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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

82 related articles for article (PubMed ID: 7550240)

  • 1. An Alu1- polymorphism in the HEXA gene is common in Ashkenazi and Sephardic Jews, Israeli Arabs, and French Canadians of Quebec and northern New England.
    Grinshpun J; Khosravi R; Peleg L; Goldman B; Kaplan F; Triggs-Raine B; Navon R
    Hum Mutat; 1995; 6(1):89-90. PubMed ID: 7550240
    [No Abstract]   [Full Text] [Related]  

  • 2. Screening for genetic disorders among Jews: how should the Tay-Sachs screening program be continued?
    Zlotogora J; Leventhal A
    Isr Med Assoc J; 2000 Sep; 2(9):665-7. PubMed ID: 11062764
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tay-Sachs disease in persons of French-Canadian heritage in northern New England.
    Palomaki GE; Williams J; Haddow JE; Natowicz MR
    Am J Med Genet; 1995 May; 56(4):409-12. PubMed ID: 7604851
    [TBL] [Abstract][Full Text] [Related]  

  • 4. NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease.
    Karban A; Waterman M; Panhuysen CI; Pollak RD; Nesher S; Datta L; Weiss B; Suissa A; Shamir R; Brant SR; Eliakim R
    Am J Gastroenterol; 2004 Jun; 99(6):1134-40. PubMed ID: 15180737
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular basis of heat labile hexosaminidase B among Jews and Arabs.
    Narkis G; Adam A; Jaber L; Pennybacker M; Proia RL; Navon R
    Hum Mutat; 1997; 10(6):424-9. PubMed ID: 9401004
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel HEXA mutation in a Bedouin Tay-Sachs patient associated with exon skipping and reduced transcript level.
    Drucker L; Golan A; Boles DJ; el Bedour K; Proia RL; Navon R
    Hum Mutat; 1997; 9(3):260-4. PubMed ID: 9090529
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tay-Sachs disease and HEXA mutations among Moroccan Jews.
    Kaufman M; Grinshpun-Cohen J; Karpati M; Peleg L; Goldman B; Akstein E; Adam A; Navon R
    Hum Mutat; 1997; 10(4):295-300. PubMed ID: 9338583
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A mutation analysis of the phenylalanine hydroxylase (PAH) gene in the Israeli population.
    Bercovich D; Elimelech A; Yardeni T; Korem S; Zlotogora J; Gal N; Goldstein N; Vilensky B; Segev R; Avraham S; Loewenthal R; Schwartz G; Anikster Y
    Ann Hum Genet; 2008 May; 72(Pt 3):305-9. PubMed ID: 18294361
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation in the HEXA gene specific to Tay-Sachs disease carriers of Jewish Iraqi origin.
    Karpati M; Peleg L; Gazit E; Akstein E; Goldman B
    Clin Genet; 2000 May; 57(5):398-400. PubMed ID: 10852376
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Orosomucoid (ORM1) polymorphism in Arabs and Jews of Israel: more evidence for a middle eastern origin of the Jews.
    Nevo S; Picornell A; Miguel A; Castro JA; Joel A; Heno N; Liron M; Ramon MM
    Hum Biol; 1996 Apr; 68(2):217-29. PubMed ID: 8838913
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Different mutations in Ashkenazi Jewish and non-Jewish French Canadians with Tay-Sachs disease.
    Myerowitz R; Hogikyan ND
    Science; 1986 Jun; 232(4758):1646-8. PubMed ID: 3754980
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Common HEXB polymorphisms reduce serum HexA and HexB enzymatic activities, potentially masking Tay-Sachs disease carrier identification.
    Vallance H; Morris TJ; Coulter-Mackie M; Lim-Steele J; Kaback M
    Mol Genet Metab; 2006 Feb; 87(2):122-7. PubMed ID: 16352452
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers.
    Peleg L; Frisch A; Goldman B; Karpaty M; Narinsky R; Bronstein S; Frydman M
    Eur J Hum Genet; 1998; 6(2):185-6. PubMed ID: 9781065
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hexosaminidase A deficiency is an uncommon cause of a syndrome mimicking amyotrophic lateral sclerosis.
    Drory VE; Birnbaum M; Peleg L; Goldman B; Korczyn AD
    Muscle Nerve; 2003 Jul; 28(1):109-12. PubMed ID: 12811781
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Screening for carriers of Tay-Sachs disease in the ultraorthodox Ashkenazi Jewish community in Israel.
    Broide E; Zeigler M; Eckstein J; Bach G
    Am J Med Genet; 1993 Aug; 47(2):213-5. PubMed ID: 8213907
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel mutation at the invariant acceptor splice site of intron 9 in the HEXA gene [IVS9-1 G-->T] detected by a PCR-based diagnostic test.
    Brown DH; Triggs-Raine BL; McGinniss MJ; Kaback MM
    Hum Mutat; 1995; 5(2):173-4. PubMed ID: 7749415
    [No Abstract]   [Full Text] [Related]  

  • 17. Tay-Sachs genes in Acadians.
    Thurmon TF
    Am J Hum Genet; 1993 Sep; 53(3):781-3. PubMed ID: 8352284
    [No Abstract]   [Full Text] [Related]  

  • 18. Tay-Sachs disease in an Israeli Arab family: Trp26-->stop in the alpha-subunit of hexosaminidase A.
    Drucker L; Navon R
    Hum Mutat; 1993; 2(5):415-7. PubMed ID: 8257995
    [No Abstract]   [Full Text] [Related]  

  • 19. Homozygosity for the common Ashkenazi jewish Tay-Sachs +1 IVS-12 splice-junction mutation: first report.
    Strasberg P; Warren I; Skomorowski MA; Feigenbaum A
    Hum Mutat; 1997; 10(1):82-3. PubMed ID: 9222766
    [No Abstract]   [Full Text] [Related]  

  • 20. High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews.
    Nebel A; Filon D; Weiss DA; Weale M; Faerman M; Oppenheim A; Thomas MG
    Hum Genet; 2000 Dec; 107(6):630-41. PubMed ID: 11153918
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.