Double Msp I RFLP in the human LDL receptor gene

Geisel J, Weisshaar B, Oette K, Mechtel M, Doerfler W (1987)
Nucleic Acids Research 15(9): 3943.

Zeitschriftenaufsatz | Veröffentlicht| Englisch
 
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Autor/in
Geisel, J; Weisshaar, BerndUniBi ; Oette, K; Mechtel, M; Doerfler, W
Erscheinungsjahr
1987
Zeitschriftentitel
Nucleic Acids Research
Band
15
Ausgabe
9
Seite(n)
3943
ISSN
0305-1048
eISSN
1362-4962
Page URI
https://pub.uni-bielefeld.de/record/1990311

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Geisel J, Weisshaar B, Oette K, Mechtel M, Doerfler W. Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research. 1987;15(9):3943.
Geisel, J., Weisshaar, B., Oette, K., Mechtel, M., & Doerfler, W. (1987). Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research, 15(9), 3943. doi:10.1093/nar/15.9.3943
Geisel, J., Weisshaar, B., Oette, K., Mechtel, M., and Doerfler, W. (1987). Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research 15, 3943.
Geisel, J., et al., 1987. Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research, 15(9), p 3943.
J. Geisel, et al., “Double Msp I RFLP in the human LDL receptor gene”, Nucleic Acids Research, vol. 15, 1987, pp. 3943.
Geisel, J., Weisshaar, B., Oette, K., Mechtel, M., Doerfler, W.: Double Msp I RFLP in the human LDL receptor gene. Nucleic Acids Research. 15, 3943 (1987).
Geisel, J, Weisshaar, Bernd, Oette, K, Mechtel, M, and Doerfler, W. “Double Msp I RFLP in the human LDL receptor gene”. Nucleic Acids Research 15.9 (1987): 3943.

15 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

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Komarova TY, Korneva VA, Kuznetsova TY, Golovina AS, Vasilyev VB, Mandelshtam MY., BMC Med Genet 14(), 2013
PMID: 24373485
A rare polymorphism in the low density lipoprotein (LDL) gene that affects mRNA splicing.
Bourbon M, Sun XM, Soutar AK., Atherosclerosis 195(1), 2007
PMID: 17335829
Three novel small deletion mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemia.
Chae JJ, Kim SH, Kim UK, Han KH, Kim HS, Kastner DL, Namkoong Y, Park YB, Lee CC., Clin Genet 55(5), 1999
PMID: 10422802
Mutation analysis of exon 3 of the LDL receptor gene in patients with severe hypercholesterolemia.
Geisel J, Gielen J, Oette K, Herrmann W, Wielckens K., Clin Chem Lab Med 36(5), 1998
PMID: 9676383
The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark.
Jensen HK, Jensen LG, Hansen PS, Faergeman O, Gregersen N., Atherosclerosis 120(1-2), 1996
PMID: 8645371
Severe hypercholesterolaemia: unusual inheritance in an Italian pedigree.
Zuliani G, Vigna GB, Corsini A, Maioli M, Romagnoni F, Fellin R., Eur J Clin Invest 25(5), 1995
PMID: 7628519
Type III dyslipoproteinemia in patients heterozygous for familial hypercholesterolemia and apolipoprotein E2. Evidence for a gene-gene interaction.
Hopkins PN, Wu LL, Schumacher MC, Emi M, Hegele RM, Hunt SC, Lalouel JM, Williams RR., Arterioscler Thromb 11(5), 1991
PMID: 1680391
Effects of three genetic loci in a pedigree with multiple lipoprotein phenotypes.
Emi M, Hegele RM, Hopkins PN, Wu LL, Plaetke R, Williams RR, Lalouel JM., Arterioscler Thromb 11(5), 1991
PMID: 1655017
Four DNA polymorphisms in the LDL-receptor gene and their use in diagnosis of familial hypercholesterolemia.
Schuster H, Stiefenhofer B, Wolfram G, Keller C, Humphries S, Huber A, Zöllner N., Hum Genet 82(1), 1989
PMID: 2565869
Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus.
Kotze MJ, Langenhoven E, Retief AE, Seftel HC, Henderson HE, Weich HF., J Med Genet 26(4), 1989
PMID: 2565980
Multiple mutations underlying familial hypercholesterolemia in the South African population.
Henderson HE, Kotze MJ, Berger GM., Hum Genet 83(1), 1989
PMID: 2570020
TaqI polymorphism in the LDL receptor gene and a TaqI 1.5-kb band associated with familial hypercholesterolemia.
Yamakawa K, Okafuji T, Iwamura Y, Yuzawa K, Satoh J, Hattori N, Yamanouchi Y, Yanagi H, Kawai K, Tsuchiya S., Hum Genet 80(1), 1988
PMID: 2901393

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