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Denise Yan

Showing results (41-50 of 103) with videos related to

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International Journal of Pediatric Otorhinolaryngology|March 12, 2011
Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African populationRosemary I Kabahuma, Xiaomei Ouyang, Li Lin Du, et al.
Journal of Human Genetics|February 7, 2009
The genetic bases for non-syndromic hearing loss among ChineseXiao Mei Ouyang, Denise Yan, Hui Jun Yuan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 22, 2021
Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant PatientsEric Nisenbaum, Sandra Prentiss, Denise Yan, et al.
Genes|March 6, 2021
Spectrum of <i>MYO7A</i> Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous MutationsRosemary Ida Kabahuma, Wolf-Dieter Schubert, Christiaan Labuschagne, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 24, 2017
The genetic basis of deafness in populations of African descentJason R Rudman, Rosemary I Kabahuma, Sara E Bressler, et al.
Scientific Reports|July 27, 2019
Otopathogenic Staphylococcus aureus Invades Human Middle Ear Epithelial Cells Primarily through Cholesterol Dependent PathwayRahul Mittal, Luca H Debs, Amit P Patel, et al.
Genes|May 28, 2025
Whole-Genome DNA Methylation Analysis in Age-Related Hearing LossMarie Valerie Roche, Denise Yan, Yan Guo, et al.
Hearing, Balance and Communication|February 26, 2019
Genetic screening revealed usher syndrome in a paediatric Chinese patientChunyan Qu, Fenghe Liang, Qin Long, et al.
Genome Research|February 5, 2003
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure programXiaofeng Zhu, Denise Yan, Richard S Cooper, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 30, 2009
Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueductSamuel Reyes, Guojian Wang, Xiaomei Ouyang, et al.
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
International Journal of Pediatric Otorhinolaryngology|March 12, 2011
Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African populationRosemary I Kabahuma, Xiaomei Ouyang, Li Lin Du, et al.
Journal of Human Genetics|February 7, 2009
The genetic bases for non-syndromic hearing loss among ChineseXiao Mei Ouyang, Denise Yan, Hui Jun Yuan, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|April 22, 2021
Screening Strategies for Deafness Genes and Functional Outcomes in Cochlear Implant PatientsEric Nisenbaum, Sandra Prentiss, Denise Yan, et al.
Genes|March 6, 2021
Spectrum of <i>MYO7A</i> Mutations in an Indigenous South African Population Further Elucidates the Nonsyndromic Autosomal Recessive Phenotype of DFNB2 to Include Both Homozygous and Compound Heterozygous MutationsRosemary Ida Kabahuma, Wolf-Dieter Schubert, Christiaan Labuschagne, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 24, 2017
The genetic basis of deafness in populations of African descentJason R Rudman, Rosemary I Kabahuma, Sara E Bressler, et al.
Scientific Reports|July 27, 2019
Otopathogenic Staphylococcus aureus Invades Human Middle Ear Epithelial Cells Primarily through Cholesterol Dependent PathwayRahul Mittal, Luca H Debs, Amit P Patel, et al.
Genes|May 28, 2025
Whole-Genome DNA Methylation Analysis in Age-Related Hearing LossMarie Valerie Roche, Denise Yan, Yan Guo, et al.
Hearing, Balance and Communication|February 26, 2019
Genetic screening revealed usher syndrome in a paediatric Chinese patientChunyan Qu, Fenghe Liang, Qin Long, et al.
Genome Research|February 5, 2003
Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure programXiaofeng Zhu, Denise Yan, Richard S Cooper, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 30, 2009
Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueductSamuel Reyes, Guojian Wang, Xiaomei Ouyang, et al.
Pageof 11