(Q51923232)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16354937%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

title

A genetic screen for mutations that affect cranial nerve development in the mouse (English)

1 reference

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10 January 2020

author name string

Lynn Mar

1

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10 January 2020

Elena Rivkin

2

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10 January 2020

Dennis Y Kim

3

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10 January 2020

Joanna Y Yu

4

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10 January 2020

Sabine P Cordes

5

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10 January 2020

language of work or name

English

0 references

publication date

1 December 2005

1 reference

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10 January 2020

published in

Journal of Neuroscience

1 reference

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10 January 2020

volume

25

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10 January 2020

issue

50

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10 January 2020

page(s)

11787-11795

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16354937%20AND%20SRC:MED&resulttype=core&format=json

Surface densities of ephrin-B1 determine EphB1-coupled activation of cell attachment through alphavbeta3 and alpha5beta1 integrins

10 January 2020

cites work

1 reference

12 December 2020

Symmetrical mutant phenotypes of the receptor EphB4 and its specific transmembrane ligand ephrin-B2 in cardiovascular development

1 reference

12 December 2020

A requirement for neuropilin-1 in embryonic vessel formation.

1 reference

12 December 2020

oto is a homeotic locus with a role in anteroposterior development that is partially redundant with Lim1

1 reference

12 December 2020

The receptor tyrosine kinase EphB4 and ephrin-B ligands restrict angiogenic growth of embryonic veins in Xenopus laevis.

1 reference

12 December 2020

Slit proteins: key regulators of axon guidance, axonal branching, and cell migration

1 reference

12 December 2020

Finding the genes that direct mammalian development : ENU mutagenesis in the mouse.

1 reference

12 December 2020

Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells

1 reference

12 December 2020

Identification of a novel mutation in the paired domain of PAX3 in an Iranian family with waardenburg syndrome type I

1 reference

12 December 2020

A homeodomain protein code specifies progenitor cell identity and neuronal fate in the ventral neural tube

1 reference

12 December 2020

The development and subsequent elimination of aberrant peripheral axon projections in Semaphorin3A null mutant mice

1 reference

12 December 2020

Clinical and molecular characterisation of 80 patients with 5p deletion: genotype-phenotype correlation

1 reference

12 December 2020

Defining brain wiring patterns and mechanisms through gene trapping in mice.

1 reference

12 December 2020

A highly efficient Escherichia coli-based chromosome engineering system adapted for recombinogenic targeting and subcloning of BAC DNA

1 reference

12 December 2020

Genetics of craniofacial development and malformation

1 reference

12 December 2020

Functional analysis of secreted and transmembrane proteins critical to mouse development.

1 reference

12 December 2020

Rab23 is an essential negative regulator of the mouse Sonic hedgehog signalling pathway

1 reference

12 December 2020

DelBank: a mouse ES-cell resource for generating deletions

1 reference

12 December 2020

Molecular genetics of cranial nerve development in mouse

1 reference

12 December 2020

Engineering chromosomal rearrangements in mice

1 reference

12 December 2020

Assigning the positional identity of spinal motor neurons: rostrocaudal patterning of Hox-c expression by FGFs, Gdf11, and retinoids.

1 reference

12 December 2020

Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis

1 reference

12 December 2020

A gene-driven approach to the identification of ENU mutants in the mouse

1 reference

12 December 2020

Abnormal development of the hippocampal dentate gyrus in mice lacking the CXCR4 chemokine receptor

1 reference

12 December 2020

The chemokine SDF1 regulates migration of dentate granule cells

1 reference

12 December 2020

Engineering the mouse genome with bacterial artificial chromosomes to create multipurpose alleles.

1 reference

12 December 2020

The morphogen sonic hedgehog is an axonal chemoattractant that collaborates with netrin-1 in midline axon guidance

1 reference

12 December 2020

High-throughput engineering of the mouse genome coupled with high-resolution expression analysis

1 reference

12 December 2020

CXCR4 regulates interneuron migration in the developing neocortex.

1 reference

12 December 2020

Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome

1 reference

12 December 2020

Functional genetic analysis of mouse chromosome 11

1 reference

12 December 2020

Essential role of glycosaminoglycans in Fgf signaling during mouse gastrulation.

1 reference

12 December 2020

A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development

1 reference

12 December 2020

The axonal attractant Netrin-1 is an angiogenic factor.

1 reference

12 December 2020

Semaphorin 3E and plexin-D1 control vascular pattern independently of neuropilins

1 reference

12 December 2020

Role of SDF1 chemokine in the development of lateral line efferent and facial motor neurons

1 reference

12 December 2020

Communicating with Hedgehogs

1 reference

12 December 2020

The chemokine stromal cell-derived factor-1 regulates the migration of sensory neuron progenitors

1 reference

12 December 2020

1 reference

12 December 2020

Assembly of trigeminal sensory ganglia by chemokine signaling.

1 reference

12 December 2020

A Cxcl12-CXCR4 chemokine signaling pathway defines the initial trajectory of mammalian motor axons

1 reference

12 December 2020

N-ethyl-N-nitrosourea mutagenesis: boarding the mouse mutant express

1 reference

12 December 2020

Segmental patterns of neuronal development in the chick hindbrain

1 reference

12 December 2020

Spatial regulation of axonal glycoprotein expression on subsets of embryonic spinal neurons

1 reference

12 December 2020

Topographic organization of embryonic motor neurons defined by expression of LIM homeobox genes

1 reference

12 December 2020

Molecular definition of deletions of different segments of distal 5p that result in distinct phenotypic features.

1 reference

12 December 2020

Homozygosity for Waardenburg syndrome

1 reference

12 December 2020

Floor plate and motor neuron induction by vhh-1, a vertebrate homolog of hedgehog expressed by the notochord

1 reference

12 December 2020

Forward and reverse genetic approaches to behavior in the mouse

1 reference

12 December 2020

Two rhombomeres are altered in Hoxa-1 mutant mice

1 reference

12 December 2020

Overexpression of a membrane protein, neuropilin, in chimeric mice causes anomalies in the cardiovascular system, nervous system and limbs.

1 reference

12 December 2020

Sonic hedgehog: a common signal for ventral patterning along the rostrocaudal axis of the neural tube.

1 reference

12 December 2020

Transcription factors in disease

1 reference

12 December 2020

Sonic hedgehog regulates patterning in early embryos

1 reference

12 December 2020

Chromosomal deletion complexes in mice by radiation of embryonic stem cells

1 reference

12 December 2020

Presenilin 1 is required for Notch1 and DII1 expression in the paraxial mesoderm

1 reference

12 December 2020

A high-resolution physical and transcript map of the Cri du chat region of human chromosome 5p.

1 reference

12 December 2020

Reciprocal effect of Waardenburg syndrome mutations on DNA binding by the Pax-3 paired domain and homeodomain

1 reference

12 December 2020

Receptive and expressive language skills in children with cri-du-chat syndrome

1 reference

12 December 2020

Using targeted large deletions and high-efficiency N-ethyl-N-nitrosourea mutagenesis for functional analyses of the mammalian genome

1 reference

12 December 2020

Molecular distinction and angiogenic interaction between embryonic arteries and veins revealed by ephrin-B2 and its receptor Eph-B4

1 reference

12 December 2020

A phenotype-based screen for embryonic lethal mutations in the mouse

1 reference

12 December 2020

Reduced apoptosis and cytochrome c-mediated caspase activation in mice lacking caspase 9

1 reference

12 December 2020

Differential requirement for caspase 9 in apoptotic pathways in vivo.

1 reference

12 December 2020

Apaf1 (CED-4 homolog) regulates programmed cell death in mammalian development

1 reference

12 December 2020

1 reference

12 December 2020

Ephrin-A1 is expressed at sites of vascular development in the mouse

1 reference

12 December 2020

Pax3 and Pax7 are expressed in commissural neurons and restrict ventral neuronal identity in the spinal cord

1 reference

12 December 2020

Roles of ephrinB ligands and EphB receptors in cardiovascular development: demarcation of arterial/venous domains, vascular morphogenesis, and sprouting angiogenesis

1 reference

12 December 2020

10.1523/JNEUROSCI.3813-05.2005

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16354937%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16354937%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

PubMed publication ID

16354937

1 reference