Prince MA - Search Results

1

Detection of growth hormone gene defects by dideoxy fingerprinting (ddF).

Miyata I, Cogan JD, Prince MA, Kamijo T, Ogawa M, Phillips JA 3rd. Miyata I, et al. Among authors: prince ma. Endocr J. 1997 Feb;44(1):149-54. doi: 10.1507/endocrj.44.149. Endocr J. 1997. PMID: 9152628 Free article.

2

A novel mechanism of aberrant pre-mRNA splicing in humans.

Cogan JD, Prince MA, Lekhakula S, Bundey S, Futrakul A, McCarthy EM, Phillips JA 3rd. Cogan JD, et al. Among authors: prince ma. Hum Mol Genet. 1997 Jun;6(6):909-12. doi: 10.1093/hmg/6.6.909. Hum Mol Genet. 1997. PMID: 9175738

3

Allelic variations in the human growth hormone-1 gene promoter of growth hormone-deficient patients and normal controls.

Wagner JK, Eblé A, Cogan JD, Prince MA, Phillips JA 3rd, Mullis PE. Wagner JK, et al. Among authors: prince ma. Eur J Endocrinol. 1997 Nov;137(5):474-81. doi: 10.1530/eje.0.1370474. Eur J Endocrinol. 1997. PMID: 9405026

4

A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study.

Cogan JD, Ramel B, Lehto M, Phillips J 3rd, Prince M, Blizzard RM, de Ravel TJ, Brammert M, Groop L. Cogan JD, et al. J Clin Endocrinol Metab. 1995 Dec;80(12):3591-5. doi: 10.1210/jcem.80.12.8530604. J Clin Endocrinol Metab. 1995. PMID: 8530604

5

An exon splice enhancer mutation causes autosomal dominant GH deficiency.

Moseley CT, Mullis PE, Prince MA, Phillips JA 3rd. Moseley CT, et al. Among authors: prince ma. J Clin Endocrinol Metab. 2002 Feb;87(2):847-52. doi: 10.1210/jcem.87.2.8236. J Clin Endocrinol Metab. 2002. PMID: 11836331

6

Applications of new genetic approaches to growth hormone-releasing hormone receptor defects.

Phillips JA, Prince MA. Phillips JA, et al. Among authors: prince ma. Growth Horm IGF Res. 1999 Apr;9 Suppl A:45-9. doi: 10.1016/s1096-6374(99)80009-4. Growth Horm IGF Res. 1999. PMID: 10429880 Review. No abstract available.

7

High frequency of BMPR2 exonic deletions/duplications in familial pulmonary arterial hypertension.

Cogan JD, Pauciulo MW, Batchman AP, Prince MA, Robbins IM, Hedges LK, Stanton KC, Wheeler LA, Phillips JA 3rd, Loyd JE, Nichols WC. Cogan JD, et al. Among authors: prince ma. Am J Respir Crit Care Med. 2006 Sep 1;174(5):590-8. doi: 10.1164/rccm.200602-165OC. Epub 2006 May 25. Am J Respir Crit Care Med. 2006. PMID: 16728714 Free PMC article.

8

Isolated growth hormone (GH) deficiency due to compound heterozygosity for two new mutations in the GH-releasing hormone receptor gene.

Salvatori R, Fan X, Phillips JA 3rd, Prince M, Levine MA. Salvatori R, et al. Among authors: prince m. Clin Endocrinol (Oxf). 2001 May;54(5):681-7. doi: 10.1046/j.1365-2265.2001.01273.x. Clin Endocrinol (Oxf). 2001. PMID: 11380500

9

Proteomics of transformed lymphocytes from a family with familial pulmonary arterial hypertension.

Meyrick BO, Friedman DB, Billheimer DD, Cogan JD, Prince MA, Phillips JA 3rd, Loyd JE. Meyrick BO, et al. Among authors: prince ma. Am J Respir Crit Care Med. 2008 Jan 1;177(1):99-107. doi: 10.1164/rccm.200703-499OC. Epub 2007 Oct 11. Am J Respir Crit Care Med. 2008. PMID: 17932379 Free PMC article.

10

Pulmonary veno-occlusive disease caused by an inherited mutation in bone morphogenetic protein receptor II.

Runo JR, Vnencak-Jones CL, Prince M, Loyd JE, Wheeler L, Robbins IM, Lane KB, Newman JH, Johnson J, Nichols WC, Phillips JA 3rd. Runo JR, et al. Am J Respir Crit Care Med. 2003 Mar 15;167(6):889-94. doi: 10.1164/rccm.200208-861OC. Epub 2002 Nov 21. Am J Respir Crit Care Med. 2003. PMID: 12446270

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