Johnson K - Search Results

1

A c-DNA probe for the oncogene c-MEL (pC7-1) recognises a polymorphism with NcoI.

Nimmo ER, Padua RA, Hughes D, Williamson R, Johnson K. Nimmo ER, et al. Among authors: johnson k. Nucleic Acids Res. 1987 May 11;15(9):3940. doi: 10.1093/nar/15.9.3940. Nucleic Acids Res. 1987. PMID: 2884641 Free PMC article.

2

Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping.

Nimmo E, Padua RA, Hughes D, Brook JD, Williamson R, Johnson KJ. Nimmo E, et al. Among authors: johnson kj. Hum Genet. 1989 Mar;81(4):382-4. doi: 10.1007/BF00283697. Hum Genet. 1989. PMID: 2564840

3

Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy.

Johnson KJ, Jones PJ, Spurr N, Nimmo E, Davies J, Creed H, Weiss M, Williamson R. Johnson KJ, et al. Cytogenet Cell Genet. 1988;48(1):13-5. doi: 10.1159/000132577. Cytogenet Cell Genet. 1988. PMID: 2460293

4

The MEL gene: a new member of the RAB/YPT class of RAS-related genes.

Nimmo ER, Sanders PG, Padua RA, Hughes D, Williamson R, Johnson KJ. Nimmo ER, et al. Among authors: johnson kj. Oncogene. 1991 Aug;6(8):1347-51. Oncogene. 1991. PMID: 1886711

5

Constructing a complete restriction map of human chromosome 19.

Johnson KJ, Jones CP, Williamson R, Kaneda Y, Miki T. Johnson KJ, et al. Adv Neurol. 1988;48:163-6. Adv Neurol. 1988. PMID: 2891254 No abstract available.

6

A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.

Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Siciliano MJ, Bachinski LL, Anvret M, Harley H, Rundle S, et al. Johnson K, et al. Am J Hum Genet. 1990 Jun;46(6):1073-81. Am J Hum Genet. 1990. PMID: 1971149 Free PMC article.

7

The use of cloned gene probes to diagnose human genetic disease.

Williamson R, Moore G, Johnson K. Williamson R, et al. Among authors: johnson k. Rev Med Brux. 1987 Apr;8(4):240-1. Rev Med Brux. 1987. PMID: 3589275 No abstract available.

8

Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.

Johnson K, Nimmo E, Jones P, Weiss M, Savontaus ML, Anvret M, Bartlett R, Roses A, Shaw D, Harper PS, et al. Johnson K, et al. Hum Genet. 1988 Dec;80(4):379-81. doi: 10.1007/BF00273655. Hum Genet. 1988. PMID: 3198115

9

D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q.

Tsilfidis C, MacKenzie AE, Shutler G, Leblond S, Bailly J, Johnson K, Williamson R, Siegel-Bartelt J, Korneluk RG, Shelbourne P. Tsilfidis C, et al. Among authors: johnson k. Am J Hum Genet. 1991 Nov;49(5):961-5. Am J Hum Genet. 1991. PMID: 1928101 Free PMC article.

10

Recombination events that locate myotonic dystrophy distal to APOC2 on 19q.

Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Anvret M, Bonduelle M, Williamson B, Savontaus ML. Johnson K, et al. Genomics. 1989 Nov;5(4):746-51. doi: 10.1016/0888-7543(89)90116-x. Genomics. 1989. PMID: 2591962

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