Cogan JD - Search Results

1

Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein.

Cogan JD, Phillips JA 3rd, Schenkman SS, Milner RD, Sakati N. Cogan JD, et al. J Clin Endocrinol Metab. 1994 Nov;79(5):1261-5. doi: 10.1210/jcem.79.5.7962317. J Clin Endocrinol Metab. 1994. PMID: 7962317

2

Genetic basis of endocrine disease. 6. Molecular basis of familial human growth hormone deficiency.

Phillips JA 3rd, Cogan JD. Phillips JA 3rd, et al. Among authors: cogan jd. J Clin Endocrinol Metab. 1994 Jan;78(1):11-6. doi: 10.1210/jcem.78.1.8288694. J Clin Endocrinol Metab. 1994. PMID: 8288694 Review. No abstract available.

3

Heterogeneous growth hormone (GH) gene mutations in familial GH deficiency.

Cogan JD, Phillips JA 3rd, Sakati N, Frisch H, Schober E, Milner RD. Cogan JD, et al. J Clin Endocrinol Metab. 1993 May;76(5):1224-8. doi: 10.1210/jcem.76.5.8496314. J Clin Endocrinol Metab. 1993. PMID: 8496314

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

Genetic mapping of the human pituitary-specific transcriptional factor gene and its analysis in familial panhypopituitary dwarfism.

Raskin S, Cogan JD, Summar ML, Moreno A, Krishnamani MR, Phillips JA 3rd. Raskin S, et al. Among authors: cogan jd. Hum Genet. 1996 Dec;98(6):703-5. doi: 10.1007/s004390050289. Hum Genet. 1996. PMID: 8931705

6

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: cogan jd. Endocr J. 1997 Feb;44(1):149-54. doi: 10.1507/endocrj.44.149. Endocr J. 1997. PMID: 9152628 Free article.

7

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. Hum Mol Genet. 1997 Jun;6(6):909-12. doi: 10.1093/hmg/6.6.909. Hum Mol Genet. 1997. PMID: 9175738

8

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: cogan jd. Eur J Endocrinol. 1997 Nov;137(5):474-81. doi: 10.1530/eje.0.1370474. Eur J Endocrinol. 1997. PMID: 9405026

9

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. Wu W, et al. Among authors: cogan jd. Nat Genet. 1998 Feb;18(2):147-9. doi: 10.1038/ng0298-147. Nat Genet. 1998. PMID: 9462743

10

Clinical and molecular characterization of Brazilian patients with growth hormone gene deletions.

Arnhold IJ, Osorio MG, Oliveira SB, Estefan V, Kamijo T, Krishnamani MR, Cogan JD, Phillips JA 3rd, Mendonca BB. Arnhold IJ, et al. Among authors: cogan jd. Braz J Med Biol Res. 1998 Apr;31(4):491-7. doi: 10.1590/s0100-879x1998000400003. Braz J Med Biol Res. 1998. PMID: 9698799

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