Back to Search
SCOTT LEIKIN, D.O.
D.O.
Critical Care Medicine (Internal Medicine) Physician
NPI: 1588079479IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
T4413(TX)125065761(IL)
Critical Care Medicine (Internal Medicine) PhysicianPrimary
Internal Medicine — Critical Care Medicine
Code: 207RC0200X
T4413(TX)
Education
OTHER
Class of 2014
Research & Publications (20)
Variable bone fragility associated with an Amish COL1A2 variant and a knock-in mouse model.
PMID 19594296·J Bone Miner Res·2010
7-preclinical
Laboratory interferences with the newer cyanide antidote: hydroxocobalamin.
PMID 19292028·Semin Diagn Pathol·2009
8-other
In utero transplantation of adult bone marrow decreases perinatal lethality and rescues the bone phenotype in the knockin murine model for classical, dominant osteogenesis imperfecta.
PMID 19414862·Blood·2009
7-preclinical
Defective C-propeptides of the proalpha2(I) chain of type I procollagen impede molecular assembly and result in osteogenesis imperfecta.
PMID 18375391·J Biol Chem·2008
8-other
Structural heterogeneity of type I collagen triple helix and its role in osteogenesis imperfecta.
PMID 18073209·J Biol Chem·2008
8-other
DNA double helices recognize mutual sequence homology in a protein free environment.
PMID 18181611·J Phys Chem B·2008
8-other
Segregation of type I collagen homo- and heterotrimers in fibrils.
PMID 18721810·J Mol Biol·2008
7-preclinical
Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta.
PMID 17277775·Nat Genet·2007
5-case
Procollagen triple helix assembly: an unconventional chaperone-assisted folding paradigm.
PMID 17925877·PLoS One·2007
8-other
Selective retention and degradation of molecules with a single mutant alpha1(I) chain in the Brtl IV mouse model of OI.
PMID 17662583·Matrix Biol·2007
7-preclinical
Y-position cysteine substitution in type I collagen (alpha1(I) R888C/p.R1066C) is associated with osteogenesis imperfecta/Ehlers-Danlos syndrome phenotype.
PMID 17206620·Hum Mutat·2007
8-other
Deficiency of cartilage-associated protein in recessive lethal osteogenesis imperfecta.
PMID 17192541·N Engl J Med·2006
5-case
Molecular mechanism of alpha 1(I)-osteogenesis imperfecta/Ehlers-Danlos syndrome: unfolding of an N-anchor domain at the N-terminal end of the type I collagen triple helix.
PMID 16407265·J Biol Chem·2006
8-other
Direct observation of azimuthal correlations between DNA in hydrated aggregates.
PMID 16241694·Phys Rev Lett·2005
8-other
Mutations near amino end of alpha1(I) collagen cause combined osteogenesis imperfecta/Ehlers-Danlos syndrome by interference with N-propeptide processing.
PMID 15728585·J Biol Chem·2005
8-other
Torsional deformation of double helix in interaction and aggregation of DNA.
PMID 18950140·J Phys Chem B·2004
8-other
Interactions of inorganic phosphate and sulfate anions with collagen.
PMID 15554697·Biochemistry·2004
7-preclinical
Structure, stability and interactions of type I collagen with GLY349-CYS substitution in alpha 1(I) chain in a murine Osteogenesis Imperfecta model.
PMID 15246109·Matrix Biol·2004
7-preclinical
Five-year incidence of age-related maculopathy: the Visual Impairment Project.
PMID 15177968·Ophthalmology·2004
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 6720 BERTNER AVE
HOUSTON, TX 77030 - Phone
- (832) 355-2666
Quick Facts
- NPI
- 1588079479
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 3
- Locations
- 2
- Years in Practice
- 12
- Publications
- 20
Are you this provider?
Claim Your Profile