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Similar articles for PubMed (Select 14523376)

1.

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis.

Aretz S, Uhlhaas S, Caspari R, Mangold E, Pagenstecher C, Propping P, Friedl W.

Eur J Hum Genet. 2004 Jan;12(1):52-8.

2.

De novo mutations in familial adenomatous polyposis (FAP).

Ripa R, Bisgaard ML, Bülow S, Nielsen FC.

Eur J Hum Genet. 2002 Oct;10(10):631-7. Erratum in: Eur J Hum Genet. 2002 Dec;10(12):887-8.

3.

Mutation spectrum of the APC gene in 83 Korean FAP families.

Kim DW, Kim IJ, Kang HC, Park HW, Shin Y, Park JH, Jang SG, Yoo BC, Lee MR, Hong CW, Park KJ, Oh NG, Kim NK, Sung MK, Lee BW, Kim YJ, Lee H, Park JG.

Hum Mutat. 2005 Sep;26(3):281.

PMID:
16088911
4.
5.

Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.

Friedl W, Caspari R, Sengteller M, Uhlhaas S, Lamberti C, Jungck M, Kadmon M, Wolf M, Fahnenstich J, Gebert J, Möslein G, Mangold E, Propping P.

Gut. 2001 Apr;48(4):515-21.

6.

APC germline mutations identified in Czech patients with familial adenomatous polyposis.

Kohoutová M, Stekrová J, Jirásek V, Kapras J.

Hum Mutat. 2002 Apr;19(4):460-1.

PMID:
11933206
7.

APC mutation and phenotypic spectrum of Singapore familial adenomatous polyposis patients.

Cao X, Eu KW, Seow-Choen F, Zao Y, Cheah PY.

Eur J Hum Genet. 2000 Jan;8(1):42-8.

8.

Should children at risk for familial adenomatous polyposis be screened for hepatoblastoma and children with apparently sporadic hepatoblastoma be screened for APC germline mutations?

Aretz S, Koch A, Uhlhaas S, Friedl W, Propping P, von Schweinitz D, Pietsch T.

Pediatr Blood Cancer. 2006 Nov;47(6):811-8.

PMID:
16317745
9.

Rare mutations predisposing to familial adenomatous polyposis in Greek FAP patients.

Mihalatos M, Apessos A, Dauwerse H, Velissariou V, Psychias A, Koliopanos A, Petropoulos K, Triantafillidis JK, Danielidis I, Fountzilas G, Agnantis NJ, Nasioulas G.

BMC Cancer. 2005 Apr 15;5:40.

11.

Founder mutation in familial adenomatous polyposis (FAP) in the Balearic Islands.

González S, Blanco I, Campos O, Julià M, Reyes J, Llompart A, Cabeza E, Germà JR, Obrador A, Capellá G.

Cancer Genet Cytogenet. 2005 Apr 1;158(1):70-4.

PMID:
15771908
12.

The mutation spectrum of the APC gene in FAP patients from southern Italy: detection of known and four novel mutations.

De Rosa M, Scarano MI, Panariello L, Morelli G, Riegler G, Rossi GB, Tempesta A, Romano G, Renda A, Pettinato G, Izzo P.

Hum Mutat. 2003 Jun;21(6):655-6.

PMID:
14961559
13.

APC haploinsufficiency, but not CTNNB1 or CDH1 gene mutations, accounts for a fraction of familial adenomatous polyposis patients without APC truncating mutations.

Venesio T, Balsamo A, Rondo-Spaudo M, Varesco L, Risio M, Ranzani GN.

Lab Invest. 2003 Dec;83(12):1859-66.

PMID:
14691304
14.

Frequency of common and novel inactivating APC mutations in 202 families with familial adenomatous polyposis.

Mandl M, Paffenholz R, Friedl W, Caspari R, Sengteller M, Propping P.

Hum Mol Genet. 1994 Jan;3(1):181-4.

PMID:
8162022
15.

[Germline mutation of adenomatous polyposis coli gene in Chinese patients with familial adenomatous polyposis].

Wang TT, Chen SQ, Zhang XM.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Apr;25(2):199-202. Chinese.

PMID:
18393246
16.

[Hereditary forms of colorectal adenomatous polyposis].

Kohoutová M, Stekrová J, Sulová M, Zidková K, Kleibl Z, Vandrovcová J, Kebrdlová V, Kotlas J, Jirásek V.

Cas Lek Cesk. 2006;145(6):475-9. Czech.

PMID:
16836001
17.

Different phenotype manifestation of familial adenomatous polyposis in families with APC mutation at codon 1309.

Wachsmannova-Matelova L, Stevurkova V, Adamcikova Z, Holec V, Zajac V.

Neoplasma. 2009;56(6):486-9.

PMID:
19728755
18.

Genomic rearrangements of the APC tumor-suppressor gene in familial adenomatous polyposis.

Su LK, Steinbach G, Sawyer JC, Hindi M, Ward PA, Lynch PM.

Hum Genet. 2000 Jan;106(1):101-7.

PMID:
10982189
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