Citation Impact
Citing Papers
Histone demethylase KDM6A directly senses oxygen to control chromatin and cell fate
2019 StandoutScienceNobel
Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
2005 Standout
Hypoxia Induces Trimethylated H3 Lysine 4 by Inhibition of JARID1A Demethylase
2010
A cryo-ET survey of microtubules and intracellular compartments in mammalian axons
2021
A Neuroligin-3 Mutation Implicated in Autism Increases Inhibitory Synaptic Transmission in Mice
2007 StandoutScienceNobel
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
Cerebral cortex expansion and folding: what have we learned?
2016
Notch signalling controls pancreatic cell differentiation
1999 StandoutNatureNobel
X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family
2004
CeMyoD accumulation defines the body wall muscle cell fate during C. elegans embryogenesis
1990 StandoutNobel
A novel mutation in JARID1C gene associated with mental retardation
2006
Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage ofXLMRgenes
2007
Targeted inactivation of the muscle regulatory gene Myf-5 results in abnormal rib development and perinatal death
1992
Role for the p53 homologue p73 in E2F-1-induced apoptosis
2000 StandoutNatureNobel
Combinatorial Marking of Cells and Organelles with Reconstituted Fluorescent Proteins
2004 StandoutNobel
Influence of Metabolism on Epigenetics and Disease
2013 StandoutNobel
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases
1993 StandoutNature
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
1989
Eomesodermin, a Key Early Gene in Xenopus Mesoderm Differentiation
1996 StandoutNobel
Monocyte/Macrophage-derived IGF-1 Orchestrates Murine Skeletal Muscle Regeneration and Modulates Autocrine Polarization
2015
Developments in Quantitative PCR
1998
Live Imaging at the Onset of Cortical Neurogenesis Reveals Differential Appearance of the Neuronal Phenotype in Apical versus Basal Progenitor Progeny
2008
Nomenclature of the ARID family of DNA-binding proteins
2005
A new mathematical model for relative quantification in real-time RT-PCR
2001 Standout
In vitro genetic analysis of the Tetrahymena self-splicing intron
1990 StandoutNatureNobel
Growth and folding of the mammalian cerebral cortex: from molecules to malformations
2014
TRIBE: Hijacking an RNA-Editing Enzyme to Identify Cell-Specific Targets of RNA-Binding Proteins
2016 StandoutNobel
RNA-binding proteins in human genetic disease
2008
AMPKα1 Regulates Macrophage Skewing at the Time of Resolution of Inflammation during Skeletal Muscle Regeneration
2013
The Oncogenic Cysteine-rich LIM domain protein Rbtn2 is essential for erythroid development
1994 StandoutNobel
Enrichment of brain-related genes on the mammalian X chromosome is ancient and predates the divergence of synapsid and sauropsid lineages
2009
Positional cloning of the mouse obese gene and its human homologue
1994 StandoutNature
MyoD or Myf-5 is required for the formation of skeletal muscle
1993 Standout
Immunoblot analysis of dystrophin-related protein (DRP)
1993
JmjC-domain-containing proteins and histone demethylation
2006
A role for the Drosophila neurogenic genes in mesoderm differentiation
1991 StandoutNobel
Inactivation of MyoD in mice leads to up-regulation of the myogenic HLH gene Myf-5 and results in apparently normal muscle development
1992
Expression of β amyloid protein precursor mRNAs: Recognition of a novel alternatively spliced form and quantitation in alzheimer's disease using PCR
1990
Macrophages in Tissue Repair, Regeneration, and Fibrosis
2016 Standout
Searching for ways out of the autism maze: genetic, epigenetic and environmental clues
2006
Differential regulation of natriuretic peptide receptor messenger RNAs during the development of cardiac hypertrophy in the rat.
1993
Synthetic Par polarity induces cytoskeleton asymmetry in unpolarized mammalian cells
2023 StandoutNobel
Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPase
1993
Stabilization of Xist RNA Mediates Initiation of X Chromosome Inactivation
1997
The hexosamine signaling pathway: O-GlcNAc cycling in feast or famine
2009
Mechanisms involved in the regulation of histone lysine demethylases
2008
Expression of full-length utrophin prevents muscular dystrophy in mdx mice
1998
Isolation of genes from complex sources of mammalian genomic DNA using exon amplification
1994
Neuroligins and neurexins link synaptic function to cognitive disease
2008 StandoutNatureNobel
The MyoD family of transcription factors and skeletal myogenesis
1995
Maintenance of somite borders in mice requires the Delta homologue Dll1
1997 Nature
CASK Functions as a Mg2+-Independent Neurexin Kinase
2008 StandoutNobel
An altered repertoire of (AP-1) at the onset of replicative senescence
1992
Microtubule Minus-End Stabilization by Polymerization-Driven CAMSAP Deposition
2014
A common E2F-1 and p73 pathway mediates cell death induced by TCR activation
2000 StandoutNatureNobel
The Retinoblastoma Binding Protein RBP2 Is an H3K4 Demethylase
2007 StandoutNobel
Human Menkes X‐chromosome disease and the staphylococcal cadmium‐resistance ATPase: a remarkable similarity in protein sequences
1993
The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene
1993 Standout
Nilotinib reduces muscle fibrosis in chronic muscle injury by promoting TNF-mediated apoptosis of fibro/adipogenic progenitors
2015
The evolution of gene expression levels in mammalian organs
2011 StandoutNatureNobel
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method
2001 Standout
MyoD family: a paradigm for development?
1990
Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays
2000 Standout
Generation of Lymphohematopoietic Cells from Embryonic Stem Cells in Culture
1994 StandoutScienceNobel
The Hexosamine Signaling Pathway: Deciphering the "O-GlcNAc Code"
2005
Metabolic cross-talk allows labeling of O-linked β- N -acetylglucosamine-modified proteins via the N -acetylgalactosamine salvage pathway
2011 StandoutNobel
In Vitro Development of Primitive and Definitive Erythrocytes from Different Precursors
1996 StandoutScienceNobel
Quantitation of mRNA by the polymerase chain reaction.
1989
Dynamics of mitochondrial DNA evolution in animals: amplification and sequencing with conserved primers.
1989 StandoutNobel
Expression level, allelic origin, and mutation analysis of the p73 gene in neuroblastoma tumors and cell lines.
1998
Chromatin and oxygen sensing in the context of JmjC histone demethylases
2014
The future of cloning
1999 StandoutNatureNobel
Expression of the unc-4 homeoprotein in Caenorhabditis elegans motor neurons specifies presynaptic input
1995
The polymerase chain reaction
1989
Hematopoietic Commitment During Embryonic Stem Cell Differentiation in Culture
1993
A chemical approach for identifying O -GlcNAc-modified proteins in cells
2003 StandoutNobel
Reactivation of the Paternal X Chromosome in Early Mouse Embryos
2004 StandoutScienceNobel
Early expression of the myogenic regulatory gene, myf-5, in precursor cells of skeletal muscle in the mouse embryo
1991
Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration
2004
Neural Science
2000 StandoutNobel
Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function
2011 StandoutNobel
Human TKTL1 implies greater neurogenesis in frontal neocortex of modern humans than Neanderthals
2022 StandoutScienceNobel
X-CHROMOSOME INACTIVATION IN MAMMALS
1997
Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides.
1993
Quantitative analysis of MDR1 (multidrug resistance) gene expression in human tumors by polymerase chain reaction.
1990
Aspm specifically maintains symmetric proliferative divisions of neuroepithelial cells
2006 StandoutNobel
Prions
1998 StandoutNobel
NMR solution structure of the human prion protein
2000 StandoutNobel
Direct detection of dystrophin gene rearrangements by analysis of dystrophin mRNA in peripheral blood lymphocytes.
1991
Body-Wall Muscle Formation in Caenorhabditis elegans Embryos that Lack the MyoD Homolog hlh-1
1992 StandoutScienceNobel
Xist RNA and the Mechanism of X Chromosome Inactivation
2002
Flip and Flop: A Cell-Specific Functional Switch in Glutamate-Operated Channels of the CNS
1990 StandoutScienceNobel
NMR structure of the bovine prion protein
2000 StandoutNobel
Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein
2001 StandoutNobel
The RNA Component of Human Telomerase
1995 StandoutScienceNobel
Identification of MRF4: a new member of the muscle regulatory factor gene family.
1989
The natriuretic peptide clearance receptor locally modulates the physiological effects of the natriuretic peptide system
1999 StandoutNobel
Transcription-based amplification system and detection of amplified human immunodeficiency virus type 1 with a bead-based sandwich hybridization format.
1989
Hematopoietic commitment during embryonic stem cell differentiation in culture.
1993
Prion Protein Selectively Binds Copper(II) Ions
1998 Nobel
Glycan‐dependent signaling: O‐linked N‐acetylglucosamine
2001
Quantitative or semi-quantitative PCR: reality versus myth.
1992
Systemic delivery of antisense oligoribonucleotide restores dystrophin expression in body-wide skeletal muscles
2004 StandoutNobel
Reduced growth, abnormal kidney structure, and type 2 (AT 2 ) angiotensin receptor-mediated blood pressure regulation in mice lacking both AT 1A and AT 1B receptors for angiotensin II
1998 StandoutNobel
Chemical Glycoproteomics
2016 StandoutNobel
Works of Jamel Chelly being referenced
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia
2005
Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects
2009
Mechanism of Microtubule Stabilization by Doublecortin
2004
Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
2005
A new model of experimental fibrosis in hindlimb skeletal muscle of adult mdx mouse mimicking muscular dystrophy
2012
DXS106 and DXS559 Flank the X-Linked Dystonia-Parkinsonism Syndrome Locus (DYT3)
1994
Doublecortin Is a Developmentally Regulated, Microtubule-Associated Protein Expressed in Migrating and Differentiating Neurons
1999
Transcription of the dystrophin gene in human muscle and non-muscle tissues
1988 Nature
A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome
1998
Quantitative estimation of minor mRNAs by cDNA‐polymerase chain reaction
1990
Homozygous truncating mutation of the KBP gene, encoding a KIF1B-binding protein, in a familial case of fetal polymicrogyria
2013
Monogenic causes of X-linked mental retardation
2001
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex
2010
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
1993
Dystrophin gene transcribed from different promoters in neuronal and glial cells
1990 Nature
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia
1994
Doublecortin, a Stabilizer of Microtubules
1999
Immunolocalization and developmental expression of dystrophin related protein in skeletal muscle
1991
Distinct roles of doublecortin modulating the microtubule cytoskeleton
2006
CFTR illegitimate transcription in lymphoid cells: quantification and applications to the investigation of pathological transcripts
1992
2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes
1993
Expression of MyoD1 coincides with terminal differentiation in determined but inducible muscle cells.
1989
Assignment of the dystonia-parkinsonism syndrome locus, DYT3, to a small region within a 1.8-Mb YAC contig of Xq13.1.
1995
Illegitimate transcription: transcription of any gene in any cell type.
1989
Developmental patterns in the expression of Myf5, MyoD, myogenin, and MRF4 during myogenesis.
1991
A "G" to "A" mutation at position -1 of a 5' splice site in a late infantile form of Tay-Sachs disease.
1990
Differentially Activated Macrophages Orchestrate Myogenic Precursor Cell Fate During Human Skeletal Muscle Regeneration
2012