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pro vyhledávání: '"H. Holme"'
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Autor:
Ralph H. Holme, Karen P. Steel
Publikováno v:
JARO - Journal of the Association for Research in Otolaryngology. 5:66-79
Exposure to intense noise can damage the stereocilia of sensory hair cells in the inner ear. Since stereocilia play a vital role in the transduction of sound from a mechanical stimulus into an electrical one, this pathology is thought to contribute t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf484b98b2fc9055fcebd41434a6840e
https://doi.org/10.1007/s10162-003-4021-2
https://doi.org/10.1007/s10162-003-4021-2
Publikováno v:
Experimental Eye Research. 77:731-739
Mutations in the cadherin 23 gene (CDH23) cause Usher syndrome type 1D in humans, a disease that results in retinitis pigmentosa and deafness. Cdh23 is also mutated in the waltzer mouse. In order to determine if the retina of the waltzer mouse underg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d90ac95085fcb134d55f2275de332cf6
https://doi.org/10.1016/j.exer.2003.07.007
https://doi.org/10.1016/j.exer.2003.07.007
Autor:
Federica Di Palma, Bechara Kachar, Karen P. Steel, Inna A. Belyantseva, Konrad Noben-Trauth, Ralph H. Holme, Richard Pellegrino, Elizabeth C. Bryda
Publikováno v:
Nature Genetics. 27:103-107
Mouse chromosome 10 harbors several loci associated with hearing loss, including waltzer (v), modifier-of deaf waddler (mdfw) and Age-related hearing loss1 (Ahl). The human region that is orthologous to the mouse 'waltzer' region is located at 10q21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e4f249e58d93d8ee6b351749c8d5f13
https://doi.org/10.1038/83660
https://doi.org/10.1038/83660
Publikováno v:
Mechanisms of Development. 91:175-187
During the initial stages of vertebrate retinogenesis, cells of the optic vesicle adopt one of two alternate cell fates. Cells in the distal-most part of the vesicle, immediately beneath the surface ectoderm, undergo neural differentiation; cells in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19004eb67255279f7ccff7cb26b60447
https://doi.org/10.1016/s0925-4773(99)00296-8
https://doi.org/10.1016/s0925-4773(99)00296-8
Autor:
Ralph H. Holme, Karen P Steelt
Publikováno v:
Current Opinion in Genetics & Development. 9:309-314
Remarkable progress has been made over the past few years in the field of hereditary deafness. To date, mutations in at least 35 genes are known to cause hearing loss. We are now beginning to understand the function of many of these genes, which affe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9182b207b88a296c4cab0fd93331c88
https://doi.org/10.1016/s0959-437x(99)80046-x
https://doi.org/10.1016/s0959-437x(99)80046-x
Publikováno v:
Archives of Disease in Childhood. 101:A189.3-A191
Aims To prospectively evaluate the Neonatal Trigger Score (NTS) to determine optimum threshold scores for medical intervention and intensive care (ICU) admission. Methods All neonates on the postnatal ward with a set of pre-defined risk factors were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1f288a8ccbfb86a9ca94e19e10e4652
https://doi.org/10.1136/archdischild-2016-310863.318
https://doi.org/10.1136/archdischild-2016-310863.318
Autor:
Timothy W. R. Briggs, H. Holme, A Cassoni, Roberto Tirabosco, G Erturan, Robin Pollock, C.B. Westbury, Daniel A. Morgenstern, Maria Michelagnoli
Publikováno v:
Clinical oncology (Royal College of Radiologists (Great Britain)). 25(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c546b8d8f323b4cf44c3da206b32201
https://pubmed.ncbi.nlm.nih.gov/23098387
https://pubmed.ncbi.nlm.nih.gov/23098387
Akademický článek
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