Citation Impact
Citing Papers
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosis.
1989 StandoutNobel
A microtransfection method using the luciferase-encoding reporter gene for the assay of human immunodeficiency virus LTR promoter activity
1990 StandoutNobel
A deletion hot spot in the Duchenne muscular dystrophy gene
1988
The muscular dystrophies
2002 Standout
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
Mitochondrial fusion and fission in cell life and death
2010 Standout
Behavior of Mitochondria in the Living Cell
1990
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology
2006 StandoutNobel
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
2007 Standout
Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy
2007 StandoutNobel
Dystrophin: The protein product of the duchenne muscular dystrophy locus
1987 Standout
A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations
1990 Standout
Molecular cloning oflin-29, a heterochronic gene required for the differentiation of hypodermal cells and the cessation of molting inC.elegans
1991 StandoutNobel
Sister-chromatid exchange: second report of the Gene-Tox program
1993
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
1990 Standout
Molecular genetics and genetic counselling for Duchenne/Becker muscular dystrophy
1993
Dynamics of mitochondria in living cells: Shape changes, dislocations, fusion, and fission of mitochondria
1994
The Saccharomyces cerevisiae RAD9, RAD17, RAD24 and MEC3 Genes Are Required for Tolerating Irreparable, Ultraviolet-Induced DNA Damage
1998 StandoutNobel
Molecular analysis of the armadillo locus: uniformly distributed transcripts and a protein with novel internal repeats are associated with a Drosophila segment polarity gene.
1989 StandoutNobel
FORMATION OF MITOCHONDRIA IN NEUROSPORA CRASSA
1963
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
THE CONCEPTS OF MEMBRANE FLOW AND MEMBRANE VESICULATION AS MECHANISMS FOR ACTIVE TRANSPORT AND ION PUMPING
1956
GENETICS OF HUMAN CELL LINES, IV. DNA-MEDIATED HERITABLE TRANSFORMATION OF A BIOCHEMICAL TRAIT
1962
Telomere shortening associated with chromosome instability is arrested in immortal cells which express telomerase activity.
1992 StandoutNobel
The Fine Structure of Brown Adipose Tissue in the Newborn Mouse and Rat
1958
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
1988
A giant locus for the Duchenne and Becker muscular dystrophy gene
1987
An appraisal of the application of recombinant DNA techniques to chromosome defects
1985
Duchenne Muscular Dystrophy Involving Translocation of the dmd Gene Next to Ribosomal RNA Genes
1984 Science
Cytoplasmic fibrils in living cultured cells
1967
Immunometabolism governs dendritic cell and macrophage function
2015 Standout
The effects of actinomycin D on growth of Rous sarcoma virus in vitro
1963 StandoutNobel
Oxygen-Dependent Microbial Killing by Phagocytes
1978 Standout
Transformation of Cells in vitro by Viruses
1963 StandoutScienceNobel
STUDIES ON INFLAMMATION
1961 StandoutNobel
Telomeric association of chromosomes in B-cell lymphoid leukemia
1984
The control of cellular morphology in embryonic cells infected with Rous sarcoma virus in vitro
1960 StandoutNobel
Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy
1985 Nature
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
2014 Standout
A Maelll polymorphism near the dystrophin gene promoter by restriction of amplified DNA
1990 StandoutNobel
PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs
1985
Subcellular localization of the b-cytochrome component of the human neutrophil microbicidal oxidase: translocation during activation.
1983 Standout
Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.
1985
Light Inactivation of Focus Formation by Chicken Embryo Fibroblasts infected with Avian Sarcoma Virus in the Presence of 5-Bromodeoxyuridine
1970 StandoutNatureNobel
Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
1981
A genetic analysis of dicentric minichromosomes in saccharomyces cerevisiae
1987 StandoutNobel
The first seven amino acids encoded by the v-src oncogene act as a myristylation signal: lysine 7 is a critical determinant.
1988 StandoutNobel
Enzymatic Amplification of β-Globin Genomic Sequences and Restriction Site Analysis for Diagnosis of Sickle Cell Anemia
1985 StandoutScienceNobel
Primary mouse myoblast purification, characterization, and transplantation for cell-mediated gene therapy.
1994 Standout
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1987 Standout
Flow cytometric studies of oxidative product formation by neutrophils: a graded response to membrane stimulation.
1983 Standout
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
1990 StandoutScience
The First Seven Amino Acids Encoded by the v-src Oncogene Act as a Myristylation Signal: Lysine 7 is a Critical Determinant
1988 StandoutNobel
Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.
1985
Intracellular Aspects of the Process of Protein Synthesis
1975 StandoutScienceNobel
Microfilaments in Cellular and Developmental Processes
1971 StandoutScience
Coordinate modulation of transfected HSV thymidine kinase and human globin genes
1983 StandoutNobel
INTRAMITOCHONDRIAL FIBERS WITH DNA CHARACTERISTICS
1963
THE ORGANIZATION OF LIVING MATTER
1964 StandoutNobel
EVIDENCE FOR RECYCLING OF SYNAPTIC VESICLE MEMBRANE DURING TRANSMITTER RELEASE AT THE FROG NEUROMUSCULAR JUNCTION
1973 Standout
BIOGENESIS OF CHLOROPLAST MEMBRANES
1967 StandoutNobel
Patterns of Integration of DNA Microinjected into Cultured Mammalian Cells: Evidence for Homologous Recombination Between Injected Plasmid DNA Molecules
1982 StandoutNobel
The structural gene for yeast cytochrome C.
1966 StandoutNobel
Oxidative Metabolism in Cells Isolated from Brown Adipose Tissue
1968 StandoutNobel
Characteristics of an assay for Rous sarcoma virus and Rous sarcoma cells in tissue culture
1958 StandoutNobel
RESOLUTION OF GRANULES FROM RABBIT HETEROPHIL LEUKOCYTES INTO DISTINCT POPULATIONS BY ZONAL SEDIMENTATION
1969 StandoutNobel
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy
1987
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Fusion of two apparently intact human X chromosomes
1976
Apparently isodicentric but functionally monocentric X chromosome in man.
1974
ELECTRON MICROSCOPE STUDIES ON THE DEGRANULATION OF RABBIT PERITONEAL LEUKOCYTES DURING PHAGOCYTOSIS
1964
Spectroscopic Evidence for the Control of Respiration Prior to Phosphorylation in Hamster Brown Fat Cells
1970 StandoutNobel
Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development
2003 Standout
CHANGES IN THE METABOLIC PATTERN OF POLYMORPHO-NUCLEAR LEUCOCYTES DURING PHAGOCYTOSIS.
1964
A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome
1986
Mitochondrial Cristae Revealed with Focused Light
2009 StandoutNobel
Myeloperoxidase: Contribution to the Microbicidal Activity of Intact Leukocytes
1970 Science
CINEMICROPHOTOGRAPHIC OBSERVATIONS ON GRANULE LYSIS IN POLYMORPHONUCLEAR LEUCOCYTES DURING PHAGOCYTOSIS
1962
Results of a Triple Blind Clinical Study of Myoblast Transplantations without Immunosuppressive Treatment in Young Boys with Duchenne Muscular Dystrophy
1993
Works of J Frédéric being referenced
ACTION OF VARIOUS SUBSTANCES ON THE MITOCHONDRIA OF LIVING CELLS CULTIVATED IN VITRO
1954
An abnormal large human chromosome identified as an end‐to‐end fusion of two X's by combined results of the new banding techniques and microdensitometry
1972
CONTRIBUTION A L’ÉTUDE DE L’ÉPITHÉLIUM HÉPATIQUE CULTIVÉ IN VITRO
1952
[Contribution to the study of neutrophil granulations of the polynuclears by phase contrast microcinematography].
1955
[X-chromosome translocations. Examination based on treatment with BUDR and staining with acridine orange].
1974
Sister chromatid exchange frequency in workers exposed to high levels of ethylene oxide, in a hospital sterilization service
1984
[Cytological research on the normal chondriome or the chondriome subjected to experimentation in living cells cultivated in vitro].
1958
[Investigations on the chondriosomes of living cells by phase contrast microscopy and microcinematography].
1952
CONTRIBUTION A L’ÉTUDE DE LA PRÉPARATION A LA MITOSE
1957
[Modifications of the chromosomes and of the karyotype in chicken cells cultured in vitro in the presence of calf desoxyribonucleic acids].
1962
Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome
1984