Citation Impact
Citing Papers
A genomic region associated with protection against severe COVID-19 is inherited from Neandertals
2021 StandoutNobel
Limits of long-term selection against Neandertal introgression
2019 StandoutNobel
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe
2018 StandoutNobel
Distinct MutS DNA-binding Modes That Are Differentially Modulated by ATP Binding and Hydrolysis
2001 StandoutNobel
Covalent inhibitors of glycosidases and their applications in biochemistry and biology
2008
Dynamic O-Glycosylation of Nuclear and Cytosolic Proteins
2001
Identification of a DAF-16 Transcriptional Target Gene, scl-1, that Regulates Longevity and Stress Resistance in Caenorhabditis elegans
2003
WAF1, a potential mediator of p53 tumor suppression
1993 Standout
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
1993 Standout
Mesenchymal Nuclear factor I B regulates cell proliferation and epithelial differentiation during lung maturation
2011
Epigenetics in human disease and prospects for epigenetic therapy
2004 StandoutNature
Evidence for archaic adaptive introgression in humans
2015
A Haplotype at STAT2 Introgressed from Neanderthals and Serves as a Candidate of Positive Selection in Papua New Guinea
2012
The genomic landscape of Neanderthal ancestry in present-day humans
2014 StandoutNatureNobel
An X-Linked Haplotype of Neandertal Origin Is Present Among All Non-African Populations
2011
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
1992 Standout
Lung Cancer
2008 Standout
Mutagenic and epigenetic effects of DNA methylation
1997
MutS and MutL Activate DNA Helicase II in a Mismatch-dependent Manner
1998 StandoutNobel
ESDN, a Novel Neuropilin-like Membrane Protein Cloned from Vascular Cells with the Longest Secretory Signal Sequence among Eukaryotes, Is Up-regulated after Vascular Injury
2001 StandoutNobel
Human Exonuclease I Is Required for 5′ and 3′ Mismatch Repair
2002 StandoutNobel
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Regulated expression and phosphorylation of a possible mammalian cell-cycle control protein
1988 StandoutNatureNobel
Crystal structure of the Hhal DNA methyltransferase complexed with S-adenosyl-l-methionine
1993 StandoutNobel
Gene Silencing in Cancer in Association with Promoter Hypermethylation
2003 Standout
The fission yeast gene pmt1+encodes a DNA methyltransferase homologue
1995 StandoutNobel
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals
2003 Standout
Nuclear import by karyopherin-βs: Recognition and inhibition
2010
The formation of internal 6-methyladenine residues in eucaryotic messenger rna
1992
Expression of Antisense to DNA Methyltransferase mRNA Induces DNA Demethylation and Inhibits Tumorigenesis
1995
Chemical Approaches To Perturb, Profile, and Perceive Glycans
2009 StandoutNobel
MECHANISMS AND BIOLOGICAL EFFECTS OF MISMATCH REPAIR
1991 StandoutNobel
Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer
1994 StandoutNature
Repair of Large Insertion/Deletion Heterologies in Human Nuclear Extracts Is Directed by a 5′ Single-strand Break and Is Independent of the Mismatch Repair System
1999 StandoutNobel
DNA-dependent Activation of the hMutSα ATPase
1998 StandoutNobel
N6-methyladenosine-dependent regulation of messenger RNA stability
2013 StandoutNature
Inference of human population history from individual whole-genome sequences
2011 StandoutNature
The LCCL module
2000
Cross-cultural estimation of the human generation interval for use in genetics-based population divergence studies
2005
Isolation and characterization of the cDNA encoding human DNA methyltransferase
1992
The MutL ATPase Is Required for Mismatch Repair
2000 StandoutNobel
Genes that act downstream of DAF-16 to influence the lifespan of Caenorhabditis elegans
2003 StandoutNature
Redundant Exonuclease Involvement in Escherichia coli Methyl-directed Mismatch Repair
2001 StandoutNobel
Hypermutability and mismatch repair deficiency in RER+ tumor cells
1993 StandoutNobel
Lysosomal storage diseases
1995
An alkylation-tolerant, mutator human cell line is deficient in strand-specific mismatch repair.
1993 StandoutNobel
Metabolic cross-talk allows labeling of O-linked β- N -acetylglucosamine-modified proteins via the N -acetylgalactosamine salvage pathway
2011 StandoutNobel
High expression of the DNA methyltransferase gene characterizes human neoplastic cells and progression stages of colon cancer.
1991
Removal of polymerase-produced mutant sequences from PCR products
1997 StandoutNobel
Alterations in DNA Methylation: A Fundamental Aspect of Neoplasia
1997 Standout
Control of thymidine kinase mRNA during the cell cycle.
1987
Aggregation-Induced Emission: Together We Shine, United We Soar!
2015 Standout
Oxidative Nucleobase Modifications Leading to Strand Scission
1998 Standout
Initiation of methyl-directed mismatch repair.
1992 StandoutNobel
In vivo requirement for RecJ, ExoVII, ExoI, and ExoX in methyl-directed mismatch repair
2001 StandoutNobel
Substrate spectrum of human excinuclease: repair of abasic sites, methylated bases, mismatches, and bulky adducts.
1994 StandoutNobel
A chemical approach for identifying O -GlcNAc-modified proteins in cells
2003 StandoutNobel
Human MutSalpha recognizes damaged DNA base pairs containing O6-methylguanine, O4-methylthymine, or the cisplatin-d(GpG) adduct.
1996 StandoutNobel
Selective suppression of human papillomavirus transcription in non-tumorigenic cells by 5-azacytidine.
1988 StandoutNobel
The Caenorhabditis elegans mucolipin-like gene cup-5 is essential for viability and regulates lysosomes in multiple cell types
2002 StandoutNobel
DNA methyltransferase polypeptides in mouse and human cells
1986
Influence of Pre-existing Methylation on the de Novo Activity of Eukaryotic DNA Methyltransferase
1998
DNA methyltransferase levels in tumorigenic and nontumorigenic cells in culture.
1986
Inhibition of DNA methylation and histone deacetylation prevents murine lung cancer.
2003
The Role of DNA Methylation in Mammalian Epigenetics
2001 StandoutScience
Differential Display of Eukaryotic Messenger RNA by Means of the Polymerase Chain Reaction
1992 StandoutScience
G 1 Events and Regulation of Cell Proliferation
1989 StandoutScience
Morphological, Biochemical and Molecular Biology Approaches for the Diagnosis of Lysosomal Storage Diseases
2000
Restoration of mismatch repair to nuclear extracts of H6 colorectal tumor cells by a heterodimer of human MutL homologs.
1995 StandoutNobel
Gene expression during the mammalian cell cycle
1986
Replacement of 5-methylcytosine by cytosine: a possible mechanism for transient DNA demethylation during differentiation.
1986
CpG island methylator phenotype in colorectal cancer
1999 Standout
Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs.
1994 StandoutNobel
Changes in DNA Methylation in Neoplasia: Pathophysiology and Therapeutic Implications
2001
Generation times in wild chimpanzees and gorillas suggest earlier divergence times in great ape and human evolution
2012 StandoutNobel
Metabolic labeling enables selective photocrosslinking of O-GlcNAc-modified proteins to their binding partners
2012 StandoutNobel
Redox ribonucleosides. Isolation and characterization of 5-hydroxyuridine, 8-hydroxyguanosine, and 8-hydroxyadenosine from Torula yeast RNA.
1992
Works of Feige Kaplan being referenced
More than one mutant allele causes infantile Tay-Sachs disease in French-Canadians.
1990
Interaction between importin 13 and myopodin suggests a nuclear import pathway for myopodin
2007
Novel Tay-Sachs disease mutations from China
1992
A glycine250 → aspartate substitution in the α-subunit of hexosaminidase a causes juvenile-onset Tay-Sachs disease in a Lebanese-Canadian family
1992
The intron 7 donor splice site transition: a second Tay-Sachs disease mutation in French Canada
1992
Haplotypes in the Dystrophin DNA Segment Point to a Mosaic Origin of Modern Human Diversity
2003
A new Tay-Sachs disease B1 allele in exon 7 in two compound heterozygotes each with a second novel mutation
1992
Identification of Candidate Active Site Residues in Lysosomal β-Hexosaminidase A
1997
Reduced Viability of Mice with Lung Epithelial-Specific Knockout of Glucocorticoid Receptor
2009
A Chronic GM(2) Gangliosidosis Variant with a HEXA Splicing Defect: Quantitation of HEXA mRNAs in Normal and Mutant Fibroblasts
1997
DNA methylation pattern is determined by the intracellular level of the methylase.
1984
A chronic GM2 gangliosidosis variant with a HEXA splicing defect: quantitation of HEXA mRNAs in normal and mutant fibroblasts.
1997
Purification and properties of a DPNH-TPNH diaphorase from Clostridium kluyverii
1969
A novel developmentally regulated gene in lung mesenchyme: homology to a tumor-derived trypsin inhibitor
1999
Cell cycle-dependent regulation of eukaryotic DNA methylase level.
1985