Disruption of planar cell polarity activity leads to developmental biliary defects

Por Cui, Shuang, Capecci, Louis M., Matthews, Randolph P.
Publicado em 2011

Interferon-Gamma Directly Mediates Developmental Biliary Defects

Por Cui, Shuang, EauClaire, Steven F., Matthews, Randolph P.
Publicado em 2013

p53-Mediated Biliary Defects Caused by Knockdown of cirh1a, the Zebrafish Homolog of the Gene Responsible for North American Indian Childhood Cirrhosis

Por Wilkins, Benjamin J., Lorent, Kristin, Matthews, Randolph P., Pack, Michael
Publicado em 2013

Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish

Por Tang, Vivian, Cofer, Zenobia C., Cui, Shuang, Sapp, Valerie, Loomes, Kathleen M., Matthews, Randolph P.
Publicado no J Pediatr Gastroenterol Nutr (2016)

The microRNA-30 family is required for vertebrate hepatobiliary development

Por Hand, Nicholas J., Master, Zankhana R., EauClaire, Steven F., Weinblatt, Daniel E., Matthews, Randolph P., Friedman, Joshua R.
Publicado em 2008

TNFα-dependent hepatic steatosis and liver degeneration caused by mutation of zebrafish s-adenosylhomocysteine hydrolase

Por Matthews, Randolph P., Lorent, Kristin, Mañoral-Mobias, Rafael, Huang, Yuehua, Gong, Weilong, Murray, Ian V. J., Blair, Ian A., Pack, Michael
Publicado em 2009

DNA hypomethylation causes bile duct defects in zebrafish and is a distinguishing feature of infantile biliary atresia

Por Matthews, Randolph P., EauClaire, Steven F., Mugnier, Monica, Lorent, Kristin, Cui, Shuang, Ross, Megan M., Zhang, Zhe, Russo, Pierre, Pack, Michael
Publicado em 2011

Methylation Microarray Studies Highlight PDGFA Expression as a Factor in Biliary Atresia

Por Cofer, Zenobia C., Cui, Shuang, EauClaire, Steven F., Kim, Cecilia, Tobias, John W., Hakonarson, Hakon, Loomes, Kathleen M., Matthews, Randolph P.
Publicado no PLoS One (2016)

CCBE1 Mutation in Two Siblings, One Manifesting Lymphedema-Cholestasis Syndrome, and the Other, Fetal Hydrops

Por Shah, Sohela, Conlin, Laura K., Gomez, Luis, Aagenaes, Øystein, Eiklid, Kristin, Knisely, A. S., Mennuti, Michael T., Matthews, Randolph P., Spinner, Nancy B., Bull, Laura N.
Publicado em 2013

Evidence From Human and Zebrafish That GPC1 Is a Biliary Atresia Susceptibility Gene

Por Cui, Shuang, Leyva-Vega, Melissa, Tsai, Ellen A., Eauclaire, Steven F., Glessner, Joseph T., Hakonarson, Hakon, Devoto, Marcella, Haber, Barbara A., Spinner, Nancy B., Matthews, Randolph P.
Publicado em 2013

Mutations in vacuolar H(+)-ATPase subunits lead to biliary developmental defects in zebrafish

Por EauClaire, Steven F., Cui, Shuang, Ma, Liyuan, Matous, James, Marlow, Florence L., Gupta, Tripti, Burgess, Harold A., Abrams, Elliott W., Kapp, Lee D., Granato, Michael, Mullins, Mary C., Matthews, Randolph P.
Publicado em 2012

Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization

Por Cullinane, Andrew R, Straatman-Iwanowska, Anna, Zaucker, Andreas, Wakabayashi, Yoshiyuki, Bruce, Christopher K, Luo, Guanmei, Rahman, Fatimah, Gürakan, Figen, Utine, Eda, Özkan, Tanju B, Denecke, Jonas, Vukovic, Jurica, Di Rocco, Maja, Mandel, Hanna, Cangul, Hakan, Matthews, Randolph P, Thomas, Steve G, Rappoport, Joshua Z, Arias, Irwin M, Wolburg, Hartwig, Knisely, A S, Kelly, Deirdre A, Müller, Ferenc, Maher, Eamonn R, Gissen, Paul
Publicado no Nat Genet (2010)