(Q37278613)

19 August 2017

Skin cancers, blindness, and anterior tongue mass in African brothers (English)

1 reference

19 August 2017

Priya Mahindra

1

1 reference

19 August 2017

John J DiGiovanna

2

1 reference

19 August 2017

Deborah Tamura

3

1 reference

19 August 2017

Jaime S Brahim

4

1 reference

19 August 2017

Thomas J Hornyak

5

1 reference

19 August 2017

Jere B Stern

6

1 reference

19 August 2017

Chyi-Chia Richard Lee

7

1 reference

19 August 2017

Sikandar G Khan

8

1 reference

19 August 2017

Brian P Brooks

9

1 reference

19 August 2017

Janine A Smith

10

1 reference

19 August 2017

Brian P Driscoll

11

1 reference

19 August 2017

Andrew D Montemarano

12

1 reference

19 August 2017

Kate Sugarman

13

1 reference

19 August 2017

Kenneth H Kraemer

14

1 reference

19 August 2017

language of work or name

English

0 references

publication date

1 November 2008

1 reference

Journal of the American Academy of Dermatology

19 August 2017

1 reference

19 August 2017

59

1 reference

19 August 2017

5

1 reference

19 August 2017

881-886

1 reference

Keratocystic odontogenic tumour: reclassification of the odontogenic keratocyst from cyst to tumour

19 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Heterozygous individuals bearing a founder mutation in the XPA DNA repair gene comprise nearly 1% of the Japanese population

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Ocular manifestations in the inherited DNA repair disorders.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Xeroderma pigmentosum--bridging a gap between clinic and laboratory.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Cockayne syndrome and xeroderma pigmentosum

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Squamous cell carcinoma of the tongue in young adults: increasing incidence and factors that predict treatment outcomes

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Xeroderma pigmentosum in Libya

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Characterization of molecular defects in xeroderma pigmentosum group C

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Oculocutaneous manifestations in xeroderma pigmentosa

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

The role of sunlight and DNA repair in melanoma and nonmelanoma skin cancer. The xeroderma pigmentosum paradigm

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published cases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Human skin responses to UV radiation: pigment in the upper epidermis protects against DNA damage in the lower epidermis and facilitates apoptosis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

DNA repair protects against cutaneous and internal neoplasia: evidence from xeroderma pigmentosum

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

UV-induced DNA damage and melanin content in human skin differing in racial/ethnic origin

26 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Mutations in the XPC gene in families with xeroderma pigmentosum and consequences at the cell, protein, and transcript levels.

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2717011

Normal vitamin D levels can be maintained despite rigorous photoprotection: six years' experience with xeroderma pigmentosum

3 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19119101

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevention of skin cancer in xeroderma pigmentosum: the physician as advocate

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19119101

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19119101

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.JAAD.2008.06.030

1 reference

19 August 2017

1 reference

19 August 2017

PubMed publication ID

19119101

1 reference