Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Samples, J R"'
Autor:
Samples, J. R.
Publikováno v:
Indianapolis Business Journal. 9/13/2024, Vol. 45 Issue 30, p15A-15A. 1/8p.
Autor:
Jeffers, Tim, Samples, J. R.
Publikováno v:
Indianapolis Business Journal. 3/15/2024, Vol. 45 Issue 4, p15A-15A. 1/4p.
Autor:
Kitsos, G., Petrou, Z., Grigoriadou, M., Samples, J. R., Hewitt, A. W., Kokotas, H., Giannoulia-Karantana, A., Mackey, D. A., Wirtz, M. K., Moschou, M., Ioannidis, J. P., Petersen, M. B.
BACKGROUND: Mutations in the MYOC gene have been shown to explain 5% of unrelated primary open angle glaucoma (POAG) in different populations. In particular, the T377M MYOC mutation has arisen at least three separate times in history, in Great Britai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::8c97b5986022cb64d9fe8620ca50862b
http://olympias.lib.uoi.gr/jspui/handle/123456789/19048
http://olympias.lib.uoi.gr/jspui/handle/123456789/19048
Autor:
Petersen, M. B., Kitsos, G., Samples, J. R., Gaudette, N. D., Economou-Petersen, E., Sykes, R., Rust, K., Grigoriadou, M., Aperis, G., Choi, D., Psilas, K., Craig, J. E., Kramer, P. L., Mackey, D. A., Wirtz, M. K.
PURPOSE: POAG is a complex disease; therefore, families in which a glaucoma gene has been mapped may carry additional POAG genes. The goal of this study was to determine whether mutations in the myocilin (MYOC) gene on chromosome 1 are present in two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::538d1b174b7613b4e9112790d640b31c
http://olympias.lib.uoi.gr/jspui/handle/123456789/24335
http://olympias.lib.uoi.gr/jspui/handle/123456789/24335
Autor:
Samples, J. R., Kitsos, G., Economou-Petersen, E., Steinkamp, P., Sykes, R., Rust, K., Patzer, C., Grigoriadou, M., Aperis, G., Psilas, K., Petersen, M. B., Wirtz, M. K.
The GLC1C locus for primary open-angle glaucoma (POAG) is inherited as an autosomal dominant trait. This region on chromosome 3 is 11 cM long. DNA samples from members of a Greek and an American GLC1C family were obtained to determine whether additio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::c7b227a2fca7ea82736fc10907b72c46
http://olympias.lib.uoi.gr/jspui/handle/123456789/18727
http://olympias.lib.uoi.gr/jspui/handle/123456789/18727
Autor:
Wirtz, M K, Samples, J R, Kramer, P L, Rust, K, Topinka, J R, Yount, J, Koler, R D, Acott, T S
Glaucoma is the third-leading cause of blindness in the world, affecting >13.5 million people. Adult-onset primary open-angle glaucoma (POAG) is the most common form of glaucoma in the United States. We present a family in which adult-onset POAG is i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3102da73dcd4fd44d04583ddb4fe086d
https://europepmc.org/articles/PMC1712411/
https://europepmc.org/articles/PMC1712411/
Akademický článek
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Publikováno v:
British Journal of Ophthalmology; Jan2004, Vol. 88 Issue 1, p125-30, 6p
Autor:
Faivere, L., Gorlin, R. J., Wirtz, M. K., Godfrey, M., Dagoneau, N., Samples, J. R., Le Merrer, M., Collod-Beroud, G., Boileau, C., Munnich, A., Cormier-Daire, V.
Publikováno v:
Journal of Medical Genetics; Jan2003, Vol. 40 Issue 1, p34-36, 3p, 1 Diagram
Autor:
Hewitt, A. W., Samples, J. R., Allingham, R. R., Jarvela, I., Kitsos, G., Krishnadas, S. R., Richards, J. E., Lichter, P. R., Petersen, M. B., Sundaresan, P., Wiggs, J. L., David Mackey AO, Wirtz, M. K.
Publikováno v:
University of Michigan Symplectic Elements
Scopus-Elsevier
University of Western Australia
Scopus-Elsevier
University of Western Australia
PURPOSE: The aim of this study was to determine if there is a common founder for the Thr377Met myocilin mutation in primary open angle glaucoma (POAG) families with various ethnic backgrounds. METHODS: Genomic DNA of 24 POAG-affected individuals from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::30779d8d9989600ac8cad3231afdb1ce
https://app.dimensions.ai/details/publication/pub.1077396692
https://app.dimensions.ai/details/publication/pub.1077396692