Thomas M Glaser mostly deals with Gene, Genetics, Molecular biology, Mutation and Wilms' tumor. His study looks at the relationship between Gene and topics such as DNA, which overlap with PAX2, Alternative splicing and Gene isoform. He mostly deals with Haploinsufficiency in his studies of Genetics.
His Molecular biology research integrates issues from Regulation of gene expression, Mutant and Ribosomal protein. His Mutation research includes elements of Ribosome biogenesis, Aniridia and WAGR syndrome. His Wilms' tumor study deals with Zinc finger intersecting with Wilms Tumor Protein and Gene expression.
His main research concerns Genetics, Gene, Molecular biology, Cell biology and Retinal ganglion cell. His Genetics and Chromosome, Locus, Aniridia, Gene mapping and Restriction fragment length polymorphism investigations all form part of his Genetics research activities. His work deals with themes such as DNA and Wilms' tumor, which intersect with Gene.
In his research on the topic of Wilms' tumor, Wilms Tumor Protein is strongly related with Zinc finger. His work focuses on many connections between Molecular biology and other disciplines, such as Regulation of gene expression, that overlap with his field of interest in Xenopus. He combines subjects such as Progenitor cell and Transcription factor with his study of Retinal ganglion cell.
Thomas M Glaser spends much of his time researching Cell biology, Retinal, Retinal ganglion cell, Retinal ganglion and Retina. His Cell biology research includes themes of Gene targeting, Genetically modified mouse, PAX6 and Null allele. His research investigates the link between Retinal and topics such as Optic nerve that cross with problems in Chromatin, Enhancer, Messenger RNA and Transcription.
In his research, Transcription factor is intimately related to Neurogenesis, which falls under the overarching field of Retinal ganglion. His research investigates the connection between Retina and topics such as Muller glia that intersect with problems in Cell cycle. Cell cycle is a subfield of Genetics that Thomas M Glaser tackles.
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Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus.
Katherine M. Call;Thomas M Glaser;Caryn Y. Ito;Alan J. Buckler.
Cell (1990)
Cloning of human mineralocorticoid receptor complementary DNA: structural and functional kinship with the glucocorticoid receptor
Jeffrey L. Arriza;Jeffrey L. Arriza;Cary Weinberger;Cary Weinberger;Gail Cerelli;Thomas M Glaser.
Science (1987)
An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor.
Daniel A. Haber;Daniel A. Haber;Alan J. Buckler;Thomas M Glaser;Katherine M. Call.
Cell (1990)
PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects
Tom Glaser;Lisa Jepeal;Janice G. Edwards;S. Robert Young.
Nature Genetics (1994)
Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene.
Tom Glaser;David S. Walton;Richard L. Maas.
Nature Genetics (1992)
WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour
Jerry Pelletier;Jerry Pelletier;Wendy Bruening;Frederick P. Li;Daniel A. Haber;Daniel A. Haber.
Nature (1991)
Math5 is required for retinal ganglion cell and optic nerve formation
Nadean L. Brown;Nadean L. Brown;Sima Patel;Joseph Brzezinski;Tom Glaser.
Development (2001)
Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing.
Jonathan A. Epstein;Thomas M Glaser;Jiexing Cai;Lisa Jepeal.
Genes & Development (1994)
Identification of a Pax paired domain recognition sequence and evidence for DNA-dependent conformational changes.
Jonathan Epstein;Jiexing Cai;Thomas M Glaser;Lisa Jepeal.
Journal of Biological Chemistry (1994)
Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development.
Alan J. Buckler;Jerry Pelletier;Daniel A. Haber;Thomas M Glaser.
Molecular and Cellular Biology (1991)
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