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Human Mutation|January 9, 2008
Mutation spectrum of MYO7A and evaluation of a novel nonsyndromic deafness DFNB2 allele with residual functionSaima Riazuddin, Sabiha Nazli, Zubair M Ahmed, et al.
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education|September 2, 2022
Implementation During a Pandemic: Findings, Successes, and Lessons Learned from Community GranteesWilhelmenia Mathias, Karen A Nichols, Jewel Golden-Wright, et al.
Human Genetics|June 11, 2011
Mutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19pAtteeq U Rehman, Khitab Gul, Robert J Morell, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|March 29, 2023
Stakeholder engagement in European brain research: Experiences of the Lifebrain consortiumIsabelle Budin-Ljøsne, Barbara B Friedman, William F C Baaré, et al.
The Journal of Cell Biology|February 17, 2022
ANKRD24 organizes TRIOBP to reinforce stereocilia insertion pointsJocelyn F Krey, Chang Liu, Inna A Belyantseva, et al.
Proteomics|March 12, 2011
The ABRF Proteomics Research Group studies: educational exercises for qualitative and quantitative proteomic analysesDavid B Friedman, Tracy M Andacht, Maureen K Bunger, et al.
Molecular Biology of the Cell|December 10, 2016
Harnessing molecular motors for nanoscale pulldown in live cellsJonathan E Bird, Melanie Barzik, Meghan C Drummond, et al.
Annals of Surgical Oncology|March 6, 2014
A randomized prospective study of lumpectomy margin assessment with use of MarginProbe in patients with nonpalpable breast malignanciesFreya Schnabel, Susan K Boolbol, Mark Gittleman, et al.
Nature Communications|April 8, 2017
Defective Gpsm2/Gαi3 signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Human Molecular Genetics|August 13, 2003
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationTamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, et al.
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