Examination of Smad2 and Smad4 copy-number variations in skin cancers (Q42501534)

1 November 2017

title

Examination of Smad2 and Smad4 copy-number variations in skin cancers (English)

1 reference

1 November 2017

Yong Shao

1

1 reference

1 November 2017

Jie Zhang

2

1 reference

1 November 2017

Richu Zhang

3

1 reference

1 November 2017

Jun Wan

4

1 reference

1 November 2017

Wei Zhang

5

1 reference

1 November 2017

Bo Yu

6

1 reference

1 November 2017

publication date

1 February 2012

1 reference

Clinical and Translational Oncology

1 November 2017

published in

1 reference

1 November 2017

volume

14

1 reference

1 November 2017

issue

2

1 reference

1 November 2017

page(s)

138-142

1 reference

The logic of TGFbeta signaling.

1 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Smad transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Distinct mechanisms of TGF-beta1-mediated epithelial-to-mesenchymal transition and metastasis during skin carcinogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Targeted disruption of Smad4 in mouse epidermis results in failure of hair follicle cycling and formation of skin tumors.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Distinct genetic alterations in colorectal cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Acquired variation outweighs inherited variation in whole genome analysis of methotrexate polyglutamate accumulation in leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Mapping and sequencing of structural variation from eight human genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Association of a germ-line copy number variation at 2p24.3 and risk for aggressive prostate cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Lack of somatic alterations of MC1R in primary melanoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Allelic imbalances and microdeletions affecting the PTPRD gene in cutaneous squamous cell carcinomas detected using single nucleotide polymorphism microarray analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

A method for accurate detection of genomic microdeletions using real-time quantitative PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Copy-number variation: the end of the human genome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Excessive genomic DNA copy number variation in the Li-Fraumeni cancer predisposition syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

The roles of Smad2 and Smad3 in the development of chemically induced skin tumors in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12094-012-0773-7

Hair follicle defects and squamous cell carcinoma formation in Smad4 conditional knockout mouse skin

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22301403

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

https://pubmed.ncbi.nlm.nih.gov/22301403

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S12094-012-0773-7

1 reference

1 November 2017

1 reference