Kruyer H - Search Results

1

A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers.

Wainwright B, Lench N, Davies K, Scambler P, Kruyer H, Williamson R, Jahnsen T, Farrall M. Wainwright B, et al. Among authors: kruyer h. Cytogenet Cell Genet. 1987;45(3-4):237-9. doi: 10.1159/000132461. Cytogenet Cell Genet. 1987. PMID: 3691190 No abstract available.

2

The application of molecular genetics to the study of the basic defect causing cystic fibrosis.

Estivill X, Bates G, Bell G, Farrall M, Frederick P, Hawley K, Kruyer H, Lench N, Scrambler P, Stanier P, et al. Estivill X, et al. Among authors: kruyer h. Prog Clin Biol Res. 1987;254:181-90. Prog Clin Biol Res. 1987. PMID: 2893385 Review.

3

Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene.

Lathrop GM, Farrall M, O'Connell P, Wainwright B, Leppert M, Nakamura Y, Lench N, Kruyer H, Dean M, Park M, et al. Lathrop GM, et al. Among authors: kruyer h. Am J Hum Genet. 1988 Jan;42(1):38-44. Am J Hum Genet. 1988. PMID: 2892400 Free PMC article.

4

Further data supporting linkage between cystic fibrosis and the met oncogene and haplotype analysis with met and pJ3.11.

Farrall M, Watson E, Bates G, Bell G, Bell J, Davies KA, Estivill X, Kruyer H, Law HY, Lench N, et al. Farrall M, et al. Among authors: kruyer h. Am J Hum Genet. 1986 Dec;39(6):713-9. Am J Hum Genet. 1986. PMID: 3467586 Free PMC article.

5

Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator gene.

Tata F, Stanier P, Wicking C, Halford S, Kruyer H, Lench NJ, Scambler PJ, Hansen C, Braman JC, Williamson R, et al. Tata F, et al. Among authors: kruyer h. Genomics. 1991 Jun;10(2):301-7. doi: 10.1016/0888-7543(91)90312-3. Genomics. 1991. PMID: 1712752

6

Linkage of COL1A2 collagen gene to cystic fibrosis, and its clinical implications.

Scambler PJ, Wainwright BJ, Farrall M, Bell J, Stanier P, Lench NJ, Bell G, Kruyer H, Ramirez F, Williamson R. Scambler PJ, et al. Among authors: kruyer h. Lancet. 1985 Nov 30;2(8466):1241-2. doi: 10.1016/s0140-6736(85)90765-2. Lancet. 1985. PMID: 2866313 No abstract available.

7

Molecular genetics and the basic defect causing cystic fibrosis.

Williamson R, Bell G, Bell J, Bates G, Davies KA, Estivill X, Farrall M, Kruyer H, Law HY, Lench N, et al. Williamson R, et al. Among authors: kruyer h. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:309-15. doi: 10.1101/sqb.1986.051.01.036. Cold Spring Harb Symp Quant Biol. 1986. PMID: 3472728 No abstract available.

8

A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.

Estivill X, Farrall M, Scambler PJ, Bell GM, Hawley KM, Lench NJ, Bates GP, Kruyer HC, Frederick PA, Stanier P, et al. Estivill X, et al. Among authors: kruyer hc. Nature. 1987 Apr 30-May 6;326(6116):840-5. doi: 10.1038/326840a0. Nature. 1987. PMID: 2883581

9

MspI restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) gene.

Bosch A, Kruyer H, Nunes V, Estivill X. Bosch A, et al. Among authors: kruyer h. Nucleic Acids Res. 1991 Apr 11;19(7):1719. doi: 10.1093/nar/19.7.1719-a. Nucleic Acids Res. 1991. PMID: 1709281 Free PMC article.

10

Carrier detection and microsatellite analysis of Duchenne and Becker muscular dystrophy in Spanish families.

Kruyer H, Miranda M, Volpini V, Estivill X. Kruyer H, et al. Prenat Diagn. 1994 Feb;14(2):123-30. doi: 10.1002/pd.1970140208. Prenat Diagn. 1994. PMID: 7910399

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