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NATALIE SPECK, MD
MD
Family Medicine Physician
NPI: 1902061898IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
LL18121(OR)MD153081(OR)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
LL18121(OR)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF VERMONT COLLEGE OF MEDICINE
Class of 2008
Research & Publications (20)
Low-dose 5-fluorouracil adjuvant in laser therapy for HPV lesions in immunosuppressed patients and cases of difficult control.
PMID 15493174·Eur J Gynaecol Oncol·2004
8-other
Fas/CD95 promoter polymorphism gene and its relationship with cervical carcinoma.
PMID 19480241·Eur J Gynaecol Oncol·2009
8-other
Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter.
PMID 19129762·Nature·2009
7-preclinical
Structure of the AML1-ETO eTAFH domain-HEB peptide complex and its contribution to AML1-ETO activity.
PMID 19204326·Blood·2009
7-preclinical
Core binding factors are necessary for natural killer cell development and cooperate with Notch signaling during T-cell specification.
PMID 18390836·Blood·2008
7-preclinical
Leukemia and hematopoietic stem cells: balancing proliferation and quiescence.
PMID 18239455·Cell Cycle·2008
6-review
Of lineage and legacy: the development of mammalian hematopoietic stem cells.
PMID 18204427·Nat Immunol·2008
6-review
PU.1 is a major downstream target of AML1 (RUNX1) in adult mouse hematopoiesis.
PMID 17994017·Nat Genet·2008
7-preclinical
Allosteric inhibition of the protein-protein interaction between the leukemia-associated proteins Runx1 and CBFbeta.
PMID 17961830·Chem Biol·2007
8-other
Structural basis for recognition of SMRT/N-CoR by the MYND domain and its contribution to AML1/ETO's activity.
PMID 17560331·Cancer Cell·2007
7-preclinical
A novel RUNX2 missense mutation predicted to disrupt DNA binding causes cleidocranial dysplasia in a large Chinese family with hyperplastic nails.
PMID 18166138·BMC Med Genet·2007
5-case
Disease mutations in RUNX1 and RUNX2 create nonfunctional, dominant-negative, or hypomorphic alleles.
PMID 17290219·EMBO J·2007
4-observational
T-lymphoid, megakaryocyte, and granulocyte development are sensitive to decreases in CBFbeta dosage.
PMID 16940420·Blood·2007
7-preclinical
Endogenous cortisol elevations are related to memory facilitation only in individuals who are emotionally aroused.
PMID 16225997·Psychoneuroendocrinology·2006
3-trial
The tetramer structure of the Nervy homology two domain, NHR2, is critical for AML1/ETO's activity.
PMID 16616331·Cancer Cell·2006
7-preclinical
The allantois and chorion, when isolated before circulation or chorio-allantoic fusion, have hematopoietic potential.
PMID 17038514·Development·2006
7-preclinical
A mutation in the S-switch region of the Runt domain alters the dynamics of an allosteric network responsible for CBFbeta regulation.
PMID 17059830·J Mol Biol·2006
8-other
Runx1 function in hematopoiesis is required in cells that express Tek.
PMID 16174759·Blood·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 849 PACIFIC AVENUE
HOOD RIVER, OR 97031 - Phone
- (541) 386-6380
Quick Facts
- NPI
- 1902061898
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 1
- Years in Practice
- 18
- Publications
- 20
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