DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Pejvakin
Pejvakin
1 INVITED REVIEW Mechanisms of Gasdermin Family Members in Inflammasome Signaling and Cell Death Shouya Feng,* Daniel Fox,* Si M
The Functional Annotation of Mammalian Genomes: the Challenge of Phenotyping
Pejvakin, a Candidate Stereociliary Rootlet Protein, Regulates Hair Cell Function in a Cell-Autonomous Manner
Biochemical Studies of the Synaptic Protein Otoferlin
Mechanisms and Functions of Pexophagy in Mammalian Cells
Diaphanous Causes Hearing Defects in Humans with Auditory Neuropathy and in Drosophila
Auditory Neuropathy Spectrum Disorder (ANSD)
AN ALPORT SYNDROME MUTATION in MOUSE Col4a4 IDENTIFIED by WHOLE GENOME SEQUENCING and BULK SEGREGATION ANALYSIS
Curriculum Vitae
SACGHS Report on Gene Patents And
The Many Faces of DFNB9: Relating OTOF Variants to Hearing Impairment
A Forward Genetics Screen in Mice Identifies Recessive Deafness Traits and Reveals That Pejvakin Is Essential for Outer Hair Cell Function
The Gasdermins, a Protein Family Executing Cell Death And
Įtaka Patogenezei Ir Fenotipinei Išraiškai Lietuvos Populiacijoje
CNV) Em Pacientes Com Surdez Sindrômica
Channelling Inflammation: Gasdermins in Physiology and Disease
Finding New Genes for Non-Syndromic Hearing Loss Through an in Silico Prioritization Study
Gene Expression Profiles of the Cochlea and Vestibular Endorgans
Top View
Mouse Pjvk Knockout Project (CRISPR/Cas9)
Genome-Wide Analysis Reveals a Novel Autosomal-Recessive Hearing Loss Locus DFNB80 on Chromosome 2P16.1-P21
A Novel Allele of Myosin Viia Reveals a Critical Function for the C-Terminal FERM Domain for Melanosome Transport in Retinal Pigment Epithelial Cells
Curriculum Vitae
Gasdermin E-Mediated Programmed Cell Death: an Unpaved Path to Tumor Suppression Yueyuan Wang1, Jingyu Peng1, Xiao Xie1, Zhihao Zhang1, Mingxi Li2, Ming Yang1
T.C. Istanbul Üniversitesi Sağlik Bilimleri Enstitüsü
Spectrum of DNA Variants for Nonsyndromic Deafness in a Large Cohort from Multiple Continents
A Novel ENU-Induced Mutation in Myo6 Causes Vestibular Dysfunction and Deafness
A Catechol-O-Methyltransferase That Is Essential for Auditory Function in Mice and Humans
Genetics of Peripheral Vestibular Dysfunction: Lessons from Mutant Mouse Strains Sherri M