Wolfgang Hofmeister

发表

Loss of ctnnd2b affects neuronal differentiation and behavior in zebrafish

A. Lindstrand, W. Hofmeister, Steven Edwards, 2023, Frontiers in Neuroscience.

Loss of zebrafish ctnnd2b results in disorganised forebrain neuron clusters

A. Lindstrand, W. Hofmeister, R. Vaz, 2018, bioRxiv.

Zebrafish Models of Neurodevelopmental Disorders: Limitations and Benefits of Current Tools and Techniques

A. Lindstrand, W. Hofmeister, R. Vaz, 2019, International journal of molecular sciences.

Whole‐Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation

Daniel Nilsson, Anna Lindstrand, Francesco Vezzi, 2017, Human mutation.

Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene

D. Nilsson, A. Lindstrand, G. Barker, 2019, Molecular genetics & genomic medicine.

WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.

D. Nilsson, A. Lindstrand, G. Barker, 2015, Human molecular genetics.

WNT 3 involvement in human bladder exstrophy and cloaca development in zebra fi sh

D. Nilsson, A. Lindstrand, G. Barker, 2015 .

Apex Resection in Zebrafish (Danio rerio) as a Model of Heart Regeneration: A Video-Assisted Guide

E. Ober, D. C. Andersen, D. Ellman, 2021, International journal of molecular sciences.

A Systematic Exposition of Methods used for Quantification of Heart Regeneration after Apex Resection in Zebrafish

D. C. Andersen, W. Hofmeister, Helene Juul Belling, 2020, Cells.

CTNND2—a candidate gene for reading problems and mild intellectual disability

J. Kere, T. Klingberg, F. Vezzi, 2014, Journal of Medical Genetics.

Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish

J. Eisfeldt, A. Lindstrand, N. Papadogiannakis, 2018, Human mutation.

Frizzled-3a and slit2 genetically interact to modulate midline axon crossing in the telencephalon

J. Rothnagel, B. Key, W. Hofmeister, 2012, Mechanisms of Development.

Different mutations in PDE4D associated with developmental disorders with mirror phenotypes

O. Mäkitie, A. Nordgren, D. Nilsson, 2013, Journal of Medical Genetics.

Chemoattractant axon guidance cues regulate de novo axon trajectories in the embryonic forebrain of zebrafish.

B. Key, W. Hofmeister, Arnaud Gaudin, 2012, Developmental biology.

Identification of three novel FGF16 mutations in X-linked recessive fusion of the fourth and fifth metacarpals and possible correlation with heart disease

O. Mäkitie, A. Nordgren, N. Ahituv, 2014, Molecular genetics & genomic medicine.