Glycerol Hypersensitivity in a Drosophila Model for Glycerol Kinase Deficiency Is Affected by Mutations in Eye Pigmentation Genes

Por Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Publicado em 2012

Disruption of Glycerol Metabolism by RNAi Targeting of Genes Encoding Glycerol Kinase Results in a Range of Phenotype Severity in Drosophila

Por Wightman, Patrick J., Jackson, George R., Dipple, Katrina M.
Publicado em 2013

Genetic Screening in Patients with Craniofacial Malformations

Por Yoon, Amanda J., Pham, Binh N., Dipple, Katrina M.
Publicado no J Pediatr Genet (2016)

Clinical Findings Associated with a De Novo Partial Trisomy 10p11.22p15.3 and Monosomy 7p22.3 Detected by Chromosomal Microarray Analysis

Por Kohannim, Omid, Peredo, Jane, Dipple, Katrina M., Quintero-Rivera, Fabiola
Publicado em 2011

Moonlighting function of glycerol kinase causes systems-level changes in rat hepatoma cells

Por Sriram, Ganesh, Parr, Lilly S., Rahib, Lola, Liao, James C., Dipple, Katrina M.
Publicado em 2010

Transcriptomic and network component analysis of glycerol kinase in skeletal muscle using a mouse model of glycerol kinase deficiency

Por Rahib, Lola, Sriram, Ganesh, Harada, Melissa K., Liao, James C., Dipple, Katrina M.
Publicado em 2009

Ensemble Modeling of Hepatic Fatty Acid Metabolism with a Synthetic Glyoxylate Shunt

Por Dean, Jason T., Rizk, Matthew L., Tan, Yikun, Dipple, Katrina M., Liao, James C.
Publicado em 2010

Mathematical Modeling of the Insulin Signal Transduction Pathway for Prediction of Insulin Sensitivity from Expression Data

Por Ho, Clark K, Rahib, Lola, Liao, James C, Sriram, Ganesh, Dipple, Katrina M
Publicado no Mol Genet Metab (2014)

Suicide Risk in Adolescents with Fetal Alcohol Spectrum Disorders

Por O’Connor, Mary J., Portnoff, Larissa C., Lebsack-Coleman, Michael, Dipple, Katrina M.
Publicado no Birth Defects Res (2019)

Gestational diabetes associated with a novel mutation (378–379insTT) in the glycerol kinase gene

Por Zhang, Yao H., Van Hove, Johan L., McCabe, Edward R.B., Dipple, Katrina M.
Publicado no Mol Genet Metab Rep (2015)

Modeling craniofacial and skeletal congenital birth defects to advance therapies

Por Neben, Cynthia L., Roberts, Ryan R., Dipple, Katrina M., Merrill, Amy E., Klein, Ophir D.
Publicado no Hum Mol Genet (2016)

Single-Gene Disorders: What Role Could Moonlighting Enzymes Play?

Por Sriram, Ganesh, Martinez, Julian A., McCabe, Edward R. B., Liao, James C., Dipple, Katrina M.
Publicado em 2005

Resistance to Diet-Induced Obesity in Mice with Synthetic Glyoxylate Shunt

Por Dean, Jason T., Tran, Linh, Beaven, Simon, Tontonoz, Peter, Reue, Karen, Dipple, Katrina M., Liao, James C.
Publicado no Cell Metab (2009)

Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndrome

Por Yazdani, Shahram, Badjatiya, Anish, Dorrani, Naghmeh, Lee, Hane, Grody, Wayne W., Nelson, Stanley F., Dipple, Katrina M.
Publicado no Mol Genet Metab Rep (2020)

Global Metabolic Effects of Glycerol Kinase Overexpression in Rat Hepatoma Cells

Por Sriram, Ganesh, Rahib, Lola, He, Jian-Sen, Campos, Allison E., Parr, Lilly S., Liao, James C., Dipple, Katrina M.
Publicado em 2007

Development of catecholamine and cortisol stress responses in zebrafish()()

Por Eto, Kaoru, Mazilu-Brown, Jaime K., Henderson-MacLennan, Nicole, Dipple, Katrina M., McCabe, Edward R.B.
Publicado no Mol Genet Metab Rep (2014)

Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders

Por Lee, Hane, Deignan, Joshua L., Dorrani, Naghmeh, Strom, Samuel P., Kantarci, Sibel, Quintero-Rivera, Fabiola, Das, Kingshuk, Toy, Traci, Harry, Bret, Yourshaw, Michael, Fox, Michelle, Fogel, Brent L., Martinez-Agosto, Julian A., Wong, Derek A., Chang, Vivian Y., Shieh, Perry B., Palmer, Christina G. S., Dipple, Katrina M., Grody, Wayne W., Vilain, Eric, Nelson, Stanley F.
Publicado no JAMA (2014)

The Impact of Rapid Exome Sequencing on Medical Management of Critically Ill Children

Por Freed, Amanda S., Candadai, Sarah V. Clowes, Sikes, Megan C., Thies, Jenny, Byers, Heather M., Dines, Jennifer N., Ndugga-Kabuye, Mesaki Kenneth, Smith, Mallory B., Fogus, Katie, Mefford, Heather C., Lam, Christina, Adam, Margaret P., Sun, Angela, McGuire, John K., DiGeronimo, Robert, Dipple, Katrina M., Deutsch, Gail H., Billimoria, Zeenia C., Bennett, James T.
Publicado no J Pediatr (2020)

Validation of Candidate Causal Genes for Abdominal Obesity Which Affect Shared Metabolic Pathways and Networks

Por Yang, Xia, Deignan, Joshua L., Qi, Hongxiu, Zhu, Jun, Qian, Su, Zhong, Judy, Torosyan, Gevork, Majid, Sana, Falkard, Brie, Kleinhanz, Robert R., Karlsson, Jenny, Castellani, Lawrence W., Mumick, Sheena, Wang, Kai, Xie, Tao, Coon, Michael, Zhang, Chunsheng, Estrada-Smith, Daria, Farber, Charles R., Wang, Susanna S., Van Nas, Atila, Ghazalpour, Anatole, Zhang, Bin, MacNeil, Douglas J., Lamb, John R., Dipple, Katrina M., Reitman, Marc L., Mehrabian, Margarete, Lum, Pek Y., Schadt, Eric E., Lusis, Aldons J., Drake, Thomas A.
Publicado em 2009

Mandibulofacial Dysostosis with Microcephaly: Mutation and Database Update

Por Huang, Lijia, Vanstone, Megan R., Hartley, Taila, Osmond, Matthew, Barrowman, Nick, Allanson, Judith, Baker, Laura, Dabir, Tabib A., Dipple, Katrina M., Dobyns, William B., Estrella, Jane, Faghfoury, Hanna, Favaro, Francine P., Goel, Himanshu, Gregersen, Pernille A., Gripp, Karen W., Grix, Art, Guion-Almeida, Maria-Leine, Harr, Margaret H., Hudson, Cindy, Hunter, Alasdair G.W., Johnson, John, Joss, Shelagh K., Kimball, Amy, Kini, Usha, Kline, Antonie D., Lauzon, Julie, Lildballe, Dorte L., López-González, Vanesa, Martinezmoles, Johanna, Meldrum, Cliff, Mirzaa, Ghayda M., Morel, Chantal F., Morton, Jenny E.V., Pyle, Louise C., Quintero-Rivera, Fabiola, Richer, Julie, Scheuerle, Angela E., Schönewolf-Greulich, Bitten, Shears, Deborah J., Silver, Josh, Smith, Amanda C., Temple, I. Karen, van de Kamp, Jiddeke M., van Dijk, Fleur S., Vandersteen, Anthony M., White, Sue M., Zackai, Elaine H., Zou, Ruobing, Bulman, Dennis E., Boycott, Kym M., Lines, Matthew A.
Publicado no Hum Mutat (2015)