about
The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.In vivo wall shear measurements within the developing zebrafish heartMorphogenesis and cell fate determination within the adaxial cell equivalence group of the zebrafish myotomeVariants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar DisorganizationUsing Touch-evoked Response and Locomotion Assays to Assess Muscle Performance and Function in ZebrafishThe zebrafish dystrophic mutant softy maintains muscle fibre viability despite basement membrane rupture and muscle detachmentZebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle functionAnalysis of protein sequence and interaction data for candidate disease gene prediction.FishNet: an online database of zebrafish anatomy.The structure and evolution of the melanocortin and MCH receptors in fish and mammals.Sequence characterization of teleost fish melanocortin receptors.Zebrafish prox1b mutants develop a lymphatic vasculature, and prox1b does not specifically mark lymphatic endothelial cells.The eIF4G-homolog p97 can activate translation independent of caspase cleavageGenome-wide identification of conserved intronic non-coding sequences using a Bayesian segmentation approach.Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy.The genetics of vertebrate myogenesis.The quail anatomy portal.Production of zebrafish cardiospheres and cardiac progenitor cells in vitro and three-dimensional culture of adult zebrafish cardiac tissue in scaffolds.The Zebrafish Anatomy Portal: a novel integrated resource to facilitate zebrafish research.Filamin C is a highly dynamic protein associated with fast repair of myofibrillar microdamage.Comparison of different numerical treatments for x-ray phase tomography of soft tissue from differential phase projections.FLNC myofibrillar myopathy results from impaired autophagy and protein insufficiency.Sample drift correction following 4D confocal time-lapse imagingLarge-scale analysis of gene structure in rhodopsin-like GPCRs: evidence for widespread loss of an ancient intron.Met and Hgf signaling controls hypaxial muscle and lateral line development in the zebrafish.Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo.Developmentally restricted actin-regulatory molecules control morphogenetic cell movements in the zebrafish gastrula.Characterization and investigation of zebrafish models of filamin-related myofibrillar myopathy.Whole-somite rotation generates muscle progenitor cell compartments in the developing zebrafish embryo.Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein.Immuno correlative light and electron microscopy on Tokuyasu cryosections.The Driving Mechanism for Unidirectional Blood Flow in the Tubular Embryonic Heart.The Role of ADHD Associated Genes in Neurodevelopment.Cardiac-phase filtering in intracardiac particle image velocimetry.Analysis of RNA Expression in Adult Zebrafish Skeletal Muscle.Myosin heavy chain expression in zebrafish and slow muscle composition.Cadherin-mediated differential cell adhesion controls slow muscle cell migration in the developing zebrafish myotome.Bone morphogenetic protein/retinoic acid inducible neural-specific protein (brinp) expression during Danio rerio development.Testing of therapies in a novel nebulin nemaline myopathy model demonstrate a lack of efficacy.Zebrafish models of BAG3 myofibrillar myopathy suggest a toxic gain of function leading to BAG3 insufficiency
P50
Q24681141-6BE666B4-D08A-4549-9CE8-33B0C5F961C5Q27305114-FC174659-542D-4031-8BCC-09BC49EC98B4Q27330465-48E14118-11FB-498E-86DE-098797F4C128Q28771758-A38109C0-0374-40A4-A653-74706956B6BAQ28817560-F54D48A1-5A77-4472-BA58-C9883CA11474Q30490034-074CBF49-DC6F-486D-BFF6-9D91C513F5A2Q30661724-2D999F58-5A70-4CBF-820D-3EF35E34CAE0Q31064465-48909EA5-C471-4F70-A9C4-ADAD47F1BBBBQ33294513-8EACBBE9-BF4C-414E-A8C0-0308CCEB5E1FQ33964758-CC2884F7-18F3-45EA-893B-1560808C5C34Q33967041-5EC02115-A835-4F62-98A2-46BF993A3D3AQ34117087-B0F36F77-78B9-4AFD-A665-064F665D5DAFQ35641230-A6D7A091-054E-4134-886D-A14DE9884008Q36324277-92B7891D-5554-4F85-99D1-76C3979EDCBBQ37010363-EB4508AB-206D-433C-B1B5-4E25F001F348Q37219522-7F2B3D4F-315C-4BD9-8220-BC9AD6E90AADQ37689554-E1A40E9C-1DDE-4883-A5B1-F24D29EFC5E1Q38704706-99CE0577-30EE-4FF2-A9D2-95CFC8B39449Q39552227-EC0496A7-D24B-4D2F-8383-28B423B625F8Q39748665-6F32BF31-73DD-4A25-B2C7-3D8D329FD034Q41172290-36918070-15E8-412B-938B-95D5F79A5A52Q41600270-7F1B677F-B173-4F59-84B0-80449936E5E3Q41845879-6F696349-F467-426E-A6E0-085103F1FD68Q44161459-6F11B0E0-876B-454D-B56D-7622458CA54EQ45040913-C6E11AE1-AC49-4947-A4DB-07B2C4242349Q47073103-301F15A2-E062-4056-B2B7-C535E8A29654Q47073595-6A045C77-FBE9-413F-9C25-9422EED993C9Q47073660-79D7C494-690B-47CB-AEF1-0AC58D1873D5Q48919496-FD91D4BE-9E78-4D85-85E7-CD10F7A2C8C4Q50114679-3B6774E4-31FE-4F65-A909-5816C8482D70Q50448382-12D1E8B3-88F8-4BF9-A3CC-9BF7EEBCC587Q51357548-25A5E798-F147-4AB8-9D54-D576AA7E5099Q51730963-1AB31521-44F2-4319-ACF1-4F8A99431178Q51793848-8F7A4529-B558-4979-AF58-261833ED8D6DQ51800682-BE8B19CD-197D-47DD-B13B-1AF37BF549BFQ52052475-28A9AEF5-2333-4FF8-8731-A2926261B77FQ52096461-7C603C80-15E9-4F90-A47C-6C70D869F9B7Q53504215-454E0A96-589B-476B-8835-5114B1FF1D5BQ55268192-CF8B2215-72E9-435B-ABCD-702C554A9649Q57651547-CD2A5513-0C6C-4879-A40C-3FFB23F7309D
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Robert J. Bryson-Richardson
@ast
Robert J. Bryson-Richardson
@en
Robert J. Bryson-Richardson
@es
Robert J. Bryson-Richardson
@nl
Robert J. Bryson-Richardson
@sl
type
label
Robert J. Bryson-Richardson
@ast
Robert J. Bryson-Richardson
@en
Robert J. Bryson-Richardson
@es
Robert J. Bryson-Richardson
@nl
Robert J. Bryson-Richardson
@sl
prefLabel
Robert J. Bryson-Richardson
@ast
Robert J. Bryson-Richardson
@en
Robert J. Bryson-Richardson
@es
Robert J. Bryson-Richardson
@nl
Robert J. Bryson-Richardson
@sl
P1053
B-7556-2008
P106
P1153
6507924982
P21
P31
P4012
P496
0000-0002-9501-8208