About: Ilja Demuth

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

About: Ilja Demuth Goto Sponge NotDistinct Permalink

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

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq)
rdfs:label	Ilja Demuth (en) Ilja Demuth (es) Ilja Demuth (nl) Ilja Demuth (sl) Ilja Demuth (ast)
skos:prefLabel	Ilja Demuth (en) Ilja Demuth (es) Ilja Demuth (nl) Ilja Demuth (sl) Ilja Demuth (ast)
name	Ilja Demuth (en) Ilja Demuth (es) Ilja Demuth (nl) Ilja Demuth (sl) Ilja Demuth (ast)
Scopus author ID	wds:Q47502509-71C2C9F7-CE13-4F17-9A71-591955ACD921
Scopus author ID	6602464740
instance of	wds:Q47502509-47120CBA-4B64-4A00-8B89-1D45CD495960
instance of	Homo sapiens
skos:altLabel	Demuth I (en) I Demuth (en)
occupation	wds:Q47502509-21AB109E-12EE-4349-B463-2E760D5BFC20
employer	wds:Q47502509-B090ECEE-3588-465A-A07E-7ABE0678F7EE
sex or gender	wds:Q47502509-4EB6130B-3EA8-4D35-8FD1-CA0302516FB8
ISNI	wds:Q47502509-744E9285-BAFE-4946-AE95-E3524F15C003
VIAF ID	wds:Q47502509-F8F12F8B-02BE-4A19-9250-B383D07D807E
GND ID	wds:Q47502509-94A08011-4542-48F5-8A10-5950114B0952
date of birth	wds:Q47502509-2110BC34-0F6C-4B44-AC32-656D80347940
family name	wds:Q47502509-449EA4A1-CB09-49E7-8C6C-A3350158FD6B
WorldCat Identities ID (superseded)	wds:Q47502509-B6015C56-E4D3-4BF2-958D-8A51F946BF86
VIAF ID	http://viaf.org/viaf/47623427
GND ID	https://d-nb.info/gnd/121639460
occupation	researcher
employer	Charité
sex or gender	male
ISNI	0000000023176341
VIAF ID	47623427
GND ID	121639460
date of birth	1967-01-01 00:00:00Z (xsd:dateTime)
family name	Demuth
WorldCat Identities ID (superseded)	viaf-47623427
ORCID iD	wds:Q47502509-6333FF43-6631-45D6-B6E3-F25C1D6B1B13
ORCID iD	https://orcid.org/0000-0002-4340-2523
ORCID iD	0000-0002-4340-2523
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q47502509
is author of	The nuclease hSNM1B/Apollo is linked to the Fanconi anemia pathway via its interaction with FANCP/SLX4. The Fanconi anaemia group G gene FANCG is identical with XRCC9 The Fanconi anemia group A protein modulates homologous repair of DNA double-strand breaks in mammalian cells. An inducible null mutant murine model of Nijmegen breakage syndrome proves the essential function of NBS1 in chromosomal stability and cell viability. Expression pattern of the Nijmegen breakage syndrome gene, Nbs1, during murine development Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9 Secular changes in late-life cognition and well-being: Towards a long bright future with a short brisk ending? Cohort Differences in Psychosocial Function over 20 Years: Current Older Adults Feel Less Lonely and Less Dependent on External Circumstances DNA-repair in mild cognitive impairment and Alzheimer's disease. PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study Selenium-binding protein 2, the major hepatic target for acetaminophen, shows sex differences in protein abundance MicroRNA-138 is a potential regulator of memory performance in humans Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease Human SNM1B is required for normal cellular response to both DNA interstrand crosslink-inducing agents and ionizing radiation Directional dominance on stature and cognition in diverse human populations An essential function for NBS1 in the prevention of ataxia and cerebellar defects New mutations in the ATM gene and clinical data of 25 AT patients Nibrin functions in Ig class-switch recombination Exercise at Different Ages and Appendicular Lean Mass and Strength in Later Life: Results From the Berlin Aging Study II. Clinical utility gene card for: hyperlipoproteinemia, TYPE II. Endogenous hSNM1B/Apollo interacts with TRF2 and stimulates ATM in response to ionizing radiation Genetic heterogeneity for a Nijmegen breakage‐like syndrome Assessment of mitomycin C sensitivity in Fanconi anemia complementation group C gene (Fac) knock-out mouse cells Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants Cancer incidence in Nijmegen breakage syndrome is modulated by the amount of a variant NBS protein. The clinical manifestation of a defective response to DNA double-strand breaks as exemplified by Nijmegen breakage syndrome. Mutations causing Greenberg dysplasia but not Pelger anomaly uncouple enzymatic from structural functions of a nuclear membrane protein Clinical variability and novel mutations in the NHEJ1 gene in patients with a Nijmegen breakage syndrome-like phenotype. New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk Genome-wide association study identifies 74 loci associated with educational attainment Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Association of Low Lean Mass With Frailty and Physical Performance: A Comparison Between Two Operational Definitions of Sarcopenia-Data From the Berlin Aging Study II (BASE-II). The inflammatory markers CRP, IL-6, and IL-10 are associated with cognitive function--data from the Berlin Aging Study II. Correction: A Systematic Proteomic Study of Irradiated DNA Repair Deficient Nbn-Mice. Cohort profile: The Berlin Aging Study II (BASE-II). Large meta-analysis of genome-wide association studies identifies five loci for lean body mass A common Fanconi anemia mutation in black populations of sub-Saharan Africa No strong correlations between serum cytokine levels, CMV serostatus and hand-grip strength in older subjects in the Berlin BASE-II cohort Adherence to a Mediterranean-Style Diet and Appendicular Lean Mass in Community-Dwelling Older People: Results From the Berlin Aging Study II. The Subjective Health Horizon Questionnaire (SHH-Q): Assessing Future Time Perspectives for Facets of an Active Lifestyle

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, 188 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software