Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Sigrid, Wayne"'
Autor:
Matthew J. Provenzano, Mark R. Ver Meer, Frederick E. Domann, Michael J. Hitchler, Robert A. Robinson, Sigrid Wayne, Matthew P. Fitzgerald, Lei Yu
Publikováno v:
Experimental and Molecular Pathology. 83:277-282
Amyloid precursor protein (APP) has been implicated in squamous cell carcinoma. In this study we show that forced expression of the transcription factor activating protein 2alpha (AP-2alpha) results in significantly increased steady state levels of A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd886222e9c36999408a4f4c16dabd4d
https://doi.org/10.1016/j.yexmp.2007.06.001
https://doi.org/10.1016/j.yexmp.2007.06.001
Autor:
Sigrid, Wayne, Robert A, Robinson
Publikováno v:
Archives of Pathology & Laboratory Medicine. 130:1309-1314
Context.—Differential expression of cell cycle–associated proteins may correlate with human papillomavirus status and may help delineate degree of dysplasia in upper aerodigestive tract squamous lesions. Objective.—To determine intraepithelial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::720b6e54857e8e01c98424f07d3b01b9
https://doi.org/10.5858/2006-130-1309-uatsdc
https://doi.org/10.5858/2006-130-1309-uatsdc
Autor:
Kristien Verhoeven, Sai Prasad, Sigrid Wayne, Nancy Chen, Frank DeClau, Lisbeth Tranebjärg, Nahid G. Robertson, Cynthia C. Morton, Guy Van Camp, Richard Smith, Allen F. Ryan
Publikováno v:
Human molecular genetics
We identified Eyes absent 4 (EYA4), a member of the vertebrate Eya family of transcriptional activators, as the causative gene of postlingual, progressive, autosomal dominant hearing loss at the DFNA10 locus. In two unrelated families from Belgium an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72a2f37d82868e1b25793c4d260c294c
https://doi.org/10.1093/hmg/10.3.195
https://doi.org/10.1093/hmg/10.3.195
Autor:
Lisbeth Tranebjärg, Bjorn Solem, Paul Van de Heyning, Sai Prasad, Wendy Balemans, Kristien Verhoeven, Guy Van Camp, Isabelle Schatteman, Frank De Clau, Toril Fagerheim, Richard J.H. Smith, M. Verstreken, Sigrid Wayne
Publikováno v:
Human genetics
DFNA10 originally was mapped to the long arm of chromosome 6 in a large American family segregating for autosomal dominant progressive nonsyndromic hearing impairment. By extending this American family, we have reduced the original DFNA10 candidate r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91a6b4ff1eb7a5bf50378fdeb6b24687
https://doi.org/10.1007/s004390000319
https://doi.org/10.1007/s004390000319
Autor:
M. L. Kraft, Guy Van Camp, Paul Coucke, Sigrid Wayne, John H. Greinwald, Ross I. S. Zbar, Achih H. Chen, Richard J.H. Smith, C. R. Srikumari Srisailapathy, Michael Lovett, Sai Prasad, Daryl A. Scott, Arabandi Ramesh
Publikováno v:
American journal of medical genetics
Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of hereditary hearing impairment (HHI). To date, 16 different loci have been reported, making ARNSHL an extremely heterogeneous disorder. One of these loci, DFNB4, was map
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74a168e9b0034112b8e626e282081d52
https://doi.org/10.1002/(sici)1096-8628(19980630)78:2<107::aid-ajmg2>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19980630)78:2<107::aid-ajmg2>3.0.co
Autor:
Kunihiro Fukushima, C. R. Srikumari Srisailapathy, Arabandi Ramesh, Richard J.H. Smith, Sigrid Wayne, Ross I. S. Zbar
Publikováno v:
Otolaryngology–Head and Neck Surgery. 118:333-337
Hereditary hearing impairment affects approximately 0.05% of all children born in the United States. It is most commonly autosomal recessive, nonsyndromic, and monogenic [autosomal recessive nonsyndromic hearing loss (ARNSHL)]. Although the number of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1407159d5924c68d4ae61903f2118bc1
https://doi.org/10.1016/s0194-59989870311-0
https://doi.org/10.1016/s0194-59989870311-0
Autor:
Peter Van Hauwe, Arabandi Ramesh, Daryl A. Scott, Ross I. S. Zbar, Michael Lovett, Val C. Sheffield, C. R. Srikumari Srisailapathy, Achih Chen, Sigrid Wayne, Adam M. Bell, Guy Van Camp, Richard J.H. Smith, Jennifer Ashley
Publikováno v:
Scopus-Elsevier
American journal of medical genetics
American journal of medical genetics
Autosomal recessive non-syndromic hearing loss (ARNSHL) is the most common form of prelingual inherited hearing impairment. A small consanguineous family with this disorder was ascertained through the Institute of Basic Medical Sciences in Madras, In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26299c0502bbbaf53336fdf34f3dc129
https://doi.org/10.1002/(sici)1096-8628(19970905)71:4<467::aid-ajmg18>3.0.co
https://doi.org/10.1002/(sici)1096-8628(19970905)71:4<467::aid-ajmg18>3.0.co
Autor:
Vazken M. Der Kaloustian, Val C. Sheffield, Robert C. Polomeno, Daryl A. Scott, Melvin D. Schloss, J. Fielding Hejtmancik, Richard J.H. Smith, Sigrid Wayne
Publikováno v:
Human Molecular Genetics. 5:1689-1692
The Usher syndromes (USH) are a group of autosomal recessive diseases characterized by progressive pigmentary retinopathy and sensorineural hearing loss. Five USH genes have been mapped and at least one additional gene is known to exist. By homozygos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3581545d0aed08aea4670c7aebec0a75
https://doi.org/10.1093/hmg/5.10.1689
https://doi.org/10.1093/hmg/5.10.1689
Autor:
Ross I. S. Zbar, Dilip Deshmukh, Kunihiro Fukushima, Hana Skarka, Elizabeth A. Thomas, Anil K. Lalwani, Arabandi Ramesh, Ishwar C. Verma, Edward R. Wilcox, Subrinder Kumar, C. R. Srikumari Srisailapathy, Richard J.H. Smith, Pawan K. Jain, Sigrid Wayne, Barbara Ploplis
Publikováno v:
Human Molecular Genetics. 4:2391-2394
A locus for recessive neurosensory nonsyndromic hearing impairment maps to chromosome 9q13-q21 in two regionally separate consanguineous families from India. Each family demonstrates a LOD score greater than 4.5 to this region. D9S15, tightly linked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e6eb5bdfe2b48a14309e09cf30fd94
https://doi.org/10.1093/hmg/4.12.2391
https://doi.org/10.1093/hmg/4.12.2391
Autor:
Sigrid Wayne
Publikováno v:
Molecular Pathology Library ISBN: 9781441917065
Autoimmunity is defined as an immune response directed against a self-antigen - an antigen of host origin, within host tissue. Autoimmunity encompasses nonpathologic, naturally occurring immune responses, such as cold autoantibodies to red blood cell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::beb260a243f7fc44b44062ee25a31fa2
https://doi.org/10.1007/978-1-4419-1707-2_2
https://doi.org/10.1007/978-1-4419-1707-2_2
