Mitochondrial DNA mutations and age.
Annals of the New York Academy of Sciences | 1998-11-20 | PMID 9928426
Ozawa T
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.
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Publications
Page 1097 of 10600
Tissue-specific distribution of multiple mitochondrial DNA rearrangements during human aging.
Annals of the New York Academy of Sciences | 1998-11-20 | PMID 9928428
Kovalenko S A, Kopsidas G, Kelso J and 2 more
The role of the FHIT/FRA3B locus in cancer.
Annual review of genetics | 1998-01-01 | PMID 9928473
Huebner K, Garrison P N, Barnes L D and 1 more
Genes: FHIT
The genetics of breast cancer susceptibility.
Annual review of genetics | 1998-01-01 | PMID 9928476
Rahman N, Stratton M R
Genes: BRCA1, BRCA2
The ethylene gas signal transduction pathway: a molecular perspective.
Annual review of genetics | 1998-01-01 | PMID 9928480
Johnson P R, Ecker J R
Molecular mechanisms of bacteriocin evolution.
Annual review of genetics | 1998-01-01 | PMID 9928481
Riley M A
Kinetochores and the checkpoint mechanism that monitors for defects in the chromosome segregation machinery.
Annual review of genetics | 1998-01-01 | PMID 9928483
Skibbens R V, Hieter P
Genes: APC
The diverse and dynamic structure of bacterial genomes.
Annual review of genetics | 1998-01-01 | PMID 9928484
Casjens S
Recombination and recombination-dependent DNA replication in bacteriophage T4.
Annual review of genetics | 1998-01-01 | PMID 9928485
Mosig G
Natural selection at major histocompatibility complex loci of vertebrates.
Annual review of genetics | 1998-01-01 | PMID 9928486
Hughes A L, Yeager M
Alzheimer's disease: genetic studies and transgenic models.
Annual review of genetics | 1998-01-01 | PMID 9928488
Price D L, Tanzi R E, Borchelt D R and 1 more
Early patterning of the C. elegans embryo.
Annual review of genetics | 1998-01-01 | PMID 9928490
Rose L S, Kemphues K J
Update on breast cancer susceptibility genes.
Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer | 1998-01-01 | PMID 9928546
Weber B L
Genes: BRCA1, BRCA2
Distribution of the CCR5 gene 32-base pair deletion in Israeli ethnic groups.
Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association | 1999-01-01 | PMID 9928734
Kantor R, Gershoni J M
Genes: CCR5
Immunohistochemical study on phenotypical changes of hepatocytes in liver disease with reference to extracellular matrix composition.
Liver | 1999-02-01 | PMID 9928763
Matsumoto S, Yamamoto K, Nagano T and 4 more
Markedly different course of Friedreich's ataxia in sib pairs with similar GAA repeat expansions in the frataxin gene.
Acta neuropathologica | 1999-02-01 | PMID 9928824
Klopstock T, Chahrokh-Zadeh S, Holinski-Feder E and 4 more
Genes: GAA
Binocular interactions and spatial disparity sensitivity in the superior colliculus of the Siamese cat.
Experimental brain research | 1999-01-01 | PMID 9928841
Bacon B A, Lepore F, Guillemot J P
Molecular characterization of methicillin-resistant Staphylococcus aureus (MRSA) in a university hospital in Italy.
European journal of epidemiology | 1998-12-01 | PMID 9928877
Villari P, Farullo C, Torre I and 1 more
Analysis of a polymorphism in the tuberous sclerosis (TSC2) gene does not predispose to schizophrenia.
European archives of psychiatry and clinical neuroscience | 1998-01-01 | PMID 9928911
Przkora R, Falkai P, von Deimling A and 5 more
Genes: TSC2
Dynamic organization of the beta-heterochromatin in the Drosophila melanogaster polytene X chromosome.
Molecular & general genetics : MGG | 1999-01-01 | PMID 9928929
Koryakov D E, Alekseyenko A A, Zhimulev I F
The S/M checkpoint at 37 degrees C and the recovery of viability of the mutant poldeltats3 require the crb2+/rhp9+ gene in fission yeast.
Molecular & general genetics : MGG | 1999-01-01 | PMID 9928931
Grenon M, Tillit J, Piard K and 2 more
Genes: PCNA
The Saccharomyces cerevisiae protein YJR043C (Pol32) interacts with the catalytic subunit of DNA polymerase alpha and is required for cell cycle progression in G2/M.
Molecular & general genetics : MGG | 1999-01-01 | PMID 9928933
Huang M E, Le Douarin B, Henry C and 1 more
The protease activity of a calpain-like cysteine protease in Saccharomyces cerevisiae is required for alkaline adaptation and sporulation.
Molecular & general genetics : MGG | 1999-01-01 | PMID 9928935
Futai E, Maeda T, Sorimachi H and 3 more
Gene stability in transgenic aspen (Populus). I. Flanking DNA sequences and T-DNA structure.
Molecular & general genetics : MGG | 1999-01-01 | PMID 9928937
Fladung M
C-terminal domains of human translation termination factors eRF1 and eRF3 mediate their in vivo interaction.
FEBS letters | 1999-01-22 | PMID 9928949
Merkulova T I, Frolova L Y, Lazar M and 2 more
The aminoacceptor stem of the yeast tRNA(Lys) contains determinants of mitochondrial import selectivity.
FEBS letters | 1999-01-15 | PMID 9929000
Kazakova H A, Entelis N S, Martin R P and 1 more
Colocalization of phospholipase D1 and GTP-binding-defective mutant of ADP-ribosylation factor 6 to endosomes and lysosomes.
FEBS letters | 1999-01-15 | PMID 9929005
Toda K, Nogami M, Murakami K and 2 more
Genes: PLD1, ARF6, PLD2
Induction of cytokines in a human colon epithelial cell line by Shiga toxin 1 (Stx1) and Stx2 but not by non-toxic mutant Stx1 which lacks N-glycosidase activity.
FEBS letters | 1999-01-15 | PMID 9929007
Yamasaki C, Natori Y, Zeng X T and 4 more
Conformational stabilities of the rat alpha- and beta-parvalbumins.
FEBS letters | 1999-01-15 | PMID 9929009
Henzl M T, Graham J S
p53 inactivating mutations in Chinese nasopharyngeal carcinomas.
Cancer letters | 1998-11-13 | PMID 9929165
Lung M L, Hu Y, Cheng Y and 4 more
Creation and maintenance of Helix, a Web based database of medical genetics laboratories, to serve the needs of the genetics community.
Proceedings. AMIA Symposium | 1998-01-01 | PMID 9929238
Tarczy-Hornoch P, Covington M L, Edwards J and 3 more
Accelerated evolution and molecular surface of venom phospholipase A2 enzymes.
Journal of molecular evolution | 1999-02-01 | PMID 9929380
Kini R M, Chan Y M
Phylogeny of organisms investigated by the base-pair changes in the stem regions of small and large ribosomal subunit RNAs.
Journal of molecular evolution | 1999-02-01 | PMID 9929391
Otsuka J, Terai G, Nakano T
Ca2+ sparks in embryonic mouse skeletal muscle selectively deficient in dihydropyridine receptor alpha1S or beta1a subunits.
Biophysical journal | 1999-02-01 | PMID 9929471
Conklin M W, Powers P, Gregg R G and 1 more
Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotonia.
Biophysical journal | 1999-02-01 | PMID 9929487
Takahashi M P, Cannon S C
Central olfactory structures in Pax-6 mutant mice.
Annals of the New York Academy of Sciences | 1998-11-30 | PMID 9929589
López-Mascaraque L, García C, Valverde F and 1 more
Apolipoprotein E and Alzheimer's disease. The tip of the susceptibility iceberg.
Annals of the New York Academy of Sciences | 1998-11-30 | PMID 9929679
Roses A D
Genes: APOE
Apolipoprotein E status is associated with odor identification deficits in nondemented older persons.
Annals of the New York Academy of Sciences | 1998-11-30 | PMID 9929680
Murphy C, Bacon A W, Bondi M W and 1 more
New knowledge of genetic pathogenesis of hemochromatosis and Wilson's disease.
Advances in internal medicine | 1999-01-01 | PMID 9929706
Bacon B R, Schilsky M L
Ethics and genetic testing.
Advances in internal medicine | 1999-01-01 | PMID 9929717
Grady C
[Expression of mutant horse cytochrome c genes in Escherichia coli].
Bioorganicheskaia khimiia | 1998-10-01 | PMID 9929736
Dolgikh D A, Latypov R F, Abdullaev Z Kh and 3 more
[Interaction between three types of variation and fluctuating asymmetry in the population of malaria mosquito Anopheles messeae Fall].
Genetika | 1998-10-01 | PMID 9929828
Burlak V A
[Allozyme variation of lactate dehydrogenase (EC1.1.1.27) in a series of vertebrate animals].
Genetika | 1998-10-01 | PMID 9929829
Mezhzherin S V
[Selective structure of the gene pool. III. Technology of determination from F(ST)-statistics using numerical resampling].
Genetika | 1998-10-01 | PMID 9929832
Balanovskaia E V, Nurbaev S D
Genes: FST
[The behavior of mice from 6 genotypes in 2 tests for anxiety].
Zhurnal vysshei nervnoi deiatelnosti imeni I P Pavlova | 2000-01-01 | PMID 9929918
Avgustinovich D F, Alekseenko O V, Popova N K
Repeat-directed isolation of a novel gene preferentially expressed from the maternal allele in human placenta.
Journal of human genetics | 1999-01-01 | PMID 9929968
Miura K, Miyoshi O, Yun K and 8 more
Anxiety traits associated with a polymorphism in the serotonin transporter gene regulatory region in the Japanese.
Journal of human genetics | 1999-01-01 | PMID 9929970
Murakami F, Shimomura T, Kotani K and 3 more
Allelic variations of the D2 dopamine receptor gene in children with idiopathic short stature.
Journal of human genetics | 1999-01-01 | PMID 9929973
Miyake H, Nagashima K, Onigata K and 3 more
Genes: DRD2
Four novel mutations of the Fanconi anemia group A gene (FAA) in Japanese patients.
Journal of human genetics | 1999-01-01 | PMID 9929978
Nakamura A, Matsuura S, Tauchi H and 9 more
Autosomal dominant onychodystrophy and congenital sensorineural deafness.
Journal of human genetics | 1999-01-01 | PMID 9929981
Kondoh T, Tsuru A, Matsumoto T and 2 more
A single-nucleotide polymorphism in the human bone morphogenetic protein-4 (BMP 4) gene.
Journal of human genetics | 1999-01-01 | PMID 9929985
Mangino M, Torrente I, De Luca A and 3 more
Genes: BMP4
Hepatitis C virus genotypes and quantification of serum hepatitis C RNA in liver transplant recipients. Relationship with histologic outcome of recurrent hepatitis C.
American journal of clinical pathology | 1999-02-01 | PMID 9930149
Costes V, Durand L, Pageaux G P and 6 more
Immunolocalization of beta ig-h3 protein in 5q31-linked corneal dystrophies and normal corneas.
Archives of ophthalmology (Chicago, Ill. : 1960) | 1999-01-01 | PMID 9930162
Streeten B W, Qi Y, Klintworth G K and 3 more
Hepatitis B virus genomic sequence in the circulation of hepatocellular carcinoma patients: comparative analysis of 40 full-length isolates.
Archives of virology | 1998-01-01 | PMID 9930189
Takahashi K, Akahane Y, Hino K and 2 more
Determinants of pantropism of the F1-R mutant of Sendai virus: specific mutations involved are in the F and M genes.
Archives of virology | 1998-01-01 | PMID 9930191
Okada H, Seto J T, McQueen N L and 3 more
Localizations of NS3 and E proteins in mouse brain infected with mutant strain of Japanese encephalitis virus.
Archives of virology | 1998-01-01 | PMID 9930192
Wang J J, Liao C L, Yang C I and 3 more
The Swedish snus and the Sudanese toombak: are they different?
Oral oncology | 1998-11-01 | PMID 9930371
Idris A M, Ibrahim S O, Vasstrand E N and 6 more
Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosis.
Journal of neurochemistry | 1999-02-01 | PMID 9930742
Bruening W, Roy J, Giasson B and 3 more
Presenilin mutations associated with Alzheimer disease cause defective intracellular trafficking of beta-catenin, a component of the presenilin protein complex.
Nature medicine | 1999-02-01 | PMID 9930863
Nishimura M, Yu G, Levesque G and 22 more
Carbonic anhydrase II and H+ -ATPase in osteoclasts of four osteopetrotic mutations in the rat.
Histochemistry and cell biology | 1999-01-01 | PMID 9930884
Sundquist K T, Väänänen H K, Marks S C
A high incidence of apolipoprotein E epsilon4 allele in middle-aged non-demented subjects with cerebral amyloid beta protein deposits.
Acta neuropathologica | 1999-01-01 | PMID 9930898
Arai T, Ikeda K, Akiyama H and 5 more
Walker mutations reveal loose relationship between catalytic and channel-gating activities of purified CFTR (cystic fibrosis transmembrane conductance regulator).
Biochemistry | 1999-02-02 | PMID 9931011
Ramjeesingh M, Li C, Garami E and 4 more
Genes: CFTR
Site-directed mutagenesis of basic arginine residues 305 and 342 in the CP 43 protein of photosystem II affects oxygen-evolving activity in Synechocystis 6803.
Biochemistry | 1999-02-02 | PMID 9931025
Knoepfle N, Bricker T M, Putnam-Evans C
Efficiency of two different nine-loci short tandem repeat systems for DNA typing purposes.
Clinical chemistry | 1999-02-01 | PMID 9931038
Sacchetti L, Calcagno G, Coto I and 3 more
Genes: FGA
Role of the alpha2B-adrenergic receptor in the development of salt-induced hypertension.
Hypertension (Dallas, Tex. : 1979) | 1999-01-01 | PMID 9931075
Makaritsis K P, Handy D E, Johns C and 3 more
Effect of chromosome 19 transfer on blood pressure in the spontaneously hypertensive rat.
Hypertension (Dallas, Tex. : 1979) | 1999-01-01 | PMID 9931113
St Lezin E, Zhang L, Yang Y and 11 more
Role of chromosome X in the Sabra rat model of salt-sensitive hypertension.
Hypertension (Dallas, Tex. : 1979) | 1999-01-01 | PMID 9931114
Yagil C, Sapojnikov M, Kreutz R and 3 more
Genes encoding atrial and brain natriuretic peptides as candidates for sensitivity to brain ischemia in stroke-prone hypertensive rats.
Hypertension (Dallas, Tex. : 1979) | 1999-01-01 | PMID 9931119
Brosnan M J, Clark J S, Jeffs B and 8 more
Renal mechanoreceptor dysfunction: an intermediate phenotype in spontaneously hypertensive rats.
Hypertension (Dallas, Tex. : 1979) | 1999-01-01 | PMID 9931150
DiBona G F, Jones S Y, Kopp U C
Bed rest increases the amount of mismatched fibers in human skeletal muscle.
Journal of applied physiology (Bethesda, Md. : 1985) | 1999-02-01 | PMID 9931176
Andersen J L, Gruschy-Knudsen T, Sandri C and 2 more
Effect of mutations in the A site of 16 S rRNA on aminoglycoside antibiotic-ribosome interaction.
Journal of molecular biology | 1999-02-12 | PMID 9931247
Recht M I, Douthwaite S, Dahlquist K D and 1 more
Using loop length variants to dissect the folding pathway of a four-helix-bundle protein.
Journal of molecular biology | 1999-02-12 | PMID 9931264
Nagi A D, Anderson K S, Regan L
Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis.
Human molecular genetics | 1999-02-01 | PMID 9931323
Al-Chalabi A, Andersen P M, Nilsson P and 6 more
Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism.
Human molecular genetics | 1999-02-01 | PMID 9931325
Leeflang E P, Tavaré S, Marjoram P and 8 more
PTEN is inversely correlated with the cell survival factor Akt/PKB and is inactivated via multiple mechanismsin haematological malignancies.
Human molecular genetics | 1999-02-01 | PMID 9931326
Dahia P L, Aguiar R C, Alberta J and 8 more
Genes: PTEN
A full genome scan for late onset Alzheimer's disease.
Human molecular genetics | 1999-02-01 | PMID 9931331
Kehoe P, Wavrant-De Vrieze F, Crook R and 20 more
Genes: APOE
Increased expression of the NF2 tumor suppressor gene product, merlin, impairs cell motility, adhesionand spreading.
Human molecular genetics | 1999-02-01 | PMID 9931334
Gutmann D H, Sherman L, Seftor L and 3 more
AIRE encodes a nuclear protein co-localizing with cytoskeletal filaments: altered sub-cellular distribution of mutants lacking the PHD zinc fingers.
Human molecular genetics | 1999-02-01 | PMID 9931335
Rinderle C, Christensen H M, Schweiger S and 2 more
Genes: AIRE
Isolation and characterization of human patched 2 (PTCH2), a putative tumour suppressor gene inbasal cell carcinoma and medulloblastoma on chromosome 1p32.
Human molecular genetics | 1999-02-01 | PMID 9931336
Smyth I, Narang M A, Evans T and 6 more
Genes: PTCH2
Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function.
Human molecular genetics | 1999-02-01 | PMID 9931337
Swaroop A, Wang Q L, Wu W and 6 more
Genes: CRX, NRL
Association of ulcerative colitis with rare VNTR alleles of the human intestinal mucin gene, MUC3.
Human molecular genetics | 1999-02-01 | PMID 9931338
Kyo K, Parkes M, Takei Y and 10 more
Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions.
Human molecular genetics | 1999-02-01 | PMID 9931339
Wu Y Q, Heilstedt H A, Bedell J A and 5 more
The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness.
Human molecular genetics | 1999-02-01 | PMID 9931340
Feng L, Seymour A B, Jiang S and 9 more
Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-I gene in the population: a population-based survey.
Human molecular genetics | 1999-02-01 | PMID 9931341
Yamakawa-Kobayashi K, Yanagi H, Fukayama H and 6 more
A novel protein tyrosine phosphatase gene is mutated in progressive myoclonus epilepsy of the Lafora type (EPM2).
Human molecular genetics | 1999-02-01 | PMID 9931343
Serratosa J M, Gómez-Garre P, Gallardo M E and 11 more
Thiopurine methyltransferase alleles in British and Ghanaian populations.
Human molecular genetics | 1999-02-01 | PMID 9931345
Ameyaw M M, Collie-Duguid E S, Powrie R H and 2 more
Genes: TPMT
Polymorphism of the thiopurine S-methyltransferase gene in African-Americans.
Human molecular genetics | 1999-02-01 | PMID 9931346
Hon Y Y, Fessing M Y, Pui C H and 3 more
Genes: TPMT
Evidence of decreased adhesion between the neural retina and retinal pigmented epithelium of the Mitfvit (vitiligo) mutant mouse.
Cell and tissue research | 1999-01-01 | PMID 9931354
Bora N, Defoe D, Smith S B
Genes: RPE
Protein tyrosine phosphatases: counting the trees in the forest.
Gene | 1998-12-28 | PMID 9931406
Hooft van Huijsduijnen R
Triplet repeat variability in the signal peptide sequence of the Xmrk receptor tyrosine kinase gene in Xiphophorus fish.
Gene | 1998-12-11 | PMID 9931413
Schartl M, Wilde B, Hornung U
Dissociable and nondissociable forms of platelet-activating factor acetylhydrolase in human plasma LDL: implications for LDL oxidative susceptibility.
Biochimica et biophysica acta | 1999-01-29 | PMID 9931415
McCall M R, La Belle M, Forte T M and 3 more
Expression cloning in Fe2+ transport defective yeast of a novel maize MYC transcription factor.
Gene | 1998-12-28 | PMID 9931428
Loulergue C, Lebrun M, Briat J F
Genes: MYC, MYB
Identification and molecular characterization of a gene homologous to epr (endopeptidase resistance gene) in Staphylococcus aureus.
Gene | 1998-12-11 | PMID 9931440
Sugai M, Fujiwara T, Komatsuzawa H and 1 more
Isolation of hMRE11B: failure to complement yeast mre11 defects due to species-specific protein interactions.
Gene | 1998-12-28 | PMID 9931460
Chamankhah M, Wei Y F, Xiao W
Genes: MRE11
Both neuronal NO synthase and nitric oxide are required for PC12 cell differentiation: a cGMP independent pathway.
Brain research. Molecular brain research | 1999-02-05 | PMID 9931481
Phung Y T, Bekker J M, Hallmark O G and 1 more
Genes: NGF
Genetic mechanisms for duplication and multiduplication of the human CYP2D6 gene and methods for detection of duplicated CYP2D6 genes.
Gene | 1999-01-21 | PMID 9931507
Lundqvist E, Johansson I, Ingelman-Sundberg M
House-fly cytochrome P450 CYP6D1: 5' flanking sequences and comparison of alleles.
Gene | 1999-01-21 | PMID 9931509
Scott J G, Liu N, Wen Z and 3 more
Medical complications in long-term survivors with X-linked myotubular myopathy.
The Journal of pediatrics | 1999-02-01 | PMID 9931531
Herman G E, Finegold M, Zhao W and 2 more
Genes: MTM1
Treatment of ataxia in isolated vitamin E deficiency caused by alpha-tocopherol transfer protein deficiency.
The Journal of pediatrics | 1999-02-01 | PMID 9931538
Schuelke M, Mayatepek E, Inter M and 5 more
[Basic molecular biology of colon and rectal carcinoma--when differential diagnosis?].
Langenbecks Archiv fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft fur Chirurgie. Kongress | 1998-01-01 | PMID 9931632
Schackert H K, Kruppa C, Hahn M
Genes: FAP