about
Low-density lipoprotein receptor-related protein 8 (apolipoprotein E receptor 2) gene polymorphisms in Alzheimer's diseaseThree endothelial nitric oxide (NOS3) gene polymorphisms in hypertensive and normotensive individuals: meta-analysis of 53 studies reveals evidence of publication biasPharmacogenetic analysis of lipid responses to rosuvastatin in Chinese patientsEffects of Huanglian-Jie-Du-Tang and its modified formula on the modulation of amyloid-β precursor protein processing in Alzheimer's disease modelsHighly stabilized curcumin nanoparticles tested in an in vitro blood-brain barrier model and in Alzheimer's disease Tg2576 miceCurcumin-conjugated magnetic nanoparticles for detecting amyloid plaques in Alzheimer's disease mice using magnetic resonance imaging (MRI).Isolation and enrichment of human genomic CpG islands by methylation-sensitive mirror orientation selection.Variants conferring risk of atrial fibrillation on chromosome 4q25.Multidrug-resistant genotype (ABCB1) and seizure recurrence in newly treated epilepsy: data from international pharmacogenetic cohorts.A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.Modulation of amyloid beta-protein clearance and Alzheimer's disease susceptibility by the LDL receptor-related protein pathway.A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.Outcomes of Phacoemulsification Using Different Size of Clear Corneal Incision in Eyes with Previous Radial Keratotomy.Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.EDN1 Lys198Asn is associated with diabetic retinopathy in type 2 diabetes.Serum multivalent cationic pattern: speculation on the efficient approach for detection of Alzheimer's disease.Effects of 17-allylamino-17-demethoxygeldanamycin (17-AAG) in transgenic mouse models of frontotemporal lobar degeneration and Alzheimer's disease.Association of 8q24.21 loci with the risk of colorectal cancer: a systematic review and meta-analysis.GABRG2 rs211037 polymorphism and epilepsy: a systematic review and meta-analysis.Developing the use of mismatch binding proteins for discovering rare somatic mutations.SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.In vitro transport assays of rufinamide, pregabalin, and zonisamide by human P-glycoprotein.The potential role of CAMSAP1L1 in symptomatic epilepsy.Potential role for human P-glycoprotein in the transport of lacosamide.In vitro transport profile of carbamazepine, oxcarbazepine, eslicarbazepine acetate, and their active metabolites by human P-glycoprotein.SCN1A IVS5N+5 polymorphism and response to sodium valproate: a multicenter study.Neuroprotective effect of honokiol and magnolol, compounds from Magnolia officinalis, on beta-amyloid-induced toxicity in PC12 cells.In vitro concentration dependent transport of phenytoin and phenobarbital, but not ethosuximide, by human P-glycoprotein.Trophism of neural progenitor cells to embryonic stem cells: neural induction and transplantation in a mouse ischemic stroke model.Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis.Pathogenic mutations of the lipoprotein lipase gene in Chinese patients with hypertriglyceridemic type 2 diabetes.Overexpressed tau protein in cultured cells is phosphorylated without formation of PHF: implication of phosphoprotein phosphatase involvement.The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.Genetic polymorphisms of Chinese patients with ischemic stroke and concurrent stenoses of extracranial and intracranial vessels.Simple and practical staining of DNA with GelRed in agarose gel electrophoresis.ABCG2 polymorphism is associated with the low-density lipoprotein cholesterol response to rosuvastatin.Serum zinc is decreased in Alzheimer's disease and serum arsenic correlates positively with cognitive ability.Failure to detect association between polymorphisms of the sodium channel gene SCN1A and febrile seizures in Chinese patients with epilepsy.Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposis.Casein kinase II is associated with neurofibrillary tangles but is not an intrinsic component of paired helical filaments.
P50
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P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Larry Baum
@ast
Larry Baum
@en
Larry Baum
@es
Larry Baum
@nl
Larry Baum
@sl
type
label
Larry Baum
@ast
Larry Baum
@en
Larry Baum
@es
Larry Baum
@nl
Larry Baum
@sl
prefLabel
Larry Baum
@ast
Larry Baum
@en
Larry Baum
@es
Larry Baum
@nl
Larry Baum
@sl
P106
P1153
7103310839
P21
P2798
P31
P496
0000-0002-5345-9355