The Dread Disease: Cancer and Modern American Culture

por Griffith, Andrew J.
Publicado 1990

Psychopathology in Epilepsy: Social Dimensions

por Griffith, Andrew J.
Publicado 1986

DNA Replication and Recombination

por Griffith, Andrew J.
Publicado 1987

Dissection of the Endolymphatic Sac from Mice

por Honda, Keiji, Lee, Hyun Jae, Griffith, Andrew J., Roux, Isabelle
Publicado 2021

Influence of dietary iodine deficiency on the thyroid gland in Slc26a4-null mutant mice

por Iwata, Tomoyuki, Yoshida, Tadao, Teranishi, Masaaki, Murata, Yoshiharu, Hayashi, Yoshitaka, Kanou, Yasuhiko, Griffith, Andrew J, Nakashima, Tsutomu
Publicado 2011

Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function

por Nakanishi, Hiroshi, Kurima, Kiyoto, Pan, Bifeng, Wangemann, Philine, Fitzgerald, Tracy S., Géléoc, Gwenaëlle S., Holt, Jeffrey R., Griffith, Andrew J.
Publicado 2018

Genetic Hearing Loss Associated With Autoinflammation

por Nakanishi, Hiroshi, Prakash, Pragya, Ito, Taku, Kim, H. Jeffrey, Brewer, Carmen C., Harrow, Danielle, Roux, Isabelle, Hosokawa, Seiji, Griffith, Andrew J.
Publicado 2020

AAV8BP2 and AAV8 transduce the mammalian cochlear lateral wall and endolymphatic sac with high efficiency

por Isgrig, Kevin, Ishibashi, Yasuko, Lee, Hyun Jae, Zhu, Jianliang, Grati, Mhamed, Bennett, Jean, Griffith, Andrew J., Roux, Isabelle, Chien, Wade W.
Publicado 2022

SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct

por Chao, Janet R., Chattaraj, Parna, Munjal, Tina, Honda, Keiji, King, Kelly A., Zalewski, Christopher K., Chien, Wade W., Brewer, Carmen C., Griffith, Andrew J.
Publicado 2019

Cell Type–Specific Transcriptome Analysis Reveals a Major Role for Zeb1 and miR-200b in Mouse Inner Ear Morphogenesis

por Hertzano, Ronna, Elkon, Ran, Kurima, Kiyoto, Morrisson, Annie, Chan, Siaw-Lin, Sallin, Michelle, Biedlingmaier, Andrew, Darling, Douglas S., Griffith, Andrew J., Eisenman, David J., Strome, Scott E.
Publicado 2011

Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria Vascularis

por Strepay, Dillon, Olszewski, Rafal T., Nixon, Sydney, Korrapati, Soumya, Adadey, Samuel, Griffith, Andrew J., Su, Yijun, Liu, Jiamin, Vishwasrao, Harshad, Gu, Shoujun, Saunders, Thomas, Roux, Isabelle, Hoa, Michael
Publicado 2023

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome

por Riazuddin, Saima, Ahmed, Zubair M, Hegde, Rashmi S, Khan, Shaheen N, Nasir, Idrees, Shaukat, Uzma, Riazuddin, Sheikh, Butman, John A, Griffith, Andrew J, Friedman, Thomas B, Choi, Byung Yoon
Publicado 2011

SLC26A4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc26a4 Mutant Mice

por Li, Xiangming, Sanneman, Joel D., Harbidge, Donald G., Zhou, Fei, Ito, Taku, Nelson, Raoul, Picard, Nicolas, Chambrey, Régine, Eladari, Dominique, Miesner, Tracy, Griffith, Andrew J., Marcus, Daniel C., Wangemann, Philine
Publicado 2013

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 2017

A Noncoding Point Mutation of Zeb1 Causes Multiple Developmental Malformations and Obesity in Twirler Mice

por Kurima, Kiyoto, Hertzano, Ronna, Gavrilova, Oksana, Monahan, Kelly, Shpargel, Karl B., Nadaraja, Garani, Kawashima, Yoshiyuki, Lee, Kyu Yup, Ito, Taku, Higashi, Yujiro, Eisenman, David J., Strome, Scott E., Griffith, Andrew J.
Publicado 2011

CHD7 variants associated with hearing loss and enlargement of the vestibular aqueduct

por 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.
Publicado 2023

Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome

por Sethna, Saumil, Zein, Wadih M, Riaz, Sehar, Giese, Arnaud PJ, Schultz, Julie M, Duncan, Todd, Hufnagel, Robert B, Brewer, Carmen C, Griffith, Andrew J, Redmond, T Michael, Riazuddin, Saima, Friedman, Thomas B, Ahmed, Zubair M
Publicado 2021

Vestibular phenotype‐genotype correlation in a cohort of 90 patients with Usher syndrome

por Wafa, Talah T., Faridi, Rabia, King, Kelly A., Zalewski, Christopher, Yousaf, Rizwan, Schultz, Julie M., Morell, Robert J., Muskett, Julie, Turriff, Amy, Tsilou, Ekaterini, Griffith, Andrew J., Friedman, Thomas B., Zein, Wadih M., Brewer, Carmen C.
Publicado 2020

Genomic analysis of childhood hearing loss in the Yoruba population of Nigeria

por Adeyemo, Adebolajo, Faridi, Rabia, Chattaraj, Parna, Yousaf, Rizwan, Tona, Risa, Okorie, Samuel, Bharadwaj, Thashi, Nouel-Saied, Liz M., Acharya, Anushree, Schrauwen, Isabelle, Morell, Robert J., Leal, Suzanne M., Friedman, Thomas B., Griffith, Andrew J., Roux, Isabelle
Publicado 2021

Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss

por Patel, Mayher J, DiStefano, Marina T, Oza, Andrea M, Hughes, Madeline Y, Wilcox, Emma H, Hemphill, Sarah E, Cushman, Brandon J, Grant, Andrew R, Siegert, Rebecca K, Shen, Jun, Chapin, Alex, Boczek, Nicole J, Schimmenti, Lisa A, Nara, Kiyomitsu, Kenna, Margaret, Azaiez, Hela, Booth, Kevin T, Avraham, Karen B, Kremer, Hannie, Griffith, Andrew J., Rehm, Heidi L, Amr, Sami S, Tayoun, Ahmad N Abou
Publicado 2021