Search Results - "Park, Vicki M"
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Cloning and characterization of the promoter for the liver isoform of the rat carnitine palmitoyltransferase I (L-CPT I) gene
Published in Biochemical journal (15-02-1998)“…Carnitine palmitoyltransferase I (CPTI) catalyses the transfer of long chain fatty acids to carnitine for translocation across the mitochondrial inner…”
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Introductory TBL Exercise on Genetic Risk
Published in MedEdPORTAL (22-04-2016)“…Abstract Introduction Team-based learning (TBL) has gained favor in medical education as an applied approach to learning that promotes teamwork and…”
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Hypercoagulable state mutation analysis in white patients with early first-trimester recurrent pregnancy loss
Published in Fertility and sterility (01-06-1999)“…Antiphospholipid antibodies (APA) and other coagulation abnormalities have been associated with an increased risk of venous, arterial, and placental thrombosis…”
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Hepatitis C hypervariable region 1 : Association of reduced selection pressure in African Americans with treatment failure
Published in Digestive diseases and sciences (01-10-2007)“…In a prospective therapeutic trial, features of the hepatitis C quasispecies were investigated as possible markers of therapeutic response. Individuals…”
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Genetic Risk for Recessively Inherited Disease (Duchenne Muscular Dystrophy and Congenital Hearing Loss)
Published in MedEdPORTAL (13-08-2012)“…Abstract Introduction This resource is a team-based learning (TBL) module on genetic risk and was developed for use in the inaugural semester of our revised…”
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Naturally occurring dominant resistance mutations to hepatitis C virus protease and polymerase inhibitors in treatment‐naïve patients
Published in Hepatology (Baltimore, Md.) (01-12-2008)“…Resistance mutations to hepatitis C virus (HCV) nonstructural protein 3 (NS3) protease inhibitors in <1% of the viral quasispecies may still allow >1000‐fold…”
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Factor V Leiden and other hypercoagulable state mutations are not associated with osteonecrosis during or after treatment for pediatric malignancy
Published in The Journal of pediatrics (01-03-1999)“…Objective: Osteonecrosis (ON) is a debilitating complication of cancer treatment in children and is usually associated with systemic steroid therapy. Defects…”
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A model system using fetal hemoglobin to distinguish fetal cells enriched from maternal blood
Published in Annals of the New York Academy of Sciences (01-09-1994)Get more information
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Naturally occurring dominant resistance mutations to HCV protease and polymerase inhibitors in treatment-naïve patients
Published in Hepatology (Baltimore, Md.) (01-12-2008)“…Resistance mutations to HCV NS3 protease inhibitors in <1% of the viral quasispecies may still allow >1000-fold viral load reductions upon treatment,…”
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Risk of fetal mosaicism when placental mosaicism is diagnosed by chorionic villus sampling
Published in American journal of obstetrics and gynecology (01-03-1996)“…OBJECTIVE: Our purpose was to determine the risk of fetal mosaicism when placental mosaicism is found on chorionic villus sampling. STUDY DESIGN: We present a…”
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Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21
Published in Journal of medical genetics (01-08-1995)“…We describe a prenatally detected case of double trisomy involving chromosome 21 and the X chromosome (48,XXX,+21) along with determination of the segregation…”
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A jumping Robertsonian translocation : a molecular and cytogenetic study
Published in Human genetics (01-09-1996)“…We report a patient with mosaicism for two different Robertsonian translocations, both involving chromosome 21. She carries an unbalanced cell line with an…”
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Primary structure of the 5 S subunit of transcarboxylase as deduced from the genomic DNA sequence
Published in FEBS letters (13-09-1993)“…Transcarboxylase from Propionibacterium shermanii is a complex biotin-containing enzyme composed of 30 polypeptides of three different types. It is composed of…”
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Sex chromosome markers: Characterization using fluorescence in situ hybridization and review of the literature
Published in American journal of medical genetics (11-07-1997)“…Fluorescence in situ hybridization (FISH) using biotin labeled X‐ and Y‐chromosome DNA probes was utilized in the analysis of 23 sex chromosome‐derived…”
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