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12ŒŽ18“ú Allele-specific silencing of dominant disease genes.
Miller VM et al., PNAS 2003 100:7195-7200
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11ŒŽ27“ú Sex hormone-regulated renal transport of perfluorooctanoic acid(PFOA).
Kudo N et al., Chem Biol Interact. 2002 139:301-16
Interactions of fluorochemicals with rat liver fatty acid-binding protein.
Luebker DJ et al., Toxicology. 2002 176:175-85
Binding of perfluorooctanoic acid(PFOA) to rat and human plasma proteins.
Han X et al., Chem Res Toxicol. 2003 16:775-81
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11ŒŽ13“ú Family-based association study of markers on chromosome 22 in schizophrenia using African-American, European-American, and Chinese families.
Takahashi S, Am J Hum Genet. 2003 120B(1):11-7

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10ŒŽ16“ú Mutations of the RNA-Specific Adenosine Deaminase Gene are Involved in Dyschromatosis Synmetrica Hereditaria.
Miyamura Y, Am J Hum Genet. 2003 73:693-9.

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10ŒŽ2“ú The Molecular Biology Database Collection: 2003 update.
Baxevanis AD, Nucleic Acids Res. 2003 31(1):1-12.

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9ŒŽ24“ú Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.
EA Otto et al., Nat genet, 2003, 34:413-20

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9ŒŽ17“ú In Vitro Refolding of Human Proinsulin.
ZS Qiao et al., J Biol Chem, 2003, 278:17800-9
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9ŒŽ11“ú Extracellular matrix remodeling and matrix metalloproteinases in the vascular wall during aging and in pathological conditions.
MP Jacob, Biomed Pharmacother, 2003, 57:195-202
Regulation of Matrix Metalloproteinase (Matrixin) Genes in Blood Vessels: A Multi-Step Recruitment Model for Pathological Remodelling.
Chase AJ, Newby AC, J Vasc Res, 2003
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9ŒŽ4“ú Operative morbidity of living liver donors in Japan.
K Umeshita et al., Lancet, 2003, 362:687-690
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P¼ Living Donor Liver Transplantation
7ŒŽ31“ú Association of the T-cell Regulatory Gene CTLA4 with Susceptibility to Autoimmune Disease.
H Ueda et al., Nature, 2003; 423:506-511
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7ŒŽ24“ú Evaluating the Results of Genomewide Linkage Scans of Complex Traits by Locus Counting.
S Wiltshire et al., Am J Hum Genet, 2002; 71:1175-1182
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7ŒŽ10“ú A surbey of liver transplantation from living adult donors in the united states.
R S Brown et al., N Engl J Med, 2003; 348:818-25
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7ŒŽ3“ú Association of mutation position in polycystic kidney disease 1(PKD1) and development of a vascular phenotype.
Lancet, 2003; 36:12196-201
Cardiovascular skeletal, and renal defects in mice with a targeted disruption of the PKD1 gene.
PNAS, 2001; 98:12174-79
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6ŒŽ26“ú Persistent toxic chemicals in the US food supply.
K S Schafer et al., J Epidemiol Community Health, 2002; 56:813-7
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6ŒŽ5“ú [Exposure to Lead in Children -How Low is Low Enough?-]
Intellectual Impairment in Children with Blood Lead Concentrations below 10ug per Deciliter.
Richard LC et al., N Engl J Med, 2003 Apr; 348(16):1517-26
Blood Lead Concentration and Delayed Puberty in Girls.
Sherry GS et al., N Engl J Med, 2003 Apr; 348(16):1527-36
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5ŒŽ29“ú Improving Risk Communication.
National Research Council, 1989
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5ŒŽ22“ú Mutations in RAI1 associated with Smith-Magenis syndrome.
Slager RE et al., Nat Genet, 2003 Mar; 33(4):466-8
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5ŒŽ15“ú Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.
Vamsi K. Mootha et al., PNAS, 2003 Jan; 100(2):605-610
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5ŒŽ8“ú Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells.
Nauli SM et al., Nat Genet, 2003 Feb; 33:129-137
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5ŒŽ1“ú Combating omission errors through task analysis and good reminders.
J Reason Qual Saf Health Care 2002; 11:40-44
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4ŒŽ17“ú Discovering Genotype Underlying Human Phenotypes: Past Successes for Mendelian Disease, Future Approaches for Complex Disease.
David B & Neil R Nat Genet 2003 Mar; 33:228-237
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4ŒŽ10“ú Role of the Connecting Peptide in Insulin Biosynthesis.
Ming L.et al. J Biol Chem 2003 Feb;
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4ŒŽ3“ú Linkage studies in familial Alzheimer disease: evidence for chromosome 19 linkage.
Pericak-Vance MA. et al. Am J Hum Genet 1991 Jun; 48(6):1034-50
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3ŒŽ13“ú Dominant Negative Pathogenesis by Mutant Proinsulin in the Akita Diabetic Mouse.
Izumi T et al. Diabetes 2003 52:409-416
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2ŒŽ27“ú Germline Mutations of TSH Receptor Gene as Cause of Nonautoimmune Subclinical Hypothyroidism.
Luisella A et al. J Clin Endcrinol Metabol 2002 87(6):2549-2555
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2ŒŽ20“ú Distribution and Characterization of Regulatory Elements in the Human Genome.
Majewski & Ott J. Genome Res 2002 Dec; 12(12):1827-36
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2ŒŽ13“ú Detecting Recent Positive Selection in the Human Genome from Haplotype Structure.
Sabeti PC et al. Nature 2002 419:832-837
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2ŒŽ6“ú Hospital Nurse Staffing and Patient Mortality, Nurse Burnout, and Job Dissatisfaction.
Linda H et al. JAMA 2002; 288:1987-1993
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1ŒŽ30“ú Gene-environmental Interaction: An example -Neural Tube Defect
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1ŒŽ20“ú Magnetic Resonance Angiographic Evidence of Sex-linked Variations in the Circle of Willis and the Occurence of Cerebral Aneurysms.
Horikoshi T et al. J Neurosurg 2002 Apr; 96:697-703
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