-
1
-
-
0017119580
-
Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
-
Tiepolo L., and Zuffardi O. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum Genet 34 (1976) 119-124
-
(1976)
Hum Genet
, vol.34
, pp. 119-124
-
-
Tiepolo, L.1
Zuffardi, O.2
-
2
-
-
0007272350
-
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
-
Vogt P.H., Edelmann A., Kirsch S., Henegariu O., Hirschmann P., Kiesewetter F., et al. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum Mol Genet 5 (1996) 933-943
-
(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
Kiesewetter, F.6
-
3
-
-
0031432996
-
Genetics of idiopathic male infertility: Y chromosomal azoospermia factors (AZFa, AZFb, AZFc)
-
Vogt P.H. Genetics of idiopathic male infertility: Y chromosomal azoospermia factors (AZFa, AZFb, AZFc). Baillieres Clin Obstet Gynaecol 11 (1997) 773-795
-
(1997)
Baillieres Clin Obstet Gynaecol
, vol.11
, pp. 773-795
-
-
Vogt, P.H.1
-
4
-
-
33645409448
-
Reevaluation of azoospermic factor c microdeletions using sequence-tagged site markers with confirmed physical positions from the GenBank database
-
Fukushima M., Koh E., Choi J., Maeda Y., Namiki M., and Yoshida A. Reevaluation of azoospermic factor c microdeletions using sequence-tagged site markers with confirmed physical positions from the GenBank database. Fertil Steril 85 (2006) 965-971
-
(2006)
Fertil Steril
, vol.85
, pp. 965-971
-
-
Fukushima, M.1
Koh, E.2
Choi, J.3
Maeda, Y.4
Namiki, M.5
Yoshida, A.6
-
5
-
-
79961162523
-
Multiplex sequence-tagged site PCR for efficient screening of microdeletions in Y chromosome in infertile males with azoospermia or severe oligozoospermia
-
Nakashima M., Koh E., Namiki M., and Yoshida A. Multiplex sequence-tagged site PCR for efficient screening of microdeletions in Y chromosome in infertile males with azoospermia or severe oligozoospermia. Arch Androl 48 (2002) 351-358
-
(2002)
Arch Androl
, vol.48
, pp. 351-358
-
-
Nakashima, M.1
Koh, E.2
Namiki, M.3
Yoshida, A.4
-
6
-
-
0034641881
-
Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events
-
Kamp C., Hirschmann P., Voss H., Huellen K., and Vogt P.H. Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events. Hum Mol Genet 9 (2000) 2563-2572
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2563-2572
-
-
Kamp, C.1
Hirschmann, P.2
Voss, H.3
Huellen, K.4
Vogt, P.H.5
-
7
-
-
0034703178
-
Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses
-
Sun C., Skaletsky H., Rozen S., Gromoll J., Nieschlag E., Oates R., et al. Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses. Hum Mol Genet 9 (2000) 2291-2296
-
(2000)
Hum Mol Genet
, vol.9
, pp. 2291-2296
-
-
Sun, C.1
Skaletsky, H.2
Rozen, S.3
Gromoll, J.4
Nieschlag, E.5
Oates, R.6
-
8
-
-
0032727618
-
An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y
-
Sun C., Skaletsky H., Birren B., Devon K., Tang Z., Silber S., et al. An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y. Nat Genet 23 (1999) 429-432
-
(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
-
9
-
-
0034194140
-
Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility
-
Foresta C., Ferlin A., and Moro E. Deletion and expression analysis of AZFa genes on the human Y chromosome revealed a major role for DBY in male infertility. Hum Mol Genet 9 (2000) 1161-1169
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1161-1169
-
-
Foresta, C.1
Ferlin, A.2
Moro, E.3
-
10
-
-
0033836470
-
AZFa deletions in Sertoli cell-only syndrome: a retrospective study
-
Blagosklonova O., Fellmann F., Clavequin M.C., Roux C., and Bresson J.L. AZFa deletions in Sertoli cell-only syndrome: a retrospective study. Mol Hum Reprod 6 (2000) 795-799
-
(2000)
Mol Hum Reprod
, vol.6
, pp. 795-799
-
-
Blagosklonova, O.1
Fellmann, F.2
Clavequin, M.C.3
Roux, C.4
Bresson, J.L.5
-
11
-
-
0029131041
-
The Y chromosome: a graveyard for endogenous retroviruses
-
Kjellman C., Sjogren H.O., and Widegren B. The Y chromosome: a graveyard for endogenous retroviruses. Gene 161 (1995) 163-170
-
(1995)
Gene
, vol.161
, pp. 163-170
-
-
Kjellman, C.1
Sjogren, H.O.2
Widegren, B.3
-
13
-
-
4043092052
-
EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004
-
Simoni M., Bakker E., and Krausz C. EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int J Androl 27 (2004) 240-249
-
(2004)
Int J Androl
, vol.27
, pp. 240-249
-
-
Simoni, M.1
Bakker, E.2
Krausz, C.3
-
14
-
-
0032787762
-
Human male infertility and Y chromosome deletions: role of the AZF-candidate genes DAZ, RBM and DFFRY
-
Ferlin A., Moro E., Garolla A., and Foresta C. Human male infertility and Y chromosome deletions: role of the AZF-candidate genes DAZ, RBM and DFFRY. Hum Reprod 14 (1999) 1710-1716
-
(1999)
Hum Reprod
, vol.14
, pp. 1710-1716
-
-
Ferlin, A.1
Moro, E.2
Garolla, A.3
Foresta, C.4
-
15
-
-
0034749439
-
AZFa candidate gene deletions in Taiwanese patients with spermatogenic failure
-
Lin Y.M., Teng Y.N., Lee P.C., Lin Y.H., Hsu C.C., Lin J.S., et al. AZFa candidate gene deletions in Taiwanese patients with spermatogenic failure. J Formos Med Assoc 100 (2001) 592-597
-
(2001)
J Formos Med Assoc
, vol.100
, pp. 592-597
-
-
Lin, Y.M.1
Teng, Y.N.2
Lee, P.C.3
Lin, Y.H.4
Hsu, C.C.5
Lin, J.S.6
-
16
-
-
0034883093
-
Y-chromosome microdeletion and phenotype in cytogenetically normal men with idiopathic azoospermia
-
Fujisawa M., Shirakawa T., Kanzaki M., Okada H., Arakawa S., and Kamidono S. Y-chromosome microdeletion and phenotype in cytogenetically normal men with idiopathic azoospermia. Fertil Steril 76 (2001) 491-495
-
(2001)
Fertil Steril
, vol.76
, pp. 491-495
-
-
Fujisawa, M.1
Shirakawa, T.2
Kanzaki, M.3
Okada, H.4
Arakawa, S.5
Kamidono, S.6
-
17
-
-
0035012270
-
Y chromosome microdeletions and alterations of spermatogenesis
-
Foresta C., Moro E., and Ferlin A. Y chromosome microdeletions and alterations of spermatogenesis. Endocr Rev 22 (2001) 226-239
-
(2001)
Endocr Rev
, vol.22
, pp. 226-239
-
-
Foresta, C.1
Moro, E.2
Ferlin, A.3
-
18
-
-
0034795056
-
High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome
-
Kamp C., Huellen K., Fernandes S., Sousa M., Schlegel P.N., Mielnik A., et al. High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome. Mol Hum Reprod 7 (2001) 987-994
-
(2001)
Mol Hum Reprod
, vol.7
, pp. 987-994
-
-
Kamp, C.1
Huellen, K.2
Fernandes, S.3
Sousa, M.4
Schlegel, P.N.5
Mielnik, A.6
-
19
-
-
0033785321
-
Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism
-
Blanco P., Shlumukova M., Sargent C.A., Jobling M.A., Affara N., and Hurles M.E. Divergent outcomes of intrachromosomal recombination on the human Y chromosome: male infertility and recurrent polymorphism. J Med Genet 37 (2000) 752-758
-
(2000)
J Med Genet
, vol.37
, pp. 752-758
-
-
Blanco, P.1
Shlumukova, M.2
Sargent, C.A.3
Jobling, M.A.4
Affara, N.5
Hurles, M.E.6
-
20
-
-
8444223551
-
Origins of chromosomal rearrangement hotspots in the human genome: evidence from the AZFa deletion hotspots
-
[Epub 2004 July 14]
-
Hurles M.E., Willey D., Matthews L., and Hussain S.S. Origins of chromosomal rearrangement hotspots in the human genome: evidence from the AZFa deletion hotspots. Genome Biol 5 (2004) R55 [Epub 2004 July 14]
-
(2004)
Genome Biol
, vol.5
-
-
Hurles, M.E.1
Willey, D.2
Matthews, L.3
Hussain, S.S.4
-
21
-
-
0033692865
-
Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions
-
Paracchini S., Stuppia L., Gatta V., Palka G., Moro E., Foresta C., et al. Y-chromosomal DNA haplotypes in infertile European males carrying Y-microdeletions. J Endocrinol Investig 23 (2000) 671-676
-
(2000)
J Endocrinol Investig
, vol.23
, pp. 671-676
-
-
Paracchini, S.1
Stuppia, L.2
Gatta, V.3
Palka, G.4
Moro, E.5
Foresta, C.6
-
22
-
-
0031792256
-
Genetic evidence for a higher female migration rate in humans
-
Seielstad M.T., Minch E., and Cavalli-Sforza L.L. Genetic evidence for a higher female migration rate in humans. Nat Genet 20 (1998) 278-280
-
(1998)
Nat Genet
, vol.20
, pp. 278-280
-
-
Seielstad, M.T.1
Minch, E.2
Cavalli-Sforza, L.L.3
-
23
-
-
0028960407
-
Y chromosomal DNA variation and the peopling of Japan
-
Hammer M.F., and Horai S. Y chromosomal DNA variation and the peopling of Japan. Am J Hum Genet 56 (1995) 951-962
-
(1995)
Am J Hum Genet
, vol.56
, pp. 951-962
-
-
Hammer, M.F.1
Horai, S.2
-
24
-
-
31544453951
-
Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes
-
Hammer M.F., Karafet T.M., Park H., Omoto K., Harihara S., Stoneking M., et al. Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes. J Hum Genet 51 (2006) 47-58
-
(2006)
J Hum Genet
, vol.51
, pp. 47-58
-
-
Hammer, M.F.1
Karafet, T.M.2
Park, H.3
Omoto, K.4
Harihara, S.5
Stoneking, M.6
-
25
-
-
0034744362
-
The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations
-
Underhill P.A., Passarino G., Lin A.A., Shen P., Mirazon Lahr M., Foley R.A., et al. The phylogeography of Y chromosome binary haplotypes and the origins of modern human populations. Ann Hum Genet 65 (2001) 43-62
-
(2001)
Ann Hum Genet
, vol.65
, pp. 43-62
-
-
Underhill, P.A.1
Passarino, G.2
Lin, A.A.3
Shen, P.4
Mirazon Lahr, M.5
Foley, R.A.6
-
26
-
-
0242298320
-
Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection
-
Repping S., Skaletsky H., Brown L., van Daalen S.K., Korver C.M., Pyntikova T., et al. Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection. Nat Genet 35 (2003) 247-251
-
(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
-
27
-
-
0031889383
-
High frequency of well-defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome
-
Foresta C., Ferlin A., Garolla A., Moro E., Pistorello M., Barbaux S., et al. High frequency of well-defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome. Hum Reprod 13 (1998) 302-307
-
(1998)
Hum Reprod
, vol.13
, pp. 302-307
-
-
Foresta, C.1
Ferlin, A.2
Garolla, A.3
Moro, E.4
Pistorello, M.5
Barbaux, S.6
-
28
-
-
1242306489
-
AZF microdeletions of the Y chromosome and in vitro fertilization outcome
-
Choi J.M., Chung P., Veeck L., Mielnik A., Palermo G.D., and Schlegel P.N. AZF microdeletions of the Y chromosome and in vitro fertilization outcome. Fertil Steril 81 (2004) 337-341
-
(2004)
Fertil Steril
, vol.81
, pp. 337-341
-
-
Choi, J.M.1
Chung, P.2
Veeck, L.3
Mielnik, A.4
Palermo, G.D.5
Schlegel, P.N.6
-
29
-
-
0033763693
-
Microsurgical TESE and the distribution of spermatogenesis in non-obstructive azoospermia
-
Silber S.J. Microsurgical TESE and the distribution of spermatogenesis in non-obstructive azoospermia. Hum Reprod 15 (2000) 2278-2284
-
(2000)
Hum Reprod
, vol.15
, pp. 2278-2284
-
-
Silber, S.J.1
-
30
-
-
0030029393
-
Correlation between testicular histology and outcome after intracytoplasmic sperm injection using testicular spermatozoa
-
Tournaye H., Liu J., Nagy P.Z., Camus M., Goossens A., Silber S., et al. Correlation between testicular histology and outcome after intracytoplasmic sperm injection using testicular spermatozoa. Hum Reprod 11 (1996) 127-132
-
(1996)
Hum Reprod
, vol.11
, pp. 127-132
-
-
Tournaye, H.1
Liu, J.2
Nagy, P.Z.3
Camus, M.4
Goossens, A.5
Silber, S.6
|