA-gene: cosegregation with hypertension and mapping to rat chromsome 1. J. Hypertension 11, 19-23 (1993).
-
(1993)
J. Hypertension
, vol.11
, pp. 19-23
-
-
Lindpaintner, K.1
-
29
-
-
0028900806
-
Evaluation of the SA locus in human hypertension
-
Nabika, T. et al. Evaluation of the SA locus in human hypertension. Hypertension. 25, 6-13 (1995).
-
(1995)
Hypertension
, vol.25
, pp. 6-13
-
-
Nabika, T.1
-
30
-
-
0023555546
-
Cosmid vectors for genomic walking and rapid restriction mapping
-
Evans, G. A. & Wahl, G. M. Cosmid vectors for genomic walking and rapid restriction mapping. Meth. Enzymol. 152, 604-610 (1987).
-
(1987)
Meth. Enzymol
, vol.152
, pp. 604-610
-
-
Evans, G.A.1
Wahl, G.M.2
-
31
-
-
0025146957
-
Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: Identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene
-
Hata, A., Robertson, M., Emi, M. & Lalouel, J.-M. Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene. Nucl. Acids Res. 18, 5407-5411 (1990).
-
(1990)
Nucl. Acids Res
, vol.18
, pp. 5407-5411
-
-
Hata, A.1
Robertson, M.2
Emi, M.3
Lalouel, J.-M.4
-
32
-
-
0028231090
-
The 1993-94 Généthon human genetic linkage map
-
Gyapay, G. et al. The 1993-94 Généthon human genetic linkage map. Nature Genet. 7, 246-339 (1994).
-
(1994)
Nature Genet
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
-
33
-
-
0345128844
-
Polymorphic DNA region adjacent to the 5' end of the human insulin gene
-
Bell, G., Karam, J. & Rutter, W. Polymorphic DNA region adjacent to the 5' end of the human insulin gene. Proc. natn. Acad. Sci. U. S. A. 78, 5759-5763 (1981).
-
(1981)
Proc. natn. Acad. Sci. U.S.A
, vol.78
, pp. 5759-5763
-
-
Bell, G.1
Karam, J.2
Rutter, W.3
-
34
-
-
0003903343
-
-
Cold Spring Harbor Laboratories, Cold Spring Harbor
-
Sambrook, J., Fritsch, E. F. & Maniatis, T. Molecular Cloning: A Laboratory Manual. Cold Spring Harbor Laboratories, Cold Spring Harbor, 1989.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
35
-
-
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. natn. Acad. Sci. U. S. A. 81, 3443-3446 (1984).
-
(1984)
Proc. natn. Acad. Sci. U.S.A
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
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