Ribosomal protein L24 defect in Belly spot and tail (Bst), a mouse Minute
Oliver, Edward R, Saunders, Thomas L, Tarlé, Susan A, Glaser, Tom
Published in Development (Cambridge) (01.08.2004)
Published in Development (Cambridge) (01.08.2004)
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Journal Article
Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease
Kaukonen, Maria, Woods, Sean, Ahonen, Saija, Lemberg, Seppo, Hellman, Maarit, Hytönen, Marjo K., Permi, Perttu, Glaser, Tom, Lohi, Hannes
Published in Cell reports (Cambridge) (29.05.2018)
Published in Cell reports (Cambridge) (29.05.2018)
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ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous
PRASOV, Lev, MASUD, Tehmina, KELBERMAN, Daniel, SOWDEN, Jane C, DATTANI, Mehul T, GLASER, Tom, KHALIQ, Shagufta, QASIM MEHDI, S, ABID, Aiysha, OLIVER, Edward R, SILVA, Eduardo D, LEWANDA, Amy, BRODSKY, Michael C, BORCHERT, Mark
Published in Human molecular genetics (15.08.2012)
Published in Human molecular genetics (15.08.2012)
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Targeting of GFP to Newborn Rods by Nrl Promoter and Temporal Expression Profiling of Flow-Sorted Photoreceptors
Akimoto, Masayuki, Cheng, Hong, Zhu, Dongxiao, Brzezinski, Joseph A., Khanna, Ritu, Filippova, Elena, Oh, Edwin C. T., Jing, Yuezhou, Linares, Jose-Luis, Brooks, Matthew, Zareparsi, Sepideh, Mears, Alan J., Hero, Alfred, Glaser, Tom, Swaroop, Anand
Published in Proceedings of the National Academy of Sciences - PNAS (07.03.2006)
Published in Proceedings of the National Academy of Sciences - PNAS (07.03.2006)
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Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens
Lam, Phuong T, Padula, Stephanie L, Hoang, Thanh V, Poth, Justin E, Liu, Lin, Liang, Chun, LeFever, Adam S, Wallace, Lindsay M, Ashery-Padan, Ruth, Riggs, Penny K, Shields, Jordan E, Shaham, Ohad, Rowan, Sheldon, Brown, Nadean L, Glaser, Tom, Robinson, Michael L
Published in Human genomics (15.02.2019)
Published in Human genomics (15.02.2019)
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Journal Article
Math5 expression and function in the central auditory system
Saul, Sara M., Brzezinski, Joseph A., Altschuler, Richard A., Shore, Susan E., Rudolph, Dellaney D., Kabara, Lisa L., Halsey, Karin E., Hufnagel, Robert B., Zhou, Jianxun, Dolan, David F., Glaser, Tom
Published in Molecular and cellular neuroscience (01.01.2008)
Published in Molecular and cellular neuroscience (01.01.2008)
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Journal Article
3' Deletions Cause Aniridia by Preventing PAX6 Gene Expression
Lauderdale, J D, Wilensky, J S, Oliver, E R, Walton, D S, Glaser, T
Published in Proceedings of the National Academy of Sciences - PNAS (05.12.2000)
Published in Proceedings of the National Academy of Sciences - PNAS (05.12.2000)
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Journal Article
The eyeless mouse mutation (ey1) removes an alternative start codon from the Rx/rax homeobox gene
Tucker, Priscilla, Laemle, Lois, Munson, Amanda, Kanekar, Shami, Oliver, Edward R., Brown, Nadean, Schlecht, Hans, Vetter, Monica, Glaser, Tom
Published in Genesis (New York, N.Y. : 2000) (01.09.2001)
Published in Genesis (New York, N.Y. : 2000) (01.09.2001)
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Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
Call, Katherine M., Glaser, Tom, Ito, Caryn Y., Buckler, Alan J., Pelletier, Jerry, Haber, Daniel A., Rose, Elise A., Kral, Astrid, Yeger, Herman, Lewis, William H., Jones, Carol, Housman, David E.
Published in Cell (09.02.1990)
Published in Cell (09.02.1990)
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Genomic, Transcriptional and Mutational Analysis of the Mouse microphthalmia Locus
Hallsson, Jon H, Favor, Jack, Hodgkinson, Colin, Glaser, Tom, Lamoreux, M. Lynn, Magnusdottir, Rannveig, Gunnarsson, Gunnar J, Sweet, Hope O, Copeland, Neal G, Jenkins, Nancy A, Steingrimsson, Eirikur
Published in Genetics (Austin) (01.05.2000)
Published in Genetics (Austin) (01.05.2000)
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Journal Article
An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor
Haber, Daniel A., Buckler, Alan J., Glaser, Tom, Call, Katherine M., Pelletier, Jerry, Sohn, Robert L., Douglass, Edwin C., Housman, David E.
Published in Cell (29.06.1990)
Published in Cell (29.06.1990)
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Cloning of Human Mineralocorticoid Receptor Complementary DNA: Structural and Functional Kinship with the Glucocorticoid Receptor
Arriza, Jeffrey L., Weinberger, Cary, Cerelli, Gail, Glaser, Tom M., Handelin, Barbara L., Housman, David E., Evans, Ronald M.
Published in Science (American Association for the Advancement of Science) (17.07.1987)
Published in Science (American Association for the Advancement of Science) (17.07.1987)
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