(Q35909588)

11 August 2017

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title

Colorectal cancer and inherited mutations in base-excision repair (English)

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11 August 2017

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1 reference

3

Finlay Macrae

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11 August 2017

Elizabeth Chow

1

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11 August 2017

Christina Thirlwell

series ordinal

2

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11 August 2017

Lara Lipton

series ordinal

4

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11 August 2017

publication date

1 October 2004

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Lancet Oncology Commission

11 August 2017

published in

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11 August 2017

volume

5

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11 August 2017

issue

10

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11 August 2017

page(s)

600-606

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Alleles of the APC gene: an attenuated form of familial polyposis

11 August 2017

cites work

1 reference

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7 January 2021

Inherited variants of MYH associated with somatic G:C-->T:A mutations in colorectal tumors

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Autosomal recessive colorectal adenomatous polyposis due to inherited mutations of MYH

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7 January 2021

Multiple colorectal adenomas, classic adenomatous polyposis, and germ-line mutations in MYH

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Lessons from hereditary colorectal cancer

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7 January 2021

Hereditary nonpolyposis colorectal cancer: review of clinical, molecular genetics, and counseling aspects

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Molecular analysis of the APC gene in 105 Dutch kindreds with familial adenomatous polyposis: 67 germline mutations identified by DGGE, PTT, and southern analysis

1 reference

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7 January 2021

Familial adenomatous polyposis and MYH.

1 reference

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7 January 2021

Comprehensive analysis of SMAD4 mutations and protein expression in juvenile polyposis: evidence for a distinct genetic pathway and polyp morphology in SMAD4 mutation carriers

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Germline mutations of the gene encoding bone morphogenetic protein receptor 1A in juvenile polyposis.

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7 January 2021

A serine/threonine kinase gene defective in Peutz-Jeghers syndrome

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7 January 2021

Repair of oxidative DNA damage: mechanisms and functions

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7 January 2021

Formation of 8‐hydroxy‐2′‐deoxyguanosine and 4‐hydroxy‐2‐nonenal‐modified proteins in human renal‐cell carcinoma

1 reference

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7 January 2021

DNA base modifications in chromatin of human cancerous tissues

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7 January 2021

Oxidative DNA base damage and antioxidant enzyme activities in human lung cancer

1 reference

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7 January 2021

Replication-associated repair of adenine:8-oxoguanine mispairs by MYH.

1 reference

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7 January 2021

Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Regulation of intracellular localization of human MTH1, OGG1, and MYH proteins for repair of oxidative DNA damage

1 reference

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7 January 2021

Cloning and sequencing a human homolog (hMYH) of the Escherichia coli mutY gene whose function is required for the repair of oxidative DNA damage

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Human homolog of the MutY repair protein (hMYH) physically interacts with proteins involved in long patch DNA base excision repair

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Biallelic germline mutations in MYH predispose to multiple colorectal adenoma and somatic G:C-->T:A mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Insight into the functional consequences of inherited variants of the hMYH adenine glycosylase associated with colorectal cancer: complementation assays with hMYH variants and pre-steady-state kinetics of the corresponding mutated E.coli enzymes

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

A single nucleotide polymorphism at the splice donor site of the human MYH base excision repair genes results in reduced translation efficiency of its transcripts

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Proportion and phenotype of MYH-associated colorectal neoplasia in a population-based series of Finnish colorectal cancer patients

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Germline mutations but not somatic changes at the MYH locus contribute to the pathogenesis of unselected colorectal cancers.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Comprehensive analysis of the contribution of germline MYH variation to early-onset colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Allelic loss of a common microsatellite marker MYCL1: a useful prognostic factor of poor outcomes in colorectal cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Defective human MutY phosphorylation exists in colorectal cancer cell lines with wild-type MutY alleles

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Role of inherited defects of MYH in the development of sporadic colorectal cancer

1 reference

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7 January 2021

Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Inherited variants in MYH are unlikely to contribute to the risk of lung carcinoma.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

Duodenal adenomatosis in familial adenomatous polyposis.

1 reference

https://api.crossref.org/works/10.1016%2FS1470-2045%2804%2901595-5

7 January 2021

10.1016/S1470-2045(04)01595-5

Identifiers

DOI

1 reference

11 August 2017

1 reference