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MICHAEL D'ADAMO, PH.D.
PH.D.
Psychologist
NPI: 1417041971Individual
Specialties, Licenses & Credentials
PsychologistPrimary
Psychologist
Code: 103T00000X
2645(NJ)
Research & Publications (19)
Increased release and activity of matrix metalloproteinase-9 in patients with mandibuloacral dysplasia type A, a rare premature ageing syndrome.
PMID 18554282·Clin Genet·2008
8-other
Insulin resistance affects gene expression in endothelium.
PMID 18216326·Arterioscler Thromb Vasc Biol·2008
8-other
A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1.
PMID 18926884·Neuroscience·2008
7-preclinical
Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvbeta1.1.
PMID 16956965·Am J Physiol Cell Physiol·2007
7-preclinical
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype.
PMID 17848409·J Clin Endocrinol Metab·2007
5-case
Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.
PMID 17156368·Eur J Neurosci·2006
7-preclinical
C-174G polymorphism in the promoter of the interleukin-6 gene is associated with insulin resistance.
PMID 16043746·Diabetes Care·2005
4-observational
Gene expression profiling of fibroblasts from a human progeroid disease (mandibuloacral dysplasia, MAD #248370) through cDNA microarrays.
PMID 15473259·Gene Expr·2004
8-other
The -866A/A genotype in the promoter of the human uncoupling protein 2 gene is associated with insulin resistance and increased risk of type 2 diabetes.
PMID 15220218·Diabetes·2004
8-other
Identification of a heteromeric interaction that influences the rectification, gating, and pH sensitivity of Kir4.1/Kir5.1 potassium channels.
PMID 12923169·J Biol Chem·2003
7-preclinical
Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels.
PMID 12799903·Pflugers Arch·2003
7-preclinical
A common polymorphism in the promoter of UCP2 contributes to the variation in insulin secretion in glucose-tolerant subjects.
PMID 12716765·Diabetes·2003
8-other
Relationship between plasma free fatty acids and uncoupling protein-3 gene expression in skeletal muscle of obese subjects: in vitro evidence of a causal link.
PMID 12153598·Clin Endocrinol (Oxf)·2002
8-other
Expression in E. coli and purification of recombinant fragments of wild type and mutant human prion protein.
PMID 11918972·Neurochem Int·2002
8-other
Experimental arterial thrombosis in genetically or diet induced hyperlipidemia in rats--role of vitamin K-dependent clotting factors and prevention by low-intensity oral anticoagulation.
PMID 11776312·Thromb Haemost·2001
4-observational
Differential pH sensitivity of Kir4.1 and Kir4.2 potassium channels and their modulation by heteropolymerisation with Kir5.1.
PMID 11306656·J Physiol·2001
7-preclinical
Role of receptor protein tyrosine phosphatase alpha (RPTPalpha) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels.
PMID 11211111·Pflugers Arch·2000
7-preclinical
pH dependence of the inwardly rectifying potassium channel, Kir5.1, and localization in renal tubular epithelia.
PMID 10764726·J Biol Chem·2000
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
- 295 ROUTE 22 EAST, SUITE 3
WHITEHOUSE STATION, NJ 08889 - Phone
- (908) 534-5850
Quick Facts
- NPI
- 1417041971
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 19
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