About: Jochen Graw

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researcher

Attributes	Values
rdf:type	Item
description	ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Jochen Graw (en) Jochen Graw (es) Jochen Graw (nl) Jochen Graw (sl) Jochen Graw (ast)
skos:prefLabel	Jochen Graw (en) Jochen Graw (es) Jochen Graw (nl) Jochen Graw (sl) Jochen Graw (ast)
name	Jochen Graw (en) Jochen Graw (es) Jochen Graw (nl) Jochen Graw (sl) Jochen Graw (ast)
Scopus author ID	wds:Q53815836-57289FBC-61AF-45DC-9C35-A59C48476767
Scopus author ID	7006618540
given name	wds:Q53815836-201BF529-6DFE-4CFA-960B-E6A5AC775126
given name	Jochen
instance of	wds:Q53815836-7AE40D36-746D-41CC-A247-3191E59CF2FE
instance of	Homo sapiens
occupation	wds:Q53815836-08D8EBDB-3FB1-4A29-8562-2C4623F6023A
sex or gender	wds:Q53815836-AA806079-4582-488B-9535-0A1641E9CD4C
VIAF ID	wds:Q53815836-1978D3EE-1AC9-458F-8661-3B348619A817
GND ID	wds:Q53815836-04d27dd8-784e-456b-ae35-e750b0f2e43b
WorldCat Identities ID (superseded)	wds:Q53815836-23112BD5-23C7-444B-9CF5-F804E0C905B9
VIAF ID	http://viaf.org/viaf/20789686
GND ID	https://d-nb.info/gnd/130388637
occupation	researcher
sex or gender	male
VIAF ID	20789686
GND ID	130388637
WorldCat Identities ID (superseded)	viaf-20789686
ORCID iD	wds:Q53815836-3CCA383A-4871-495F-AA06-C001AC35DC52
ORCID iD	https://orcid.org/0000-0003-0298-9660
ORCID iD	0000-0003-0298-9660
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q53815836
is author of	Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2G257D mutant mouse. "Sighted C3H" mice--a tool for analysing the influence of vision on mouse behaviour? Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype Molecular dissection of Pax6 function: the specific roles of the paired domain and homeodomain in brain development Rapamycin extends murine lifespan but has limited effects on aging Regulation of the human SIX3 gene promoter. Altered aggregation properties of mutant gamma-crystallins cause inherited cataract Cancer-retina antigens as potential paraneoplastic antigens in melanoma-associated retinopathy V76D mutation in a conserved gD-crystallin region leads to dominant cataracts in mice Innovations in phenotyping of mouse models in the German Mouse Clinic Microphthalmia, parkinsonism, and enhanced nociception in Pitx3 ( 416insG ) mice CRYBA4, a novel human cataract gene, is also involved in microphthalmia A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice Mouse phenotyping Systemic first-line phenotyping Introducing the German Mouse Clinic: open access platform for standardized phenotyping. The KORA Eye Study: a population-based study on eye diseases in Southern Germany (KORA F4). Clinical and experimental advances in congenital and paediatric cataracts. Mouse mutants as models for congenital retinal disorders Functional compensation among HMGN variants modulates the DNase I hypersensitive sites at enhancers Germ-line mutations in p27Kip1 cause a multiple endocrine neoplasia syndrome in rats and humans Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genes. Reduced levels of gamma-crystallin transcripts during embryonic development of murine Cat2nop mutant lenses Genomic sequences of murine gamma B- and gamma C-crystallin-encoding genes: promoter analysis and complete evolutionary pattern of mouse, rat and human gamma-crystallins. Induction of gene mutations in mice: the multiple endpoint approach. Histological and biochemical characterization of the murine cataract mutant Nop Characterization of Scat (suture cataract), a dominant cataract mutation in mice Genetical and biochemical studies of a dominant cataract mutant in mice Close linkage of the dominant cataract mutations (Cat-2) with Idh-1 and cryge on mouse chromosome 1 Effects of UV-B radiation on a hereditary suture cataract in mice Cat3vl and Cat3vao cataract mutations on mouse chromosome 10: phenotypic characterization, linkage studies and analysis of candidate genes Radiation cataractogenesis: a review of recent studies. Nuclear breakdown during terminal differentiation of primary lens fibres in mice: a transmission electron microscopic study Requirement of the RNA-editing enzyme ADAR2 for normal physiology in mice Betacellulin overexpression in transgenic mice causes disproportionate growth, pulmonary hemorrhage syndrome, and complex eye pathology Agonistic and antagonistic action of AP2, Msx2, Pax6, Prox1 AND Six3 in the regulation of Sox2 expression. Genetics of crystallins: cataract and beyond. Pleiotropic effects in Eya3 knockout mice Electroretinography as a screening method for mutations causing retinal dysfunction in mice Variations of eye size parameters among different strains of mice. Aphakia (ak), a mouse mutation affecting early eye development: fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern. On the use of Tono-Pen XL for the measurement of intraocular pressure in mice The German Mouse Clinic: a platform for systemic phenotype analysis of mouse models. Cataract mutations and lens development A comparative phenotypic and genomic analysis of C57BL/6J and C57BL/6N mouse strains Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function First mutation in the βA2-crystallin encoding gene is associated with small lenses and age-related cataracts Permanent neonatal diabetes in INS(C94Y) transgenic pigs. An in vivo doxycycline-controlled expression system for functional studies of the retina Relative roles of the different Pax6 domains for pancreatic alpha cell development Large-scale phenotyping of an accurate genetic mouse model of JNCL identifies novel early pathology outside the central nervous system

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