About: Ronald Gregg

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Ronald Gregg Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

American biochemistry professor

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) গবেষক (bn) 研究者 (ja) ഗവേഷകൻ (ml) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) American biochemistry professor (en)
rdfs:label	Ronald Gregg (en) Ronald Gregg (es) Ronald Gregg (it) Ronald Gregg (nl) Ronald Gregg (sl) Ronald Gregg (ast)
skos:prefLabel	Ronald Gregg (en) Ronald Gregg (es) Ronald Gregg (it) Ronald Gregg (nl) Ronald Gregg (sl) Ronald Gregg (ast)
name	Ronald Gregg (en) Ronald Gregg (es) Ronald Gregg (it) Ronald Gregg (nl) Ronald Gregg (sl) Ronald Gregg (ast)
LinkedIn personal profile ID	wds:Q42650166-14962660-452c-4e62-8e48-0bb808fabad0
LinkedIn personal profile ID	ron-gregg-1a29023a
given name	wds:Q42650166-1D3FFF52-527D-4C50-8164-85746FA3ECBD
given name	Ronald
instance of	wds:Q42650166-E1E4F0B9-407B-41FB-AC48-A81554FB42AF
instance of	Homo sapiens
ResearchGate profile ID	wds:Q42650166-d9148ef2-4f6e-4ee9-7742-2d89c86fcd66
ResearchGate profile ID	Ronald_Gregg
skos:altLabel	Ronald G. Gregg (en)
occupation	wds:Q42650166-016891A1-68CC-41F9-B668-945F81203943 wds:Q42650166-5b9f0406-4a3a-33ea-a6d1-1951f7101a92
employer	wds:Q42650166-E326094E-4DD2-4BFE-AE41-AB53A7A50585
sex or gender	wds:Q42650166-2CCD998F-0284-47B8-B1C5-34ABDD67E57A
educated at	wds:Q42650166-3f14a064-457f-074a-f32a-49bf409cf38e
family name	wds:Q42650166-5614D286-7749-4545-818D-EFD2CCA2F561
occupation	researcher biochemist
employer	University of Louisville
sex or gender	male
educated at	University of Queensland
family name	Gregg
ORCID iD	wds:Q42650166-BD195030-D32E-422A-A515-51155544A957
Dimensions author ID	wds:Q42650166-0DB3D2CE-1241-470D-8435-444F3AA47821
ORCID iD	https://orcid.org/0000-0001-5805-224X
ORCID iD	0000-0001-5805-224X
Dimensions author ID	01003531571.49
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q42650166
is author of	Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation Targeted modification of human chromosomal genes A transient receptor potential-like channel mediates synaptic transmission in rod bipolar cells. Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32 Positional cloning of the young mutation identifies an essential role for the Brahma chromatin remodeling complex in mediating retinal cell differentiation Molecular characterization and expression patterns of a B-type nuclear lamin during sea urchin embryogenesis. Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome Inversion of the Williams syndrome region is a common polymorphism found more frequently in parents of children with Williams syndrome Failure to maintain eye-specific segregation in nob, a mutant with abnormally patterned retinal activity. Genetic heterogeneity in families with hereditary multiple exostoses Localization of a non-specific X-linked mental retardation gene, MRX23, to Xq23-q24. Muscle contractions guide rohon-beard peripheral sensory axons Anesthetic requirement is increased in redheads GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells. GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish. Morphological and Physiological Consequences of the Selective Elimination of Rod Photoreceptors in Transgenic Mice A calcium channel mutation causing hypokalemic periodic paralysis Modulation of L-type Ca2+ current but not activation of Ca2+ release by the gamma1 subunit of the dihydropyridine receptor of skeletal muscle Involvement of the carboxy-terminus region of the dihydropyridine receptor beta1a subunit in excitation-contraction coupling of skeletal muscle GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region. Elimination of the rho1 subunit abolishes GABA(C) receptor expression and alters visual processing in the mouse retina The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1) Mutations in TRPM1 are a common cause of complete congenital stationary night blindness Role of the beta(2) subunit of voltage-dependent calcium channels in the retinal outer plexiform layer The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses Nyctalopin expression in retinal bipolar cells restores visual function in a mouse model of complete X-linked congenital stationary night blindness A role for nyctalopin, a small leucine-rich repeat protein, in localizing the TRP melastatin 1 channel to retinal depolarizing bipolar cell dendrites Comparisons of structural and functional abnormalities in mouse b-wave mutants. Immunohistochemical analysis of the outer plexiform layer in the nob mouse shows no abnormalities The Ca2+ channel subunit beta2 regulates Ca2+ channel abundance and function in inner hair cells and is required for hearing Insertion of DNA sequences into the human chromosomal beta-globin locus by homologous recombination Targetted correction of a mutant HPRT gene in mouse embryonic stem cells Localization of the mouse nob (no b-wave) gene to the centromeric region of the X chromosome Analysis of the Zebrafish perplexed mutation reveals tissue-specific roles for de novo pyrimidine synthesis during development Using mutant mice to study the role of voltage-gated calcium channels in the retina. Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11. Genetic localization of an autosomal dominant leukodystrophy mimicking chronic progressive multiple sclerosis to chromosome 5q31

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 183 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2025 OpenLink Software