Spiral ganglion deficiency in adult-onset deafness-dystonia syndrome

por Hoa, Michael, Linthicum, Fred H.
Publicado em 2013

Applications of single‐cell sequencing for the field of otolaryngology: A contemporary review

por Pyle, Madeline P., Hoa, Michael
Publicado no Laryngoscope Investig Otolaryngol (2020)

Petrous Apex Cholesterol Granuloma: Maintenance of Drainage Pathway, the Histopathology of Surgical Management and Histopathologic Evidence for the Exposed Marrow Theory

por Hoa, Michael, House, John, Linthicum, Fred H.
Publicado em 2012

Surgical Management of Endolymphatic Sac Tumors

por Friedman, Rick A., Hoa, Michael, Brackmann, Derald E.
Publicado em 2012

Radiologic anatomy of the round window relevant to cochlear implantation and inner ear drug delivery

por Nguy, Peter L., Saidha, Sheela, Jay, Ann, Jeffrey Kim, H., Hoa, Michael
Publicado no World J Otorhinolaryngol Head Neck Surg (2020)

Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear

por Burns, Joseph C., Kelly, Michael C., Hoa, Michael, Morell, Robert J., Kelley, Matthew W.
Publicado no Nat Commun (2015)

Supporting Cell Survival After Cochlear Implant Surgery

por deTorres, Alvin, Olszewski, Rafal T., Lopez, Ivan A., Ishiyama, Akira, Linthicum, Fred, Hoa, Michael
Publicado no Laryngoscope (2018)

Characterization of rare spindle and root cell transcriptional profiles in the stria vascularis of the adult mouse cochlea

por Gu, Shoujun, Olszewski, Rafal, Taukulis, Ian, Wei, Zheng, Martin, Daniel, Morell, Robert J., Hoa, Michael
Publicado no Sci Rep (2020)

Identification of Potential Meniere's Disease Targets in the Adult Stria Vascularis

por Gu, Shoujun, Olszewski, Rafal, Nelson, Lacey, Gallego-Martinez, Alvaro, Lopez-Escamez, Jose Antonio, Hoa, Michael
Publicado no Front Neurol (2021)

Deafness and loss of cochlear hair cells in the absence of thyroid hormone transporters Slc16a2 (Mct8) and Slc16a10 (Mct10)

por Sharlin, David S., Ng, Lily, Verrey, François, Visser, Theo J., Liu, Ye, Olszewski, Rafal T., Hoa, Michael, Heuer, Heike, Forrest, Douglas
Publicado no Sci Rep (2018)

Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis

por Korrapati, Soumya, Taukulis, Ian, Olszewski, Rafal, Pyle, Madeline, Gu, Shoujun, Singh, Riya, Griffiths, Carla, Martin, Daniel, Boger, Erich, Morell, Robert J., Hoa, Michael
Publicado no Front Mol Neurosci (2019)

VEGFA165 gene therapy ameliorates blood-labyrinth barrier breakdown and hearing loss

por Zhang, Jinhui, Hou, Zhiqiang, Wang, Xiaohan, Jiang, Han, Neng, Lingling, Zhang, Yunpei, Yu, Qing, Burwood, George, Song, Junha, Auer, Manfred, Fridberger, Anders, Hoa, Michael, Shi, Xiaorui
Publicado no JCI Insight (2021)

Corrigendum: Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the...

por Hoa, Michael, Olszewski, Rafal, Li, Xiaoyi, Taukulis, Ian, Gu, Shoujun, DeTorres, Alvin, Lopez, Ivan A., Linthicum, Fred H., Ishiyama, Akira, Martin, Daniel, Morell, Robert J., Kelley, Matthew W.
Publicado no Front Mol Neurosci (2021)

Molecular architecture underlying fluid absorption by the developing inner ear

por Honda, Keiji, Kim, Sung Huhn, Kelly, Michael C, Burns, Joseph C, Constance, Laura, Li, Xiangming, Zhou, Fei, Hoa, Michael, Kelley, Matthew W, Wangemann, Philine, Morell, Robert J, Griffith, Andrew J
Publicado no eLife (2017)

Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human...

por 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.
Publicado no Front Mol Neurosci (2020)

Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness

por Tona, Risa, Lopez, Ivan A., Fenollar-Ferrer, Cristina, Faridi, Rabia, Anselmi, Claudio, Khan, Asma A., Shahzad, Mohsin, Morell, Robert J., Gu, Shoujun, Hoa, Michael, Dong, Lijin, Ishiyama, Akira, Belyantseva, Inna A., Riazuddin, Sheikh, Friedman, Thomas B.
Publicado no Genes (Basel) (2020)

Mutational and Phenotypic Spectra of KCNE1 deficiency in Jervell and Lange-Nielsen Syndrome and Romano-Ward Syndrome

por Faridi, Rabia, Tona, Risa, Brofferio, Alessandra, Hoa, Michael, Olszewski, Rafal, Schrauwen, Isabelle, Assir, Muhammad Z.K., Bandesha, Akhtar A., Khan, Asma A., Rehman, Atteeq U., Brewer, Carmen, Ahmed, Wasim, Leal, Suzanne M., Riazuddin, Sheikh, Boyden, Steven E., Friedman, Thomas B.
Publicado no Hum Mutat (2018)

Noncoding Microdeletion in Mouse Hgf Disrupts Neural Crest Migration into the Stria Vascularis, Reduces the Endocochlear Potential, and Suggests the Neuropathology for Human Nonsyn...

por 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
Publicado no J Neurosci (2020)

NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy

por Nakanishi, Hiroshi, Kawashima, Yoshiyuki, Kurima, Kiyoto, Chae, Jae Jin, Ross, Astin M., Pinto-Patarroyo, Gineth, Patel, Seema K., Muskett, Julie A., Ratay, Jessica S., Chattaraj, Parna, Park, Yong Hwan, Grevich, Sriharsha, Brewer, Carmen C., Hoa, Michael, Kim, H. Jeffrey, Butman, John A., Broderick, Lori, Hoffman, Hal M., Aksentijevich, Ivona, Kastner, Daniel L., Goldbach-Mansky, Raphaela, Griffith, Andrew J.
Publicado no Proc Natl Acad Sci U S A (2017)

CDC14A phosphatase is essential for hearing and male fertility in mouse and human

por Imtiaz, Ayesha, Belyantseva, Inna A, Beirl, Alisha J, Fenollar-Ferrer, Cristina, Bashir, Rasheeda, Bukhari, Ihtisham, Bouzid, Amal, Shaukat, Uzma, Azaiez, Hela, Booth, Kevin T, Kahrizi, Kimia, Najmabadi, Hossein, Maqsood, Azra, Wilson, Elizabeth A, Fitzgerald, Tracy S, Tlili, Abdelaziz, Olszewski, Rafal, Lund, Merete, Chaudhry, Taimur, Rehman, Atteeq U, Starost, Matthew F, Waryah, Ali M, Hoa, Michael, Dong, Lijin, Morell, Robert J, Smith, Richard J H, Riazuddin, Sheikh, Masmoudi, Saber, Kindt, Katie S, Naz, Sadaf, Friedman, Thomas B
Publicado no Hum Mol Genet (2018)