UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 126

Sortiert nach

Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14

American journal of human genetics, 2012-07, Vol.91 (1), p.163-170

2012

Volltextzugriff (PDF)

Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies

Human molecular genetics, 2011-11, Vol.20 (21), p.4175-4186

2011

Volltextzugriff (PDF)

The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation

The Journal of clinical investigation, 2014-06, Vol.124 (6), p.2640-2650

2014

Volltextzugriff (PDF)

Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene

Journal of human genetics, 2023-04, Vol.68 (4), p.273-279

2023

Volltextzugriff (PDF)

Acquired resistance to the Hedgehog pathway inhibitor vismodegib due to smoothened mutations in treatment of locally advanced basal cell carcinoma

Journal of the American Academy of Dermatology, 2014-11, Vol.71 (5), p.1005-1008

2014

Volltextzugriff (PDF)

Spectrum of oncogenic driver mutations in lung adenocarcinomas from East Asian never smokers

PloS one, 2011-11, Vol.6 (11), p.e28204-e28204

2011

Volltextzugriff (PDF)

A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis

American journal of human genetics, 2010-04, Vol.86 (4), p.596-603

2010

Volltextzugriff (PDF)

The effect of topical diclofenac 3% and calcitriol 3 μg/g on superficial basal cell carcinoma (sBCC) and nodular basal cell carcinoma (nBCC): A phase II, randomized controlled trial

Journal of the American Academy of Dermatology, 2016-07, Vol.75 (1), p.126-134

2016

Volltextzugriff (PDF)

Kidney cancer characteristics and genotype-phenotype-correlations in Birt-Hogg-Dubé syndrome

PloS one, 2018-12, Vol.13 (12), p.e0209504-e0209504

2018

Volltextzugriff (PDF)

A Homozygous Missense Mutation in TGM5 Abolishes Epidermal Transglutaminase 5 Activity and Causes Acral Peeling Skin Syndrome

American journal of human genetics, 2005-12, Vol.77 (6), p.909-917

2005

Volltextzugriff (PDF)

Benefit Cost Analysis of Three Skin Cancer Public Education Mass-Media Campaigns Implemented in New South Wales, Australia

PloS one, 2016-01, Vol.11 (1), p.e0147665-e0147665

2016

Volltextzugriff (PDF)

Role of the keratin 1 and keratin 10 tails in the pathogenesis of ichthyosis hystrix of Curth Macklin

PloS one, 2018-04, Vol.13 (4), p.e0195792

2018

Volltextzugriff (PDF)

Novel Mutations in the BHD Gene and Absence of Loss of Heterozygosity in Fibrofolliculomas of Birt-Hogg-Dubé Patients

Journal of investigative dermatology, 2007-03, Vol.127 (3), p.588-593

2007

Volltextzugriff (PDF)

Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation

Human molecular genetics, 2006-08, Vol.15 (16), p.2509-2522

2006

Volltextzugriff (PDF)

Cutaneous HPV23 E6 prevents p53 phosphorylation through interaction with HIPK2

PloS one, 2011-11, Vol.6 (11), p.e27655

2011

Volltextzugriff (PDF)

A Novel Missense Mutation in the Second Extracellular Domain of GJB2 , p.Ser183Phe, Causes a Syndrome of Focal Palmoplantar Keratoderma with Deafness

The American journal of pathology, 2008-10, Vol.173 (4), p.1113-1119

2008

Volltextzugriff (PDF)

Identification of a KEAP1 germline mutation in a family with multinodular goitre

PloS one, 2013-05, Vol.8 (5), p.e65141-e65141

2013

Volltextzugriff (PDF)

Neuroendocrinology and neurobiology of sebaceous glands

Biological reviews of the Cambridge Philosophical Society, 2020-06, Vol.95 (3), p.592-624

2020

Volltextzugriff (PDF)

Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey–Hailey Disease

Human mutation, 2017-04, Vol.38 (4), p.343-356

2017

Volltextzugriff (PDF)

DNA dosimetry assessment for sunscreen genotoxic photoprotection

PloS one, 2012-06, Vol.7 (6), p.e40344

2012

Volltextzugriff (PDF)

The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress

Journal of cellular and molecular medicine, 2009-05, Vol.13 (5), p.959-971

2009

Volltextzugriff (PDF)

Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle

Journal of investigative dermatology, 2022-10, Vol.142 (10), p.2603-2612.e6

2022

Volltextzugriff (PDF)

Cutibacterium acnes: Much ado about maybe nothing much

Experimental dermatology, 2021-10, Vol.30 (10), p.1471-1476

2021

Volltextzugriff (PDF)

1 – 25 von 126

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(117)
Mit Volltextzugriff
(115)

Publikationsform

Sprache

Englisch
(124)
Japanisch
(20)
Deutsch
(1)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14

Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies

The tumor suppressor folliculin regulates AMPK-dependent metabolic transformation

Gram-positive anaerobe cocci (GPAC) are underrepresented in the microbiome of filaggrin-deficient human skin

Familial multiple discoid fibromas is linked to a locus on chromosome 5 including the FNIP1 gene

Acquired resistance to the Hedgehog pathway inhibitor vismodegib due to smoothened mutations in treatment of locally advanced basal cell carcinoma

Spectrum of oncogenic driver mutations in lung adenocarcinomas from East Asian never smokers

Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis

A Single-Nucleotide Deletion in the POMP 5′ UTR Causes a Transcriptional Switch and Altered Epidermal Proteasome Distribution in KLICK Genodermatosis

The effect of topical diclofenac 3% and calcitriol 3 μg/g on superficial basal cell carcinoma (sBCC) and nodular basal cell carcinoma (nBCC): A phase II, randomized controlled trial

Kidney cancer characteristics and genotype-phenotype-correlations in Birt-Hogg-Dubé syndrome

A Homozygous Missense Mutation in TGM5 Abolishes Epidermal Transglutaminase 5 Activity and Causes Acral Peeling Skin Syndrome

Benefit Cost Analysis of Three Skin Cancer Public Education Mass-Media Campaigns Implemented in New South Wales, Australia

Role of the keratin 1 and keratin 10 tails in the pathogenesis of ichthyosis hystrix of Curth Macklin

Novel Mutations in the BHD Gene and Absence of Loss of Heterozygosity in Fibrofolliculomas of Birt-Hogg-Dubé Patients

Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation

Cutaneous HPV23 E6 prevents p53 phosphorylation through interaction with HIPK2

A Novel Missense Mutation in the Second Extracellular Domain of GJB2 , p.Ser183Phe, Causes a Syndrome of Focal Palmoplantar Keratoderma with Deafness

Identification of a KEAP1 germline mutation in a family with multinodular goitre

Neuroendocrinology and neurobiology of sebaceous glands

Mendelian Disorders of Cornification Caused by Defects in Intracellular Calcium Pumps: Mutation Update and Database for Variants in ATP2A2 and ATP2C1 Associated with Darier Disease and Hailey–Hailey Disease

DNA dosimetry assessment for sunscreen genotoxic photoprotection

The R439C mutation in LMNA causes lamin oligomerization and susceptibility to oxidative stress

Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle

Cutibacterium acnes: Much ado about maybe nothing much

Suchergebnisse filtern