Targeting collagen expression in alcoholic liver disease

Por Thompson, Kyle J, McKillop, Iain H, Schrum, Laura W
Publicado em 2011

Withaferin A Effectively Targets Soluble Vimentin in the Glaucoma Filtration Surgical Model of Fibrosis

Por Bargagna-Mohan, Paola, Deokule, Sunil P., Thompson, Kyle, Wizeman, John, Srinivasan, Cidambi, Vooturi, Sunil, Kompella, Uday B., Mohan, Royce
Publicado em 2013

Leptin inhibits hepatocellular carcinoma proliferation via p38-MAPK-dependent signalling

Por Thompson, Kyle J, Lau, Kwan N, Johnson, Sarah, Martinie, John B, Iannitti, David A, McKillop, Iain H, Sindram, David
Publicado em 2011

Microwave ablation using 915-MHz and 2.45-GHz systems: what are the differences?

Por Simo, Kerri A, Tsirline, Victor B, Sindram, David, McMillan, Matthew T, Thompson, Kyle J, Swan, Ryan Z, McKillop, Iain H, Martinie, John B, Iannitti, David A
Publicado em 2013

Dihydroceramide Desaturase Knockdown Impacts Sphingolipids and Apoptosis after Photodamage in Human Head and Neck Squamous Carcinoma Cells

Por BREEN, PAUL, JOSEPH, NICHOLAS, THOMPSON, KYLE, KRAVEKA, JACQUELINE M., GUDZ, TATYANA I., LI, LI, RAHMANIYAN, MEHRDAD, BIELAWSKI, JACEK, PIERCE, JASON S., VAN BUREN, ERIC, BHATTI, GAURAV, SEPAROVIC, DUSKA
Publicado em 2013

Synergistic Effects of Secretory Phospholipase A(2) from the Venom of Agkistrodon piscivorus piscivorus with Cancer Chemotherapeutic Agents

Por Nelson, Jennifer, Barlow, Kristen, Beck, D. Olin, Berbert, Amanda, Eshenroder, Nathan, Francom, Lyndee, Pruitt, Mark, Thompson, Kina, Thompson, Kyle, Thurber, Brian, Yeung, Celestine H.-Y., Judd, Allan M., Bell, John D.
Publicado em 2013

Altered lysophosphatidic acid (LPA) receptor expression during hepatic regeneration in a mouse model of partial hepatectomy

Por Simo, Kerri A, Niemeyer, David J, Hanna, Erin M, Swet, Jacob H, Thompson, Kyle J, Sindram, David, Iannitti, David A, Eheim, Ashley L, Sokolov, Eugene, Zuckerman, Valentina, McKillop, Iain H
Publicado em 2014

The Use of a Novel MUC1 Antibody to Identify Cancer Stem Cells and Circulating MUC1 in Mice and Patients With Pancreatic Cancer

Por CURRY, JENNIFER M., THOMPSON, KYLE J., RAO, SHANTI G., BESMER, DAHLIA M., MURPHY, ANDREA M., GRDZELISHVILI, VALERY Z., AHRENS, WILLIAM A., MCKILLOP, IAIN H., SINDRAM, DAVID, IANNITTI, DAVID A., MARTINIE, JOHN B., MUKHERJEE, PINKU
Publicado em 2013

Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

Por Brito, Sara, Thompson, Kyle, Campistol, Jaume, Colomer, Jaime, Hardy, Steven A., He, Langping, Fernández-Marmiesse, Ana, Palacios, Lourdes, Jou, Cristina, Jiménez-Mallebrera, Cecilia, Armstrong, Judith, Montero, Raquel, Artuch, Rafael, Tischner, Christin, Wenz, Tina, McFarland, Robert, Taylor, Robert W.
Publicado no Front Genet (2015)

Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

Por Brito, Sara, Thompson, Kyle, Campistol, Jaume, Colomer, Jaime, Hardy, Steven A., He, Langping, Fernández-Marmiesse, Ana, Palacios, Lourdes, Jou, Cristina, Jiménez-Mallebrera, Cecilia, Armstrong, Judith, Montero, Raquel, Artuch, Rafael, Tischner, Christin, Wenz, Tina, McFarland, Robert, Taylor, Robert W.
Publicado no Front Genet (2015)

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

Por Metodiev, Metodi D., Thompson, Kyle, Alston, Charlotte L., Morris, Andrew A.M., He, Langping, Assouline, Zarah, Rio, Marlène, Bahi-Buisson, Nadia, Pyle, Angela, Griffin, Helen, Siira, Stefan, Filipovska, Aleksandra, Munnich, Arnold, Chinnery, Patrick F., McFarland, Robert, Rötig, Agnès, Taylor, Robert W.
Publicado no Am J Hum Genet (2016)

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

Por Metodiev, Metodi D., Thompson, Kyle, Alston, Charlotte L., Morris, Andrew A.M., He, Langping, Assouline, Zarah, Rio, Marlène, Bahi-Buisson, Nadia, Pyle, Angela, Griffin, Helen, Siira, Stefan, Filipovska, Aleksandra, Munnich, Arnold, Chinnery, Patrick F., McFarland, Robert, Rötig, Agnès, Taylor, Robert W.
Publicado no Am J Hum Genet (2016)

Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduria

Por Oláhová, Monika, Thompson, Kyle, Hardy, Steven A., Barbosa, Inês A., Besse, Arnaud, Anagnostou, Maria-Eleni, White, Kathryn, Davey, Tracey, Simpson, Michael A., Champion, Michael, Enns, Greg, Schelley, Susan, Lightowlers, Robert N., Chrzanowska-Lightowlers, Zofia M. A., McFarland, Robert, Deshpande, Charu, Bonnen, Penelope E., Taylor, Robert W.
Publicado no J Inherit Metab Dis (2016)

Alcoholic and non-alcoholic steatohepatitis

Por Neuman, Manuela G., French, Samuel W., French, Barbara A., Seitz, Helmut K., Cohen, Lawrence B., Mueller, Sebastian, Osna, Natalia A., Kharbanda, Kusum K., Seth, Devanshi, Bautista, Abraham, Thompson, Kyle J., McKillop, Iain H., Kirpich, Irina A., McClain, Craig J., Bataller, Ramon, Nanau, Radu M., Voiculescu, Mihai, Opris, Mihai, Shen, Hong, Tillman, Brittany, Li, Jun, Liu, Hui, Thomas, Paul G., Ganesan, Murali, Malnick, Steve
Publicado no Exp Mol Pathol (2014)

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

Por Thompson, Kyle, Majd, Homa, Dallabona, Christina, Reinson, Karit, King, Martin S., Alston, Charlotte L., He, Langping, Lodi, Tiziana, Jones, Simon A., Fattal-Valevski, Aviva, Fraenkel, Nitay D., Saada, Ann, Haham, Alon, Isohanni, Pirjo, Vara, Roshni, Barbosa, Inês A., Simpson, Michael A., Deshpande, Charu, Puusepp, Sanna, Bonnen, Penelope E., Rodenburg, Richard J., Suomalainen, Anu, Õunap, Katrin, Elpeleg, Orly, Ferrero, Ileana, McFarland, Robert, Kunji, Edmund R.S., Taylor, Robert W.
Publicado no Am J Hum Genet (2016)

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

Por Thompson, Kyle, Majd, Homa, Dallabona, Cristina, Reinson, Karit, King, Martin S., Alston, Charlotte L., He, Langping, Lodi, Tiziana, Jones, Simon A., Fattal-Valevski, Aviva, Fraenkel, Nitay D., Saada, Ann, Haham, Alon, Isohanni, Pirjo, Vara, Roshni, Barbosa, Inês A., Simpson, Michael A., Deshpande, Charu, Puusepp, Sanna, Bonnen, Penelope E., Rodenburg, Richard J., Suomalainen, Anu, Õunap, Katrin, Elpeleg, Orly, Ferrero, Ileana, McFarland, Robert, Kunji, Edmund R.S., Taylor, Robert W.
Publicado no Am J Hum Genet (2016)