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T-complex-associated-testis-expressed 1

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Top mentioned proteins: MHC, p21, Lactoylglutathione Lyase, IgE, DGKH
Papers on TCTE1
Comparative analysis of testis transcriptomes from triploid and fertile diploid cyprinid fish.
Liu et al., Changsha, China. In Biol Reprod, Apr 2015
A series of genes (DNAHs, DNAL1, IFTs, and DNAAF1) associated with sperm flagellar assembly and motility, and testis-specific candidate markers (Tcte1, Tekt1, Tekt4, Spag17, Spag5, Spag9a, Spag1b, and Spef2), had low expression levels in the testis of triploid fish.
Pheochromocytoma in rats with multiple endocrine neoplasia (MENX) shares gene expression patterns with human pheochromocytoma.
Pellegata et al., M√ľnchen, Germany. In Proc Natl Acad Sci U S A, 2010
The expression of GAL, DGKH, BMP7, PHOX2A, L1CAM, TCTE1, EBF3, SOX4, and HASH1 was up-regulated, although with different frequencies.
Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex.
Ragoussis et al., London, United Kingdom. In Genome Res, 1998
The GLO1 gene was mapped further centromeric in the 6p21.2-6p21.1 region toward TCTE-1.
Sequence divergence within the sperm-specific polypeptide TCTE1 is correlated with species-specific differences in sperm binding to zona-intact eggs.
Silver et al., Princeton, United States. In J Androl, 1998
The T-complex-associated testes-expressed (TCTE1) gene encodes a novel sperm cell-specific polypeptide (TCTE1) that is conserved across vertebrate species.
Cloning, expression, and mapping of TCTEL1, a putative human homologue of murine Tcte1, to 6q.
Hirai et al., Tokushima, Japan. In Cytogenet Cell Genet, 1995
From a human fetal-brain cDNA library we isolated a putative human homologue of the murine Tcte1 gene.
Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family.
Olsen et al., Boston, United States. In Hum Mol Genet, 1995
Linkage was established between CCD and four loci (D6S426, D6S451, D6S459, TCTE1) that span a region of 10 cM on chromosome 6p.
Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele.
Johnson et al., Newark, United States. In Am J Med Genet, 1994
Members of a 5-generation family with sacral defect and anterior meningocele (SDAM) were typed with polymorphic markers (dinucleotide repeats D6S89, D6S105, D6S109, and TCTE1) linked to HLA.
Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.
Gardiner et al., London, United Kingdom. In Am J Hum Genet, 1993
Family members were typed for eight polymorphic loci on chromosome 6p: F13A, D6S89, D6S109, D6S105, D6S10, C4B, DQA1/A2, and TCTE1.
Linkage mapping and fluorescence in situ hybridization of TCTE1 on human chromosome 6p: analysis of dinucleotide polymorphisms on native gels.
Zoghbi et al., Houston, United States. In Genomics, 1991
Highly informative dinucleotide repeat polymorphisms were identified at the T-complex-associated-testes-expressed-1 (TCTE1) locus on human chromosome 6p.
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.
Cann et al., Houston, United States. In Am J Hum Genet, 1991
These two loci are D6S89, which is telomeric to the HLA region, and T complex-associated testes-expressed 1 (TCTE1), centromeric to HLA.
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