J. Brigande

发表

Probing the Functional Equivalence of Otoferlin and Synaptotagmin 1 in Exocytosis

Chris S Bresee, Chris S. Bresee, S. Kügler, 2011, The Journal of Neuroscience.

Lineage Analysis of the Late Otocyst Stage Mouse Inner Ear by Transuterine Microinjection of A Retroviral Vector Encoding Alkaline Phosphatase and an Oligonucleotide Library

Kevin T. Beier, C. Cepko, D. Fekete, 2013, PloS one.

A neonatal nonhuman primate model of gestational Zika virus infection with evidence of microencephaly, seizures and cardiomyopathy

J. B. Kempton, C. Kroenke, Xiaojie Wang, 2020, PloS one.

Inhibition of Glycosphingolipid Biosynthesis Does Not Impair Growth or Morphogenesis of the Postimplantation Mouse Embryo

T. Seyfried, F. Platt, T. Seyfried, 1998, Journal of neurochemistry.

Glycosphingolipid Biosynthesis May Not Be Necessary for Vertebrate Brain Development a

T. Seyfried, J. Brigande, 1998, Annals of the New York Academy of Sciences.

Electroporation-mediated gene transfer to the developing mouse inner ear.

S. Gubbels, J. Brigande, David W. Woessner, 2009, Methods in molecular biology.

In vivo delivery of recombinant viruses to the fetal murine cochlea: transduction characteristics and long-term effects on auditory function.

J. Bennett, M. Gratton, J. Brigande, 2006, Molecular therapy : the journal of the American Society of Gene Therapy.

Requirement for scleraxis in the recruitment of mesenchymal progenitors during embryonic tendon elongation

Brendon M. Baker, B. Baker, R. Schweitzer, 2019, Development.

Deleterious mtDNA mutations are common in mature oocytes

A. Terzic, S. Mitalipov, S. Yamada, 2019, Biology of Reproduction.

CRISPR/Cas9 editing of the MYO7A gene in rhesus macaque embryos to generate a primate model of Usher syndrome type 1B

E. Porsov, B. Burwitz, J. Hennebold, 2022, Scientific Reports.

Ganglioside biosynthesis in mouse embryos: sialyltransferase IV and the asialo pathway.

A. M. Novikov, T. Seyfried, J. Brigande, 1994, Journal of lipid research.

Gene Therapy in Mouse Models of Deafness and Balance Dysfunction

J. Brigande, Lingyan Wang, J. Kempton, 2018, Front. Mol. Neurosci..

Antisense oligonucleotides delivered to the amniotic cavity in utero modulate gene expression in the postnatal mouse

J. Lentz, F. Rigo, Francine M. Jodelka, 2016, Nucleic acids research.

Tgfβ signaling is critical for maintenance of the tendon cell fate

R. Schweitzer, D. Keene, Guak-Kim Tan, 2019, bioRxiv.

Fetal antisense oligonucleotide therapy for congenital deafness and vestibular dysfunction

J. Lentz, F. Rigo, Rachel A Dumont, 2020, Nucleic acids research.

Gipc1 has a dual role in Vangl2 trafficking and hair bundle integrity in the inner ear

J. Reboul, M. Montcouquiol, M. Kelley, 2012, Development.

Optogenetic Control of Mouse Outer Hair Cells.

Hrebesh Subhash, Yuan Zhang, Sarah Foster, 2016, Biophysical journal.

The development of semicircular canals in the inner ear: role of FGFs in sensory cristae

Doris K. Wu, D. Fekete, J. Brigande, 2004, Development.

Fetal gene therapy and pharmacotherapy to treat congenital hearing loss and vestibular dysfunction

J. Brigande, M. Hastings, 2020, Hearing Research.

Quo vadis, hair cell regeneration?

Stefan Heller, S. Heller, J. Brigande, 2009, Nature Neuroscience.

Hearing in the mouse of Usher

J. Brigande, 2017, Nature Biotechnology.

Biochemical Correlates of Epilepsy in the El Mouse: Analysis of Glial Fibrillary Acidic Protein and Gangliosides

T. Seyfried, A. Wieraszko, J. Brigande, 1992, Journal of neurochemistry.

Scleraxis is Required for Differentiation of the Stapedius and Tensor Tympani Tendons of the Middle Ear

Chris S. Bresee, T. Ren, R. Schweitzer, 2011, Journal of the Association for Research in Otolaryngology.

Repositioning forelimb superficialis muscles: tendon attachment and muscle activity enable active relocation of functional myofibers.

R. Schweitzer, A. Huang, E. Zelzer, 2013, Developmental cell.

Optimizing Auditory Brainstem Response Acquisition Using Interleaved Frequencies

B. N. Buran, S. Elkins, J. B. Kempton, 2019, bioRxiv.

Tgfβ signaling is critical for maintenance of the tendon cell fate

R. Schweitzer, D. Keene, Guak-Kim Tan, 2020, eLife.

Functional auditory hair cells produced in the mammalian cochlea by in utero gene transfer

John C. Mitchell, J. Mitchell, S. Gubbels, 2008, Nature.

Molecular genetics of pattern formation in the inner ear: do compartment boundaries play a role?

A. Kiernan, D. Fekete, D M Fekete, 2000, Proceedings of the National Academy of Sciences of the United States of America.

A fate map of chick otic cup closure reveals lineage boundaries in the dorsal otocyst.

D. Fekete, J. Brigande, L. Iten, 2000, Developmental biology.

Prolyl 3-hydroxylase-1 null mice exhibit hearing impairment and abnormal morphology of the middle ear bone joints.

Chris S Bresee, Chris S. Bresee, E. Pokidysheva, 2013, Matrix biology : journal of the International Society for Matrix Biology.

Gene transfer to the developing mouse inner ear by in vivo electroporation.

J. Brigande, Han Jiang, Lingyan Wang, 2012, Journal of visualized experiments : JoVE.