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...

MicroRNA analysis of childhood atopic dermatitis reveals a role for miR‐451a

British journal of dermatology (1951), 2021-03, Vol.184 (3), p.514-523

2021

Volltextzugriff (PDF)

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes

British journal of dermatology (1951), 2014-12, Vol.171 (6), p.1521-1524

2014

Volltextzugriff (PDF)

CEDNIK syndrome results from loss-of-function mutations in SNAP29

British journal of dermatology (1951), 2011-03, Vol.164 (3), p.610-616

2011

Volltextzugriff (PDF)

New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome

Clinical and experimental dermatology, 2014-04, Vol.39 (3), p.361-367

2014

Volltextzugriff (PDF)

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris

British journal of dermatology (1951), 2014-05, Vol.170 (5), p.1196-1198

2014

Volltextzugriff (PDF)

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia

Clinical and experimental dermatology, 2012-03, Vol.37 (2), p.186-188

2012

Volltextzugriff (PDF)

757 MiRNA signature in atopic dermatitis

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S129-S129

2018

Volltextzugriff (PDF)

Infantile Mitochondrial Hepatopathy Is a Cardinal Feature of MEGDEL Syndrome (3-Methylglutaconic Aciduria Type IV With Sensorineural Deafness, Encephalopathy and Leigh-Like Syndrome) Caused by Novel Mutations in S epsilon RAC1

American journal of medical genetics. Part A, 2013-09, Vol.161A (9), p.2204-2215

2013

Volltextzugriff (PDF)

774 Focal facial dermal dysplasia type I caused by a duplication on 1p36.22

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S131-S131

2018

Volltextzugriff (PDF)

Transcriptional regulation of human microsomal triglyceride transfer protein by hepatocyte nuclear factor-4α

Journal of lipid research, 2005-02, Vol.46 (2), p.328-341

2005

Volltextzugriff (PDF)

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia: Correspondence

Clinical and experimental dermatology, 2012-03, Vol.37 (2), p.186-188

2012

Volltextzugriff (PDF)

Transcriptional suppression of human microsomal triglyceride transfer protein by hypolipidemic insulin sensitizers

Biochemical pharmacology, 2005-11, Vol.70 (11), p.1548-1559

2005

Volltextzugriff (PDF)

CEDNIK syndrome results from loss-of-function mutations in SNAP29: CEDNIK syndrome

British journal of dermatology (1951), 2011-02, p.no-no

2011

Volltextzugriff (PDF)

Negative autoregulation of HNF-4 alpha gene expression by HNF-4 alpha 1

Biochemical journal, 2005-05, Vol.388 (1), p.325-332

2005

Volltextzugriff (PDF)

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia

Clinical and experimental dermatology, 2012, Vol.37 (2), p.186-188

2012

Volltextzugriff (PDF)

1 – 15 von 15

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(14)
Mit Volltextzugriff
(15)

Publikationsform

Artikel
(14)
Berichte
(1)

Sprache

Englisch
(15)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(10)
Science & Technology
(10)
Dermatology
(6)
Humans
(6)
Biological And Medical Sciences
(4)
Medical Sciences
(4)
Adult
(3)
Female
(3)
Male
(3)
Mutation - Genetics
(3)
Biochemistry & Molecular Biology
(2)
Child
(2)
Child, Preschool
(2)
Membrane Proteins - Genetics
(2)
Promoter Regions, Genetic - Genetics
(2)
Adolescent
(1)
Aged
(1)
Aged, 80 And Over
(1)
Animals
(1)
Atopic Dermatitis
(1)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

MicroRNA analysis of childhood atopic dermatitis reveals a role for miR‐451a

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes

CEDNIK syndrome results from loss-of-function mutations in SNAP29

New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia

757 MiRNA signature in atopic dermatitis

Infantile Mitochondrial Hepatopathy Is a Cardinal Feature of MEGDEL Syndrome (3-Methylglutaconic Aciduria Type IV With Sensorineural Deafness, Encephalopathy and Leigh-Like Syndrome) Caused by Novel Mutations in S epsilon RAC1

774 Focal facial dermal dysplasia type I caused by a duplication on 1p36.22

Transcriptional regulation of human microsomal triglyceride transfer protein by hepatocyte nuclear factor-4α

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia: Correspondence

Transcriptional suppression of human microsomal triglyceride transfer protein by hypolipidemic insulin sensitizers

CEDNIK syndrome results from loss-of-function mutations in SNAP29: CEDNIK syndrome

Negative autoregulation of HNF-4 alpha gene expression by HNF-4 alpha 1

Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasia

Suchergebnisse filtern