Citation Impact
Citing Papers
Accelerated Evolution of Conserved Noncoding Sequences in Humans
2006 StandoutScienceNobel
2013 AHA/ACC Guideline on Lifestyle Management to Reduce Cardiovascular Risk
2013 Standout
No health without mental health
2007 Standout
Functions of DNA methylation: islands, start sites, gene bodies and beyond
2012 Standout
A refined restriction map of YAC clones spanning the entire human dystrophin gene
1994
Physical mapping across the fragile X: Hypermethylation and clinical expression of the fragile X syndrome
1991
Expression of the glial glutamate transporter EAAT2 in the human CNS: an immunohistochemical study
1997
The combined role of P- and E-selectins in atherosclerosis.
1998
Disease-Specific Induced Pluripotent Stem Cells
2008 Standout
The high-affinity glutamate transporters GLT1, GLAST, and EAAT4 are regulated via different signalling mechanisms
2000
Mutations in the glutamate transporter EAAT2 gene do not cause abnormal EAAT2 transcripts in amyotrophic lateral sclerosis
1998 StandoutNobel
Glutamate uptake
2001 Standout
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
1989
Aberrant RNA Processing in a Neurodegenerative Disease: the Cause for Absent EAAT2, a Glutamate Transporter, in Amyotrophic Lateral Sclerosis
1998
Severe cognitive impairment in DMD: obvious clinical evidence for Dp71 isoform point mutations screening
2000
Cellular senescence in aging and age-related disease: from mechanisms to therapy
2015 Standout
Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification
1988
A deletion hot spot in the Duchenne muscular dystrophy gene
1988
The EAAT2 (GLT-1) gene in motor neuron disease: absence of mutations in amyotrophic lateral sclerosis and a point mutation in patients with hereditary spastic paraplegia
1998
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
1991 Standout
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies
1988
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements.
1990 StandoutNobel
Effect of Lifestyle Changes on Atherogenic Lipids and Endothelial Cell Adhesion Molecules in Young Adults With Familial Premature Coronary Heart Disease
2005
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
1991 StandoutNature
High Affinity Glutamate Transporters: Regulation of Expression and Activity
1997
Systemic delivery of morpholino oligonucleotide restores dystrophin expression bodywide and improves dystrophic pathology
2006 StandoutNobel
Indigenous Bacteria from the Gut Microbiota Regulate Host Serotonin Biosynthesis
2015 Standout
Dmdmdx-βgeo: A new allele for the mouse dystrophin gene
1998
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
1990 StandoutNature
β-Lactam antibiotics offer neuroprotection by increasing glutamate transporter expression
2005 StandoutNature
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
Activation of microglial N‐methyl‐D‐aspartate receptors triggers inflammation and neuronal cell death in the developing and mature brain
2012
Molecular cloning oflin-29, a heterochronic gene required for the differentiation of hypodermal cells and the cessation of molting inC.elegans
1991 StandoutNobel
NEUROTOXIC MECHANISMS OF DEGENERATION IN MOTOR NEURON DISEASES*
1999
Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels
1987 Nature
A physical map around the WAGR complex on the short arm of chromosome 11
1989
Telomere Shortening in Kidneys with Age
2000
A DNA sequence (LD1) which occurs in several genomic organizations in Leishmania
1991
Amyotrophic Lateral Sclerosis-linked Glutamate Transporter Mutant Has Impaired Glutamate Clearance Capacity
2001
Inflammation in atherosclerosis
2002 StandoutNature
Deletions and a translocation interrupt a cloned gene at the neurofibromatosis type 1 locus
1990 Standout
The RNA of the glutamate transporter EAAT2 is variably spliced in amyotrophic lateral sclerosis and normal individuals
1999
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin
1990 Nature
Prenatal Valproate Exposure and Risk of Autism Spectrum Disorders and Childhood Autism
2013 Standout
Atherosclerosis
2000 StandoutNature
Cytochrome P450 ω-Hydroxylase Pathway of Tocopherol Catabolism
2002 Standout
Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A
1998
Common Genetic Vulnerability to Depressive Symptoms and Coronary Artery Disease: A Review and Development of Candidate Genes Related to Inflammation and Serotonin
2006
Telomere shortening during aging of human osteoblasts in vitro and leukocytes in vivo: lack of excessive telomere loss in osteoporotic patients
1999
Atherosclerosis
2001 Standout
Alternative splicing of the glutamate transporter EAAT2 (GLT-1)
1998
CLIP170-like tip1p Spatially Organizes Microtubular Dynamics in Fission Yeast
2000 StandoutNobel
Matrix Crosslinking Forces Tumor Progression by Enhancing Integrin Signaling
2009 Standout
Amyotrophic Lateral Sclerosis
2001 Standout
Cognitive/behavioral teratogenetic effects of antiepileptic drugs
2007
Replicative senescence in organ transplantation—mechanisms and significance
2002
Identification of alternative splicing forms of GLT-1 mRNA in the spinal cord of amyotrophic lateral sclerosis patients
1998
Excitatory amino acid transporter 1 and 2 immunoreactivity in the spinal cord in amyotrophic lateral sclerosis
2000
Physical mapping of the cystic fibrosis region by pulsed-field gel electrophoresis
1988
Age-Dependent Changes in Material Properties of the Brain and Braincase of the Rat
2003
Identification of the Cystic Fibrosis Gene: Chromosome Walking and Jumping
1989 StandoutScience
Interphase and Metaphase Resolution of Different Distances Within the Human Dystrophin Gene
1990 Science
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1991 Standout
A giant locus for the Duchenne and Becker muscular dystrophy gene
1987
An α-syntrophin-dependent pool of AQP4 in astroglial end-feet confers bidirectional water flow between blood and brain
2003 StandoutNobel
Detection of specific polymerase chain reaction product by utilizing the 5'----3' exonuclease activity of Thermus aquaticus DNA polymerase.
1991 Standout
Telomere length is paternally inherited and is associated with parental lifespan
2007 StandoutNobel
Expression of a Variant Form of the Glutamate Transporter GLT1 in Neuronal Cultures and in Neurons and Astrocytes in the Rat Brain
2002
Glutamate transporter EAAT2 splice variants occur not only in ALS, but also in AD and controls
2000
Preferential deletion of exons in Duchenne and Becker muscular dystrophies
1987 Nature
The Calpain System
2003 Standout
Vitamin E: function and metabolism
1999
Near-Field Optics: Microscopy, Spectroscopy, and Surface Modification Beyond the Diffraction Limit
1992 StandoutScienceNobel
P-Selectin or Intercellular Adhesion Molecule (Icam)-1 Deficiency Substantially Protects against Atherosclerosis in Apolipoprotein E–Deficient Mice
2000
Neural Science
2000 StandoutNobel
Identification of the Cystic Fibrosis Gene: Genetic Analysis
1989 StandoutScience
Mechanisms of Muscle Degeneration, Regeneration, and Repair in the Muscular Dystrophies
2008
Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals
1987 Standout
Type 1 Neurofibromatosis Gene: Identification of a Large Transcript Disrupted in Three NF1 Patients
1990 StandoutScience
Decreased platelet glutamate uptake in patients with amyotrophic lateral sclerosis
2001
Telomerase in kinetoplastid parasitic protozoa
1999 StandoutNobel
Fusion of a Kinase Gene, ALK , to a Nucleolar Protein Gene, NPM , in Non-Hodgkin's Lymphoma
1994 StandoutScience
Delayed onset of brain edema and mislocalization of aquaporin-4 in dystrophin-null transgenic mice
2002 StandoutNobel
Defects in mRNA 3'-end formation, transcription initiation, and mRNA transport associated with the yeast mutation prp20: possible coupling of mRNA processing and chromatin structure.
1992 StandoutNobel
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands.
1992 Standout
To shape a cell: an inquiry into the causes of morphogenesis of microorganisms
1990
Generation of skeletal muscle stem/progenitor cells from murine induced pluripotent stem cells
2010 StandoutNobel
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles
2004 StandoutNobel
Organoselenium and Organotellurium Compounds: Toxicology and Pharmacology
2004 Standout
Physiology of Microglia
2011 Standout
A functional mRNA polyadenylation signal is required for transcription termination by RNA polymerase II.
1988
Works of Astrid Speer being referenced
Apoptotic neurodegeneration following trauma is markedly enhanced in the immature brain
1999
Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients
1993
Examination of Telomere Lengths in Muscle Tissue Casts Doubt on Replicative Aging as Cause of Progression in Duchenne Muscular Dystrophy
1997
Treatment of ataxia in isolated vitamin E deficiency caused by α-tocopherol transfer protein deficiency
1999
Genomic organization of the human excitatory amino acid transporter gene GLT-1
1997
DMA polymorphisms in adhesion molecule genes ? a new risk factor for early atherosclerosis
1996
The glial glutamate transporter complementary DNA in patients with amyotrophic lateral sclerosis
1996
Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis
1987
E-selectin polymorphism and atherosclerosis: an association study
1994
Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients
1987
A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A
1998