-
1
-
-
0030011808
-
Report of the second international workshop on Y chromosome mapping 1995
-
Affara, N., Lau, Y., 1996. Report of the second international workshop on Y chromosome mapping 1995. Cytogenet. Cell. Genet.
-
(1996)
Cytogenet. Cell. Genet.
-
-
Affara, N.1
Lau, Y.2
-
2
-
-
0028124953
-
Congenital bilateral absence of the vas deferens in the absence of cystic fibrosis
-
Augarten A., Yahav Y., Kerem B.S., Halle D., Laufer J., Szeinberg A., Dor J., Mashiach S., Gazit E., Madgar I. Congenital bilateral absence of the vas deferens in the absence of cystic fibrosis. Lancet. 344:1994;1473-1474.
-
(1994)
Lancet
, vol.344
, pp. 1473-1474
-
-
Augarten, A.1
Yahav, Y.2
Kerem, B.S.3
Halle, D.4
Laufer, J.5
Szeinberg, A.6
Dor, J.7
Mashiach, S.8
Gazit, E.9
Madgar, I.10
-
4
-
-
0028049607
-
-
Caceres C., Ribes E., Muller S., Cornudella L., Chiva M. Mol. Reprod. Dev. 38(4):1994;440-452.
-
(1994)
Mol. Reprod. Dev.
, vol.38
, Issue.4
, pp. 440-452
-
-
Caceres, C.1
Ribes, E.2
Muller, S.3
Cornudella, L.4
Chiva, M.5
-
5
-
-
0030726761
-
Multiple functional copies of the RBM gene family, a spermatogenesis candidate of the human Y chromosome
-
Chai N.N., Salido E.C., Yen P.H. Multiple functional copies of the RBM gene family, a spermatogenesis candidate of the human Y chromosome. Genetics. 45:1997;355-361.
-
(1997)
Genetics
, vol.45
, pp. 355-361
-
-
Chai, N.N.1
Salido, E.C.2
Yen, P.H.3
-
6
-
-
0016558147
-
Cytogenetics and infertility in man. Results of a 5 year study of men attending a subfertility clinic: Karyotype and seminal analysis
-
Chandley A.C., Edmond P.E., Christie S., Gowans I., Fletcher J., Frackiewicz A., Newton M. Cytogenetics and infertility in man. Results of a 5 year study of men attending a subfertility clinic: Karyotype and seminal analysis. Ann. Hum. Genet. 39:1975;231-254.
-
(1975)
Ann. Hum. Genet.
, vol.39
, pp. 231-254
-
-
Chandley, A.C.1
Edmond, P.E.2
Christie, S.3
Gowans, I.4
Fletcher, J.5
Frackiewicz, A.6
Newton, M.7
-
7
-
-
0029025333
-
Mutations in cystic fibrosis gene in patients with congenital absence of the vas deferens
-
Chillon M., Casals T., Mercier B., Bassas L., Lissens W., Silber S., Rorney M.C., Ruiz-Romero J., Verlingue C., Claustres M. et al. Mutations in cystic fibrosis gene in patients with congenital absence of the vas deferens. New. Eng. J. Med. 332:1995;1475-1480.
-
(1995)
New. Eng. 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
Rorney, M.C.7
Ruiz-Romero, J.8
Verlingue, C.9
Claustres, M.10
-
8
-
-
0028158533
-
Achievement of meiosis in XXY germ cells: Study of 543 sperm karyotypes from an XY/XXY mosaic patient
-
Cozzi J., Chevret E., Rousseaux S. et al. Achievement of meiosis in XXY germ cells: study of 543 sperm karyotypes from an XY/XXY mosaic patient. Hum. Genet. 93:1994;32-34.
-
(1994)
Hum. Genet.
, vol.93
, pp. 32-34
-
-
Cozzi, J.1
Chevret, E.2
Rousseaux, S.3
-
9
-
-
0030225318
-
Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens
-
De Braekelleer M., Ferec C. Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens. Mol. Hum. Reprod. 2:1996;669-677.
-
(1996)
Mol. Hum. Reprod.
, vol.2
, pp. 669-677
-
-
De Braekelleer, M.1
Ferec, C.2
-
10
-
-
0028220333
-
Heterogeneity in the severity of cystic fibrosis and the role of the CFTR gene mutations
-
Dean M., Santis G. Heterogeneity in the severity of cystic fibrosis and the role of the CFTR gene mutations. Hum. Genet. 93(4):1994;364-368.
-
(1994)
Hum. Genet.
, vol.93
, Issue.4
, pp. 364-368
-
-
Dean, M.1
Santis, G.2
-
11
-
-
85046165594
-
A human candidate spermatogenesis gene, RBM1, is conserved and amplified on the marsupial Y chromosome
-
Delbridge M.L., Harry J.L., Toder R., O'Neill R.J., Ma K., Chandley A.C., Graves J.A. A human candidate spermatogenesis gene, RBM1, is conserved and amplified on the marsupial Y chromosome. Nat. Genet. 4:(April 15) 1997;411.
-
(1997)
Nat. Genet.
, vol.4
, pp. 411
-
-
Delbridge, M.L.1
Harry, J.L.2
Toder, R.3
O'Neill, R.J.4
Ma, K.5
Chandley, A.C.6
Graves, J.A.7
-
14
-
-
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., Hargreave T.B. The incidence of cystic fibrosis gene mutations in patients with congenital bilateral absence of the vas deferens in Scotland. Br. J. Urol. 79:1997;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
-
15
-
-
0030410836
-
Absent vas deferens and ipsilateral multicystic dysplastic kidney in a child
-
Drake M.J., Quinn F.M. Absent vas deferens and ipsilateral multicystic dysplastic kidney in a child. Br. J. Urol. 77:1996;756-757.
-
(1996)
Br. J. Urol.
, vol.77
, pp. 756-757
-
-
Drake, M.J.1
Quinn, F.M.2
-
16
-
-
0022402180
-
Lymphocyte sub-populations in the male genital tract
-
El-Demiry M.I.M., Hargreave T.B., Busuttil A., James K., Ritchie A.W.S., Chisholm G.D. Lymphocyte sub-populations in the male genital tract. Br. J. Urol. 57:1985;769-774.
-
(1985)
Br. J. Urol.
, vol.57
, pp. 769-774
-
-
El-Demiry, M.I.M.1
Hargreave, T.B.2
Busuttil, A.3
James, K.4
Ritchie, A.W.S.5
Chisholm, G.D.6
-
17
-
-
12644310287
-
Expression of RBM in the nuclei of human germ cell is dependent on a critical region of the Y chromosome long arm
-
Elliot D.J., Millar M.R., Oghene K., Ross A., Kiesewelter F., Pryor J., McIntyre M., Hargreave T.B., Saunders P.T., Vogt P.H., Chandley A.C., Cooke H. Expression of RBM in the nuclei of human germ cell is dependent on a critical region of the Y chromosome long arm. Proc. Natl. Acad. Sci. USA. 94(8):(15 April) 1997;3848-3853.
-
(1997)
Proc. Natl. Acad. Sci. USA.
, vol.94
, Issue.8
, pp. 3848-3853
-
-
Elliot, D.J.1
Millar, M.R.2
Oghene, K.3
Ross, A.4
Kiesewelter, F.5
Pryor, J.6
McIntyre, M.7
Hargreave, T.B.8
Saunders, P.T.9
Vogt, P.H.10
Chandley, A.C.11
Cooke, H.12
-
18
-
-
0030072658
-
Germline gene therapy: Its time is near
-
Fiddler M., Pergament E. Germline gene therapy: its time is near. Mol. Hum. Reprod. 2:1996;75-76.
-
(1996)
Mol. Hum. Reprod.
, vol.2
, pp. 75-76
-
-
Fiddler, M.1
Pergament, E.2
-
19
-
-
0030471118
-
Male infertility and ICSI: Are there limits?
-
Foresta, C., Rossato, M., Garolla, Ferlin, A., 1996. Male infertility and ICSI: are there limits? Hum. Reprod. 11 2347-2348.
-
(1996)
Hum. Reprod.
, vol.11
, pp. 2347-2348
-
-
Foresta, C.1
Rossato, M.2
Garolla Ferlin, A.3
-
20
-
-
0025248381
-
Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X-Y translocation
-
Gabriel-Robez O., Rumpler Y., Ratomponirina C., Petit C., Levilliers J., Croquette M.F., Couturier J. Deletion of the pseudoautosomal region and lack of sex-chromosome pairing at pachytene in two infertile men carrying an X-Y translocation. Cytogenet. Cell. Genet. 54:1990;38-42.
-
(1990)
Cytogenet. Cell. Genet.
, vol.54
, pp. 38-42
-
-
Gabriel-Robez, O.1
Rumpler, Y.2
Ratomponirina, C.3
Petit, C.4
Levilliers, J.5
Croquette, M.F.6
Couturier, J.7
-
21
-
-
0001062056
-
An azoospermic man with a submicroscopic interstitial deletion on the Xp pseudoautosomal region
-
Gonialves, J., McElreavey, K., Carreiro, H., Vale, F., Marques, R., Simaoi, L., Boieiro, F., Fellous, M., Lavinha, J., 1996. An azoospermic man with a submicroscopic interstitial deletion on the Xp pseudoautosomal region. Hum. Reprod. 11 158. 12th Annual meeting of the European Society of Human Reproduction.
-
(1996)
Hum. Reprod. 11 158. 12th Annual Meeting of the European Society of Human Reproduction
-
-
Gonialves, J.1
McElreavey, K.2
Carreiro, H.3
Vale, F.4
Marques, R.5
Simaoi, L.6
Boieiro, F.7
Fellous, M.8
Lavinha, J.9
-
22
-
-
0001779058
-
Localisation of an SPGY gene product in human spermatozoa
-
Abstract 115 in Hum. Reprod. 11.
-
Haberman, B., Mi, H., Krause, W., Vogt, P.H., 1996. Localisation of an SPGY gene product in human spermatozoa. Abstract 115 in Hum. Reprod. 11. Proceedings of the 12th Annual meeting of the European Society of Human Reproduction, pp. 54.
-
(1996)
Proceedings of the 12th Annual Meeting of the European Society of Human Reproduction
, pp. 54
-
-
Haberman, B.1
Mi, H.2
Krause, W.3
Vogt, P.H.4
-
24
-
-
0019813869
-
Searching for the infertile man with hyperprolactinaemia
-
Hargreave T.B., Richmond J.D., Liakatas J., Elton R.A., Brown N.S. Searching for the infertile man with hyperprolactinaemia. Fertil. Steril. 36:1981;630-632.
-
(1981)
Fertil. Steril.
, vol.36
, pp. 630-632
-
-
Hargreave, T.B.1
Richmond, J.D.2
Liakatas, J.3
Elton, R.A.4
Brown, N.S.5
-
25
-
-
0012339765
-
Randomised trial of Tamoxifen versus vitamin C for male infertility. Advances in fertility and sterility, vol. 4. Infertility male and female
-
In: Ratnam, S.S., Teoh, E., Anandakumar, C. (Eds.) Singapore, October 1986. Perthenon Publishing Group, Carnforth, Lancs, UK
-
Hargreave, T.B., Sweeting, V.M., Elton, R.A., 1987. Randomised trial of Tamoxifen versus vitamin C for male infertility. Advances in fertility and sterility, vol. 4. Infertility male and female. In: Ratnam, S.S., Teoh, E., Anandakumar, C. (Eds.), Proceedings of the 12th World Congress on Fertility and Sterility, Singapore, October 1986. Perthenon Publishing Group, Carnforth, Lancs, UK, PP. 51-57.
-
(1987)
Proceedings of the 12th World Congress on Fertility and Sterility
, vol.4
, pp. 51-57
-
-
Hargreave, T.B.1
Sweeting, V.M.2
Elton, R.A.3
-
26
-
-
0028360261
-
Rapid screening of the Y chromosome in idiopathic sterile men, diagnostic for deletions in AZF, a genetic Y factor expressed during spermatogenesis
-
Henegariu O., Hirschmann P., Killian K., Kirsch S., Lengauer C., Maiwald R., Mielke K., Vogt P. Rapid screening of the Y chromosome in idiopathic sterile men, diagnostic for deletions in AZF, a genetic Y factor expressed during spermatogenesis. Andrologia. 26:1994;97-106.
-
(1994)
Andrologia
, vol.26
, pp. 97-106
-
-
Henegariu, O.1
Hirschmann, P.2
Killian, K.3
Kirsch, S.4
Lengauer, C.5
Maiwald, R.6
Mielke, K.7
Vogt, P.8
-
27
-
-
0026928949
-
Menkes disease: An X-linked neurological disorder of copper metabolism
-
Horn N., Tonnesen T., Tumer Z. Menkes disease: an X-linked neurological disorder of copper metabolism. Brain Pathol. 2:1992;351-362.
-
(1992)
Brain Pathol.
, vol.2
, pp. 351-362
-
-
Horn, N.1
Tonnesen, T.2
Tumer, Z.3
-
28
-
-
0025282069
-
Retinitis pigmentosa: Genetic mapping in X-linked and autosomal forms of the disease
-
Humphries P., Farrar G.J., Kenna P., McWilliam P. Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease. Clin. Genet. 38:1990;1-13.
-
(1990)
Clin. Genet.
, vol.38
, pp. 1-13
-
-
Humphries, P.1
Farrar, G.J.2
Kenna, P.3
McWilliam, P.4
-
29
-
-
0029147090
-
Sex chromosomal abnormalities and intracytoplasmic sperm injection
-
(letter)
-
In't Veld P., Brandenburg H., Verhoeff A., Dhont M., Los F. Sex chromosomal abnormalities and intracytoplasmic sperm injection. Lancet. 346:1995;773. (letter).
-
(1995)
Lancet
, vol.346
, pp. 773
-
-
In't Veld, P.1
Brandenburg, H.2
Verhoeff, A.3
Dhont, M.4
Los, F.5
-
30
-
-
0001101706
-
Germ-line therapy: Back to basics
-
Jeungst E.T. Germ-line therapy: back to basics. J. Med. Philos. 16:1991;593-612.
-
(1991)
J. Med. Philos.
, vol.16
, pp. 593-612
-
-
Jeungst, E.T.1
-
31
-
-
0002166383
-
Development of a large highly diagnostic panel of multiplexed sequence tagged sites (STS'S) which cover key regions on human Yq: Its application in fertile and infertile (azoospermic and oligozoospermic) populations
-
Organised by the National institutes of Health USA and Human genome organisation Medical Research Council UK. Asilomar conference centre, Pacific Grove, California, Sept 17-20, 1995
-
Kent, F., Muallem, M.G., Agulnik, A., 1995. Development of a large highly diagnostic panel of multiplexed sequence tagged sites (STS'S) which cover key regions on human Yq: its application in fertile and infertile (azoospermic and oligozoospermic) populations. Proceedings of the second international workshop on the Y chromosome. Organised by the National institutes of Health USA and Human genome organisation Medical Research Council UK. Asilomar conference centre, Pacific Grove, California, Sept 17-20, 1995, pp. 24-25.
-
(1995)
Proceedings of the Second International Workshop on the Y Chromosome
, pp. 24-25
-
-
Kent, F.1
Muallem, M.G.2
Agulnik, A.3
-
32
-
-
0013519634
-
PCR analysis of the Y chromosome long arm in azoospermic patients: Evidence of a second locus required for spermatogenesis
-
Kobayashi K., Mizuno K., Hida A., Komaki R., Tomita K., Matsushita I., Namiki M., Iwamoto T., Tamura S., Minowada S., Nakhori Y., Nakogome Y. PCR analysis of the Y chromosome long arm in azoospermic patients: evidence of a second locus required for spermatogenesis. Cell. 75:1994;1287-1295.
-
(1994)
Cell
, vol.75
, pp. 1287-1295
-
-
Kobayashi, K.1
Mizuno, K.2
Hida, A.3
Komaki, R.4
Tomita, K.5
Matsushita, I.6
Namiki, M.7
Iwamoto, T.8
Tamura, S.9
Minowada, S.10
Nakhori, Y.11
Nakogome, Y.12
-
33
-
-
0002675673
-
Prevalence of microdeletions in the azoospermic factor region of the Y chromosome in cases of azoospermia and severe oligoasthenoteratozoospermia
-
Hum. Reprod. 11. Abstract no 121
-
Kupker W., Ludwig M., Hahn K., Al-Hasani S., Montzka P., Felberbaum R., Sturm R., Yilmaz A., Diedrich, K., 1996. Prevalence of microdeletions in the azoospermic factor region of the Y chromosome in cases of azoospermia and severe oligoasthenoteratozoospermia. Hum. Reprod. 11. Abstract no 121, pp. 57, Annual meeting of the European Society of Human Reproduction.
-
(1996)
Annual Meeting of the European Society of Human Reproduction
, pp. 57
-
-
Kupker, W.1
Ludwig, M.2
Hahn, K.3
Al-Hasani, S.4
Montzka, P.5
Felberbaum, R.6
Sturm, R.7
Yilmaz, A.8
Diedrich, K.9
-
34
-
-
0030662441
-
Birth defects in infants conceived by intracytoplasmic sperm injection: An alternative interpretation
-
Kurinczuk J.J., Bower C. Birth defects in infants conceived by intracytoplasmic sperm injection: an alternative interpretation. Br. Med. J. 315:1997;1260-1266.
-
(1997)
Br. Med. J.
, vol.315
, pp. 1260-1266
-
-
Kurinczuk, J.J.1
Bower, C.2
-
35
-
-
0028128358
-
Case control study of whether subfertility in men is familial
-
Lilford R., Jones A.M., Bishop D.T., Thornton J., Mueller R. Case control study of whether subfertility in men is familial. Br. Med. J. 309:1994;570-573.
-
(1994)
Br. Med. J.
, vol.309
, pp. 570-573
-
-
Lilford, R.1
Jones, A.M.2
Bishop, D.T.3
Thornton, J.4
Mueller, R.5
-
36
-
-
0026849360
-
Towards the molecular localisation of the AZF locus: Mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome
-
Ma K., . Sharkey A., Kirsch S., Vogt P., Keil R., Hargreave T.B., McBeath S., Chandley A.C. Towards the molecular localisation of the AZF locus: mapping of microdeletions in azoospermic men within 14 subintervals of interval 6 of the human Y chromosome. Hum. Mol. Genet. 1:1992;29-33.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 29-33
-
-
Ma, K.1
Sharkey, A.2
Kirsch, S.3
Vogt, P.4
Keil, R.5
Hargreave, T.B.6
McBeath, S.7
Chandley, A.C.8
-
37
-
-
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. 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
-
38
-
-
0013519639
-
Reports of the second international workshop on Y chromosome mapping 1995
-
In: Lau, et al. (Eds.) (in press).
-
Maiwald, R., Seebacher, T., Edelmann, A., Hirschmann, P., Kohler, M.R., Kirsch, S., Vogt, P., 1995. In: Lau, et al. (Eds.), Reports of the second international workshop on Y chromosome mapping 1995. Cytogenet. Cell. Genet. (in press).
-
(1995)
Cytogenet. Cell. Genet.
-
-
Maiwald, R.1
Seebacher, T.2
Edelmann, A.3
Hirschmann, P.4
Kohler, M.R.5
Kirsch, S.6
Vogt, P.7
-
39
-
-
0001931536
-
The incidence of the deleted azoospermia gene in infertile men
-
Hum. Reprod. 11. Abstract no. 120
-
Mallidis, C., Loveland, K., Najmabadi, H., McLaughlin, R., Baker, G., Basin, S., de Kretser, D.M., 1996. The incidence of the deleted azoospermia gene in infertile men. Hum. Reprod. 11. Abstract no. 120 pp. 56, 12th Annual meeting of the European Society of Human Reproduction.
-
(1996)
12th Annual Meeting of the European Society of Human Reproduction
, pp. 56
-
-
Mallidis, C.1
Loveland, K.2
Najmabadi, H.3
McLaughlin, R.4
Baker, G.5
Basin, S.6
De Kretser, D.M.7
-
40
-
-
0028794627
-
Is congenital bilateral absence of vas deferens primary form of cystic fibrosis? Analysis of the CFTR gene in 67 patients
-
Mercier B., Verlingue C., Lissens W., Silber S.J., Noveli G., Bonduelle M., Audrezet M.P., Ferec C. Is congenital bilateral absence of vas deferens primary form of cystic fibrosis? Analysis of the CFTR gene in 67 patients. Am. J. Hum. Genet. 56:1995;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
Noveli, G.5
Bonduelle, M.6
Audrezet, M.P.7
Ferec, C.8
-
41
-
-
0000399387
-
Karyotypes of men involved in ICSI programmes: The Maastricht experience
-
April 1994 to date. Hum. Reprod. 11. Abstract T089
-
Moog, U., Coonen, E., Dumoulin, J.C.M., Engelen, 1996. Karyotypes of men involved in ICSI programmes: The Maastricht experience, April 1994 to date. Hum. Reprod. 11. Abstract T089 pp. 223, 12th Annual meeting of the European Society of Human Reproduction.
-
(1996)
12th Annual Meeting of the European Society of Human Reproduction
, pp. 223
-
-
Moog, U.1
Coonen, E.2
Dumoulin, J.C.M.3
Engelen4
-
42
-
-
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
-
Najmabadi H., Huang V., Yen P., Subbarao M.N., Bhasinb D., Banaag L., Nasseeruddin S., de kretser D.M., Baker H.W., McLachlan R.I. et al. 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. 81:1996;1347-1352.
-
(1996)
J. Clin. Endocrinol. Metab.
, vol.81
, pp. 1347-1352
-
-
Najmabadi, H.1
Huang, V.2
Yen, P.3
Subbarao, M.N.4
Bhasinb, D.5
Banaag, L.6
Nasseeruddin, S.7
De Kretser, D.M.8
Baker, H.W.9
McLachlan, R.I.10
-
43
-
-
0028069337
-
The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis
-
Oates R.D., Amos J.A. The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis. J. Andol. 15:1994;1-8.
-
(1994)
J. Andol.
, vol.15
, pp. 1-8
-
-
Oates, R.D.1
Amos, J.A.2
-
44
-
-
0027215085
-
An autosomal factor from Drosophila mojavensis restores normal spermatogenesis in Drosophila males carrying the D arizonae Y chromosome
-
Pantazidis A.C., Galanopoulos V.K., Zouros E. An autosomal factor from Drosophila mojavensis restores normal spermatogenesis in Drosophila males carrying the D arizonae Y chromosome. Genetics. 134:1993;309-318.
-
(1993)
Genetics
, vol.134
, pp. 309-318
-
-
Pantazidis, A.C.1
Galanopoulos, V.K.2
Zouros, E.3
-
45
-
-
0029973468
-
Is ICSI associated with risks of genetic disease? Implications for counseling, practice and research
-
Persson J.W., Peters G.B., Saunders D.M. Is ICSI associated with risks of genetic disease? Implications for counseling, practice and research. Hum. Reprod. 11:1996;921-924.
-
(1996)
Hum. Reprod.
, vol.11
, pp. 921-924
-
-
Persson, J.W.1
Peters, G.B.2
Saunders, D.M.3
-
46
-
-
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., Roberts K.P. Microdeletions in the Y chromosome of infertile men. New Engl. J. Med. 336:1997;534-539.
-
(1997)
New 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
Roberts, K.P.7
-
47
-
-
0030253042
-
Polymerase chain reaction screening for Y chromosome microdeletions: A first step towards the diagnosis of genetically determined spermatogenetic failure in men
-
Qureshi S.J., Ross A.R., Ma K., Cooke H.J., McIntrye M.A., Chandley A.C., Hargreave T.B. Polymerase chain reaction screening for Y chromosome microdeletions: a first step towards the diagnosis of genetically determined spermatogenetic 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
McIntrye, M.A.5
Chandley, A.C.6
Hargreave, T.B.7
-
48
-
-
0029088061
-
Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
-
Reijo R., Lee T.Y., Salo P., Alagappan R., Brown L.G., Rosenberg M. et al. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene. Nature Genet. 10:1995;383-393.
-
(1995)
Nature Genet.
, vol.10
, pp. 383-393
-
-
Reijo, R.1
Lee, T.Y.2
Salo, P.3
Alagappan, R.4
Brown, L.G.5
Rosenberg, M.6
-
49
-
-
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. 34:1996;1290-1293.
-
(1996)
Lancet
, vol.34
, pp. 1290-1293
-
-
Reijo, R.1
Alagappan, P.K.2
Patrizio, P.3
Page, D.C.4
-
50
-
-
16044372544
-
Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification
-
Roest H.P., Van Klaveren J., de Wit J., van Gurp C.G., Koken M.H.M., Vermey M., van Roijen J.H., Hoogerbrugge J.W., Vreeburg J.T.M., Baarends W.M., Bootsma D., Grootegoed J.A., Hoeijmakers J.H.J. Inactivation of the HR6B ubiquitin-conjugating DNA repair enzyme in mice causes male sterility associated with chromatin modification. Cell. 86:1996;799-810.
-
(1996)
Cell
, vol.86
, pp. 799-810
-
-
Roest, H.P.1
Van Klaveren, J.2
De Wit, J.3
Van Gurp, C.G.4
Koken, M.H.M.5
Vermey, M.6
Van Roijen, J.H.7
Hoogerbrugge, J.W.8
Vreeburg, J.T.M.9
Baarends, W.M.10
Bootsma, D.11
Grootegoed, J.A.12
Hoeijmakers, J.H.J.13
-
51
-
-
0030885623
-
The mouse DAZLA gene encodes a cytoplasmic protein essential for gametogenesis
-
Ruggiu M., Speed R., Taggart M., McKay S.J., Kilanowski F., Saunders P., Dorin J., Cooke H.J. The mouse DAZLA gene encodes a cytoplasmic protein essential for gametogenesis. Nature. 389(6646):1997;73-77.
-
(1997)
Nature
, vol.389
, Issue.6646
, 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
-
52
-
-
0027317070
-
HnRNP G: Sequence and characterization of a glycosylated RNA-binding protein
-
Saulard M., Della Valle V., Siomi M.C., Pinol-Roma S., Codogna P., Bauvy C. et al. hnRNP G: sequence and characterization of a glycosylated RNA-binding protein. Nucleic Acids Res. 21(18):1993;4210-4217.
-
(1993)
Nucleic Acids Res.
, vol.21
, Issue.18
, pp. 4210-4217
-
-
Saulard, M.1
Della Valle, V.2
Siomi, M.C.3
Pinol-Roma, S.4
Codogna, P.5
Bauvy, C.6
-
53
-
-
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., Reijo R., Rozen S., Dinulos M.B., Disteche C.M., Page D.C. The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned. Nat. Genet. 14(3):1996;292-299.
-
(1996)
Nat. Genet.
, vol.14
, Issue.3
, pp. 292-299
-
-
Saxena, R.1
Brown, L.G.2
Hawkins, T.3
Alagappan, R.K.4
Skaletsky, H.5
Reeve, M.P.6
Reijo, R.7
Rozen, S.8
Dinulos, M.B.9
Disteche, C.M.10
Page, D.C.11
-
54
-
-
0029032452
-
Comparative mapping of YRRM and TSPY related cosmids in man and hominoid apes
-
Schempp W., Binkele A., Arnemann J., Glaser B., Ma K., Taylor K., Toder R., Wolfe J., Zeitler S., Chandley A.C. Comparative mapping of YRRM and TSPY related cosmids in man and hominoid apes. Chromosome Res. 3:1995;227-234.
-
(1995)
Chromosome Res.
, vol.3
, pp. 227-234
-
-
Schempp, W.1
Binkele, A.2
Arnemann, J.3
Glaser, B.4
Ma, K.5
Taylor, K.6
Toder, R.7
Wolfe, J.8
Zeitler, S.9
Chandley, A.C.10
-
55
-
-
0020396956
-
Randomised trial of clomiphene citrate treatment and vitamin C for male infertility
-
Abel B.J., Carswell G., Elton R., Hargreave T.B., Kyle K., Orr S., Rogers A., Baxby K., Yates A. Randomised trial of clomiphene citrate treatment and vitamin C for male infertility. Br. J. Urol. 54:1982;780-784.
-
(1982)
Br. J. Urol.
, vol.54
, pp. 780-784
-
-
Abel, B.J.1
Carswell, G.2
Elton, R.3
Hargreave, T.B.4
Kyle, K.5
Orr, S.6
Rogers, A.7
Baxby, K.8
Yates, A.9
-
56
-
-
0021748462
-
Randomised trial of mesterolone versus vitamin C for male infertility
-
Hargreave T.B., Kyle K.F., Baxby K., Rogers A.C.N., Scott R., Tolley D.A., Abel B.J., Orr P.S., Elton R.A. Randomised trial of mesterolone versus vitamin C for male infertility. Br. J. Urol. 56:1984;740-744.
-
(1984)
Br. J. Urol.
, vol.56
, pp. 740-744
-
-
Hargreave, T.B.1
Kyle, K.F.2
Baxby, K.3
Rogers, A.C.N.4
Scott, R.5
Tolley, D.A.6
Abel, B.J.7
Orr, P.S.8
Elton, R.A.9
-
57
-
-
0028901601
-
The paternal inheritance of the centrosome, the cells microtubular organizing center in humans, and the implications for infertility
-
Simmerly C., Wu G.J., Zoran S., Ord T., Rawlins R., Jones J., Navara C., Gerrity M., Rinehart J., Binor Z., Asch R., Shcatten G. The paternal inheritance of the centrosome, the cells microtubular organizing center in humans, and the implications for infertility. Nat. Med. 1:1995;45-47.
-
(1995)
Nat. Med.
, vol.1
, pp. 45-47
-
-
Simmerly, C.1
Wu, G.J.2
Zoran, S.3
Ord, T.4
Rawlins, R.5
Jones, J.6
Navara, C.7
Gerrity, M.8
Rinehart, J.9
Binor, Z.10
Asch, R.11
Shcatten, G.12
-
58
-
-
0031024316
-
Screening for deletions of the Y chromosome involving the DAZ (deleted in azoospermia) gene in severe oligozoospermia
-
Simoni M., Grommoll J., Dworniczak B., Rolf C., Abshagen K., Kamischke A., Carani C., Meschede D., Behre H.M., Horst J., Nieschlag E. Screening for deletions of the Y chromosome involving the DAZ (deleted in azoospermia) gene in severe oligozoospermia. Fertil. Steril. 67(3):1979;542-547.
-
(1979)
Fertil. Steril.
, vol.67
, Issue.3
, pp. 542-547
-
-
Simoni, M.1
Grommoll, J.2
Dworniczak, B.3
Rolf, C.4
Abshagen, K.5
Kamischke, A.6
Carani, C.7
Meschede, D.8
Behre, H.M.9
Horst, J.10
Nieschlag, E.11
-
59
-
-
0031266759
-
Preliminary investigations on androgen receptor gene mutations in infertile men
-
Tincello D.G., Saunders P.T.K., Hargreave T.B. Preliminary investigations on androgen receptor gene mutations in infertile men. Mol. Hum. Reprod. 3(11):1997;941-943.
-
(1997)
Mol. Hum. Reprod.
, vol.3
, Issue.11
, pp. 941-943
-
-
Tincello, D.G.1
Saunders, P.T.K.2
Hargreave, T.B.3
-
60
-
-
0028234356
-
Microsurgical epididymal sperm aspiration and intracytoplasmic sperm injection: A new effective approach to infertility as a result of congenital bilateral absence of the vas deferens
-
Tournaye H., Devroey P., Liu J., Nagy Z., Lissens W., Van Steirteghem A. Microsurgical epididymal sperm aspiration and intracytoplasmic sperm injection: a new effective approach to infertility as a result of congenital bilateral absence of the vas deferens. Fert. Steril. 61(6):1994;1045-1051.
-
(1994)
Fert. Steril.
, vol.61
, Issue.6
, pp. 1045-1051
-
-
Tournaye, H.1
Devroey, P.2
Liu, J.3
Nagy, Z.4
Lissens, W.5
Van Steirteghem, A.6
-
61
-
-
0029187431
-
Intracytoplasmic sperm injection: The Brussels experience
-
Tournaye A., Liu J., Nagy Z. et al. Intracytoplasmic sperm injection: the Brussels experience. Reprod. Fertil. Dev. 7:1995;269-279.
-
(1995)
Reprod. Fertil. Dev.
, vol.7
, pp. 269-279
-
-
Tournaye, A.1
Liu, J.2
Nagy, Z.3
-
62
-
-
0029883545
-
Cystic fibrosis mutation screening in healthy men with reduced sperm quality
-
van der Ven K., Messer L., van der Ven H., Jeyendran R.S., Ober C. Cystic fibrosis mutation screening in healthy men with reduced sperm quality. Hum. Reprod. 11:1996;513-517.
-
(1996)
Hum. Reprod.
, vol.11
, pp. 513-517
-
-
Van Der Ven, K.1
Messer, L.2
Van Der Ven, H.3
Jeyendran, R.S.4
Ober, C.5
-
63
-
-
0030634920
-
Absence of DAZ gene mutations in cases of non obstructed azoospermia
-
Vereb M., Agulnik A.I., Houston J.T., Lipschultz L.I., Lamb D.J., Bishop C.E. Absence of DAZ gene mutations in cases of non obstructed azoospermia. Mol. Human. Reprod. 3(1):1997;55-59.
-
(1997)
Mol. Human. Reprod.
, vol.3
, Issue.1
, pp. 55-59
-
-
Vereb, M.1
Agulnik, A.I.2
Houston, J.T.3
Lipschultz, L.I.4
Lamb, D.J.5
Bishop, C.E.6
-
64
-
-
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., Sharkley 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
Sharkley, A.6
-
65
-
-
0007272350
-
Human Y chromosome azoospermic factors AZF mapped to different regions in Ya11
-
Vogt P., Elemann A., Kirsch S. et al. Human Y chromosome azoospermic factors AZF mapped to different regions in Ya11. Hum. Mol. Genet. 5:1996;933-943.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 933-943
-
-
Vogt, P.1
Elemann, A.2
Kirsch, S.3
-
66
-
-
0024353060
-
Mesterolone and Idiopathic male infertility: A double blind study
-
Manuscript prepared by T.B. Hargreave and T.N.M. Farley.
-
World Health Organisation Task Force on the Diagnosis and Treatment of Infertility, 1989. Mesterolone and Idiopathic male infertility: a double blind study. Manuscript prepared by T.B. Hargreave and T.N.M. Farley. Int. J. Androl. 12 254-264.
-
(1989)
Int. J. Androl.
, vol.12
, pp. 254-264
-
-
-
67
-
-
0013512701
-
Clomiphene and idiopathic male infertility: A double blind study
-
Manuscript prepared by T.B. Hargreave, T.N.M. Farley and F. Comhaire.
-
World Health Organisation Task Force on the Diagnosis and Treatment of Infertility, 1991. Clomiphene and idiopathic male infertility: a double blind study. Manuscript prepared by T.B. Hargreave, T.N.M. Farley and F. Comhaire. Int. J. Androl. 15 299-307.
-
(1991)
Int. J. Androl.
, vol.15
, pp. 299-307
-
-
|