prop-es:autor
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- Gerhard DS, Wagner L, Feingold EA, et al. (es)
- Strausberg RL, Feingold EA, Grouse LH, et al. (es)
- Miyoshi I, Kasai N, Hayashizaki Y (es)
- Pierce JG (es)
- Atzmon G, Barzilai N, Surks MI, Gabriely I (es)
- Benhadi N, Wiersinga WM, Reitsma JB, et al. (es)
- Bonomi M, Proverbio MC, Weber G, et al. (es)
- Borck G, Topaloglu AK, Korsch E, et al. (es)
- Brumm H, Pfeufer A, Biebermann H, et al. (es)
- Clark AG, Glanowski S, Nielsen R, et al. (es)
- Comings DE, Gade-Andavolu R, Gonzalez N, et al. (es)
- Kabadi UM, Premachandra BN (es)
- Karges B, LeHeup B, Schoenle E, et al. (es)
- Landa I, Ruiz-Llorente S, Montero-Conde C, et al. (es)
- Loinder K, Söderström M (es)
- Luttrell LM (es)
- Miyai S, Yoshimura S, Iwasaki Y, et al. (es)
- Pohlenz J, Dumitrescu A, Aumann U, et al. (es)
- Schaefer JS, Klein JR (es)
- Vuissoz JM, Deladoëy J, Buyukgebiz A, et al. (es)
- Gerhard DS, Wagner L, Feingold EA, et al. (es)
- Strausberg RL, Feingold EA, Grouse LH, et al. (es)
- Miyoshi I, Kasai N, Hayashizaki Y (es)
- Pierce JG (es)
- Atzmon G, Barzilai N, Surks MI, Gabriely I (es)
- Benhadi N, Wiersinga WM, Reitsma JB, et al. (es)
- Bonomi M, Proverbio MC, Weber G, et al. (es)
- Borck G, Topaloglu AK, Korsch E, et al. (es)
- Brumm H, Pfeufer A, Biebermann H, et al. (es)
- Clark AG, Glanowski S, Nielsen R, et al. (es)
- Comings DE, Gade-Andavolu R, Gonzalez N, et al. (es)
- Kabadi UM, Premachandra BN (es)
- Karges B, LeHeup B, Schoenle E, et al. (es)
- Landa I, Ruiz-Llorente S, Montero-Conde C, et al. (es)
- Loinder K, Söderström M (es)
- Luttrell LM (es)
- Miyai S, Yoshimura S, Iwasaki Y, et al. (es)
- Pohlenz J, Dumitrescu A, Aumann U, et al. (es)
- Schaefer JS, Klein JR (es)
- Vuissoz JM, Deladoëy J, Buyukgebiz A, et al. (es)
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prop-es:título
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- The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection . (es)
- Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (es)
- Eli Lilly lecture. The subunits of pituitary thyrotropin--their relationship to other glycoprotein hormones. (es)
- [Structure and regulation of human thyroid-stimulating hormone gene] (es)
- Compound heterozygous and homozygous mutations of the TSHbeta gene as a cause of congenital central hypothyroidism in Europe. (es)
- New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism. (es)
- Reviews in molecular biology and biotechnology: transmembrane signaling by G protein-coupled receptors. (es)
- Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene. (es)
- Higher maternal TSH levels in pregnancy are associated with increased risk for miscarriage, fetal or neonatal death. (es)
- A multivariate analysis of 59 candidate genes in personality traits: the temperament and character inventory. (es)
- Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect. (es)
- Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect. (es)
- Induction of GH, PRL, and TSH beta mRNA by transfection of Pit-1 in a human pituitary adenoma-derived cell line. (es)
- Serum thyrotropin in Graves' disease: a more reliable index of circulating thyroid-stimulating immunoglobulin level than thyroid function? (es)
- A novel thyroid stimulating hormone beta-subunit isoform in human pituitary, peripheral blood leukocytes, and thyroid. (es)
- An LXXLL motif in nuclear receptor corepressor mediates ligand-induced repression of the thyroid stimulating hormone-beta gene. (es)
- The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors. (es)
- 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. (es)
- Genetic predisposition to elevated serum thyrotropin is associated with exceptional longevity. (es)
- Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios. (es)
- The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection . (es)
- Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. (es)
- Eli Lilly lecture. The subunits of pituitary thyrotropin--their relationship to other glycoprotein hormones. (es)
- [Structure and regulation of human thyroid-stimulating hormone gene] (es)
- Compound heterozygous and homozygous mutations of the TSHbeta gene as a cause of congenital central hypothyroidism in Europe. (es)
- New autosomal recessive mutation of the TSH-beta subunit gene causing central isolated hypothyroidism. (es)
- Reviews in molecular biology and biotechnology: transmembrane signaling by G protein-coupled receptors. (es)
- Congenital secondary hypothyroidism caused by exon skipping due to a homozygous donor splice site mutation in the TSHbeta-subunit gene. (es)
- Higher maternal TSH levels in pregnancy are associated with increased risk for miscarriage, fetal or neonatal death. (es)
- A multivariate analysis of 59 candidate genes in personality traits: the temperament and character inventory. (es)
- Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect. (es)
- Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect. (es)
- Induction of GH, PRL, and TSH beta mRNA by transfection of Pit-1 in a human pituitary adenoma-derived cell line. (es)
- Serum thyrotropin in Graves' disease: a more reliable index of circulating thyroid-stimulating immunoglobulin level than thyroid function? (es)
- A novel thyroid stimulating hormone beta-subunit isoform in human pituitary, peripheral blood leukocytes, and thyroid. (es)
- An LXXLL motif in nuclear receptor corepressor mediates ligand-induced repression of the thyroid stimulating hormone-beta gene. (es)
- The variant rs1867277 in FOXE1 gene confers thyroid cancer susceptibility through the recruitment of USF1/USF2 transcription factors. (es)
- 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. (es)
- Genetic predisposition to elevated serum thyrotropin is associated with exceptional longevity. (es)
- Inferring nonneutral evolution from human-chimp-mouse orthologous gene trios. (es)
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