Deletion mapping of interval 6 of the human Y chromosome

1991 ◽  
Vol 87 (2) ◽  
pp. 234-236 ◽  
Author(s):  
Maciej Kotecki ◽  
Jadwiga Jaruzelska ◽  
Malgorzata Skowrońska ◽  
Piotr Fichna
Keyword(s):  
Y Chromosome ◽  
Deletion Mapping ◽  
Human Y Chromosome

Mapping the human Y chromosome

1988 ◽  
Vol 322 (1208) ◽  
pp. 125-131 ◽  
Keyword(s):  
Y Chromosome ◽  
Dna Sequences ◽  
Physical Map ◽  
Sex Reversal ◽  
Chromosomal Anomalies ◽  
Deletion Mapping ◽  
Molecular Analyses ◽  
Large Size ◽  
Definition Of ◽  
Human Y Chromosome

This paper reviews past and present trends in mapping the human Y chromosome. So far, mapping has essentially used a combination of cytogenetic and molecular analyses of Y-chromosomal anomalies and sex reversal syndromes. This deletion mapping culminated recently in the isolation of the putative sex-determining locus TDF . With the availability of new separation and cloning techniques suited for large size fragments (over 100 kilobases), the next step will consist rather in the establishment of a physical map of fragments of known physical sizes. This may allow the definition of several variants of the human Y chromosome differing by the order or location of DNA sequences along the molecule.

scholarly journals Deletion mapping of H-Y antigen to the long arm of the human Y chromosome

Genomics ◽  
1992 ◽  
Vol 13 (4) ◽  
pp. 1255-1260 ◽  
Author(s):  
Michael A. Cantrell ◽  
Jonathan S. Bogan ◽  
Elizabeth Simpson ◽  
James N. Bicknell ◽  
Els Goulmy ◽  
...  
Keyword(s):  
Y Chromosome ◽  
Deletion Mapping ◽  
Human Y Chromosome

The azoospermia factor (AZF) of the human Y chromosome in Yq11: function and analysis in spermatogenesis

1995 ◽  
Vol 7 (4) ◽  
pp. 685 ◽  
Author(s):  
PH Vogt ◽  
A Edelmann ◽  
P Hirschmann ◽  
MR Kohler
Keyword(s):  
Y Chromosome ◽  
Chromatin Structure ◽  
De Novo ◽  
Screening Programme ◽  
Deletion Mapping ◽  
Azoospermia Factor ◽  
Its Analysis ◽  
Human Y Chromosome

Different Y mutations in Yq11 occurring de novo in sterile males were first described 19 years ago. Since the phenotype of the patients was always associated with azoospermia or severe oligospermia, it was postulated that these mutations interrupt a Y spermatogenesis locus in the euchromatic Y region (Yq11) called azoospermia factor (AZF). Recently, it became possible to map AZF mutations to different subregions in Yq11 by molecular deletion mapping. This indicated that azoospermia is possibly caused by more than one Y gene in Yq11 and the Yq11 chromatin structure. The frequency of AZF mutations in idiopathic sterile males (5-20%) may indicate a need for a general screening programme for its analysis in infertility clinics.

scholarly journals Association of the Human Y Chromosome with Cholesterol Levels in the General Population

2004 ◽  
Vol 24 (2) ◽  
pp. 308-312 ◽  
Author(s):  
Fadi J. Charchar ◽  
Maciej Tomaszewski ◽  
Beata Lacka ◽  
Jaroslaw Zakrzewski ◽  
Ewa Zukowska-Szczechowska ◽  
...  
Keyword(s):  
General Population ◽  
Y Chromosome ◽  
Cholesterol Levels ◽  
Human Y Chromosome

scholarly journals A Back Migration from Asia to Sub-Saharan Africa Is Supported by High-Resolution Analysis of Human Y-Chromosome Haplotypes

2002 ◽  
Vol 70 (5) ◽  
pp. 1197-1214 ◽  
Author(s):  
Fulvio Cruciani ◽  
Piero Santolamazza ◽  
Peidong Shen ◽  
Vincent Macaulay ◽  
Pedro Moral ◽  
...  
Keyword(s):  
High Resolution ◽  
Y Chromosome ◽  
Sub Saharan Africa ◽  
High Resolution Analysis ◽  
Resolution Analysis ◽  
Sub Saharan ◽  
Human Y Chromosome

DA/DAPI-Fluorescent heteromorphism of human Y chromosome

1988 ◽  
Vol 79 (1) ◽  
pp. 36-38 ◽  
Author(s):  
M. S. Lin ◽  
A. Zhang ◽  
M. G. Wilson ◽  
A. Fujimoto
Keyword(s):  
Y Chromosome ◽  
Human Y Chromosome

Human Y chromosome isn't wasting away

Lab Animal ◽  
2012 ◽  
Vol 41 (4) ◽  
pp. 89-89
Author(s):  
Monica Harrington
Keyword(s):  
Y Chromosome ◽  
Human Y Chromosome
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