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Items: 19

1.

Coronary artery disease and dyslipidemia within Europe: genetic variants in lipid transport gene loci in German subjects with premature coronary artery disease.

Kay A, März W, Hoffmann MM, Zhang Q, Masana Ll, Cavanna J, Baroni MG, Shine B, Galton DJ.

Atheroscler Suppl. 2002 May;3(1):27-33.

PMID:
12044583
2.

Common genetic variants that relate to disorders of lipid transport in Spanish subjects with premature coronary artery disease.

Masana L, Febrer G, Cavanna J, Baroni MG, Marz W, Hoffmann MM, Shine B, Galton DJ.

Clin Sci (Lond). 2001 Feb;100(2):183-90.

PMID:
11171287
3.
4.

Acute hypertriglyceridaemic pancreatitis in a pregnant Indian: a new lipoprotein lipase gene mutation.

Murugasu CG, Armstrong G, Creedon G, Cavanna JS, Galton DJ, Tomkin GH.

J R Soc Med. 1998 Apr;91(4):205-7. No abstract available.

5.

Human cloning: safety is the issue.

Galton DJ, Kay A, Cavanna JS.

Nat Med. 1998 Jun;4(6):644. No abstract available.

PMID:
9623951
6.

Mutations at the lipoprotein lipase gene locus in subjects with diabetes mellitus, obesity and lipaemia.

Zhang Q, Cavallero E, Hoffmann MM, Cavanna J, Kay A, Charles A, Braschi S, Marz W, Perlemuter L, Jacotot B, Galton DJ.

Clin Sci (Lond). 1997 Oct;93(4):335-41.

PMID:
9404225
7.

Lipid transport genes and their relation to the syndrome of insulin resistance.

Galton DJ, Zhang Q, Cavallero E, Cavanna J, Kay A, Charles A, Braschi S, Perlemuter L, Jacotot B.

Ann N Y Acad Sci. 1997 Sep 20;827:100-9. No abstract available.

PMID:
9329745
8.

Identification of putative beneficial mutations for lipid transport.

Galton DJ, Mattu R, Needham EW, Cavanna J.

Z Gastroenterol. 1996 Jun;34 Suppl 3:56-8.

PMID:
8767463
9.

Common genetic variants of lipoprotein lipase that relate to lipid transport in patients with premature coronary artery disease.

Zhang Q, Cavanna J, Winkelman BR, Shine B, Gross W, Marz W, Galton DJ.

Clin Genet. 1995 Dec;48(6):293-8.

PMID:
8835323
10.

Coronary artery disease in Europe: what are the genetic risk factors?

Galton DJ, Cavanna J, Kay A, Zhang Q.

J R Coll Physicians Lond. 1995 Sep-Oct;29(5):429-30. No abstract available.

11.

Polymorphisms of the lipoprotein lipase gene and premature atherosclerosis.

Galton DJ, Mattu RK, Cavanna J.

J Intern Med Suppl. 1994;736:63-8. Review.

PMID:
7986311
12.

Mapping the Hrc gene to proximal mouse chromosome 7: delineation of a conserved linkage group with human 19q.

Brown SD, Chartier F, Johnson K, Cavanna JS.

Genomics. 1993 Nov;18(2):459-61. No abstract available.

PMID:
8288260
13.

Reverse genetic approaches to cloning deafness genes.

Brown SD, Brown KA, Sutcliffe MJ, Cavanna JS, Greenfield AJ, Steel KP.

Ann N Y Acad Sci. 1991;630:93-9. No abstract available.

PMID:
1952627
14.

Establishment of the mouse chromosome 7 region with homology to the myotonic dystrophy region of human chromosome 19q.

Cavanna JS, Greenfield AJ, Johnson KJ, Marks AR, Nadal-Ginard B, Brown SD.

Genomics. 1990 May;7(1):12-8.

PMID:
1970795
15.

Molecular and genetic mapping of the mouse mdx locus.

Cavanna JS, Coulton G, Morgan JE, Brockdorff N, Forrest SM, Davies KE, Brown SD.

Genomics. 1988 Nov;3(4):337-41.

PMID:
3243547
16.

The long-range mapping of mammalian chromosomes.

Brown SD, Brockdorff N, Cavanna JS, Fisher EM, Greenfield AJ, Lyon MF, Nasir J.

Curr Top Microbiol Immunol. 1988;137:3-12. No abstract available.

PMID:
3416640
17.

Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses.

Brockdorff N, Fisher EM, Cavanna JS, Lyon MF, Brown SD.

EMBO J. 1987 Nov;6(11):3291-7.

18.

The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome.

Brockdorff N, Cross GS, Cavanna JS, Fisher EM, Lyon MF, Davies KE, Brown SD.

Nature. 1987 Jul 9-15;328(6126):166-8.

PMID:
3600793
19.

Microdissection and microcloning of the mouse X chromosome.

Fisher EM, Cavanna JS, Brown SD.

Proc Natl Acad Sci U S A. 1985 Sep;82(17):5846-9.

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