Showing search results for "Saitoh S"
Kurume University, Japan
Patients, Chromosome, Cell, Syndrome, Centromere, Plays, Role, Phenotype, Epilepsy, Time, Mitosis, Patient,
, Chromatin, Human, Proteins,
, Kinase, Adenosine,
Information and abstracts for author publications
Hsk1- and SCF(Pof3)-dependent proteolysis of S. pombe Ams2 ensures histone homeostasis and centromere function.
Current biology : CB
Epigenetic inactivation and subsequent heterochromatinization of a centromere stabilize dicentric chromosomes.
HbA1c and the risks for all-cause and cardiovascular mortality in the general Japanese population: NIPPON DATA90.
Molecular and cellular biology
CENP-A reduction induces a p53-dependent cellular senescence response to protect cells from executing defective mitoses.
The Journal of pediatrics
Maternal uniparental disomy 14 syndrome demonstrates prader-willi syndrome-like phenotype.
Increased protein stability of CDKN1C causes a gain-of-function phenotype in patients with IMAGe syndrome.
Direct correlation between the facial nerve nucleus and hemifacial seizures associated with a gangliocytoma of the floor of the fourth ventricle: a case report.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
A loss-of-function mutation in the SLC9A6 gene causes X-linked mental retardation resembling Angelman syndrome.
Biochemical Society transactions
Switching the centromeres on and off: epigenetic chromatin alterations provide plasticity in centromere activity stabilizing aberrant dicentric chromosomes.
Chaperones and transport proteins regulate TLR4 trafficking and activation.
Journal of magnetic resonance imaging : JMRI
Diffusion analysis with triexponential function in liver cirrhosis.
European journal of pharmacology
Metabolic regulation of coronary vascular tone: role of hydrogen peroxide, purinergic components, and angiotensin.
American journal of medical genetics. Part A
West syndrome associated with mosaic duplication of FOXG1 in a patient with maternal uniparental disomy of chromosome 14.
MEG time-frequency analyses for pre- and post-surgical evaluation of patients with epileptic rhythmic fast activity.
The applications of time-frequency analyses to ictal magnetoencephalography in neocortical epilepsy.
Magnetoencephalographic analysis of paroxysmal fast activity in patients with epileptic spasms.
Brain & development
Childhood-onset anti-MuSK antibody positive myasthenia gravis demonstrates a distinct clinical course.
Micromanipulation of Chromosomes in Insect Spermatocytes
Micromanipulation of Chromosom…
Transdermal Measurement of Glomerular Filtration Rate in Mice
Transdermal Measurement of Glo…
Gene Expression Analysis of Endothelial Cells Exposed to Shear Stress Using Multiple Parallel-plate Flow Chambers
Gene Expression Analysis of En…
Pore-scale Imaging and Characterization of Hydrocarbon Reservoir Rock Wettability at Subsurface Conditions Using X-ray Microtomography
Pore-scale Imaging and Charact…
Contrast-Matching Detergent in Small-Angle Neutron Scattering Experiments for Membrane Protein Structural Analysis and
Contrast-Matching Detergent in…
Construction of a Multilayered Mesenchymal Stem Cell Sheet with a 3D Dynamic Culture System
Construction of a Multilayered…
Method for Evaluating the Gut-Blood Barrier and Liver Metabolism of Microbiota Products
Scalable Fabrication of Stretchable, Dual Channel, Microfluidic Organ Chips
Scalable Fabrication of Stretc…
Detection of Heterodimerization of Protein Isoforms Using an
Proximity Ligation Assay
Detection of Heterodimerizatio…
Preparation of Chloroplast Sub-compartments from Arabidopsis for the Analysis of Protein Localization by Immunoblotting or Proteomics
Preparation of Chloroplast Sub…
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