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Expansion explosion: new clues to the pathogenesis of repeat expansion neurodegenerative diseases
TRENDS IN MOLECULAR MEDICINE
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2
NATURE GENETICS
Tetraploid state induces p53-dependent arrest of nontransformed mammalian cells in G1
MOLECULAR BIOLOGY OF THE CELL
Cerebellum and psychiatry
INTERNATIONAL REVIEW OF PSYCHIATRY
Psychiatric syndromes in cerebellar degeneration
INTERNATIONAL REVIEW OF PSYCHIATRY
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion (vol 50, pg 373, 2001)
ANNALS OF NEUROLOGY
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion
ANNALS OF NEUROLOGY
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study ofan Indian family
ANNALS OF NEUROLOGY
SCA12: An unusual mutation leads to an unusual spinocerebellar ataxia
BRAIN RESEARCH BULLETIN
Familial influence on age of onset among siblings with Huntington disease
AMERICAN JOURNAL OF MEDICAL GENETICS
SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion
NEUROLOGY
Mammalian mad2 and bub1/bubR1 recognize distinct spindle-attachment and kinetochore-tension checkpoints
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
The Gln-Ala repeat transcriptional activator CA150 interacts with huntingtin: Neuropathologic and genetic evidence for a role in Huntington's diseasepathogenesis
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Neither p21(WAF1) nor 14-3-3 sigma prevents G(2) progression to mitotic catastrophe in human colon carcinoma cells after DNA damage, but p21(WAF1) induces stable G(1) arrest in resulting tetraploid cells
CANCER RESEARCH
Tubulin detyrosination is a frequent occurrence in breast cancers of poor prognosis
CANCER RESEARCH
Allelic distribution of CTG18.1 in Caucasian populations: association studies in bipolar disorder, schizophrenia, and ataxia
MOLECULAR PSYCHIATRY
Crystal structure of human survivin reveals a bow tie-shaped dimer with two unusual alpha-helical extensions
MOLECULAR CELL
Organization of the human synphilin-1 gene, a candidate for Parkinson's disease
MAMMALIAN GENOME
Human huntingtin-associated protein (HAP-1) gene: genomic organisation andan intragenic polymorphism
GENE
Human survivin is a kinetochore-associated passenger protein
JOURNAL OF CELL BIOLOGY
Family-based association analysis of the hSKCa3 potassium channel gene in bipolar disorder
MOLECULAR PSYCHIATRY
Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization
NATURE MEDICINE
Expansion of a novel CAG trinucleotide repeat in the 5 ' region of PPP2R2Bis associated with SCA12
NATURE GENETICS
Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions
NATURE GENETICS
Polyglutamine pathogenesis
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES
Chromosomal localization of the Huntingtin associated protein (HAP-1) genein mouse and humans with radiation hybrid and interspecific backcross mapping
MAMMALIAN GENOME
Nuclear accumulation of truncated atrophin-1 fragments in a transgenic mouse model of DRPLA
NEURON
Genetics of childhood disorders: IX. Triplet repeat disorders
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY
The role of the telophasic disc in the regulation of cytokinesis.
PATHOLOGIE BIOLOGIE
CCG repeats in cDNAs from human brain (vol 103, pg 666, 1998)
HUMAN GENETICS
Mitogen-activated protein kinase kinase activity is required for the G(2)/M transition of the cell cycle in mammalian fibroblasts
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of asecond pedigree and effect on protein expression
JOURNAL OF MEDICAL GENETICS
Cleavage of atrophin-1 at caspase site aspartic acid 109 modulates cytotoxicity
JOURNAL OF BIOLOGICAL CHEMISTRY
Trinucleotide repeat expansion and neuropsychiatric disease
ARCHIVES OF GENERAL PSYCHIATRY
Two novel single-base-pair substitutions adjacent to the CAG repeat in theHuntington disease gene (IT15): Implications for diagnostic testing
AMERICAN JOURNAL OF HUMAN GENETICS
ATROPHIN-1, THE DRPLA GENE-PRODUCT, INTERACTS WITH 2 FAMILIES OF WW DOMAIN-CONTAINING PROTEINS
Molecular and cellular neurosciences (Print)
DOES CAG REPEAT NUMBER PREDICT THE RATE OF PATHOLOGICAL-CHANGES IN HUNTINGTONS-DISEASE
Annals of neurology
CCG repeats in cDNAs from human brain
HUMAN GENETICS
MICROTUBULE TREADMILLING - WHAT GOES AROUND COMES AROUND
BioEssays
PATIENTS WITH FEATURES SIMILAR TO HUNTINGTONS-DISEASE, WITHOUT CAG EXPANSION IN HUNTINGTIN
Neurology
NONNEURONAL ISOFORMS OF STOP PROTEIN ARE RESPONSIBLE FOR MICROTUBULE COLD STABILITY IN MAMMALIAN FIBROBLASTS
Proceedings of the National Academy of Sciences of the United Statesof America
SUPPRESSION OF TUBULIN TYROSINE LIGASE DURING TUMOR-GROWTH
Journal of Cell Science
STEPWISE RECONSTITUTION OF INTERPHASE MICROTUBULE DYNAMICS IN PERMEABILIZED CELLS AND COMPARISON TO DYNAMIC MECHANISMS IN INTACT-CELLS
The Journal of cell biology
DIFFERENTIAL SUBCELLULAR-LOCALIZATION OF PROTEIN-PHOSPHATASE-1-ALPHA,PROTEIN-PHOSPHATASE-1-GAMMA-1, AND PROTEIN-PHOSPHATASE-1-DELTA ISOFORMS DURING BOTH INTERPHASE AND MITOSIS IN MAMMALIAN-CELLS
The Journal of cell biology
CASPASE CLEAVAGE OF GENE-PRODUCTS ASSOCIATED WITH TRIPLET EXPANSION DISORDERS GENERATES TRUNCATED FRAGMENTS CONTAINING THE POLYGLUTAMINE TRACT
The Journal of biological chemistry
Colocalization of TD-60 and INCENP throughout G2 and mitosis: evidence fortheir possible interaction in signalling cytokinesis
CHROMOSOMA
Dual function C-terminal domain of dynamin-1: Modulation of self-assembly by interaction of the assembly site with SH3 domains
BIOCHEMISTRY
PUZZLES OF PSYCHIATRIC GENETICS - NEW CANDIDATE GENE APPROACHES
Molecular psychiatry
A NOVEL, HERITABLE, EXPANDING CTG REPEAT IN AN INTRON OF THE SEF2-1 GENE ON CHROMOSOME 18Q21.1
Human molecular genetics
THE ROLE OF THE PH DOMAIN AND SH3 BINDING DOMAINS IN DYNAMIN FUNCTION
Cellular signalling
SOUTHERN ANALYSIS FOR DETECTION OF CAG REPEAT EXPANSIONS ASSOCIATED WITH DENTATORUBRAL PALLIDOLUYSIAN ATROPHY
Human genetics
CDNAS WITH LONG CAG TRINUCLEOTIDE REPEATS FROM HUMAN BRAIN
Human genetics
ANALYSIS OF 13 TRINUCLEOTIDE REPEAT LOCI AS CANDIDATE GENES FOR SCHIZOPHRENIA AND BIPOLAR-DISORDER
American journal of medical genetics
TRINUCLEOTIDE REPEATS AND NEUROPSYCHIATRIC DISORDERS
American journal of medical genetics
HUNTINGTON-DISEASE AND THE RELATED DISORDER, DENTATORUBRAL-PALLIDOLUYSIAN ATROPHY (DRPLA)
Medicine
CHROMOSOMES WITH 2 INTACT AXIAL CORES ARE INDUCED BY G(2) CHECKPOINT OVERRIDE - EVIDENCE THAT DNA DECATENATION IS NOT REQUIRED TO TEMPLATE THE CHROMOSOME STRUCTURE
The Journal of cell biology
2-AMINOPURINE INDUCES SPINDLE-CELL MORPHOLOGY IN MM14 MYOBLASTS IN THE ABSENCE OF DIFFERENTIATION SIGNALS
Experimental cell research
CASPASE CLEAVAGE OF HUNTINGTIN, ATROPHIN-1 AND ANDROGEN RECEPTOR
American journal of human genetics
ATROPHIN-1, THE DRPLA GENE-PRODUCT, INTERACTS WITH A NUMBER OF WW DOMAIN-CONTAINING PROTEINS
American journal of human genetics
TRINUCLEOTIDE REPEATS AND NEUROPSYCHIATRIC DISORDERS
American journal of human genetics
CDNA CLONING AND CHARACTERIZATION OF AN ATROPHIN-1 (DRPLA DISEASE GENE)-RELATED PROTEIN
Neurobiology of disease
CDNA CLONING OF A HUMAN HOMOLOG OF THE CAENORHABDITIS-ELEGANS CELL FATE-DETERMINING GENE MAB-21 - EXPRESSION, CHROMOSOMAL LOCALIZATION AND ANALYSIS OF A HIGHLY POLYMORPHIC (CAG)(N) TRINUCLEOTIDE REPEAT
Human molecular genetics
OCCUPATIONAL-THERAPY TASK OBSERVATION SCALE (OTTOS)(C) - A RAPID METHOD FOR RATING TASK GROUP-FUNCTION OF PSYCHIATRIC-PATIENTS
The American journal of occupational therapy
DISTINCT SPECIFICITY IN THE RECOGNITION OF PHOSPHOINOSITIDES BY THE PLECKSTRIN HOMOLOGY DOMAINS OF DYNAMIN AND BRUTONS TYROSINE KINASE
EMBO journal
DRPLA GENE (ATROPHIN-1) SEQUENCE AND MESSENGER-RNA EXPRESSION IN HUMAN BRAIN
Molecular brain research
ANALYSIS OF 13 TRINUCLEOTIDE REPEAT LOCI AS CANDIDATE GENES FOR SCHIZOPHRENIA AND BIPOLAR AFFECTIVE-DISORDER
American journal of medical genetics
CLONING, EXPRESSION, AND PROPERTIES OF THE MICROTUBULE-STABILIZING PROTEIN STOP
Proceedings of the National Academy of Sciences of the United Statesof America
CHEMICAL INDUCTION OF MITOTIC CHECKPOINT OVERRIDE IN MAMMALIAN-CELLS RESULTS IN ANEUPLOIDY FOLLOWING A TRANSIENT TETRAPLOID STATE
Mutation research
MICROSATELLITE EVOLUTION - EVIDENCE FOR DIRECTIONALITY AND VARIATION IN RATE BETWEEN SPECIES
Nature genetics
NEURONAL STOP CDNA CLONING AND EXPRESSION - DEMONSTRATION THAT STOP ASSOCIATES WITH MICROTUBULES AND INDUCES MICROTUBULE COLD AND DRUG STABILITY IN CULTURED-MAMMALIAN-CELLS
Molecular biology of the cell
CHARACTERIZATION OF CDNA CLONES CONTAINING CCA TRINUCLEOTIDE REPEATS DERIVED FROM HUMAN BRAIN
Somatic cell and molecular genetics
POLYMORPHIC (AAT)N TRINUCLEOTIDE REPEATS DERIVED FROM A HUMAN BRAIN CDNA LIBRARY
Human genetics
ACTIVATION-INDUCED T-CELL DEATH IS CELL-CYCLE DEPENDENT AND REGULATEDBY CYCLIN-B
Molecular and cellular biology
DELAY OF HELA-CELL CLEAVAGE INTO INTERPHASE USING DIHYDROCYTOCHALASIN-B - RETENTION OF A POSTMITOTIC SPINDLE AND TELOPHASE DISC CORRELATES WITH SYNCHRONOUS CLEAVAGE RECOVERY
The Journal of cell biology
CHANGES IN THE SUBCELLULAR-LOCALIZATION OF REPLICATION INITIATION PROTEINS AND CELL-CYCLE PROTEINS DURING G1-PHASE TO S-PHASE TRANSITION INMAMMALIAN-CELLS
Chromosoma
CARBAMAZEPINE INDUCTION OF APOPTOSIS IN CULTURED CEREBELLAR NEURONS -EFFECTS OF N-METHYL-D-ASPARTATE, AURINTRICARBOCYLIC ACID AND CYCLOHEXIMIDE
Brain research
MICROSATELLITES ARE GENERALLY LONGER IN HUMANS COMPARED TO THEIR HOMOLOGS IN NONHUMAN-PRIMATES - EVIDENCE FOR DIRECTIONAL EVOLUTION AT MICROSATELLITE LOCI
American journal of human genetics
LONG CAG TRINUCLEOTIDE REPEATS IN HUMAN BRAIN CDNA
American journal of human genetics
GROWTH FACTOR-INDUCED BINDING OF DYNAMIN TO SIGNAL-TRANSDUCTION PROTEINS INVOLVES SORTING TO DISTINCT AND SEPARATE PROLINE-RICH DYNAMIN SEQUENCES
EMBO journal
NONPSYCHIATRIST HOUSE STAFF FREQUENTLY MISDIAGNOSE PSYCHIATRIC-DISORDERS IN GENERAL-HOSPITAL INPATIENTS
Psychosomatics
MICROTUBULE STABILITY IN NEURONS - MARKERS AND MECHANISMS
Journal of neurochemistry
MICROTUBULE DEPENDENCY OF P34(CDC2) INACTIVATION AND MITOTIC EXIT IN MAMMALIAN-CELLS
The Journal of cell biology
MICROTUBULE DEPENDENCY OF P34(CDC2) INACTIVATION AND MITOTIC EXIT IN MAMMALIAN-CELLS
The Journal of cell biology
PROGRAMMED CELL-DEATH - IMPLICATIONS FOR NEUROPSYCHIATRIC DISORDERS
Biological psychiatry
HUNTINGTONS-DISEASE GENE (IT-15) IS WIDELY EXPRESSED IN HUMAN AND RAT-TISSUES
Neuron
NOVEL TRIPLET REPEAT CONTAINING GENES IN HUMAN BRAIN - CLONING, EXPRESSION, AND LENGTH POLYMORPHISMS
Genomics
A RAPID METHOD FOR SEQUENCING TRINUCLEOTIDE REPEATS
Nucleic acids research
GENES WITH TRIPLET REPEATS - CANDIDATE MEDIATORS OF NEUROPSYCHIATRIC DISORDERS
Trends in neurosciences
EFFECT OF COCAINE, LIDOCAINE KINDLING AND CARBAMAZEPINE ON BATRACHOTOXIN-INDUCED PHOSPHOINOSITIDE HYDROLYSIS IN RAT-BRAIN SLICES
Brain research
EXPRESSION OF IT-15 AND LACK OF REDUCTION IN HUNTINGTONS-DISEASE (HD)
American journal of human genetics
IDENTIFICATION OF NOVEL CDNA CLONES CONTAINING CAG OR CCG TRINUCLEOTIDE REPEATS FROM HUMAN BRAIN
American journal of human genetics
IDENTIFICATION OF NOVEL CDNA CLONES CONTAINING AAT OR CCA TRINUCLEOTIDE REPEATS
American journal of human genetics