UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

The evolving universe of BRAF mutations in melanoma

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.893-893

2017

Volltextzugriff (PDF)

Skin colour and skin cancer - MC1R, the genetic link

Melanoma research, 2002-09, Vol.12 (5), p.405-416

Sturm, R A

2002

Volltextzugriff (PDF)

Characterization of Melanocyte Stimulating Hormone Receptor Variant Alleles in Twins with Red Hair

Human molecular genetics, 1997-10, Vol.6 (11), p.1891-1897

1997

Volltextzugriff (PDF)

Melanocortin-1 Receptor Polymorphisms and Risk of Melanoma: Is the Association Explained Solely by Pigmentation Phenotype?

American journal of human genetics, 2000-01, Vol.66 (1), p.176-186

2000

Volltextzugriff (PDF)

High naevus count and MC1R red hair alleles contribute synergistically to increased melanoma risk

British journal of dermatology (1951), 2019-11, Vol.181 (5), p.1009-1016

2019

Volltextzugriff (PDF)

Inverse expression states of the BRN2 and MITF transcription factors in melanoma spheres and tumour xenografts regulate the NOTCH pathway

Oncogene, 2011-07, Vol.30 (27), p.3036-3048

2011

Volltextzugriff (PDF)

The BRAF and NRAS mutation prevalence in dermoscopic subtypes of acquired naevi reveals constitutive mitogen‐activated protein kinase pathway activation

British journal of dermatology (1951), 2018-01, Vol.178 (1), p.191-197

2018

Volltextzugriff (PDF)

The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls

British journal of dermatology (1951), 2020-08, Vol.183 (2), p.357-366

2020

Volltextzugriff (PDF)

Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case–control study

British journal of dermatology (1951), 2018-05, Vol.178 (5), p.1119-1127

2018

Volltextzugriff (PDF)

Rufous Oculocutaneous Albinism in Southern African Blacks Is Caused by Mutations in the TYRP1 Gene

American journal of human genetics, 1997-11, Vol.61 (5), p.1095-1101

1997

Volltextzugriff (PDF)

Genetic Association and Cellular Function of MC1R Variant Alleles in Human Pigmentation

Annals of the New York Academy of Sciences, 2003-06, Vol.994 (1), p.348-358

2003

Volltextzugriff (PDF)

Phenotypic and genotypic analysis of amelanotic and hypomelanotic melanoma patients

Journal of the European Academy of Dermatology and Venereology, 2019-06, Vol.33 (6), p.1076-1083

2019

Volltextzugriff (PDF)

Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles

Human molecular genetics, 2007-09, Vol.16 (18), p.2249-2260

2007

Volltextzugriff (PDF)

GSTP1 and MC1R in melanoma susceptibility

British journal of dermatology (1951), 2012-06, Vol.166 (6), p.1155-1156

Sturm, R.A.

2012

Volltextzugriff (PDF)

The ubiquitous octamer-binding protein Oct-1 contains a POU domain with a homeo box subdomain

Genes & development, 1988-12, Vol.2 (12A), p.1582-1599

1988

Volltextzugriff (PDF)

Naevus count and MC1R R alleles contribute to melanoma risk

British journal of dermatology (1951), 2019-11, Vol.181 (5), p.e119-e119

2019

Volltextzugriff (PDF)

Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism : A new subtype of albinism classified as OCA3

American journal of human genetics, 1996-06, Vol.58 (6), p.1145-1156

1996

Volltextzugriff (PDF)

CDKN2A testing threshold in a high‐risk Australian melanoma cohort: number of primaries, family history and young age of onset impact risk

Journal of the European Academy of Dermatology and Venereology, 2020-12, Vol.34 (12), p.e797-e798

2020

Volltextzugriff (PDF)

Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: a cross-sectional study

British journal of dermatology (1951), 2016-02, Vol.174 (2), p.356-363

2016

Volltextzugriff (PDF)

Point mutation in p14ARF‐specific exon 1β of CDKN2A causing familial melanoma and astrocytoma

British journal of dermatology (1951), 2018-04, Vol.178 (4), p.e263-e264

2018

Volltextzugriff (PDF)

The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products

Genes & development, 1988-12, Vol.2 (12A), p.1513-1516

1988

Volltextzugriff (PDF)

Human pigmentation genes: identification, structure and consequences of polymorphic variation

Gene, 2001-10, Vol.277 (1), p.49-62

2001

Volltextzugriff (PDF)

Lack of protection from development of multiple melanomas by an injected melanocortin analogue in a combined high-risk MC1R/CDKN2A genotype patient

Journal of the European Academy of Dermatology and Venereology, 2016-10, Vol.30 (10), p.e65-e67

2016

Volltextzugriff (PDF)

Molecular genetics of human pigmentation diversity

Human molecular genetics, 2009-04, Vol.18 (R1), p.R9-R17

Sturm, Richard A.

2009

Volltextzugriff (PDF)

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes

Human molecular genetics, 2004-02, Vol.13 (4), p.447-461

2004

Volltextzugriff (PDF)

1 – 25 von 3.421

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.819)
Mit Volltextzugriff
(2.825)

Publikationsform

4 weitere anzeigen...

Weniger anzeigen...

Sprache

7 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.056)
Life Sciences & Biomedicine
(1.211)
Humans
(938)
Physical Sciences
(635)
Female
(503)
Male
(500)
Biological And Medical Sciences
(456)
Technology
(380)
Physics
(364)
Medical Sciences
(335)
Animals
(315)
Middle Aged
(313)
Adult
(310)
Aged
(232)
Astronomy & Astrophysics
(230)
Exact Sciences And Technology
(196)
Neurosciences & Neurology
(144)
Fundamental And Applied Biological Sciences. Psychology
(141)
Engineering
(139)
Adolescent
(120)

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

The evolving universe of BRAF mutations in melanoma

Skin colour and skin cancer - MC1R, the genetic link

Characterization of Melanocyte Stimulating Hormone Receptor Variant Alleles in Twins with Red Hair

Melanocortin-1 Receptor Polymorphisms and Risk of Melanoma: Is the Association Explained Solely by Pigmentation Phenotype?

High naevus count and MC1R red hair alleles contribute synergistically to increased melanoma risk

Inverse expression states of the BRN2 and MITF transcription factors in melanoma spheres and tumour xenografts regulate the NOTCH pathway

The BRAF and NRAS mutation prevalence in dermoscopic subtypes of acquired naevi reveals constitutive mitogen‐activated protein kinase pathway activation

The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls

Iris pigmented lesions as a marker of cutaneous melanoma risk: an Australian case–control study

Rufous Oculocutaneous Albinism in Southern African Blacks Is Caused by Mutations in the TYRP1 Gene

Genetic Association and Cellular Function of MC1R Variant Alleles in Human Pigmentation

Phenotypic and genotypic analysis of amelanotic and hypomelanotic melanoma patients

Receptor function, dominant negative activity and phenotype correlations for MC1R variant alleles

GSTP1 and MC1R in melanoma susceptibility

The ubiquitous octamer-binding protein Oct-1 contains a POU domain with a homeo box subdomain

Naevus count and MC1R R alleles contribute to melanoma risk

Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism : A new subtype of albinism classified as OCA3

CDKN2A testing threshold in a high‐risk Australian melanoma cohort: number of primaries, family history and young age of onset impact risk

Heritability of naevus patterns in an adult twin cohort from the Brisbane Twin Registry: a cross-sectional study

Point mutation in p14ARF‐specific exon 1β of CDKN2A causing familial melanoma and astrocytoma

The POU domain: a large conserved region in the mammalian pit-1, oct-1, oct-2, and Caenorhabditis elegans unc-86 gene products

Human pigmentation genes: identification, structure and consequences of polymorphic variation

Lack of protection from development of multiple melanomas by an injected melanocortin analogue in a combined high-risk MC1R/CDKN2A genotype patient

Molecular genetics of human pigmentation diversity

Interactive effects of MC1R and OCA2 on melanoma risk phenotypes

Suchergebnisse filtern