Citation Impact

Citing Papers

MutL traps MutS at a DNA mismatch
2015 StandoutNobel
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
A possible mechanism for exonuclease 1-independent eukaryotic mismatch repair
2009 StandoutNobel
Protein roadblocks and helix discontinuities are barriers to the initiation of mismatch repair
2007 StandoutNobel
Saccharomyces cerevisiae MutLα Is a Mismatch Repair Endonuclease
2007 StandoutNobel
Mismatch Repair-dependent Iterative Excision at Irreparable O6-Methylguanine Lesions in Human Nuclear Extracts
2006 StandoutNobel
Human Mismatch Repair
2005 StandoutNobel
Mispair-specific Recruitment of the Mlh1-Pms1 Complex Identifies Repair Substrates of the Saccharomyces cerevisiae Msh2-Msh3 Complex
2014
Mechanisms in Eukaryotic Mismatch Repair
2006 StandoutNobel
Discovery of archaeal fusexins homologous to eukaryotic HAP2/GCS1 gamete fusion proteins
2022 StandoutNobel
The DNA-damage response in human biology and disease
2009 StandoutNature
The molecular hallmarks of epigenetic control
2016 Standout
RNA Methylation by the MIS Complex Regulates a Cell Fate Decision in Yeast
2012
Identification of new components of the RipC-FtsEX cell separation pathway of Corynebacterineae
2019 StandoutNobel
Microsatellite Instability in Colorectal Cancer
2010 Standout
The β Sliding Clamp Binds to Multiple Sites within MutL and MutS
2006 StandoutNobel
Kinetochore Function from the Bottom Up
2017
High-Resolution Mapping Reveals a Conserved, Widespread, Dynamic mRNA Methylation Program in Yeast Meiosis
2013 StandoutNobel
Design and Analysis of Single-Cell Sequencing Experiments
2015
N6-methyladenosine Modulates Messenger RNA Translation Efficiency
2015 Standout
Mechanisms of regulation of G protein-coupled receptor kinases (GRKs) and cardiovascular disease
2005
Post-transcriptional gene regulation by mRNA modifications
2016 Standout
Direct Visualization of Asymmetric Adenine Nucleotide-Induced Conformational Changes in MutLα
2008 StandoutNobel
DNA repair mechanisms in dividing and non-dividing cells
2013
Interactions of Human Mismatch Repair Proteins MutSα and MutLα with Proteins of the ATR-Chk1 Pathway
2009 StandoutNobel
The MutSα-Proliferating Cell Nuclear Antigen Interaction in Human DNA Mismatch Repair
2008 StandoutNobel
Anti–β1-adrenergic receptor antibodies and heart failure: causation, not just correlation
2004 StandoutNobel
Endonucleolytic Function of MutLα in Human Mismatch Repair
2006 StandoutNobel
Mismatch repair proteins: key regulators of genetic recombination
2004
The multifaceted mismatch-repair system
2006
Molecular mechanisms of cisplatin resistance
2011 Standout
Predicting and interpreting large-scale mutagenesis data using analyses of protein stability and conservation
2022
Structure of the Human MutSα DNA Lesion Recognition Complex
2007 StandoutNobel
Exploring in vitro expression and immune potency in mice using mRNA encoding the Plasmodium falciparum malaria antigen, CelTOS
2022 StandoutNobel
The DNA Damage Response: Making It Safe to Play with Knives
2010 Standout
Sequential assembly of the septal cell envelope prior to V snapping in Corynebacterium glutamicum
2019 StandoutNobel
The causes and consequences of genetic heterogeneity in cancer evolution
2013 StandoutNature
MutLα and Proliferating Cell Nuclear Antigen Share Binding Sites on MutSβ
2010 StandoutNobel
Transcription of Two Long Noncoding RNAs Mediates Mating-Type Control of Gametogenesis in Budding Yeast
2012
Characterization of the Interactome of the Human MutL Homologues MLH1, PMS1, and PMS2
2006
Reading, writing and erasing mRNA methylation
2019 Standout
Functions of MutLα, Replication Protein A (RPA), and HMGB1 in 5′-Directed Mismatch Repair
2009 StandoutNobel
Analysis of the Excision Step in Human DNA Mismatch Repair
2006 StandoutNobel
De novo design of tyrosine and serine kinase-driven protein switches
2021 StandoutNobel
A Defined Human System That Supports Bidirectional Mismatch-Provoked Excision
2004 StandoutNobel
DNA mismatch repair: Molecular mechanism, cancer, and ageing
2008
A Unique Microglia Type Associated with Restricting Development of Alzheimer’s Disease
2017 Standout
Long Noncoding RNAs: Cellular Address Codes in Development and Disease
2013 Standout
A Phylogenomic Inventory of Meiotic Genes
2005
PhyloGene server for identification and visualization of co-evolving proteins using normalized phylogenetic profiles
2015 StandoutNobel
N6-methyladenosine-dependent RNA structural switches regulate RNA–protein interactions
2015 StandoutNature
Involvement of the β Clamp in Methyl-directed Mismatch Repair in Vitro
2009 StandoutNobel
PCNA function in the activation and strand direction of MutLα endonuclease in mismatch repair
2010 StandoutNobel
The scaffold protein Nde1 safeguards the brain genome during S phase of early neural progenitor differentiation
2014
DNA MISMATCH REPAIR
2005
Genomes in Focus: Development and Applications of CRISPR‐Cas9 Imaging Technologies
2017 StandoutNobel
Stronger together for in-cell translation: natural and unnatural base modified mRNA
2022
DNA Mismatch Repair:  Functions and Mechanisms
2005 StandoutNobel
Longer metaphase and fewer chromosome segregation errors in modern human than Neanderthal brain development
2022 StandoutNobel
Localization of MMR proteins on meiotic chromosomes in mice indicates distinct functions during prophase I
2005
DNA Mismatch Repair: Molecular Mechanisms and Biological Function
2003
PMS2 endonuclease activity has distinct biological functions and is essential for genome maintenance
2010 StandoutNobel
Oufti: an integrated software package for high‐accuracy, high‐throughput quantitative microscopy analysis
2015
Walking the tightrope: proteostasis and neurodegenerative disease
2016
Phosphodiesterase 4D is required for β 2 adrenoceptor subtype-specific signaling in cardiac myocytes
2005 StandoutNobel
EGF Regulates the Interaction of Tks4 with Src through Its SH2 and SH3 Domains
2018
Expression of the MutL Homologue hMLH3 in Human Cells and its Role in DNA Mismatch Repair
2005
Anti–β1-adrenergic receptor antibodies and heart failure: causation, not just correlation
2004 StandoutNobel
Extrahelical (CAG)/(CTG) triplet repeat elements support proliferating cell nuclear antigen loading and MutLα endonuclease activation
2013 StandoutNobel
Trafficking of G Protein–Coupled Receptors
2006 StandoutNobel
Defective Mismatch Repair, Microsatellite Mutation Bias, and Variability in Clinical Cancer Phenotypes
2010
What Is the Role of β-Adrenergic Signaling in Heart Failure?
2003
Accurate proteome-wide missense variant effect prediction with AlphaMissense
2023 StandoutScienceNobel

Works of Eva R. Hoffmann being referenced

Cmr1/WDR76 defines a nuclear genotoxic stress body linking genome integrity and protein quality control
2015
A Mec1- and PP4-Dependent Checkpoint Couples Centromere Pairing to Meiotic Recombination
2010
Monopolin Subunit Csm1 Associates with MIND Complex to Establish Monopolar Attachment of Sister Kinetochores at Meiosis I
2013
A role for the MutL homologue <i>MLH2</i> in controlling heteroduplex formation and in regulating between two different crossover pathways in budding yeast
2004
The G67E mutation in hMLH1 is associated with an unusual presentation of Lynch syndrome
2009
Genome-wide maps of recombination and chromosome segregation in human oocytes and embryos show selection for maternal recombination rates
2015
Meiotic recombination intermediates and mismatch repair proteins
2004
Requirement for DNA Ligase IV during Embryonic Neuronal Development
2011
FindFoci: A Focus Detection Algorithm with Automated Parameter Training That Closely Matches Human Assignments, Reduces Human Inconsistencies and Increases Speed of Analysis
2014
Effects of two Gβγ-binding proteins – N-terminally truncated phosducin and β-adrenergic receptor kinase C terminus (βARKct) – in heart failure
2003
Strategies for Covalent Labeling of Long RNAs
2021
Computational and cellular studies reveal structural destabilization and degradation of MLH1 variants in Lynch syndrome
2019
MLH1 Mutations Differentially Affect Meiotic Functions in Saccharomyces cerevisiae
2003
Rankless by CCL
2026