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...

ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response

Nature communications, 2019-07, Vol.10 (1), p.3195-12, Article 3195

2019

Volltextzugriff (PDF)

BBS4 is necessary for ciliary localization of TrkB receptor and activation by BDNF

PloS one, 2014-05, Vol.9 (5), p.e98687-e98687

2014

Volltextzugriff (PDF)

RFX transcription factors are essential for hearing in mice

Nature communications, 2015-10, Vol.6 (1), p.8549-8549, Article 8549

2015

Volltextzugriff (PDF)

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Nature genetics, 2005-03, Vol.37 (3), p.275-281

2005

Volltextzugriff (PDF)

Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response

Nature genetics, 2007-11, Vol.39 (11), p.1350-1360

2007

Volltextzugriff (PDF)

Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators

The Journal of clinical investigation, 2014-05, Vol.124 (5), p.2059-2070

2014

Volltextzugriff (PDF)

Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome

Proceedings of the National Academy of Sciences - PNAS, 2010-06, Vol.107 (23), p.10602-10607

2010

Volltextzugriff (PDF)

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

Nature, 2003-10, Vol.425 (6958), p.628-633

2003

Volltextzugriff (PDF)

Dissection of epistasis in oligogenic Bardet-Biedl syndrome

Nature, 2006-01, Vol.439 (7074), p.326-330

2006

Volltextzugriff (PDF)

Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse

Nature genetics, 2004-09, Vol.36 (9), p.994-998

2004

Volltextzugriff (PDF)

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Nature communications, 2016-04, Vol.7 (1), p.10953-10953, Article 10953

2016

Volltextzugriff (PDF)

Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio rerio

G3 : genes - genomes - genetics, 2018-07, Vol.8 (7), p.2215-2223

2018

Volltextzugriff (PDF)

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

Nature genetics, 2004-05, Vol.36 (5), p.462-470

2004

Volltextzugriff (PDF)

Identification of a Novel BBS Gene ( BBS12) Highlights the Major Role of a Vertebrate-Specific Branch of Chaperonin-Related Proteins in Bardet-Biedl Syndrome

American journal of human genetics, 2007-01, Vol.80 (1), p.1-11

2007

Volltextzugriff (PDF)

Exocrine pancreas proteases regulate β-cell proliferation in zebrafish ciliopathy models and in murine systems

Biology open, 2021-06, Vol.10 (6)

2021

Volltextzugriff (PDF)

MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis

Journal of cell science, 2005-03, Vol.118 (5), p.1007-1020

2005

Volltextzugriff (PDF)

An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes

PLoS genetics, 2008-03, Vol.4 (3), p.e1000044-e1000044

2008

Volltextzugriff (PDF)

Basal body proteins regulate Notch signaling through endosomal trafficking

Journal of cell science, 2014-06, Vol.127 (Pt 11), p.2407-2419

2014

Volltextzugriff (PDF)

Genetic deletion of trkB.T1 increases neuromuscular function

American Journal of Physiology: Cell Physiology, 2012-01, Vol.302 (1), p.C141-C153

2012

Volltextzugriff (PDF)

Differential effects on β-cell mass by disruption of Bardet-Biedl syndrome or Alstrom syndrome genes

Human molecular genetics, 2016-01, Vol.25 (1), p.57-68

2016

Volltextzugriff (PDF)

Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome

Nature genetics, 2008-04, Vol.40 (4), p.443-448

2008

Volltextzugriff (PDF)

TM6SF2 rs58542926 impacts lipid processing in liver and small intestine

Hepatology (Baltimore, Md.), 2017-05, Vol.65 (5), p.1526-1542

2017

Volltextzugriff (PDF)

In Vivo Evidence that Truncated Trkb.T1 Participates in Nociception

Molecular pain, 2009-10, Vol.5 (1), p.61-61

2009

Volltextzugriff (PDF)

Genomic knockout of alms1 in zebrafish recapitulates Alström syndrome and provides insight into metabolic phenotypes

Human molecular genetics, 2019-07, Vol.28 (13), p.2212-2223

2019

Volltextzugriff (PDF)

Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene

Cell, 2004-05, Vol.117 (4), p.541-552

2004

Volltextzugriff (PDF)

1 – 25 von 44

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(44)
Mit Volltextzugriff
(44)

Publikationsform

Artikel
(44)

Sprache

Englisch
(44)

Erscheinungsjahr

n.n

Thema

Science & Technology
(32)
Animals
(27)
Life Sciences & Biomedicine
(25)
Humans
(23)
Male
(16)
Mutation
(16)
Genetics & Heredity
(14)
Proteins
(14)
Biological And Medical Sciences
(13)
Mice
(13)
Bardet-Biedl Syndrome - Genetics
(12)
Female
(12)
Bardet-Biedl Syndrome
(11)
Danio Rerio
(11)
Medical Sciences
(11)
Proteins - Genetics
(11)
Zebrafish
(11)
Fundamental And Applied Biological Sciences. Psychology
(10)
Genetics
(9)
Medical Genetics
(9)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response

BBS4 is necessary for ciliary localization of TrkB receptor and activation by BDNF

RFX transcription factors are essential for hearing in mice

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Disruption of the basal body compromises proteasomal function and perturbs intracellular Wnt response

Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators

Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndrome

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

Dissection of epistasis in oligogenic Bardet-Biedl syndrome

Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio rerio

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

Identification of a Novel BBS Gene ( BBS12) Highlights the Major Role of a Vertebrate-Specific Branch of Chaperonin-Related Proteins in Bardet-Biedl Syndrome

Exocrine pancreas proteases regulate β-cell proliferation in zebrafish ciliopathy models and in murine systems

MKKS/BBS6, a divergent chaperonin-like protein linked to the obesity disorder Bardet-Biedl syndrome, is a novel centrosomal component required for cytokinesis

An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes

Basal body proteins regulate Notch signaling through endosomal trafficking

Genetic deletion of trkB.T1 increases neuromuscular function

Differential effects on β-cell mass by disruption of Bardet-Biedl syndrome or Alstrom syndrome genes

Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome

TM6SF2 rs58542926 impacts lipid processing in liver and small intestine

In Vivo Evidence that Truncated Trkb.T1 Participates in Nociception

Genomic knockout of alms1 in zebrafish recapitulates Alström syndrome and provides insight into metabolic phenotypes

Comparative Genomics Identifies a Flagellar and Basal Body Proteome that Includes the BBS5 Human Disease Gene

Suchergebnisse filtern