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RICHARD WENSTRUP, M.D.
M.D.
Pediatrics Physician
NPI: 1841221280Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
35-06-5950(OH)
Research & Publications (20)
Effect of enzyme replacement therapy with imiglucerase on BMD in type 1 Gaucher disease.
PMID 17032149·J Bone Miner Res·2007
3-trial
Murine model of the Ehlers-Danlos syndrome. col5a1 haploinsufficiency disrupts collagen fibril assembly at multiple stages.
PMID 16492673·J Biol Chem·2006
7-preclinical
Type V collagen controls the initiation of collagen fibril assembly.
PMID 15383546·J Biol Chem·2004
7-preclinical
Reduced type I collagen utilization: a pathogenic mechanism in COL5A1 haplo-insufficient Ehlers-Danlos syndrome.
PMID 15095409·J Cell Biochem·2004
8-other
Gaucher disease: alendronate disodium improves bone mineral density in adults receiving enzyme therapy.
PMID 15010365·Blood·2004
3-trial
COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDS.
PMID 10777716·Am J Hum Genet·2000
8-other
BRCA1 and BRCA2 mutations in women of different ethnicities undergoing testing for hereditary breast-ovarian cancer.
PMID 19241424·Cancer·2009
8-other
Three-dimensional in vitro effects of compression and time in culture on aggregate modulus and on gene expression and protein content of collagen type II in murine chondrocytes.
PMID 19231914·Tissue Eng Part A·2009
7-preclinical
Tensile stimulation of murine stem cell-collagen sponge constructs increases collagen type I gene expression and linear stiffness.
PMID 19191514·Tissue Eng Part A·2009
7-preclinical
Multiple rare nonsynonymous variants in the adenomatous polyposis coli gene predispose to colorectal adenomas.
PMID 18199528·Cancer Res·2008
8-other
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
PMID 17924331·Am J Hum Genet·2007
8-other
A multicenter study of the frequency and distribution of GJB2 and GJB6 mutations in a large North American cohort.
PMID 17666888·Genet Med·2007
4-observational
Familial haemophagocytic lymphohistiocytosis in patients who are heterozygous for the A91V perforin variation is often associated with other genetic defects.
PMID 17627755·Int J Immunogenet·2007
8-other
ColVa1 and ColXIa1 are required for myocardial morphogenesis and heart valve development.
PMID 17029294·Dev Dyn·2006
7-preclinical
Structural abnormalities of the cornea and lid resulting from collagen V mutations.
PMID 16431952·Invest Ophthalmol Vis Sci·2006
7-preclinical
A genetic approach to fracture epidemiology in childhood.
PMID 16278883·Am J Med Genet C Semin Med Genet·2005
8-other
Endogenously expressed multimeric self-cleaving hammerhead ribozymes ablate mutant collagen in cellulo.
PMID 15963928·Mol Ther·2005
7-preclinical
Mesenchymal stem cells used for rabbit tendon repair can form ectopic bone and express alkaline phosphatase activity in constructs.
PMID 15304271·J Orthop Res·2004
7-preclinical
Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss.
PMID 15286157·J Med Genet·2004
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 3333 BURNET AVE, ML 4006
CINCINNATI, OH 45229 - Phone
- (513) 636-4760
Quick Facts
- NPI
- 1841221280
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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