List of works - Elisabeth M. Busch-Nentwich

A high-resolution mRNA expression time course of embryonic development in zebrafish

scientific article published on 16 November 2017

A point mutation decouples the lipid transfer activities of microsomal triglyceride transfer protein

scientific article published on 06 August 2020

A systematic genome-wide analysis of zebrafish protein-coding gene function

scientific article published on 17 April 2013

Author Correction: Chemokine receptor trafficking coordinates neutrophil clustering and dispersal at wounds in zebrafish

scientific article published on 21 January 2020

Chemokine receptor trafficking coordinates neutrophil clustering and dispersal at wounds in zebrafish

scientific article published on 14 November 2019

Common and distinct transcriptional signatures of mammalian embryonic lethality

scientific article published on 26 June 2019

Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specification

scientific article published on 19 February 2019

Control of crystal size and lattice formation by starmaker in otolith biomineralization.

scientific article published in October 2003

Deep phenotyping in zebrafish reveals genetic and diet-induced adiposity changes that may inform disease risk

scientific article published on 23 May 2018

Efficient identification of CRISPR/Cas9-induced insertions/deletions by direct germline screening in zebrafish

scientific article

High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping

scientific article published on 5 August 2015

Identification of slit3 as a locus affecting nicotine preference in zebrafish and human smoking behaviour

scientific article published on 25 March 2020

Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt).

scientific article

Large-scale mapping of mutations affecting zebrafish development.

scientific article published on 9 January 2007

Loss of the chromatin modifier Kdm2aa causes BrafV600E-independent spontaneous melanoma in zebrafish.

scientific article published on 14 August 2017

Multi-allelic phenotyping--a systematic approach for the simultaneous analysis of multiple induced mutations

scientific article published on 23 April 2013

Report of a Meeting on Contemporary Topics in Zebrafish Husbandry and Care

scientific article published on 18 August 2016

The age of heterozygous telomerase mutant parents influences the adult phenotype of their offspring irrespective of genotype in zebrafish.

scientific article

The deafness gene dfna5 is crucial for ugdh expression and HA production in the developing ear in zebrafish.

scientific article

The gene regulatory basis of genetic compensation during neural crest induction

scientific article published on 14 June 2019

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment

scientific article

Vesicular glutamate transporter 3 is required for synaptic transmission in zebrafish hair cells.

scientific article

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

scientific article

gemini encodes a zebrafish L-type calcium channel that localizes at sensory hair cell ribbon synapses.

scientific article published in April 2004

mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay

scientific article published on 21 November 2017

scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling

scientific article published on 25 January 2019

List of works by Elisabeth M. Busch-Nentwich

A high-resolution mRNA expression time course of embryonic development in zebrafish

A point mutation decouples the lipid transfer activities of microsomal triglyceride transfer protein

A systematic genome-wide analysis of zebrafish protein-coding gene function

Author Correction: Chemokine receptor trafficking coordinates neutrophil clustering and dispersal at wounds in zebrafish

Chemokine receptor trafficking coordinates neutrophil clustering and dispersal at wounds in zebrafish

Common and distinct transcriptional signatures of mammalian embryonic lethality

Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specification

Control of crystal size and lattice formation by starmaker in otolith biomineralization.

Deep phenotyping in zebrafish reveals genetic and diet-induced adiposity changes that may inform disease risk

Efficient identification of CRISPR/Cas9-induced insertions/deletions by direct germline screening in zebrafish

High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenotyping

Identification of slit3 as a locus affecting nicotine preference in zebrafish and human smoking behaviour

Integration of Tmc1/2 into the mechanotransduction complex in zebrafish hair cells is regulated by Transmembrane O-methyltransferase (Tomt).

Large-scale mapping of mutations affecting zebrafish development.

Loss of the chromatin modifier Kdm2aa causes BrafV600E-independent spontaneous melanoma in zebrafish.

Multi-allelic phenotyping--a systematic approach for the simultaneous analysis of multiple induced mutations

Report of a Meeting on Contemporary Topics in Zebrafish Husbandry and Care

The age of heterozygous telomerase mutant parents influences the adult phenotype of their offspring irrespective of genotype in zebrafish.

The deafness gene dfna5 is crucial for ugdh expression and HA production in the developing ear in zebrafish.

The gene regulatory basis of genetic compensation during neural crest induction

The zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachment

Vesicular glutamate transporter 3 is required for synaptic transmission in zebrafish hair cells.

Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function

gemini encodes a zebrafish L-type calcium channel that localizes at sensory hair cell ribbon synapses.

mRNA processing in mutant zebrafish lines generated by chemical and CRISPR-mediated mutagenesis produces unexpected transcripts that escape nonsense-mediated decay

scRNA-Seq reveals distinct stem cell populations that drive hair cell regeneration after loss of Fgf and Notch signaling