Y microdeletions and male infertility;Microdélétions du chromosome Y et infertilité masculine

References en Gynecologie Obstetrique

Volumn 8, Issue 1, 2001, Pages 13-20

  Patrat, C ^a   Bienvenu, T ^a   Jouannet, P ^a  

^a UNIVERSITÉ PARIS DESCARTES   (France)

Author keywords

Male infertility; Microdeletion; Y chromosome

Indexed keywords

AZOOSPERMIA; CHROMOSOME DELETION Y; CRYPTORCHISM; GENETIC COUNSELING; HUMAN; INCIDENCE; MALE; MALE INFERTILITY; OLIGOSPERMIA; REVIEW; SPERMATOGENESIS; SPERMATOZOON; VARICOCELE;

EID: 0035048624     PISSN: 12448168     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

References (49)

1. Male infertility
2. Localization of factors controlling spermatogenesis in the non-fluorescent portion of the human Y chromosome long arm
3. 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
4. The human Y chromosome: A 43-interval map based on naturally occuring deletions
5. Human male fertility-Y linked genes and spermatogenesis
6. Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11
7. Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection
8. Characterisation of the coding sequence and fine mapping of the DFFRY gene and comparative Dffry gene
9. Functional coherence of the human Y chromosome
10. A Y chromosome gene family with RNA-binding protein homology: Candidates for the azoospermia factor AZF controlling spermatogenesis
11. Expression of RBM in the nuclei of human germ cells is dependent on a critical region of the Y chromosome long arm
12. Expression of DAZ, an Azoospermia factor candidate, in human spermatogonia
13. The human DAZ genes, a putative male infertility factor on the Y chromosome, are highly polymorphic in the DAZ repeat regions
14. Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome
15. Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene
16. An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y
17. Microdeletions of the Y chromosome and intracytoplasmic sperm injection: From gene to clinic
18. Microdeletions in the Y chromosome of infertile men
19. Y chromosome microdeletions, in azoospermic and near-azoospermic subjects, are located in AZFc (DAZ) subregion
20. Prevalence of Y chromosome microdeletions in oligospermic and azoospermic candidates for intracytoplasmic sperm injection
21. Human male infertility and Y chromosome deletions: Role of the AZF-candidate genes DAZ, RBM and DFFRY
22. Polymerase chain reaction screening for Y chromosome microdeletions: A first step towards the diagnosis of genetically-determined spermatogenic failure in men
23. Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome
24. Microdeletions in interval 6 of the Y chromosome detected by STS-PCR in 6 of 33 patients with idiopathic oligo-or azoospermia
25. Submicroscopic deletions in the Y chromosome of infertile men
26. Azoospermic men with deletion in 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
27. Screening for deletions of the Y chromosome involving the DAZ gene in azoospermia and severe oligozoospermia
28. Combined cytogenetic and Y chromosome microdeletion screening in males undergoing intracytoplasmic sperm injection
29. Absence of DAZ gene mutations in cases of non-obstructed azoospermia
30. High frequency of well-defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome
31. Genetic evaluation of infertile men
32. Screening for microdeletions on the long arm of chromosome Y in 53 infertile men
33. Screening for microdeletions of Y chromosome genes in patients undergoig intracytoplasmic sperm injection
34. Microdeletions within the azoospermia factor subregions of the Y chromosome in patients with idiopathic azoospermia
35. Absence of microdeletions in the Y chromosome in patients with a history of cryptorchidism and azoospermia or oligospermia
36. Screening for AZF deletion in a large series of severely impaired spermatogenesis patients
37. Low number of Y-chromosome deletions in infertile azoospermic men at a Swedish andrology centre
38. Validation of a simple Yq deletions screening programme in an ICSI candidate population
39. Principles of sequence-tagged site selection in screening for Y deletions
40. AZFb deletions predict the absence of spermatozoa with testicular sperm extraction: Preliminary report of a prognostic genetic test
41. Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplsmic sperm injection after testicular sperm extraction
42. Current status of the molecular diagnosis of Y-chromosomal microdeletions in the work-up of male infertility
43. Y chromosome microdeletion in a father and his four infertile sons
44. Human chromosome deletions in Yq11, AZF candidate genes ans male infertility: History and update
45. Infertilité masculine: Des anomalies moléculaires aux possibiltés thérapeutiques
46. Prognostic value of Y deletion analysis
47. Men with infertility caused by AZFc deletion can produce sons by intracytoplasmic sperm injection, but are likely to transmit the deletion and infertility
48. Three-Generation evaluation of Y-chromosome microdeletion
49. Genetic counselling for infertile male patients