Stewart C - Search Results

1

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients.

Dean M, White MB, Amos J, Gerrard B, Stewart C, Khaw KT, Leppert M. Dean M, et al. Among authors: stewart c. Cell. 1990 Jun 1;61(5):863-70. doi: 10.1016/0092-8674(90)90196-l. Cell. 1990. PMID: 2344617

2

Detection of three rare frameshift mutations in the cystic fibrosis gene in an African-American (CF444delA), an Italian (CF2522insC), and a Soviet (CF3821delT).

White MB, Krueger LJ, Holsclaw DS Jr, Gerrard BC, Stewart C, Quittell L, Dolganov G, Baranov V, Ivaschenko T, Kapronov NI, et al. White MB, et al. Among authors: stewart c. Genomics. 1991 May;10(1):266-9. doi: 10.1016/0888-7543(91)90510-l. Genomics. 1991. PMID: 1710600

3

Identification of cystic fibrosis mutations.

Dean M, Gerrard B, Stewart C, Krueger L, Holsclaw D, Quittell L, Baranov V, Kapronov N, Leppert M, Amos J, et al. Dean M, et al. Among authors: stewart c. Adv Exp Med Biol. 1991;290:45-51. doi: 10.1007/978-1-4684-5934-0_6. Adv Exp Med Biol. 1991. PMID: 1719771 No abstract available.

4

Approaches to localizing disease genes as applied to cystic fibrosis.

Dean M, Drumm ML, Stewart C, Gerrard B, Perry A, Hidaka N, Cole JL, Collins FS, Iannuzzi MC. Dean M, et al. Among authors: stewart c. Nucleic Acids Res. 1990 Jan 25;18(2):345-50. doi: 10.1093/nar/18.2.345. Nucleic Acids Res. 1990. PMID: 1970161 Free PMC article.

5

Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis.

Anguiano A, Oates RD, Amos JA, Dean M, Gerrard B, Stewart C, Maher TA, White MB, Milunsky A. Anguiano A, et al. Among authors: stewart c. JAMA. 1992 Apr 1;267(13):1794-7. JAMA. 1992. PMID: 1545465

6

Typing of HLA-DQA1 and DQB1 using DNA single-strand conformation polymorphism.

Carrington M, Miller T, White M, Gerrard B, Stewart C, Dean M, Mann D. Carrington M, et al. Among authors: stewart c. Hum Immunol. 1992 Mar;33(3):208-12. doi: 10.1016/0198-8859(92)90073-v. Hum Immunol. 1992. PMID: 1618658

7

A de novo cystic fibrosis mutation: CGA (Arg) to TGA (stop) at codon 851 of the CFTR gene.

White MB, Leppert M, Nielsen D, Zielenski J, Gerrard B, Stewart C, Dean M. White MB, et al. Among authors: stewart c. Genomics. 1991 Nov;11(3):778-9. doi: 10.1016/0888-7543(91)90092-s. Genomics. 1991. PMID: 1723056 No abstract available.

8

Genetic markers for oncogenes, growth factors, and cystic fibrosis.

Dean M, Stewart C, Perry A, Gerrard B, Beck T, Rapp U, Drumm M, Iannuzzi M, Collins F, O'Brien S. Dean M, et al. Among authors: stewart c. Haematol Blood Transfus. 1989;32:360-5. doi: 10.1007/978-3-642-74621-5_63. Haematol Blood Transfus. 1989. PMID: 2576235 No abstract available.

9

Analysis of Mdr50: a Drosophila P-glycoprotein/multidrug resistance gene homolog.

Gerrard B, Stewart C, Dean M. Gerrard B, et al. Among authors: stewart c. Genomics. 1993 Jul;17(1):83-8. doi: 10.1006/geno.1993.1286. Genomics. 1993. PMID: 7691715

10

Mapping and sequencing of two yeast genes belonging to the ATP-binding cassette superfamily.

Dean M, Allikmets R, Gerrard B, Stewart C, Kistler A, Shafer B, Michaelis S, Strathern J. Dean M, et al. Among authors: stewart c. Yeast. 1994 Mar;10(3):377-83. doi: 10.1002/yea.320100310. Yeast. 1994. PMID: 7912468

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