Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Taryn M Phippen"'
Autor:
Andreas Rechtsteiner, Sevinc Ercan, Teruaki Takasaki, Taryn M Phippen, Thea A Egelhofer, Wenchao Wang, Hiroshi Kimura, Jason D Lieb, Susan Strome
Publikováno v:
PLoS Genetics, Vol 6, Iss 9, p e1001091 (2010)
Methylation of histone H3K36 in higher eukaryotes is mediated by multiple methyltransferases. Set2-related H3K36 methyltransferases are targeted to genes by association with RNA Polymerase II and are involved in preventing aberrant transcription init
Externí odkaz:
https://doaj.org/article/22760d6767a24ab5ad8e51c72b532913
Autor:
Taryn M Phippen, Amir Orian, Mona Abed, Jeffrey J. Delrow, Bella Koltun, Kevin C. Barry, Susan M. Parkhurst, Dorit Kenyagin
Publikováno v:
The EMBO Journal. 30:1289-1301
Transcriptional cofactors are essential for proper embryonic development. One such cofactor in Drosophila, Degringolade (Dgrn), encodes a RING finger/E3 ubiquitin ligase. Dgrn and its mammalian ortholog RNF4 are SUMO-targeted ubiquitin ligases (STUbL
Autor:
Mona, Abed, Kevin C, Barry, Dorit, Kenyagin, Bella, Koltun, Taryn M, Phippen, Jeffrey J, Delrow, Susan M, Parkhurst, Amir, Orian
Publikováno v:
The EMBO journal. 30(7)
Transcriptional cofactors are essential for proper embryonic development. One such cofactor in Drosophila, Degringolade (Dgrn), encodes a RING finger/E3 ubiquitin ligase. Dgrn and its mammalian ortholog RNF4 are SUMO-targeted ubiquitin ligases (STUbL
Autor:
Gustavo D. Aguirre, Gregory M. Acland, David R. Sargan, Duska J. Sidjanin, John L. McElwee, Jennifer K. Lowe, Elaine A. Ostrander, B.S. Milne, Taryn M. Phippen
Publikováno v:
Human molecular genetics. 11(16)
Cone degeneration (cd ) is an autosomal recessive canine disease that occurs naturally in the Alaskan Malamute and German Shorthaired Pointer breeds. It is phenotypically similar to human achromatopsia, a heterogeneous autosomal recessive disorder as