Similarities between mice and humans with hereditary deafness

Genetic deafness of central origin.

Brain research·2013

Pitpnm1 is expressed in hair cells during development but is not required for hearing.

Neuroscience·2013

Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip link formation.

Neuroscience·2008

The roles of unconventional myosins in hearing and deafness.

Essays in biochemistry·2002

Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations.

Nature neuroscience·2001

The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects.

Developmental biology·2001

LKB1 Dysregulation in Duchenne Muscular Dystrophy Models: Disease Specificity and Epigenetic Control by HDAC Inhibitors.

Annals of the New York Academy of Sciences·2026

Three-Day Bi-Hemispheric tDCS With Motor Training Shows No Improvement in Pianist's With Musician's Dystonia: A Pilot Study.

Annals of the New York Academy of Sciences·2026

Experience-Tuned Predictive Coding in Monocultural Brains: A Visual Mismatch Response Study.

Annals of the New York Academy of Sciences·2026

Real-Time Gear Surface Defect Detection via Multi-Order Feature Aggregation and Spatial-Frequency Dual-Domain Enhancement.

Annals of the New York Academy of Sciences·2026

Global Attention Mechanism-Enhanced Deep Learning for Multi-Sequence MRI Diagnosis of Early Femoral Head Osteonecrosis.

Annals of the New York Academy of Sciences·2026

A (Political) Battle of the Sexes: Gender Polarization on Gender-Related Attitudes Across 14 Societies.

Annals of the New York Academy of Sciences·2026

Single-cell multiomic mapping of genetic predisposition to childhood B-cell acute lymphoblastic leukemia.

bioRxiv : the preprint server for biology·2026

Identifying the causal allele in the CD40 autoimmune locus enables discovery of context-specific trans-effects in B cells.

bioRxiv : the preprint server for biology·2026

Shared genetic architecture between Crohn's disease and IgA nephropathy: implications for a gut-immune-kidney axis.

Frontiers in immunology·2026

Congenital goitrous hypothyroidism due to thyroglobulin deficiency associated with angioinvasive follicular thyroid carcinoma: comprehensive and integral analysis of the p.Cys1897_Glu1900 deletion.

Endocrine·2026

Determinants of HIV testing intentions among heterosexual men in the Bolgatanga Municipality of Ghana: Evidence from the theory of planned behaviour.

PLOS global public health·2026

The First Iranian Patient with West Syndrome Due to a RYR3 Gene Variant: A Case Report and Literature Review.

Archives of Iranian medicine·2026

Related Experiment Videos

Similarities between mice and humans with hereditary deafness

Related Concept Videos

Genetic deafness of central origin.

Pitpnm1 is expressed in hair cells during development but is not required for hearing.

Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip link formation.

The roles of unconventional myosins in hearing and deafness.

Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations.

The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects.

LKB1 Dysregulation in Duchenne Muscular Dystrophy Models: Disease Specificity and Epigenetic Control by HDAC Inhibitors.

Three-Day Bi-Hemispheric tDCS With Motor Training Shows No Improvement in Pianist's With Musician's Dystonia: A Pilot Study.

Experience-Tuned Predictive Coding in Monocultural Brains: A Visual Mismatch Response Study.

Real-Time Gear Surface Defect Detection via Multi-Order Feature Aggregation and Spatial-Frequency Dual-Domain Enhancement.

Global Attention Mechanism-Enhanced Deep Learning for Multi-Sequence MRI Diagnosis of Early Femoral Head Osteonecrosis.

A (Political) Battle of the Sexes: Gender Polarization on Gender-Related Attitudes Across 14 Societies.

Single-cell multiomic mapping of genetic predisposition to childhood B-cell acute lymphoblastic leukemia.

Identifying the causal allele in the CD40 autoimmune locus enables discovery of context-specific trans-effects in B cells.

Shared genetic architecture between Crohn's disease and IgA nephropathy: implications for a gut-immune-kidney axis.

Congenital goitrous hypothyroidism due to thyroglobulin deficiency associated with angioinvasive follicular thyroid carcinoma: comprehensive and integral analysis of the p.Cys1897_Glu1900 deletion.

Determinants of HIV testing intentions among heterosexual men in the Bolgatanga Municipality of Ghana: Evidence from the theory of planned behaviour.

The First Iranian Patient with West Syndrome Due to a RYR3 Gene Variant: A Case Report and Literature Review.

Related Experiment Videos

Similarities between mice and humans with hereditary deafness

Related Concept Videos

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