Lista de obras - Hatasu Kobayashi - Dominio Público Uruguay

A new horizon of moyamoya disease and associated health risks explored through RNF213

artículo científico publicado en 2016

A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians

artículo científico publicado en 2009

Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo

scientific journal article

Biological Monitoring of Human Exposure to Neonicotinoids Using Urine Samples, and Neonicotinoid Excretion Kinetics

artículo científico publicado en 2016

Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).

artículo científico publicado en 2012

Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan ⬇️

artículo científico publicado el 21 de febrero de 2012

Combined linkage analysis and exome sequencing identifies novel genes for familial goiter.

artículo científico publicado en 2013

Damage to cellular and isolated DNA induced by a metabolite of aspirin.

artículo científico publicado en 2008

Downregulation of Securin by the variant RNF213 R4810K (rs112735431, G>A) reduces angiogenic activity of induced pluripotent stem cell-derived vascular endothelial cells from moyamoya patients.

artículo científico publicado en 2013

Dysregulation of RNF213 promotes cerebral hypoperfusion.

artículo científico publicado en 2018

Early onset of moyamoya syndrome in a Down syndrome patient with the genetic variant RNF213 p.R4810K.

artículo científico publicado en 2014

Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement ⬇️

artículo científico publicado el 16 de junio de 2011

Familial episodic limb pain in kindreds with novel Nav1.9 mutations ⬇️

artículo científico publicado en 2018

Frequency of RNF213 p.R4810K, a susceptibility variant for moyamoya disease, and health characteristics of carriers in the Japanese population

artículo científico publicado en 2016

Genes associated with moyamoya syndrome and disease

artículo científico publicado el 1 de febrero de 2012

Genetic study of intracranial aneurysms

artículo científico

Genomewide association study identifies no major founder variant in Caucasian moyamoya disease.

artículo científico publicado en 2013

Identification of MMP1 as a novel risk factor for intracranial aneurysms in ADPKD using iPSC models

artículo científico publicado en 2016

Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development

artículo científico publicado en 2011

Importance of molecular diagnosis in the accurate diagnosis of systemic carnitine deficiency

artículo científico publicado en 2015

Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

artículo científico publicado en 2016

Mechanism of DNA damage and apoptosis induced by tetrahydropapaveroline, a metabolite of dopamine

artículo científico publicado en 2006

Mechanism of metal-mediated DNA damage and apoptosis induced by 6-hydroxydopamine in neuroblastoma SH-SY5Y cells

artículo científico publicado en 2008

Metal-mediated oxidative damage to cellular and isolated DNA by gallic acid, a metabolite of antioxidant propyl gallate.

artículo científico publicado en 2004

Moyamoya Disease Susceptibility Variant RNF213 p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis

artículo científico publicado en 2019

Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial Fibrillation

scientific article published on 01 April 2019

Nitrative DNA damage and Oct3/4 expression in urinary bladder cancer with Schistosoma haematobium infection

scientific article published on 17 September 2011

P.R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure.

artículo científico publicado en 2012

Perfluorinated carboxylic acids discharged from the Yodo River Basin, Japan

artículo científico publicado en 2015

Preliminary assessment of ecological exposure of adult residents in Fukushima Prefecture to radioactive cesium through ingestion and inhalation

artículo científico publicado en 2011

Prevalence of RNF213 p.R4810K Variant in Early-Onset Stroke With Intracranial Arterial Stenosis

scientific article published on 07 May 2019

Proteomic analysis of carbonylated proteins in the monkey substantia nigra after ischemia-reperfusion.

artículo científico publicado en 2014

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

artículo científico publicado en 2016

RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients

artículo científico publicado en 2016

RNF213 p.R4810K Variant and Intracranial Arterial Stenosis or Occlusion in Relatives of Patients with Moyamoya Disease.

artículo científico publicado en 2017

Rapid contralateral progression of focal cerebral arteriopathy distinguished from RNF213-related moyamoya disease and fibromuscular dysplasia.

artículo científico publicado en 2017

Rapid progression of unilateral moyamoya disease in a patient with a family history and an RNF213 risk variant

scientific article published on 11 September 2013

Rare variants in RNF213, a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in mice.

artículo científico publicado en 2018

Significant Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease.

artículo científico publicado en 2016

Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease

artículo científico publicado en 2017

Suppressed phosphorylation of collapsin response mediator protein-2 in the hippocampus of HCNP precursor transgenic mice

artículo científico publicado en 2010

Temporal trend and age-dependent serum concentration of phenolic organohalogen contaminants in Japanese men during 1989-2010.

artículo científico publicado en 2013

The mechanisms of oxidative DNA damage and apoptosis induced by norsalsolinol, an endogenous tetrahydroisoquinoline derivative associated with Parkinson's disease.

artículo científico publicado en 2008

The moyamoya disease susceptibility variant RNF213 R4810K (rs112735431) induces genomic instability by mitotic abnormality

artículo científico publicado en 2013

Whole-exome sequencing reveals genetic variants associated with chronic kidney disease characterized by tubulointerstitial damages in North Central Region, Sri Lanka.

artículo científico publicado en 2015

β-cell-specific overexpression of adiponectin receptor 1 does not improve diabetes mellitus in Akita mice.

artículo científico publicado en 2018

Lista de obras de Hatasu Kobayashi

A new horizon of moyamoya disease and associated health risks explored through RNF213

A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians

Biochemical and Functional Characterization of RNF213 (Mysterin) R4810K, a Susceptibility Mutation of Moyamoya Disease, in Angiogenesis In Vitro and In Vivo

Biological Monitoring of Human Exposure to Neonicotinoids Using Urine Samples, and Neonicotinoid Excretion Kinetics

Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).

Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan ⬇️

Combined linkage analysis and exome sequencing identifies novel genes for familial goiter.

Damage to cellular and isolated DNA induced by a metabolite of aspirin.

Downregulation of Securin by the variant RNF213 R4810K (rs112735431, G>A) reduces angiogenic activity of induced pluripotent stem cell-derived vascular endothelial cells from moyamoya patients.

Dysregulation of RNF213 promotes cerebral hypoperfusion.

Early onset of moyamoya syndrome in a Down syndrome patient with the genetic variant RNF213 p.R4810K.

Expansion of Intronic GGCCTG Hexanucleotide Repeat in NOP56 Causes SCA36, a Type of Spinocerebellar Ataxia Accompanied by Motor Neuron Involvement ⬇️

Familial episodic limb pain in kindreds with novel Nav1.9 mutations ⬇️

Frequency of RNF213 p.R4810K, a susceptibility variant for moyamoya disease, and health characteristics of carriers in the Japanese population

Genes associated with moyamoya syndrome and disease

Genetic study of intracranial aneurysms

Genomewide association study identifies no major founder variant in Caucasian moyamoya disease.

Identification of MMP1 as a novel risk factor for intracranial aneurysms in ADPKD using iPSC models

Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development

Importance of molecular diagnosis in the accurate diagnosis of systemic carnitine deficiency

Infantile Pain Episodes Associated with Novel Nav1.9 Mutations in Familial Episodic Pain Syndrome in Japanese Families

Mechanism of DNA damage and apoptosis induced by tetrahydropapaveroline, a metabolite of dopamine

Mechanism of metal-mediated DNA damage and apoptosis induced by 6-hydroxydopamine in neuroblastoma SH-SY5Y cells

Metal-mediated oxidative damage to cellular and isolated DNA by gallic acid, a metabolite of antioxidant propyl gallate.

Moyamoya Disease Susceptibility Variant RNF213 p.R4810K Increases the Risk of Ischemic Stroke Attributable to Large-Artery Atherosclerosis

Mutant KCNJ3 and KCNJ5 Potassium Channels as Novel Molecular Targets in Bradyarrhythmias and Atrial Fibrillation

Nitrative DNA damage and Oct3/4 expression in urinary bladder cancer with Schistosoma haematobium infection

P.R4810K, a polymorphism of RNF213, the susceptibility gene for moyamoya disease, is associated with blood pressure.

Perfluorinated carboxylic acids discharged from the Yodo River Basin, Japan

Preliminary assessment of ecological exposure of adult residents in Fukushima Prefecture to radioactive cesium through ingestion and inhalation

Prevalence of RNF213 p.R4810K Variant in Early-Onset Stroke With Intracranial Arterial Stenosis

Proteomic analysis of carbonylated proteins in the monkey substantia nigra after ischemia-reperfusion.

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

RNF213 Rare Variants in Slovakian and Czech Moyamoya Disease Patients

RNF213 p.R4810K Variant and Intracranial Arterial Stenosis or Occlusion in Relatives of Patients with Moyamoya Disease.

Rapid contralateral progression of focal cerebral arteriopathy distinguished from RNF213-related moyamoya disease and fibromuscular dysplasia.

Rapid progression of unilateral moyamoya disease in a patient with a family history and an RNF213 risk variant

Rare variants in RNF213, a susceptibility gene for moyamoya disease, are found in patients with pulmonary hypertension and aggravate hypoxia-induced pulmonary hypertension in mice.

Significant Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease.

Significant association of RNF213 p.R4810K, a moyamoya susceptibility variant, with coronary artery disease

Suppressed phosphorylation of collapsin response mediator protein-2 in the hippocampus of HCNP precursor transgenic mice

Temporal trend and age-dependent serum concentration of phenolic organohalogen contaminants in Japanese men during 1989-2010.

The mechanisms of oxidative DNA damage and apoptosis induced by norsalsolinol, an endogenous tetrahydroisoquinoline derivative associated with Parkinson's disease.

The moyamoya disease susceptibility variant RNF213 R4810K (rs112735431) induces genomic instability by mitotic abnormality

Whole-exome sequencing reveals genetic variants associated with chronic kidney disease characterized by tubulointerstitial damages in North Central Region, Sri Lanka.

β-cell-specific overexpression of adiponectin receptor 1 does not improve diabetes mellitus in Akita mice.