scholarly article | Q13442814 |
P50 | author | Pascal Haffter | Q84381030 |
P2093 | author name string | Dawid IB | |
Fricke C | |||
Toyama R | |||
Rebagliati MR | |||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Danio rerio | Q169444 |
P304 | page(s) | 261-272 | |
P577 | publication date | 1998-07-01 | |
P1433 | published in | Developmental Biology | Q3025402 |
P1476 | title | Zebrafish nodal-related genes are implicated in axial patterning and establishing left-right asymmetry | |
P478 | volume | 199 |
Q36442060 | 21st century neontology and the comparative development of the vertebrate skull |
Q46052521 | A Nodal-independent and tissue-intrinsic mechanism controls heart-looping chirality |
Q41697654 | A molecular pathway leading to endoderm formation in zebrafish |
Q39864308 | A protein disulfide isomerase expressed in the embryonic midline is required for left/right asymmetries |
Q41697625 | A role for the extraembryonic yolk syncytial layer in patterning the zebrafish embryo suggested by properties of the hex gene. |
Q34165989 | An amphioxus nodal gene (AmphiNodal) with early symmetrical expression in the organizer and mesoderm and later asymmetrical expression associated with left-right axis formation |
Q21128790 | An essential role for maternal control of Nodal signaling |
Q90568619 | Analysis of novel domain-specific mutations in the zebrafish ndr2/cyclops gene generated using CRISPR-Cas9 RNPs |
Q50478787 | Antagonistic interactions in the zebrafish midline prior to the emergence of asymmetric gene expression are important for left-right patterning. |
Q36936122 | Anteriorward shifting of asymmetric Xnr1 expression and contralateral communication in left-right specification in Xenopus |
Q36783121 | Anteroposterior and dorsoventral patterning are coordinated by an identical patterning clock |
Q36815556 | Araf kinase antagonizes Nodal-Smad2 activity in mesendoderm development by directly phosphorylating the Smad2 linker region |
Q34419767 | Association of valproate-induced teratogenesis with histone deacetylase inhibition in vivo |
Q24602687 | Asymmetric and node-specific nodal expression patterns are controlled by two distinct cis-acting regulatory elements |
Q91790367 | Brain and Behavioral Asymmetry: A Lesson From Fish |
Q81154543 | Cardiac development |
Q52117440 | Cell death along the embryo midline regulates left-right sidedness. |
Q52916524 | Characterization and genomic structure of Dnah9, and its roles in nodal signaling pathways in the Japanese flounder (Paralichthys olivaceus). |
Q28312164 | Characterization of an lhx1a transgenic reporter in zebrafish |
Q47919138 | Characterization of zebrafish smad1, smad2 and smad5: the amino-terminus of smad1 and smad5 is required for specific function in the embryo. |
Q47073475 | Cloning and characterization of zebrafish smad2, smad3 and smad4. |
Q26752209 | CncRNAs: RNAs with both coding and non-coding roles in development |
Q34865346 | Conservation defines functional motifs in the squint/nodal-related 1 RNA dorsal localization element. |
Q28512508 | Conserved requirement for EGF-CFC genes in vertebrate left-right axis formation |
Q27334688 | Conserved roles for cytoskeletal components in determining laterality |
Q47073117 | Cooperative roles of Bozozok/Dharma and Nodal-related proteins in the formation of the dorsal organizer in zebrafish. |
Q35197449 | Coregulation of anterior and posterior mesendodermal development by a hairy-related transcriptional repressor |
Q33901600 | Correct anteroposterior patterning of the zebrafish neurectoderm in the absence of the early dorsal organizer. |
Q34735355 | Deep mRNA sequencing analysis to capture the transcriptome landscape of zebrafish embryos and larvae |
Q47436511 | Development and connectivity of the habenular nuclei. |
Q52140982 | Development of the Neuroendocrine Hypothalamus. |
Q52127586 | Diffusion of nodal signaling activity in the absence of the feedback inhibitor Lefty2. |
Q36264710 | Distinct requirements for Wntless in habenular development |
Q33712592 | Diverse initiation in a conserved left-right pathway? |
Q39227258 | Early left-right asymmetries during axial morphogenesis in the chick embryo |
Q34518401 | Embryonic mesoderm and endoderm induction requires the actions of non-embryonic Nodal-related ligands and Mxtx2 |
Q30480122 | Environmental and genetic modifiers of squint penetrance during zebrafish embryogenesis. |
Q34114827 | Establishment of left-right asymmetry |
Q39038824 | Establishment of the Vertebrate Germ Layers. |
Q28218181 | Establishment of vertebrate left-right asymmetry |
Q34347339 | Evolution of vertebrate forebrain development: how many different mechanisms? |
Q28661032 | Evolutionary conservation of early mesoderm specification by mechanotransduction in Bilateria |
Q45917677 | Expression and regulation of miR-17a and miR-430b in zebrafish ovarian follicles. |
Q52163856 | Expression of three zebrafish Six4 genes in the cranial sensory placodes and the developing somites. |
Q35728277 | Expression profiling and comparative genomics identify a conserved regulatory region controlling midline expression in the zebrafish embryo |
Q28829653 | Extracellular interactions and ligand degradation shape the nodal morphogen gradient |
Q38562948 | FGF signaling is required for brain left-right asymmetry and brain midline formation |
Q37342278 | Forming and interpreting gradients in the early Xenopus embryo |
Q34629093 | Functional knowledge transfer for high-accuracy prediction of under-studied biological processes |
Q47876440 | Genes dependent on zebrafish cyclops function identified by AFLP differential gene expression screen |
Q47073617 | Heterogeneity across the dorso-ventral axis in zebrafish EVL is regulated by a novel module consisting of sox, snail1a and max genes |
Q36672098 | Human embryonic stem cells: an in vitro model to study mechanisms controlling pluripotency in early mammalian development |
Q37152621 | Identification of common and unique modifiers of zebrafish midline bifurcation and cyclopia |
Q48021528 | Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signalling |
Q45263246 | Interaction of Wnt and caudal-related genes in zebrafish posterior body formation |
Q42067932 | Is left-right asymmetry a form of planar cell polarity? |
Q26770629 | Keeping a lid on nodal: transcriptional and translational repression of nodal signalling |
Q24658310 | Lateralization of the vertebrate brain: taking the side of model systems |
Q36313478 | Left-right asymmetry and congenital cardiac defects: getting to the heart of the matter in vertebrate left-right axis determination |
Q34770342 | Left-right asymmetry in the nervous system: the Caenorhabditis elegans model |
Q44259972 | Lefty antagonism of Squint is essential for normal gastrulation |
Q52110869 | Lefty proteins are long-range inhibitors of squint-mediated nodal signaling. |
Q47566361 | Lefty-dependent inhibition of Nodal- and Wnt-responsive organizer gene expression is essential for normal gastrulation |
Q36682973 | Lethal giant larvae 2 regulates development of the ciliated organ Kupffer's vesicle |
Q47718684 | Local tissue interactions across the dorsal midline of the forebrain establish CNS laterality |
Q43890494 | Localization of transcripts of the zebrafish morphogen Squint is dependent on egg activation and the microtubule cytoskeleton |
Q48600458 | Maternal Eomesodermin regulates zygotic nodal gene expression for mesendoderm induction in zebrafish embryos |
Q47417320 | Maternal Gdf3 is an obligatory cofactor in Nodal signaling for embryonic axis formation in zebrafish. |
Q77152628 | Mechanisms of left-right asymmetry: what's right and what's left? |
Q33897938 | Mechanisms of left-right determination in vertebrates |
Q52182135 | Molecular mechanisms of vertebrate left-right development. |
Q50066731 | Molecular regulation of Nodal signaling during mesendoderm formation |
Q52174020 | Mouse Lefty2 and zebrafish antivin are feedback inhibitors of nodal signaling during vertebrate gastrulation. |
Q34271462 | Nodal Signaling in Vertebrate Development |
Q24644638 | Nodal morphogens |
Q38304615 | Nodal signaling activates differentiation genes during zebrafish gastrulation |
Q34446545 | Nodal signaling and the evolution of deuterostome gastrulation |
Q34101865 | Nodal signaling in early vertebrate embryos: themes and variations |
Q36063112 | Nodal signaling is required for mesodermal and ventral but not for dorsal fates in the indirect developing hemichordate, Ptychodera flava |
Q40994506 | Nodal signalling in Xenopus: the role of Xnr5 in left/right asymmetry and heart development. |
Q33833716 | Nodal signalling in vertebrate development. |
Q36097374 | Nodal signals mediate interactions between the extra-embryonic and embryonic tissues in zebrafish |
Q24291289 | Nodal signals to Smads through Cripto-dependent and Cripto-independent mechanisms |
Q52014275 | Nodal-related gene Xnr5 is amplified in the Xenopus genome. |
Q37348560 | Normal function of Myf5 during gastrulation is required for pharyngeal arch cartilage development in zebrafish embryos |
Q39895384 | Notch activity induces Nodal expression and mediates the establishment of left-right asymmetry in vertebrate embryos |
Q47744464 | Nuclear movement regulated by non-Smad Nodal signaling via JNK is associated with Smad signaling during zebrafish endoderm specification. |
Q43083653 | Odd skipped related 1 is a negative feedback regulator of nodal-induced endoderm development |
Q44590145 | One-eyed pinhead regulates cell motility independent of Squint/Cyclops signaling |
Q35213262 | Patterning of the zebrafish embryo by nodal signals |
Q40875538 | Phenotypic effects in Xenopus and zebrafish suggest that one-eyed pinhead functions as antagonist of BMP signalling |
Q47904024 | Pitx2 isoforms: involvement of Pitx2c but not Pitx2a or Pitx2b in vertebrate left-right asymmetry |
Q79149757 | Pitx2c attenuation results in cardiac defects and abnormalities of intestinal orientation in developing Xenopus laevis |
Q38764247 | Plasticity underlies tumor progression: role of Nodal signaling |
Q47073937 | Polaris and Polycystin-2 in dorsal forerunner cells and Kupffer's vesicle are required for specification of the zebrafish left-right axis |
Q47944974 | Promoter activity of the zebrafish bhikhari retroelement requires an intact activin signaling pathway |
Q33314901 | Rasl11b knock down in zebrafish suppresses one-eyed-pinhead mutant phenotype |
Q104558909 | Reassembling gastrulation |
Q34141423 | Regulation of neural determination by evolutionarily conserved signals: anti-BMP factors and what next? |
Q28312220 | Regulation of the Lim-1 gene is mediated through conserved FAST-1/FoxH1 sites in the first intron |
Q36526592 | Role of the iroquois3 homeobox gene in organizer formation |
Q28590722 | Rotatin is a novel gene required for axial rotation and left-right specification in mouse embryos |
Q90648594 | Scale-invariant patterning by size-dependent inhibition of Nodal signalling |
Q42275631 | Six3 represses nodal activity to establish early brain asymmetry in zebrafish |
Q46380548 | TAEL: a zebrafish-optimized optogenetic gene expression system with fine spatial and temporal control. |
Q34467808 | TGF-beta superfamily signaling and left-right asymmetry |
Q38733048 | TGF-β Family Signaling in Early Vertebrate Development |
Q42931463 | Tbx2b is required for the development of the parapineal organ |
Q34587480 | Teratogenesis of holoprosencephaly |
Q77310951 | The EGF-CFC protein one-eyed pinhead is essential for nodal signaling |
Q50658342 | The evolutionary origin of nodal-related genes in teleosts. |
Q47225172 | The formation and positioning of cilia in Ciona intestinalis embryos in relation to the generation and evolution of chordate left-right asymmetry |
Q27320128 | The integrator complex subunit 6 (Ints6) confines the dorsal organizer in vertebrate embryogenesis |
Q47073723 | The nodal pathway acts upstream of hedgehog signaling to specify ventral telencephalic identity |
Q24600802 | The orphan receptor ALK7 and the Activin receptor ALK4 mediate signaling by Nodal proteins during vertebrate development |
Q47073492 | The role of maternal Activin-like signals in zebrafish embryos |
Q46851653 | The zebrafish dorsal axis is apparent at the four-cell stage. |
Q24646790 | The zebrafish dyrk1b gene is important for endoderm formation |
Q34932142 | The zebrafish maternal-effect gene mission impossible encodes the DEAH-box helicase Dhx16 and is essential for the expression of downstream endodermal genes |
Q47073169 | The zebrafishnodal-related genesouthpawis required for visceral and diencephalic left-right asymmetry |
Q33280298 | Time-dependent patterning of the mesoderm and endoderm by Nodal signals in zebrafish |
Q52166646 | Transforming growth factor-beta5 expression during early development of Xenopus laevis. |
Q37462633 | Trb3 regulates LR axis formation in zebrafish embryos. |
Q36970265 | Xenopus kielin: A dorsalizing factor containing multiple chordin-type repeats secreted from the embryonic midline. |
Q37390067 | Xenopus, an ideal model system to study vertebrate left-right asymmetry |
Q102071890 | Zebrafish Cdx1b modulates epithalamic asymmetry by regulating ndr2 and lft1 expression |
Q35176811 | Zebrafish hearts and minds: nodal signaling in cardiac and neural left-right asymmetry |
Q47073698 | Zebrafish nma is involved in TGFbeta family signaling |
Q48021535 | Zebrafish organizer development and germ-layer formation require nodal-related signals |
Q43106466 | Zic-associated holoprosencephaly: zebrafish Zic1 controls midline formation and forebrain patterning by regulating Nodal, Hedgehog, and retinoic acid signaling |
Q31454949 | alpha(1)-Adrenergic stimulation perturbs the left-right asymmetric expression pattern of nodal during rat embryogenesis |
Q35079257 | casanova encodes a novel Sox-related protein necessary and sufficient for early endoderm formation in zebrafish |
Q38615610 | cncRNAs: Bi-functional RNAs with protein coding and non-coding functions |
Q36280774 | cyclops encodes a nodal-related factor involved in midline signaling |
Q37295278 | hnRNP I is required to generate the Ca2+ signal that causes egg activation in zebrafish |
Q46891841 | smad2 and smad3 are required for mesendoderm induction by transforming growth factor-beta/nodal signals in zebrafish |