These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

96 related items for PubMed ID: 2600496

  • 1. [Recent trend in the research of hyperlipidemia in Japan. Three mutations including two deletions of the low density lipoprotein receptor gene in Japanese patients with homozygous familial hypercholesterolemia].
    Funahashi T, Miyake Y, Yamamoto A.
    Nihon Naika Gakkai Zasshi; 1989 Oct; 78(10):1406-7. PubMed ID: 2600496
    [No Abstract] [Full Text] [Related]

  • 2. Mutations in the low density lipoprotein receptor gene in Japanese patients with familial hypercholesterolemia.
    Mabuchi H, Kajinami K, Fujita H, Koizumi J, Takeda R.
    Ann N Y Acad Sci; 1990 Oct; 598():393-7. PubMed ID: 2248452
    [No Abstract] [Full Text] [Related]

  • 3. Three novel partial deletions of the low-density lipoprotein (LDL) receptor gene in familial hypercholesterolemia.
    Yamakawa K, Takada K, Yanagi H, Tsuchiya S, Kawai K, Nakagawa S, Kajiyama G, Hamaguchi H.
    Hum Genet; 1989 Jul; 82(4):317-21. PubMed ID: 2544509
    [Abstract] [Full Text] [Related]

  • 4. Mutations of the low density lipoprotein receptor in Japanese kindreds with familial hypercholesterolemia.
    Funahashi T, Miyake Y, Yamamoto A, Matsuzawa Y, Kishino B.
    Hum Genet; 1988 Jun; 79(2):103-8. PubMed ID: 3391611
    [Abstract] [Full Text] [Related]

  • 5. A novel mutation in exon 2 of the low-density lipoprotein-receptor gene in a patient with homozygous familial hypercholesterolemia.
    Takahashi M, Ikeda U, Takahashi S, Hattori H, Iwasaki T, Ishihara M, Egashira T, Honma S, Asano Y, Shimada K.
    Clin Genet; 2001 Apr; 59(4):290-2. PubMed ID: 11298688
    [No Abstract] [Full Text] [Related]

  • 6. Deletion in the gene for the low-density-lipoprotein receptor in a majority of French Canadians with familial hypercholesterolemia.
    Hobbs HH, Brown MS, Russell DW, Davignon J, Goldstein JL.
    N Engl J Med; 1987 Sep 17; 317(12):734-7. PubMed ID: 3627182
    [Abstract] [Full Text] [Related]

  • 7. Novel gene mutations at the low density lipoprotein receptor locus: FH-Kanazawa and FH-Okayama.
    Kajinami K, Mabuchi H, Inazu A, Fujita H, Koizumi J, Takeda R, Matsue T, Kibata M.
    J Intern Med; 1990 Apr 17; 227(4):247-51. PubMed ID: 2324680
    [Abstract] [Full Text] [Related]

  • 8. Mutations of the low density lipoprotein receptor in familial hypercholesterolemia--analysis of 21 homozygotes.
    Yamamoto A.
    Jpn J Med; 1988 May 17; 27(2):225-8. PubMed ID: 3418993
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. DNA deletions in the low density lipoprotein (LDL) receptor gene in Danish families with familial hypercholesterolemia.
    Rüdiger NS, Heinsvig EM, Hansen FA, Faergeman O, Bolund L, Gregersen N.
    Clin Genet; 1991 Jun 17; 39(6):451-62. PubMed ID: 1863993
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. The Low-Density Lipoprotein Receptor Genotype Is a Significant Determinant of the Rebound in Low-Density Lipoprotein Cholesterol Concentration After Lipoprotein Apheresis Among Patients With Homozygous Familial Hypercholesterolemia.
    Drouin-Chartier JP, Tremblay AJ, Bergeron J, Lamarche B, Couture P.
    Circulation; 2017 Aug 29; 136(9):880-882. PubMed ID: 28847800
    [No Abstract] [Full Text] [Related]

  • 13. Multiple crm- mutations in familial hypercholesterolemia. Evidence for 13 alleles, including four deletions.
    Hobbs HH, Leitersdorf E, Goldstein JL, Brown MS, Russell DW.
    J Clin Invest; 1988 Mar 29; 81(3):909-17. PubMed ID: 3343347
    [Abstract] [Full Text] [Related]

  • 14. Identification of recurrent and novel mutations in the LDL receptor gene in Japanese familial hypercholesterolemia. Mutation in brief no. 248. Online.
    Hattori H, Nagano M, Iwata F, Homma Y, Egashira T, Okada T.
    Hum Mutat; 1999 Mar 29; 14(1):87. PubMed ID: 10447263
    [Abstract] [Full Text] [Related]

  • 15. FH-Freiburg: a novel missense mutation (C317Y) in growth factor repeat A of the low density lipoprotein receptor gene in a German patient with homozygous familial hypercholesterolemia.
    Nauck MS, Scharnagl H, Nissen H, Schürmann C, Matern D, Nauck MA, Wieland H, März W.
    Atherosclerosis; 2000 Aug 29; 151(2):525-34. PubMed ID: 10924730
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Molecular genetic analysis of familial hypercholesterolemia: spectrum and regional difference of LDL receptor gene mutations in Japanese population.
    Yu W, Nohara A, Higashikata T, Lu H, Inazu A, Mabuchi H.
    Atherosclerosis; 2002 Dec 29; 165(2):335-42. PubMed ID: 12417285
    [Abstract] [Full Text] [Related]

  • 20. Identification of deletions in the human low density lipoprotein receptor gene.
    Horsthemke B, Dunning A, Humphries S.
    J Med Genet; 1987 Mar 29; 24(3):144-7. PubMed ID: 3572996
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.