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Items: 1 to 20 of 108

1.

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
2.

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
3.

Identification and analysis of prophet of Pit-1-binding sites in human Pit-1 gene.

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

Endocrinology. 2008 Nov;149(11):5491-9. doi: 10.1210/en.2008-0030. Epub 2008 Jul 24.

PMID:
18653712
4.

Conserved amino acid sequences confer nuclear localization upon the Prophet of Pit-1 pituitary transcription factor protein.

Guy JC, Hunter CS, Showalter AD, Smith TP, Charoonpatrapong K, Sloop KW, Bidwell JP, Rhodes SJ.

Gene. 2004 Jul 21;336(2):263-73.

PMID:
15246537
6.
7.

Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).

Turton JP, Mehta A, Raza J, Woods KS, Tiulpakov A, Cassar J, Chong K, Thomas PQ, Eunice M, Ammini AC, Bouloux PM, Starzyk J, Hindmarsh PC, Dattani MT.

Clin Endocrinol (Oxf). 2005 Jul;63(1):10-8.

PMID:
15963055
8.

[Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].

Halász Z.

Orv Hetil. 2011 Feb 6;152(6):221-32. doi: 10.1556/OH.2011.29032. Hungarian.

PMID:
21278027
9.

PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.

de Graaff LC, Argente J, Veenma DC, Drent ML, Uitterlinden AG, Hokken-Koelega AC.

Horm Res Paediatr. 2010;73(5):363-71. doi: 10.1159/000308169. Epub 2010 Apr 14.

PMID:
20389107
10.

Candidate genes for panhypopituitarism identified by gene expression profiling.

Mortensen AH, MacDonald JW, Ghosh D, Camper SA.

Physiol Genomics. 2011 Oct 6;43(19):1105-16. doi: 10.1152/physiolgenomics.00080.2011. Epub 2011 Aug 9.

11.

Mutations in PROP1 cause familial combined pituitary hormone deficiency.

Wu W, Cogan JD, Pfäffle RW, Dasen JS, Frisch H, O'Connell SM, Flynn SE, Brown MR, Mullis PE, Parks JS, Phillips JA 3rd, Rosenfeld MG.

Nat Genet. 1998 Feb;18(2):147-9.

PMID:
9462743
12.

PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.

Lemos MC, Gomes L, Bastos M, Leite V, Limbert E, Carvalho D, Bacelar C, Monteiro M, Fonseca F, Agapito A, Castro JJ, Regateiro FJ, Carvalheiro M.

Clin Endocrinol (Oxf). 2006 Oct;65(4):479-85.

PMID:
16984240
13.

Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.

Abrão MG, Leite MV, Carvalho LR, Billerbeck AE, Nishi MY, Barbosa AS, Martin RM, Arnhold IJ, Mendonca BB.

Clin Endocrinol (Oxf). 2006 Sep;65(3):294-300. Review.

PMID:
16918947
14.

A critical functional missense mutation (H173R) in the bovine PROP1 gene significantly affects growth traits in cattle.

Pan C, Wu C, Jia W, Xu Y, Lei C, Hu S, Lan X, Chen H.

Gene. 2013 Dec 1;531(2):398-402. doi: 10.1016/j.gene.2013.09.002. Epub 2013 Sep 10.

PMID:
24029076
15.

Novel function of the transactivation domain of a pituitary-specific transcription factor, Pit-1.

Kishimoto M, Okimura Y, Yagita K, Iguchi G, Fumoto M, Iida K, Kaji H, Okamura H, Chihara K.

J Biol Chem. 2002 Nov 22;277(47):45141-8. Epub 2002 Aug 27.

16.

Amino-terminal enhancer of split (AES) interacts with the oncoprotein NUP98-HOXA9 and enhances its transforming ability.

Sarma NJ, Yaseen NR.

J Biol Chem. 2011 Nov 11;286(45):38989-9001. doi: 10.1074/jbc.M111.297952. Epub 2011 Sep 21.

17.

Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD).

Kelberman D, Turton JP, Woods KS, Mehta A, Al-Khawari M, Greening J, Swift PG, Otonkoski T, Rhodes SJ, Dattani MT.

Clin Endocrinol (Oxf). 2009 Jan;70(1):96-103. doi: 10.1111/j.1365-2265.2008.03326.x. Epub 2008 Jun 25.

PMID:
19128366
18.

Involvement of Prop1 homeobox gene in the early development of fish pituitary gland.

Angotzi AR, Mungpakdee S, Stefansson S, Male R, Chourrout D.

Gen Comp Endocrinol. 2011 May 1;171(3):332-40. doi: 10.1016/j.ygcen.2011.02.026. Epub 2011 Mar 21.

PMID:
21362424
19.

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.

20.

Cloning of a protein binding to the most proximal Pit-1 binding element of prolactin gene from human pituitary cDNA library.

Fumoto M, Okimura Y, Sakagami Y, Iguchi G, Kishimoto M, Takahashi Y, Kaji H, Chihara K.

Mol Cell Endocrinol. 2003 Sep 30;207(1-2):31-8.

PMID:
12972181
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