Citation Impact
Citing Papers
GPCR Engineering Yields High-Resolution Structural Insights into β 2 -Adrenergic Receptor Function
2007 StandoutScienceNobel
Structure of the 70 S Ribosome Complexed with mRNA and tRNA
2006 StandoutScienceNobel
Crystal structure of a replication fork single-stranded DNA binding protein (T4 gp32) complexed to DNA
1995 StandoutNatureNobel
Alpha-B Crystallin Gene (CRYAB) Mutation Causes Dominant Congenital Posterior Polar Cataract in Humans
2001
Replicative form of Encephalomyocarditis Virus Ribonucleic Acid
1963 StandoutNatureNobel
Characterization of the pufferfish (Fugu) genome as a compact model vertebrate genome
1993 StandoutNatureNobel
CRYBA3/A1 Gene Mutation Associated with Suture-Sparing Autosomal Dominant Congenital Nuclear Cataract: A Novel Phenotype
2004
Genetic analysis of NF1: Identification of close flanking markers on chromosome 17
1987
Projection structure of rhodopsin
1993 StandoutNatureNobel
Presynaptic Ca2+ Channels Compete for Channel Type-Preferring Slots in Altered Neurotransmission Arising from Ca2+ Channelopathy
2004
Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4
1996 Standout
New CRISPR–Cas systems from uncultivated microbes
2016 StandoutNatureNobel
Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndrome
1990 Nobel
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
1991 Standout
Phylogenetic and genetic evidence for base-triples in the catalytic domain of group I introns
1990 StandoutNatureNobel
What recent ribosome structures have revealed about the mechanism of translation
2009 StandoutNatureNobel
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
A genetic map of human chromosome 17p
1990
The CRISPR-associated DNA-cleaving enzyme Cpf1 also processes precursor CRISPR RNA
2016 StandoutNatureNobel
A missense mutation in the αB-crystallin chaperone gene causes a desmin-related myopathy
1998
Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract
2004
The conservation of dinucleotide microsatellites among mammalian genomes allows the use of heterologous PCR primer pairs in closely related species
1991
The function of alpha-crystallin in vision
2000
Mutations in the p53 gene occur in diverse human tumour types
1989 StandoutNature
A genetic linkage map of the human genome
1987
Transit of tRNA through the Escherichia coli ribosome: cross‐linking of the 3′ end of tRNA to ribosomal proteins at the P and E sites
2002
A locus control region adjacent to the human red and green visual pigment genes
1992
Male–female differences in fertility and blood pressure in ACE-deficient mice
1995 StandoutNatureNobel
Cloning of the T gene required in mesoderm formation in the mouse
1990 Nature
Link between a novel human gammaD-crystallin allele and a unique cataract phenotype explained by protein crystallography
2000
mRNA Helicase Activity of the Ribosome
2005
Crystallin γB-I4F Mutant Protein Binds to α-Crystallin and Affects Lens Transparency
2005 StandoutNobel
A Temperature-sensitive Mutation of Crygs in the Murine Opj Cataract
2001
DNA-PKcs has KU-dependent function in rRNA processing and haematopoiesis
2020 StandoutNatureNobel
The chemical repertoire of natural ribozymes
2002 StandoutNatureNobel
A mapped set of DNA markers for human chromosome 15
1988
Absence of linkage between the angiotensin converting enzyme locus and human essential hypertension
1992
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
Allelic inactivation regulates olfactory receptor gene expression
1994 StandoutNobel
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia
1996 StandoutNature
Mfold web server for nucleic acid folding and hybridization prediction
2003 Standout
Mutation in the βA3/A1-Crystallin Encoding Gene Cryba1 Causes a Dominant Cataract in the Mouse
1999
Eomesodermin is required for mouse trophoblast development and mesoderm formation
2000 StandoutNatureNobel
Mechanism of Chaperone Function in Small Heat Shock Proteins
2002
The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer
1999
GENETICS OF MIGRAINE
1997
Alpha-crystallin
2003
The Enzymic Synthesis of Amino Acyl Derivatives of Ribonucleic Acid
1961 StandoutNobel
The Complete Atomic Structure of the Large Ribosomal Subunit at 2.4 Å Resolution
2000 StandoutScienceNobel
Defining the Inside and Outside of a Catalytic RNA Molecule
1989 StandoutScienceNobel
The human T-cell receptor α-chain gene maps to chromosome 14
1985 StandoutNatureNobel
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
The Enzymic Synthesis of Amino Acyl Derivatives of Ribonucleic Acid
1961 StandoutNobel
MECHANISTIC ASPECTS OF ENZYMATIC CATALYSIS: Lessons from Comparison of RNA and Protein Enzymes
1997
Functional Modification of 16S Ribosomal RNA by Kethoxal
1972
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
1990 Standout
Familial Hemiplegic Migraine: A Clinical Comparison of Families Linked and Unlinked to Chromosome 19
1996
Crystallization of Pure Species of Bacterial tRNA for X‐Ray Diffraction Studies
1972 StandoutNobel
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17.
1990
Topography of 16S RNA in 30S ribosomal subunits. Nucleotide sequences and location of sites of reaction with kethoxal
1974
Detailed Molecular Model for Transfer Ribonucleic Acid
1969 StandoutNatureNobel
An Unstable Intermediate Carrying Information from Genes to Ribosomes for Protein Synthesis
1961 StandoutNatureNobel
Cell Cycle Control and Cancer
1994 StandoutScienceNobel
A missense mutation in the gammaD crystallin gene (CRYGD) associated with autosomal dominant "coral-like" cataract linked to chromosome 2q.
2004
The Deoxyribonucleases of Escherichia coli
1960
Structure of catabolite gene activator protein at 2.9 Å resolution suggests binding to left-handed B-DNA
1981 StandoutNatureNobel
Characterization of RNA synthesized in Escherichia coli after bacteriophage T2 infection
1960
Structural Motifs in RNA
1999
Incorporation of Amino Acids into Ribonucleic Acid
1960
Novel Proteinaceous Infectious Particles Cause Scrapie
1982 StandoutScienceNobel
Complete nucleotide sequence of a 16S ribosomal RNA gene from Escherichia coli.
1978 Standout
Special fasciculiform cataract caused by a mutation in the gammaD-crystallin gene.
2004
Assignment of the Charcot-Marie-Tooth neuropathy type 1 (CMT 1a) gene to 17p11.2-p12.
1990
The isolation and properties of deoxyribonucleoprotein particles containing single nucleic acid molecules
1959
T4 Bacteriophage Gene 32: A Structural Protein in the Replication and Recombination of DNA
1970 Nature
A procedure for the isolation of deoxyribonucleic acid from micro-organisms
1961 Standout
Assembly of functional rhodopsin requires a disulfide bond between cysteine residues 110 and 187.
1990
Aey2, a new mutation in the betaB2-crystallin-encoding gene of the mouse.
2001
Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
2001
Biochemical and physical characterization of an unmodified yeast phenylalanine transfer RNA transcribed in vitro.
1988
Bruchpilot Promotes Active Zone Assembly, Ca 2+ Channel Clustering, and Vesicle Release
2006 StandoutScienceNobel
Global Patterns of Linkage Disequilibrium at the CD4 Locus and Modern Human Origins
1996 StandoutScienceNobel
Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21
1990 StandoutScience
Enzymatic Synthesis of Deoxyribonucleic Acid
1964
A general method for site-directed mutagenesis in prokaryotes
1981 StandoutNatureNobel
Protection of specific sites in 16 S RNA from chemical modification by association of 30 S and 50 S ribosomes
1977
Chromatin Structure: Oligomers of the Histones
1974 StandoutScienceNobel
Origin of Antibody Variation
1966 StandoutNatureNobel
Rhodopsin, photoreceptor of the rod cell. An emerging pattern for structure and function.
1992
Hydrodynamic changes accompanying the thermal denaturation of transfer ribonucleic acid.
1966 StandoutNobel
THE BUOYANT BEHAVIOR OF VIRAL AND BACTERIAL DNA IN ALKALINE CsCl
1963
Correlation between chemical modification and surface accessibility in yeast phenylalanine transfer RNA
1983
Variable Number of Tandem Repeat (VNTR) Markers for Human Gene Mapping
1987 Science
Structure of nucleosome core particles of chromatin
1977 StandoutNatureNobel
Survey of human and rat microsatellites
1992
Some properties of soluble ribonucleic acid from Escherichia coli
1959
A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family.
2000
Seven-helix receptors
1991
STUDIES ON ISOLATED NUCLEI
1963 StandoutNobel
HELIX FORMATION BY GUANYLIC ACID
1962 Standout
Molecular analysis of spontaneous somatic mutants
1977 StandoutNatureNobel
Familial periodic cerebellar ataxia without myokymia maps to a 19-cM region on 19p13.
1995
Domains and the hinge region of an immunoglobulin heavy chain are encoded in separate DNA segments
1979 StandoutNatureNobel
Evolution of haplotypes at the DRD2 locus.
1995
Integrating Genetic Approaches into the Discovery of Anticancer Drugs
1997 StandoutScienceNobel
Molecular Biology of Prion Diseases
1991 StandoutScienceNobel
Interactions of metal ions with polynucleotides and related compounds. IV. Degradation of polyribonucleotides by zinc and other divalent metal ions,
1965
Altered topography of 16S RNA in the inactive form of Escherichia coli 30S ribosomal subunits
1978
Unstable Ribonucleic Acid Revealed by Pulse Labelling of Escherichia Coli
1961 StandoutNatureNobel
AlphaB-crystallin in lens development and muscle integrity: a gene knockout approach.
2001
An immunoglobulin deletion mutant with implications for the heavy-chain switch and RNA splicing
1980 StandoutNatureNobel
Allelotype of Colorectal Carcinomas
1989 Science
Human c-fos oncogene mapped within chromosomal region 14q21----q31.
1984
A hypervariable microsatellite revealed by in vitro amplification of a dinucleotide repeat within the cardiac muscle actin gene.
1989
CRYSTALLIZATION OF DNA FROM DILUTE SOLUTION
1969
Works of M. Litt being referenced
Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA
1998
Cosmid 1–26 defines four RFLPs on chromosome 17q23-qter [HGM9 No. D17S20]
1987
Detection and characterization of additional DNA polymorphisms in the dopamine D2 receptor gene
1991
Autosomal Dominant Cerulean Cataract Is Associated with a Chain Termination Mutation in the Human -Crystallin Gene CRYBB2
1997
Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
1994
A hypervariable RFLP on chromosome 17pl3 is defined by an arbitrary single copy probe pl44-D6 [HGM9 No. D17S34]
1987
1988
A mapped set of DNA markers for human chromosome 17
1988
Autosomal-Dominant Congenital Cataract Associated with a Deletion Mutation in the Human Beaded Filament Protein Gene BFSP2
2000
A Second Gene for Cerulean Cataracts Maps to the β Crystallin Region on Chromosome 22
1996
Five polymorphic microsatellite VNTRs on the human X chromosome.
1990
The human dopamine D2 receptor gene is located on chromosome 11 at q22-q23 and identifies a TaqI RFLP.
1989
A hypervariable region at the D19S11 locus
1987
A highly polymorphic locus in human DNA revealed by cosmid-derived probes.
1985
A 3-Mb Region for the FamilialHemiplegie Migraine Locus on19p13.1-p13.2: Exclusion ofPRKCSH as a Candidate Gene
1996
Molecular Genetics of Human Blue Cone Monochromacy
1989 Science
THE DEPENDENCE OF PNEUMOCOCCAL TRANSFORMATION ON THE MOLECULAR WEIGHT OF DEOXYRIBOSE NUCLEIC ACID
1958
Structural studies on transfer ribonucleic acid. I. Labeling of exposed guanine sites in yeast phenylalanine transfer ribonucleic acid with kethoxal
1969
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds.
1991
A simple procedure for the purification of yeast phenylalanine transfer RNA
1968
Localization of the restriction fragment length polymorphism D14S1 (pAW-101) to chromosome 14q32.1 leads to 32.2 by in situ hybridization.
1983
SECONDARY STRUCTURE IN RIBONUCLEIC ACIDS
1959
Report of the committee on the genetic constitution of chromosomes 20 and 21
1988
ISOLATION AND PROPERTIES OF LIVER CELL NUCLEOLI
1956
Kethoxal—A Potentially Useful Reagent for the Determination of Nucleotide Sequences in Single-Stranded Regions of Transfer Ribonucleic Acid*
1967
A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library
1986
A new locus for autosomal dominant congenital cataracts maps to chromosome 3.
2000
A gene for episodic ataxia/myokymia maps to chromosome 12p13.
1994
Morphological Features of DNA Macromolecules as Seen with the Electron Microscope
1958
Kethoxal inactivation of three transfer ribonucleic acids chargeable by yeast phenylalanyl transfer ribonucleic acid synthetase
1972
A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia
1999
Hemoglobin casper: β 106 (G8) Leu→Pro
1973