-
1
-
-
0000026508
-
-
Seriver, C.R., Beaudet, A.L., Sly, W.S. and Valle, D. (eds), New York, McGraw-Hill
-
Welsh, M.J., Tsui, L.-C., Boat, T.F. and Beaudet, A.L. (1995) In Seriver, C.R., Beaudet, A.L., Sly, W.S. and Valle, D. (eds), The Metabolic and Molecular Bases of Inherited Disease. New York, McGraw-Hill, Vol 3, pp.3799-3876.
-
(1995)
The Metabolic and Molecular Bases of Inherited Disease
, vol.3
, pp. 3799-3876
-
-
Welsh, M.J.1
Tsui, L.-C.2
Boat, T.F.3
Beaudet, A.L.4
-
2
-
-
0014411090
-
Reproductive failure in males with cystic fibrosis
-
Kaplan, E., Shwachman, H., Perlmutter, A.D., Rule, A., Khaw, K.T. and Holsclaw, D.S. (1968) Reproductive failure in males with cystic fibrosis. N. Engl. J. Med., 279, 65-69.
-
(1968)
N. Engl. J. Med.
, vol.279
, pp. 65-69
-
-
Kaplan, E.1
Shwachman, H.2
Perlmutter, A.D.3
Rule, A.4
Khaw, K.T.5
Holsclaw, D.S.6
-
3
-
-
0014673648
-
The vas deferens in cystic fibrosis
-
Valman, H.B. and France, N.E. (1969) The vas deferens in cystic fibrosis. Lancet, ii, 566-567.
-
(1969)
Lancet
, vol.2
, pp. 566-567
-
-
Valman, H.B.1
France, N.E.2
-
4
-
-
0014638684
-
Abnormality of the epididymis and vas deferens in cystic fibrosis
-
Landing, B.H., Wells, T.R. and Wang, C.-I. (1969) Abnormality of the epididymis and vas deferens in cystic fibrosis. Arch. Path., 88, 569-580.
-
(1969)
Arch. Path.
, vol.88
, pp. 569-580
-
-
Landing, B.H.1
Wells, T.R.2
Wang, C.-I.3
-
5
-
-
0015518771
-
Fertility in males with cystic fibrosis
-
Taussig, L.M., Lobeck, C.C., di Sant' Agnese, P.A., Ackerman, D.R. and Kattwinkel, J. (1972) Fertility in males with cystic fibrosis. N. Engl. J. Med., 287, 586-589.
-
(1972)
N. Engl. J. Med.
, vol.287
, pp. 586-589
-
-
Taussig, L.M.1
Lobeck, C.C.2
Di Sant' Agnese, P.A.3
Ackerman, D.R.4
Kattwinkel, J.5
-
6
-
-
0026562867
-
Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis
-
Anguiano, A., Oates, R.D., Amos, J.A., Dean, M., Gerrard, B., Stewart, C., Maher, T.A., White, M.B. and Milunsky, A. (1992) Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis. JAMA. 267, 1794-1797.
-
(1992)
JAMA
, vol.267
, pp. 1794-1797
-
-
Anguiano, A.1
Oates, R.D.2
Amos, J.A.3
Dean, M.4
Gerrard, B.5
Stewart, C.6
Maher, T.A.7
White, M.B.8
Milunsky, A.9
-
7
-
-
0027503539
-
Aetiology of congenital absence of vas deferens: Genetic study of three generations
-
Patrizio, P., Asch, R.H., Handelin, B. and Silber, SJ. (1993) Aetiology of congenital absence of vas deferens: genetic study of three generations. Hum. Reprod., 8, 215-220.
-
(1993)
Hum. Reprod.
, vol.8
, pp. 215-220
-
-
Patrizio, P.1
Asch, R.H.2
Handelin, B.3
Silber, S.J.4
-
8
-
-
0027438374
-
Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens
-
Osbome, L.R., Lynch, M., Middleton, P.G., Alton, E.W.F.W., Geddes, D.M., Pryor, J.P., Hodson, M.E. and Santis, G.K. (1993) Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferens. Hum. Mol. Genet., 2, 1605-1609.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1605-1609
-
-
Osbome, L.R.1
Lynch, M.2
Middleton, P.G.3
Alton, E.W.F.W.4
Geddes, D.M.5
Pryor, J.P.6
Hodson, M.E.7
Santis, G.K.8
-
9
-
-
0028281799
-
Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens
-
Culard, J.-F., Desgeorges, M., Costa, P., Laussel, M., Razakatzara, G., Navratil, H., Demaille, J. and Claustres, M. (1994) Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens. Hum. Genet., 93, 467-470.
-
(1994)
Hum. Genet.
, vol.93
, pp. 467-470
-
-
Culard, J.-F.1
Desgeorges, M.2
Costa, P.3
Laussel, M.4
Razakatzara, G.5
Navratil, H.6
Demaille, J.7
Claustres, M.8
-
10
-
-
0028069337
-
The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis
-
Oates, R.D. and Amos, J. A. (1994) The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis. J. Androl., 15, 1-8.
-
(1994)
J. Androl.
, vol.15
, pp. 1-8
-
-
Oates, R.D.1
Amos, J.A.2
-
11
-
-
0028794627
-
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients
-
Mercier, B., Verlingue, C., Lissens, W., Silber, S.J., Novelli, G., Bonduelle, M., Audrezet, M.P. and Ferec, C. (1995) Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients. Am. J. Hum. Genet., 56, 272-277.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 272-277
-
-
Mercier, B.1
Verlingue, C.2
Lissens, W.3
Silber, S.J.4
Novelli, G.5
Bonduelle, M.6
Audrezet, M.P.7
Ferec, C.8
-
12
-
-
0029025333
-
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
-
Chillon, M., Casals, T., Mercier, B., Bassas, L., Lissens, W., Silber, S., Romey, M.-C., Ruiz-Romero, J., Verlingue, C., Claustres, M., Nunes, V., Ferec, C. and Estivill, X. (1995) Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N. Engl. J. Med., 332, 1475-1480.
-
(1995)
N. Engl. J. Med.
, vol.332
, pp. 1475-1480
-
-
Chillon, M.1
Casals, T.2
Mercier, B.3
Bassas, L.4
Lissens, W.5
Silber, S.6
Romey, M.-C.7
Ruiz-Romero, J.8
Verlingue, C.9
Claustres, M.10
Nunes, V.11
Ferec, C.12
Estivill, X.13
-
13
-
-
0029151485
-
CFTR gene variant for patients with congenital absence of vas deferens
-
Zielenski, J., Patrizio, P., Corey, M., Handelin, B., Markiewicz, D., Asch, R. and Tsui, L.-C. (1995) CFTR gene variant for patients with congenital absence of vas deferens. Am. J. Hum. Genet., 57, 958-960.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 958-960
-
-
Zielenski, J.1
Patrizio, P.2
Corey, M.3
Handelin, B.4
Markiewicz, D.5
Asch, R.6
Tsui, L.-C.7
-
14
-
-
0028791190
-
Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens
-
Costes, B., Girodon, E., Ghanem, N., Flori, E., Jardin, A., Soufir, J.C. and Goossens, M. (1995) Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens. Eur. J. Hum. Genet., 3, 285-93.
-
(1995)
Eur. J. Hum. Genet.
, vol.3
, pp. 285-293
-
-
Costes, B.1
Girodon, E.2
Ghanem, N.3
Flori, E.4
Jardin, A.5
Soufir, J.C.6
Goossens, M.7
-
15
-
-
0029883879
-
Urogenital anomalies in men with congenital absence of the vas deferens
-
Schlegel, P.N., Shin, D. and Goldstein, M. (1996) Urogenital anomalies in men with congenital absence of the vas deferens. J. Urol., 155, 1644-1648.
-
(1996)
J. Urol.
, vol.155
, pp. 1644-1648
-
-
Schlegel, P.N.1
Shin, D.2
Goldstein, M.3
-
16
-
-
0031397371
-
The incidence of cystic fibrosis gene mutations in patients with congenital bilateral absence of the vas deferens in Scotland
-
Donat, R., McNeill, A.S., Fitzpatrick, D.R. and Hargreave, T.B. (1997) The incidence of cystic fibrosis gene mutations in patients with congenital bilateral absence of the vas deferens in Scotland. Br. J. Urol., 79, 74-77.
-
(1997)
Br. J. Urol.
, vol.79
, pp. 74-77
-
-
Donat, R.1
McNeill, A.S.2
Fitzpatrick, D.R.3
Hargreave, T.B.4
-
17
-
-
0029019461
-
Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia
-
Jarvi, K., Zielenski, J., Wilschanski, M., Durie, P., Buckspan, M., Tullis, E., Markiewicz, D. and Tsui, L.-C. (1995) Cystic fibrosis transmembrane conductance regulator and obstructive azoospermia. Lancet, 345, 1578.
-
(1995)
Lancet
, vol.345
, pp. 1578
-
-
Jarvi, K.1
Zielenski, J.2
Wilschanski, M.3
Durie, P.4
Buckspan, M.5
Tullis, E.6
Markiewicz, D.7
Tsui, L.-C.8
-
18
-
-
0025906695
-
Variable deletion of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium
-
Chu, C.-S., Trapnell, B.C., Murtagh, J.J., Moss, J., Dalemans, W., Jallat, S., Mercenier, A., Pavirani, A., Lecocq, J.-P., Cutting, G.R., Guggino, W.B. and Crystal, R.G. (1991) Variable deletion of exon 9 coding sequences in cystic fibrosis transmembrane conductance regulator gene mRNA transcripts in normal bronchial epithelium. EMBO J., 10, 1355-1363.
-
(1991)
EMBO J.
, vol.10
, pp. 1355-1363
-
-
Chu, C.-S.1
Trapnell, B.C.2
Murtagh, J.J.3
Moss, J.4
Dalemans, W.5
Jallat, S.6
Mercenier, A.7
Pavirani, A.8
Lecocq, J.-P.9
Cutting, G.R.10
Guggino, W.B.11
Crystal, R.G.12
-
19
-
-
0026656343
-
Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis
-
Chu, C.-S., Trapnell, B.C., Curristin, S.M., Cutting, G.R. and Crystal, R.G. (1992) Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis. J. Clin. Invest. 90, 785-790.
-
(1992)
J. Clin. Invest.
, vol.90
, pp. 785-790
-
-
Chu, C.-S.1
Trapnell, B.C.2
Curristin, S.M.3
Cutting, G.R.4
Crystal, R.G.5
-
20
-
-
0027502580
-
Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA
-
Chu, C.-S., Trapnell, B.C., Curristin, S.M., Cutting, G.R. and Crystal, R.G. (1993) Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA. Nature Genet., 3, 151-156.
-
(1993)
Nature Genet.
, vol.3
, pp. 151-156
-
-
Chu, C.-S.1
Trapnell, B.C.2
Curristin, S.M.3
Cutting, G.R.4
Crystal, R.G.5
-
21
-
-
0027310434
-
Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance
-
Strong, T.V., Wilkinson, d.J., Mansoura, M.K., Devor, D.C., Genze, K., Yang, Y., Wilson, J.M., Cohn, J.A., Dawaon, D.C., Frizzell, R.A. and Collins, F.S. (1993) Expression of an abundant alternatively spliced form of the cystic fibrosis transmembrane conductance regulator (CFTR) gene is not associated with a cAMP-activated chloride conductance. Hum. Mol. Genet., 2, 225-230.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 225-230
-
-
Strong, T.V.1
Wilkinson, D.J.2
Mansoura, M.K.3
Devor, D.C.4
Genze, K.5
Yang, Y.6
Wilson, J.M.7
Cohn, J.A.8
Dawaon, D.C.9
Frizzell, R.A.10
Collins, F.S.11
-
22
-
-
0027249601
-
Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels
-
Delaney, S.J., Rich, D.P., Thomson, S.A., Hargrave, M.R., Lovelock, P.K., Welsh, M.J. and Wainwright, B.J. (1993) Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels. Nature Genet., 4, 426-431.
-
(1993)
Nature Genet.
, vol.4
, pp. 426-431
-
-
Delaney, S.J.1
Rich, D.P.2
Thomson, S.A.3
Hargrave, M.R.4
Lovelock, P.K.5
Welsh, M.J.6
Wainwright, B.J.7
-
23
-
-
0027521663
-
A mutation in CFTR produces different phenotypes depending on chromosomal background
-
Kiesewetter, S., Macek, M Jr., Davis, C., Curristin, S. M., Chu, C.S., Graham, C., Shrimpton, A.E., Cashman, S.M., Tsui L.-C., Mickle, J., Amos, J., Highsmith, W.E., Shuber, A., Witt, D.R., Crystal, R.G. and Cutting, G.R. (1993) A mutation in CFTR produces different phenotypes depending on chromosomal background. Nature Genet., 5, 274-278.
-
(1993)
Nature Genet.
, vol.5
, pp. 274-278
-
-
Kiesewetter, S.1
Macek Jr., M.2
Davis, C.3
Curristin, S.M.4
Chu, C.S.5
Graham, C.6
Shrimpton, A.E.7
Cashman, S.M.8
Tsui, L.-C.9
Mickle, J.10
Amos, J.11
Highsmith, W.E.12
Shuber, A.13
Witt, D.R.14
Crystal, R.G.15
Cutting, G.R.16
-
24
-
-
0028196665
-
CFTR haplotype backgrounds on normal and mutant CFTR genes
-
Cuppens, H., Teng, H., Raeymaekers, P., De Boeck, C. and Cassiman, J.J. (1994) CFTR haplotype backgrounds on normal and mutant CFTR genes. Hum. Mol. Genet., 3, 607-614.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 607-614
-
-
Cuppens, H.1
Teng, H.2
Raeymaekers, P.3
De Boeck, C.4
Cassiman, J.J.5
-
25
-
-
0028140183
-
Exon 9 of the CFTR gene: Splice site haplotypes and cystic fibrosis mutations
-
Dork, T., Fislage, R., Neumann, T., Wulf, B. and Tummler, B. (1994) Exon 9 of the CFTR gene: splice site haplotypes and cystic fibrosis mutations. Hum. Genet., 93, 67-73.
-
(1994)
Hum. Genet.
, vol.93
, pp. 67-73
-
-
Dork, T.1
Fislage, R.2
Neumann, T.3
Wulf, B.4
Tummler, B.5
-
26
-
-
0031023970
-
Increased proportion of exon 9 alternatively spliced CFTR transcripts in vas deferens compared with nasal epithelial cells
-
Teng, H., Jorissen, M., Van Poppel, H., Legius, E., Cassiman, J.-J. and Cuppens, H. (1997) Increased proportion of exon 9 alternatively spliced CFTR transcripts in vas deferens compared with nasal epithelial cells. Hum. Mol. Genet., 6, 85-90.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 85-90
-
-
Teng, H.1
Jorissen, M.2
Van Poppel, H.3
Legius, E.4
Cassiman, J.-J.5
Cuppens, H.6
-
27
-
-
0031037337
-
The molecular basis of partial penetrance of splicing mutations in cystic fibrosis
-
Rave-Harel, N., Kerem, E., Nissim-Rafinia, M., Madjar, I., Goshen, R., Augarten, A., Rahat, A., Hurwitz, A., Darvasi, A. and Kerem, B. (1997) The molecular basis of partial penetrance of splicing mutations in cystic fibrosis. Am. J. Hum. Genet., 60, 87-94.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 87-94
-
-
Rave-Harel, N.1
Kerem, E.2
Nissim-Rafinia, M.3
Madjar, I.4
Goshen, R.5
Augarten, A.6
Rahat, A.7
Hurwitz, A.8
Darvasi, A.9
Kerem, B.10
-
28
-
-
0026734588
-
Genetic determination of exocrine pancreatic function in cystic fibrosis
-
Kristidis, P., Bozon, D., Corey, M., Markiewicz, D., Rommens, J., Tsui, L.-C. and Durie, P. (1992) Genetic determination of exocrine pancreatic function in cystic fibrosis. Am. J. Hum. Genet., 50, 1178-1184.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 1178-1184
-
-
Kristidis, P.1
Bozon, D.2
Corey, M.3
Markiewicz, D.4
Rommens, J.5
Tsui, L.-C.6
Durie, P.7
-
29
-
-
0027517995
-
Correlation between genotype and phenotype in patients with cystic fibrosis
-
Hamosh, A., Corey, M. and the Cystic fibrosis genotype/phenotype consortium. (1994) Correlation between genotype and phenotype in patients with cystic fibrosis. N. Engl. J. Med., 329, 1308-1313.
-
(1994)
N. Engl. J. Med.
, vol.329
, pp. 1308-1313
-
-
Hamosh, A.1
Corey, M.2
-
30
-
-
0027408231
-
- channels with altered pore properties
-
- channels with altered pore properties. Nature, 362, 160-164.
-
(1993)
Nature
, vol.362
, pp. 160-164
-
-
Sheppard, D.N.1
Rich, D.P.2
Ostedgaard, L.S.3
Gregory, R.J.4
Smith, A.E.5
Welsh, M.J.6
-
31
-
-
0026865024
-
Preferential PCR amplification of alleles: Mechanisms and solutions
-
Walsh, P.S., Erlich, H.A. and Higuchi, R. (1992) Preferential PCR amplification of alleles: mechanisms and solutions. PCR Methods Appl., 1, 241-242.
-
(1992)
PCR Methods Appl.
, vol.1
, pp. 241-242
-
-
Walsh, P.S.1
Erlich, H.A.2
Higuchi, R.3
-
32
-
-
0003382345
-
Transcription termination, RNA processing, and posttranscriptional control
-
Edited by H. Lodish, D.Baltimore, A. Berk, Zipursky, S.L., P. Matsudaira and J. Darnell. New York: W.H. Freeman and Company
-
Lodish, H., Baltimore, D., Berk, A., Zipursky, S.L., Matsudaira, P. and Darnell, J. (1995) Transcription termination, RNA processing, and posttranscriptional control. In: Molecular Cell Biology. Edited by H. Lodish, D.Baltimore, A. Berk, Zipursky, S.L., P. Matsudaira and J. Darnell. New York: W.H. Freeman and Company, pp. 485-542.
-
(1995)
Molecular Cell Biology
, pp. 485-542
-
-
Lodish, H.1
Baltimore, D.2
Berk, A.3
Zipursky, S.L.4
Matsudaira, P.5
Darnell, J.6
-
33
-
-
0002571603
-
RNA splicing
-
Edited by B.D. Hames and D.M. Glover. Oxford: IRL Press
-
Krainer, A.R. and Maniatis, T. (1988) RNA splicing. In: Transcription and Splicing. Edited by B.D. Hames and D.M. Glover. Oxford: IRL Press, pp. 131-206.
-
(1988)
Transcription and Splicing
, pp. 131-206
-
-
Krainer, A.R.1
Maniatis, T.2
-
34
-
-
0024390066
-
Branch point selection in alternative splicing of tropomyosin pre-mRNAs
-
Helfman, D.M. and Ricci, W.M. (1989) Branch point selection in alternative splicing of tropomyosin pre-mRNAs. Nucleic Acids Res., 17, 5633.
-
(1989)
Nucleic Acids Res.
, vol.17
, pp. 5633
-
-
Helfman, D.M.1
Ricci, W.M.2
-
35
-
-
0024594710
-
Mutually exclusive splicing of alpha-tropomyosin exons enforced by an unusual lariat branch point location: Implications for constitutive splicing
-
Smith, C.W.J. and Nadal-Ginard, B. (1989) Mutually exclusive splicing of alpha-tropomyosin exons enforced by an unusual lariat branch point location: implications for constitutive splicing. Cell, 56, 749.
-
(1989)
Cell
, vol.56
, pp. 749
-
-
Smith, C.W.J.1
Nadal-Ginard, B.2
-
36
-
-
0022413541
-
The stepwise assembly of a pre-mRNA splicing complex requires U-snRNPs and specific intron sequences
-
Frendeway, D. and Keller, W. (1985) The stepwise assembly of a pre-mRNA splicing complex requires U-snRNPs and specific intron sequences. Cell, 42, 355.
-
(1985)
Cell
, vol.42
, pp. 355
-
-
Frendeway, D.1
Keller, W.2
-
37
-
-
0022516779
-
A role for exon sequences and splice-site proximity in splice-site selection
-
Reed, R. and Maniatis, T. (1986) A role for exon sequences and splice-site proximity in splice-site selection. Cell, 46, 681.
-
(1986)
Cell
, vol.46
, pp. 681
-
-
Reed, R.1
Maniatis, T.2
-
38
-
-
0022380943
-
Role of the 3′ splice site consensus sequence in mammalian pre-mRNA splicing
-
Ruskin, B. and Green, M.R. (1985) Role of the 3′ splice site consensus sequence in mammalian pre-mRNA splicing. Nature, 317, 732.
-
(1985)
Nature
, vol.317
, pp. 732
-
-
Ruskin, B.1
Green, M.R.2
-
39
-
-
0023834880
-
A factor, U2AF, is required for U2 snRNP binding and splicing complex assembly
-
Ruskin, B., Zamore, P.D. and Green, M.R. (1988) A factor, U2AF, is required for U2 snRNP binding and splicing complex assembly. Cell, 52, 207.
-
(1988)
Cell
, vol.52
, pp. 207
-
-
Ruskin, B.1
Zamore, P.D.2
Green, M.R.3
-
40
-
-
0023659494
-
Developmentally induced, muscle specific trans factors control the differential splicing of alternative and constitutive troponin-T exons
-
Breibart, R.E. and Nadal-Ginard, B. (1987) Developmentally induced, muscle specific trans factors control the differential splicing of alternative and constitutive troponin-T exons. Cell, 49, 793.
-
(1987)
Cell
, vol.49
, pp. 793
-
-
Breibart, R.E.1
Nadal-Ginard, B.2
-
41
-
-
0023848561
-
The rat α-tropomyosin gene generates a minimum of six different mRN As coding for striated, smooth and non-muscle isoforms by alternative splicing
-
Wieczorek, D., Smith, C.W.J. and Nadal-Ginard, B. (1988) The rat α-tropomyosin gene generates a minimum of six different mRN As coding for striated, smooth and non-muscle isoforms by alternative splicing. Mol. Cell Biol., 8, 679.
-
(1988)
Mol. Cell Biol.
, vol.8
, pp. 679
-
-
Wieczorek, D.1
Smith, C.W.J.2
Nadal-Ginard, B.3
-
42
-
-
0029792944
-
The genetics of male infertility
-
Mak, V. and Jarvi, K.A. (1996) The genetics of male infertility. J. Urol., 156, 1245-1257.
-
(1996)
J. Urol.
, vol.156
, pp. 1245-1257
-
-
Mak, V.1
Jarvi, K.A.2
-
43
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, S.A., Dykes, D.D. and Polesky, H.F. (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res., 16, 1215.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
44
-
-
0022965004
-
Specific enzymatic amplication of DNA in vitro: The polymerase chain reaction
-
Mullis, K., Faloona, F., Scharf, S., Saiki, R., Horn, G. and Erlich, H. (1986) Specific enzymatic amplication of DNA in vitro: the polymerase chain reaction. Cold Spring Harbor Symp. Quant. Biol., 51, 263-273.
-
(1986)
Cold Spring Harbor Symp. Quant. Biol.
, vol.51
, pp. 263-273
-
-
Mullis, K.1
Faloona, F.2
Scharf, S.3
Saiki, R.4
Horn, G.5
Erlich, H.6
-
45
-
-
0025760318
-
Genomic DNA sequence of the cystic fibrosis transmembrane regulator (CFTR) gene
-
Zielenski, J., Rozmahel, R., Bozon, D., Kerem, B., Grzelczak, Z., Riordan, J.R., Rommens, J. and Tsui, L.-C. (1991) Genomic DNA sequence of the cystic fibrosis transmembrane regulator (CFTR) gene. Genomics, 10, 214-228.
-
(1991)
Genomics
, vol.10
, pp. 214-228
-
-
Zielenski, J.1
Rozmahel, R.2
Bozon, D.3
Kerem, B.4
Grzelczak, Z.5
Riordan, J.R.6
Rommens, J.7
Tsui, L.-C.8
-
46
-
-
0025807911
-
cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator
-
Rommens, J.M., Dho, S., Bear, C.E., Kartner, N., Kennedy, D., Riordin, J.R., Tsui, L.-C. and Foskett. J.K. (1991) cAMP-inducible chloride conductance in mouse fibroblast lines stably expressing the human cystic fibrosis transmembrane conductance regulator. Proc. Natl. Acad. Sci. USA, 88, 7500-7504.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 7500-7504
-
-
Rommens, J.M.1
Dho, S.2
Bear, C.E.3
Kartner, N.4
Kennedy, D.5
Riordin, J.R.6
Tsui, L.-C.7
Foskett, J.K.8
-
47
-
-
0016700864
-
Detection of specific sequences among DNA fragments separated by gel electrophoresis
-
Southern, E.M. (1975) Detection of specific sequences among DNA fragments separated by gel electrophoresis. J. Mol. Biol., 98, 503-517.
-
(1975)
J. Mol. Biol.
, vol.98
, pp. 503-517
-
-
Southern, E.M.1
|