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 *

72 related articles for article (PubMed ID: 8807331)

  • 21. [Analysis of the A/C polymorphic site within the phenylalanine hydroxylase gene].
    Huang S; Li Hui ; Miao S; Xu L; Fang B; Liu G; Luo H
    Yi Chuan Xue Bao; 1996; 23(3):169-73. PubMed ID: 8950848
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, Brazil.
    Santos LL; Magalhães Mde C; Reis Ade O; Starling AL; Januário JN; Fonseca CG; Aguiar MJ; Carvalho MR
    Genet Mol Res; 2006 Mar; 5(1):16-23. PubMed ID: 16755493
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Phenylketonuria in The Netherlands: 93% of the mutations are detected by single-strand conformation analysis.
    van der Sijs-Bos CJ; Diepstraten CM; Juyn JA; Plaisier M; Giltay JC; van Spronsen FJ; Smit GP; Berger R; Smeitink JA; Poll-The BT; Ploos van Amstel JK
    Hum Hered; 1996; 46(4):185-90. PubMed ID: 8807319
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Gypsy phenylketonuria: a point mutation of the phenylalanine hydroxylase gene in Gypsy families from Slovakia.
    Kalanin J; Takarada Y; Kagawa S; Yamashita K; Ohtsuka N; Matsuoka A
    Am J Med Genet; 1994 Jan; 49(2):235-9. PubMed ID: 8116675
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutation spectrum and phenylalanine hydroxylase RFLP/VNTR background in 44 Romanian phenylketonuric alleles.
    Popescu T; Blazkova M; Kozak L; Jebeleanu G; Popescu A
    Hum Mutat; 1998; 12(5):314-9. PubMed ID: 9792407
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Screening for mutations in the PAH gene in Chinese: a new splice and a novel polymorphic mutation].
    Xu L; Miao S; Liu G
    Zhonghua Yi Xue Za Zhi; 1996 Jun; 76(6):451-4. PubMed ID: 9275491
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Molecular genetic aspects of phenylketonuria (PKU)].
    Giltay JC; van Hoef AM; de Weger R; Duran M; Berger R; Beemer FA
    Tijdschr Kindergeneeskd; 1991 Jun; 59(3):77-80. PubMed ID: 1677790
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular analysis of the phenylalanine hydroxylase gene in Mexican phenylketonuric patients.
    Nicolini H; Cruz C; Camarena B; Fernanda Merino M; Bilbao G; Vela M; Velázquez A; Pérez B; Desviat L; Ugarte M
    Arch Med Res; 1995; 26(1):53-7. PubMed ID: 7711448
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Validation of PAH genotype-based predictions of metabolic phenylalanine hydroxylase deficiency phenotype: investigation of PKU/MHP patients from Lithuania.
    Kasnauskiene J; Cimbalistiene L; Kucinskas V
    Med Sci Monit; 2003 Mar; 9(3):CR142-6. PubMed ID: 12640344
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutation analysis of phenylketonuria patients from Morocco: high prevalence of mutation G352fsdelG and detection of a novel mutation p.K85X.
    Dahri S; Desviat LR; Pérez B; Leal F; Ugarte M; Chabraoui L
    Clin Biochem; 2010 Jan; 43(1-2):76-81. PubMed ID: 19786003
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Analysis of mutations in the phenylalanine hydroxylase gene in Ukrainian families at high risk for phenylketonuria].
    Nechiporenko MV; Lalivshits LA
    Tsitol Genet; 2000; 34(6):59-63. PubMed ID: 11391893
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Analysis of mutations in exon 7 of phenylalanine hydroxylase gene among children with phenylketonuria in Ningxia, China].
    Mao XM; He J; Liu Y; Li XQ; Yu WZ; Gao ZH; Cai J
    Zhongguo Dang Dai Er Ke Za Zhi; 2014 Mar; 16(3):259-62. PubMed ID: 24661517
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular characterization of phenylketonuric mutations in Japanese by analysis of phenylalanine hydroxylase mRNA from lymphoblasts.
    Okano Y; Hase Y; Shintaku H; Araki K; Furuyama J; Oura T; Isshiki G
    Hum Mol Genet; 1994 Apr; 3(4):659. PubMed ID: 7915167
    [No Abstract]   [Full Text] [Related]  

  • 34. Mutation spectrum of phenylketonuria in Iranian population.
    Zare-Karizi Sh; Hosseini-Mazinani SM; Khazaei-Koohpar Z; Seifati SM; Shahsavan-Behboodi B; Akbari MT; Koochmeshgi J
    Mol Genet Metab; 2011 Jan; 102(1):29-32. PubMed ID: 20920871
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Ten novel mutations in the phenylalanine hydroxylase gene (PAH) observed in Brazilian patients with phenylketonuria.
    Acosta AX; Silva WA; Carvalho TM; Zago MA
    Hum Mutat; 2001; 17(1):77. PubMed ID: 11139255
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Analysis of mutations and VNTR-polymorphism in the phenylalanine hydroxylase gene].
    Hechyporenko MV; Kravchenko SA; Livshyts LA
    Ukr Biokhim Zh (1999); 2001; 73(2):63-7. PubMed ID: 11642047
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Characterization of mutations at the mouse phenylalanine hydroxylase locus.
    McDonald JD; Charlton CK
    Genomics; 1997 Feb; 39(3):402-5. PubMed ID: 9119379
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The molecular basis of phenylketonuria in Lithuania.
    Kasnauskiene J; Giannattasio S; Lattanzio P; Cimbalistiene L; Kucinskas V
    Hum Mutat; 2003 Apr; 21(4):398. PubMed ID: 12655550
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Advances in the studies of molecular heredity of phenylketonuria].
    Zhang Z; He YS
    Yi Chuan; 2004 Sep; 26(5):729-34. PubMed ID: 15640093
    [TBL] [Abstract][Full Text] [Related]  

  • 40. R252W/E178G phenylalanine hydroxylase genotype in a Romanian non-PKU hyperphenylalaninaemic patient.
    Popescu T; Popescu A; Kozak L; Blazkova M; Jebeleanu G
    Acta Paediatr; 1998 Oct; 87(10):1103-4. PubMed ID: 9825986
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.