Associate Professor, Pediatrics, UCLA School of Medicine
Medical Genetics
Dr. Katrina M. Dipple, MD
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Katrina Dipple is an expert in the field of Medical Genetics. He attended Indiana University School of Medicine. Indiana University School of Medicine is ranked 45 in research and 47 in primary care medicine Katrina M. Dipple is a published physician. He published 48 publications, including: 'Binding and activation of the human aldehyde dehydrogenase 2 promoter by hepatocyte nuclear factor 4.'
Publications
- Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update.
- Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders.
- Duodenal atresia in 17q12 microdeletion including HNF1B: A new associated malformation in this syndrome.
- 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.
- Glycerol hypersensitivity in a Drosophila model for glycerol kinase deficiency is affected by mutations in eye pigmentation genes.
- Pontocerebellar hypoplasia in association with de novo 19p13.11p13.12 microdeletion.
- Glycerol homeostasis and metabolism in glycerol kinase carrier mice.
- Ensemble modeling of hepatic fatty acid metabolism with a synthetic glyoxylate shunt.
- Weighted gene co-expression network analysis identifies biomarkers in glycerol kinase deficient mice.
- Becoming a woman physician scientist.
- Resistance to diet-induced obesity in mice with synthetic glyoxylate shunt.
- Validation of candidate causal genes for obesity that affect shared metabolic pathways and networks.
- Transcriptomic and network component analysis of glycerol kinase in skeletal muscle using a mouse model of glycerol kinase deficiency.
- Global metabolic effects of glycerol kinase overexpression in rat hepatoma cells.
- In vivo time-resolved autofluorescence measurements to test for glycation of human skin.
- Asymptomatic isolated human glycerol kinase deficiency associated with splice-site mutations and nonsense-mediated decay of mutant RNA.
- Single-gene disorders: what role could moonlighting enzymes play?
- Human and murine glycerol kinase: influence of exon 18 alternative splicing on function.
- IL1RAPL1 is associated with mental retardation in patients with complex glycerol kinase deficiency who have deletions extending telomeric of DAX1.
- Characterization of the human glycerol kinase promoter: identification of a functional HNF-4alpha binding site and evidence for transcriptional activation.
- Disruption of Glycerol Metabolism by RNAi Targeting of Genes Encoding Glycerol Kinase Results in a Range of Phenotype Severity in Drosophila.
- Carnitine membrane transporter deficiency: a long-term follow up and OCTN2 mutation in the first documented case of primary carnitine deficiency.
- Human ARX gene: genomic characterization and expression.
- Consequences of complexity within biological networks: robustness and health, or vulnerability and disease.
- Glycerol kinase deficiency: evidence for complexity in a single gene disorder.
- Modifier genes convert "simple" Mendelian disorders to complex traits.
- Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics.
- AluY insertion (IVS4-52ins316alu) in the glycerol kinase gene from an individual with benign glycerol kinase deficiency.
- Activity of the human aldehyde dehydrogenase 2 promoter is influenced by the balance between activation by hepatocyte nuclear factor 4 and repression by perosixome pro...
- Binding and activation of the human aldehyde dehydrogenase 2 promoter by hepatocyte nuclear factor 4.
- The resident's column.
- The role of nuclear factor NF-Y/CP1 in the transcriptional regulation of the human aldehyde dehydrogenase 2-encoding gene.
- Modulation of hepatic and renal alcohol dehydrogenase activity and mRNA by steroid hormones in vivo.
- Effects of thyroxine on the expression of alcohol dehydrogenase in rat liver and kidney.
- Alcohol sensitivity, alcohol metabolism, risk of alcoholism, and the role of alcohol and aldehyde dehydrogenase genotypes.
- The novel aldehyde dehydrogenase gene, ALDH5, encodes an active aldehyde dehydrogenase enzyme.
- The mitochondrial aldehyde dehydrogenase gene resides in an HTF island but is expressed in a tissue-specific manner.
- Tissue-specific expression and preliminary functional analysis of the 5' flanking regions of the human mitochondrial aldehyde dehydrogenase (ALDH2) gene.
- Endocrine regulation and methylation patterns of rat class I alcohol dehydrogenase in liver and kidney.
- Moonlighting function of glycerol kinase causes systems-level changes in rat hepatoma cells.
- Targeted disruption of glycerol kinase gene in mice: expression analysis in liver shows alterations in network partners related to glycerol kinase activity.
- Duplication of the Down syndrome critical region does not predict facial phenotype in a baby with a ring chromosome 21.
- Gene therapy for murine glycerol kinase deficiency: importance of murine ortholog.
- Glycerol kinase deficiency alters expression of genes involved in lipid metabolism, carbohydrate metabolism, and insulin signaling.
- Duplication 8q22.1-q24.1 associated with bipolar disorder and speech delay.
- Ocular manifestations of oblique facial clefts.
Schools
Indiana University School Of Medicine
University Of California Los Angeles
Doctors Specialties
- Clinical Biochemical Genetics
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Blue Card PPO
- CaliforniaCare HMO
- Advantage Preferred DirectAccess Plus PPO
- Blue Cross Blue Shield of California PPO
- Pathway X Direct Access PPO
- Pathway X Tiered Direct Access
- Select Plus HMO
- Select PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- First Health (Coventry Health Care) PPO
- Medicare MCR
- Kaiser PHCS Network PPO
- MultiPlan PPO
- PHCS Network PPO
- Heritage Signature
- Principal Life
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- PacifiCare HMO
Education
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Cedars-Sinai Medical Center -
UCLA Medical Center -
Indiana University School of Medicine
Hospital
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Mattel Children's Hospital UCLA -
Ronald Reagan UCLA Medical Center -
Santa Monica-UCLA Medical Center and Orthopaedic Hospital
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