Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma (Q33383292)

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English	Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Alterations in candidate genes PHF2, FANCC, PTCH1 and XPA at chromosomal 9q22.3 region: pathological significance in early- and late-onset breast carcinoma (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

breast carcinoma

1 reference

based on heuristic

inferred from title

author name string

Satyabrata Sinha

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Ratnesh K Singh

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Neyaz Alam

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Anup Roy

4

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Susanta Roychoudhury

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Chinmay Kumar Panda

6

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

publication date

6 November 2008

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Molecular Cancer

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

84

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Hedgehog signalling in medulloblastoma, glioblastoma and neuroblastoma.

1 reference

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21 June 2018

Disruption of the FA/BRCA pathway in bladder cancer

1 reference

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21 June 2018

Nucleotide excision repair pathway genes and oral premalignant lesions

1 reference

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21 June 2018

Downregulation of Fanconi anemia genes in sporadic head and neck squamous cell carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

XPA, haplotypes, and risk of basal and squamous cell carcinoma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

Patched1 functions as a gatekeeper by promoting cell cycle progression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization

1 reference

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21 June 2018

Deciphering a subgroup of breast carcinomas with putative progression of grade during carcinogenesis revealed by comparative genomic hybridisation (CGH) and immunohistochemistry.

1 reference

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21 June 2018

Methylation and silencing of the retinoic acid receptor-beta 2 gene in cervical cancer

1 reference

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21 June 2018

Xeroderma pigmentosum complementation group A protein (XPA) modulates RPA-DNA interactions via enhanced complex stability and inhibition of strand separation activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

1 reference

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21 June 2018

Loss of heterozygosity of nucleotide excision repair factors in sporadic ovarian, colon and lung carcinomas: implication for their roles of carcinogenesis in human solid tumors

1 reference

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21 June 2018

Quantitative analysis of chromosomal CGH in human breast tumors associates copy number abnormalities with p53 status and patient survival

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

Coincident PTCH and BRCA1 germline mutations in a patient with nevoid basal cell carcinoma syndrome and familial breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

PHF2, a novel PHD finger gene located on human chromosome 9q22

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

A breakpoint map of recurrent chromosomal rearrangements in human neoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

Identification of a damaged-DNA binding domain of the XPA protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

The XPA protein is a zinc metalloprotein with an ability to recognize various kinds of DNA damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

21 June 2018

Deregulation of the p14ARF/MDM2/p53 pathway is a prerequisite for human astrocytic gliomas with G1-S transition control gene abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

28 July 2018

Unmasking of epigenetically silenced genes reveals DNA promoter methylation and reduced expression of PTCH in breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Molecular basis of basal cell carcinogenesis in the atomic-bomb survivor population: p53 and PTCH gene alterations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Functional interplay between BRCA2/FancD1 and FancC in DNA repair.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Breast cancer in young Asian women: study on survival

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

[Methylation of the promoter region of the RASSF1A gene, a candidate tumor suppressor, in primary epithelial tumors]

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Frequent loss of heterozygosity on chromosome 9 in Chinese esophageal squamous cell carcinomas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Deletion mapping of chromosome 1 in early onset and late onset breast tumors--a comparative study in eastern India

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Mapping of the candidate tumor suppressor genes' loci on human chromosome 3 in head and neck squamous cell carcinoma of an Indian patient population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Overexpression of the p16 cell cycle inhibitor in breast cancer is associated with a more malignant phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Loss of FancC function results in decreased hematopoietic stem cell repopulating ability.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2633285

31 October 2018

Fanconi anemia gene mutations in young-onset pancreatic cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential alterations of the genes in the CDKN2A-CCND1-CDK4-RB1 pathway are associated with the development of head and neck squamous cell carcinoma in Indian patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of different deleted regions in chromosome 11 and their interrelations in early- and late-onset breast tumors: association with cyclin D1 amplification and survival

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Younger women with breast carcinoma have a poorer prognosis than older women

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Four tumor suppressor loci on chromosome 9q in bladder cancer: evidence for two novel candidate regions at 9q22.3 and 9q31

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential association of BRCA1 and BRCA2 genes with some breast cancer-associated genes in early and late onset breast tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ line Fanconi anemia complementation group C mutations and pancreatic cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lack of self-renewal capacity in Fancc-/- stem cells after ex vivo expansion

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A girl with deletion 9q22.1-q22.32 including the PTCH and ROR2 genes identified by genome-wide array-CGH

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple self-healing squamous epithelioma in different ethnic groups: more than a founder mutation disorder?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequent deletion and methylation in SH3GL2 and CDKN2A loci are associated with early- and late-onset breast carcinoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 9 deletions and recurrence of superficial bladder cancer: identification of four regions of prognostic interest

1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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1 reference

https://pubmed.ncbi.nlm.nih.gov/18990233

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1476-4598-7-84

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Dimensions Publication ID

1 reference

https://scigraph.springernature.com/pub.10.1186/1476-4598-7-84

9 September 2019

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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