Published in Genomics on November 01, 1991
Two Y genes can replace the entire Y chromosome for assisted reproduction in the mouse. Science (2013) 1.66
Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent. Behav Brain Res (2002) 1.44
The Y-encoded gene zfy2 acts to remove cells with unpaired chromosomes at the first meiotic metaphase in male mice. Curr Biol (2011) 1.22
Mouse Y-linked Zfy1 and Zfy2 are expressed during the male-specific interphase between meiosis I and meiosis II and promote the 2nd meiotic division. PLoS Genet (2014) 0.93
Human and mouse ZFY genes produce a conserved testis-specific transcript encoding a zinc finger protein with a short acidic domain and modified transactivation potential. Hum Mol Genet (2012) 0.91
Spermatid development in XO male mice with varying Y chromosome short-arm gene content: evidence for a Y gene controlling the initiation of sperm morphogenesis. Reproduction (2012) 0.87
Y chromosome short arm-Sxr recombination in XSxr/Y males causes deletion of Rbm and XY female sex reversal. Proc Natl Acad Sci U S A (1995) 0.85
Mouse Y-Encoded Transcription Factor Zfy2 Is Essential for Sperm Formation and Function in Assisted Fertilization. PLoS Genet (2015) 0.84
Recombination between the mouse Y chromosome short arm and an additional Y short arm-derived chromosomal segment attached distal to the X chromosome PAR. Chromosoma (2015) 0.80
Mouse Y-Encoded Transcription Factor Zfy2 Is Essential for Sperm Head Remodelling and Sperm Tail Development. PLoS One (2016) 0.77
Mouse Y chromosome. Mamm Genome (1992) 0.76
An STS-based map of the human genome. Science (1995) 17.72
A gene map of the human genome. Science (1996) 14.32
Four evolutionary strata on the human X chromosome. Science (1999) 7.13
An abundance of X-linked genes expressed in spermatogonia. Nat Genet (2001) 5.87
Severe oligozoospermia resulting from deletions of azoospermia factor gene on Y chromosome. Lancet (1996) 4.28
The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men. Nat Genet (2001) 4.24
Functional coherence of the human Y chromosome. Science (1997) 4.15
The human Y chromosome: a 43-interval map based on naturally occurring deletions. Science (1992) 3.09
A deletion map of the human Y chromosome based on DNA hybridization. Am J Hum Genet (1986) 3.03
Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome. Cell (1990) 2.70
The human Y chromosome: overlapping DNA clones spanning the euchromatic region. Science (1992) 2.66
Unexpectedly similar rates of nucleotide substitution found in male and female hominids. Nature (2000) 2.39
Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution. Nature (1984) 2.21
Four DAZ genes in two clusters found in the AZFc region of the human Y chromosome. Genomics (2000) 2.16
The DAZ gene cluster on the human Y chromosome arose from an autosomal gene that was transposed, repeatedly amplified and pruned. Nat Genet (1996) 2.16
A map of 75 human ribosomal protein genes. Genome Res (1998) 2.15
A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination. Cell (1987) 1.93
An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y. Nat Genet (1999) 1.91
ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation. Cell (1989) 1.90
Multipoint linkage map of the human pseudoautosomal region, based on single-sperm typing: do double crossovers occur during male meiosis? Am J Hum Genet (1994) 1.78
Retroposition of autosomal mRNA yielded testis-specific gene family on human Y chromosome. Nat Genet (1999) 1.72
A proposed path by which genes common to mammalian X and Y chromosomes evolve to become X inactivated. Nature (1998) 1.69
DAZ family proteins exist throughout male germ cell development and transit from nucleus to cytoplasm at meiosis in humans and mice. Biol Reprod (2000) 1.64
Functional equivalence of human X- and Y-encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome. Nat Genet (1993) 1.63
Expression of a mouse Zfy-1/lacZ transgene in the somatic cells of the embryonic gonad and germ cells of the adult testis. Development (1994) 1.62
A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators. Hum Mol Genet (1999) 1.61
A physical map of the human Y chromosome. Nature (2001) 1.58
Deletion of azoospermia factor a (AZFa) region of human Y chromosome caused by recombination between HERV15 proviruses. Hum Mol Genet (2000) 1.53
The human UTY gene encodes a novel HLA-B8-restricted H-Y antigen. J Immunol (2000) 1.49
XY chromosome nondisjunction in man is associated with diminished recombination in the pseudoautosomal region. Am J Hum Genet (1991) 1.47
Sex reversal: deletion mapping the male-determining function of the human Y chromosome. Cold Spring Harb Symp Quant Biol (1986) 1.43
Two closely related human nuclear export factors utilize entirely distinct export pathways. Mol Cell (2001) 1.43
Linkage of an X-chromosome cleft palate gene. Nature (1987) 1.42
Putative transcription activator with alternative isoforms encoded by human ZFX gene. Nature (1989) 1.39
The sex-determining region of the mouse Y chromosome encodes a protein with a highly acidic domain and 13 zinc fingers. Cell (1989) 1.34
Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX males. Science (1986) 1.32
Mouse autosomal homolog of DAZ, a candidate male sterility gene in humans, is expressed in male germ cells before and after puberty. Genomics (1996) 1.30
Sex-determining genes on mouse autosomes identified by linkage analysis of C57BL/6J-YPOS sex reversal. Nat Genet (1996) 1.27
Small deletions of the short arm of the Y chromosome in 46,XY females. Proc Natl Acad Sci U S A (1986) 1.27
Turner syndrome: the case of the missing sex chromosome. Trends Genet (1993) 1.27
Chromosome Y-specific DNA in related human XX males. Nature (1985) 1.26
Sequences homologous to ZFY, a candidate human sex-determining gene, are autosomal in marsupials. Nature (1989) 1.25
Zfx mutation results in small animal size and reduced germ cell number in male and female mice. Development (1997) 1.22
Gonadoblastoma: molecular definition of the susceptibility region on the Y chromosome. Am J Hum Genet (1995) 1.22
A human sex-chromosomal gene family expressed in male germ cells and encoding variably charged proteins. Hum Mol Genet (2000) 1.21
Exchange of terminal portions of X- and Y-chromosomal short arms in human XX males. Nature (1987) 1.20
Reconstructing hominid Y evolution: X-homologous block, created by X-Y transposition, was disrupted by Yp inversion through LINE-LINE recombination. Hum Mol Genet (1998) 1.19
Duplication, deletion, and polymorphism in the sex-determining region of the mouse Y chromosome. Science (1989) 1.17
Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers. Mol Cell Biol (1990) 1.15
The parental origin of X chromosomes in XX males determined using restriction fragment length polymorphisms. Am J Hum Genet (1984) 1.12
Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype. Nat Genet (1994) 1.11
Inactivation of the Zfx gene on the mouse X chromosome. Proc Natl Acad Sci U S A (1991) 1.11
Familial premature ovarian failure due to an interstitial deletion of the long arm of the X chromosome. N Engl J Med (1987) 1.10
Y chromosome sequences in Turner's syndrome and risk of gonadoblastoma or virilisation. Lancet (1994) 1.08
Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12. Genomics (1995) 1.07
Molecular mapping of the putative gonadoblastoma locus on the Y chromosome. Genes Chromosomes Cancer (1995) 1.06
XX true hermaphroditism in southern African blacks: an enigma of primary sexual differentiation. Am J Hum Genet (1988) 1.05
An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome. Nucleic Acids Res (1989) 1.05
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females. Hum Mol Genet (1997) 1.05
Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia. Hum Genet (1988) 1.04
Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes. Mol Cell Biol (1994) 1.04
The Dazh gene is expressed in male and female embryonic gonads before germ cell sex differentiation. Biochem Biophys Res Commun (1998) 1.03
Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11. Hum Genet (1988) 1.02
Expression of DAZ, an azoospermia factor candidate, in human spermatogonia. Am J Hum Genet (1997) 1.01
The Old World monkey DAZ (Deleted in AZoospermia) gene yields insights into the evolution of the DAZ gene cluster on the human Y chromosome. Hum Mol Genet (1999) 1.00
Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. Hum Reprod (1998) 1.00
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes. Hum Genet (1992) 1.00
Reconstructing the evolution of vertebrate sex chromosomes. Cold Spring Harb Symp Quant Biol (2010) 0.98
Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male. Hum Genet (1988) 0.95
Inactivation of the Rps4 gene on the mouse X chromosome. Genomics (1991) 0.92
We're off to see the genome. Nat Genet (1998) 0.90
Dazl protein expression in adult rat testis is up-regulated at meiosis and not hormonally regulated. Int J Androl (2000) 0.89
Deletion mapping of stature determinants on the long arm of the Y chromosome. Hum Genet (1995) 0.89
Evidence that the SRY protein is encoded by a single exon on the human Y chromosome. Genomics (1993) 0.89
Regional assignments of three polymorphic DNA segments on human chromosome 15. Genet Epidemiol (1986) 0.89
A bird zinc-finger protein closely related to ZFY. New Biol (1990) 0.87
The origin of 45,X males. Am J Hum Genet (1986) 0.87
Optical mapping of BAC clones from the human Y chromosome DAZ locus. Genome Res (2000) 0.87
Four PCR-based polymorphisms in the pseudoautosomal region of the human X and Y chromosomes. Hum Mol Genet (1993) 0.86
A unique dicentric X;Y translocation with Xq and Yp breakpoints: cytogenetic and molecular studies. Am J Hum Genet (1987) 0.85
Human sex-chromosome-specific repeats within a region of pseudoautosomal/Yq homology. Genomics (1990) 0.85
Molecular detection of a translocation (Y;15) in a 45,X male. Hum Genet (1986) 0.85
CpG islands in human ZFX and ZFY and mouse Zfx genes: sequence similarities and methylation differences. Genomics (1995) 0.84
Separation of the genetic loci for the H-Y antigen and for testis determination on human Y chromosome. Nature (1987) 0.84
Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. Genomics (1988) 0.83
Rps4 maps near the inactivation center on the mouse X chromosome. Genomics (1992) 0.82
A 45,X male with Y-specific DNA translocated onto chromosome 15. Am J Hum Genet (1987) 0.81
Characterization of the murine Zfy1 and Zfy2 promoters. Genomics (1994) 0.81
Ovary? Testis?--A mammalian dilemma. Cell (1994) 0.81
Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe. Hum Genet (1989) 0.81
Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome. Am J Med Genet (1989) 0.81
The parental origin and mechanism of formation of three dicentric X chromosomes. Hum Genet (1988) 0.80
The structure of the Zfx gene on the mouse X chromosome. Genomics (1994) 0.79
Steroid sulfatase gene in XX males. Am J Hum Genet (1990) 0.78
Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion. J Med Genet (2001) 0.78
Intron/exon structure confirms that mouse Zfy1 and Zfy2 are members of the ZFY gene family. Genomics (1997) 0.77
Mapping of ribosomal protein S3 and internally nested snoRNA U15A gene to human chromosome 11q13.3-q13.5. Genomics (1995) 0.76
Save the males! Nat Genet (1997) 0.75
Early orthodontic care. J Am Dent Assoc (2000) 0.75
An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunction. Am J Hum Genet (1987) 0.75