The Role of DNA Methylation in Regulation of the Murine Lhx3 Gene

Por Malik, Raleigh E., Rhodes, Simon J.
Publicado em 2013

Identification and expression of Hop, an atypical homeobox gene expressed late in lens fiber cell terminal differentiation

Por Vasiliev, Oleg, Rhodes, Simon J., Beebe, David C.
Publicado em 2007

A Distal Modular Enhancer Complex Acts to Control Pituitary- and Nervous System-Specific Expression of the LHX3 Regulatory Gene

Por Mullen, Rachel D., Park, Soyoung, Rhodes, Simon J.
Publicado em 2012

Cell-Specific Actions of a Human LHX3 Gene Enhancer During Pituitary and Spinal Cord Development

Por Park, Soyoung, Mullen, Rachel D., Rhodes, Simon J.
Publicado em 2013

BMP7 and SHH Regulate Pax2 in Mouse Retinal Astrocytes by Relieving TLX Repression

Por Sehgal, Rachna, Sheibani, Nader, Rhodes, Simon J, Adams, Teri L Belecky
Publicado em 2009

LHX3 Interacts with Inhibitor of Histone Acetyltransferase Complex Subunits LANP and TAF-1β to Modulate Pituitary Gene Regulation

Por Hunter, Chad S., Malik, Raleigh E., Witzmann, Frank A., Rhodes, Simon J.
Publicado em 2013

Model of pediatric pituitary hormone deficiency separates the endocrine and neural functions of the LHX3 transcription factor in vivo

Por Colvin, Stephanie C., Malik, Raleigh E., Showalter, Aaron D., Sloop, Kyle W., Rhodes, Simon J.
Publicado em 2011

Developmental Analysis and Influence of Genetic Background on the Lhx3 W227ter Mouse Model of Combined Pituitary Hormone Deficiency Disease

Por Prince, Kelly L., Colvin, Stephanie C., Park, Soyoung, Lai, Xianyin, Witzmann, Frank A., Rhodes, Simon J.
Publicado em 2013

Mutations in the LHX3 gene cause dysregulation of pituitary and neural target genes that reflect patient phenotypes

Por Savage, Jesse J., Hunter, Chad S., Clark-Sturm, Surilda L., Jacob, Tanya M., Pfaeffle, Roland W., Rhodes, Simon J.
Publicado em 2007

A Recessive Mutation Resulting in a Disabling Amino Acid Substitution (T194R) in the LHX3 Homeodomain Causes Combined Pituitary Hormone Deficiency

Por Bechtold-Dalla Pozza, Susanne, Hiedl, Stefan, Roeb, Julia, Lohse, Peter, Malik, Raleigh E., Park, Soyoung, Durán-Prado, Mario, Rhodes, Simon J.
Publicado em 2012

Identification of the Single Base Change Causing the Callipyge Muscle Hypertrophy Phenotype, the Only Known Example of Polar Overdominance in Mammals

Por Freking, Brad A., Murphy, Susan K., Wylie, Andrew A., Rhodes, Simon J., Keele, John W., Leymaster, Kreg A., Jirtle, Randy L., Smith, Timothy P.L.
Publicado em 2002

Roles of the LHX3 and LHX4 LIM-Homeodomain Factors in Pituitary Development

Por Mullen, Rachel D., Colvin, Stephanie C., Hunter, Chad S., Savage, Jesse J., Walvoord, Emily C., Bhangoo, Amrit P.S., Ten, Svetlana, Weigel, Johannes, Pfäffle, Roland W., Rhodes, Simon J.
Publicado em 2007

Phosphatase of Regenerating Liver 2 (PRL2) Is Essential for Placental Development by Down-regulating PTEN (Phosphatase and Tensin Homologue Deleted on Chromosome 10) and Activating...

Por Dong, Yuanshu, Zhang, Lujuan, Zhang, Sheng, Bai, Yunpeng, Chen, Hanying, Sun, Xiaoxin, Yong, Weidong, Li, Wei, Colvin, Stephanie C., Rhodes, Simon J., Shou, Weinian, Zhang, Zhong-Yin
Publicado em 2012

Comparative genomics reveals functional transcriptional control sequences in the Prop1 gene

Por Ward, Robert D., Davis, Shannon W., Cho, MinChul, Esposito, Constance, Lyons, Robert H., Cheng, Jan-Fang, Rubin, Edward M., Rhodes, Simon J., Raetzman, Lori T., Smith, Timothy P. L., Camper, Sally A.
Publicado em 2007

Three Novel Missense Mutations within the LHX4 Gene Are Associated with Variable Pituitary Hormone Deficiencies

Por Pfaeffle, Roland W., Hunter, Chad S., Savage, Jesse J., Duran-Prado, Mario, Mullen, Rachel D., Neeb, Zachary P., Eiholzer, Urs, Hesse, Volker, Haddad, Nadine G., Stobbe, Heike M., Blum, Werner F., Weigel, Johannes F. W., Rhodes, Simon J.
Publicado em 2008

The Transcription Factor Encyclopedia

Por Yusuf, Dimas, Butland, Stefanie L, Swanson, Magdalena I, Bolotin, Eugene, Ticoll, Amy, Cheung, Warren A, Cindy Zhang, Xiao Yu, Dickman, Christopher TD, Fulton, Debra L, Lim, Jonathan S, Schnabl, Jake M, Ramos, Oscar HP, Vasseur-Cognet, Mireille, de Leeuw, Charles N, Simpson, Elizabeth M, Ryffel, Gerhart U, Lam, Eric W-F, Kist, Ralf, Wilson, Miranda SC, Marco-Ferreres, Raquel, Brosens, Jan J, Beccari, Leonardo L, Bovolenta, Paola, Benayoun, Bérénice A, Monteiro, Lara J, Schwenen, Helma DC, Grontved, Lars, Wederell, Elizabeth, Mandrup, Susanne, Veitia, Reiner A, Chakravarthy, Harini, Hoodless, Pamela A, Mancarelli, M Michela, Torbett, Bruce E, Banham, Alison H, Reddy, Sekhar P, Cullum, Rebecca L, Liedtke, Michaela, Tschan, Mario P, Vaz, Michelle, Rizzino, Angie, Zannini, Mariastella, Frietze, Seth, Farnham, Peggy J, Eijkelenboom, Astrid, Brown, Philip J, Laperrière, David, Leprince, Dominique, de Cristofaro, Tiziana, Prince, Kelly L, Putker, Marrit, del Peso, Luis, Camenisch, Gieri, Wenger, Roland H, Mikula, Michal, Rozendaal, Marieke, Mader, Sylvie, Ostrowski, Jerzy, Rhodes, Simon J, Van Rechem, Capucine, Boulay, Gaylor, Olechnowicz, Sam WZ, Breslin, Mary B, Lan, Michael S, Nanan, Kyster K, Wegner, Michael, Hou, Juan, Mullen, Rachel D, Colvin, Stephanie C, Noy, Peter John, Webb, Carol F, Witek, Matthew E, Ferrell, Scott, Daniel, Juliet M, Park, Jason, Waldman, Scott A, Peet, Daniel J, Taggart, Michael, Jayaraman, Padma-Sheela, Karrich, Julien J, Blom, Bianca, Vesuna, Farhad, O'Geen, Henriette, Sun, Yunfu, Gronostajski, Richard M, Woodcroft, Mark W, Hough, Margaret R, Chen, Edwin, Europe-Finner, G Nicholas, Karolczak-Bayatti, Magdalena, Bailey, Jarrod, Hankinson, Oliver, Raman, Venu, LeBrun, David P, Biswal, Shyam, Harvey, Christopher J, DeBruyne, Jason P, Hogenesch, John B, Hevner, Robert F, Héligon, Christophe, Luo, Xin M, Blank, Marissa Cathleen, Millen, Kathleen Joyce, Sharlin, David S, Forrest, Douglas, Dahlman-Wright, Karin, Zhao, Chunyan, Mishima, Yuriko, Sinha, Satrajit, Chakrabarti, Rumela, Portales-Casamar, Elodie, Sladek, Frances M, Bradley, Philip H, Wasserman, Wyeth W
Publicado em 2012