-
1
-
-
0017119580
-
Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
-
Tiepolo L., 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
-
-
0026018317
-
A deletion map of the human Yq11 region: Implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis
-
Bardoni B., Zuffardi O., Guioli S., Ballabio A., Simi P., Cavalli P., et al. A deletion map of the human Yq11 region implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesis. Genomics. 11:1991;443-451.
-
(1991)
Genomics
, vol.11
, pp. 443-451
-
-
Bardoni, B.1
Zuffardi, O.2
Guioli, S.3
Ballabio, A.4
Simi, P.5
Cavalli, P.6
-
3
-
-
0027715823
-
A Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling human spermatogenesis
-
Ma K., Inglis J.D., Sharkey A., Bickmore W.A., Hill R.E., Prosser E.J., et al. A Y chromosome gene family with RNA-binding protein homology candidates for the azoospermia factor AZF controlling human spermatogenesis. Cell. 75:1993;1287-1295.
-
(1993)
Cell
, vol.75
, pp. 1287-1295
-
-
Ma, K.1
Inglis, J.D.2
Sharkey, A.3
Bickmore, W.A.4
Hill, R.E.5
Prosser, E.J.6
-
4
-
-
0026726199
-
Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene
-
Vogt P., Chandley A.C., Hargreave T.B., Keil R., Ma K., Sharkey A. Microdeletions in interval 6 of the Y chromosome of males with idiopathic sterility point to disruption of AZF, a human spermatogenesis gene. Hum Genet. 89:1992;491-496.
-
(1992)
Hum Genet
, vol.89
, pp. 491-496
-
-
Vogt, P.1
Chandley, A.C.2
Hargreave, T.B.3
Keil, R.4
Ma, K.5
Sharkey, A.6
-
5
-
-
0028059593
-
Human male infertility Y-linked genes and spermatogenesis
-
Chandley A.C., Cooke H.J. Human male infertility Y-linked genes and spermatogenesis. Hum Mol Genet. 3:1994;1449-1452.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1449-1452
-
-
Chandley, A.C.1
Cooke, H.J.2
-
6
-
-
0029088061
-
Diverse spermatogenic defect in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
-
Reijo R., Lee T.-Y., Salo P., Alagappan R.K., Brown L.G., Rosenberg M., et al. Diverse spermatogenic defect in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat Genet. 10:1995;383-393.
-
(1995)
Nat Genet
, vol.10
, pp. 383-393
-
-
Reijo, R.1
Lee, T.-Y.2
Salo, P.3
Alagappan, R.K.4
Brown, L.G.5
Rosenberg, M.6
-
7
-
-
0029871858
-
Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome
-
Reijo R., Alagappan P.K., Patrizio P., Page D.C. Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome. Lancet. 347:1996;1290-1293.
-
(1996)
Lancet
, vol.347
, pp. 1290-1293
-
-
Reijo, R.1
Alagappan, P.K.2
Patrizio, P.3
Page, D.C.4
-
8
-
-
0028114292
-
PCR analysis of the Y chromosome long arm in azoospermic patients: Evidence for a second locus required for spermatogenesis
-
Kobayashi K., Mizuno K., Hida A., Komaki R., Tomita K., Matsushita I., et al. PCR analysis of the Y chromosome long arm in azoospermic patients evidence for a second locus required for spermatogenesis. Hum Mol Genet. 3:1994;1965-1967.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1965-1967
-
-
Kobayashi, K.1
Mizuno, K.2
Hida, A.3
Komaki, R.4
Tomita, K.5
Matsushita, I.6
-
9
-
-
0030292382
-
The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned
-
Saxena R., Brown L.G., Hawkins T., Alagappan R.K., Skaletsky H., Reeve M.P., et al. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned. Nat Genet. 14:1996;292-299.
-
(1996)
Nat Genet
, vol.14
, pp. 292-299
-
-
Saxena, R.1
Brown, L.G.2
Hawkins, T.3
Alagappan, R.K.4
Skaletsky, H.5
Reeve, M.P.6
-
10
-
-
0007272350
-
Human Y-chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
-
Vogt P.H., Edelman 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
Edelman, A.2
Kirsch, S.3
Henegariu, O.4
Hirschmann, P.5
Kiesewetter, F.6
-
11
-
-
0031135612
-
The molecular genetics of male infertility
-
Meschede D., Horst J. The molecular genetics of male infertility. Mol Hum Reprod. 3:1997;419-430.
-
(1997)
Mol Hum Reprod
, vol.3
, pp. 419-430
-
-
Meschede, D.1
Horst, J.2
-
12
-
-
0031050740
-
Microdeletions in the Y chromosome of infertile men
-
Pryor J.L., Kent-First M., Muallem A., Van Bergen A.H., Nolten W.E., Meisner L., et al. Microdeletions in the Y chromosome of infertile men. N Engl J Med. 336:1997;534-539.
-
(1997)
N Engl J Med
, vol.336
, pp. 534-539
-
-
Pryor, J.L.1
Kent-First, M.2
Muallem, A.3
Van Bergen, A.H.4
Nolten, W.E.5
Meisner, L.6
-
13
-
-
0030253042
-
Polymerase chain reaction screening for Y chromosome microdeletions: A first step towards the diagnosis of genetically-determined spermatogenic failure in men
-
Qureshi S.J., Ross A.R., Ma K., Cooke H.J., Intyre M.A., Chandley A.C., et al. Polymerase chain reaction screening for Y chromosome microdeletions a first step towards the diagnosis of genetically-determined spermatogenic failure in men. Mol Hum Reprod. 2:1996;775-779.
-
(1996)
Mol Hum Reprod
, vol.2
, pp. 775-779
-
-
Qureshi, S.J.1
Ross, A.R.2
Ma, K.3
Cooke, H.J.4
Intyre, M.A.5
Chandley, A.C.6
-
14
-
-
0030904952
-
Y-chromosome deletions in idiopathic severe testiculopathies
-
Foresta C., Ferlin A., Garolla A., Rossato M., Barbaux S., De Bortoli A. Y-chromosome deletions in idiopathic severe testiculopathies. J Clin Endocrinol Metab. 82:1997;1075-1080.
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 1075-1080
-
-
Foresta, C.1
Ferlin, A.2
Garolla, A.3
Rossato, M.4
Barbaux, S.5
De Bortoli, A.6
-
16
-
-
0026756965
-
The human Y chromosome: A 43-interval map based on naturally occurring deletions
-
Vollrath D., Foote S., Hilton A., Brown L.G., Beer-Romero P., Bogan J.S., et al. The human Y chromosome a 43-interval map based on naturally occurring deletions. Science. 258:1992;52-59.
-
(1992)
Science
, vol.258
, pp. 52-59
-
-
Vollrath, D.1
Foote, S.2
Hilton, A.3
Brown, L.G.4
Beer-Romero, P.5
Bogan, J.S.6
-
17
-
-
0026726412
-
The human Y chromosome: Overlapping DNA clones spanning the euchromatic region
-
Foote S., Vollrath D., Hilton A., Page D.C. The human Y chromosome overlapping DNA clones spanning the euchromatic region. Science. 258:1992;60-66.
-
(1992)
Science
, vol.258
, pp. 60-66
-
-
Foote, S.1
Vollrath, D.2
Hilton, A.3
Page, D.C.4
-
18
-
-
0023921510
-
Y; Autosome translocations and mosaicism in the aetiology of 45, X maleness: Assignment of fertility factor to distal Yq11
-
Andersson M., Page D.C., Pettay D., Subrt I., Turleau C., de Grouchy J., et al. Y; autosome translocations and mosaicism in the aetiology of 45, X maleness: assignment of fertility factor to distal Yq11. Hum Genet. 79:1988;2-7.
-
(1988)
Hum Genet
, vol.79
, pp. 2-7
-
-
Andersson, M.1
Page, D.C.2
Pettay, D.3
Subrt, I.4
Turleau, C.5
De Grouchy, J.6
-
19
-
-
0029965983
-
Microdeletions in interval 6 of the Y chromosome detected by STS-PCR in 6 of 33 patients with idiopathic oligo- or azoospermia
-
Stuppia L., Mastroprimiano G., Calabrese G., Peila R., Tenaglia R., Palka G. Microdeletions in interval 6 of the Y chromosome detected by STS-PCR in 6 of 33 patients with idiopathic oligo- or azoospermia. Cytogenet Cell Genet. 72:1996;155-158.
-
(1996)
Cytogenet Cell Genet
, vol.72
, pp. 155-158
-
-
Stuppia, L.1
Mastroprimiano, G.2
Calabrese, G.3
Peila, R.4
Tenaglia, R.5
Palka, G.6
-
20
-
-
0031024316
-
Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia
-
Simoni M., Gromoll J., Dworniczak B., Rolf C., Abshagen K., Kamischke A., et al. Screening for deletions of the Y chromosome involving the DAZ (Deleted in AZoospermia) gene in azoospermia and severe oligozoospermia. Fertil Steril. 67:1997;542-547.
-
(1997)
Fertil Steril
, vol.67
, pp. 542-547
-
-
Simoni, M.1
Gromoll, J.2
Dworniczak, B.3
Rolf, C.4
Abshagen, K.5
Kamischke, A.6
-
21
-
-
0031467546
-
Part of the RBM gene cluster is located distally to the DAZ gene cluster in human Yq11.23
-
Pasantes J.J., Rottger S., Schempp W. Part of the RBM gene cluster is located distally to the DAZ gene cluster in human Yq11.23. Chromosome Res. 5:1997;537-540.
-
(1997)
Chromosome Res
, vol.5
, pp. 537-540
-
-
Pasantes, J.J.1
Rottger, S.2
Schempp, W.3
-
22
-
-
0030726761
-
Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome
-
Chai N.N., Salido E.C., Yen P.H. Multiple functional copies of the RBM gene family, a spermatogenesis candidate on the human Y chromosome. Genomics. 45:1997;355-361.
-
(1997)
Genomics
, vol.45
, pp. 355-361
-
-
Chai, N.N.1
Salido, E.C.2
Yen, P.H.3
-
23
-
-
0030914159
-
Azoospermic men with deletion of the DAZ gene cluster are capable of completing spermatogenesis: Fertilization, normal embryonic development and pregnancy occur when retrieved testicular spermatozoa are used for intracytoplasmic sperm injection
-
Mulhall J.P., Reijo R., Alagappan R., Brown L., Page D., Carson R., et al. Azoospermic men with deletion of the DAZ gene cluster are capable of completing spermatogenesis fertilization, normal embryonic development and pregnancy occur when retrieved testicular spermatozoa are used for intracytoplasmic sperm injection. Hum Reprod. 12:1997;503-508.
-
(1997)
Hum Reprod
, vol.12
, pp. 503-508
-
-
Mulhall, J.P.1
Reijo, R.2
Alagappan, R.3
Brown, L.4
Page, D.5
Carson, R.6
-
24
-
-
0029842285
-
The human autosomal gene Dazla: Testis specificity and a candidate for male infertility
-
Yen P.H., Chai N.N., Salido E.C. The human autosomal gene Dazla testis specificity and a candidate for male infertility. Hum Mol Genet. 5:1996;2013-2017.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 2013-2017
-
-
Yen, P.H.1
Chai, N.N.2
Salido, E.C.3
-
25
-
-
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
|