-
2
-
-
0022102922
-
Reproductive impairments in the United States, 1965-1982
-
Mosher, W.D., Reproductive impairments in the United States, 1965-1982. Demography. 22: 415-430.
-
Demography
, vol.22
, pp. 415-430
-
-
Mosher, W.D.1
-
3
-
-
84867545171
-
Yq microdeletions-azoospermia factor candidate genes and spermatogenic arrest
-
Dada, R., N.P. Gupta and K. Kucheria, 2004. Yq microdeletions-azoospermia factor candidate genes and spermatogenic arrest. J. Biomol. Tech., 15: 176-183.
-
(2004)
J. Biomol. Tech
, vol.15
, pp. 176-183
-
-
Dada, R.1
Gupta, N.P.2
Kucheria, K.3
-
4
-
-
84861933191
-
Ychromosomal microdeletions in a local infertile male population of Pakistan
-
Siddique, A., H.J. Qureshi, S. Siddique and A. Husnain, 2009. Ychromosomal microdeletions in a local infertile male population of Pakistan. Pak J. Physiol., 5(1): 29-33.
-
(2009)
Pak J. Physiol
, vol.5
, Issue.1
, pp. 29-33
-
-
Siddique, A.1
Qureshi, H.J.2
Siddique, S.3
Husnain, A.4
-
5
-
-
84883112075
-
Detection of azoospermia factor (AZF) microdeletion on Y chromosome in infertile men with azoospermia or severe oligozoospermia
-
Abobakr, R.A.M., R.M. Mostafa, S.H. Mahmoud, H.Y. Abdallah and G.H. Ibrahim, 2009. Detection of azoospermia factor (AZF) microdeletion on Y chromosome in infertile men with azoospermia or severe oligozoospermia. Egypt. J. Derm & Androl., 29(2): 65-72.
-
(2009)
Egypt J. Derm & Androl
, vol.29
, Issue.2
, pp. 65-72
-
-
Abobakr, R.A.M.1
Mostafa, R.M.2
Mahmoud, S.H.3
Abdallah, H.Y.4
Ibrahim, G.H.5
-
6
-
-
0033803789
-
Prognostic value of Y deletion analysis: What is the clinical prognostic value of Y chromosome microdeletion analysis?
-
Krausz, C., L. Quintana-Murci and K. McElreavey, 2000. Prognostic value of Y deletion analysis: What is the clinical prognostic value of Y chromosome microdeletion analysis? Hum Reprod., 15: 1431-1434.
-
(2000)
Hum Reprod
, vol.15
, pp. 1431-1434
-
-
Krausz, C.1
Quintana-Murci, L.2
McElreavey, K.3
-
7
-
-
0034844179
-
Male infertility genetics-the future
-
Cram, D.S., M.K. O'Bryan and D.M. de Kretser, 2001. Male infertility genetics-the future. J. Androl., 22(5): 738-746.
-
(2001)
J. Androl
, vol.22
, Issue.5
, pp. 738-746
-
-
Cram, D.S.1
O'Bryan, M.K.2
de Kretser, D.M.3
-
8
-
-
0033981975
-
Human male infertility: Chromosome anomalies meiotic disorders, abnormal spermatozoa and recurrent abortion
-
Egozcue, S., J. Blanco, J.M. Vendrell, F. Garcia, A. Veiga, B. Aran, P.N. Barri, F. Vidal and J. Egozcue, 2000. Human male infertility: chromosome anomalies meiotic disorders, abnormal spermatozoa and recurrent abortion. Hum. Reprod., 6: 93-105.
-
(2000)
Hum Reprod
, vol.6
, pp. 93-105
-
-
Egozcue, S.1
Blanco, J.2
Vendrell, J.M.3
Garcia, F.4
Veiga, A.5
Aran, B.6
Barri, P.N.7
Vidal, F.8
Egozcue, J.9
-
9
-
-
44849109997
-
Genetics of azoospermia: Current knowledge, Clinical implications and future directions
-
Sadeghi-Nejad, H. and F. Farrokhi, 2007. Genetics of azoospermia: Current knowledge, Clinical implications and future directions. Part II. Urol J., 4: 192-206.
-
(2007)
Part II. Urol J
, vol.4
, pp. 192-206
-
-
Sadeghi-Nejad, H.1
Farrokhi, F.2
-
10
-
-
0017119580
-
Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm
-
Tiepolo, L. and O. Zuffardi, 1976. Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human Y chromosome long arm. Hum. Gene., 34: 119-124.
-
(1976)
Hum. Gene
, vol.34
, pp. 119-124
-
-
Tiepolo, L.1
Zuffardi, O.2
-
11
-
-
0026756965
-
The human Y chromosome: A 43-interval map based on naturally occurring deletions
-
Vollrath, D., S. Foote, A. Hilton, L.G. Brown, P. Beer-Romero, J.S. Bogan and D.C. Page, 1992. The human Y chromosome: a 43-interval map based on naturally occurring deletions. Science, 258: 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
Page, D.C.7
-
12
-
-
0007272350
-
Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq 11
-
Vogt, P.H., A. Edelmann, S. Kirsch, O. Henegariu, P. Hirschmann, F. Kiesewetter, F.M. Kohn, W.B. Schill, S. Farah, C. Ramos, M. Hartmann, W. Hartschuh, D. Meschede, H.M. Behre, A. Castel, E. Nieschalg, W. Weidncr, H.J. Grone, A. Jung, W. Engel and G. Haidl, 1996. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq 11. Hum Mol Gene. 5: 933-943.
-
(1996)
Hum Mol Gene
, vol.5
, pp. 933-943
-
-
Vogt, P.H.1
Edelmann, A.2
Kirsch, S.3
Henegariu, O.4
Hirschmann, P.5
Kiesewetter, F.6
Kohn, F.M.7
Schill, W.B.8
Farah, S.9
Ramos, C.10
Hartmann, M.11
Hartschuh, W.12
Meschede, D.13
Behre, H.M.14
Castel, A.15
Nieschalg, E.16
Weidncr, W.17
Grone, H.J.18
Jung, A.19
Engel, W.20
Haidl, G.21
more..
-
13
-
-
0032924325
-
Defining Regions of the Y chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection
-
Kent-First, M., A. Muallem, J. Shultz, J. Pryor, K. Roberts, W. Nolten, et al., 1999. Defining Regions of the Y chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection. MolReprod Dev., 53: 27-41.
-
(1999)
MolReprod Dev
, vol.53
, pp. 27-41
-
-
Kent-First, M.1
Muallem, A.2
Shultz, J.3
Pryor, J.4
Roberts, K.5
Nolten, W.6
-
14
-
-
4043092052
-
EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions. State of the art 2004
-
Simoni, M., E. Bakker and C. Krausz, 2004. EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions. State of the art 2004. Int. J. Androl., 27(4): 240-249.
-
(2004)
Int. J. Androl
, vol.27
, Issue.4
, pp. 240-249
-
-
Simoni, M.1
Bakker, E.2
Krausz, C.3
-
15
-
-
0037967242
-
The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes
-
Skaletsky, H., T. Kuroda-Kawaguchi, P.J. Minx et al., 2003. The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes. Nature., 423: 825-837.
-
(2003)
Nature
, vol.423
, pp. 825-837
-
-
Skaletsky, H.1
Kuroda-Kawaguchi, T.2
Minx, P.J.3
-
16
-
-
0031196792
-
Combined cytogenetic and Y chromosome Microdeletion screening in males undergoing intracytoplasmic sperm injection
-
Van der Ven, K., M. Montag, B. Peschka, J. Leygraaf, G. Schwanitz, G. Haidl, D. Krebs and H. Van der Ven, 1997. Combined cytogenetic and Y chromosome Microdeletion screening in males undergoing intracytoplasmic sperm injection. Molecular Reproduction, 3: 699-704.
-
(1997)
Molecular Reproduction
, vol.3
, pp. 699-704
-
-
van der Ven, K.1
Montag, M.2
Peschka, B.3
Leygraaf, J.4
Schwanitz, G.5
Haidl, G.6
Krebs, D.7
van der Ven, H.8
-
17
-
-
0031889383
-
High frequency of well defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome
-
Foresta, C., A. Ferlin, A. Garolla, E. Moro, M. Pistorello, S. Barbaux and M. Rossato, 1998. High frequency of well defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome. Human Reproduction., 13: 302-307.
-
(1998)
Human Reproduction
, vol.13
, pp. 302-307
-
-
Foresta, C.1
Ferlin, A.2
Garolla, A.3
Moro, E.4
Pistorello, M.5
Barbaux, S.6
Rossato, M.7
-
18
-
-
34547113096
-
The putative tumor suppressor gene PTPN13/PTPL1 induces apoptosis through insulin receptor substrate-1 dephosphorylation
-
Dromard, M., G. Bompard, M. Glondu-Lassis, C. Puech, D. Chalbos and G. Freiss, 2007. The putative tumor suppressor gene PTPN13/PTPL1 induces apoptosis through insulin receptor substrate-1 dephosphorylation. Cancer Research. 67(14): 6806-6813.
-
(2007)
Cancer Research
, vol.67
, Issue.14
, pp. 6806-6813
-
-
Dromard, M.1
Bompard, G.2
Glondu-Lassis, M.3
Puech, C.4
Chalbos, D.5
Freiss, G.6
-
19
-
-
77955408331
-
Genetic dissection of the AZF regions of the human Y chromosome: Thriller or filler for male (in)fertility
-
Navarro-Costa, P., C.E. Plancha and J. Goncalves, 2010. Genetic dissection of the AZF regions of the human Y chromosome: thriller or filler for male (in)fertility. J. Biomed Biotech., 2010: 1-18.
-
(2010)
J. Biomed Biotech
, vol.2010
, pp. 1-18
-
-
Navarro-Costa, P.1
Plancha, C.E.2
Goncalves, J.3
-
20
-
-
0037173065
-
Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis
-
Lahn, B.T., Z.L. Tang, J. Zhou et al., 2002. Previously uncharacterized histone acetyltransferases implicated in mammalian spermatogenesis. PANS., 99(13): 8707-8712.
-
(2002)
PANS
, vol.99
, Issue.13
, pp. 8707-8712
-
-
Lahn, B.T.1
Tang, Z.L.2
Zhou, J.3
-
21
-
-
33947608938
-
Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases
-
Peng, J., C.M. Redman, X. Wu et al., 2007. Insights into extensive deletions around the XK locus associated with McLeod phenotype and characterization of two novel cases. Gene., 392: 142-150.
-
(2007)
Gene
, vol.392
, pp. 142-150
-
-
Peng, J.1
Redman, C.M.2
Wu, X.3
-
22
-
-
0030725069
-
Functional coherence of the human Y chromosome
-
Lahn, B.T. and D.C. Page, 1997. Functional coherence of the human Y chromosome. Science, 278(5338): 675-680.
-
(1997)
Science
, vol.278
, Issue.5338
, pp. 675-680
-
-
Lahn, B.T.1
Page, D.C.2
-
23
-
-
0034508903
-
Genetic basis of male fertility
-
Hargreave, T.B., 2000. Genetic basis of male fertility. Br. Med. Bull., 56: 650-671.
-
(2000)
Br. Med. Bull
, vol.56
, pp. 650-671
-
-
Hargreave, T.B.1
-
24
-
-
84861950541
-
Prevalence of Y chromosome microdeletions in Iranian infertile men
-
Akbari Asbagh, F., A. Sina, H. Najmabadi, et al., 2003. Prevalence of Y chromosome microdeletions in Iranian infertile men. Acta Medica Iranica, 41: 3.
-
(2003)
Acta Medica Iranica
, vol.41
, pp. 3
-
-
Akbari, A.F.1
Sina, A.2
Najmabadi, H.3
-
25
-
-
0027715823
-
A Y chromosome gene family with RNA-binding protein homology: Candidates for the azospermia factor AZF controlling human spermatogenesis
-
Ma, K., J.D. Inglis, A. Sharkey, et al., 1993. A Y chromosome gene family with RNA-binding protein homology: candidates for the azospermia factor AZF controlling human spermatogenesis. Cell., 75: 1287-1295.
-
(1993)
Cell
, vol.75
, pp. 1287-1295
-
-
Ma, K.1
Inglis, J.D.2
Sharkey, A.3
-
26
-
-
6844252248
-
Characterization of the Coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxr interval of the mouse Y chromosome of the Dffry gene
-
Brown, G.M., R.A. Furlong, C.A. Sargent, R.P. Erickson, G. Longepied, M. Mitchell, M.H. Jones, T.B. Hargreave, H.J. Cooke and N.A. Affara, 1998. Characterization of the Coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxr interval of the mouse Y chromosome of the Dffry gene. Hum. Mol. Genet., 7: 97-107.
-
(1998)
Hum. Mol Genet
, vol.7
, pp. 97-107
-
-
Brown, G.M.1
Furlong, R.A.2
Sargent, C.A.3
Erickson, R.P.4
Longepied, G.5
Mitchell, M.6
Jones, M.H.7
Hargreave, T.B.8
Cooke, H.J.9
Affara, N.A.10
-
27
-
-
0035682067
-
Study of microdeletions in the Y chromosome of infertile men with idiopathic oligo-or Azoospermia
-
Yao, G., G. Chen and T. Pan, 2001. Study of microdeletions in the Y chromosome of infertile men with idiopathic oligo-or Azoospermia. J. Assist Reprod and Genet., 18(11): 612-616.
-
(2001)
J. Assist Reprod and Genet
, vol.18
, Issue.11
, pp. 612-616
-
-
Yao, G.1
Chen, G.2
Pan, T.3
-
28
-
-
0029088061
-
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
-
Reijo, R., T.Y. Lee, P. Salo, et al., 1995. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nat Genet. 10: 383-393.
-
(1995)
Nat Genet
, vol.10
, pp. 383-393
-
-
Reijo, R.1
Lee, T.Y.2
Salo, P.3
-
29
-
-
0032110611
-
Current status of the molecular diagnosis of Y-chromosomal microdeletions in the work-up of male infertility-Initiative for international quality control
-
Simoni, M., A. Kamischke and E. Nieschlag, 1998. Current status of the molecular diagnosis of Y-chromosomal microdeletions in the work-up of male infertility-Initiative for international quality control. Hum Reprod., 13: 1764-1767.
-
(1998)
Hum Reprod
, vol.13
, pp. 1764-1767
-
-
Simoni, M.1
Kamischke, A.2
Nieschlag, E.3
-
30
-
-
0031745195
-
A quarter of men with idioazoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq 11
-
Stuppia, L., V. Gatta, G. Calabrase, et al., 1998. A quarter of men with idioazoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq 11. Hum Genet., 102: 566-570.
-
(1998)
Hum Genet
, vol.102
, pp. 566-570
-
-
Stuppia, L.1
Gatta, V.2
Calabrase, G.3
-
31
-
-
0029798989
-
The Y chromosome region essential for spermatogenesis
-
Nakahori, Y., Y. Kuroki, R. Komaki, et al., 1996. The Y chromosome region essential for spermatogenesis. Horm Res., 46(suppl 1): 20-23.
-
(1996)
Horm Res
, vol.46
, Issue.1 SUPPL.
, pp. 20-23
-
-
Nakahori, Y.1
Kuroki, Y.2
Komaki, R.3
-
32
-
-
0026726412
-
The human Y chromosome: Overlapping DNA clones spanning the euchromatic region
-
Foote, S., D. Vollrath, A. Hilton and D.C. Page, 1992. The human Y chromosome: overlapping DNA clones spanning the euchromatic region. Science. 258: 60-66.
-
(1992)
Science
, vol.258
, pp. 60-66
-
-
Foote, S.1
Vollrath, D.2
Hilton, A.3
Page, D.C.4
-
33
-
-
0030883296
-
Submicroscopic deletions in the Y chromosome of infertile men
-
Girardi, S.K., A. Mielnik and P.N. Schlegel, 1997. Submicroscopic deletions in the Y chromosome of infertile men. Hum. Reprod. 12: 1635-l641.
-
(1997)
Hum Reprod
, vol.12
-
-
Girardi, S.K.1
Mielnik, A.2
Schlegel, P.N.3
-
34
-
-
84861445685
-
A Comparative Study of AZF Deletions and TSPY Gene Variation in Czech and Indian Infertile Men
-
Singh, A.R., R. Vrtel, R. Vodicka, et al. 2006. A Comparative Study of AZF Deletions and TSPY Gene Variation in Czech and Indian Infertile Men. Int. J. Hum Genet., 6: 209-217.
-
(2006)
Int. J. Hum Genet
, vol.6
, pp. 209-217
-
-
Singh, A.R.1
Vrtel, R.2
Vodicka, R.3
-
35
-
-
0031050740
-
Microdeletions in the Y chromosome of infertile men
-
Pryor, J.L., M. Kent-First, A. Muallem, et al. Microdeletions in the Y chromosome of infertile men. N Engl. J. Med., 336: 534-539.
-
N Engl. J. Med
, vol.336
, pp. 534-539
-
-
Pryor, J.L.1
Kent-First, M.2
Muallem, A.3
|