Rescue from early-onset hearing loss in a mouse model lacking the cyclin-dependent kinase inhibitor p19Ink4d

Cell Death Dis. 2016 Mar 10;7(3):e2131. doi: 10.1038/cddis.2016.38.

Authors

Q Ma¹, M Grati¹, F Bai², J Pei¹, X-H Pei², X Liu^{1

3}

Affiliations

¹ Department of Otolaryngology (D-48), University of Miami Miller School of Medicine, Miami, FL, USA.
² Molecular Oncology Program, Department of Surgery, University of Miami Miller School of Medicine, Miami, FL, USA.
³ Department of Otolaryngology, Xiangya Hospital, Central South University, Changsha, China.

No abstract available

Publication types

Letter
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

Animals
Cyclin-Dependent Kinase Inhibitor p19 / deficiency*
Cyclin-Dependent Kinase Inhibitor p19 / metabolism
Disease Models, Animal
Hair Cells, Auditory / metabolism*
Hearing Loss* / genetics
Hearing Loss* / metabolism
Hearing Loss* / prevention & control
Mice
Mice, Knockout

Substances

Cdkn2d protein, mouse
Cyclin-Dependent Kinase Inhibitor p19

Grants and funding