(Q42494105)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16645598%20AND%20SRC:MED&resulttype=core&format=json

20 January 2020

title

MC1R and PTCH gene polymorphism in French patients with basal cell carcinomas (English)

1 reference

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20 January 2020

5

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20 January 2020

author name string

Muriel Liboutet

1

1 reference

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20 January 2020

Marc Portela

2

1 reference

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20 January 2020

Gisèle Delestaing

3

1 reference

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20 January 2020

Catherine Vilmer

4

1 reference

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20 January 2020

Isabelle Gorin

6

1 reference

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20 January 2020

Philippe Saiag

7

1 reference

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20 January 2020

Céleste Lebbé

8

1 reference

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20 January 2020

Delphine Kerob

9

1 reference

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20 January 2020

Louis Dubertret

10

1 reference

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20 January 2020

Bernard Grandchamp

11

1 reference

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20 January 2020

Nicole Basset-Seguin

12

1 reference

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20 January 2020

Nadem Soufir

13

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20 January 2020

language of work or name

English

0 references

publication date

27 April 2006

1 reference

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Journal of Investigative Dermatology

20 January 2020

published in

1 reference

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20 January 2020

volume

126

1 reference

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20 January 2020

issue

7

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20 January 2020

page(s)

1510-1517

1 reference

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PTCH codon 1315 polymorphism and risk for nonmelanoma skin cancer

20 January 2020

cites work

1 reference

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7 January 2021

Melanocortin-1 receptor gene variants determine the risk of nonmelanoma skin cancer independently of fair skin and red hair

1 reference

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7 January 2021

Melanocortin-1 receptor genotype is a risk factor for basal and squamous cell carcinoma

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7 January 2021

https://api.crossref.org/works/10.1038%2FSJ.JID.5700263

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7 January 2021

Does the addition of information on genotype improve prediction of the risk of melanoma and nonmelanoma skin cancer beyond that obtained from skin phenotype?

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7 January 2021

The Validity and Practicality of Sun-Reactive Skin Types I Through VI

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7 January 2021

Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor

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7 January 2021

Nevoid basal cell carcinoma (Gorlin) syndrome

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7 January 2021

Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

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7 January 2021

Polymorphisms in DNA double-strand break repair genes and skin cancer risk

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7 January 2021

Functional variation of MC1R alleles from red-haired individuals.

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7 January 2021

Thr40 and Met122 are new partial loss-of-function natural mutations of the human melanocortin 1 receptor.

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7 January 2021

The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene

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7 January 2021

The melanocyte stimulating hormone receptor polymorphism: association of the V92M and A294H alleles with basal cell carcinoma

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7 January 2021

Melanocortin 1 Receptor (MC1R) Gene Variants are Associated with an Increased Risk for Cutaneous Melanoma Which is Largely Independent of Skin Type and Hair Color

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7 January 2021

Sun exposure and non-melanocytic skin cancer

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7 January 2021

Multiple cutaneous basal cell carcinomas: glutathione S-transferase (GSTM1, GSTT1) and cytochrome P450 (CYP2D6, CYP1A1) polymorphisms influence tumour numbers and accrual.

1 reference

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7 January 2021

Polymorphism in the nuclear excision repair gene ERCC2/XPD: association between an exon 6-exon 10 haplotype and susceptibility to cutaneous basal cell carcinoma.

1 reference

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7 January 2021

Xeroderma pigmentosum: from symptoms and genetics to gene-based skin therapy

1 reference

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7 January 2021

Melanocortin 1 receptor (MC1R) gene variants may increase the risk of melanoma in France independently of clinical risk factors and UV exposure

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7 January 2021

A simple salting out procedure for extracting DNA from human nucleated cells

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7 January 2021

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7 January 2021

Melanocortin-1 receptor polymorphisms and risk of melanoma: is the association explained solely by pigmentation phenotype?

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7 January 2021

Basal cell carcinomas: association of allelic variants with a high-risk subgroup of patients with the multiple presentation phenotype.

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7 January 2021

The genetics of sun sensitivity in humans

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7 January 2021

Pharmacological characterization of loss of function mutations of the human melanocortin 1 receptor that are associated with red hair

1 reference

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7 January 2021

Loss of function mutations of the human melanocortin 1 receptor are common and are associated with red hair

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JID.5700263

7 January 2021

PTCH polymorphism is associated with the rate of increase in basal cell carcinoma numbers during follow-up: preliminary data on the influence of an exon 12-exon 23 haplotype

1 reference

https://api.crossref.org/works/10.1038%2FSJ.JID.5700263

7 January 2021

Susceptibility to basal cell carcinoma: associations with PTCH polymorphisms.

1 reference

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7 January 2021

Skin colour and skin cancer - MC1R, the genetic link

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7 January 2021

The role of melanocortin-1 receptor polymorphism in skin cancer risk phenotypes.

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7 January 2021

Genetic association and cellular function of MC1R variant alleles in human pigmentation

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7 January 2021

The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanoma

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7 January 2021

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7 January 2021