相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Exomic analysis of myxoid liposarcomas, synovial sarcomas, and osteosarcomas
Christine G. Joseph et al.
GENES CHROMOSOMES & CANCER (2014)
Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability
Katrina Tatton-Brown et al.
NATURE GENETICS (2014)
Mutations in SETD2 and genes affecting histone H3K36 methylation target hemispheric high-grade gliomas
Adam M. Fontebasso et al.
ACTA NEUROPATHOLOGICA (2013)
The NSD1 and EZH2 Overgrowth Genes, Similarities and Differences
Katrina Tatton-Brown et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2013)
Mutations in EZH2 Cause Weaver Syndrome
William T. Gibson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
The transcriptional landscape and mutational profile of lung adenocarcinoma
Jeong-Sun Seo et al.
GENOME RESEARCH (2012)
Epigenetic protein families: a new frontier for drug discovery
Cheryl H. Arrowsmith et al.
NATURE REVIEWS DRUG DISCOVERY (2012)
Histone methylation: a dynamic mark in health, disease and inheritance
Eric L. Greer et al.
NATURE REVIEWS GENETICS (2012)
Understanding the language of Lys36 methylation at histone H3
Eric J. Wagner et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2012)
The Structure of NSD1 Reveals an Autoregulatory Mechanism Underlying Histone H3K36 Methylation
Qi Qiao et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
H3K36 Methylation Antagonizes PRC2-mediated H3K27 Methylation
Wen Yuan et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2011)
What can exome sequencing do for you?
Jacek Majewski et al.
JOURNAL OF MEDICAL GENETICS (2011)
The Polycomb complex PRC2 and its mark in life
Raphael Margueron et al.
NATURE (2011)
The functional spectrum of low-frequency coding variation
Gabor T. Marth et al.
GENOME BIOLOGY (2011)
Histone Methyltransferase Gene SETD2 Is a Novel Tumor Suppressor Gene in Clear Cell Renal Cell Carcinoma
Gerben Duns et al.
CANCER RESEARCH (2010)
Sotos syndrome and de novo balanced autosomal translocation (t(3;6)(p21;p21))
C. T. R. M. Schrander-Stumpel et al.
CLINICAL GENETICS (2010)
Detection of nonneutral substitution rates on mammalian phylogenies
Katherine S. Pollard et al.
GENOME RESEARCH (2010)
Histone H3 lysine 36 methyltransferase Hypb/Setd2 is required for embryonic vascular remodeling
Ming Hu et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Differential chromatin marking of introns and expressed exons by H3K36me3
Paulina Kolasinska-Zwierz et al.
NATURE GENETICS (2009)
The Iws1:Spt6:CTD complex controls cotranscriptional mRNA biosynthesis and HYPB/Setd2-mediated histone H3K36 methylation
Sunnie M. Yoh et al.
GENES & DEVELOPMENT (2008)
Dynamic histone H3 methylation during gene induction: HYPB/Setd2 mediates all H3K36 trimethylation
John W. Edmunds et al.
EMBO JOURNAL (2008)
Sotos syndrome
Genevieve Baujat et al.
ORPHANET JOURNAL OF RARE DISEASES (2007)
Genome-wide maps of chromatin state in pluripotent and lineage-committed cells
Tarjei S. Mikkelsen et al.
NATURE (2007)
Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth
Jenny Douglas et al.
NATURE GENETICS (2007)
High-resolution profiling of histone methylations in the human genome
Artern Barski et al.
CELL (2007)
Chromatin modifications and their function
Tony Kouzarides
CELL (2007)
Histone H3 methylation by Set2 directs deacetylation of coding regions by Rpd3S to suppress spurious intragenic transcription
MJ Carrozza et al.
CELL (2005)
Clinical and molecular overlap in overgrowth syndromes
G Baujat et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2005)
Genotype-phenotype associations in Sotos syndrome:: An analysis of 266 individuals with NSD1 aberrations
K Tatton-Brown et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
The SET-domain protein superfamily: protein lysine methyltransferases
SC Dillon et al.
GENOME BIOLOGY (2005)
Spectrum of NSD1 mutations in Sotos and Weaver syndromes
M Rio et al.
JOURNAL OF MEDICAL GENETICS (2003)
NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of weaver syndrome but are rare in other overgrowth phenotypes
J Douglas et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Haploinsufficiency of NSD1 causes Sotos syndrome
N Kurotaki et al.
NATURE GENETICS (2002)
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia
RJ Jaju et al.
BLOOD (2001)
Predicting deleterious amino acid substitutions
PC Ng et al.
GENOME RESEARCH (2001)
dbSNP: the NCBI database of genetic variation
ST Sherry et al.
NUCLEIC ACIDS RESEARCH (2001)
分享论文
