3D spheroid defects in NPHP knockdown cells are rescued by the somatostatin receptor agonist octreotide

Por Ghosh, Amiya K., Hurd, Toby, Hildebrandt, Friedhelm
Publicado em 2012

An essential role of ubiquitination in Cbl-mediated negative regulation of the Src-family kinase Fyn

Por Rao, Navin, Ghosh, Amiya K., Douillard, Patrice, Andoniou, Christopher E., Zhou, Pengcheng, Band, Hamid
Publicado em 2002

Functional Analysis of Retinitis Pigmentosa 2 (RP2) Protein Reveals Variable Pathogenic Potential of Disease-Associated Missense Variants

Por Patil, Suresh B., Hurd, Toby W., Ghosh, Amiya K., Murga-Zamalloa, Carlos A., Khanna, Hemant
Publicado em 2011

Human retinopathy-associated ciliary protein retinitis pigmentosa GTPase regulator mediates cilia-dependent vertebrate development

Por Ghosh, Amiya K., Murga-Zamalloa, Carlos A., Chan, Lansze, Hitchcock, Peter F., Swaroop, Anand, Khanna, Hemant
Publicado em 2010

The non-receptor tyrosine kinase Syk is a target of Cbl-mediated ubiquitylation upon B-cell receptor stimulation

Por Rao, Navin, Ghosh, Amiya K., Ota, Satoshi, Zhou, Pengcheng, Reddi, Alagarsamy Lakku, Hakezi, Kaoru, Druker, Brian K., Wu, Jiong, Band, Hamid
Publicado em 2001

Negative regulation of Lck by Cbl ubiquitin ligase

Por Rao, Navin, Miyake, Sachiko, Reddi, Alagarsamy Lakku, Douillard, Patrice, Ghosh, Amiya K., Dodge, Ingrid L., Zhou, Pengcheng, Fernandes, Norvin D., Band, Hamid
Publicado em 2002

Accumulation of the Raf-1 Kinase Inhibitory Protein (Rkip) Is Associated with Cep290-mediated Photoreceptor Degeneration in Ciliopathies

Por Murga-Zamalloa, Carlos A., Ghosh, Amiya K., Patil, Suresh B., Reed, Nathan A., Chan, Lan Sze, Davuluri, Supriya, Peränen, Johan, Hurd, Toby W., Rachel, Rivka A., Khanna, Hemant
Publicado em 2011

Nephronophthisis-Associated CEP164 Regulates Cell Cycle Progression, Apoptosis and Epithelial-to-Mesenchymal Transition

Por Slaats, Gisela G., Ghosh, Amiya K., Falke, Lucas L., Le Corre, Stéphanie, Shaltiel, Indra A., van de Hoek, Glenn, Klasson, Timothy D., Stokman, Marijn F., Logister, Ive, Verhaar, Marianne C., Goldschmeding, Roel, Nguyen, Tri Q., Drummond, Iain A., Hildebrandt, Friedhelm, Giles, Rachel H.
Publicado em 2014

Mutation Analysis of 18 Nephronophthisis-associated Ciliopathy Disease Genes using a DNA Pooling and Next-Generation Sequencing Strategy

Por Otto, Edgar A., Ramaswami, Gokul, Janssen, Sabine, Chaki, Moumita, Allen, Susan J., Zhou, Weibin, Airik, Rannar, Hurd, Toby W., Ghosh, Amiya K., Wolf, Matthias T., Hoppe, Bernd, Neuhaus, Thomas J., Bockenhauer, Detlef, Milford, David V., Soliman, Neveen A., Saunier, Sophie, Johnson, Colin A., Hildebrandt, Friedhelm
Publicado em 2010

FAN1 mutations cause karyomegalic interstitial nephritis, linking chronic kidney failure to defective DNA damage repair

Por Zhou, Weibin, Otto, Edgar A., Cluckey, Andrew, Airik, Rannar, Hurd, Toby W., Chaki, Moumita, Diaz, Katrina, Lach, Francis P., Bennett, Geoffrey R., Gee, Heon Y., Ghosh, Amiya K., Natarajan, Sivakumar, Thongthip, Supawat, Veturi, Uma, Allen, Susan J., Janssen, Sabine, Ramaswami, Gokul, Dixon, Joanne, Burkhalter, Felix, Spoendlin, Martin, Moch, Holger, Mihatsch, Michael J., Verine, Jerome, Reade, Richard, Soliman, Hany, Godin, Michel, Kiss, Denes, Monga, Guido, Mazzucco, Gianna, Amann, Kerstin, Artunc, Ferruh, Newland, Ronald C., Wiech, Thorsten, Zschiedrich, Stefan, Huber, Tobias B., Friedl, Andreas, Slaats, Gisela G., Joles, Jaap A., Goldschmeding, Roel, Washburn, Joseph, Giles, Rachel H., Levy, Shawn, Smogorzewska, Agata, Hildebrandt, Friedhelm
Publicado em 2012

Candidate exome capture identifies mutation of SDCCAG8 as the cause of a retinal-renal ciliopathy

Por Otto, Edgar A., Hurd, Toby W., Airik, Rannar, Chaki, Moumita, Zhou, Weibin, Stoetzel, Corinne, Patil, Suresh B., Levy, Shawn, Ghosh, Amiya K., Murga-Zamalloa, Carlos A., van Reeuwijk, Jeroen, Letteboer, Stef J.F., Sang, Liyun, Giles, Rachel H., Liu, Qin, Coene, Karlien L. M., Estrada-Cuzcano, Alejandro, Collin, Rob W. J., McLaughlin, Heather M., Held, Susanne, Kasanuki, Jennifer M., Ramaswami, Gokul, Conte, Jinny, Lopez, Irma, Washburn, Joseph, MacDonald, James, Hu, Jinghua, Yamashita, Yukiko, Maher, Eamonn R., Guay-Woodford, Lisa, Neumann, Hartmut P.H., Obermüller, Nicholas, Koenekoop, Robert K., Bergmann, Carsten, Bei, Xiaoshu, Lewis, Richard A., Katsanis, Nicholas, Lopes, Vanda, Williams, David S., Lyons, Robert H., Dang, Chi V., Brito, Daniela A., Dias, Mónica Bettencourt, Zhang, Xinmin, Nürnberg, Gudrun, Nürnberg, Peter, Pierce, Eric, Jackson, Peter, Antignac, Corinne, Saunier, Sophie, Roepman, Ronald, Dollfus, Helene, Khanna, Hemant, Hildebrandt, Friedhelm
Publicado em 2010

Exome capture reveals ZNF423 and CEP164 mutations, linking renal ciliopathies to DNA damage response signaling

Por Chaki, Moumita, Airik, Rannar, Ghosh, Amiya K., Giles, Rachel H., Chen, Rui, Slaats, Gisela G., Wang, Hui, Hurd, Toby W., Zhou, Weibin, Cluckey, Andrew, Gee, Heon-Yung, Ramaswami, Gokul, Hong, Chen-Jei, Hamilton, Bruce A., Červenka, Igor, Ganji, Ranjani Sri, Bryja, Vitezslav, Arts, Heleen H., van Reeuwijk, Jeroen, Oud, Machteld M., Letteboer, Stef J.F., Roepman, Ronald, Husson, Hervé, Ibraghimov-Beskrovnaya, Oxana, Ysunaga, Takayuki, Walz, Gerd, Eley, Lorraine, Sayer, John A., Schermer, Bernhard, Liebau, Max C., Benzing, Thomas, Le Corre, Stephanie, Drummond, Iain, Joles, Jaap A., Janssen, Sabine, Allen, Susan J., Natarajan, Sivakumar, O Toole, John F., Attanasio, Massimo, Saunier, Sophie, Antignac, Corinne, Koenekoop, Robert K., Ren, Huanan, Lopez, Irma, Nayir, Ahmet, Stoetzel, Corinne, Dollfus, Helene, Massoudi, Rustin, Gleeson, Joseph G., Andreoli, Sharon P., Doherty, Dan G., Lindstrad, Anna, Golzio, Christelle, Katsanis, Nicholas, Pape, Lars, Abboud, Emad B., Al-Rajhi, Ali A., Lewis, Richard A., Lupski, James R., Omran, Heymut, Lee, Eva, Wang, Shaohui, Sekiguchi, JoAnn M., Saunders, Rudel, Johnson, Colin A., Garner, Elizabeth, Vanselow, Katja, Andersen, Jens S., Shlomai, Joseph, Nurnberg, Gudrun, Nurnberg, Peter, Levy, Shawn, Smogorzewska, Agata, Otto, Edgar A., Hildebrandt, Friedhelm
Publicado em 2012