These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
101 related articles for article (PubMed ID: 3595213)
1. Under what circumstances is the human XY bivalent tangled? A note on chromosomally-derived sterility. Rosenmann A; Wahrman J; Richler C; Madgar I; Weissenberg R; Chaki R Cytogenet Cell Genet; 1987; 45(1):58-61. PubMed ID: 3595213 [TBL] [Abstract][Full Text] [Related]
2. Chromosomally derived sterile mice have a 'fertile' active XY chromatin conformation but no XY body. Richler C; Uliel E; Rosenmann A; Wahrman J Chromosoma; 1989 May; 97(6):465-74. PubMed ID: 2743828 [TBL] [Abstract][Full Text] [Related]
3. Meiotic association between the XY chromosomes and unpaired autosomal elements as a cause of human male sterility. Rosenmann A; Wahrman J; Richler C; Voss R; Persitz A; Goldman B Cytogenet Cell Genet; 1985; 39(1):19-29. PubMed ID: 3979116 [TBL] [Abstract][Full Text] [Related]
4. Chromosomal anomalies and disturbance of transcriptional activity at the pachytene stage of meiosis: relationship to male sterility. Jaafar H; Gabriel-Robez O; Rumpler Y Cytogenet Cell Genet; 1993; 64(3-4):273-80. PubMed ID: 8404054 [TBL] [Abstract][Full Text] [Related]
5. Meiotic behaviour and sperm aneuploidy in an infertile man with a mosaic 45,X/46,XY karyotype. Ren H; Chow V; Ma S Reprod Biomed Online; 2015 Dec; 31(6):783-9. PubMed ID: 26511872 [TBL] [Abstract][Full Text] [Related]
6. A balanced autosomal reciprocal translocation in an azoospermic bull. Ansari HA; Jung HR; Hediger R; Fries R; König H; Stranzinger G Cytogenet Cell Genet; 1993; 62(2-3):117-23. PubMed ID: 8428509 [TBL] [Abstract][Full Text] [Related]
7. Altered bivalent positioning in metaphase I human spermatocytes from Robertsonian translocation carriers. Solé M; Blanco J; Valero O; Vergés L; Vidal F; Sarrate Z J Assist Reprod Genet; 2017 Jan; 34(1):131-138. PubMed ID: 27655390 [TBL] [Abstract][Full Text] [Related]
8. Meiotic association between the XY chromosomes and the autosomal quadrivalent of a reciprocal translocation in two infertile men, 46,XY,t(19;22) and 46,XY,t(17;21). Gabriel-Robez O; Ratomponirina C; Dutrillaux B; Carré-Pigeon F; Rumpler Y Cytogenet Cell Genet; 1986; 43(3-4):154-60. PubMed ID: 3802918 [TBL] [Abstract][Full Text] [Related]
9. Cytogenetics and infertility in man. II. Testicular histology and meiosis. Chandley AC; Maclean N; Edmond P; Fletcher J; Watson GS Ann Hum Genet; 1976 Nov; 40(2):165-76. PubMed ID: 1015811 [TBL] [Abstract][Full Text] [Related]
10. Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation. Guichaoua MR; Quack B; Speed RM; Noel B; Chandley AC; Luciani JM Hum Genet; 1990 Dec; 86(2):162-6. PubMed ID: 2265828 [TBL] [Abstract][Full Text] [Related]
11. Acrocentric bivalents positioned preferentially nearby to the XY pair in metaphase I human spermatocytes. Sarrate Z; Blanco J; Vidal F Fertil Steril; 2012 Nov; 98(5):1241-5. PubMed ID: 22884015 [TBL] [Abstract][Full Text] [Related]
13. Pachytene analysis in a 17;21 reciprocal translocation carrier: role of the acrocentric chromosomes in male sterility. Luciani JM; Guichaoua MR; Delafontaine D; North MO; Gabriel-Robez O; Rumpler Y Hum Genet; 1987 Nov; 77(3):246-50. PubMed ID: 3679209 [TBL] [Abstract][Full Text] [Related]
14. Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man. Speed RM; Faed MJ; Batstone PJ; Baxby K; Barnetson W Hum Genet; 1991 Aug; 87(4):416-20. PubMed ID: 1879828 [TBL] [Abstract][Full Text] [Related]
15. Two different XY-quadrivalent associations and impairment of fertility in men. Johannisson R; Löhrs U; Wolff HH; Schwinger E Cytogenet Cell Genet; 1987; 45(3-4):222-30. PubMed ID: 3319437 [TBL] [Abstract][Full Text] [Related]
16. On the nature and extent of XY pairing at meiotic prophase in man. Chandley AC; Goetz P; Hargreave TB; Joseph AM; Speed RM Cytogenet Cell Genet; 1984; 38(4):241-7. PubMed ID: 6542485 [TBL] [Abstract][Full Text] [Related]
17. Ubiquitin ligase Rad18Sc localizes to the XY body and to other chromosomal regions that are unpaired and transcriptionally silenced during male meiotic prophase. van der Laan R; Uringa EJ; Wassenaar E; Hoogerbrugge JW; Sleddens E; Odijk H; Roest HP; de Boer P; Hoeijmakers JH; Grootegoed JA; Baarends WM J Cell Sci; 2004 Oct; 117(Pt 21):5023-33. PubMed ID: 15383616 [TBL] [Abstract][Full Text] [Related]
18. [Analysis of synaptonemal complex from a carrier with 46,XY,t(11;18) balanced translocation]. Liu JY; Wang XR; Zeng XL; Zhang CS; Song YC Yi Chuan Xue Bao; 2004 Feb; 31(2):125-31. PubMed ID: 15473301 [TBL] [Abstract][Full Text] [Related]
19. Synaptonemal complexes in a subfertile man with a pericentric inversion in chromosome 21. Heterosynapsis without previous homosynapsis. Gabriel-Robez O; Ratomponirina C; Croquette M; Couturier J; Rumpler Y Cytogenet Cell Genet; 1988; 48(2):84-7. PubMed ID: 3197453 [TBL] [Abstract][Full Text] [Related]
20. Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effect. Batanian J; Hulten MA Hum Genet; 1987 May; 76(1):81-9. PubMed ID: 3570302 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]