Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear
Burns, Joseph C., Kelly, Michael C., Hoa, Michael, Morell, Robert J., Kelley, Matthew W.
Published in Nature communications (15.10.2015)
Published in Nature communications (15.10.2015)
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Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea
Gu, Shoujun, Olszewski, Rafal, Taukulis, Ian, Wei, Zheng, Martin, Daniel, Morell, Robert J., Hoa, Michael
Published in Scientific reports (22.10.2020)
Published in Scientific reports (22.10.2020)
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A comparative analysis of library prep approaches for sequencing low input translatome samples
Song, Yang, Milon, Beatrice, Ott, Sandra, Zhao, Xuechu, Sadzewicz, Lisa, Shetty, Amol, Boger, Erich T, Tallon, Luke J, Morell, Robert J, Mahurkar, Anup, Hertzano, Ronna
Published in BMC genomics (21.09.2018)
Published in BMC genomics (21.09.2018)
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Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease
Jenkinson, Emma M., Rehman, Atteeq U., Walsh, Tom, Clayton-Smith, Jill, Lee, Kwanghyuk, Morell, Robert J., Drummond, Meghan C., Khan, Shaheen N., Naeem, Muhammad Asif, Rauf, Bushra, Billington, Neil, Schultz, Julie M., Urquhart, Jill E., Lee, Ming K., Berry, Andrew, Hanley, Neil A., Mehta, Sarju, Cilliers, Deirdre, Clayton, Peter E., Kingston, Helen, Smith, Miriam J., Warner, Thomas T., Black, Graeme C., Trump, Dorothy, Davis, Julian R.E., Ahmad, Wasim, Leal, Suzanne M., Riazuddin, Sheikh, King, Mary-Claire, Friedman, Thomas B., Newman, William G.
Published in American journal of human genetics (04.04.2013)
Published in American journal of human genetics (04.04.2013)
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Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis
Korrapati, Soumya, Taukulis, Ian, Olszewski, Rafal, Pyle, Madeline, Gu, Shoujun, Singh, Riya, Griffiths, Carla, Martin, Daniel, Boger, Erich, Morell, Robert J, Hoa, Michael
Published in Frontiers in molecular neuroscience (20.12.2019)
Published in Frontiers in molecular neuroscience (20.12.2019)
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Journal Article
Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouse
Fan, Jianguo, Jia, Li, Li, Yan, Ebrahim, Seham, May-Simera, Helen, Wood, Alynda, Morell, Robert J., Liu, Pinghu, Lei, Jingqi, Kachar, Bechara, Belluscio, Leonardo, Qian, Haohua, Li, Tiansen, Li, Wei, Wistow, Graeme, Dong, Lijin
Published in Proceedings of the National Academy of Sciences - PNAS (23.05.2017)
Published in Proceedings of the National Academy of Sciences - PNAS (23.05.2017)
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Journal Article
Defects in the Alternative Splicing-Dependent Regulation of REST Cause Deafness
Nakano, Yoko, Kelly, Michael C., Rehman, Atteeq U., Boger, Erich T., Morell, Robert J., Kelley, Matthew W., Friedman, Thomas B., Bánfi, Botond
Published in Cell (26.07.2018)
Published in Cell (26.07.2018)
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Journal Article
Modifier variant of METTL13 suppresses human GAB1-associated profound deafness
Yousaf, Rizwan, Ahmed, Zubair M, Giese, Arnaud Pj, Morell, Robert J, Lagziel, Ayala, Dabdoub, Alain, Wilcox, Edward R, Riazuddin, Sheikh, Friedman, Thomas B, Riazuddin, Saima
Published in The Journal of clinical investigation (01.04.2018)
Published in The Journal of clinical investigation (01.04.2018)
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Journal Article
Homozygous novel truncating variant of CLPP associated with severe Perrault syndrome
Faridi, Rabia, Stratton, Pamela, Salmeri, Noemi, Morell, Robert J, Khan, Asma Ali, Usmani, Muhammad A, Newman, William G, Riazuddin, Sheikh, Friedman, Thomas B
Published in Clinical genetics (01.05.2024)
Published in Clinical genetics (01.05.2024)
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TGF-β uncouples glycolysis and inflammation in macrophages and controls survival during sepsis
Gauthier, Thierry, Yao, Chen, Dowdy, Tyrone, Jin, Wenwen, Lim, Yun-Ji, Patiño, Liliana C, Liu, Na, Ohlemacher, Shannon I, Bynum, Andrew, Kazmi, Rida, Bewley, Carole A, Mitrovic, Mladen, Martin, Daniel, Morell, Robert J, Eckhaus, Michael, Larion, Mioara, Tussiwand, Roxane, O'Shea, John J, Chen, WanJun
Published in Science signaling (08.08.2023)
Published in Science signaling (08.08.2023)
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G protein–coupled receptor Gpr115 (Adgrf4) is required for enamel mineralization mediated by ameloblasts
Chiba, Yuta, Yoshizaki, Keigo, Saito, Kan, Ikeuchi, Tomoko, Iwamoto, Tsutomu, Rhodes, Craig, Nakamura, Takashi, de Vega, Susana, Morell, Robert J., Boger, Erich T., Martin, Daniel, Hino, Ryoko, Inuzuka, Hiroyuki, Bleck, Christopher K.E., Yamada, Aya, Yamada, Yoshihiko, Fukumoto, Satoshi
Published in The Journal of biological chemistry (06.11.2020)
Published in The Journal of biological chemistry (06.11.2020)
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Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyndromic Deafness DFNB39
Morell, Robert J, Olszewski, Rafal, Tona, Risa, Leitess, Samuel, Wafa, Talah T, Taukulis, Ian, Schultz, Julie M, Thomason, Elizabeth J, Richards, Keri, Whitley, Brittany N, Hill, Connor, Saunders, Thomas, Starost, Matthew F, Fitzgerald, Tracy, Wilson, Elizabeth, Ohyama, Takahiro, Friedman, Thomas B, Hoa, Michael
Published in The Journal of neuroscience (08.04.2020)
Published in The Journal of neuroscience (08.04.2020)
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Journal Article
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct
Roux, Isabelle, Fenollar-Ferrer, Cristina, Lee, Hyun Jae, Chattaraj, Parna, Lopez, Ivan A., Han, Kyungreem, Honda, Keiji, Brewer, Carmen C., Butman, John A., Morell, Robert J., Martin, Donna M., Griffith, Andrew J.
Published in Human genetics (01.10.2023)
Published in Human genetics (01.10.2023)
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Journal Article
Single-Cell RNA-Sequencing From Mouse Incisor Reveals Dental Epithelial Cell-Type Specific Genes
Chiba, Yuta, Saito, Kan, Martin, Daniel, Boger, Erich T, Rhodes, Craig, Yoshizaki, Keigo, Nakamura, Takashi, Yamada, Aya, Morell, Robert J, Yamada, Yoshihiko, Fukumoto, Satoshi
Published in Frontiers in cell and developmental biology (01.09.2020)
Published in Frontiers in cell and developmental biology (01.09.2020)
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Targeted Capture and Next-Generation Sequencing Identifies C9orf75, Encoding Taperin, as the Mutated Gene in Nonsyndromic Deafness DFNB79
Rehman, Atteeq Ur, Morell, Robert J., Belyantseva, Inna A., Khan, Shahid Y., Boger, Erich T., Shahzad, Mohsin, Ahmed, Zubair M., Riazuddin, Saima, Khan, Shaheen N., Riazuddin, Sheikh, Friedman, Thomas B.
Published in American journal of human genetics (12.03.2010)
Published in American journal of human genetics (12.03.2010)
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Journal Article
Mutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86
Rehman, Atteeq U., Santos-Cortez, Regie Lyn P., Morell, Robert J., Drummond, Meghan C., Ito, Taku, Lee, Kwanghyuk, Khan, Asma A., Basra, Muhammad Asim R., Wasif, Naveed, Ayub, Muhammad, Ali, Rana A., Raza, Syed I., Nickerson, Deborah A., Shendure, Jay, Bamshad, Michael, Riazuddin, Saima, Billington, Neil, Khan, Shaheen N., Friedman, Penelope L., Griffith, Andrew J., Ahmad, Wasim, Riazuddin, Sheikh, Leal, Suzanne M., Friedman, Thomas B.
Published in American journal of human genetics (02.01.2014)
Published in American journal of human genetics (02.01.2014)
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The phenotypic landscape of a Tbc1d24 mutant mouse includes convulsive seizures resembling human early infantile epileptic encephalopathy
Tona, Risa, Chen, Wenqian, Nakano, Yoko, Reyes, Laura D, Petralia, Ronald S, Wang, Ya-Xian, Starost, Matthew F, Wafa, Talah T, Morell, Robert J, Cravedi, Kevin D, du Hoffmann, Johann, Miyoshi, Takushi, Munasinghe, Jeeva P, Fitzgerald, Tracy S, Chudasama, Yogita, Omori, Koichi, Pierpaoli, Carlo, Banfi, Botond, Dong, Lijin, Belyantseva, Inna A, Friedman, Thomas B
Published in Human molecular genetics (01.05.2019)
Published in Human molecular genetics (01.05.2019)
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Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea
Hoa, Michael, Olszewski, Rafal, Li, Xiaoyi, Taukulis, Ian, Gu, Shoujun, DeTorres, Alvin, Lopez, Ivan A, Linthicum, Jr, Fred H, Ishiyama, Akira, Martin, Daniel, Morell, Robert J, Kelley, Matthew W
Published in Frontiers in molecular neuroscience (05.02.2020)
Published in Frontiers in molecular neuroscience (05.02.2020)
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