Dr. Katrina Dipple practices Genetic Medicine in Los Angeles, CA. As a geneticist, Dr. Dipple performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients? with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Dipple carries out studies, tests, and counsels patients with genetic diseases.
Medical GeneticsAmerican Board of Medical GeneticsABMG
- Characterization of the human glycerol kinase promoter: identification of a functional HNF-4alpha binding site and evidence for transcriptional activation.
- IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric of DAX1.
- Single-gene disorders: what role could moonlighting enzymes play?
- Targeted disruption of glycerol kinase gene in mice: expression analysis in liver shows alterations in network partners related to glycerol kinase activity.
- Asymptomatic isolated human glycerol kinase deficiency associated with splice-site mutations and nonsense-mediated decay of mutant RNA.
- Duplication 8q22.1-q24.1 associated with bipolar disorder and speech delay.
- Endocrine regulation and methylation patterns of rat class I alcohol dehydrogenase in liver and kidney.
- Glycerol kinase deficiency alters expression of genes involved in lipid metabolism, carbohydrate metabolism, and insulin signaling.
- Global metabolic effects of glycerol kinase overexpression in rat hepatoma cells.
- Transcriptomic and network component analysis of glycerol kinase in skeletal muscle using a mouse model of glycerol kinase deficiency.
- Validation of candidate causal genes for obesity that affect shared metabolic pathways and networks.
- Resistance to diet-induced obesity in mice with synthetic glyoxylate shunt.
- Becoming a woman physician scientist.
- Moonlighting function of glycerol kinase causes systems-level changes in rat hepatoma cells.
- Ensemble modeling of hepatic fatty acid metabolism with a synthetic glyoxylate shunt.
- Pontocerebellar hypoplasia in association with de novo 19p13.11p13.12 microdeletion.
- Glycerol hypersensitivity in a Drosophila model for glycerol kinase deficiency is affected by mutations in eye pigmentation genes.
- Cleft Lip and Palate in a Patient with 5q35.2-q35.3 Microdeletion: The Importance of Chromosomal Microarray Testing in the Craniofacial Clinic.
- Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis.
- Familial microdeletion of 17q24.3 upstream of SOX9 is associated with isolated Pierre Robin sequence due to position effect.
- First report of a de novo 18q11.2 microdeletion including GATA6 associated with complex congenital heart disease and renal abnormalities.
- Disruption of glycerol metabolism by RNAi targeting of genes encoding glycerol kinase results in a range of phenotype severity in Drosophila.
- Duodenal atresia in 17q12 microdeletion including HNF1B: a new associated malformation in this syndrome.
- Mathematical modeling of the insulin signal transduction pathway for prediction of insulin sensitivity from expression data.
- Structure and expression of the rat class I alcohol dehydrogenase gene.
- Gestational Diabetes Associated with a Novel Mutation (378-379insTT) in the Glycerol Kinase Gene.
- Alcohol Intervention for Adolescents with Fetal Alcohol Spectrum Disorders: Project Step Up, a Treatment Development Study.
- Insulin sensitivity predictions in individuals with obesity and type II diabetes
- Genetic Screening in Patients with Craniofacial Malformations.
- Tissue-specific expression and preliminary functional analysis of the 5' flanking regions of the human mitochondrial aldehyde dehydrogenase (ALDH2) gene.
- The mitochondrial aldehyde dehydrogenase gene resides in an HTF island but is expressed in a tissue-specific manner.
- The novel aldehyde dehydrogenase gene, ALDH5, encodes an active aldehyde dehydrogenase enzyme.
- Alcohol sensitivity, alcohol metabolism, risk of alcoholism, and the role of alcohol and aldehyde dehydrogenase genotypes.
- Effects of thyroxine on the expression of alcohol dehydrogenase in rat liver and kidney.
- Modulation of hepatic and renal alcohol dehydrogenase activity and mRNA by steroid hormones in vivo.
- The role of nuclear factor NF-Y/CP1 in the transcriptional regulation of the human aldehyde dehydrogenase 2-encoding gene.
- The resident's column.
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