Published in Hum Mol Genet on November 01, 1996
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function. Proc Natl Acad Sci U S A (2004) 7.70
Improved breast cancer prognosis through the combination of clinical and genetic markers. Bioinformatics (2006) 1.93
Epigenetics of gene expression in human hepatoma cells: expression profiling the response to inhibition of DNA methylation and histone deacetylation. BMC Genomics (2006) 1.20
TSPY, the candidate gonadoblastoma gene on the human Y chromosome, has a widely expressed homologue on the X - implications for Y chromosome evolution. Chromosome Res (2004) 1.14
A large interstitial deletion encompassing the amelogenin gene on the short arm of the Y chromosome. Hum Genet (2005) 1.13
Gonadoblastoma, testicular and prostate cancers, and the TSPY gene. Am J Hum Genet (1999) 1.08
TSPY potentiates cell proliferation and tumorigenesis by promoting cell cycle progression in HeLa and NIH3T3 cells. BMC Cancer (2006) 1.07
TSPY1 copy number variation influences spermatogenesis and shows differences among Y lineages. J Clin Endocrinol Metab (2009) 1.04
The origin and evolution of human ampliconic gene families and ampliconic structure. Genome Res (2006) 1.03
Ovarian dysgerminomas are characterised by frequent KIT mutations and abundant expression of pluripotency markers. Mol Cancer (2007) 0.98
The Y-encoded TSPY protein: a significant marker potentially plays a role in the pathogenesis of testicular germ cell tumors. Hum Pathol (2007) 0.97
TSPY is a cancer testis antigen expressed in human hepatocellular carcinoma. Br J Cancer (2005) 0.94
Delayed Recognition of Disorders of Sex Development (DSD): A Missed Opportunity for Early Diagnosis of Malignant Germ Cell Tumors. Int J Endocrinol (2012) 0.89
Simian Y chromosomes: species-specific rearrangements of DAZ, RBM, and TSPY versus contiguity of PAR and SRY. Mamm Genome (1998) 0.86
A murine TSPY. Chromosome Res (1998) 0.86
Testicular cancer: biology and biomarkers. Virchows Arch (2014) 0.86
A novel SRY missense mutation affecting nuclear import in a 46,XY female patient with bilateral gonadoblastoma. Eur J Hum Genet (2009) 0.84
Y genetic variation and phenotypic diversity in health and disease. Biol Sex Differ (2015) 0.84
Organization and expression of bovine TSPY. Mamm Genome (1997) 0.83
TTY2: a multicopy Y-linked gene family. Genome Res (2001) 0.82
An Exceptional Gene: Evolution of the TSPY Gene Family in Humans and Other Great Apes. Genes (Basel) (2011) 0.82
TSPYL2 is important for G1 checkpoint maintenance upon DNA damage. PLoS One (2011) 0.81
Molecular characterization of a polymorphic 3-Mb deletion at chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations. Hum Genet (2007) 0.79
Human Y chromosome copy number variation in the next generation sequencing era and beyond. Hum Genet (2017) 0.79
TSPY and Male Fertility. Genes (Basel) (2010) 0.79
Retracted Testis-specific protein on Y chromosome (TSPY) represses the activity of the androgen receptor in androgen-dependent testicular germ-cell tumors. Proc Natl Acad Sci U S A (2010) 0.79
Transgenic Mouse Studies to Understand the Regulation, Expression and Function of the Testis-Specific Protein Y-Encoded (TSPY) Gene. Genes (Basel) (2010) 0.79
Roles of the Y chromosome genes in human cancers. Asian J Androl (2015) 0.78
Etiology and early pathogenesis of malignant testicular germ cell tumors: towards possibilities for preinvasive diagnosis. Asian J Androl (2015) 0.78
The rat Tspy is preferentially expressed in elongated spermatids and interacts with the core histones. Biochem Biophys Res Commun (2006) 0.78
Expression of the Y-Encoded TSPY is Associated with Progression of Prostate Cancer. Genes (Basel) (2010) 0.77
Molecular analysis of testis biopsy and semen pellet as complementary methods with histopathological analysis of testis in non-obstructive azoospermia. J Assist Reprod Genet (2014) 0.77
Conserved Y-chromosomal location of TSPY in Bovidae. Chromosome Res (1997) 0.76
Molecular mining of alleles in water buffalo Bubalus bubalis and characterization of the TSPY1 and COL6A1 genes. PLoS One (2011) 0.76
A novel hypothesis for histone-to-protamine transition in Bos taurus spermatozoa. Reproduction (2016) 0.75
Copy number variation and microdeletions of the Y chromosome linked genes and loci across different categories of Indian infertile males. Sci Rep (2015) 0.75
Characterization of genome-wide segmental duplications reveals a common genomic feature of association with immunity among domestic animals. BMC Genomics (2017) 0.75
DAZLA: an important candidate gene in male subfertility? J Assist Reprod Genet (2001) 0.75
Localization of cystic fibrosis locus to human chromosome 7cen-q22. Nature (1985) 7.77
Report of the DNA committee and catalogs of cloned and mapped genes and DNA polymorphisms. Cytogenet Cell Genet (1989) 5.48
Immunoglobulins on the surface of lymphocytes. II. The bone marrow as the main source of lymphocytes with detectable surface-bound immunoglobulin. J Exp Med (1971) 5.43
Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes. Am J Hum Genet (1998) 5.24
Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping. EMBO J (2001) 5.23
Orbital and millennial Antarctic climate variability over the past 800,000 years. Science (2007) 5.10
Virus-specific cytotoxic T-lymphocyte responses select for amino-acid variation in simian immunodeficiency virus Env and Nef. Nat Med (1999) 4.93
The leader peptide of yeast gene CPA1 is essential for the translational repression of its expression. Cell (1987) 4.91
An estimate of unique DNA sequence heterozygosity in the human genome. Hum Genet (1985) 4.75
Quantitative gene expression analysis in microdissected archival formalin-fixed and paraffin-embedded tumor tissue. Am J Pathol (2001) 4.18
The hormone regulatory element of mouse mammary tumour virus mediates progesterone induction. EMBO J (1986) 4.04
A clinical pathway to accelerate recovery after colonic resection. Ann Surg (2000) 3.04
Adenocarcinoma of the esophagogastric junction: results of surgical therapy based on anatomical/topographic classification in 1,002 consecutive patients. Ann Surg (2000) 2.85
Experience with 100 cases treated with botulinum-A toxin injections in the detrusor muscle for idiopathic overactive bladder syndrome refractory to anticholinergics. J Urol (2006) 2.84
Heterogeneity in breast cancer and the problem of relevance of findings. Anal Cell Pathol (1999) 2.81
DNA restriction fragment length polymorphisms and heterozygosity in the human genome. Hum Genet (1984) 2.79
Characterisation of a human Y chromosome repeated sequence and related sequences in higher primates. Chromosoma (1982) 2.67
Acceleration of Alzheimer's fibril formation by apolipoprotein E in vitro. Am J Pathol (1994) 2.66
Low prevalence of SPINK1 gene mutations in adult patients with chronic idiopathic pancreatitis. J Med Genet (2001) 2.55
Biopsy surveillance is still necessary in patients with Barrett's oesophagus despite new endoscopic imaging techniques. Gut (2003) 2.49
Inactivation of the protein phosphatase 2A regulatory subunit A results in morphological and transcriptional defects in Saccharomyces cerevisiae. Mol Cell Biol (1992) 2.33
Positron emission tomography using [(18)F]Fluorodeoxyglucose for monitoring primary chemotherapy in breast cancer. J Clin Oncol (2000) 2.28
Regional mapping of six cloned DNA sequences on human chromosome 7. Am J Hum Genet (1986) 2.26
Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms. Cytogenet Cell Genet (1990) 2.21
Ethical problems in medical practice. A protocol for the guidance of physicians. West J Med (1982) 2.19
A protein-protein interaction map of yeast RNA polymerase III. Proc Natl Acad Sci U S A (1999) 2.18
Resectional surgery of hilar cholangiocarcinoma: a multivariate analysis of prognostic factors. J Clin Oncol (1997) 2.16
The Gorham-Stout syndrome (Gorham's massive osteolysis). A report of six cases with histopathological findings. J Bone Joint Surg Br (1999) 2.07
Neoadjuvant therapy of esophageal squamous cell carcinoma: response evaluation by positron emission tomography. Ann Surg (2001) 2.04
Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts. Hum Genet (1992) 1.94
Suppression of yeast RNA polymerase III mutations by FHL1, a gene coding for a fork head protein involved in rRNA processing. Mol Cell Biol (1994) 1.91
Desmosomal glycoprotein DGI, a component of intercellular desmosome junctions, is related to the cadherin family of cell adhesion molecules. Proc Natl Acad Sci U S A (1991) 1.91
Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitis. Am J Gastroenterol (2000) 1.90
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III. Am J Hum Genet (2000) 1.80
Long-term results of the co-operative German-Austrian-Swiss osteosarcoma study group's protocol COSS-86 of intensive multidrug chemotherapy and surgery for osteosarcoma of the limbs. Ann Oncol (1998) 1.79
Human gene cloning: the storm before the lull? Nature (1986) 1.78
Differential gene activation by glucocorticoids and progestins through the hormone regulatory element of mouse mammary tumor virus. Cell (1988) 1.78
Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. Proc Natl Acad Sci U S A (1996) 1.76
The C-terminal domain of the regulatory protein NOVH is sufficient to promote interaction with fibulin 1C: a clue for a role of NOVH in cell-adhesion signaling. Proc Natl Acad Sci U S A (1999) 1.69
Characterization of ATM gene mutations in 66 ataxia telangiectasia families. Hum Mol Genet (1999) 1.66
From first base: the sequence of the tip of the X chromosome of Drosophila melanogaster, a comparison of two sequencing strategies. Genome Res (2001) 1.64
Effect of histamine H2-receptor blockade on vagally induced gastric secretion in man. Br Med J (1974) 1.63
Search for supersymmetry using final states with one lepton, jets, and missing transverse momentum with the ATLAS detector in √s=7 TeV pp collisions. Phys Rev Lett (2011) 1.60
Intratumoral heterogeneity in breast carcinoma revealed by laser-microdissection and comparative genomic hybridization. Cancer Genet Cytogenet (1999) 1.59
Apolipoprotein E protects against bacterial lipopolysaccharide-induced lethality. A new therapeutic approach to treat gram-negative sepsis. J Biol Chem (2001) 1.59
Chromosomal imbalances in Barrett's adenocarcinoma and the metaplasia-dysplasia-carcinoma sequence. Am J Pathol (2000) 1.57
Serum protein changes during the acute phase reaction. Clin Chim Acta (1969) 1.57
Antimicrobial susceptibilities of Campylobacter jejuni and Campylobacter coli isolated in Sweden: a 10-year follow-up report. Antimicrob Agents Chemother (1992) 1.57
LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome. J Med Genet (2006) 1.56
Networking for rare diseases: a necessity for Europe. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz (2007) 1.53
Anaerobic pericarditis: case report and review. Clin Infect Dis (1994) 1.52
Early diagnosis and prevention of sporadic colorectal cancer. Endoscopy (2001) 1.51
Dual role of the C34 subunit of RNA polymerase III in transcription initiation. EMBO J (1997) 1.51
Diagnosis of genetic disease using recombinant DNA. Supplement. Hum Genet (1987) 1.50
The nature of giant cell tumor of bone. J Cancer Res Clin Oncol (2001) 1.47
Desmosomal glycoproteins II and III. Cadherin-like junctional molecules generated by alternative splicing. J Biol Chem (1991) 1.47
A universally conserved region of the largest subunit participates in the active site of RNA polymerase III. EMBO J (1995) 1.45
The yeast RNA polymerase III transcription machinery: a paradigm for eukaryotic gene activation. Cold Spring Harb Symp Quant Biol (1998) 1.45
Pathobiology of NPM-ALK and variant fusion genes in anaplastic large cell lymphoma and other lymphomas. Leukemia (2000) 1.45
What constitutes long-term survival after surgery for hilar cholangiocarcinoma? Cancer (1997) 1.43
A segment of mRNA encoding the leader peptide of the CPA1 gene confers repression by arginine on a heterologous yeast gene transcript. Mol Cell Biol (1994) 1.43
Case 3--1999. Severe fetal bradycardia in a pregnant woman undergoing hypothermic cardiopulmonary bypass. J Cardiothorac Vasc Anesth (1999) 1.42
Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis. Lancet (1993) 1.42
Observation of a centrality-dependent dijet asymmetry in lead-lead collisions at sqrt[S(NN)] =2.76 TeV with the ATLAS detector at the LHC. Phys Rev Lett (2010) 1.41
Segregation of all four major fibrillar collagen genes in the Marfan syndrome. Am J Hum Genet (1987) 1.41
A cystic fibrosis patient homozygous for the nonsense mutation R553X. J Med Genet (1991) 1.41
Limited resection for early adenocarcinoma in Barrett's esophagus. Ann Surg (2000) 1.41
[Thoracic pain in a power athlete]. Internist (Berl) (1997) 1.39
Molecular diagnosis of a Mycobacterium chelonae infection. Pathol Res Pract (2001) 1.39
Measurement of dijet azimuthal decorrelations in pp collisions at sqrt(s)=7 TeV. Phys Rev Lett (2011) 1.39
Sex difference in D7S8 marker allele distribution in adult cystic fibrosis patients. Lancet (1989) 1.39
A mutation in the C31 subunit of Saccharomyces cerevisiae RNA polymerase III affects transcription initiation. EMBO J (1995) 1.38
Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens. Hum Genet (1997) 1.38
N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma. Hum Mol Genet (1999) 1.35
Evaluation of neoadjuvant therapy response of osteogenic sarcoma using FDG PET. J Nucl Med (1999) 1.35
Intravenous infusion of apolipoprotein E accelerates clearance of plasma lipoproteins in rabbits. J Clin Invest (1989) 1.35
Determination of the strange-quark density of the proton from ATLAS measurements of the W→ℓν and Z→ℓℓ cross sections. Phys Rev Lett (2012) 1.34
MRI-guided prostate biopsy detects clinically significant cancer: analysis of a cohort of 100 patients after previous negative TRUS biopsy. World J Urol (2011) 1.32
Search for new particles in two-jet final states in 7 TeV proton-proton collisions with the ATLAS detector at the LHC. Phys Rev Lett (2010) 1.32
Kinetic modeling and simulation of in vitro transcription by phage T7 RNA polymerase. Biotechnol Bioeng (2001) 1.30
Histopathological classification of nonneoplastic and neoplastic gastrointestinal submucosal lesions. Endoscopy (2005) 1.30
Recombination between endogenous and exogenous simian virus 40 genes. III. Rescue of SV40 tsA and tsBC mutants by passage in permissive transformed monkey lines. Virology (1980) 1.29
A novel donor splice site in intron 11 of the CFTR gene, created by mutation 1811+1.6kbA-->G, produces a new exon: high frequency in Spanish cystic fibrosis chromosomes and association with severe phenotype. Am J Hum Genet (1995) 1.29
Restriction fragment length polymorphisms at the human parathyroid hormone gene locus. Hum Genet (1984) 1.27
Polymerase chain reaction: replication errors and reliability of gene diagnosis. Nucleic Acids Res (1989) 1.27
Observation of associated near-side and away-side long-range correlations in sqrt[s(NN)]=5.02 TeV proton-lead collisions with the ATLAS detector. Phys Rev Lett (2013) 1.27
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene. Hum Genet (1992) 1.27
Intraepithelial CD8-positive T lymphocytes predict survival for patients with serous stage III ovarian carcinomas: relevance of clonal selection of T lymphocytes. Br J Cancer (2009) 1.25
Human apolipoprotein E expression in Escherichia coli: structural and functional identity of the bacterially produced protein with plasma apolipoprotein E. Proc Natl Acad Sci U S A (1985) 1.25
Is Alzheimer's disease an apolipoprotein E amyloidosis? Lancet (1995) 1.25
Interaction of f1 histone with superhelical DNA. Proc Natl Acad Sci U S A (1975) 1.24
Assignment of the human parathyroid hormone gene to chromosome 11. Hum Genet (1983) 1.23
Recombination between endogenous and exogenous simian virus 40 genes. II. Biochemical evidence for genetic exchange. J Virol (1977) 1.23
Human gene cloning and disease analysis. Lancet (1987) 1.22
Murine and human TSPYL genes: novel members of the TSPY-SET-NAP1L1 family. Cytogenet Cell Genet (1998) 1.21
Heparin- and sulfatide-binding peptides from the type I repeats of human thrombospondin promote melanoma cell adhesion. Proc Natl Acad Sci U S A (1992) 1.20
Mutational analysis of PHEX gene in X-linked hypophosphatemia. J Clin Endocrinol Metab (1998) 1.20
Regional assignment of a 2.1-kb repetitive sequence to the distal part of the human Y heterochromatin. Hum Genet (1980) 1.20
Diagnosis of genetic disease using recombinant DNA. Hum Genet (1986) 1.20