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 *

661 related articles for article (PubMed ID: 8941012)

  • 1. Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutations.
    Valanzano R; Cama A; Volpe R; Curia MC; Mencucci R; Palmirotta R; Battista P; Ficari F; Mariani-Costantini R; Tonelli F
    Cancer; 1996 Dec; 78(11):2400-10. PubMed ID: 8941012
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in two Chinese families with familial adenomatous polyposis.
    Pang CP; Keung JW; Tang NL; Fan DS; Lau JW; Lam DS
    Eye (Lond); 2000 Feb; 14 ( Pt 1)():18-22. PubMed ID: 10755094
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Incidence and predictive value of congenital hypertrophy of retinal pigment epithelium in Chinese familial adenomatous polyposis patients.
    Lam DS; Kwok SP; Kwok AK; Liew CT; Lau JW; Pang CC
    Chin Med J (Engl); 1998 Mar; 111(3):278-81. PubMed ID: 10374435
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The presence of congenital hypertrophy of the retinal pigment epithelium in a subgroup of patients with adenomatous polyposis coli mutations.
    Reck AC; Bunyan D; Eccles D; Humphry R
    Eye (Lond); 1997; 11 ( Pt 3)():298-300. PubMed ID: 9373466
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of APC exon 15 mutations in families suspected of familial adenomatous polyposis (FAP).
    Kirchhoff T; Zajac V; Krizan P; Repiská V; Stevurková V; Friedl W
    Folia Biol (Praha); 1997; 43(5):203-9. PubMed ID: 9595262
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The most frequent APC mutations among Slovak familial adenomatous polyposis patients. Adenomatous polyposis coli.
    Zajac V; Kovác M; Kirchhoff T; Stevurková V; Tomka M
    Neoplasma; 2002; 49(6):356-61. PubMed ID: 12584582
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Congenital hypertrophy of the retinal pigment epithelium serves as a clinical marker in a family with familial adenomatous polyposis.
    Parisi ML
    J Am Optom Assoc; 1995 Feb; 66(2):106-12. PubMed ID: 7714311
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Transcript dosage effect in familial adenomatous polyposis: model offered by two kindreds with exon 9 APC gene mutations.
    Curia MC; Esposito DL; Aceto G; Palmirotta R; Crognale S; Valanzano R; Ficari F; Tonelli F; Battista P; Mariani-Costantini R; Cama A
    Hum Mutat; 1998; 11(3):197-201. PubMed ID: 9521420
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutations in the APC gene and clinical features in Swedish patients with polyposis coli.
    Nordling M; Engwall Y; Wahlström J; Wiklund L; Eriksson MA; Gustavsson B; Fasth S; Larsson PA; Martinsson T
    Anticancer Res; 1997; 17(6D):4275-80. PubMed ID: 9494520
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Correlations between mutation site in APC and phenotype of familial adenomatous polyposis (FAP): a review of the literature.
    Nieuwenhuis MH; Vasen HF
    Crit Rev Oncol Hematol; 2007 Feb; 61(2):153-61. PubMed ID: 17064931
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposis.
    Pang CP; Fan DS; Keung JW; Baum L; Tang NL; Lau JW; Lam DS
    Ophthalmologica; 2001; 215(6):408-11. PubMed ID: 11741105
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotype-phenotype correlation between position of constitutional APC gene mutation and CHRPE expression in familial adenomatous polyposis.
    Wallis YL; Macdonald F; Hultén M; Morton JE; McKeown CM; Neoptolemos JP; Keighley M; Morton DG
    Hum Genet; 1994 Nov; 94(5):543-8. PubMed ID: 7959691
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid RT-PCR-based protein truncation test in the screening for 5' located mutations of the APC gene.
    Kraus C; Günther K; Vogler A; Hohenberger W; Pfeiffer RA; Ballhausen WG
    Mol Cell Probes; 1998 Jun; 12(3):143-7. PubMed ID: 9664575
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Nine novel APC mutations in Italian FAP patients.
    Resta N; Stella A; Susca F; Montera M; Gentile M; Cariola F; Prete F; Tenconi R; Tibiletti MG; Logrieco G; Mattina T; Andriulli G; Caruso ML; Fiorente P; Russo S; Caputi-Jambrenghi O; Mareni C; Guanti G
    Hum Mutat; 2001 May; 17(5):434-5. PubMed ID: 11317365
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Familial adenomatous polyposis coli in the Czech population. I. Detection of an additional 3 mutations out of a total of 7 in exon 15 of the APC gene].
    Jirásek V; Olschwang S; Boisson C; Janda J; Thomas G; Martásek P
    Cas Lek Cesk; 1997 Dec; 136(23):733-8. PubMed ID: 9476377
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Value of congenital hypertrophy of the retinal pigment epithelium as diagnostic marker in familial adenomatous polyposis].
    Chagas C; Fidalgo P; Martins A; Barata A; Leitão CN; Mira FC; Ramalho PS
    Acta Med Port; 1993 Jul; 6(7):303-6. PubMed ID: 8397471
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular and clinical study of familial adenomatous polyposis for genetic testing and management.
    Li G; Tamura K; Yamamoto Y; Sashio H; Utsunomiya J; Yamamura T; Shimoyama T; Furuyama J
    J Exp Clin Cancer Res; 1999 Dec; 18(4):519-29. PubMed ID: 10746979
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Congenital hypertrophy of retinal pigment epithelium: a marker in familial adenomatous polyposis].
    Szwarcberg J; Limacher JM; Fricker JP; Flament J
    J Fr Ophtalmol; 1999 Apr; 22(3):364-70. PubMed ID: 10337595
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exceptions to the rule: individuals with FAP specific CHRPE and mutations in exon 6 of the APC gene.
    Pack K; Smith-Ravin I; Phillips RK; Hodgson SV
    Clin Genet; 1996 Aug; 50(2):110-1. PubMed ID: 8937774
    [No Abstract]   [Full Text] [Related]  

  • 20. Assessment of the value of congenital hypertrophy of the retinal pigment epithelium as an ocular marker for familial adenomatous polyposis coli.
    Hickey-Dwyer MU; Willoughby CE
    Eye (Lond); 1993; 7 ( Pt 4)():562-4. PubMed ID: 8253239
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 34.