(Q28206127)

2

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Kazuhito Matsuzaki

3

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Tadashi Anan

4

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Mitsuhiro Matsumoto

5

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Masayuki Ando

6

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Hideyuki Saya

7

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Mitsuyoshi Nakao

Journal of Biological Chemistry

8

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language of work or name

English

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publication date

1 February 2002

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published in

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volume

277

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page(s)

3599-605

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issue

5

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cites work

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The lore of the RINGs: substrate recognition and catalysis by ubiquitin ligases

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A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase

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Genetic and molecular analysis of hyperplastic discs, a gene whose product is required for regulation of cell proliferation in Drosophila melanogaster imaginal discs and germ cells

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Identification of a human HECT family protein with homology to the Drosophila tumor suppressor gene hyperplastic discs

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Conserved BRCT regions of TopBP1 and of the tumor suppressor BRCA1 bind strand breaks and termini of DNA

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A DNA-topoisomerase-II-binding protein with eight repeating regions similar to DNA-repair enzymes and to a cell-cycle regulator

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Damage and replication checkpoint control in fission yeast is ensured by interactions of Crb2, a protein with BRCT motif, with Cut5 and Chk1.

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Human ubiquitin-protein ligase Nedd4: expression, subcellular localization and selective interaction with ubiquitin-conjugating enzymes

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Nedd4-like proteins: an emerging family of ubiquitin-protein ligases implicated in diverse cellular functions

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Megabase chromatin domains involved in DNA double-strand breaks in vivo

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DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139

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The DNA damage response: putting checkpoints in perspective

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Keratinocytes exposed to ultraviolet radiation reveal three down-regulated genes with potential function in differentiation and cell cycle control

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Identification of HHR23A as a substrate for E6-associated protein-mediated ubiquitination.

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De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.

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UBE3A/E6-AP mutations cause Angelman syndrome

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BRCT domain-containing protein TopBP1 functions in DNA replication and damage response

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The stabilization mechanism of mutant-type p53 by impaired ubiquitination: the loss of wild-type p53 function and the hsp90 association

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