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

od Leitch, Carmen C., Zaghloul, Norann A.
Izdano 2014

In vivo evidence that truncated trkB.T1 participates in nociception

od Renn, Cynthia L, Leitch, Carmen C, Dorsey, Susan G
Izdano 2009

Basal body proteins regulate Notch signaling through endosomal trafficking

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

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

od Lodh, Sukanya, Hostelley, Timothy L., Leitch, Carmen C., O'Hare, Elizabeth A., Zaghloul, Norann A.
Izdano u Hum Mol Genet (2016)

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

od Badano, José L., Ansley, Stephen J., Leitch, Carmen C., Lewis, Richard Alan, Lupski, James R., Katsanis, Nicholas
Izdano 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

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

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

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

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

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

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

od 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
Izdano u Hum Mol Genet (2019)

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

od 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
Izdano 2010

Ciliopathy proteins regulate paracrine signaling by modulating proteasomal degradation of mediators

od 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
Izdano 2014

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

od 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.
Izdano 2008

TM6SF2 rs58542926 impacts lipid processing in liver and small intestine

od 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.
Izdano u Hepatology (2017)

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

od 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
Izdano u 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

od 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
Izdano 2007

RFX transcription factors are essential for hearing in mice

od 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
Izdano u Nat Commun (2015)

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

od 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.
Izdano u Nat Commun (2019)

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

od 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
Izdano u Clin Genet (2020)

Genetic deletion of trkB.T1 increases neuromuscular function

od 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.
Izdano 2012