Camper SA - Search Results

1

The phenotypic spectrum associated with OTX2 mutations in humans.

Gregory LC, Gergics P, Nakaguma M, Bando H, Patti G, McCabe MJ, Fang Q, Ma Q, Ozel AB, Li JZ, Poina MM, Jorge AAL, Benedetti AFF, Lerario AM, Arnhold IJP, Mendonca BB, Maghnie M, Camper SA, Carvalho LRS, Dattani MT. Gregory LC, et al. Among authors: camper sa. Eur J Endocrinol. 2021 May 25;185(1):121-135. doi: 10.1530/EJE-20-1453. Eur J Endocrinol. 2021. PMID: 33950863 Free PMC article.

2

Ames dwarf mice exhibit somatotrope commitment but lack growth hormone-releasing factor response.

Gage PJ, Lossie AC, Scarlett LM, Lloyd RV, Camper SA. Gage PJ, et al. Among authors: camper sa. Endocrinology. 1995 Mar;136(3):1161-7. doi: 10.1210/endo.136.3.7867569. Endocrinology. 1995. PMID: 7867569

3

Differential expression of corticotropin-releasing hormone in developing mouse embryos and adult brain.

Keegan CE, Herman JP, Karolyi IJ, O'Shea KS, Camper SA, Seasholtz AF. Keegan CE, et al. Among authors: camper sa. Endocrinology. 1994 Jun;134(6):2547-55. doi: 10.1210/endo.134.6.8194481. Endocrinology. 1994. PMID: 8194481

4

Role of prophet of Pit1 (PROP1) in gonadotrope differentiation and puberty.

Vesper AH, Raetzman LT, Camper SA. Vesper AH, et al. Among authors: camper sa. Endocrinology. 2006 Apr;147(4):1654-63. doi: 10.1210/en.2005-1080. Epub 2005 Dec 29. Endocrinology. 2006. PMID: 16384867

5

Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.

Mustapha M, Fang Q, Gong TW, Dolan DF, Raphael Y, Camper SA, Duncan RK. Mustapha M, et al. Among authors: camper sa. J Neurosci. 2009 Jan 28;29(4):1212-23. doi: 10.1523/JNEUROSCI.4957-08.2009. J Neurosci. 2009. PMID: 19176829 Free PMC article.

6

Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes.

Davis SW, Castinetti F, Carvalho LR, Ellsworth BS, Potok MA, Lyons RH, Brinkmeier ML, Raetzman LT, Carninci P, Mortensen AH, Hayashizaki Y, Arnhold IJ, Mendonça BB, Brue T, Camper SA. Davis SW, et al. Among authors: camper sa. Mol Cell Endocrinol. 2010 Jul 8;323(1):4-19. doi: 10.1016/j.mce.2009.12.012. Epub 2009 Dec 16. Mol Cell Endocrinol. 2010. PMID: 20025935 Free PMC article. Review.

7

Corepressors TLE1 and TLE3 interact with HESX1 and PROP1.

Carvalho LR, Brinkmeier ML, Castinetti F, Ellsworth BS, Camper SA. Carvalho LR, et al. Among authors: camper sa. Mol Endocrinol. 2010 Apr;24(4):754-65. doi: 10.1210/me.2008-0359. Epub 2010 Feb 24. Mol Endocrinol. 2010. PMID: 20181723 Free PMC article.

8

A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice.

Fang Q, Longo-Guess C, Gagnon LH, Mortensen AH, Dolan DF, Camper SA, Johnson KR. Fang Q, et al. Among authors: camper sa. Genetics. 2011 Oct;189(2):665-73. doi: 10.1534/genetics.111.130633. Epub 2011 Aug 11. Genetics. 2011. PMID: 21840860 Free PMC article.

9

Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.

Fang Q, Giordimaina AM, Dolan DF, Camper SA, Mustapha M. Fang Q, et al. Among authors: camper sa. J Assoc Res Otolaryngol. 2012 Apr;13(2):173-184. doi: 10.1007/s10162-011-0302-3. Epub 2011 Dec 6. J Assoc Res Otolaryngol. 2012. PMID: 22143287 Free PMC article.

10

Deletion of OTX2 in neural ectoderm delays anterior pituitary development.

Mortensen AH, Schade V, Lamonerie T, Camper SA. Mortensen AH, et al. Among authors: camper sa. Hum Mol Genet. 2015 Feb 15;24(4):939-53. doi: 10.1093/hmg/ddu506. Epub 2014 Oct 14. Hum Mol Genet. 2015. PMID: 25315894 Free PMC article.

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