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Subject Item

dbr:TSHB

owl:sameAs

dbpedia-es:TSHB

Subject Item

dbpedia-es:Tirotropina

prop-es:name

dbpedia-es:TSHB

Subject Item

wikipedia-es:TSHB

foaf:primaryTopic

dbpedia-es:TSHB

Subject Item

dbpedia-es:TSHB

rdf:type

owl:Thing wikidata:Q206229 wikidata:Q8054 dbo:Biomolecule dbo:Protein

rdfs:label

TSHB

rdfs:comment

La hormona estimulante de la tiroides, beta, también conocida como TSHB (del inglés: Thyroid stimulating hormone, beta) es una proteína que en humanos es codificada por el gen TSHB.​​

owl:sameAs

n15:05mz2q4

dct:subject

category-es:Proteínas_humanas

foaf:isPrimaryTopicOf

wikipedia-es:TSHB

prop-es:autor

Bonomi M, Proverbio MC, Weber G, et al. Kabadi UM, Premachandra BN Landa I, Ruiz-Llorente S, Montero-Conde C, et al. Strausberg RL, Feingold EA, Grouse LH, et al. Brumm H, Pfeufer A, Biebermann H, et al. Gerhard DS, Wagner L, Feingold EA, et al. Vuissoz JM, Deladoëy J, Buyukgebiz A, et al. Luttrell LM Clark AG, Glanowski S, Nielsen R, et al. Benhadi N, Wiersinga WM, Reitsma JB, et al. Borck G, Topaloglu AK, Korsch E, et al. Miyoshi I, Kasai N, Hayashizaki Y Schaefer JS, Klein JR Karges B, LeHeup B, Schoenle E, et al. Loinder K, Söderström M Atzmon G, Barzilai N, Surks MI, Gabriely I Comings DE, Gade-Andavolu R, Gonzalez N, et al. Pierce JG Pohlenz J, Dumitrescu A, Aumann U, et al. Miyai S, Yoshimura S, Iwasaki Y, et al.

prop-es:año

2002 2003 2000 2001 1994 1971 2008 2009 2007 2004 2005

prop-es:banda

13

prop-es:brazo

p

prop-es:cromosoma

1

prop-es:doi

101210 101034 101016 101007 101101 101530 101073 101371 101159 101126

prop-es:entrezgene

7252

prop-es:hgncid

12372

prop-es:name

Hormona estimulante de la tiroides, beta

prop-es:número

10.0 5652 8 9 10 12 1 2 3 4 5 6 26

prop-es:omim

188540

prop-es:pmc

2795660 2727793 2689139 139241 528928

prop-es:pmid

15489334 12477932 16216492 17954417 16133148 19730683 15297803 12364478 11140838 11549695 19273570 14671302 19837933 18240029 8196184 19364510 15292359 11297590 5002675 11788671

prop-es:publicación

Cell Tissue Res. J. Steroid Biochem. Mol. Biol. Horm. Res. Endocr Pract Endocrinology Gen. Comp. Endocrinol. J. Clin. Endocrinol. Metab. Eur. J. Endocrinol. Mol. Biotechnol. Nippon Rinsho Genome Res. Clin. Genet. Science Proc. Natl. Acad. Sci. U.S.A. PLoS Genet.

prop-es:páginas

239 1960 4136 e1000637 149 985 1331 1600 940 375 336 615 322 4811 2121 16899 269 4768 241 4468

prop-es:refseq

NM_000549

prop-es:símbolo

TSHB

prop-es:título

A novel thyroid stimulating hormone beta-subunit isoform in human pituitary, peripheral blood leukocytes, and thyroid. Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect. [Structure and regulation of human thyroid-stimulating hormone gene] Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism. Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection . Higher maternal TSH levels in pregnancy are associated with increased risk for miscarriage, fetal or neonatal death. Genetic predisposition to elevated serum thyrotropin is associated with exceptional longevity. Reviews in molecular biology and biotechnology: transmembrane signaling by G protein-coupled receptors. Serum thyrotropin in Graves' disease: a more reliable index of circulating thyroid-stimulating immunoglobulin level than thyroid function? Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect. Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios. A multivariate analysis of 59 candidate genes in personality traits: the temperament and character inventory. Compound heterozygous and homozygous mutations of the TSHbeta gene as a cause of congenital central hypothyroidism in Europe. The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors. Induction of GH, PRL, and TSH beta mRNA by transfection of Pit-1 in a human pituitary adenoma-derived cell line. Hyperplastic pituitary gland, high serum glycoprotein hormone alpha-subunit, and variable circulating thyrotropin levels as hallmark of central hypothyroidism due to mutations of the TSH beta gene. An LXXLL motif in nuclear receptor corepressor mediates ligand-induced repression of the thyroid stimulating hormone-beta gene. Eli Lilly lecture. The subunits of pituitary thyrotropin--their relationship to other glycoprotein hormones.

prop-es:uniprot

P01222

prop-es:volumen

162 160 322 94 89 86 87 99 97 14 13 302 5 39 62 58 52

dbo:wikiPageID

4872769

dbo:wikiPageRevisionID

120687473

dbo:wikiPageLength

8696

dbo:arm

p

dbo:band

13

dbo:chromosome

1

dbo:entrezgene

7252

dbo:hgncid

12372

dbo:omim

188540

dbo:refseq

NM_000549

dbo:symbol

TSHB

dbo:uniprot

P01222

prov:wasDerivedFrom

n11:0

dbo:abstract

La hormona estimulante de la tiroides, beta, también conocida como TSHB (del inglés: Thyroid stimulating hormone, beta) es una proteína que en humanos es codificada por el gen TSHB.​​