scholarly article | Q13442814 |
P356 | DOI | 10.1007/S00412-005-0029-1 |
P698 | PubMed publication ID | 16240122 |
P2093 | author name string | Timothy F Lane | |
Brian P Chadwick | |||
P2860 | cites work | Chromatin dynamics at DNA replication, transcription and repair | Q22065678 |
BRCA1 is associated with a human SWI/SNF-related complex: linking chromatin remodeling to breast cancer | Q24273430 | ||
Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant | Q24291187 | ||
BRCA1-induced large-scale chromatin unfolding and allele-specific effects of cancer-predisposing mutations | Q24291985 | ||
Role of histone H2A ubiquitination in Polycomb silencing | Q24305090 | ||
BRCA1 participates in DNA decatenation | Q24305584 | ||
BRCA1 supports XIST RNA concentration on the inactive X chromosome | Q24316340 | ||
Stable X chromosome inactivation involves the PRC1 Polycomb complex and requires histone MACROH2A1 and the CULLIN3/SPOP ubiquitin E3 ligase | Q24529056 | ||
Factors associated with the mammalian RNA polymerase II holoenzyme | Q24546284 | ||
Time-Sequence of Human Chromosome Duplication | Q59066816 | ||
The human X-inactivation centre is not required for maintenance of X-chromosome inactivation | Q59073076 | ||
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia | Q60641474 | ||
Impaired meiotic DNA-damage repair and lack of crossing-over during spermatogenesis in BRCA1 full-length isoform deficient mice | Q73139875 | ||
Conditional deletion of Xist disrupts histone macroH2A localization but not maintenance of X inactivation | Q78079159 | ||
Ring1b-mediated H2A ubiquitination associates with inactive X chromosomes and is involved in initiation of X inactivation | Q80918747 | ||
The BRCA1-associated protein BACH1 is a DNA helicase targeted by clinically relevant inactivating mutations | Q24622650 | ||
Cell cycle-dependent colocalization of BARD1 and BRCA1 proteins in discrete nuclear domains | Q24645684 | ||
XIST RNA paints the inactive X chromosome at interphase: evidence for a novel RNA involved in nuclear/chromosome structure | Q24672147 | ||
Cell cycle-dependent localization of macroH2A in chromatin of the inactive X chromosome | Q24672610 | ||
Synergism of Xist RNA, DNA methylation, and histone hypoacetylation in maintaining X chromosome inactivation | Q24678487 | ||
DNA double-stranded breaks induce histone H2AX phosphorylation on serine 139 | Q28131715 | ||
Replication-dependent marking of DNA by PCNA facilitates CAF-1-coupled inheritance of chromatin | Q28138029 | ||
Association of BRCA1 with the hRad50-hMre11-p95 complex and the DNA damage response | Q28140763 | ||
A critical role for histone H2AX in recruitment of repair factors to nuclear foci after DNA damage | Q28144576 | ||
H2AX: the histone guardian of the genome | Q28274279 | ||
Histone macroH2A1 is concentrated in the inactive X chromosome of female mammals | Q28274301 | ||
BRCA1 is a 220-kDa nuclear phosphoprotein that is expressed and phosphorylated in a cell cycle-dependent manner | Q28287385 | ||
Association of BRCA1 with Rad51 in mitotic and meiotic cells | Q28302118 | ||
Polycomb group proteins Ring1A/B link ubiquitylation of histone H2A to heritable gene silencing and X inactivation | Q28505166 | ||
The human XIST gene: analysis of a 17 kb inactive X-specific RNA that contains conserved repeats and is highly localized within the nucleus | Q29614336 | ||
The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus | Q29617834 | ||
Gene action in the X-chromosome of the mouse (Mus musculus L.) | Q29618263 | ||
Co-localization of chicken DNA topoisomerase IIalpha, but not beta, with sites of DNA replication and possible involvement of a C-terminal region of alpha through its binding to PCNA. | Q30687752 | ||
A shift from reversible to irreversible X inactivation is triggered during ES cell differentiation | Q33908327 | ||
PCNA connects DNA replication to epigenetic inheritance in yeast. | Q33926058 | ||
The human decatenation checkpoint. | Q33946976 | ||
H2AX is required for chromatin remodeling and inactivation of sex chromosomes in male mouse meiosis | Q33965393 | ||
ATM-dependent DNA damage-independent mitotic phosphorylation of H2AX in normally growing mammalian cells. | Q34049864 | ||
Xist RNA and the mechanism of X chromosome inactivation | Q34158806 | ||
The multiple nuclear functions of BRCA1: transcription, ubiquitination and DNA repair | Q34203060 | ||
Distribution and dynamics of chromatin modification induced by a defined DNA double-strand break | Q34354650 | ||
Maintenance of chromatin states: an open-and-shut case | Q35145809 | ||
Barring gene expression after XIST: maintaining facultative heterochromatin on the inactive X. | Q35688633 | ||
BRCA1 and transcription | Q35836752 | ||
DNA repair: the importance of phosphorylating histone H2AX. | Q36032031 | ||
Developmentally regulated alterations in Polycomb repressive complex 1 proteins on the inactive X chromosome | Q36322853 | ||
Asynchronous duplication of human chromosomes and the origin of sex chromatin | Q36394766 | ||
Multiple spatially distinct types of facultative heterochromatin on the human inactive X chromosome | Q37694528 | ||
Inhibition of DNA decatenation, but not DNA damage, arrests cells at metaphase | Q40512889 | ||
BRCA1, histone H2AX phosphorylation, and male meiotic sex chromosome inactivation. | Q52064286 | ||
THE GENETICS OF BREAST CANCER SUSCEPTIBILITY | Q57272243 | ||
P433 | issue | 6 | |
P921 | main subject | phosphorylation | Q242736 |
P304 | page(s) | 432-439 | |
P577 | publication date | 2005-11-15 | |
P1433 | published in | Chromosoma | Q15765851 |
P1476 | title | BRCA1 associates with the inactive X chromosome in late S-phase, coupled with transient H2AX phosphorylation | |
P478 | volume | 114 |
Q35175983 | A deletion at the mouse Xist gene exposes trans-effects that alter the heterochromatin of the inactive X chromosome and the replication time and DNA stability of both X chromosomes |
Q40251391 | Abnormalities of the inactive X chromosome are a common feature of BRCA1 mutant and sporadic basal-like breast cancer |
Q35447270 | Advancing small-molecule-based chemical biology with next-generation sequencing technologies. |
Q30480563 | BRCA1 foci in normal S-phase nuclei are linked to interphase centromeres and replication of pericentric heterochromatin |
Q33290461 | Cytometry of ATM activation and histone H2AX phosphorylation to estimate extent of DNA damage induced by exogenous agents |
Q33988971 | DNA damage and DNA damage responses in THP-1 monocytes after exposure to spores of either Stachybotrys chartarum or Aspergillus versicolor or to T-2 toxin |
Q30436771 | Double-strand DNA breaks recruit the centromeric histone CENP-A. |
Q24608343 | Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications |
Q30560450 | Loss of WSTF results in spontaneous fluctuations of heterochromatin formation and resolution, combined with substantial changes to gene expression |
Q35171563 | Multiple facets of histone variant H2AX: a DNA double-strand-break marker with several biological functions |
Q37398589 | New developments in post-translational modifications and functions of histone H2A variants |
Q36834533 | Nucleotide-resolution DNA double-strand break mapping by next-generation sequencing |
Q42738107 | Phosphorylation of the SQ H2A.X motif is required for proper meiosis and mitosis in Tetrahymena thermophila |
Q34014307 | Rad3 decorates critical chromosomal domains with gammaH2A to protect genome integrity during S-Phase in fission yeast |
Q34482956 | The WSTF-ISWI chromatin remodeling complex transiently associates with the human inactive X chromosome during late S-phase prior to BRCA1 and γ-H2AX |
Q37038673 | The gamma-H2A.X: is it just a surrogate marker of double-strand breaks or much more? |
Q37325705 | Toxoplasma H2A variants reveal novel insights into nucleosome composition and functions for this histone family |
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