Published in Biochem Biophys Res Commun on April 28, 1998
The mammalian ovary from genesis to revelation. Endocr Rev (2009) 2.31
Licensing of gametogenesis, dependent on RNA binding protein DAZL, as a gateway to sexual differentiation of fetal germ cells. Proc Natl Acad Sci U S A (2011) 1.72
Conserved and divergent patterns of expression of DAZL, VASA and OCT4 in the germ cells of the human fetal ovary and testis. BMC Dev Biol (2007) 1.49
Genetics of germ cell development. Nat Rev Genet (2012) 1.20
A human DAZ transgene confers partial rescue of the mouse Dazl null phenotype. Proc Natl Acad Sci U S A (1999) 1.10
Boule is present in fish and bisexually expressed in adult and embryonic germ cells of medaka. PLoS One (2009) 1.06
Characterization of a Dazl-GFP germ cell-specific reporter. Genesis (2009) 0.93
The roles of the DAZ family in spermatogenesis: More than just translation? Spermatogenesis (2011) 0.92
Implication of DNA demethylation and bivalent histone modification for selective gene regulation in mouse primordial germ cells. PLoS One (2012) 0.89
Uncovering gene regulatory networks during mouse fetal germ cell development. Biol Reprod (2010) 0.86
Regulation of male sex determination: genital ridge formation and Sry activation in mice. Cell Mol Life Sci (2014) 0.83
Toward a more precise and informative nomenclature describing fetal and neonatal male germ cells in rodents. Biol Reprod (2013) 0.82
Mouse Germ Cell Development in-vivo and in-vitro. Biomark Insights (2007) 0.82
Modelling germ cell development in vitro. Mol Hum Reprod (2008) 0.81
Licensing of primordial germ cells for gametogenesis depends on genital ridge signaling. PLoS Genet (2015) 0.81
Establishment and Characterization of Human Germline Stem Cell Line with Unlimited Proliferation Potentials and no Tumor Formation. Sci Rep (2015) 0.80
Transcription factor TFAP2C regulates major programs required for murine fetal germ cell maintenance and haploinsufficiency predisposes to teratomas in male mice. PLoS One (2013) 0.79
DAZ Family Proteins, Key Players for Germ Cell Development. Int J Biol Sci (2015) 0.78
Germ stem cells are active in postnatal mouse ovary under physiological conditions. Mol Hum Reprod (2016) 0.77
Local signalling environments and human male infertility: what we can learn from mouse models. Expert Rev Mol Med (2010) 0.77
A premeiotic function for boule in the planarian Schmidtea mediterranea. Proc Natl Acad Sci U S A (2016) 0.75
BCAS2 is involved in alternative mRNA splicing in spermatogonia and the transition to meiosis. Nat Commun (2017) 0.75
Is there a role for DAZL in human female fertility? Mol Hum Reprod (2016) 0.75
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
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
Cytogenetic and molecular characterization of marker chromosomes in patients with mosaic 45,X karyotypes. Hum Genet (1992) 1.00
Y chromosome deletions in azoospermic and severely oligozoospermic men undergoing intracytoplasmic sperm injection after testicular sperm extraction. Hum Reprod (1998) 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
An interstitial deletion in mouse Y chromosomal DNA created a transcribed Zfy fusion gene. Genomics (1991) 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
Deletion mapping of stature determinants on the long arm of the Y chromosome. Hum Genet (1995) 0.89
Dazl protein expression in adult rat testis is up-regulated at meiosis and not hormonally regulated. Int J Androl (2000) 0.89
Regional assignments of three polymorphic DNA segments on human chromosome 15. Genet Epidemiol (1986) 0.89
Evidence that the SRY protein is encoded by a single exon on the human Y chromosome. Genomics (1993) 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
Characterization of the murine Zfy1 and Zfy2 promoters. Genomics (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
Ovary? Testis?--A mammalian dilemma. Cell (1994) 0.81
A 45,X male with Y-specific DNA translocated onto chromosome 15. Am J Hum Genet (1987) 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
Mosaicism for 45,X cell line may accentuate the severity of spermatogenic defects in men with AZFc deletion. J Med Genet (2001) 0.78
Steroid sulfatase gene in XX males. Am J Hum Genet (1990) 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
Revealing smile. J Am Dent Assoc (1998) 0.75
Early orthodontic care. J Am Dent Assoc (2000) 0.75
Save the males! Nat Genet (1997) 0.75