Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 gene (Q28586185)

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English	Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 gene	scientific journal article

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PubMed

PubMed publication ID

11425903

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31 January 2017

title

Progressive cerebellar, auditory, and esophageal dysfunction caused by targeted disruption of the frizzled-4 gene (English)

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PubMed

PubMed publication ID

11425903

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31 January 2017

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Europe PubMed Central

PMC publication ID

6762346

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main subject

cerebellum

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Frizzled class receptor 4

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GOA release 2020-03-11

author name string

Y Wang

series ordinal

1

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Europe PubMed Central

PMC publication ID

6762346

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D Huso

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2

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PMC publication ID

6762346

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H Cahill

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3

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PMC publication ID

6762346

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D Ryugo

series ordinal

4

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Europe PubMed Central

PMC publication ID

6762346

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J Nathans

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5

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PMC publication ID

6762346

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language of work or name

English

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publication date

1 July 2001

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PubMed

PubMed publication ID

11425903

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31 January 2017

published in

Journal of Neuroscience

2 references

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PubMed

PubMed publication ID

11425903

retrieved

31 January 2017

stated in

Europe PubMed Central

PMC publication ID

6762346

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6762346&resulttype=core&format=json

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12 May 2020

volume

21

2 references

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PubMed

PubMed publication ID

11425903

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31 January 2017

stated in

Europe PubMed Central

PMC publication ID

6762346

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6762346&resulttype=core&format=json

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12 May 2020

issue

13

2 references

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PubMed

PubMed publication ID

11425903

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31 January 2017

stated in

Europe PubMed Central

PMC publication ID

6762346

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6762346&resulttype=core&format=json

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12 May 2020

page(s)

4761-4771

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Europe PubMed Central

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6762346

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12 May 2020

cites work

Axonal remodeling and synaptic differentiation in the cerebellum is regulated by WNT-7a signaling

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Identification of programmed cell death in situ via specific labeling of nuclear DNA fragmentation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Cerebellar cell degeneration in the leaner mutant mouse

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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frizzled and frizzled 2 play a partially redundant role in wingless signaling and have similar requirements to wingless in neurogenesis.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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The cells and molecules that make a cerebellum.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential expression of the Wnt putative receptors Frizzled during mouse somitogenesis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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inferred from PubMed ID database lookup

Wingless transduction by the Frizzled and Frizzled2 proteins of Drosophila.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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TECHNICAL NOTE: A SILVER METHOD FOR PARAFFIN SECTIONS OF NEURAL TISSUE.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of staggerer gene in determining cell number in cerebellar cortex. II. Granule cell death and persistence of the external granule cell layer in young mouse chimeras.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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inferred from PubMed ID database lookup

Disruption of the nuclear hormone receptor RORalpha in staggerer mice

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pathway specificity by the bifunctional receptor frizzled is determined by affinity for wingless

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Purkinje cell degeneration, a new neurological mutation in the mouse

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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A "DIRECT-COLORING" THIOCHOLINE METHOD FOR CHOLINESTERASES

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Many tumors induced by the mouse mammary tumor virus contain a provirus integrated in the same region of the host genome

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Biochemical characterization of Wnt-frizzled interactions using a soluble, biologically active vertebrate Wnt protein

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Evidence for a mitogenic effect of Wnt-1 in the developing mammalian central nervous system

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Interaction of granule, Purkinje and inferior olivary neurons in lurcher chimeric mice. II. Granule cell death

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Innervation of the esophagus in mice that lack MASH1

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Wnt-1-dependent regulation of local E-cadherin and alpha N-catenin expression in the embryonic mouse brain

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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The hem of the embryonic cerebral cortex is defined by the expression of multiple Wnt genes and is compromised in Gli3-deficient mice

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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A large family of putative transmembrane receptors homologous to the product of the Drosophila tissue polarity gene frizzled

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Signaling by wingless in Drosophila

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WNT-7a induces axonal remodeling and increases synapsin I levels in cerebellar neurons

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A local Wnt-3a signal is required for development of the mammalian hippocampus

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

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The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Control of neuronal precursor proliferation in the cerebellum by Sonic Hedgehog

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Activation of beta-catenin-Tcf signaling in colon cancer by mutations in beta-catenin or APC

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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inferred from PubMed ID database lookup

Expression of Xfz3, a Xenopus frizzled family member, is restricted to the early nervous system

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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A common human skin tumour is caused by activating mutations in beta-catenin

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Spermatid-specific expression of protamine 1 in transgenic mice

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

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Targeted disruption of the murine int-1 proto-oncogene resulting in severe abnormalities in midbrain and cerebellar development

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of staggerer gene in determining cell number in cerebellar cortex. I. Granule cell death is an indirect consequence of staggerer gene action

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Essential role of POU–domain factor Brn-3c in auditory and vestibular hair cell development

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A member of the Frizzled protein family mediating axis induction by Wnt-5A

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

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Evidence for developmentally programmed transdifferentiation in mouse esophageal muscle.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mammalian wnt gene, WNT8B, shows brain-restricted expression in early development, with sharply delimited expression boundaries in the developing forebrain

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse Wnt genes exhibit discrete domains of expression in the early embryonic CNS and limb buds.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Use of dsRNA-mediated genetic interference to demonstrate that frizzled and frizzled 2 act in the wingless pathway.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

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Wnt signaling: a common theme in animal development

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Destabilization of beta-catenin by mutations in presenilin-1 potentiates neuronal apoptosis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

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Insights from mouse models into the molecular basis of neurodegeneration

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two novel Xenopus frizzled genes expressed in developing heart and brain

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wnt-3, a gene activated by proviral insertion in mouse mammary tumors, is homologous to int-1/Wnt-1 and is normally expressed in mouse embryos and adult brain

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sonic hedgehog regulates the growth and patterning of the cerebellum

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hippocampus development and generation of dentate gyrus granule cells is regulated by LEF1

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomics and hearing impairment

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neurodegeneration in Lurcher mice caused by mutation in δ2 glutamate receptor gene

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genes involved in deafness

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frizzled and Dfrizzled-2 function as redundant receptors for Wingless during Drosophila embryonic development.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regional expression of the Wnt-3 gene in the developing mouse forebrain in relationship to diencephalic neuromeres

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wnt-1 signaling inhibits apoptosis by activating beta-catenin/T cell factor-mediated transcription

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Local control of granule cell generation by cerebellar Purkinje cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Wnt signalling required for expansion of neural crest and CNS progenitors.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural and quantitative studies on the normal C3H and Lurcher mutant mouse

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11425903

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12 December 2020

based on heuristic

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Identifiers

DOI

10.1523/JNEUROSCI.21-13-04761.2001

1 reference

stated in

Europe PubMed Central

PMC publication ID

6762346

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6762346&resulttype=core&format=json

retrieved

12 May 2020

OpenCitations bibliographic resource ID

1714552

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1714552

PMC publication ID

6762346

1 reference

stated in

Europe PubMed Central

PMC publication ID

6762346

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6762346&resulttype=core&format=json

retrieved

12 May 2020

PubMed publication ID

11425903

2 references

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1714552

stated in

Europe PubMed Central

PMC publication ID

6762346

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6762346&resulttype=core&format=json

retrieved

12 May 2020

 

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