(Q33898355)

English

Inactivation of the tumor suppressor genes causing the hereditary syndromes predisposing to head and neck cancer via promoter hypermethylation in sporadic head and neck cancers

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Inactivation of the tumor suppressor genes causing the hereditary syndromes predisposing to head and neck cancer via promoter hypermethylation in sporadic head and neck cancers (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

hypermethylation

1 reference

based on heuristic

inferred from title

head and neck cancer

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

head and neck carcinoma

1 reference

based on heuristic

inferred from title

Joseph A Califano

5

object named as

Joseph A Califano

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Ian M Smith

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Suhail K Mithani

2

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Wojciech K Mydlarz

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Steven S Chang

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

24 March 2010

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

72

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

44-50

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Impaired control of IRES-mediated translation in X-linked dyskeratosis congenita

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Promoter methylation and inactivation of tumour-suppressor genes in oral squamous-cell carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Dyskeratosis congenita: a disorder of defective telomere maintenance?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Molecular pathogenesis of Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Dyskeratosis congenita in a 40-year-old patient

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Dyskeratosis congenita vs. chronic graft versus host disease: report of a case and a review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Molecular pathology of head-and-neck cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Promoter hypermethylation of FANCF: disruption of Fanconi Anemia-BRCA pathway in cervical cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Inactivation of the Fanconi anemia/BRCA pathway in lung and oral cancers: implications for treatment and survival

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Epigenetic inactivation of RASSF1A in head and neck cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Dyskeratosis congenita with pigmentation, dystrophia unguium, and leucokeratosis oris; review of the known cases reported to date and discussion of the disease from various aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

The Fanconi road to cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

The Fanconi Anemia/BRCA signaling pathway: disruption in cisplatin-sensitive ovarian cancers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Cancer in Fanconi anemia, 1927-2001

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Genetic basis of Fanconi anemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

The role of DNA methylation in mammalian epigenetics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

The emerging genetic and molecular basis of Fanconi anaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Dyskeratosis congenita in all its forms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Genetic progression model for head and neck cancer: implications for field cancerization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

5 July 2018

5′ CpG island methylation is associated with transcriptional silencing of the tumour suppressor p16/CDKN2/MTS1 in human cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

28 July 2018

Gene promoter hypermethylation in tumors and lymph nodes of stage I lung cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

29 October 2018

Cancer incidence in persons with Fanconi anemia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

29 October 2018

Gene promoter hypermethylation in tumors and serum of head and neck cancer patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

29 October 2018

Dyskeratosis Congenita (DC) Registry: identification of new features of DC.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2881891

29 October 2018

Dyskeratosis congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita with associated periodontal disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple squamous-cell carcinomas in Fanconi's anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita with macular cutaneous amyloid deposits

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral squamous cell carcinoma in a case of dyskeratosis congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inactivation of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of p16 (CDKN2/MTS-1/INK4A) inactivation in head and neck squamous cell carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dyskeratosis congenita with pigmentation, dystrophia unguium, and leukoplakia oris; a follow-up report of two brothers

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

THE ASSOCIATION OF DYSKERATOSIS CONGENITA AND FANCONI'S ANAEMIA

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fanconi anemia: adult head and neck cancer and hematopoietic mosaicism

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Head and neck squamous cell carcinoma in patients with Fanconi anemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome-wide profiling of oral squamous cell carcinoma by array-based comparative genomic hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tongue cancer as a complication of dyskeratosis congenita in a woman

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Oral carcinoma in a young man: a case of dyskeratosis congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/20332657

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1159/000292104

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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