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Biorxiv : the Preprint Server for Biology
|
May 7, 2024
Molecular differences between neonatal and adult stria vascularis from organotypic explants and transcriptomics
Matsya Ruppari Thulasiram, Ryosuke Yamamoto, Rafal T Olszewski, et al.
Genes & Cancer
|
December 14, 2017
Alcohol, stem cells and cancer
Shoujun Gu, Bao-Ngoc Nguyen, Shuyun Rao, et al.
Frontiers in Molecular Neuroscience
|
January 11, 2020
Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis
Soumya Korrapati, Ian Taukulis, Rafal Olszewski, et al.
Frontiers in Molecular Neuroscience
|
March 3, 2020
Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea
Michael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
Scientific Reports
|
February 6, 2024
Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularis
Dillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Research Square
|
October 27, 2023
Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria Vascularis
Dillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Frontiers in Molecular Neuroscience
|
June 21, 2021
Corrigendum: Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea
Michael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
Human Genetics
|
August 2, 2021
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder
Rabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, et al.
Genes
|
July 27, 2024
Deafness DFNB128 Associated with a Recessive Variant of Human <i>MAP3K1</i> Recapitulates Hearing Loss of <i>Map3k1</i>-Deficient Mice
Rabia Faridi, Rizwan Yousaf, Sayaka Inagaki, et al.
Genes
|
September 29, 2020
Mouse Models of Human Pathogenic Variants of <i>TBC1D24</i> Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness
Risa Tona, Ivan A Lopez, Cristina Fenollar-Ferrer, et al.
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Search research articles
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Showing results (11-20 of 28) with videos related to
Sort By:
Page
of 3
Biorxiv : the Preprint Server for Biology
|
May 7, 2024
Molecular differences between neonatal and adult stria vascularis from organotypic explants and transcriptomics
Matsya Ruppari Thulasiram, Ryosuke Yamamoto, Rafal T Olszewski, et al.
Genes & Cancer
|
December 14, 2017
Alcohol, stem cells and cancer
Shoujun Gu, Bao-Ngoc Nguyen, Shuyun Rao, et al.
Frontiers in Molecular Neuroscience
|
January 11, 2020
Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria Vascularis
Soumya Korrapati, Ian Taukulis, Rafal Olszewski, et al.
Frontiers in Molecular Neuroscience
|
March 3, 2020
Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea
Michael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
Scientific Reports
|
February 6, 2024
Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularis
Dillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Research Square
|
October 27, 2023
Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria Vascularis
Dillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Frontiers in Molecular Neuroscience
|
June 21, 2021
Corrigendum: Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human Cochlea
Michael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
Human Genetics
|
August 2, 2021
New insights into Perrault syndrome, a clinically and genetically heterogeneous disorder
Rabia Faridi, Alessandro Rea, Cristina Fenollar-Ferrer, et al.
Genes
|
July 27, 2024
Deafness DFNB128 Associated with a Recessive Variant of Human <i>MAP3K1</i> Recapitulates Hearing Loss of <i>Map3k1</i>-Deficient Mice
Rabia Faridi, Rizwan Yousaf, Sayaka Inagaki, et al.
Genes
|
September 29, 2020
Mouse Models of Human Pathogenic Variants of <i>TBC1D24</i> Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness
Risa Tona, Ivan A Lopez, Cristina Fenollar-Ferrer, et al.
Page
of 3