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...

Precise Editing of the Zebrafish Genome Made Simple and Efficient

Developmental cell, 2016-03, Vol.36 (6), p.654-667

2016

Volltextzugriff (PDF)

Quadruple zebrafish mutant reveals different roles of Mesp genes in somite segmentation between mouse and zebrafish

Development (Cambridge), 2016-08, Vol.143 (15), p.2842-2852

2016

Volltextzugriff (PDF)

Simple methods for generating and detecting locus-specific mutations induced with TALENs in the zebrafish genome

PLoS genetics, 2012-08, Vol.8 (8), p.e1002861

2012

Volltextzugriff (PDF)

Efficient identification of TALEN‐mediated genome modifications using heteroduplex mobility assays

Genes to cells : devoted to molecular & cellular mechanisms, 2013-06, Vol.18 (6), p.450-458

2013

Volltextzugriff (PDF)

Localization of ammonia transporter Rhcg1 in mitochondrion-rich cells of yolk sac, gill, and kidney of zebrafish and its ionic strength-dependent expression

American journal of physiology. Regulatory, integrative and comparative physiology, 2007-10, Vol.293 (4), p.R1743-R1753

2007

Volltextzugriff (PDF)

The Paf1 complex and P-TEFb have reciprocal and antagonist roles in maintaining multipotent neural crest progenitors

Development (Cambridge), 2019-12, Vol.146 (24)

2019

Volltextzugriff (PDF)

tbx6l and tbx16 are redundantly required for posterior paraxial mesoderm formation during zebrafish embryogenesis

Developmental dynamics, 2017-10, Vol.246 (10), p.759-769

2017

Volltextzugriff (PDF)

Expression of endocrine genes in zebrafish larvae in response to environmental salinity

Journal of endocrinology, 2007-06, Vol.193 (3), p.481-491

2007

Volltextzugriff (PDF)

Interactions among ryanodine receptor isotypes contribute to muscle fiber type development and function

Disease models & mechanisms, 2020-02, Vol.13 (2)

2020

Volltextzugriff (PDF)

Close Association of Carbonic Anhydrase (CA2a and CA15a), Na(+)/H(+) Exchanger (Nhe3b), and Ammonia Transporter Rhcg1 in Zebrafish Ionocytes Responsible for Na(+) Uptake

Frontiers in physiology, 2013-01, Vol.4, p.59-59

2013

Volltextzugriff (PDF)

Intramolecular Disulfide Bond Is a Critical Check Point Determining Degradative Fates of ATP-binding Cassette (ABC) Transporter ABCG2 Protein

The Journal of biological chemistry, 2007-09, Vol.282 (38), p.27841-27846

2007

Volltextzugriff (PDF)

Mechanism of development of ionocytes rich in vacuolar-type H +-ATPase in the skin of zebrafish larvae

Developmental biology, 2009-05, Vol.329 (1), p.116-129

2009

Volltextzugriff (PDF)

Ubiquitin-mediated proteasomal degradation of non-synonymous SNP variants of human ABC transporter ABCG2

Biochemical journal, 2008-05, Vol.411 (3), p.623-631

2008

Volltextzugriff (PDF)

In Vitro Evaluation of Photosensitivity Risk Related to Genetic Polymorphisms of Human ABC Transporter ABCG2 and Inhibition by Drugs

DRUG METABOLISM AND PHARMACOKINETICS, 2007-01, Vol.22 (6), p.428-440

2007

Volltextzugriff (PDF)

Functional Analysis of OA-Associated PIEZO1 Human Variants on OA Susceptibility

Osteoarthritis and cartilage, 2024-04, Vol.32, p.S374

2024

Volltextzugriff (PDF)

530 - Functional Analysis of OA-Associated PIEZO1 Human Variants on OA Susceptibility

Osteoarthritis and cartilage, 2024-04, Vol.32, p.S374-S374

2024

Volltextzugriff (PDF)

Zebrafish foxP2 zinc finger nuclease mutant has normal axon pathfinding

PloS one, 2012-08, Vol.7 (8), p.e43968-e43968

2012

Volltextzugriff (PDF)

Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish

Developmental cell, 2019-12, Vol.51 (5), p.645-657.e4

2019

Volltextzugriff (PDF)

Zebrafish early cardiac connexin, Cx36.7/Ecx, regulates myofibril orientation and heart morphogenesis by establishing Nkx2.5 expression

Proceedings of the National Academy of Sciences - PNAS, 2008-03, Vol.105 (12), p.4763-4768

2008

Volltextzugriff (PDF)

An Interacting Network of T-Box Genes Directs Gene Expression and Fate in the Zebrafish Mesoderm

Proceedings of the National Academy of Sciences - PNAS, 2003-08, Vol.100 (16), p.9410-9415

2003

Volltextzugriff (PDF)

Identification of zebrafish Fxyd11a protein that is highly expressed in ion-transporting epithelium of the gill and skin and its possible role in ion homeostasis

Frontiers in physiology, 2010-01, Vol.1, p.129-129

2010

Volltextzugriff (PDF)

Molecular and functional characterization of adrenomedullin receptors in pufferfish

American journal of physiology. Regulatory, integrative and comparative physiology, 2006-02, Vol.290 (2), p.R467-R478

2006

Volltextzugriff (PDF)

A protein disulfide isomerase expressed in the embryonic midline is required for left/right asymmetries

Genes & development, 2002-10, Vol.16 (19), p.2518-2529

2002

Volltextzugriff (PDF)

NOD/RIPK2 signalling pathway contributes to osteoarthritis susceptibility

Annals of the rheumatic diseases, 2022-10, Vol.81 (10), p.1465-1473

2022

Volltextzugriff (PDF)

Highly efficient methods for generating deletion mutations and F0 embryos that lack gene function in zebrafish

Developmental cell, 2019-11, Vol.51 (5), p.645-657.e4

2019

Volltextzugriff (PDF)

1 – 25 von 42

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(42)
Mit Volltextzugriff
(39)

Publikationsform

Artikel
(42)

Sprache

Englisch
(42)

Erscheinungsjahr

n.n

Thema

Science & Technology
(32)
Life Sciences & Biomedicine
(26)
Animals
(25)
Zebrafish - Genetics
(11)
Danio Rerio
(10)
Developmental Biology
(9)
Molecular Sequence Data
(9)
Zebrafish
(9)
Base Sequence
(8)
Gene Expression
(8)
Humans
(8)
Zebrafish - Embryology
(8)
Biological And Medical Sciences
(7)
Fundamental And Applied Biological Sciences. Psychology
(7)
Mutation
(7)
Zebrafish Proteins - Genetics
(7)
Cell Biology
(6)
Genetics
(6)
Molecular And Cellular Biology
(6)
Multidisciplinary Sciences
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Precise Editing of the Zebrafish Genome Made Simple and Efficient

Quadruple zebrafish mutant reveals different roles of Mesp genes in somite segmentation between mouse and zebrafish

Simple methods for generating and detecting locus-specific mutations induced with TALENs in the zebrafish genome

Efficient identification of TALEN‐mediated genome modifications using heteroduplex mobility assays

Localization of ammonia transporter Rhcg1 in mitochondrion-rich cells of yolk sac, gill, and kidney of zebrafish and its ionic strength-dependent expression

The Paf1 complex and P-TEFb have reciprocal and antagonist roles in maintaining multipotent neural crest progenitors

tbx6l and tbx16 are redundantly required for posterior paraxial mesoderm formation during zebrafish embryogenesis

Expression of endocrine genes in zebrafish larvae in response to environmental salinity

Interactions among ryanodine receptor isotypes contribute to muscle fiber type development and function

Close Association of Carbonic Anhydrase (CA2a and CA15a), Na(+)/H(+) Exchanger (Nhe3b), and Ammonia Transporter Rhcg1 in Zebrafish Ionocytes Responsible for Na(+) Uptake

Intramolecular Disulfide Bond Is a Critical Check Point Determining Degradative Fates of ATP-binding Cassette (ABC) Transporter ABCG2 Protein

Mechanism of development of ionocytes rich in vacuolar-type H +-ATPase in the skin of zebrafish larvae

Ubiquitin-mediated proteasomal degradation of non-synonymous SNP variants of human ABC transporter ABCG2

In Vitro Evaluation of Photosensitivity Risk Related to Genetic Polymorphisms of Human ABC Transporter ABCG2 and Inhibition by Drugs

Functional Analysis of OA-Associated PIEZO1 Human Variants on OA Susceptibility

530 - Functional Analysis of OA-Associated PIEZO1 Human Variants on OA Susceptibility

Zebrafish foxP2 zinc finger nuclease mutant has normal axon pathfinding

Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish

Zebrafish early cardiac connexin, Cx36.7/Ecx, regulates myofibril orientation and heart morphogenesis by establishing Nkx2.5 expression

An Interacting Network of T-Box Genes Directs Gene Expression and Fate in the Zebrafish Mesoderm

Identification of zebrafish Fxyd11a protein that is highly expressed in ion-transporting epithelium of the gill and skin and its possible role in ion homeostasis

Molecular and functional characterization of adrenomedullin receptors in pufferfish

A protein disulfide isomerase expressed in the embryonic midline is required for left/right asymmetries

NOD/RIPK2 signalling pathway contributes to osteoarthritis susceptibility

Highly efficient methods for generating deletion mutations and F0 embryos that lack gene function in zebrafish

Suchergebnisse filtern