about
Mutations in the human SIX3 gene in holoprosencephaly are loss of functionCumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephalyUnique alterations of an ultraconserved non-coding element in the 3'UTR of ZIC2 in holoprosencephalyEnvironmental and genetic modifiers of squint penetrance during zebrafish embryogenesis.A model of Costeff Syndrome reveals metabolic and protective functions of mitochondrial OPA3.Transcriptional profiling of endogenous germ layer precursor cells identifies dusp4 as an essential gene in zebrafish endoderm specification.Pre-gastrula expression of zebrafish extraembryonic genes.An early requirement for maternal FoxH1 during zebrafish gastrulation.Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephalyThe second European conference on zebrafish genetics and development.Lefty antagonism of Squint is essential for normal gastrulation.Murine FGF-12 and FGF-13: expression in embryonic nervous system, connective tissue and heart.Dynamics of zebrafish somitogenesis
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description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Benjamin Feldman
@ast
Benjamin Feldman
@en
Benjamin Feldman
@es
Benjamin Feldman
@nl
Benjamin Feldman
@sl
type
label
Benjamin Feldman
@ast
Benjamin Feldman
@en
Benjamin Feldman
@es
Benjamin Feldman
@nl
Benjamin Feldman
@sl
prefLabel
Benjamin Feldman
@ast
Benjamin Feldman
@en
Benjamin Feldman
@es
Benjamin Feldman
@nl
Benjamin Feldman
@sl
P106
P1153
34874659400
P21
P31
P496
0000-0003-4838-8641