About: Kevin Eggan

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

researcher (ORCID 0000-0003-4436-8467)

Attributes	Values
rdf:type	Item
description	연구원 (ko) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) researcher (ORCID 0000-0003-4436-8467) (en)
rdfs:label	Kevin Eggan (en) Kevin Eggan (nl)
skos:prefLabel	Kevin Eggan (en) Kevin Eggan (nl)
name	Kevin Eggan (en) Kevin Eggan (nl)
given name	wds:Q91046031-C067EE43-F75E-47B0-AE6C-AE9BBA503CD1
given name	Kevin
instance of	wds:Q91046031-C4DB9922-F4B1-4C25-A157-931AB9EF8540
instance of	Homo sapiens
occupation	wds:Q91046031-B363276C-1230-4EFA-BE46-26A7209B02C9
sex or gender	wds:Q91046031-20cbb4b1-6b0a-4153-bff9-9287d27cbcb9
VIAF ID	wds:Q91046031-ffbadaad-22fe-43e4-9a3f-5e32e6f98163
IdRef ID	wds:Q91046031-2FD29DF6-C036-4ADD-8143-950F36BFCF26
National Library of Israel J9U ID	wds:Q91046031-82EF6CCD-C399-4F5D-AAA0-284FE7B2E541
VIAF ID	http://viaf.org/viaf/34780369
IdRef ID	http://www.idref.fr/119936933/id
occupation	researcher
sex or gender	male
VIAF ID	34780369
IdRef ID	119936933
National Library of Israel J9U ID	987007324505605171
ORCID iD	wds:Q91046031-F0B4DD5C-A0F1-4515-B692-D80788947977
ORCID iD	https://orcid.org/0000-0003-4436-8467
ORCID iD	0000-0003-4436-8467
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q91046031
is author of	Opportunities and challenges of pluripotent stem cell neurodegenerative disease models Directed differentiation and functional maturation of cortical interneurons from human embryonic stem cells How to make spinal motor neurons Abnormal gene expression in cloned mice derived from embryonic stem cell and cumulus cell nuclei Incomplete reactivation of Oct4-related genes in mouse embryos cloned from somatic nuclei. Somatic coding mutations in human induced pluripotent stem cells Conversion of mouse and human fibroblasts into functional spinal motor neurons The C9orf72-interacting protein Smcr8 is a negative regulator of autoimmunity and lysosomal exocytosis Progress toward the clinical application of patient-specific pluripotent stem cells Mice cloned from olfactory sensory neurons Targeted bisulfite sequencing reveals changes in DNA methylation associated with nuclear reprogramming Derivation of embryonic germ cells and male gametes from embryonic stem cells. CLP1 links tRNA metabolism to progressive motor-neuron loss Reprogramming within hours following nuclear transfer into mouse but not human zygotes Digital RNA allelotyping reveals tissue-specific and allele-specific gene expression in human Optimal timing of inner cell mass isolation increases the efficiency of human embryonic stem cell derivation and allows generation of sibling cell lines FUS is sequestered in nuclear aggregates in ALS patient fibroblasts Human embryonic stem cell-derived motor neurons are sensitive to the toxic effect of glial cells carrying an ALS-causing mutation Male and female mice derived from the same embryonic stem cell clone by tetraploid embryo complementation Efficient CRISPR-Cas9-mediated generation of knockin human pluripotent stem cells lacking undesired mutations at the targeted locus Pathways disrupted in human ALS motor neurons identified through genetic correction of mutant SOD1. Intrinsic membrane hyperexcitability of amyotrophic lateral sclerosis patient-derived motor neurons Developmental reprogramming after chromosome transfer into mitotic mouse zygotes Mediators of reprogramming: transcription factors and transitions through mitosis Constructing and deconstructing stem cell models of neurological disease The mouse C9ORF72 ortholog is enriched in neurons known to degenerate in ALS and FTD. Modeling human disease with pluripotent stem cells: from genome association to function. Nanog-independent reprogramming to iPSCs with canonical factors Recipient cell nuclear factors are required for reprogramming by nuclear transfer The role of maternal-specific H3K9me3 modification in establishing imprinted X-chromosome inactivation and embryogenesis in mice Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality Monitoring peripheral nerve degeneration in ALS by label-free stimulated Raman scattering imaging SLC52A3, A Brown-Vialetto-van Laere syndrome candidate gene is essential for mouse development, but dispensable for motor neuron differentiation Loss-of-function mutations in the C9ORF72 mouse ortholog cause fatal autoimmune disease From Dish to Bedside: Lessons Learned While Translating Findings from a Stem Cell Model of Disease to a Clinical Trial. Flp recombinase regulated lacZ expression at the ROSA26 locus Genetic validation of a therapeutic target in a mouse model of ALS. Generation of neuropeptidergic hypothalamic neurons from human pluripotent stem cells Comprehensive Protocols for CRISPR/Cas9-based Gene Editing in Human Pluripotent Stem Cells CAT7 and cat7l Long Non-coding RNAs Tune Polycomb Repressive Complex 1 Function during Human and Zebrafish Development Nuclear cloning, stem cells, and genomic reprogramming Impracticality of egg donor recruitment in the absence of compensation. A perspective on stem cell modeling of amyotrophic lateral sclerosis Dysregulated protocadherin-pathway activity as an intrinsic defect in induced pluripotent stem cell-derived cortical interneurons from subjects with schizophrenia A High-Content Screen Identifies TPP1 and Aurora B as Regulators of Axonal Mitochondrial Transport Comparison of three congruent patient-specific cell types for the modelling of a human genetic Schwann-cell disorder Two familial ALS proteins function in prevention/repair of transcription-associated DNA damage Generation of a Motor Nerve Organoid with Human Stem Cell-Derived Neurons. Effect of Ezogabine on Cortical and Spinal Motor Neuron Excitability in Amyotrophic Lateral Sclerosis: A Randomized Clinical Trial ALS-implicated protein TDP-43 sustains levels of STMN2, a mediator of motor neuron growth and repair Dipeptide repeat proteins activate a heat shock response found in C9ORF72-ALS/FTLD patients. C9orf72 suppresses systemic and neural inflammation induced by gut bacteria Molecularly cleavable bioinks facilitate high-performance digital light processing-based bioprinting of functional volumetric soft tissues Genoppi is an open-source software for robust and standardized integration of proteomic and genetic data Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein All-Optical Electrophysiology for High-Throughput Functional Characterization of a Human iPSC-Derived Motor Neuron Model of ALS. Nuclear Cloning, Epigenetic Reprogramming and Cellular Differentiation Comparative genomic analysis of embryonic, lineage-converted, and stem cell-derived motor neurons Micromanipulating dosage compensation: understanding X-chromosome inactivation through nuclear transplantation Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein Nuclear cloning, epigenetic reprogramming and cellular differentiation. Shushing down the epigenetic landscape towards stem cell differentiation. Absence of Survival and Motor Deficits in 500 Repeat C9ORF72 BAC Mice
is author of	wds:Q33559694-5A2570E7-50AE-4EC6-8129-D68C221057F7 wds:Q34545949-893E2767-C17F-4EED-82A6-A36DDE8E8066 wds:Q34353458-B1E171FC-C6A5-4C27-B871-C8B27DF71EEC wds:Q34568328-F1193EAF-2297-4005-9707-24CAB6B4722A wds:Q37879269-08D29036-0320-426A-979A-E341C6CC24D7

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