[Tokyo Centenarian Study. 4. Apolipoprotein E phenotype in Japanese centenarians living in the Tokyo Metropolitan area].
Nihon Ronen Igakkai zasshi. Japanese journal of geriatrics | 1997-04-01 | PMID 9212680
Hirose N, Homma S, Arai Y and 7 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 867 of 10600
Use of a polybrene capillary coating in capillary electrophoresis for rapid analysis of hemoglobin variants with on-line detection via an ion trap storage/reflectron time-of-flight mass spectrometer.
Analytical chemistry | 1997-07-01 | PMID 9212707
Li M X, Liu L, Wu J T and 1 more
Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
The American journal of pathology | 1997-07-01 | PMID 9212754
Sundberg J P, Boggess D, Hogan M E and 6 more
Genotoxicity monitoring of small bodies of water using two species of tadpoles and the alkaline single cell gel (comet) assay.
Environmental and molecular mutagenesis | 1997-01-01 | PMID 9212794
Ralph S, Petras M
[Cyclin and cell cycle].
Gan to kagaku ryoho. Cancer & chemotherapy | 1997-06-01 | PMID 9212797
Inoue S
[Genetic testing for cancer susceptibility: the present situation in Japan].
Gan to kagaku ryoho. Cancer & chemotherapy | 1997-06-01 | PMID 9212800
Miki Y
Portal vein thrombosis in association with factor V Leiden mutation in a patient with hepatocellular carcinoma.
Medical and pediatric oncology | 1997-09-01 | PMID 9212850
Gürgey A, Büyükpamukcu M, Baskut C and 2 more
Rat tibial osteoblasts III: propagation in vitro is accompanied by enhancement of osteoblast phenotype.
Bone | 1997-07-01 | PMID 9213005
Manduca P, Palermo C, Caruso C and 4 more
Genes: CPD
Polymorphisms of the interleukin-6 gene are associated with bone mineral density.
Bone | 1997-07-01 | PMID 9213013
Murray R E, McGuigan F, Grant S F and 2 more
Celiacomesenteric trunk.
Clinical anatomy (New York, N.Y.) | 1997-01-01 | PMID 9213038
Cavdar S, Sehirli U, Pekin B
Unreported anatomical variation of septum pellucidum.
Clinical anatomy (New York, N.Y.) | 1997-01-01 | PMID 9213041
Aldur M M, Celik H H, Sargon M F and 3 more
Scalene muscles and the brachial plexus: anatomical variations and their clinical significance.
Clinical anatomy (New York, N.Y.) | 1997-01-01 | PMID 9213042
Harry W G, Bennett J D, Guha S C
Rare case of high origin of the ulnar artery from the brachial artery.
Clinical anatomy (New York, N.Y.) | 1997-01-01 | PMID 9213043
Aharinejad S, Nourani F, Hollensteiner H
Variation in the triceps brachii muscle: a fourth muscular head.
Clinical anatomy (New York, N.Y.) | 1997-01-01 | PMID 9213044
Fabrizio P A, Clemente F R
Problem in diagnostic imaging.
Clinical anatomy (New York, N.Y.) | 1997-01-01 | PMID 9213047
Dubowitz D J
Apolipoprotein-E genotyping in Alzheimer's disease and frontotemporal dementia.
Dementia and geriatric cognitive disorders | 2000-01-01 | PMID 9213069
Gustafson L, Abrahamson M, Grubb A and 2 more
A proposed test battery and constellations of specific behavioral paradigms to investigate the behavioral phenotypes of transgenic and knockout mice.
Hormones and behavior | 1997-06-01 | PMID 9213134
Crawley J N, Paylor R
Progesterone receptor function from a behavioral perspective.
Hormones and behavior | 1997-06-01 | PMID 9213138
Mani S K, Blaustein J D, O'Malley B W
High incidence of thrombosis in Fabry's disease.
Internal medicine (Tokyo, Japan) | 1997-05-01 | PMID 9213168
Utsumi K, Yamamoto N, Kase R and 6 more
Facioscapulohumeral muscular dystrophy: clinical diversity and genetic abnormalities in Japanese patients.
Internal medicine (Tokyo, Japan) | 1997-05-01 | PMID 9213170
Nakagawa M, Matsuzaki T, Higuchi I and 6 more
Elevated serum lipoprotein (a) levels associated with ulcerative colitis in a young Japanese patient.
Internal medicine (Tokyo, Japan) | 1997-06-01 | PMID 9213183
Kawabata S, Katagiri S, Negoro H and 5 more
Phosphorylation of the G protein alpha-subunit, G alpha 2, of Dictyostelium discoideum requires a functional and activated G alpha 2.
Journal of cellular biochemistry | 1997-08-01 | PMID 9213227
Gundersen R E
Immunological evaluation in oral lichen planus with chronic hepatitis C.
Journal of gastroenterology | 1997-06-01 | PMID 9213245
Nagao Y, Sata M, Abe K and 2 more
Wild-type p53 gene-induced morphological changes and growth suppression in hepatoma cells.
Journal of gastroenterology | 1997-06-01 | PMID 9213246
Terai S, Noma T, Kimura T and 3 more
Genes: HLF, SCX
[Late centronuclear myopathy: autosomal dominant form].
Revista medica de Chile | 1996-02-01 | PMID 9213890
Cartier L, Hernández J E
Role of protein-protein interactions in the function of replication protein A (RPA): RPA modulates the activity of DNA polymerase alpha by multiple mechanisms.
Biochemistry | 1997-07-15 | PMID 9214288
Braun K A, Lao Y, He Z and 2 more
Structure of human isovaleryl-CoA dehydrogenase at 2.6 A resolution: structural basis for substrate specificity,.
Biochemistry | 1997-07-15 | PMID 9214289
Tiffany K A, Roberts D L, Wang M and 4 more
Genes: IVD
Phenotypically selected mutations in myosin's actin binding domain demonstrate intermolecular contacts important for motor function.
Biochemistry | 1997-07-15 | PMID 9214290
Giese K C, Spudich J A
A small conserved domain in the yeast Spa2p is necessary and sufficient for its polarized localization.
The Journal of cell biology | 1997-07-14 | PMID 9214378
Arkowitz R A, Lowe N
Aminopeptidase I is targeted to the vacuole by a nonclassical vesicular mechanism.
The Journal of cell biology | 1997-07-14 | PMID 9214379
Scott S V, Baba M, Ohsumi Y and 1 more
Cofilin promotes rapid actin filament turnover in vivo.
Nature | 1997-07-03 | PMID 9214506
Lappalainen P, Drubin D G
Mutations increasing autoinhibition inactivate tumour suppressors Smad2 and Smad4.
Nature | 1997-07-03 | PMID 9214507
Hata A, Lo R S, Wotton D and 2 more
DNA-replication checkpoint control at the Drosophila midblastula transition.
Nature | 1997-07-03 | PMID 9214509
Sibon O C, Stevenson V A, Theurkauf W E
Apolipoprotein E epsilon4 associated with chronic traumatic brain injury in boxing.
JAMA | 1997-07-09 | PMID 9214529
Jordan B D, Relkin N R, Ravdin L D and 3 more
Genes: APOE
Regulation of catalases in Arabidopsis.
Free radical biology & medicine | 1997-01-01 | PMID 9214587
McClung C R
Grafting assay distinguishes promotion sensitive from promotion resistant JB6 cells.
Carcinogenesis | 1997-06-01 | PMID 9214594
Strickland J, Sun Y, Dong Z and 1 more
Ki-ras mutations are an early event and correlate with tumor stage in transplacentally-induced murine lung tumors.
Carcinogenesis | 1997-06-01 | PMID 9214598
Leone-Kabler S, Wessner L L, McEntee M F and 2 more
Antigenic phenotypes common to rat oval cells, primary hepatocellular carcinomas and developing bile ducts.
Carcinogenesis | 1997-06-01 | PMID 9214599
Hixson D C, Chapman L, McBride A and 2 more
Genes: HBD
Genetic polymorphism of CYP2D6 and lung cancer risk in African-Americans and Caucasians in Los Angeles County.
Carcinogenesis | 1997-06-01 | PMID 9214604
London S J, Daly A K, Leathart J B and 3 more
Serum, plasma and paraffin-embedded tissues as sources of DNA for studying cancer susceptibility genes.
Carcinogenesis | 1997-06-01 | PMID 9214613
Blömeke B, Bennett W P, Harris C C and 1 more
Genes: NAT2, GSTM1
The thrombin E192Q-BPTI complex reveals gross structural rearrangements: implications for the interaction with antithrombin and thrombomodulin.
The EMBO journal | 1997-06-02 | PMID 9214615
van de Locht A, Bode W, Huber R and 4 more
The extent of affinity maturation differs between the memory and antibody-forming cell compartments in the primary immune response.
The EMBO journal | 1997-06-02 | PMID 9214617
Smith K G, Light A, Nossal G J and 1 more
A novel SNARE complex implicated in vesicle fusion with the endoplasmic reticulum.
The EMBO journal | 1997-06-02 | PMID 9214619
Lewis M J, Rayner J C, Pelham H R
Kinesin is essential for cell morphogenesis and polarized secretion in Neurospora crassa.
The EMBO journal | 1997-06-02 | PMID 9214620
Seiler S, Nargang F E, Steinberg G and 1 more
Dimer model for the microfibrillar protein fibulin-2 and identification of the connecting disulfide bridge.
The EMBO journal | 1997-06-02 | PMID 9214621
Sasaki T, Mann K, Wiedemann H and 5 more
Genes: EGF
Subunit interactions in ABC transporters: a conserved sequence in hydrophobic membrane proteins of periplasmic permeases defines an important site of interaction with the ATPase subunits.
The EMBO journal | 1997-06-02 | PMID 9214624
Mourez M, Hofnung M, Dassa E
IkappaB alpha is a target for the mitogen-activated 90 kDa ribosomal S6 kinase.
The EMBO journal | 1997-06-02 | PMID 9214631
Schouten G J, Vertegaal A C, Whiteside S T and 5 more
Variable telomeric repeat synthesis in Paramecium tetraurelia is consistent with misincorporation by telomerase.
The EMBO journal | 1997-06-02 | PMID 9214639
McCormick-Graham M, Haynes W J, Romero D P
Mex67p, a novel factor for nuclear mRNA export, binds to both poly(A)+ RNA and nuclear pores.
The EMBO journal | 1997-06-02 | PMID 9214641
Segref A, Sharma K, Doye V and 4 more
Extraplastidic site-specific factors mediate RNA editing in chloroplasts.
The EMBO journal | 1997-06-02 | PMID 9214643
Bock R, Koop H U
Rules for RNA recognition of GNRA tetraloops deduced by in vitro selection: comparison with in vivo evolution.
The EMBO journal | 1997-06-02 | PMID 9214644
Costa M, Michel F
Deletions at stalled replication forks occur by two different pathways.
The EMBO journal | 1997-06-02 | PMID 9214648
Bierne H, Ehrlich S D, Michel B
Transfer RNA recognition by the Escherichia coli delta2-isopentenyl-pyrophosphate:tRNA delta2-isopentenyl transferase: dependence on the anticodon arm structure.
RNA (New York, N.Y.) | 1997-07-01 | PMID 9214656
Motorin Y, Bec G, Tewari R and 1 more
In vitro optimization of truncated stem-loop II variants of the hammerhead ribozyme for cleavage in low concentrations of magnesium under non-turnover conditions.
RNA (New York, N.Y.) | 1997-07-01 | PMID 9214657
Zillmann M, Limauro S E, Goodchild J
Mutation of PTB binding sites causes misregulation of alternative 3' splice site selection in vivo.
RNA (New York, N.Y.) | 1997-07-01 | PMID 9214659
Pérez I, Lin C H, McAfee J G and 1 more
Relationship between lifetime ovulatory cycles and overexpression of mutant p53 in epithelial ovarian cancer.
Journal of the National Cancer Institute | 1997-07-02 | PMID 9214672
Schildkraut J M, Bastos E, Berchuck A
Prostate cancer susceptibility locus on chromosome 1q: a confirmatory study.
Journal of the National Cancer Institute | 1997-07-02 | PMID 9214675
Cooney K A, McCarthy J D, Lange E and 6 more
Genes: NPL
Heterologous protein production in Acremonium chrysogenum: expression of bacterial cephalosporin C acylase and human thrombomodulin genes.
Bioscience, biotechnology, and biochemistry | 1997-06-01 | PMID 9214752
Honda G, Matsuda A, Zushi M and 2 more
Genes: EGF
Genetic analysis of hydatidiform moles in paraffin wax embedded tissue using rapid, sequence specific PCR-based HLA class II typing.
Journal of clinical pathology | 1997-04-01 | PMID 9215143
Bateman A C, Hemmatpour S K, Theaker J M and 1 more
Evidence for a heterozygote advantage in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
The Journal of clinical endocrinology and metabolism | 1997-07-01 | PMID 9215278
Witchel S F, Lee P A, Suda-Hartman M and 2 more
A novel splicing junction mutation in the gene for the steroidogenic acute regulatory protein causes congenital lipoid adrenal hyperplasia.
The Journal of clinical endocrinology and metabolism | 1997-07-01 | PMID 9215316
Okuyama E, Nishi N, Onishi S and 5 more
Molecular basis of nonclassical steroid 21-hydroxylase deficiency detected by neonatal mass screening in Japan.
The Journal of clinical endocrinology and metabolism | 1997-07-01 | PMID 9215318
Tajima T, Fujieda K, Nakae J and 6 more
Multiplex polymerase chain reaction assay for genotyping Clostridium perfringens.
American journal of veterinary research | 1997-07-01 | PMID 9215442
Meer R R, Songer J G
Intrastrain variation of lipopolysaccharide of Pasteurella multocida in turkeys.
American journal of veterinary research | 1997-07-01 | PMID 9215453
Coy S L, Lee M D, Sander J
Activated protein C resistance as a "new" cause of deep venous thrombosis in aviators.
Aviation, space, and environmental medicine | 1997-07-01 | PMID 9215466
Emonson D L
Weight changes and risk of ischaemic heart disease for middle aged and elderly men. An 8-year follow-up in the Copenhagen Male study.
Journal of cardiovascular risk | 1997-02-01 | PMID 9215517
Suadicani P, Hein H O, Gyntelberg F
A variation in the apolipoprotein C-III gene is associated with an increased number of circulating VLDL and IDL particles in familial combined hyperlipidemia.
Journal of lipid research | 1997-06-01 | PMID 9215535
Ribalta J, La Ville A E, Vallvé J C and 3 more
Genes: LPL
Quantitative and compositional changes in high density lipoprotein subclasses in patients with various genotypes of cholesteryl ester transfer protein deficiency.
Journal of lipid research | 1997-06-01 | PMID 9215548
Chiba H, Akita H, Tsuchihashi K and 7 more
Genes: CETP
The conserved HR domain of the Drosophila suppressor 2 of zeste [Su(z)2] and murine bmi-1 proteins constitutes a locus-specific chromosome binding domain.
Chromosoma | 1997-07-01 | PMID 9215556
Sharp E J, Abramova N A, Park W J and 1 more
Genotypic differentiation of Gardnerella vaginalis by amplified ribosomal DNA restriction analysis (ARDRA).
FEMS immunology and medical microbiology | 1997-05-01 | PMID 9215588
Ingianni A, Petruzzelli S, Morandotti G and 1 more
Deoxycytidine kinase mRNA expression in childhood acute lymphoblastic leukemia.
Anti-cancer drugs | 1997-06-01 | PMID 9215616
Stammler G, Zintl F, Sauerbrey A and 1 more
14-3-3 proteins are essential for RAS/MAPK cascade signaling during pseudohyphal development in S. cerevisiae.
Cell | 1997-06-27 | PMID 9215628
Roberts R L, Mösch H U, Fink G R
Genes: CDC42
Protein-protein communication: structural model of the repression complex formed by CytR and the global regulator CRP.
Cell | 1997-06-27 | PMID 9215632
Kallipolitis B H, Nørregaard-Madsen M, Valentin-Hansen P
Genes: CRP
Activation of the ethylene gas response pathway in Arabidopsis by the nuclear protein ETHYLENE-INSENSITIVE3 and related proteins.
Cell | 1997-06-27 | PMID 9215635
Chao Q, Rothenberg M, Solano R and 3 more
Spinal muscular atrophy gene wobbler of the mouse: evidence from chimeric spinal cord and testis for cell-autonomous function.
Developmental dynamics : an official publication of the American Association of Anatomists | 1997-07-01 | PMID 9215643
Augustin M, Heimann P, Rathke S and 1 more
SIV/HIV-1 hybrid virus expressing the reverse transcriptase gene of HIV-1 remains sensitive to HIV-1-specific reverse transcriptase inhibitors after passage in rhesus macaques.
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association | 1997-05-01 | PMID 9215647
Balzarini J, De Clercq E, Uberla K
Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic.
Human molecular genetics | 1997-07-01 | PMID 9215664
Moutou C, Vincent M C, Biancalana V and 1 more
Evidence by allelic association-dependent methods for a type 1 diabetes polygene (IDDM6) on chromosome 18q21.
Human molecular genetics | 1997-07-01 | PMID 9215667
Merriman T, Twells R, Merriman M and 20 more
Evidence for a type 1 diabetes susceptibility locus (IDDM10) on human chromosome 10p11-q11.
Human molecular genetics | 1997-07-01 | PMID 9215668
Reed P, Cucca F, Jenkins S and 13 more
The molecular basis of the Kidd blood group polymorphism and its lack of association with type 1 diabetes susceptibility.
Human molecular genetics | 1997-07-01 | PMID 9215669
Olivès B, Merriman M, Bailly P and 5 more
Elastin point mutations cause an obstructive vascular disease, supravalvular aortic stenosis.
Human molecular genetics | 1997-07-01 | PMID 9215670
Li D Y, Toland A E, Boak B B and 4 more
Genes: ELN
Molecular basis of the brindled mouse mutant (Mo(br)): a murine model of Menkes disease.
Human molecular genetics | 1997-07-01 | PMID 9215672
Grimes A, Hearn C J, Lockhart P and 2 more
Genetic predisposition to phaeochromocytoma: analysis of candidate genes GDNF, RET and VHL.
Human molecular genetics | 1997-07-01 | PMID 9215674
Woodward E R, Eng C, McMahon R and 4 more
Genes: VHL, GDNF, RET
Single sperm analysis of the CAG repeats in the gene for Machado-Joseph disease (MJD1): evidence for non-Mendelian transmission of the MJD1 gene and for the effect of the intragenic CGG/GGG polymorphism on the intergenerational instability.
Human molecular genetics | 1997-07-01 | PMID 9215676
Takiyama Y, Sakoe K, Soutome M and 8 more
Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndrome.
Human molecular genetics | 1997-07-01 | PMID 9215678
Krebs I, Weis I, Hudler M and 8 more
Mutations in the Chediak-Higashi syndrome gene (CHS1) indicate requirement for the complete 3801 amino acid CHS protein.
Human molecular genetics | 1997-07-01 | PMID 9215679
Karim M A, Nagle D L, Kandil H H and 3 more
Identification of mutations in two major mRNA isoforms of the Chediak-Higashi syndrome gene in human and mouse.
Human molecular genetics | 1997-07-01 | PMID 9215680
Barbosa M D, Barrat F J, Tchernev V T and 11 more
Autosomal glycogenosis of liver and muscle due to phosphorylase kinase deficiency is caused by mutations in the phosphorylase kinase beta subunit (PHKB).
Human molecular genetics | 1997-07-01 | PMID 9215682
Burwinkel B, Maichele A J, Aagenaes O and 5 more
Modulation of disease severity of dystrophic epidermolysis bullosa by a splice site mutation in combination with a missense mutation in the COL7A1 gene.
Human molecular genetics | 1997-07-01 | PMID 9215684
Winberg J O, Hammami-Hauasli N, Nilssen O and 7 more
A novel human serine-threonine phosphatase related to the Drosophila retinal degeneration C (rdgC) gene is selectively expressed in sensory neurons of neural crest origin.
Human molecular genetics | 1997-07-01 | PMID 9215685
Montini E, Rugarli E I, Van de Vosse E and 7 more
Missense mutations in the human glutathione synthetase gene result in severe metabolic acidosis, 5-oxoprolinuria, hemolytic anemia and neurological dysfunction.
Human molecular genetics | 1997-07-01 | PMID 9215686
Dahl N, Pigg M, Ristoff E and 5 more
Incomplete rescue of cystic fibrosis transmembrane conductance regulator deficient mice by the human CFTR cDNA.
Human molecular genetics | 1997-07-01 | PMID 9215687
Rozmahel R, Gyömörey K, Plyte S and 5 more
Genes: CFTR
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.
Human molecular genetics | 1997-07-01 | PMID 9215690
Lemmens I, Van de Ven W J, Kas K and 22 more
Genes: MEN1, SCG2, PYGM
Increased intermale aggression and neuroendocrine response in mice deficient for the neural cell adhesion molecule (NCAM).
The European journal of neuroscience | 1997-06-01 | PMID 9215693
Stork O, Welzl H, Cremer H and 1 more
Synchronized overproduction of AMPA, kainate, and NMDA glutamate receptors during human spinal cord development.
The Journal of comparative neurology | 1997-07-28 | PMID 9215718
Kalb R G, Fox A J
Glial cells assemble hyaluronan-based pericellular matrices in vitro.
Glia | 1997-07-01 | PMID 9215728
Maleski M, Hockfield S
Genes: GFAP
Molecular genetics of glucose-6-phosphate dehydrogenase deficiency in Mexico.
Blood cells, molecules & diseases | 1997-01-01 | PMID 9215753
Medina M D, Vaca G, Lopez-Guido B and 2 more
HLA-H mutations in the Ashkenazi Jewish population.
Blood cells, molecules & diseases | 1997-01-01 | PMID 9215754
Beutler E, Gelbart T
T-cell receptor beta chain variability in bone marrow and peripheral blood in severe acquired aplastic anemia.
Blood cells, molecules & diseases | 1997-01-01 | PMID 9215756
Manz C Y, Dietrich P Y, Schnuriger V and 2 more
Genetic and clinical description of hemochromatosis probands and heterozygotes: evidence that multiple genes linked to the major histocompatibility complex are responsible for hemochromatosis.
Blood cells, molecules & diseases | 1997-01-01 | PMID 9215758
Barton J C, Shih W W, Sawada-Hirai R and 4 more