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JOSHUA A EGLY MD
MD
Emergency Medicine Physician
NPI: 1518166404IndividualAccepts Medicare
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
4301090145(MI)N6276(TX)
Education
UNIVERSITY OF TEXAS MEDICAL SCHOOL AT HOUSTON
Class of 2007
Research & Publications (20)
Deletion of 5' sequences of the CSB gene provides insight into the pathophysiology of Cockayne syndrome.
PMID 18183039·Eur J Hum Genet·2008
5-case
Sequential recruitment of the repair factors during NER: the role of XPG in initiating the resynthesis step.
PMID 18079701·EMBO J·2008
8-other
Nucleotide excision repair driven by the dissociation of CAK from TFIIH.
PMID 18614043·Mol Cell·2008
8-other
CSB protein is (a direct target of HIF-1 and) a critical mediator of the hypoxic response.
PMID 18784753·EMBO J·2008
7-preclinical
Dissection of the molecular defects caused by pathogenic mutations in the DNA repair factor XPC.
PMID 18809580·Mol Cell Biol·2008
8-other
p8/TTDA overexpression enhances UV-irradiation resistance and suppresses TFIIH mutations in a Drosophila trichothiodystrophy model.
PMID 19008953·PLoS Genet·2008
7-preclinical
The human DNA repair factor XPC-HR23B distinguishes stereoisomeric benzo[a]pyrenyl-DNA lesions.
PMID 17525733·EMBO J·2007
8-other
Solution structure and self-association properties of the p8 TFIIH subunit responsible for trichothiodystrophy.
PMID 17350038·J Mol Biol·2007
8-other
Fully automated image-guided needle insertion: application to small animal biopsies.
PMID 18001922·Annu Int Conf IEEE Eng Med Biol Soc·2007
7-preclinical
Neurological defects in trichothiodystrophy reveal a coactivator function of TFIIH.
PMID 17952069·Nat Neurosci·2007
7-preclinical
[Neurological disorders and trichothiodystrophy: when the transcription process is impaired].
PMID 18154723·Med Sci (Paris)·2007
8-other
Common XPD (ERCC2) polymorphisms have no measurable effect on nucleotide excision repair and basal transcription.
PMID 17403617·DNA Repair (Amst)·2007
7-preclinical
DNA repair and transcriptional deficiencies caused by mutations in the Drosophila p52 subunit of TFIIH generate developmental defects and chromosome fragility.
PMID 17339330·Mol Cell Biol·2007
7-preclinical
XPG stabilizes TFIIH, allowing transactivation of nuclear receptors: implications for Cockayne syndrome in XP-G/CS patients.
PMID 17466625·Mol Cell·2007
8-other
Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair.
PMID 17466626·Mol Cell·2007
8-other
Rescue of progeria in trichothiodystrophy by homozygous lethal Xpd alleles.
PMID 17020410·PLoS Biol·2006
7-preclinical
RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors.
PMID 17110932·EMBO J·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 6451 BRENTWOOD STAIR RD, SUITE #200
FORT WORTH, TX 76112 - Phone
- (817) 496-9700
Quick Facts
- NPI
- 1518166404
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 19
- Publications
- 20
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