Citation Impact
Citing Papers
Impacts of Biodiversity Loss on Ocean Ecosystem Services
2006 StandoutScience
Complement Factor H Polymorphism in Age-Related Macular Degeneration
2005 StandoutScience
2014 AHA/ACC Guideline for the Management of Patients With Valvular Heart Disease
2014 Standout
2014 AHA/ACC Guideline for the Management of Patients With Valvular Heart Disease: Executive Summary
2014 Standout
Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans
2001
Distinct MutS DNA-binding Modes That Are Differentially Modulated by ATP Binding and Hydrolysis
2001 StandoutNobel
CRYBA3/A1 Gene Mutation Associated with Suture-Sparing Autosomal Dominant Congenital Nuclear Cataract: A Novel Phenotype
2004
Racial Differences in Lens Opacity Incidence and Progression: The Salisbury Eye Evaluation (SEE) Study
2013
The Human Intestinal Microbiome in Health and Disease
2016 Standout
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
1998
A Randomized Controlled Phase IIb Trial of Beta1-Receptor Blockade for Chronic Degenerative Mitral Regurgitation
2012
Genetic factors of age-related macular degeneration
2004
Hydrolytic function of Exo1 in mammalian mismatch repair
2014 StandoutNobel
Thrombolysis with alteplase for acute ischaemic stroke in the Safe Implementation of Thrombolysis in Stroke-Monitoring Study (SITS-MOST): an observational study
2007 Standout
MutS and MutL Activate DNA Helicase II in a Mismatch-dependent Manner
1998 StandoutNobel
differential effects of the angiotensin-converting enzyme inhibitor lisinopril versus the beta-adrenergic receptor blocker atenolol on hemodynamics and left ventricular contractile function in experimental mitral regurgitation
2002
DNA helicases: Enzymes with essential roles in all aspects of DNA metabolism
1994
Interactions and chaperone function of αA‐crystallin with T5P γC‐crystallin mutant
2004
A deletion mutation in the ?A1/A3 crystallin gene (CRYBA1/A3) is associated with autosomal dominant congenital nuclear cataract in a Chinese family
2004
Human Exonuclease I Is Required for 5′ and 3′ Mismatch Repair
2002 StandoutNobel
A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q
1998
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract
2004
A conformational switch in response to Chi converts RecBCD from phage destruction to DNA repair
2020
Stroke
2008 Standout
The structure of the E. coli recA protein monomer and polymer
1992 StandoutNatureNobel
Characterization of a Mutation in the Lens-specific MP70 Encoding Gene of the Mouse Leading to a Dominant Cataract
2001
A Randomized Trial of Tenecteplase versus Alteplase for Acute Ischemic Stroke
2012
Selection of high affinity RNA ligands to the bacteriophage R17 coat protein
1992
Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography
2000
Connexin46 Mutations in Autosomal Dominant Congenital Cataract
1999
BLM–DNA2–RPA–MRN and EXO1–BLM–RPA–MRN constitute two DNA end resection machineries for human DNA break repair
2011 StandoutNobel
Human Transcription-Repair Coupling Factor CSB/ERCC6 Is a DNA-stimulated ATPase but Is Not a Helicase and Does Not Disrupt the Ternary Transcription Complex of Stalled RNA Polymerase II
1997 StandoutNobel
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
2005 StandoutNobel
Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase II
1994 StandoutNatureNobel
Initiation of genetic recombination and recombination-dependent replication
2000
Biology and Applications of CRISPR Systems: Harnessing Nature’s Toolbox for Genome Engineering
2016 StandoutNobel
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
A Point Mutation in Escherichia coli DNA Helicase II Renders the Enzyme Nonfunctional in Two DNA Repair Pathways
1997
DNA-dependent Activation of the hMutSα ATPase
1998 StandoutNobel
Pathophysiology of ischaemic stroke: insights from imaging, and implications for therapy and drug discovery
2007
The Biology of CRISPR-Cas: Backward and Forward
2018 StandoutNobel
Adaptation in CRISPR-Cas Systems
2016 StandoutNobel
Magnetic resonance imaging profiles predict clinical response to early reperfusion: The diffusion and perfusion imaging evaluation for understanding stroke evolution (DEFUSE) study
2006
Myocardial Matrix Remodeling and the Matrix Metalloproteinases: Influence on Cardiac Form and Function
2007
A Nonsense Mutation in CRYBB1 Associated with Autosomal Dominant Cataract Linked to Human Chromosome 22q
2002
Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21q
2003
Gene Replacement With Linear DNA Fragments in Wild-Type Escherichia coli: Enhancement by Chi Sites
1997
Mechanism of 5′-Directed Excision in Human Mismatch Repair
2003 StandoutNobel
Molecular evolution in the gnd locus of Salmonella enterica.
1994
Cryo-EM structure of a type IV secretion system
2022 StandoutNatureNobel
Characterizing physiological heterogeneity of infarction risk in acute human ischaemic stroke using MRI
2006
Redundant Exonuclease Involvement in Escherichia coli Methyl-directed Mismatch Repair
2001 StandoutNobel
Mutation in the βA3/A1-Crystallin Encoding Gene Cryba1 Causes a Dominant Cataract in the Mouse
1999
A multigene deletion in the human IGH constant region locus involves highly homologous hot spots of recombination
1989
The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer
1999
RecBCD Enzyme and the Repair of Double-Stranded DNA Breaks
2008
Guidelines for the Early Management of Patients With Acute Ischemic Stroke
2013 Standout
Organization of the bacterial chromosome
1990
Heteroduplex deoxyribonucleic acid base mismatch repair in bacteria
1986
Dose Escalation of Desmoteplase for Acute Ischemic Stroke (DEDAS)
2006
Coordinating Radiometals of Copper, Gallium, Indium, Yttrium, and Zirconium for PET and SPECT Imaging of Disease
2010 Standout
A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
2000
Genetic and Allelic Heterogeneity ofCrygMutations in Eight Distinct Forms of Dominant Cataract in the Mouse
2004
Requirement for d(GATC) sequences in Escherichia coli mutHLS mismatch correction.
1987 StandoutNobel
Novel folded protein domains generated by combinatorial shuffling of polypeptide segments
2000 StandoutNobel
Isolation and Characterization of the Escherichia coli mutL Gene Product
1989 StandoutNobel
Incorporation of therapeutically modified bacteria into gut microbiota inhibits obesity
2014
Isolation and characterization of the Escherichia coli mutH gene product.
1987 StandoutNobel
Mispair specificity of methyl-directed DNA mismatch correction in vitro.
1988 StandoutNobel
Escherichia coli mutY gene product is required for specific A-G----C.G mismatch correction.
1988 StandoutNobel
Methyl-directed DNA Mismatch Correction
1989 StandoutNobel
Differential Prognosis of Isolated Cortical Swelling and Hypoattenuation on CT in Acute Stroke
2007
Properties of a mutant recA-encoded protein reveal a possible role for Escherichia coli recF-encoded protein in genetic recombination.
1988
A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
2004
The effects of infaunal biodiversity on biogeochemistry of coastal marine sediments
2004
Chi, a promoter of generalized recombination in λ phage, is present in immunoglobulin genes
1981 Nature
Selection of an RNA molecule that mimics a major autoantigenic epitope of human insulin receptor.
1995 StandoutNobel
DNA Mismatch Repair: Functions and Mechanisms
2005 StandoutNobel
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products
2000 Standout
Homologous recombination in procaryotes
1988
Special fasciculiform cataract caused by a mutation in the gammaD-crystallin gene.
2004
Molecular Characterization of Novel Reciprocal Translocation t(6;14) in an Epstein-Barr Virus-Transformed B Cell Precursor
1987 StandoutNobel
Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
2001
Fibrosis — A Common Pathway to Organ Injury and Failure
2015 Standout
Postthrombolysis Blood Pressure Elevation Is Associated With Hemorrhagic Transformation
2009
2020 ACC/AHA Guideline for the Management of Patients With Valvular Heart Disease: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines
2020 Standout
Cataracts
2017 Standout
A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q.
2004
Synthesis of a Site-Specific DNA-Binding Peptide
1987 StandoutScienceNobel
DNA Mismatch Correction in a Defined System
1989 StandoutScienceNobel
Recommendations for Imaging of Acute Ischemic Stroke
2009
Hin-mediated site-specific recombination requires two 26 by recombination sites and a 60 by recombinational enhancer
1985
A novel connexin46 (GJA3) mutation in autosomal dominant congenital nuclear pulverulent cataract.
2004
Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines.
1990 StandoutNobel
A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family.
2000
Duplicated variable region genes account for double isotype expression in a human leukemic B-cell line that gives rise to single isotype-expressing cells
1991 StandoutNobel
Elevated hematocrit is associated with reduced reperfusion and tissue survival in acute stroke
2005
Human exonuclease 1 and BLM helicase interact to resect DNA and initiate DNA repair
2008 StandoutNobel
Restricted structural gene polymorphism in the Mycobacterium tuberculosis complex indicates evolutionarily recent global dissemination
1997 Standout
Optimal Definition for PWI/DWI Mismatch in Acute Ischemic Stroke Patients
2008
Mismatch repair proteins MutS and MutL inhibit RecA-catalyzed strand transfer between diverged DNAs.
1994 StandoutNobel
Ischemic Thresholds for Gray and White Matter
2006
Thrombolysis for acute ischaemic stroke
2014
A DNA exonuclease induced during meiosis of Schizosaccharomyces pombe.
1992
Rapid Assessment of Perfusion–Diffusion Mismatch
2007
Heteroduplex joint formation in Escherichia coli recombination is initiated by pairing of a 3′-ending strand
1998
recD: the gene for an essential third subunit of exonuclease V.
1986
Molecular Mechanisms of Mammalian DNA Repair and the DNA Damage Checkpoints
2004 StandoutNobel
Diverse gap junctions modulate distinct mechanisms for fiber cell formation during lens development and cataractogenesis
2006 StandoutNobel
How RecBCD Enzyme and Chi Promote DNA Break Repair and Recombination: a Molecular Biologist's View
2012
Works of David Schultz being referenced
Age-related Macular Degeneration: A Genome-wide Scan in Extended Families
2003
Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human -Crystallin Gene CRYBB2
1997
Refining the Perfusion–Diffusion Mismatch Hypothesis
2005
Roles of RecBC Enzyme and Chi Sites in Homologous Recombination
1984
Comparison of Two New Mouse Models of Polygenic Type 2 Diabetes at the Jackson Laboratory, NONcNZO10Lt/J and TALLYHO/JngJ
2013
Fishing disturbance and marine biodiversity: role of habitat structure in simple soft-sediment systems
2001
Escherichia coli RecBC pseudorevertants lacking chi recombinational hotspot activity
1983
A simple and sensitive in vivo luciferase assay for tRNA-mediated nonsense suppression
1990
Nucleotide sequence of the chi recombinational hot spot chi +D in bacteriophage lambda
1981
EPITHET
2010
Volume-overload cardiac hypertrophy is unaffected by ACE inhibitor treatment in dogs
1997
Thrombolysis for acute stroke in Australia: outcomes from the Safe Implementation of Thrombolysis in Stroke registry (2002–2008)
2010