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...

Resetting of Circadian Time in Peripheral Tissues by Glucocorticoid Signaling

Science (American Association for the Advancement of Science), 2000-09, Vol.289 (5488), p.2344-2347

2000

Volltextzugriff (PDF)

Disruption of CREB function in brain leads to neurodegeneration

Nature genetics, 2002-05, Vol.31 (1), p.47-54

2002

Volltextzugriff (PDF)

The Epithelial Glucocorticoid Receptor Is Required for the Normal Timing of Cell Proliferation during Mammary Lobuloalveolar Development but Is Dispensable for Milk Production

Molecular endocrinology (Baltimore, Md.), 2005-02, Vol.19 (2), p.340-349

2005

Volltextzugriff (PDF)

Pharmacological estrogen administration causes a FSH-independent osteo-anabolic effect requiring ER alpha in osteoblasts

PloS one, 2012-11, Vol.7 (11), p.e50301-e50301

2012

Volltextzugriff (PDF)

Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency

The Journal of clinical investigation, 2002-02, Vol.109 (4), p.475-480

2002

Volltextzugriff (PDF)

Targeted Mutation of the CREB Gene: Compensation within the CREB/ATF Family of Transcription Factors

Proceedings of the National Academy of Sciences - PNAS, 1994-06, Vol.91 (12), p.5647-5651

1994

Volltextzugriff (PDF)

The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis― ichthyosis―deafness syndrome

Human molecular genetics, 2011, Vol.20 (1), p.28-39

2011

Volltextzugriff (PDF)

Genetic Dissection of Corticosteroid Receptor Function in Mice

Hormone and metabolic research, 2004-06, Vol.36 (6), p.387-391

2004

Volltextzugriff (PDF)

Analysis of mice carrying targeted mutations of the glucocorticoid receptor gene argues against an essential role of glucocorticoid signalling for generating adrenal chromaffin cells

Development (Cambridge), 1999-07, Vol.126 (13), p.2935-2944

1999

Volltextzugriff (PDF)

Rescue of the albino phenotype by introduction of a functional tyrosinase gene into mice

The EMBO journal, 1990-09, Vol.9 (9), p.2819-2826

1990

Volltextzugriff (PDF)

Two genetically defined trans-acting loci coordinately regulate overlapping sets of liver-specific genes

Cell, 1990-06, Vol.61 (5), p.895-904

1990

Volltextzugriff (PDF)

Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections

Movement disorders, 2005-06, Vol.20 (6), p.764-767

2005

Volltextzugriff (PDF)

Impaired cardiac contraction and relaxation and decreased expression of sarcoplasmic Ca2+‐ATPase in mice lacking the CREM gene

The FASEB journal, 2003-01, Vol.17 (1), p.103-105

2003

Volltextzugriff (PDF)

The Cre/loxP system--a versatile tool to study glucocorticoid signalling in mice

Biochemical Society transactions, 1999-02, Vol.27 (2), p.78-83

1999

Volltextzugriff (PDF)

Analysis of glucocorticoid receptor function in the mouse by gene targeting

Ernst Schering Research Foundation workshop, 2002 (40), p.305

2002

Volltextzugriff (PDF)

1 – 15 von 15

Suche als RSS-Feed

Aktive Filter

ThemaMice

ThemaMutation

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(14)
Mit Volltextzugriff
(13)

Publikationsform

Artikel
(15)

Sprache

Englisch
(15)
Japanisch
(7)

Erscheinungsjahr

n.n

Menü

Weitere Dienste

Einstellungen

Resetting of Circadian Time in Peripheral Tissues by Glucocorticoid Signaling

Disruption of CREB function in brain leads to neurodegeneration

The Epithelial Glucocorticoid Receptor Is Required for the Normal Timing of Cell Proliferation during Mammary Lobuloalveolar Development but Is Dispensable for Milk Production

Pharmacological estrogen administration causes a FSH-independent osteo-anabolic effect requiring ER alpha in osteoblasts

Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency

Targeted Mutation of the CREB Gene: Compensation within the CREB/ATF Family of Transcription Factors

The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis― ichthyosis―deafness syndrome

Genetic Dissection of Corticosteroid Receptor Function in Mice

Analysis of mice carrying targeted mutations of the glucocorticoid receptor gene argues against an essential role of glucocorticoid signalling for generating adrenal chromaffin cells

Rescue of the albino phenotype by introduction of a functional tyrosinase gene into mice

Two genetically defined trans-acting loci coordinately regulate overlapping sets of liver-specific genes

Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections

Impaired cardiac contraction and relaxation and decreased expression of sarcoplasmic Ca2+‐ATPase in mice lacking the CREM gene

The Cre/loxP system--a versatile tool to study glucocorticoid signalling in mice

Analysis of glucocorticoid receptor function in the mouse by gene targeting

Aktive Filter

Suchergebnisse filtern