Chantal M. Longo-Guess

发表

Editing-defective tRNA synthetase causes protein misfolding and neurodegeneration

S. Ackerman, P. Schimmel, M. Davisson, 2006, Nature.

Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice

Richard J. Salvi, Kenneth R. Johnson, R. Salvi, 2012, Hearing Research.

The harlequin mouse mutation downregulates apoptosis-inducing factor

Wayne N. Frankel, W. Frankel, S. Ackerman, 2002, Nature.

A spontaneous mouse deletion in Mctp1 uncovers a long-range cis-regulatory region crucial for NR2F1 function during inner ear development.

K. Johnson, Chantal M. Longo-Guess, Cong Tian, 2018, Developmental biology.

Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice

K. Johnson, L. Gagnon, Chantal M. Longo-Guess, 2012, Neurobiology of Aging.

N-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in γ-glutamyl transferase 1 deficient mice

R. Salvi, D. Ding, K. Johnson, 2016, Aging.

Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts

R. Korstanje, K. Johnson, L. Gagnon, 2017, Human molecular genetics.

Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice

M. Wiles, A. Kiernan, K. Johnson, 2018, Genetics.

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

K. Johnson, L. Gagnon, Chantal M. Longo-Guess, 2005, Proceedings of the National Academy of Sciences of the United States of America.

A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9

K. Johnson, D. Bergstrom, L. Gagnon, 2007, Hearing Research.

Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice.

D. Bergstrom, W. Nauseef, Chantal M. Longo-Guess, 2008, The Journal of clinical investigation.

The Chloride Intracellular Channel Protein CLIC5 Is Expressed at High Levels in Hair Cell Stereocilia and Is Essential for Normal Inner Ear Function

Heping Yu, K. Johnson, L. Gagnon, 2006, The Journal of Neuroscience.

Protein accumulation and neurodegeneration in the woozy mutant mouse is caused by disruption of SIL1, a cochaperone of BiP

S. Ackerman, Chantal M. Longo-Guess, Chantal Longo-Guess, 2005, Nature Genetics.

A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice.

Heping Yu, Qing Yin Zheng, K. Johnson, 2008, Genomics.

Ush1c gene expression levels in the ear and eye suggest different roles for Ush1c in neurosensory organs in a new Ush1c knockout mouse

X. Liu, D. Yan, Chantal M. Longo-Guess, 2010, Brain Research.

Deletion in Catna2, encoding αN-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation

Jacqueline H. Finger, S. Ackerman, Chankyu Park, 2002, Nature Genetics.

Alström Syndrome protein ALMS1 localizes to basal bodies of cochlear hair cells and regulates cilium-dependent planar cell polarity.

D. Jagger, A. Forge, J. Naggert, 2011, Human molecular genetics.

A Modifier Gene Alleviates Hypothyroidism-Induced Hearing Impairment in Pou1f1dw Dwarf Mice

S. Camper, K. Johnson, L. Gagnon, 2011, Genetics.

A novel modifier of hypothyroidism-induced hearing impairment in Pou1f1 dw dwarf mice

S. Camper, K. Johnson, L. Gagnon, 2011 .

A Modi fi er Gene Alleviates Hypothyroidism-Induced Hearing Impairment in Pou 1 f 1 dw Dwarf Mice

S. Camper, K. Johnson, L. Gagnon, 2011 .

Hearing Impairment in Hypothyroid Dwarf Mice Caused by Mutations of the Thyroid Peroxidase Gene

K. Johnson, L. Gagnon, B. Chang, 2014, Journal of the Association for Research in Otolaryngology.

Mutations of the Mouse ELMO Domain Containing 1 Gene (Elmod1) Link Small GTPase Signaling to Actin Cytoskeleton Dynamics in Hair Cell Stereocilia

K. Johnson, L. Gagnon, Chantal M. Longo-Guess, 2012, PloS one.

NPHP4 is necessary for normal photoreceptor ribbon synapse maintenance and outer segment formation, and for sperm development.

J. Naggert, Tiansen Li, Richard S. Smith, 2011, Human molecular genetics.

A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice

K. Johnson, L. Gagnon, Chantal M. Longo-Guess, 2015, Mammalian Genome.

The R109H Variant of Fascin-2, a Developmentally Regulated Actin Crosslinker in Hair-Cell Stereocilia, Underlies Early-Onset Hearing Loss of DBA/2J Mice

K. Johnson, L. Gagnon, P. Gillespie, 2010, The Journal of Neuroscience.

Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation

Bernd Fritzsch, K. Johnson, L. Gagnon, 2007, Mammalian Genome.