BBS4 Is Necessary for Ciliary Localization of TrkB Receptor and Activation by BDNF

gan Leitch, Carmen C., Zaghloul, Norann A.
Cyhoeddwyd 2014

In vivo evidence that truncated trkB.T1 participates in nociception

gan Renn, Cynthia L, Leitch, Carmen C, Dorsey, Susan G
Cyhoeddwyd 2009

Basal body proteins regulate Notch signaling through endosomal trafficking

gan Leitch, Carmen C., Lodh, Sukanya, Prieto-Echagüe, Victoria, Badano, Jose L., Zaghloul, Norann A.
Cyhoeddwyd 2014

Differential effects on β-cell mass by disruption of Bardet–Biedl syndrome or Alstrom syndrome genes

gan Lodh, Sukanya, Hostelley, Timothy L., Leitch, Carmen C., O'Hare, Elizabeth A., Zaghloul, Norann A.
Cyhoeddwyd yn Hum Mol Genet (2016)

Identification of a Novel Bardet-Biedl Syndrome Protein, BBS7, That Shares Structural Features with BBS1 and BBS2

gan Badano, José L., Ansley, Stephen J., Leitch, Carmen C., Lewis, Richard Alan, Lupski, James R., Katsanis, Nicholas
Cyhoeddwyd 2003

Genome-Wide Screen Identifies Drug-Induced Regulation of the Gene Giant Axonal Neuropathy (Gan) in a Mouse Model of Antiretroviral-Induced Painful Peripheral Neuropathy

gan Dorsey, Susan G., Leitch, Carmen C., Renn, Cynthia L., Lessans, Sherrie, Smith, Barbara A., Wang, Xiao M., Dionne, Raymond A.
Cyhoeddwyd 2009

Exocrine pancreas proteases regulate β-cell proliferation in zebrafish ciliopathy models and in murine systems

gan Hostelley, Timothy L., Nesmith, Jessica E., Larkin, Emily, Jones, Amanda, Boyes, Daniel, Leitch, Carmen C., Fontaine, Magali, Zaghloul, Norann A.
Cyhoeddwyd yn Biol Open (2021)

Survey of Human Chromosome 21 Gene Expression Effects on Early Development in Danio rerio

gan Edie, Sarah, Zaghloul, Norann A., Leitch, Carmen C., Klinedinst, Donna K., Lebron, Janette, Thole, Joey F., McCallion, Andrew S., Katsanis, Nicholas, Reeves, Roger H.
Cyhoeddwyd yn G3 (Bethesda) (2018)

Genomic knockout of alms1 in zebrafish recapitulates Alström syndrome and provides insight into metabolic phenotypes

gan Nesmith, Jessica E, Hostelley, Timothy L, Leitch, Carmen C, Matern, Maggie S, Sethna, Saumil, McFarland, Rebecca, Lodh, Sukanya, Westlake, Christopher J, Hertzano, Ronna, Ahmed, Zubair M, Zaghloul, Norann A
Cyhoeddwyd yn Hum Mol Genet (2019)

Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet–Biedl syndrome

gan Zaghloul, Norann A., Liu, Yangjian, Gerdes, Jantje M., Gascue, Cecilia, Oh, Edwin C., Leitch, Carmen C., Bromberg, Yana, Binkley, Jonathan, Leibel, Rudolph L., Sidow, Arend, Badano, Jose L., Katsanis, Nicholas
Cyhoeddwyd 2010

Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators

gan Liu, Yangfan P., Tsai, I-Chun, Morleo, Manuela, Oh, Edwin C., Leitch, Carmen C., Massa, Filomena, Lee, Byung-Hoon, Parker, David S., Finley, Daniel, Zaghloul, Norann A., Franco, Brunella, Katsanis, Nicholas
Cyhoeddwyd 2014

An Essential Role for DYF-11/MIP-T3 in Assembling Functional Intraflagellar Transport Complexes

gan Li, Chunmei, Inglis, Peter N., Leitch, Carmen C., Efimenko, Evgeni, Zaghloul, Norann A., Mok, Calvin A., Davis, Erica E., Bialas, Nathan J., Healey, Michael P., Héon, Elise, Zhen, Mei, Swoboda, Peter, Katsanis, Nicholas, Leroux, Michel R.
Cyhoeddwyd 2008

TM6SF2 rs58542926 impacts lipid processing in liver and small intestine

gan O’Hare, Elizabeth A., Yang, Rongze, Yerges-Armstrong, Laura, Sreenivasan, Urmilla, McFarland, Rebecca, Leitch, Carmen C., Wilson, Meredith H., Narina, Shilpa, Gorden, Alexis, Ryan, Kathy, Shuldiner, Alan R., Farber, Steve A., Wood, G. Craig, Still, Christopher D., Gerhard, Glenn S., Robishaw, Janet D., Sztalryd, Carole, Zaghloul, Norann A.
Cyhoeddwyd yn Hepatology (2017)

FOXE3 contributes to Peters anomaly through transcriptional regulation of an autophagy-associated protein termed DNAJB1

gan Khan, Shahid Y., Vasanth, Shivakumar, Kabir, Firoz, Gottsch, John D., Khan, Arif O., Chaerkady, Raghothama, Lee, Mei-Chong W., Leitch, Carmen C., Ma, Zhiwei, Laux, Julie, Villasmil, Rafael, Khan, Shaheen N., Riazuddin, Sheikh, Akram, Javed, Cole, Robert N., Talbot, C. Conover, Pourmand, Nader, Zaghloul, Norann A., Hejtmancik, J. Fielding, Riazuddin, S. Amer
Cyhoeddwyd yn Nat Commun (2016)

Identification of a Novel BBS Gene (BBS12) Highlights the Major Role of a Vertebrate-Specific Branch of Chaperonin-Related Proteins in Bardet-Biedl Syndrome

gan Stoetzel, Corinne, Muller, Jean, Laurier, Virginie, Davis, Erica E., Zaghloul, Norann A., Vicaire, Serge, Jacquelin, Cécile, Plewniak, Frédéric, Leitch, Carmen C., Sarda, Pierre, Hamel, Christian, de Ravel, Thomy J. L., Lewis, Richard Alan, Friederich, Evelyne, Thibault, Christelle, Danse, Jean-Marc, Verloes, Alain, Bonneau, Dominique, Katsanis, Nicholas, Poch, Olivier, Mandel, Jean-Louis, Dollfus, Hélène
Cyhoeddwyd 2007

RFX transcription factors are essential for hearing in mice

gan Elkon, Ran, Milon, Beatrice, Morrison, Laura, Shah, Manan, Vijayakumar, Sarath, Racherla, Manoj, Leitch, Carmen C., Silipino, Lorna, Hadi, Shadan, Weiss-Gayet, Michèle, Barras, Emmanuèle, Schmid, Christoph D., Ait-Lounis, Aouatef, Barnes, Ashley, Song, Yang, Eisenman, David J., Eliyahu, Efrat, Frolenkov, Gregory I., Strome, Scott E., Durand, Bénédicte, Zaghloul, Norann A., Jones, Sherri M., Reith, Walter, Hertzano, Ronna
Cyhoeddwyd yn Nat Commun (2015)

ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response

gan Adeyemo, Adebowale A., Zaghloul, Norann A., Chen, Guanjie, Doumatey, Ayo P., Leitch, Carmen C., Hostelley, Timothy L., Nesmith, Jessica E., Zhou, Jie, Bentley, Amy R., Shriner, Daniel, Fasanmade, Olufemi, Okafor, Godfrey, Eghan, Benjamin, Agyenim-Boateng, Kofi, Chandrasekharappa, Settara, Adeleye, Jokotade, Balogun, William, Owusu, Samuel, Amoah, Albert, Acheampong, Joseph, Johnson, Thomas, Oli, Johnnie, Adebamowo, Clement, Collins, Francis, Dunston, Georgia, Rotimi, Charles N.
Cyhoeddwyd yn Nat Commun (2019)

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet-Biedl syndrome

gan Delvallée, Clarisse, Nicaise, Samuel, Antin, Manuela, Leuvrey, Anne-Sophie, Nourisson, Elsa, Leitch, Carmen C., Kellaris, Georgios, Stoetzel, Corinne, Geoffroy, Véronique, Scheidecker, Sophie, Keren, Boris, Depienne, Christel, Klar, Joakim, Dahl, Niklas, Deleuze, Jean-François, Génin, Emmanuelle, Redon, Richard, Demurger, Florence, Devriendt, Koenraad, Mathieu-Dramard, Michèle, Poitou-Bernert, Christine, Odent, Sylvie, Katsanis, Nicholas, Mandel, Jean-Louis, Davis, Erica E., Dollfus, Hélène, Muller, Jean
Cyhoeddwyd yn Clin Genet (2020)

Genetic deletion of trkB.T1 increases neuromuscular function

gan Dorsey, Susan G., Lovering, Richard M., Renn, Cynthia L., Leitch, Carmen C., Liu, Xinyue, Tallon, Luke J., Sadzewicz, Lisa DeShong, Pratap, Abhishek, Ott, Sandra, Sengamalay, Naomi, Jones, Kristie M., Barrick, Colleen, Fulgenzi, Gianluca, Becker, Jodi, Voelker, Kevin, Talmadge, Robert, Harvey, Brandon K., Wyatt, Ryan M., Vernon-Pitts, Elizabeth, Zhang, Chao, Shokat, Kevan, Fraser-Liggett, Claire, Balice-Gordon, Rita J., Tessarollo, Lino, Ward, Christopher W.
Cyhoeddwyd 2012