Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Abhiraami Kannan Sundhari"'
Autor:
Abhiraami Kannan-Sundhari, Clemer Abad, Marie E. Maloof, Nagi G. Ayad, Juan I. Young, Xue Zhong Liu, Katherina Walz
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Hair cells (HCs) play crucial roles in perceiving sound, acceleration, and fluid motion. The tonotopic architecture of the sensory epithelium recognizes mechanical stimuli and convert them into electrical signals. The expression and regulation of the
Externí odkaz:
https://doaj.org/article/b5b3e7ba0bf14d1aa1431f8ca70420d6
Autor:
Clive P Morgan, Jocelyn F Krey, M'hamed Grati, Bo Zhao, Shannon Fallen, Abhiraami Kannan-Sundhari, Xue Zhong Liu, Dongseok Choi, Ulrich Müller, Peter G Barr-Gillespie
Publikováno v:
eLife, Vol 5 (2016)
While more than 70 genes have been linked to deafness, most of which are expressed in mechanosensory hair cells of the inner ear, a challenge has been to link these genes into molecular pathways. One example is Myo7a (myosin VIIA), in which deafness
Externí odkaz:
https://doaj.org/article/3e65b5e5353b40bf98ff63ca95741554
Autor:
Xue Zhong Liu, Denise Yan, Susan H. Blanton, Kolsoum Saeidi, Afsaneh Sahebalzamani, Abhiraami Kannan-Sundhari
Publikováno v:
Genet Test Mol Biomarkers
Background: Hearing loss (HL) is one of the most common and genetically heterogeneous sensory disorders in humans. Genetic causes underlie 50–60% of all HL and the majority of these cases exhibit an autosomal recessive model of inheritance. Methods
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ced7be76effe7cdbaa192e3c64362fd5
https://doi.org/10.1089/gtmb.2020.0153
https://doi.org/10.1089/gtmb.2020.0153
Autor:
Shalini Kamu Reddy, Channabasavaiah B. Gurumurthy, Rolen M. Quadros, Katherina Walz, Abhiraami Kannan Sundhari
Early approaches to create gene-modified animal models involved chemical (e.g., N-ethyl-N-nitrosourea) and physical (e.g., radiation) mutagenesis methods; however, the precise location of the mutations in these models was not easy to discern. These f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d2287a0fa9b02cf6e3d0837897230d7
https://doi.org/10.1016/b978-0-12-816573-7.00007-9
https://doi.org/10.1016/b978-0-12-816573-7.00007-9
Autor:
Jose L. Badano, Cesar P. Canales, Paulina Carmona-Mora, Channabasavaiah B. Gurumurthy, Kevin A. Hope, Paola Lepanto, Patricia S. Pardo, Jennifer E. Posey, Rolen M. Quadros, Shalini Kamu Reddy, Lawrence T. Reiter, Abhiraami Kannan Sundhari, Andrew M. Tidball, Katherina Walz, Juan I. Young, Flavio R. Zolessi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52c066968b8dc8633fdb0a4403620618
https://doi.org/10.1016/b978-0-12-816573-7.00013-4
https://doi.org/10.1016/b978-0-12-816573-7.00013-4
Autor:
Claudia Carranza, Guney Bademci, Marianna Herrera, Majid Mojarrad, M'hamed Grati, Joseph Foster, Abhiraami Kannan-Sundhari, Yong Feng, Denise Yan, F. Basak Cengiz, Mariem Bensaid, Akeem O. Lasisi, Reza Maroofian, Saber Masmoudi, Alex M. Mawla, Mahdiyeh Behnam, Bing Zou, Duygu Duman, Rahul Mittal, Demet Tekin, Mohan Kameswaran, Waheed A. Adedeji, Xuezhong Liu, Rosemary I. Kabahuma, Alexander Nord, Mustafa Tekin, T.J. Lasisi, Andrew H. Crosby, Susan H. Blanton, Ibis Menéndez, Shengru Guo
Publikováno v:
Human genetics, vol 135, iss 8
Hearing loss is the most common sensory deficit in humans with causative variants in over 140 genes. With few exceptions, however, the population-specific distribution for many of the identified variants/genes is unclear. Until recently, the extensiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40d9d35b96efcfd3f46fd9900fa5371b
https://doi.org/10.1007/s00439-016-1697-z
https://doi.org/10.1007/s00439-016-1697-z
Autor:
Denise Yan, Prem P. Chapagain, Li Wang, Rahul Mittal, Susan H. Blanton, Litao Qin, Shixiu Liao, Abhiraami Kannan Sundhari, Yong Feng, Tao Li, Yalan Liu, M'hamed Grati, Xuezhong Liu
Identification of genes with variants causing non-syndromic hearing loss (NSHL) is challenging due to genetic heterogeneity. The difficulty is compounded by technical limitations that in the past prevented comprehensive gene identification. Recent ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17a9693d923e9377a2734e5a8077249e
https://europepmc.org/articles/PMC6560636/
https://europepmc.org/articles/PMC6560636/
Autor:
M'hamed Grati, Abhiraami Kannan-Sundhari, Ulrich Müller, Jocelyn F. Krey, Xue Zhong Liu, Peter G. Barr-Gillespie, Clive P Morgan, Dongseok Choi, Shannon Fallen, Bo Zhao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c27c7c29fb29f967cc0566ba9c612d9
https://doi.org/10.7554/elife.18312.034
https://doi.org/10.7554/elife.18312.034
Autor:
Peter G. Barr-Gillespie, Clive P Morgan, Jocelyn F. Krey, Abhiraami Kannan-Sundhari, Bo Zhao, Dongseok Choi, M'hamed Grati, Ulrich Müller, Shannon Fallen, Xue Zhong Liu
Publikováno v:
eLife
eLife, Vol 5 (2016)
eLife, Vol 5 (2016)
While more than 70 genes have been linked to deafness, most of which are expressed in mechanosensory hair cells of the inner ear, a challenge has been to link these genes into molecular pathways. One example is Myo7a (myosin VIIA), in which deafness
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a884c04e82425afa066ec5226184c4c
http://europepmc.org/articles/PMC5005036
http://europepmc.org/articles/PMC5005036
Autor:
Rahul Mittal, Jie Qing, Denise Yan, Mohan Kameswaran, Xue Zhong Liu, Subramanian Vishwanath, Abhiraami Kannan-Sundhari
Publikováno v:
Genetic testing and molecular biomarkers. 19(9)
Deafness encompasses a series of etiologically heterogeneous disorders with mutations in more than 400 independent genes. However, several studies indicate that a large proportion of both syndromic and nonsyndromic forms of deafness in the racially d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82fa56c8a34d64bc4df47f76324a81d6
https://pubmed.ncbi.nlm.nih.gov/26186295
https://pubmed.ncbi.nlm.nih.gov/26186295