Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Hilda, Tateossian"'
Autor:
Carlos Aguilar, Debbie Williams, Ramakrishna Kurapati, Rasneer S. Bains, Philomena Mburu, Andy Parker, Jackie Williams, Danilo Concas, Hilda Tateossian, Andrew R. Haynes, Gareth Banks, Pratik Vikhe, Ines Heise, Marie Hutchison, Gemma Atkins, Simon Gillard, Becky Starbuck, Simona Oliveri, Andrew Blake, Siddharth Sethi, Saumya Kumar, Tanaya Bardhan, Jing-Yi Jeng, Stuart L. Johnson, Lara F. Corns, Walter Marcotti, Michelle Simon, Sara Wells, Paul K. Potter, Heena V. Lad
Publikováno v:
iScience, Vol 27, Iss 7, Pp 110170- (2024)
Summary: Despite some evidence indicating diverse roles of whirlin in neurons, the functional corollary of whirlin gene function and behavior has not been investigated or broadly characterized. A single nucleotide variant was identified from our rece
Externí odkaz:
https://doaj.org/article/8421d27753b841d7bc0fb0382fdbd3c7
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Chronic otitis media (OM) is the most common cause of hearing loss worldwide, yet the underlying genetics and molecular pathology are poorly understood. The mouse mutant Jeff is a single gene mouse model for OM identified from a deafness screen as pa
Externí odkaz:
https://doaj.org/article/749d241dfcd341cdbd97992d5a1f73c1
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
The Jeff mouse mutant carries a mutation in the F-box only 11 gene (Fbxo11) and heterozygous animals display conductive deafness due to the development of otitis media (OM). The Fbxo11 locus is also associated with chronic otitis media with effusion
Externí odkaz:
https://doaj.org/article/fbd51b26323b4a8c8438e58f67966add
Publikováno v:
Disease Models & Mechanisms, Vol 8, Iss 12, Pp 1531-1542 (2015)
Otitis media with effusion (OME) is the most common cause of hearing loss in children, and tympanostomy (ear tube insertion) to alleviate the condition remains the commonest surgical intervention in children in the developed world. Chronic and recurr
Externí odkaz:
https://doaj.org/article/5a825f34bbd749f8883ccfcc13b75285
Autor:
Michael Crompton, Tom Purnell, Hayley E Tyrer, Andrew Parker, Greg Ball, Rachel E Hardisty-Hughes, Richard Gale, Debbie Williams, Charlotte H Dean, Michelle M Simon, Ann-Marie Mallon, Sara Wells, Mahmood F Bhutta, Martin J Burton, Hilda Tateossian, Steve D M Brown
Publikováno v:
PLoS Genetics, Vol 13, Iss 8, p e1006969 (2017)
Otitis media (OM), inflammation of the middle ear (ME), is a common cause of conductive hearing impairment. Despite the importance of the disease, the aetiology of chronic and recurrent forms of middle ear inflammatory disease remains poorly understo
Externí odkaz:
https://doaj.org/article/4037f860bf2443118801ffd0087a7524
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Chronic otitis media (OM) is the most common cause of hearing loss worldwide, yet the underlying genetics and molecular pathology are poorly understood. The mouse mutant Jeff is a single gene mouse model for OM identified from a deafness screen as pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad63de2eb0c422007c8ef4e3d61077fb
https://www.frontiersin.org/article/10.3389/fgene.2020.00498/full
https://www.frontiersin.org/article/10.3389/fgene.2020.00498/full
Autor:
Allen F. Ryan, Mahmood F. Bhutta, Joshua Chang Mell, Hilda Tateossian, Lena Hafrén, Garth D. Ehrlich, Michael E. Pichichero, Regie Lyn P. Santos-Cortez, Joshua P. Earl, Michael P. Jennings
Publikováno v:
Int J Pediatr Otorhinolaryngol
Objective: To review the most recent advances in human and bacterial genomics as applied to pathogenesis and clinical management of otitis media. Data sources: PubMed articles published since the last meeting in June 2015 up to June 2019. Review meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3791fe72a398f961cda6fb4292360dc1
https://pubmed.ncbi.nlm.nih.gov/32007292
https://pubmed.ncbi.nlm.nih.gov/32007292
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
The Jeff mouse mutant carries a mutation in the F-box only 11 gene (Fbxo11) and heterozygous animals display conductive deafness due to the development of otitis media (OM). The Fbxo11 locus is also associated with chronic otitis media with effusion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac60bb7bbb11b1ac8c33b67b35ea31b6
https://www.frontiersin.org/article/10.3389/fgene.2020.00050/full
https://www.frontiersin.org/article/10.3389/fgene.2020.00050/full
Autor:
Nick Warr, Debora Bogani, Pam Siggers, Rachel Brixey, Hilda Tateossian, Asha Dopplapudi, Sara Wells, Michael Cheeseman, Ying Xia, Harry Ostrer, Andy Greenfield
Publikováno v:
PLoS ONE, Vol 6, Iss 5, p e19572 (2011)
In mammals, the Y chromosome is a dominant male determinant, causing the bipotential gonad to develop as a testis. Recently, cases of familial and spontaneous 46,XY disorders of sex development (DSD) have been attributed to mutations in the human gen
Externí odkaz:
https://doaj.org/article/90c4c456a12b4bcdaab8107f57443116
Autor:
Nicholas Parkinson, Rachel E Hardisty-Hughes, Hilda Tateossian, Hsun-Tien Tsai, Debra Brooker, Sue Morse, Zuzanna Lalane, Francesca MacKenzie, Martin Fray, Pete Glenister, Anne-Marie Woodward, Sian Polley, Ivana Barbaric, Neil Dear, Tertius A Hough, A Jackie Hunter, Michael T Cheeseman, Steve D M Brown
Publikováno v:
PLoS Genetics, Vol 2, Iss 10, p e149 (2006)
Otitis media (OM), inflammation of the middle ear, remains the most common cause of hearing impairment in children. It is also the most common cause of surgery in children in the developed world. There is evidence from studies of the human population
Externí odkaz:
https://doaj.org/article/4e04b3f64b7f43c8b014fa9eef6c1a5c