Seltzer WK - Search Results

1

Congenital adrenal hypoplasia and selective absence of pituitary luteinizing hormone: a new autosomal recessive syndrome.

Burke BA, Wick MR, King R, Thompson T, Hansen J, Darrae BT, Francke U, Seltzer WK, McCabe ER, Scheithauer BW. Burke BA, et al. Among authors: seltzer wk. Am J Med Genet. 1988 Sep;31(1):75-97. doi: 10.1002/ajmg.1320310111. Am J Med Genet. 1988. PMID: 2906226 Review.

2

Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Francke U, Harper JF, Darras BT, Cowan JM, McCabe ER, Kohlschütter A, Seltzer WK, Saito F, Goto J, Harpey JP, et al. Francke U, et al. Among authors: seltzer wk. Am J Hum Genet. 1987 Mar;40(3):212-27. Am J Hum Genet. 1987. PMID: 2883886 Free PMC article.

3

Characterization of patients with glycerol kinase deficiency utilizing cDNA probes for the Duchenne muscular dystrophy locus.

Towbin JA, Wu DR, Chamberlain J, Larsen PD, Seltzer WK, McCabe ER. Towbin JA, et al. Among authors: seltzer wk. Hum Genet. 1989 Sep;83(2):122-6. doi: 10.1007/BF00286703. Hum Genet. 1989. PMID: 2550352

4

Human and rat adrenal glycerol kinase: subcellular distribution and bisubstrate kinetics.

Seltzer WK, McCabe ER. Seltzer WK, et al. Mol Cell Biochem. 1984 Apr;62(1):43-50. doi: 10.1007/BF00230076. Mol Cell Biochem. 1984. PMID: 6330523

5

Subcellular distribution and kinetic properties of soluble and particulate-associated bovine adrenal glycerol kinase.

Seltzer WK, McCabe ER. Seltzer WK, et al. Mol Cell Biochem. 1984 Sep;64(1):51-61. doi: 10.1007/BF00420928. Mol Cell Biochem. 1984. PMID: 6092910

6

DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis.

Towbin JA, Chamberlain JS, Wu DR, Pillers DA, Seltzer WK, McCabe ER. Towbin JA, et al. Among authors: seltzer wk. Genomics. 1990 Jul;7(3):442-4. doi: 10.1016/0888-7543(90)90181-s. Genomics. 1990. PMID: 2163974

7

Complementary DNA probes for the Duchenne muscular dystrophy locus demonstrate a previously undetectable deletion in a patient with dystrophic myopathy, glycerol kinase deficiency, and congenital adrenal hypoplasia.

McCabe ER, Towbin J, Chamberlain J, Baumbach L, Witkowski J, van Ommen GJ, Koenig M, Kunkel LM, Seltzer WK. McCabe ER, et al. Among authors: seltzer wk. J Clin Invest. 1989 Jan;83(1):95-9. doi: 10.1172/JCI113890. J Clin Invest. 1989. PMID: 2536049 Free PMC article.

8

Adrenal dysfunction in glycerol kinase deficiency.

Seltzer WK, Firminger H, Klein J, Pike A, Fennessey P, McCabe ER. Seltzer WK, et al. Biochem Med. 1985 Apr;33(2):189-99. doi: 10.1016/0006-2944(85)90027-4. Biochem Med. 1985. PMID: 2988520 Review.

9

Glycerol kinase deficiency: compartmental considerations regarding pathogenesis and clinical heterogeneity.

McCabe ER, Seltzer WK. McCabe ER, et al. Among authors: seltzer wk. Adv Exp Med Biol. 1986;194:481-93. doi: 10.1007/978-1-4684-5107-8_36. Adv Exp Med Biol. 1986. PMID: 3019103 Review. No abstract available.

10

1-Thioglycerol: inhibitor of glycerol kinase activity in vitro and in situ.

Seltzer WK, Dhariwal G, Mckelvey HA, McCabe ER. Seltzer WK, et al. Life Sci. 1986 Oct 20;39(16):1417-24. doi: 10.1016/0024-3205(86)90545-x. Life Sci. 1986. PMID: 3022087

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