-
1
-
-
0031647686
-
The genetic basis of male infertility
-
Bhasin, S., Ma, K., Sinha, I., Limbo, M., Taylor, W. E., and Salehian, B. (1998). The genetic basis of male infertility. Endocrinol. Metab. Clin. North Am. 27, 783-805.
-
(1998)
Endocrinol. Metab. Clin. North Am.
, vol.27
, pp. 783-805
-
-
Bhasin, S.1
Ma, K.2
Sinha, I.3
Limbo, M.4
Taylor, W.E.5
Salehian, B.6
-
2
-
-
0035370789
-
Systematic approaches to mouse mutagenesis
-
doi:10.1016/S0959-437X(00)00189-1
-
Brown, S., and Balling, R. (2001). Systematic approaches to mouse mutagenesis. Curr. Opin. Genet. Dev. 11, 268-273. doi:10.1016/S0959-437X(00)00189-1
-
(2001)
Curr. Opin. Genet. Dev.
, vol.11
, pp. 268-273
-
-
Brown, S.1
Balling, R.2
-
3
-
-
0029025333
-
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens
-
doi:10.1056/NEJM199506013322204
-
Chillon, M., Casals, T., Mercier, B., Bassas, L., Lissens, W., et al. (1995). Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens. N. Engl. J. Med. 332, 1475-1480. doi:10.1056/NEJM199506013322204
-
(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
-
4
-
-
0035030318
-
Haploinsufficiency of protamine-1 or -2 causes infertility in mice
-
doi:10.1038/88313
-
Cho, C., Willis, W. D., Goulding, E. H., Jung-Ha, H., Choi, Y. C., Hecht, N. B., and Eddy, E. M. (2001). Haploinsufficiency of protamine-1 or -2 causes infertility in mice. Nat. Genet. 28, 82-86. doi:10.1038/88313
-
(2001)
Nat. Genet.
, vol.28
, pp. 82-86
-
-
Cho, C.1
Willis, W.D.2
Goulding, E.H.3
Jung-Ha, H.4
Choi, Y.C.5
Hecht, N.B.6
Eddy, E.M.7
-
5
-
-
0032551674
-
The Melbourne Pre-Diabetes Study: Prediction of type 1 diabetes mellitus using antibody and metabolic testing
-
Colman, P. G., McNair, P., Margetts, H., Schmidli, R. S., Werther, G. A., Alford, F. P., Ward, G. M., Tait, B. D., Honeyman, M. C., and Harrison, L. C. (1998). The Melbourne Pre-Diabetes Study: prediction of type 1 diabetes mellitus using antibody and metabolic testing. Med. J. Aust. 169, 81-84.
-
(1998)
Med. J. Aust.
, vol.169
, pp. 81-84
-
-
Colman, P.G.1
McNair, P.2
Margetts, H.3
Schmidli, R.S.4
Werther, G.A.5
Alford, F.P.6
Ward, G.M.7
Tait, B.D.8
Honeyman, M.C.9
Harrison, L.C.10
-
6
-
-
0036787299
-
Mouse models of male infertility
-
doi:10.1038/NRG911
-
Cooke, H. J., and Saunders, P. T. (2002). Mouse models of male infertility. Nat. Rev. Genet. 3, 790-801. doi:10.1038/NRG911
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 790-801
-
-
Cooke, H.J.1
Saunders, P.T.2
-
7
-
-
0033760207
-
Y chromosome analysis of infertile men and their sons conceived through intracytoplasmic sperm injection: Vertical transmission of deletions and rarity of de novo deletions
-
doi:10.1016/S0015-0282 (00)01568-5
-
Cram, D. S., Ma, K., Bhasin, S., Arias, J., Pandjaitan, M., et al. (2000). Y chromosome analysis of infertile men and their sons conceived through intracytoplasmic sperm injection: vertical transmission of deletions and rarity of de novo deletions. Fertil. Steril. 74, 909-915. doi:10.1016/S0015-0282 (00)01568-5
-
(2000)
Fertil. Steril.
, vol.74
, pp. 909-915
-
-
Cram, D.S.1
Ma, K.2
Bhasin, S.3
Arias, J.4
Pandjaitan, M.5
-
8
-
-
0034844179
-
Male infertility genetics - The future
-
Cram, D. S., O'Bryan, M. K., and de Kretser, D. M. (2001). Male infertility genetics - the future. J. Androl. 22, 738-746.
-
(2001)
J. Androl.
, vol.22
, pp. 738-746
-
-
Cram, D.S.1
O'Bryan, M.K.2
de Kretser, D.M.3
-
9
-
-
0029991234
-
Targeted gene disruption of Hsp70-2 results in failed meiosis, germ cell apoptosis, and male infertility
-
doi:10.1073/PNAS.93.8.3264
-
Dix, D. J., Allen, J. W., Collins, B. W., Mori, C., Nakamura, N., Poorman-Allen, P., Goulding, E. H., and Eddy, E. M. (1996). Targeted gene disruption of Hsp70-2 results in failed meiosis, germ cell apoptosis, and male infertility. Proc. Natl. Acad. Sci. USA 93, 3264-3268. doi:10.1073/PNAS.93.8.3264
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 3264-3268
-
-
Dix, D.J.1
Allen, J.W.2
Collins, B.W.3
Mori, C.4
Nakamura, N.5
Poorman-Allen, P.6
Goulding, E.H.7
Eddy, E.M.8
-
10
-
-
0033592186
-
Linkage between male infertility and trinucleotide repeat expansion in the androgen-receptor gene
-
doi:10.1016/S0140-6736(98)08413-X
-
Dowsing, A. T., Yong, E. L., Clark, M., McLachlan, R. I., de Kretser, D. M., and Trounson, A. O. (1999). Linkage between male infertility and trinucleotide repeat expansion in the androgen-receptor gene. Lancet 354, 640-643. doi:10.1016/S0140-6736(98)08413-X
-
(1999)
Lancet
, vol.354
, pp. 640-643
-
-
Dowsing, A.T.1
Yong, E.L.2
Clark, M.3
McLachlan, R.I.4
de Kretser, D.M.5
Trounson, A.O.6
-
11
-
-
18244410193
-
High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia
-
doi:10.1093/MOLEHR/8.3.286
-
Fernandes, S., Huellen, K., Goncalves, J., Dukal, H., Zeisler, J., et al. (2002). High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia. Mol. Hum. Reprod. 8, 286-298. doi:10.1093/MOLEHR/8.3.286
-
(2002)
Mol. Hum. Reprod.
, vol.8
, pp. 286-298
-
-
Fernandes, S.1
Huellen, K.2
Goncalves, J.3
Dukal, H.4
Zeisler, J.5
-
12
-
-
0035012270
-
Y chromosome microdeletions and alterations of spermatogenesis
-
doi:10.1210/ER.22.2.226
-
Foresta, C., Moro, E., and Ferlin, A. (2001a). Y chromosome microdeletions and alterations of spermatogenesis. Endocr. Rev. 22, 226-239. doi:10.1210/ER.22.2.226
-
(2001)
Endocr. Rev.
, vol.22
, pp. 226-239
-
-
Foresta, C.1
Moro, E.2
Ferlin, A.3
-
13
-
-
0034889045
-
Prognostic value of Y deletion analysis. The role of current methods
-
doi:10.1093/HUMREP/16.8.1543
-
Foresta, C., Moro, E., and Ferlin, A. (2001b). Prognostic value of Y deletion analysis. The role of current methods. Hum. Reprod. 16, 1543-1547. doi:10.1093/HUMREP/16.8.1543
-
(2001)
Hum. Reprod.
, vol.16
, pp. 1543-1547
-
-
Foresta, C.1
Moro, E.2
Ferlin, A.3
-
14
-
-
0037497254
-
Partial DAZ deletions in a family with five infertile brothers
-
doi:10.1016/S0015-0282(03)00338-8
-
Gianotten, J., Hoffer, M. J., De Vries, J. W., Leschot, N. J., Gerris, J., and van der Veen, F. (2003). Partial DAZ deletions in a family with five infertile brothers. Fertil. Steril. Suppl. 79, 1652-1655. doi:10.1016/S0015-0282(03)00338-8
-
(2003)
Fertil. Steril. Suppl.
, vol.79
, pp. 1652-1655
-
-
Gianotten, J.1
Hoffer, M.J.2
De Vries, J.W.3
Leschot, N.J.4
Gerris, J.5
van der Veen, F.6
-
15
-
-
0031913144
-
DAZ (deleted in azoospermia) genes encode proteins located in human late spermatids and in sperm tails
-
doi:10.1093/HUMREP/13.2.363
-
Habermann, B., Mi, H. F., Edelmann, A., Bohring, C., Backert, I. T., Kiesewetter, F., Aumuller, G., and Vogt, P. H. (1998). DAZ (deleted in azoospermia) genes encode proteins located in human late spermatids and in sperm tails. Hum. Reprod. 13, 363A-369A. doi:10.1093/HUMREP/13.2.363
-
(1998)
Hum. Reprod.
, vol.13
-
-
Habermann, B.1
Mi, H.F.2
Edelmann, A.3
Bohring, C.4
Backert, I.T.5
Kiesewetter, F.6
Aumuller, G.7
Vogt, P.H.8
-
16
-
-
0033917014
-
Application and evaluation of denaturing HPLC for molecular genetic analysis in tuberous sclerosis
-
doi:10.1007/S004390050040
-
Jones, A. C., Sampson, J. R., Hoogendoorn, B., Cohen, D., and Cheadle, J. P. (2000). Application and evaluation of denaturing HPLC for molecular genetic analysis in tuberous sclerosis. Hum. Genet. 106, 663-668. doi:10.1007/S004390050040
-
(2000)
Hum. Genet.
, vol.106
, pp. 663-668
-
-
Jones, A.C.1
Sampson, J.R.2
Hoogendoorn, B.3
Cohen, D.4
Cheadle, J.P.5
-
17
-
-
0035991092
-
Genetic follow-up of male offspring born by ICSI, using a multiplex fluorescent PCR-based test for Yq deletions
-
doi:10.1093/MOLEHR/8.6.589
-
Katz, M. G., Chu, B., McLachlan, R., Alexopoulos, N. I., de Kretser, D. M., and Cram, D. S. (2002). Genetic follow-up of male offspring born by ICSI, using a multiplex fluorescent PCR-based test for Yq deletions. Mol. Hum. Reprod. 8, 589-595. doi:10.1093/MOLEHR/8.6.589
-
(2002)
Mol. Hum. Reprod.
, vol.8
, pp. 589-595
-
-
Katz, M.G.1
Chu, B.2
McLachlan, R.3
Alexopoulos, N.I.4
de Kretser, D.M.5
Cram, D.S.6
-
18
-
-
0042911521
-
Functional genetic analysis of mouse chromosome 11
-
doi:10.1038/NATURE01865
-
Kile, B. T., Hentes, K. E., Clark, A. T., Nakamura, H., Sallinger, A. P., et al. (2003). Functional genetic analysis of mouse chromosome 11. Nature 425, 81-86. doi:10.1038/NATURE01865
-
(2003)
Nature
, vol.425
, pp. 81-86
-
-
Kile, B.T.1
Hentes, K.E.2
Clark, A.T.3
Nakamura, H.4
Sallinger, A.P.5
-
19
-
-
0035184973
-
The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men
-
doi:10.1038/NG757
-
Kuroda-Kawaguchi, T., Skaletsky, H., Brown, L. G., Minx, P. J., Cordum, H. S., et al. (2001). The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men. Nat. Genet. 29, 279-286. doi:10.1038/NG757
-
(2001)
Nat. Genet.
, vol.29
, pp. 279-286
-
-
Kuroda-Kawaguchi, T.1
Skaletsky, H.2
Brown, L.G.3
Minx, P.J.4
Cordum, H.S.5
-
20
-
-
0030725069
-
Functional coherence of the human Y chromosome
-
doi:10.1126/SCIENCE.278.5338.675
-
Lahn, B. T., and Page, D. C. (1997). Functional coherence of the human Y chromosome. Science 278, 675-680. doi:10.1126/SCIENCE.278.5338.675
-
(1997)
Science
, vol.278
, pp. 675-680
-
-
Lahn, B.T.1
Page, D.C.2
-
21
-
-
0038420050
-
Evidence that the human X chromosome is enriched for male-specific but not female-specific genes
-
doi:10.1093/MOLBEV/MSG131
-
Lercher, M. J., Urrutia, A. O., and Hurst, L. D. (2003). Evidence that the human X chromosome is enriched for male-specific but not female-specific genes. Mol. Biol. Evol. 20, 1113-1116. doi:10.1093/MOLBEV/MSG131
-
(2003)
Mol. Biol. Evol.
, vol.20
, pp. 1113-1116
-
-
Lercher, M.J.1
Urrutia, A.O.2
Hurst, L.D.3
-
22
-
-
0032520681
-
Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations
-
doi:10.1093/NAR/26.6.1396
-
Liu, W., Smith, D. I., Rechtzigel, K. J., Thibodeau, S. N., and James, C. D. (1998). Denaturing high performance liquid chromatography (DHPLC) used in the detection of germline and somatic mutations. Nucleic Acids Res. 26, 1396-1400. doi:10.1093/NAR/26.6.1396
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 1396-1400
-
-
Liu, W.1
Smith, D.I.2
Rechtzigel, K.J.3
Thibodeau, S.N.4
James, C.D.5
-
23
-
-
0036798824
-
Genetic dissection of mammalian fertility pathways
-
Matzuk, M. M., and Lamb, D. J. (2002). Genetic dissection of mammalian fertility pathways. Nat. Cell Biol. 4(Suppl), s41-s49.
-
(2002)
Nat. Cell Biol.
, vol.4
, Issue.SUPPL.
-
-
Matzuk, M.M.1
Lamb, D.J.2
-
24
-
-
0033707093
-
Y chromosome microdeletion screening in infertile men
-
Maurer, B., and Simoni, M. (2000). Y chromosome microdeletion screening in infertile men. J. Endocrinol. Invest. 23, 664-670.
-
(2000)
J. Endocrinol. Invest.
, vol.23
, pp. 664-670
-
-
Maurer, B.1
Simoni, M.2
-
25
-
-
0036888516
-
Genetics of autoimmune diseases in humans and in animal models
-
doi:10.1016/S0952-7915(02)00401-6
-
Morahan, G., and Morel, L. (2002). Genetics of autoimmune diseases in humans and in animal models. Curr. Opin. Immunol. 14, 803-811. doi:10.1016/S0952-7915(02)00401-6
-
(2002)
Curr. Opin. Immunol.
, vol.14
, pp. 803-811
-
-
Morahan, G.1
Morel, L.2
-
26
-
-
9244243681
-
Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy
-
doi:10.1210/JC.81.4.1347
-
Najmabadi, H., Huang, V., Yen, P., Subbarao, M. N., Bhasin, D., et al. (1996). Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy. J. Clin. Endocrinol. Metab. 81, 1347-1352. doi:10.1210/JC.81.4.1347
-
(1996)
J. Clin. Endocrinol. Metab.
, vol.81
, pp. 1347-1352
-
-
Najmabadi, H.1
Huang, V.2
Yen, P.3
Subbarao, M.N.4
Bhasin, D.5
-
27
-
-
0034813659
-
Genome-wide ENU mutagenesis to reveal immune regulators
-
doi:10.1016/S1074-7613(01)00199-6
-
Nelms, K. A., and Goodnow, C. C. (2001). Genome-wide ENU mutagenesis to reveal immune regulators. Immunity 15, 409-418. doi:10.1016/S1074-7613(01)00199-6
-
(2001)
Immunity
, vol.15
, pp. 409-418
-
-
Nelms, K.A.1
Goodnow, C.C.2
-
28
-
-
0034425410
-
A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse
-
doi:10.1038/78140
-
Nolan, P. M., Peters, J., Strivens, M., Rogers, D., Hagan, J., et al. (2000). A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nat. Genet. 25, 440-443. doi:10.1038/78140
-
(2000)
Nat. Genet.
, vol.25
, pp. 440-443
-
-
Nolan, P.M.1
Peters, J.2
Strivens, M.3
Rogers, D.4
Hagan, J.5
-
29
-
-
0033979258
-
Congenital bilateral absence of the vas deferens, cystic fibrosis mutation analysis and intracytoplasmic sperm injection
-
doi:10.1093/HUMREP/15.2.431
-
Phillipson, G. T., Petrucco, O. M., and Matthews, C. D. (2000). Congenital bilateral absence of the vas deferens, cystic fibrosis mutation analysis and intracytoplasmic sperm injection. Hum. Reprod. 15, 431-435. doi:10.1093/HUMREP/15.2.431
-
(2000)
Hum. Reprod.
, vol.15
, pp. 431-435
-
-
Phillipson, G.T.1
Petrucco, O.M.2
Matthews, C.D.3
-
30
-
-
13144267780
-
Apoptosis regulator bcl-w is essential for spermatogenesis but appears otherwise redundant
-
doi:10.1073/PNAS.95.21.12424
-
Print, C. G., Loveland, K. L., Gibson, L., Meehan, T., Stylianou, A., et al. (1998). Apoptosis regulator bcl-w is essential for spermatogenesis but appears otherwise redundant. Proc. Natl Acad. Sci. USA 95, 12424-12431. doi:10.1073/PNAS.95.21.12424
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 12424-12431
-
-
Print, C.G.1
Loveland, K.L.2
Gibson, L.3
Meehan, T.4
Stylianou, A.5
-
31
-
-
0036195225
-
DHPLC screening of cystic fibrosis gene mutations
-
Ravnik-Glavac, M., Atkinson, A., Glavac, D., and Dean, M. (2002). DHPLC screening of cystic fibrosis gene mutations. Hum. Mutat. 19, 374-383.
-
(2002)
Hum. Mutat.
, vol.19
, pp. 374-383
-
-
Ravnik-Glavac, M.1
Atkinson, A.2
Glavac, D.3
Dean, M.4
-
32
-
-
0033550904
-
Genetic determination of islet cell autoimmunity in monozygotic twin, dizygotic twin, and non-twin siblings of patients with type 1 diabetes: Prospective twin study
-
Redondo, M. J., Rewers, M., Yu, L., Garg, S., Pilcher, C. C., Elliott, R. B., and Eisenbarth, G. S. (1999). Genetic determination of islet cell autoimmunity in monozygotic twin, dizygotic twin, and non-twin siblings of patients with type 1 diabetes: prospective twin study. BMJ 318, 698-702.
-
(1999)
BMJ
, vol.318
, pp. 698-702
-
-
Redondo, M.J.1
Rewers, M.2
Yu, L.3
Garg, S.4
Pilcher, C.C.5
Elliott, R.B.6
Eisenbarth, G.S.7
-
33
-
-
0242298320
-
Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
-
doi:10.1038/NG1250
-
Repping, S., Skaletsky, H., Brown, L., Van Daalen, S. K., Korver, C. M., Pyntikova, T., Kuroda-Kawaguchi, T., De Vries, J. W., Oates, R. D., and Silber, S. (2003). Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nat. Genet. 35, 247-251. doi:10.1038/NG1250
-
(2003)
Nat. Genet.
, vol.35
, pp. 247-251
-
-
Repping, S.1
Skaletsky, H.2
Brown, L.3
Van Daalen, S.K.4
Korver, C.M.5
Pyntikova, T.6
Kuroda-Kawaguchi, T.7
De Vries, J.W.8
Oates, R.D.9
Silber, S.10
-
34
-
-
0030885623
-
The mouse Dazla gene encodes a cytoplasmic protein essential for gametogenesis
-
doi:10.1038/37987
-
Ruggiu, M., Speed, R., Taggart, M., McKay, S. J., Kilanowski, F., Saunders, P., Dorin, J., and Cooke, H. J. (1997). The mouse Dazla gene encodes a cytoplasmic protein essential for gametogenesis. Nature 389, 73-77. doi:10.1038/37987
-
(1997)
Nature
, vol.389
, pp. 73-77
-
-
Ruggiu, M.1
Speed, R.2
Taggart, M.3
McKay, S.J.4
Kilanowski, F.5
Saunders, P.6
Dorin, J.7
Cooke, H.J.8
-
35
-
-
0033593570
-
An apparent excess of sex- and reproduction-related genes on the human X chromosome
-
doi:10.1098/RSPB.1999.0623
-
Saifi, G. M., and Chandra, H. S. (1999). An apparent excess of sex- and reproduction-related genes on the human X chromosome. Proc. R. Soc. Lond. B. Biol. Sci. 266, 203-209. doi:10.1098/RSPB.1999.0623
-
(1999)
Proc. R. Soc. Lond. B. Biol. Sci.
, vol.266
, pp. 203-209
-
-
Saifi, G.M.1
Chandra, H.S.2
-
36
-
-
0028608904
-
Disturbances of nuclear condensation in human spermatozoa: Search for mutations in the genes for protamine 1, protamine 2 and transition protein 1
-
Schlicker, M., Schnulle, V., Schneppel, L., Vorob'ev, V. I., and Engel, W. (1994). Disturbances of nuclear condensation in human spermatozoa: search for mutations in the genes for protamine 1, protamine 2 and transition protein 1. Hum. Reprod. 9, 2313-2317.
-
(1994)
Hum. Reprod.
, vol.9
, pp. 2313-2317
-
-
Schlicker, M.1
Schnulle, V.2
Schneppel, L.3
Vorob'ev, V.I.4
Engel, W.5
-
37
-
-
0142091380
-
A multitude of genes expressed solely in meiotic or postmeiotic spermatogenic cells offers a myriad of contraceptive targets
-
doi:10.1073/PNAS.1635054100
-
Schultz, N., Hamra, F. K., and Garbers, D. (2003). A multitude of genes expressed solely in meiotic or postmeiotic spermatogenic cells offers a myriad of contraceptive targets. Proc. Natl Acad. Sci. USA 100, 12201-12206. doi:10.1073/PNAS.1635054100
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 12201-12206
-
-
Schultz, N.1
Hamra, F.K.2
Garbers, D.3
-
38
-
-
0037967242
-
The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes
-
doi:10.1038/NATURE01722
-
Skaletsky, H., Kuroda-Kawaguchi, T., Minx, P. J., Cordum, H. S., Hillier, L., et al. (2003). The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature 423, 825-837. doi:10.1038/NATURE01722
-
(2003)
Nature
, vol.423
, pp. 825-837
-
-
Skaletsky, H.1
Kuroda-Kawaguchi, T.2
Minx, P.J.3
Cordum, H.S.4
Hillier, L.5
-
39
-
-
0032866936
-
Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions
-
doi:10.1046/11365-2605.1999.00193.X
-
Simoni, M., Bakker, E., Eurlings, M. C., Matthijs, G., Moro, E., Muller, C. R., and Vogt, P. H. (1999). Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions. Int. J. Androl. 22, 292-299. doi:10.1046/11365-2605.1999.00193.X
-
(1999)
Int. J. Androl.
, vol.22
, pp. 292-299
-
-
Simoni, M.1
Bakker, E.2
Eurlings, M.C.3
Matthijs, G.4
Moro, E.5
Muller, C.R.6
Vogt, P.H.7
-
40
-
-
0032727618
-
An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y
-
doi:10.1038/70539
-
Sun, C., Skaletsky, H., Birren, B., Devon, K., Tang, Z., Silber, S., Oates, R., and Page, D. C. (1999). An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y. Nat. Genet. 23, 429-432. doi:10.1038/70539
-
(1999)
Nat. Genet.
, vol.23
, pp. 429-432
-
-
Sun, C.1
Skaletsky, H.2
Birren, B.3
Devon, K.4
Tang, Z.5
Silber, S.6
Oates, R.7
Page, D.C.8
-
41
-
-
0037291314
-
Single nucleotide polymorphisms in the protamine-1 and -2 genes of fertile and infertile human male populations
-
doi:10.1093/MOLEHR/GAG010
-
Tanaka, H., Miyagawa, Y., Tsujimura, A., Matsumiya, K., Okuyama, A., and Nishimune, Y. (2003). Single nucleotide polymorphisms in the protamine-1 and -2 genes of fertile and infertile human male populations. Mol. Hum. Reprod. 9, 69-73. doi:10.1093/MOLEHR/GAG010
-
(2003)
Mol. Hum. Reprod.
, vol.9
, pp. 69-73
-
-
Tanaka, H.1
Miyagawa, Y.2
Tsujimura, A.3
Matsumiya, K.4
Okuyama, A.5
Nishimune, Y.6
-
42
-
-
0035895505
-
The sequence of the human genome
-
doi:10.1126/SCIENCE.1058040
-
Venter, J. C., Adams, M. D., Myers, E. W., Li, P. W., Mural, R. J., et al. (2001). The sequence of the human genome. Science 291, 1304-1351. doi:10.1126/SCIENCE.1058040
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
-
43
-
-
0007272350
-
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
-
doi:10.1093/HMG/5.7.933
-
Vogt, P. H., Edelmann, A., Kirsch, S., Henegariu, O., Hirschmann, P., et al. (1996). Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum. Mol. Genet. 5, 933-943. doi:10.1093/HMG/5.7.933
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 933-943
-
-
Vogt, P.H.1
Edelmann, A.2
Kirsch, S.3
Henegariu, O.4
Hirschmann, P.5
-
44
-
-
0242298746
-
Towards the genetics of mammalian reproduction: Induction and mapping of gametogenesis mutants in mice
-
Ward, J. O., Reinholdt, L. G., Hartford, S. A., Wilson, L. A., Munroe, R. J., Schimenti, K. J., Libby, B. J., O'Brien, M., Pendola, J. K., Eppig, J., and Schimenti, J. C. (2003). Towards the genetics of mammalian reproduction: induction and mapping of gametogenesis mutants in mice. Biol. Reprod. 69, 1615-1625.
-
(2003)
Biol. Reprod.
, vol.69
, pp. 1615-1625
-
-
Ward, J.O.1
Reinholdt, L.G.2
Hartford, S.A.3
Wilson, L.A.4
Munroe, R.J.5
Schimenti, K.J.6
Libby, B.J.7
O'Brien, M.8
Pendola, J.K.9
Eppig, J.10
Schimenti, J.C.11
-
45
-
-
0034999807
-
Denaturing high-performance liquid chromatography: A review
-
doi:10.1002/HUMU.1130.ABS
-
Xiao, W., and Oeffier, P. J. (2001). Denaturing high-performance liquid chromatography: a review. Hum. Mutat. 17, 439-474. doi:10.1002/HUMU.1130.ABS
-
(2001)
Hum. Mutat.
, vol.17
, pp. 439-474
-
-
Xiao, W.1
Oeffier, P.J.2
-
46
-
-
0034712735
-
Abnormal spermatogenesis and reduced fertility in transition nuclear protein 1-deficient mice
-
doi:10.1073/PNAS.97.9.4683
-
Yu, Y. E., Zhang, Y., Unni, E., Shirley, C. R., Deng, J. M., Russell, L. D., Weil, M. M., Behringer, R. R., and Meistrich, M. L. (2000). Abnormal spermatogenesis and reduced fertility in transition nuclear protein 1-deficient mice. Proc. Natl Acad. Sci. USA 97, 4683-4688. doi:10.1073/PNAS.97.9.4683
-
(2000)
Proc. Natl Acad. Sci. USA
, vol.97
, pp. 4683-4688
-
-
Yu, Y.E.1
Zhang, Y.2
Unni, E.3
Shirley, C.R.4
Deng, J.M.5
Russell, L.D.6
Weil, M.M.7
Behringer, R.R.8
Meistrich, M.L.9
-
47
-
-
0034797470
-
Targeted disruption of the transition protein 2 gene affects sperm chromatin structure and reduces fertility in mice
-
doi:10.1128/MCB.21.21.7243-7255.2001
-
Zhao, M., Shirley, C. R., Yu, Y. E., Mohapatra, B., Zhang, Y., et al. (2001). Targeted disruption of the transition protein 2 gene affects sperm chromatin structure and reduces fertility in mice. Mol. Cell. Biol. 21, 7243-7255. doi:10.1128/MCB.21.21.7243-7255.2001
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 7243-7255
-
-
Zhao, M.1
Shirley, C.R.2
Yu, Y.E.3
Mohapatra, B.4
Zhang, Y.5
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