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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Dec 2016.

CGA glycoprotein hormones, alpha polypeptide

TSH alpha, FSH alpha
Top mentioned proteins: FSH, HAD, CD45, ACID, Thyrotropin-Releasing Hormone
Papers on TSH alpha
Interaction between neurotrophin 4 and gonadotrophin in bovine oviducts.
Zhou et al., Changchun, China. In Theriogenology, 2012
Neurotrophin 4 may have a role in regulating the function of bovine oviducts by interacting with gonadotrophins.
TSH receptor - autoantibody interactions.
Furmaniak et al., Cardiff, United Kingdom. In Horm Metab Res, 2009
Comparison of M22 and TSH interactions with the TSHR at the atomic level reveal that M22 heavy and light chains mimic TSH alpha and beta chains, respectively, in the way they bind to the receptor, but the evolutionary forces which have caused this close molecular mimicry are as yet completely unknown.
Involvement of thyrotropin in photoperiodic signal transduction in mice.
Yoshimura et al., Nagoya, Japan. In Proc Natl Acad Sci U S A, 2008
Although most mouse strains are considered to be nonseasonal, a robust photoperiodic response comprising induced expression of TSHB (TSH beta subunit), CGA (TSH alpha subunit), and DIO2, and reduced expression of DIO3, was observed in melatonin-proficient CBA/N mice.
[A novel microbeads-based chemiluminescence immunoassay for detecting human thyrotropin].
Gu et al., Beijing, China. In Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 2004
METHODS: Thyrotropin in sera was captured by an alkaline phosphase-labeled mAb against TSH beta subunit and a FITC-labeled mAb against TSH alpha subunit.
[A case of pleomorphic TSH-producing pituitary adenoma with calcification].
Mizoi et al., Akita, Japan. In No Shinkei Geka, 2004
Postoperatively, the serum levels of FT3, FT4, TSH, and TSH alpha-subunit decreased to normal range.
Follicle-stimulating hormone interacts with exoloop 3 of the receptor.
Ji et al., Lexington, United States. In J Biol Chem, 2003
We present the evidence for the interaction of FSH and exoloop 3. A peptide mimic of exoloop 3 specifically and saturably photoaffinity-labels FSH alpha but not FSH beta.
Truncated equine LH beta and asparagine(56)-deglycosylated equine LH alpha combine to produce a potent FSH antagonist.
Bousfield et al., Wichita, United States. In J Endocrinol, 2002
Hybrid hormone preparations were prepared by combining intact and Asn(56)-deglycosylated (N(56)dg) equine (e) LH or FSH alpha subunit preparations with truncated, des(121-149)eLH beta (eLH beta t), immunopurified, intact eLH beta or equine chorionic gonadotropin beta (eCG beta) preparations, and eFSH beta.
Chromatin remodeling by the thyroid hormone receptor in regulation of the thyroid-stimulating hormone alpha-subunit promoter.
Wolffe et al., Bethesda, United States. In J Biol Chem, 2001
In contrast, the thyroid-stimulating hormone alpha-subunit (TSH alpha) gene promoter is down-regulated by TR in the presence of T(3).
Cranial irradiation and central hypothyroidism.
Rose, Cincinnati, United States. In Trends Endocrinol Metab, 2001
TRH deficiency leads to abnormal glycosylation of TSH alpha and beta subunits and loss of the normal circadian pattern of TSH secretion (low in the afternoon, a surge in the evening, higher at night).
cDNA cloning of canine common alpha gene and its co-expression with canine thyrotropin beta gene in baculovirus expression system.
Ferguson et al., Athens, United States. In Domest Anim Endocrinol, 2000
The medium from the Sf9 cultures, presumably containing canine TSH alpha and beta in native heterodimer confirmation, exhibited TSH bioactivity as indicated in the cAMP stimulation assay in FRTL-5 cells.
Effect of octreotide acetate on thyrotropin-secreting adenoma: report of two cases and review of the literature.
Oezata et al., Ankara, Turkey. In Endocr Regul, 1999
One case had no increase in the TSH alpha subunit level, while this was increased in the other one.
A novel TR beta mutation (R383H) in resistance to thyroid hormone syndrome predominantly impairs corepressor release and negative transcriptional regulation.
Chatterjee et al., Cambridge, United Kingdom. In Mol Endocrinol, 1998
Although the R383H mutant receptor activated positively regulated genes to an extent comparable to wild-type (WT), negative transcriptional regulation of human TSH alpha and TRH promoters was impaired in either TR beta 1 or TR beta 2 contexts, and WT receptor function was dominantly inhibited.
High-level expression of biologically active recombinant bovine follicle stimulating hormone in a baculovirus system.
Moormann et al., Lelystad, Netherlands. In J Mol Endocrinol, 1998
Sf21 insect cells were coinfected with two recombinant baculoviruses, containing the cDNAs of bovine FSH alpha- and beta-subunits respectively.
Salmon thyroid-stimulating hormone: isolation, characterization, and development of a radioimmunoassay.
Dickhoff et al., Seattle, United States. In Gen Comp Endocrinol, 1997
The N-terminal sequence (25 residues) of the salmon TSH alpha subunit is identical to gonadotropin alpha-II subunit.
Quantification of salmon alpha- and thyrotropin (TSH) beta-subunit messenger RNA by an RNase protection assay: regulation by thyroid hormones.
Dickhoff et al., Seattle, United States. In Gen Comp Endocrinol, 1997
These findings confirm that, as in mammals, TSH alpha- and beta-subunit expression in teleosts may be differentially regulated by negative feedback from the thyroid hormones.
Follicle-stimulating hormone in the brushtail possum (Trichosurus vulpecula): purification, characterization, and radioimmunoassay.
McNatty et al., Upper Hutt, New Zealand. In Gen Comp Endocrinol, 1997
Amino-terminal sequencing for 11 cycles indicated that the alpha subunit has the same sequence as ovine FSH except for residue 7, where the possum FSH alpha subunit contains isoleucine compared to the ovine subunit which contains threonine.
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