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Results: 1 to 20 of 78

1.

High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.

Navardauskaite R, Dusatkova P, Obermannova B, Pfaeffle RW, Blum WF, Adukauskiene D, Smetanina N, Cinek O, Verkauskiene R, Lebl J.

J Clin Endocrinol Metab. 2014 Jan;99(1):299-306. doi: 10.1210/jc.2013-3090. Epub 2013 Dec 20.

PMID:
24178788
[PubMed - indexed for MEDLINE]
2.

A PROP1-binding factor, AES cloned by yeast two-hybrid assay represses PROP1-induced Pit-1 gene expression.

Sugiyama Y, Ikeshita N, Shibahara H, Yamamoto D, Kawagishi M, Iguchi G, Iida K, Takahashi Y, Kaji H, Chihara K, Okimura Y.

Mol Cell Endocrinol. 2013 Aug 25;376(1-2):93-8. doi: 10.1016/j.mce.2013.05.022. Epub 2013 Jun 1.

PMID:
23732115
[PubMed - indexed for MEDLINE]
3.

Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency.

Kandemir N, Vurallı D, Taşkıran E, Gönç N, Özön A, Alikaşifoğlu A, Yılmaz E.

Turk J Pediatr. 2012 Nov-Dec;54(6):570-5.

PMID:
23692781
[PubMed - indexed for MEDLINE]
Free Article
4.

Isolated central hypothyroidism in young siblings as a manifestation of PROP1 deficiency: clinical impact of whole exome sequencing.

Wassner AJ, Cohen LE, Hechter E, Dauber A.

Horm Res Paediatr. 2013;79(6):379-86. doi: 10.1159/000350013. Epub 2013 May 3.

PMID:
23652424
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

PROP-1 gene mutations in a 63-year-old woman presenting with osteoporosis and hyperlipidaemia.

Andrikoula M, Sertedaki A, Andrikoula S, Dacou-Voutetakis C, Tsatsoulis A.

Hormones (Athens). 2013 Jan-Mar;12(1):128-34.

PMID:
23624138
[PubMed - indexed for MEDLINE]
Free Article
6.

Clinical Case Seminar. Peculiar prolactinomas in patients with pituitary developmental gene mutations: from an adult endocrinologist perspective.

Doknic M, Pekic S, Civcic M, Popovic V.

Hormones (Athens). 2012 Apr-Jun;11(2):189-98.

PMID:
22801565
[PubMed - indexed for MEDLINE]
Free Article
7.

Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).

Godi M, Mellone S, Tiradani L, Marabese R, Bardelli C, Salerno M, Prodam F, Bellone S, Petri A, Momigliano-Richiardi P, Bona G, Giordano M.

J Clin Endocrinol Metab. 2012 Sep;97(9):E1791-7. doi: 10.1210/jc.2012-1527. Epub 2012 Jun 28.

PMID:
22745233
[PubMed - indexed for MEDLINE]
8.

PROP1 and CTNNB1 expression in adamantinomatous craniopharyngiomas with or without β-catenin mutations.

Cani CM, Matushita H, Carvalho LR, Soares IC, Brito LP, Almeida MQ, Mendonça BB.

Clinics (Sao Paulo). 2011;66(11):1849-54.

PMID:
22086512
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Mutations and pituitary morphology in a series of 82 patients with PROP1 gene defects.

Obermannova B, Pfaeffle R, Zygmunt-Gorska A, Starzyk J, Verkauskiene R, Smetanina N, Bezlepkina O, Peterkova V, Frisch H, Cinek O, Child CJ, Blum WF, Lebl J.

Horm Res Paediatr. 2011;76(5):348-54. doi: 10.1159/000332693. Epub 2011 Oct 18.

PMID:
22024773
[PubMed - indexed for MEDLINE]
10.

CTNNB1 gene mutations, pituitary transcription factors, and MicroRNA expression involvement in the pathogenesis of adamantinomatous craniopharyngiomas.

Campanini ML, Colli LM, Paixao BM, Cabral TP, Amaral FC, Machado HR, Neder LS, Saggioro F, Moreira AC, Antonini SR, de Castro M.

Horm Cancer. 2010 Aug;1(4):187-96. doi: 10.1007/s12672-010-0041-7.

PMID:
21761366
[PubMed - indexed for MEDLINE]
11.

Detection of genetic hypopituitarism in an adult population of idiopathic pituitary insufficiency patients with growth hormone deficiency.

Nyström HF, Saveanu A, Barbosa EJ, Barlier A, Enjalbert A, Glad C, Palming J, Johannsson G, Brue T.

Pituitary. 2011 Sep;14(3):208-16. doi: 10.1007/s11102-010-0278-8.

PMID:
21132537
[PubMed - indexed for MEDLINE]
12.

Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency.

Cruz JB, Nunes VS, Clara SA, Perone D, Kopp P, Nogueira CR.

Arq Bras Endocrinol Metabol. 2010;54(5):482-7.

PMID:
20694410
[PubMed - indexed for MEDLINE]
Free Article
13.

Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study.

Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S; DREAM investigators.

Diabetes Care. 2010 Oct;33(10):2250-3. doi: 10.2337/dc10-0452. Epub 2010 Jul 13.

PMID:
20628086
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion.

Dateki S, Fukami M, Uematsu A, Kaji M, Iso M, Ono M, Mizota M, Yokoya S, Motomura K, Kinoshita E, Moriuchi H, Ogata T.

J Clin Endocrinol Metab. 2010 Aug;95(8):4043-7. doi: 10.1210/jc.2010-0150. Epub 2010 Jun 9.

PMID:
20534763
[PubMed - indexed for MEDLINE]
15.

A large deletion of PROP1 gene in patients with combined pituitary hormone deficiency from two unrelated Chinese pedigrees.

Zhang H, Wang Y, Han L, Gu X, Shi D.

Horm Res Paediatr. 2010;74(2):98-105. doi: 10.1159/000313375. Epub 2010 Apr 15.

PMID:
20395664
[PubMed - indexed for MEDLINE]
16.

W194XProp1 and S156insTProp1, both of which have intact DNA-binding domain, show a different DNA-binding activity to the Prop1-binding element in human Pit-1 gene.

Shibahara H, Ikeshita N, Sugiyama Y, Toda K, Yamamoto D, Herningtyas EH, Maki T, Kubota E, Iguchi G, Iida K, Takahashi Y, Kaji H, Chihara K, Okimura Y.

Mol Cell Endocrinol. 2010 Jul 29;323(2):167-71. doi: 10.1016/j.mce.2010.03.023. Epub 2010 Apr 8.

PMID:
20381582
[PubMed - indexed for MEDLINE]
17.

PROP1-Related Combined Pituitary Hormone Deficiency.

de Graaff LCG.

In: Pagon RA, Adam MP, Ardinger HH, Bird TD, Dolan CR, Fong CT, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2014.
2000 Dec 07 [updated 2014 Aug 07].

PMID:
20301521
[PubMed]
Books & Documents
18.

Corepressors TLE1 and TLE3 interact with HESX1 and PROP1.

Carvalho LR, Brinkmeier ML, Castinetti F, Ellsworth BS, Camper SA.

Mol Endocrinol. 2010 Apr;24(4):754-65. doi: 10.1210/me.2008-0359. Epub 2010 Feb 24.

PMID:
20181723
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip.

Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD; ASCOT investigators; NORDIL investigators; BRIGHT Consortium.

Am J Hum Genet. 2009 Nov;85(5):628-42. doi: 10.1016/j.ajhg.2009.10.014.

PMID:
19913121
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.

Yerges LM, Klei L, Cauley JA, Roeder K, Kammerer CM, Moffett SP, Ensrud KE, Nestlerode CS, Marshall LM, Hoffman AR, Lewis C, Lang TF, Barrett-Connor E, Ferrell RE, Orwoll ES, Zmuda JM; MrOS Research Group.

J Bone Miner Res. 2009 Dec;24(12):2039-49. doi: 10.1359/jbmr.090524.

PMID:
19453261
[PubMed - indexed for MEDLINE]
Free PMC Article
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