A Spectrum of FOXC1 Mutations Suggests Gene Dosage as a Mechanism for Developmental Defects of the Anterior Chamber of the Eye
Nishimura, Darryl Y., Searby, Charles C., Alward, Wallace L., Walton, David, Craig, Jamie E., Mackey, David A., Kawase, Kazuhide, Kanis, Adam B., Patil, Shivanand R., Stone, Edwin M., Sheffield, Val C.
Published in American journal of human genetics (01.02.2001)
Published in American journal of human genetics (01.02.2001)
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Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humor
JACOBSON, Nasreen, ANDREWS, Michael, ALWARD, W. L. M, STONE, Edwin M, CLARK, Abbot F, SHEFFIELD, Val C, SHEPARD, Allan R, NISHIMURA, Darryl, SEARBY, Charles, FINGERT, John H, HAGEMAN, Greg, MULLINS, Robert, DAVIDSON, Beverly L, KWON, Young H
Published in Human molecular genetics (15.01.2001)
Published in Human molecular genetics (15.01.2001)
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Identification of a Gene That Causes Primary Open Angle Glaucoma
Stone, Edwin M., Fingert, John H., Wallace L. M. Alward, Nguyen, Thai D., Polansky, Jon R., Sara L. F. Sunden, Nishimura, Darryl, Clark, Abbot F., Nystuen, Arne, Nichols, Brian E., Mackey, David A., Ritch, Robert, Kalenak, Jeffrey W., Craven, E. Randy, Sheffield, Val C.
Published in Science (American Association for the Advancement of Science) (31.01.1997)
Published in Science (American Association for the Advancement of Science) (31.01.1997)
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Journal Article
Acute Hepatitis B Virus Infection: Relation of Age to the Clinical Expression of Disease and Subsequent Development of the Carrier State
McMahon, Brian J., Alward, Wallace L. M., Hall, David B., Heyward, William L., Bender, Thomas R., Francis, Donald P., Maynard, James E.
Published in The Journal of infectious diseases (01.04.1985)
Published in The Journal of infectious diseases (01.04.1985)
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Journal Article
Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development
SMITH, R. S, ZABALETA, A, KUME, T, SAVINOVA, O. V, KIDSON, S. H, MARTIN, J. E, NISHIMURA, D. Y, ALWARD, W. L. M, HOGAN, B. L. M, JOHN, S. W. M
Published in Human molecular genetics (12.04.2000)
Published in Human molecular genetics (12.04.2000)
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Journal Article
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
Murray, Jeffrey C, Semina, Elena V, Ferrell, Robert E, Mintz-Hittner, Helen A, Bitoun, Pierre, Alward, Wallace Lee M, Reiter, Rebecca S, Funkhauser, Carrie, Daack-Hirsch, Sandra
Published in Nature genetics (01.06.1998)
Published in Nature genetics (01.06.1998)
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Cloning and characterization of a novel bicoid -related homeobox transcription factor gene, RIEG , involved in Rieger syndrome
Alward, W. Lee M, Semina, Elena V, Small, Kent W, Datson, Nicole A, Siegel-Bartelt, Jacqueline, Murray, Jeffrey C, Bierke-Nelson, Diane, Reiter, Rebecca, Zabel, Bernhard U, Carey, John C, Bitoun, Pierre, Leysens, Nancy J
Published in Nature genetics (01.12.1996)
Published in Nature genetics (01.12.1996)
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Clinical Features Associated with Mutations in the Chromosome 1 Open-Angle Glaucoma Gene (GLC1A)
Alward, Wallace L.M, Fingert, John H, Coote, Michael A, Johnson, A. Tim, Lerner, S. Fabian, Junqua, Denise, Durcan, Fiona J, McCartney, Paul J, Mackey, David A, Sheffield, Val C, Stone, Edwin M
Published in The New England journal of medicine (09.04.1998)
Published in The New England journal of medicine (09.04.1998)
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Journal Article
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
Sheffield, Val C, Nishimura, Darryl Y, Swiderski, Ruth E, Alward, Wallace L. M, Searby, Charles C, Patil, Shivanand R, Bennet, Steven R, Kanis, Adam B, Gastier, Julie M, Stone, Edwin M
Published in Nature genetics (01.06.1998)
Published in Nature genetics (01.06.1998)
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Journal Article
Nocturnal arterial hypotension and its role in optic nerve head and ocular ischemic disorders
Hayreh, S S, Zimmerman, M B, Podhajsky, P, Alward, W L
Published in American journal of ophthalmology (15.05.1994)
Published in American journal of ophthalmology (15.05.1994)
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The genetics of open-angle glaucoma: The story of GLC1A and myocilin
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Conference Proceeding
The Long-Term Serological Course of Asymptomatic Hepatitis B Virus Carriers and the Development of Primary Hepatocellular Carcinoma
Alward, Wallace L. M., McMahon, Brian J., Hall, David B., Heyward, William L., Francis, Donald P., Bender, Thomas R.
Published in The Journal of infectious diseases (01.04.1985)
Published in The Journal of infectious diseases (01.04.1985)
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Journal Article
Autosomal dominant iris hypoplasia is caused by a mutation in the rieger syndrome (rieg/pitx2) gene
Alward, Wallace L.M., Semina, Elena V., Kalenak, Jeffrey W., Héon, Elise, Sheth, Bhavna P., Stone, Edwin M., Murray, Jeffrey C.
Published in American journal of ophthalmology (1998)
Published in American journal of ophthalmology (1998)
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Journal Article
Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve head
Clark, A F, Kawase, K, English-Wright, S, Lane, D, Steely, H T, Yamamoto, T, Kitazawa, Y, Kwon, Y H, Fingert, J H, Swiderski, R E, Mullins, R F, Hageman, G S, Alward, W L, Sheffield, V C, Stone, E M
Published in The FASEB journal (01.05.2001)
Published in The FASEB journal (01.05.2001)
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Linkage of posterior polymorphous corneal dystrophy to 20q11
Héon, E, Mathers, W D, Alward, W L, Weisenthal, R W, Sunden, S L, Fishbaugh, J A, Taylor, C M, Krachmer, J H, Sheffield, V C, Stone, E M
Published in Human molecular genetics (01.03.1995)
Published in Human molecular genetics (01.03.1995)
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Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma
Johnson, A T, Drack, A V, Kwitek, A E, Cannon, R L, Stone, E M, Alward, W L
Published in Ophthalmology (Rochester, Minn.) (01.04.1993)
Published in Ophthalmology (Rochester, Minn.) (01.04.1993)
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