Lista de obras - Busch-Nentwich EM - Dominio Público Uruguay

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

artículo científico publicado en 2017

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

artículo científico publicado en 2020

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

artículo científico publicado en 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

artículo científico publicado en 2019

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

artículo científico publicado en 2019

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

artículo científico publicado en 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

artículo científico publicado en 2016

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

artículo científico publicado en 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).

artículo científico publicado en 2017

Large-scale mapping of mutations affecting zebrafish development.

artículo científico publicado en 2007

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

artículo científico

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2004

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

artículo científico publicado en 2009

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

artículo científico publicado en 2008

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

artículo científico publicado en 2015

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

artículo científico publicado en 2004

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

artículo científico publicado en 2017

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

artículo científico publicado en 2019

Lista de obras de Busch-Nentwich EM

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