Kenichi Ishibashi

The Dichotomy of MIP Family Suggests Two Separate Origins of Water Channels.

Prospect of a stanniocalcin endocrine/paracrine system in mammals.

A single amino acid mutation results in a rapid inactivation of epithelial calcium channels.

Mouse aquaporin 10 gene (AQP10) is a pseudogene.

Opening of ligand-gated cation channel families by calpain inhibitors.

Cloning and identification of a new member of water channel (AQP10) as an aquaglyceroporin.

AE4 is a DIDS-sensitive Cl(-)/HCO(-)(3) exchanger in the basolateral membrane of the renal CCD and the SMG duct.

Functional analysis of ABCA8, a new drug transporter.

A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.

Identification of a new member of type I Na/phosphate co-transporter in the rat kidney.

Successful gene transfer using adeno-associated virus vectors into the kidney: comparison among adeno-associated virus serotype 1-5 vectors in vitro and in vivo.

Surgical treatment of temporal lobe epilepsy associated with subcortical ectopic gray matter under the guidance of intraoperative electrocorticography.

Localization of aquaporin-7 in human testis and ejaculated sperm: possible involvement in maintenance of sperm quality.

Molecular mechanisms and drug development in aquaporin water channel diseases: aquaporin superfamily (superaquaporins): expansion of aquaporins restricted to multicellular organisms.

[Surgical technique and outcome of transsylvian selective amygdalohippocampectomy].

Identification of a novel aquaporin, AQP12, expressed in pancreatic acinar cells.

Expression and localization of two isoforms of AQP10 in human small intestine.

Identification of a keratinocarcinoma cell line expressing AQP3.

[Japanese CADASIL case with limited dementia who had the Notch 3 R141C mutation].

Disruption of aquaporin-11 produces polycystic kidneys following vacuolization of the proximal tubule.

Radioiodinated flavones for in vivo imaging of beta-amyloid plaques in the brain.

Small artery dementia in Japan: radiological differences between CADASIL, leukoaraiosis and Binswanger's disease.

Acute digoxin loading reduces ABCA8A mRNA expression in the mouse liver.

Aquaporin subfamily with unusual NPA boxes.

Effectiveness of cerebral hemispherotomy for improving behavioral disorders associated with intractable post-traumatic seizures.

Comparison of neuropsychological outcomes after selective amygdalohippocampectomy versus anterior temporal lobectomy.

The anterolateral partial vertebrectomy approach for ventrally located cervical intramedullary cavernous angiomas.

Schwannoma of the oculomotor nerve.

Aquaporin-11 containing a divergent NPA motif has normal water channel activity.

Cerebral vascular accumulation of Dutch-type Abeta42, but not wild-type Abeta42, in hereditary cerebral hemorrhage with amyloidosis, Dutch type.

Intracellular aquaporins: clues for intracellular water transport?

Neuromyelitis optica and anti-aquaporin-4 antibodies measured by an enzyme-linked immunosorbent assay.

Importance of fixation angle in posterior instrumented occipitocervical fusion.

Aquaporin-11 knockout mice and polycystic kidney disease animals share a common mechanism of cyst formation.

Single amino acid substitution in aquaporin 11 causes renal failure.

Aquaporin water channels in mammals.

New members of mammalian aquaporins: AQP10-AQP12.

The E693Delta mutation in amyloid precursor protein increases intracellular accumulation of amyloid beta oligomers and causes endoplasmic reticulum stress-induced apoptosis in cultured cells.

[Enlarged perivascular spaces associated with hydrocephalus: a case report].

Pancreas-specific aquaporin 12 null mice showed increased susceptibility to caerulein-induced acute pancreatitis.

Central neurocytoma presenting with massive hemorrhage leading to coma--case report.

The role of a group III AQP, AQP11 in intracellular organelle homeostasis.

The role of radical microsurgical resection in multimodal treatment for skull base meningioma.

Cost-effective gene transfection by DNA compaction at pH 4.0 using acidified, long shelf-life polyethylenimine.

A mouse model of amyloid beta oligomers: their contribution to synaptic alteration, abnormal tau phosphorylation, glial activation, and neuronal loss in vivo.

Ag nanoparticle sheet as a marker of lateral remote photocatalytic reactions.

The NPC motif of aquaporin-11, unlike the NPA motif of known aquaporins, is essential for full expression of molecular function.

The evolutionary aspects of aquaporin family.

The association of plasma prorenin level with an oxidative stress marker, 8-OHdG, in nondiabetic hemodialysis patients.

Middle skull base approach with posterolateral mobilization of the geniculate ganglion to access the clival regions.

Three-dimensional video presentation of microsurgery by the cross-eyed viewing method using a high-definition video system.

Bilateral subfrontal approach for tuberculum sellae meningiomas in long-term postoperative visual outcome.

The interaction of LFA-1 on mononuclear cells and ICAM-1 on tubular epithelial cells accelerates TGF-β1-induced renal epithelial-mesenchymal transition.

Nuclear c-Abl-mediated tyrosine phosphorylation induces chromatin structural changes through histone modifications that include H4K16 hypoacetylation.

Establishment of acute kidney injury mouse model by 0.75% adenine ingestion.

Analysis of venous drainage from sylvian veins in clinoidal meningiomas.

Long-term effects of aliskiren on blood pressure and the renin-angiotensin-aldosterone system in hypertensive hemodialysis patients.

Oncogenic osteomalacia associated with mesenchymal tumor in the middle cranial fossa: a case report.

Isolation and characterization of bacterial isolates algicidal against a harmful bloom-forming cyanobacterium Microcystis aeruginosa.

Aliskiren suppresses the renin-angiotensin-aldosterone system and reduces blood pressure and albuminuria in elderly chronic kidney disease patients with hypertension.

Nuclear ErbB4 signaling through H3K9me3 is antagonized by EGFR-activated c-Src.

Simple and safe exposure of the sigmoid sinus with presigmoid approaches.

Phosphorylation of KRAB-associated protein 1 (KAP1) at Tyr-449, Tyr-458, and Tyr-517 by nuclear tyrosine kinases inhibits the association of KAP1 and heterochromatin protein 1α (HP1α) with heterochromatin.

Analysis of progression and recurrence of meningioma using (11)C-methionine PET.

Twelve-year-old girl with intracranial epidural abscess and sphenoiditis.

Preoperative evaluation of the petrosal vein with contrast-enhanced PRESTO imaging in petroclival meningiomas to establish surgical strategy.

Formation of long and winding nuclear F-actin bundles by nuclear c-Abl tyrosine kinase.

Medication-prescribing patterns of primary care physicians in chronic kidney disease.

The role of mammalian superaquaporins inside the cell.

Association of primary care physicians' exercise habits and their age, specialty, and workplace.

Surgical outcomes of the minimum anterior and posterior combined transpetrosal approach for resection of retrochiasmatic craniopharyngiomas with complicated conditions.

Activation of the prereplication complex is blocked by mimosine through reactive oxygen species-activated ataxia telangiectasia mutated (ATM) protein without DNA damage.

Positive association of vigorous and moderate physical activity volumes with skeletal muscle mass but not bone density or metabolism markers in hemodialysis patients.

Preservation of labyrinthine structures while drilling the posterior wall of the internal auditory canal in surgery of vestibular schwannomas via the retrosigmoid suboccipital approach.

Staged 'intentional' bridging vein ligation: a safe strategy in gaining wide access to skull base tumors.

Src family kinases promote silencing of ATR-Chk1 signaling in termination of DNA damage checkpoint.

Primary care physicians' own exercise habits influence exercise counseling for patients with chronic kidney disease: a cross-sectional study.

Skeletal muscle loss is negatively associated with single-pool Kt/V and dialysis duration in hemodialysis patients.

Aberrant glycosylation and localization of polycystin-1 cause polycystic kidney in an AQP11 knockout model.

Exercise counseling of primary care physicians in metabolic syndrome and cardiovascular diseases is associated with their specialty and exercise habits.

Lyn tyrosine kinase promotes silencing of ATM-dependent checkpoint signaling during recovery from DNA double-strand breaks.

siRNAs targeted to Smad4 prevent renal fibrosis in vivo.

Cdk1-mediated phosphorylation of human ATF7 at Thr-51 and Thr-53 promotes cell-cycle progression into M phase.

Functional Preservation After Planned Partial Resection Followed by Gamma Knife Radiosurgery for Large Vestibular Schwannomas.

[Term 5: Neutrophil extracellular traps and inflammasomes].

Delivery of microRNA-146a with polyethylenimine nanoparticles inhibits renal fibrosis in vivo.

Utilization of arsenic trioxide as a treatment of cisplatin-resistant non-small cell lung cancer PC-9/CDDP and PC-14/CDDP cells.

The distribution and function of aquaporins in the kidney: resolved and unresolved questions.

Differentiation with elaidate tends to impair insulin-dependent glucose uptake and GLUT4 translocation in 3T3-L1 adipocytes.

Functional Outcomes of Salvage Surgery for Vestibular Schwannomas after Failed Gamma Knife Radiosurgery.

Reconstitution of Human Ion Channels into Solvent-free Lipid Bilayers Enhanced by Centrifugal Forces.

Aquaporin-11 (AQP11) Expression in the Mouse Brain.

Impact of Endoscopic Indocyanine Green Fluorescence Imaging on Superselective Intra-arterial Chemotherapy for Recurrent Cancer of the Skull Base.

Pediatric thalamic glioma with H3F3A K27M mutation, which was detected before and after malignant transformation: a case report.

Delayed cyst formations and/or expanding hematomas developing after Gamma Knife surgery for cerebral arteriovenous malformations.

A combination of TERT promoter mutation and MGMT methylation status predicts clinically relevant subgroups of newly diagnosed glioblastomas.

Disruption of Membranes of Extracellular Vesicles Is Necessary for ELISA Determination of Urine AQP2: Proof of Disruption and Epitopes of AQP2 Antibodies.

Enhanced Autophagy in Polycystic Kidneys of AQP11 Null Mice.

The association between soluble intercellular adhesion molecule-1 levels in drained dialysate and peritoneal injury in peritoneal dialysis.

The Evolutionary Aspects of Aquaporin Family.

Activation of PPARγ at an Early Stage of Differentiation Enhances Adipocyte Differentiation of MEFs Derived from Type II Diabetic TSOD Mice and Alters Lipid Droplet Morphology.

Aquaporin10 is a pseudogene in cattle and their relatives.

Proteomic analysis of AQP11-null kidney: Proximal tubular type polycystic kidney disease.

AQP2 in human urine is predominantly localized to exosomes with preserved water channel activities.

Protective Effects of Diuretics Against the Development of Cardiovascular Disease in Patients with Chronic Kidney Disease: A Systematic Review.

Nano-sized carriers in gene therapy for renal fibrosis .

Nano-sized carriers in gene therapy for peritoneal fibrosis .

Transgene and islet cell delivery systems using nano-sized carriers for the treatment of diabetes mellitus.

Involvement of the NADPH oxidase 2 pathway in renal oxidative stress in mice.

MicroRNAs in peritoneal fibrosis: a systematic review.

Perspectives on the evolution of aquaporin superfamily.

Phosphorylation profile of human AQP2 in urinary exosomes by LC-MS/MS phosphoproteomic analysis.

MicroRNAs in Sarcopenia: A Systematic Review.

MicroRNAs in Podocyte Injury in Diabetic Nephropathy.

Effects of osmolality on the expression of brain aquaporins in AQP11-null mice.

The role of mammalian superaquaporins inside the cell: An update.

Systematic Review and Meta-Analysis of Renin-Angiotensin-Aldosterone System Blocker Effects on the Development of Cardiovascular Disease in Patients With Chronic Kidney Disease.