Search Results - "GEBUHR, T"

Characterization of mammary tumors from Brg1 heterozygous mice by Bultman, S J, Herschkowitz, J I, Godfrey, V, Gebuhr, T C, Yaniv, M, Perou, C M, Magnuson, T

“…Mammalian SWI/SNF-related complexes have been implicated in cancer based on some of the subunits physically interacting with retinoblastoma (RB) and other…”
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Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome by Bamshad, Michael, Lin, Robert C, Law, David J, Watkins, W. Scott, Krakowiak, Patrycja A, Moore, Mary E, Franceschini, Piergiorgio, Lala, Roberto, Holmes, Lewis B, Gebuhr, Tom C, Bruneau, Benoit G, Schinzel, Albert, Seidman, J. G, Seidman, Christine E, Jorde, Lynn B

“…Ulnar-mammary syndrome is a rare pleiotropic disorder affecting limb, apocrine gland, tooth and genital development. We demonstrate that mutations in human…”
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The role of Brg1, a catalytic subunit of mammalian chromatin-remodeling complexes, in T cell development by Gebuhr, Thomas C, Kovalev, Grigoriy I, Bultman, Scott, Godfrey, Virginia, Su, Lishan, Magnuson, Terry

“…Mammalian SWI-SNF-related complexes use brahma-related gene 1 (Brg1) as a catalytic subunit to remodel nucleosomes and regulate transcription. Recent…”
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A Model System to Study Genomic Imprinting of Human Genes by Gabriel, J. M., Higgins, M. J., Gebuhr, T. C., Shows, T. B., Saitoh, S., Nicholls, R. D.

“…Somatic-cell hybrids have been shown to maintain the correct epigenetic chromatin states to study developmental globin gene expression as well as gene…”
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Identification, characterization, and localization to chromosome 17q21-22 of the human TBX2 homolog, member of a conserved developmental gene family by Law, D J, Gebuhr, T, Garvey, N, Agulnik, S I, Silver, L M

“…The T-box motif is present in a family of genes whose structural features and expression patterns support their involvement in developmental gene regulation…”
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Coiled bodies preferentially associate with U4, U11, and U12 small nuclear RNA genes in interphase HeLa cells but not with U6 and U7 genes by Jacobs, E Y, Frey, M R, Wu, W, Ingledue, T C, Gebuhr, T C, Gao, L, Marzluff, W F, Matera, A G

“…Coiled bodies (CBs) are nuclear organelles involved in the metabolism of small nuclear RNAs (snRNAs) and histone messages. Their structural morphology and…”
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Pc-G/trx-G and the SWI/SNF connection: Developmental gene regulation through chromatin remodeling by Gebuhr, Thomas C., Bultman, Scott J., Magnuson, Terry

“…Pc‐G and trx‐G genes are responsible for maintenance of transcriptional regulation and provide a cellular memory mechanism throughout development. Studies in…”
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A Brg1 Null Mutation in the Mouse Reveals Functional Differences among Mammalian SWI/SNF Complexes by Bultman, Scott, Gebuhr, Tom, Yee, Della, La Mantia, Christian, Nicholson, Jackie, Gilliam, Anita, Randazzo, Filippo, Metzger, Daniel, Chambon, Pierre, Crabtree, Gerald, Magnuson, Terry

“…Mammalian SWI/SNF complexes utilize either brahma (Brm) or brahma-related gene 1 (Brg1) catalytic subunits to remodel nucleosomes in an ATP-dependent manner…”
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Localization of the Human Estrogen-Responsive Finger Protein (EFP) Gene (ZNF147) within a YAC Contig Containing the Myeloperoxidase (MPO) Gene by Law, David J., Prasad, Madhu A., King, Stephanie E., Spranger, Kristina D., Lee, Yoon Hee, Fox, Rita E., Collins, Elizabeth E., Gebuhr, Thomas C., Miller, Diane E., Petty, Elizabeth M.

“…The estrogen-responsive finger protein (EFP) gene (ZNF-147) belongs to a family of putative transcription factors that contain RING finger, B-box, and…”
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Holt-oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family by QUAN YI LI, NEWBURY-ECOB, R. A, BONNET, D, LYONNET, S, YOUNG, I. D, RAEBURN, J. A, BUCKLER, A. J, LAW, D. J, DAVID BROOK, J, TERRETT, J. A, WILSON, D. I, CURTIS, A. R. J, CHEONG HO YI, GEBUHR, T, BULLEN, P. J, ROBSON, S. C, STRACHAN, T

“…Holt-Oram syndrome is a developmental disorder affecting the heart and upper limb, the gene for which was mapped to chromosome 12 two years ago. We have now…”
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TBX10, a member of the Tbx1-subfamily of conserved developmental genes, is located at human chromosome 11q13 and proximal mouse chromosome 19 by Law, D J, Garvey, N, Agulnik, S I, Perlroth, V, Hahn, O M, Rhinehart, R E, Gebuhr, T C, Silver, L M

“…Here we report the isolation and mapping of a new T-box family member, TBX10/Tbx10, in human and mouse…”
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A Brg1 mutation that uncouples ATPase activity from chromatin remodeling reveals an essential role for SWI/SNF-related complexes in beta-globin expression and erythroid development by Bultman, Scott J, Gebuhr, Thomas C, Magnuson, Terry

“…The Brg1 catalytic subunit of SWI/SNF-related complexes has been implicated in many developmental and physiological processes, but null homozygotes die as…”
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Mutations in human TBX3 alter limb, apocrine, and genital development in ulnar-mammary syndrome

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