Citation Impact
Citing Papers
The mucin-selective protease StcE enables molecular and functional analysis of human cancer-associated mucins
2019 StandoutNobel
Finishing the euchromatic sequence of the human genome
2004 StandoutNature
The epithelial mucin, MUC1, of milk, mammary gland and other tissues
1995
Short-Term Effects of Nose-Only Cigarette Smoke Exposure on Glutathione Redox Homeostasis, Cytochrome P450 1A1/2 and Respiratory Enzyme Activities in Mice Tissues
2013 Standout
Bcl-2 is an inner mitochondrial membrane protein that blocks programmed cell death
1990 StandoutNature
Oncogenic kinase signalling
2001 StandoutNature
Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
1994 StandoutNature
Do bilineal pedigrees represent a problem for linkage analysis? basic principles and simulation results for single‐gene diseases with no heterogeneity
1992
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
1991 Standout
Microarray analysis shows that some microRNAs downregulate large numbers of target mRNAs
2005 StandoutNature
MUSCLE: multiple sequence alignment with high accuracy and high throughput
2004 Standout
Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins
1994 StandoutNobel
Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
2001 StandoutNature
The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH
1995
The impact of microRNAs on protein output
2008 StandoutNature
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
1990 StandoutNature
RefSeq and LocusLink: NCBI gene-centered resources
2001
Nucleotide Excision Repair in Mammalian Cells
1997
Introducing RefSeq and LocusLink: curated human genome resources at the NCBI
2000
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
NCBI Reference Sequence Project: update and current status
2003
The drosophila gastrulation gene concertina encodes a Gα-like protein
1991 StandoutNobel
The origin and function of the mammalian Y chromosome and Y‐borne genes – an evolving understanding
1995
Defective Urinary Concentrating Ability Due to a Complete Deficiency of Aquaporin-1
2001 StandoutNobel
The protein tyrosine kinase family of the human genome
2000
Bcl-2 gene promotes haemopoietic cell survival and cooperates with c-myc to immortalize pre-B cells
1988 StandoutNature
Disrupted dichotomous intracellular control of human papillomavirus infection in cancer of the cervix
1994 StandoutNobel
G protein multiplicity in eukaryotic signal transduction systems
1988
A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif
1990 StandoutNature
C. elegans cell survival gene ced-9 encodes a functional homolog of the mammalian proto-oncogene bcl-2
1994 StandoutNobel
Free radicals, antioxidant enzymes, and carcinogenesis
1990
Rat gene mapping using PCR-analyzed microsatellites.
1992
Isolation, characterization, and mapping to chromosome 19 of the human apolipoprotein E gene.
1985
The Bcl-2 Protein Family: Arbiters of Cell Survival
1998 StandoutScience
The human T-cell receptor α-chain gene maps to chromosome 14
1985 StandoutNatureNobel
An abnormal terminal X-Y interchange accounts for most but not all cases of human XX maleness
1987
Exploiting Differences in Sialoside Expression for Selective Targeting of MRI Contrast Reagents
1999 StandoutNobel
DNA ligase I deficiency in Bloom's syndrome
1987 StandoutNatureNobel
Clustering by Passing Messages Between Data Points
2007 StandoutScience
Quality Control by DNA Repair
1999 StandoutScienceNobel
The genetics of peptidase C in man
1972
The T cell receptor β chain genes are located on chromosome 6 in mice and chromosome 7 in humans
1984
Apoptosis in the Pathogenesis and Treatment of Disease
1995 StandoutScience
Mitochondrial DNA and human evolution
1987 StandoutNature
Bloom's syndrome XI. Progress report for 1983
1984
Molecular cloning of a mouse DNA repair gene that complements the defect of group-A xeroderma pigmentosum.
1989
Radiation Hybrid Mapping: A Somatic Cell Genetic Method for Constructing High-Resolution Maps of Mammalian Chromosomes
1990 Science
Structural alterations of DNA ligase I in Bloom syndrome.
1987 StandoutNobel
Functional Coherence of the Human Y Chromosome
1997 StandoutScience
Human DNA ligase I cDNA: cloning and functional expression in Saccharomyces cerevisiae.
1990 StandoutNobel
Cloning the chromosomal breakpoint of t(14;18) human lymphomas: clustering around Jh on chromosome 14 and near a transcriptional unit on 18
1985
Partial deletion of distal 17q
1985
Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programed cell death
1993 Standout
Chromosomal Locations of the Murine T-Cell Receptor Alpha-Chain Gene and the T-Cell Gamma Gene
1985 StandoutScienceNobel
Expression of the T-cell-specific γ gene is unnecessary in T cells recognizing class II MHC determinants
1985 StandoutNatureNobel
Chromosome localization in normal human cells and neuroblastomas of a gene related to c-myc
1984 StandoutNatureNobel
Genealogical analysis of cystic fibrosis families and chromosome 7q RFLP haplotypes in the Hutterite Brethren.
1989
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Europium Chelate Labels in Time-Resolved Fluorescence Immunoassays and DNA Hybridization Assays
1990
Accurate and superaccurate gene mapping.
1985
A molecular solution to the riddle of the giant panda's phylogeny
1985 Nature
The proopiocortin (adrenocorticotropin/?-lipotropin) gene is located on chromosome 2 in humans
1981
Apolipoprotein E: Cholesterol Transport Protein with Expanding Role in Cell Biology
1988 StandoutScience
Viruses in Human Cancers
1991 StandoutScienceNobel
Genetic Dissection of Complex Traits
1994 StandoutScience
Assignment of the human acid α‐glucosidase gene (αGLU) to chromosome 17 using somatic cell hybrids
1979
The Molecular Genetics of Cancer
1987 StandoutScienceNobel
PTEN , a Putative Protein Tyrosine Phosphatase Gene Mutated in Human Brain, Breast, and Prostate Cancer
1997 StandoutScience
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
1987
Splice Variants of the α Subunit of the G Protein G s Activate Both Adenylyl Cyclase and Calcium Channels
1989 StandoutScienceNobel
Common polymorphism of Peptidase A. Electrophoretic variants associated with quantitative variation of red cell levels
1973
Linkage between the Colton blood group locus and ASSP11 on chromosome 7
1990
Circadian control of XPA and excision repair of cisplatin-DNA damage by cryptochrome and HERC2 ubiquitin ligase
2010 StandoutNobel
Evolution of in vitro transformation and tumorigenesis of HPV16 and HPV18 immortalized primary cervical epithelial cells.
1991
Evolution at Two Levels in Humans and Chimpanzees
1975 StandoutScience
Molecular cloning of the human nucleotide-excision-repair gene ERCC4.
1994 StandoutNobel
Localization of X-Linked Dominant Charcot-Marie-Tooth Disease (CMT 2) to Xq13
1986
A polymorphic DNA marker genetically linked to Huntington's disease
1983 StandoutNature
Diversity of G Proteins in Signal Transduction
1991 StandoutScience
Connexin Mutations in X-Linked Charcot-Marie-Tooth Disease
1993 StandoutScience
Mapping the Human Genome, Cloned Genes, DNA Polymorphisms, and Inherited Disease
1982
Isolation and sequence of a human apolipoprotein CII cDNA clone and its use to isolate and map to human chromosome 19 the gene for apolipoprotein CII.
1984
Human von Willebrand Factor (vWF): Isolation of Complementary DNA (cDNA) Clones and Chromosomal Localization
1985 Science
Structure and Function of DNA Photolyase and Cryptochrome Blue-Light Photoreceptors
2003 StandoutNobel
Cockayne syndrome group B protein enhances elongation by RNA polymerase II
1997 StandoutNobel
Works of P.J. McAlpine being referenced
The Colton blood group locus
1988
Confirmation of the assignment of MYCL to chromosome 1 in humans and its position relative to RH, UMPK, and PGM1
1988
Nomenclature of human DNA repair genes
1994
Localization of a locus for Charcot-Marie-Tooth neuropathy type la (CMT1A) to chromosome 17
1990
NOMENCLATURE
1997
The 1987 Catalog of Mapped Genes and Report of the Nomenclature Committee (Part 1 of 4)
1987
Multiplicity of genetic polymorphisms of blood in the Schmiedeleut Hutterites
1985
The 1983 catalogue of mapped human genetic markers and report of the nomenclature committee
1984
The 1988 catalog of mapped genes and report of the nomenclature committee
1988
Ring chromosome 17 in a mentally retarded young man—clinical, cytogenetic, and biochemical investigations
1982
Report of the nomenclature committee and the 1989 catalog of mapped genes (Part 1 of 3)
1989
Detection of attograms of antigen by a high-sensitivity enzyme-linked immunoabsorbent assay (HS-ELISA) using a fluorogenic substrate
1980
The 1981 catalogue of assigned human genetic markers and report of the nomenclature committee
1982
Thermostability studies on the isozymes of human phosphoglucomutase
1970
The 1979 catalog of human genes and chromosome assignments.
1980
The position of the Radin blood group locus in relation to other chromosome 1 loci
1980
The 1985 catalog of mapped genes and report of the nomenclature committee
1985
Assignment of the <i>peptidase D </i>gene locus <i>(PEP</i><i>D</i>) to chromosome 19 in man
1976
The 1991 catalog of mapped genes and report of the nomenclature committee (Part 1 of 5)
1991
Hereditary lecithin‐cholesterol acyltransferase deficiency and bloom syndrome in the same individual
1983