The high copper tolerance of Candida albicans is mediated by a P-type ATPase.
Proceedings of the National Academy of Sciences of the United States of America | 2000-03-28 | PMID 10737803
Weissman Z, Berdicevsky I, Cavari B Z and 1 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.
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Publications
Page 1303 of 10600
HIV heterosexual transmission: a hypothesis about an additional potential determinant.
International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases | 2000-01-01 | PMID 10737850
Louria D B, Skurnick J H, Palumbo P and 4 more
DNA methylation and cancer.
Journal of cellular physiology | 2000-05-01 | PMID 10737890
Momparler R L, Bovenzi V
Suppression of malignant growth potentials of v-Src-transformed human gallbladder epithelial cells by adenovirus-mediated dominant negative H-Ras.
Journal of cellular physiology | 2000-05-01 | PMID 10737897
Tokumitsu Y, Nakano S, Ueno H and 1 more
Molecular modeling of substrate binding in wild-type and mutant Corynebacteria 2,5-diketo-D-gluconate reductases.
Proteins | 2000-04-01 | PMID 10737928
Khurana S, Sanli G, Powers D B and 2 more
Aromatase inhibitor and 17alpha-methyltestosterone cause sex-reversal from genetical females to phenotypic males and suppression of P450 aromatase gene expression in Japanese flounder (Paralichthys olivaceus).
Molecular reproduction and development | 2000-05-01 | PMID 10737961
Kitano T, Takamune K, Nagahama Y and 1 more
VMD2 mutations in vitelliform macular dystrophy (Best disease) and other maculopathies.
Human mutation | 2000-01-01 | PMID 10737974
White K, Marquardt A, Weber B H
Hypophosphatasia: the mutations in the tissue-nonspecific alkaline phosphatase gene.
Human mutation | 2000-01-01 | PMID 10737975
Mornet E
Genes: ALPL
Mutation in the PAX6 gene in twenty patients with aniridia.
Human mutation | 2000-01-01 | PMID 10737978
Chao L Y, Huff V, Strong L C and 1 more
Genes: PAX6
Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously described.
Human mutation | 2000-01-01 | PMID 10737980
Lachtermacher M B, Seuánez H N, Moser A B and 2 more
beta-galactosidase gene mutations affecting the lysosomal enzyme and the elastin-binding protein in GM1-gangliosidosis patients with cardiac involvement.
Human mutation | 2000-01-01 | PMID 10737981
Morrone A, Bardelli T, Donati M A and 8 more
Genes: GLB1, EBP
SLC7A7 genomic structure and novel variants in three Japanese lysinuric protein intolerance families.
Human mutation | 2000-01-01 | PMID 10737982
Noguchi A, Shoji Y, Koizumi A and 10 more
Genes: LAT
Identification of a novel mutation (867delA) in the glucose-6-phosphatase gene in two siblings with glycogen storage disease type Ia with different phenotypes.
Human mutation | 2000-04-01 | PMID 10737986
Rake J P, ten Berge A M, Visser G and 5 more
Identification of fifteen novel PHEX gene mutations in Finnish patients with hypophosphatemic rickets.
Human mutation | 2000-04-01 | PMID 10737991
Tyynismaa H, Kaitila I, Näntö-Salonen K and 2 more
Genes: PHEX
Genetic screening of fourteen mutations in Jordanian familial Mediterranean fever patients.
Human mutation | 2000-04-01 | PMID 10737992
Medlej-Hashim M, Rawashdeh M, Chouery E and 6 more
Genes: MEFV
Bruton's tyrosine kinase mutations in 8 Chinese families with X-linked agammaglobulinemia.
Human mutation | 2000-04-01 | PMID 10737994
Yip K L, Chan S Y, Ip W K and 1 more
Genes: BTK
The E148Q mutation in the MEFV gene: is it a disease-causing mutation or a sequence variant?
Human mutation | 2000-04-01 | PMID 10737995
Ben-Chetrit E, Lerer I, Malamud E and 2 more
Genes: MEFV
Novel mutations of the RPGR gene in RP3 families.
Human mutation | 2000-04-01 | PMID 10737996
Zito I, Gorin M B, Plant C and 3 more
Genes: RPGR
Identification of six novel WASP gene mutations in patients suffering from Wiskott-Aldrich syndrome.
Human mutation | 2000-04-01 | PMID 10737997
Brooimans R A, van den Berg A J, Tamminga R Y and 3 more
Novel KCNQ1 mutations associated with recessive and dominant congenital long QT syndromes: evidence for variable hearing phenotype associated with R518X.
Human mutation | 2000-04-01 | PMID 10737999
Wei J, Fish F A, Myerburg R J and 2 more
Genes: KCNQ1
Three novel mutations and twelve polymorphisms identified in the USH2A gene in Israeli USH2 families.
Human mutation | 2000-04-01 | PMID 10738000
Adato A, Weston M D, Berry A and 2 more
TT virus infections among blood donors in Iceland: prevalence, genotypes, and lack of relationship to serum ALT levels.
Transfusion | 2000-03-01 | PMID 10738031
Löve A, Stanzeit B, Li L and 4 more
Molecular mechanisms that lead to reduced expression of duffy antigens.
Transfusion | 2000-03-01 | PMID 10738032
Yazdanbakhsh K, Rios M, Storry J R and 4 more
Methylene blue reverts multidrug resistance: sensitivity of multidrug resistant cells to this dye and its photodynamic action.
Cancer letters | 2000-04-14 | PMID 10738110
Trindade G S, Farias S L, Rumjanek V M and 1 more
Methylenetetrahydrofolate reductase polymorphism and risk of colorectal adenomas.
Cancer letters | 2000-04-14 | PMID 10738112
Marugame T, Tsuji E, Inoue H and 8 more
Genes: MTHFR
Psoriasis patients with basal cell carcinoma have more repair-mediated DNA strand-breaks after UVC damage in lymphocytes than psoriasis patients without basal cell carcinoma.
Cancer letters | 2000-04-14 | PMID 10738113
Møller P, Wallin H, Dybdahl M and 2 more
Genes: ERCC1, LIG1, XRCC1
Molecular characterization of HHV-8 positive primary effusion lymphoma reveals pathogenetic and histogenetic features of the disease.
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology | 2000-05-01 | PMID 10738140
Gaidano G, Capello D, Fassone L and 9 more
Genes: HGF
Molecular epidemiology of dengue viruses in Brazil.
Cadernos de saude publica | 2000-01-01 | PMID 10738165
Nogueira R M, Miagostovich M P, Schatzmayr H G
P53 tumor suppressor gene mutations in hepatocellular carcinoma patients in India.
Cancer | 2000-04-01 | PMID 10738214
Katiyar S, Dash B C, Thakur V and 3 more
Genes: AGT
Growth inhibitory effects of paclitaxel on human epithelioid sarcoma in vitro: heterogeneity of response and the multidrug resistance phenotype.
Cancer | 2000-04-01 | PMID 10738220
Reinecke P, Knopf C, Schmitz M and 3 more
Alterations on chromosome 3 in endemic and nonendemic nasopharyngeal carcinoma.
International journal of cancer | 2000-04-15 | PMID 10738252
Sung N S, Zeng Y, Raab-Traub N
Genes: FHIT
Fine mapping of smallest common regions of deletion on chromosome 12 in liver epithelial and hepatocellular carcinoma cell lines from B6C3F(1) and C3B6F(1) mice.
International journal of cancer | 2000-04-15 | PMID 10738253
Ishizaki K, Ogawa K
Aberrant splicing of the ATM gene associated with shortening of the intronic mononucleotide tract in human colon tumor cell lines: a novel mutation target of microsatellite instability.
International journal of cancer | 2000-04-15 | PMID 10738255
Ejima Y, Yang L, Sasaki M S
Genes: ATM, BAX
Mutation screening of the CDKN2A promoter in melanoma families.
Genes, chromosomes & cancer | 2000-05-01 | PMID 10738302
Harland M, Holland E A, Ghiorzo P and 8 more
Evidence that haploinsufficiency of Ptch leads to medulloblastoma in mice.
Genes, chromosomes & cancer | 2000-05-01 | PMID 10738305
Zurawel R H, Allen C, Wechsler-Reya R and 2 more
Cystic fibrosis diagnosed in adult patients.
The New Zealand medical journal | 2000-01-28 | PMID 10738492
McWilliams T J, Wilsher M L, Kolbe J
Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations.
Annals of human genetics | 1999-01-01 | PMID 10738516
Valente E M, Povey S, Warner T T and 2 more
Mucopolysaccharidosis type I: characterization of a common mutation that causes Hurler syndrome in Moroccan subjects.
Annals of human genetics | 1999-01-01 | PMID 10738517
Alif N, Hess K, Straczek J and 4 more
Locus and population specific evolution in HLA class II genes.
Annals of human genetics | 1999-01-01 | PMID 10738519
Valdes A M, McWeeney S K, Meyer D and 2 more
Evolution of the apolipoprotein B gene and coronary artery disease: a study in low and high risk Asians.
Annals of human genetics | 1999-01-01 | PMID 10738520
Heng C K, Saha N, Low P S
Genes: CAD
An Asian-Native American paternal lineage identified by RPS4Y resequencing and by microsatellite haplotyping.
Annals of human genetics | 1999-01-01 | PMID 10738521
Bergen A W, Wang C Y, Tsai J and 6 more
Relative efficiencies of the chi-square recombination models for gene mapping with human pedigree data.
Annals of human genetics | 1999-01-01 | PMID 10738522
Lin S, Speed T P
Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1).
Annals of human genetics | 1999-03-01 | PMID 10738524
Yip S P, Putt W, Hopkinson D A and 1 more
Genes: PGM1
Enzymatic characterization of four new mutations in the glucose-6 phosphatase (G6PC) gene which cause glycogen storage disease type 1a.
Annals of human genetics | 1999-03-01 | PMID 10738525
Bruni N, Rajas F, Montano S and 3 more
Supportive evidence for contribution of the dopamine D2 receptor gene to heritability of stature: linkage and association studies.
Annals of human genetics | 1999-03-01 | PMID 10738526
Arinami T, Iijima Y, Yamakawa-Kobayashi K and 6 more
Genes: DRD2
Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study.
Annals of human genetics | 1999-03-01 | PMID 10738527
Quintana-Murci L, Semino O, Poloni E S and 11 more
Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association.
Annals of human genetics | 1999-03-01 | PMID 10738528
Zhao H, Pakstis A J, Kidd J R and 1 more
Genes: DRD2
MUC1 gene polymorphism does not explain the different incidence of gastric cancer in Portugal and Denmark.
Annals of human genetics | 1999-05-01 | PMID 10738530
Carvalho F, Peixoto A, Steffensen R and 3 more
Genes: MUC1
Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR-SSCP: detection of a new polymorphic mutation.
Annals of human genetics | 1999-05-01 | PMID 10738531
Simonsen K, Dissing J, Rudbeck L and 1 more
Genes: HFE
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease.
Annals of human genetics | 1999-05-01 | PMID 10738533
Giordano M, Bolognesi E, D'Alfonso S and 9 more
Common HLA alleles, rather than rare mutants, confer susceptibility to coeliac disease.
Annals of human genetics | 1999-05-01 | PMID 10738534
Brett P M, Yiannakou J Y, Morris M A and 3 more
Sequence variants in the 5' flanking region of the leptin gene are associated with obesity in women.
Annals of human genetics | 1999-05-01 | PMID 10738535
Li W D, Reed D R, Lee J H and 4 more
New DNA markers with increased informativeness show diminished support for a chromosome 5q11-13 schizophrenia susceptibility locus and exclude linkage in two new cohorts of British and Icelandic families.
Annals of human genetics | 1999-05-01 | PMID 10738536
Kalsi G, Mankoo B, Curtis D and 8 more
A statistically robust variance-components approach for quantitative trait linkage analysis.
Annals of human genetics | 1999-05-01 | PMID 10738537
Wang J, Guerra R, Cohen J
Meta-analysis of genome searches.
Annals of human genetics | 1999-05-01 | PMID 10738538
Wise L H, Lanchbury J S, Lewis C M
Allelic diversity of the human plasma alpha(1,3)fucosyltransferase gene (FUT6).
Annals of human genetics | 1999-07-01 | PMID 10738539
Pang H, Koda Y, Soejima M and 3 more
Genes: FUT6
Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany.
Annals of human genetics | 1999-07-01 | PMID 10738540
Klein C, Vieregge P, Hagenah J and 7 more
Apolipoprotein E (APOE) allele distribution in the world. Is APOE*4 a 'thrifty' allele?
Annals of human genetics | 1999-07-01 | PMID 10738542
Corbo R M, Scacchi R
Genes: APOE, CAD
Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor gene.
Annals of human genetics | 1999-07-01 | PMID 10738546
Erdmann J, Riedel K, Rohde K and 4 more
Genes: AGTR1
[Deletion of chromosome 10q--a marker for metastasis of head-neck carcinomas?].
Laryngo- rhino- otologie | 2000-02-01 | PMID 10738714
Bockmühl U, Schmidt S, Petersen S and 1 more
[The craniofacial architectural factors predisposing to a skeletal Class II identified by Jean Delaire's architectural analysis].
Revue de stomatologie et de chirurgie maxillo-faciale | 2000-01-01 | PMID 10738747
Paranque A R
Dopamine D3 receptor variant and tardive dyskinesia.
European archives of psychiatry and clinical neuroscience | 2000-01-01 | PMID 10738862
Rietschel M, Krauss H, Müller D J and 10 more
Lactoferrin expression in human breast cancer.
Cancer biochemistry biophysics | 1999-07-01 | PMID 10738912
Penco S, Caligo M A, Cipollini G and 2 more
Clinical and molecular heterogeneity in very-long-chain acyl-coenzyme A dehydrogenase deficiency.
Pediatric neurology | 2000-02-01 | PMID 10738914
Pons R, Cavadini P, Baratta S and 4 more
Mitochondrial biogenesis defects and neuromuscular disorders.
Pediatric neurology | 2000-02-01 | PMID 10738917
Marin-Garcia J, Goldenthal M J
Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndrome.
Pediatric neurology | 2000-02-01 | PMID 10738921
Vajsar J, Ackerley C, Chitayat D and 1 more
Natural killer (NK) and T cell-associated surface marker expression following allogeneic and autologous bone marrow transplantation (BMT).
Journal of hematotherapy & stem cell research | 2000-02-01 | PMID 10738973
Nagler A, Rabinowitz R, Rosengolts-Rat J and 2 more
Genotyping by restriction endonuclease analysis compared to phenotyping by antibiogram for typing methicillin-resistant Staphylococcus aureus strains colonizing patients in a nursing home.
Infection control and hospital epidemiology | 2000-03-01 | PMID 10738994
Lee Y L, Thrupp L
Frequent microsatellite instability and BAX mutations in T cell acute lymphoblastic leukemia cell lines.
Leukemia research | 2000-03-01 | PMID 10739008
Inoue K, Kohno T, Takakura S and 3 more
Genes: BAX
Genetic linkage groups in the Japanese brown frog (Rana japonica).
The Journal of heredity | 2000-01-01 | PMID 10739117
Sumida M, Nishioka M
Genes: GPI, ADA, MPI
Genetic differentiation among Oregon lake populations of the Daphnia pulex species complex.
The Journal of heredity | 2000-01-01 | PMID 10739118
Straughan D J, Lehman N
Detection of RFLP markers associated with antibody response in meat-type chickens: haplotype/genotype, single-band, and multiband analyses of RFLP in the major histocompatibility complex.
The Journal of heredity | 2000-01-01 | PMID 10739120
Yonash N, Heller E D, Hillel J and 1 more
Mitochondrial DNA variation in the European otter (Lutra lutra) and the use of spatial autocorrelation analysis in conservation.
The Journal of heredity | 2000-01-01 | PMID 10739121
Cassens I, Tiedemann R, Suchentrunk F and 1 more
Establishing a captive broodstock for the endangered bonytail chub (Gila elegans).
The Journal of heredity | 2000-01-01 | PMID 10739122
Hedrick P W, Dowling T E, Minckley W L and 3 more
Turkish honeybees: genetic variation and evidence for a fourth lineage of Apis mellifera mtDNA.
The Journal of heredity | 2000-01-01 | PMID 10739124
Palmer M R, Smith D R, Kaftanoğlu O
Improved estimation of the proportion of triploids in populations with diploid and triploid individuals.
The Journal of heredity | 2000-01-01 | PMID 10739127
Ridout M S
Inheritance of unique fruit and foliage color mutation in NuMex piñata.
The Journal of heredity | 2000-01-01 | PMID 10739128
Votava E J, Balok C, Coon D and 1 more
Population genetics of geographically restricted and widespread species of Myrica (Myricaceae).
The Journal of heredity | 2000-01-01 | PMID 10739129
Cheng Y P, Chien C T, Lin T P
Chloroplast inheritance and DNA variation in sweet, sour, and ground cherry.
The Journal of heredity | 2000-01-01 | PMID 10739133
Brettin T S, Karle R, Crowe E L and 1 more
Single-locus inheritance in the allotetraploid Coffea arabica L. and interspecific hybrid C. arabica x C. canephora.
The Journal of heredity | 2000-01-01 | PMID 10739135
Lashermes P, Paczek V, Trouslot P and 3 more
CYP2D6 ultrarapid metabolizer genotype as a potential modifier of smoking behaviour.
Pharmacogenetics | 2000-02-01 | PMID 10739167
Saarikoski S T, Sata F, Husgafvel-Pursiainen K and 6 more
Variation in induced CYP1A1 levels: relationship to CYP1A1, Ah receptor and GSTM1 polymorphisms.
Pharmacogenetics | 2000-02-01 | PMID 10739168
Smart J, Daly A K
Genes: GSTM1
Association of CYP1B1 genetic polymorphism with incidence to breast and lung cancer.
Pharmacogenetics | 2000-02-01 | PMID 10739169
Watanabe J, Shimada T, Gillam E M and 5 more
Polymorphisms of NAT2 in relation to sulphasalazine-induced agranulocytosis.
Pharmacogenetics | 2000-02-01 | PMID 10739170
Wadelius M, Stjernberg E, Wiholm B E and 1 more
Genes: NAT2
Association study of dopamine receptor gene polymorphisms with drug-induced hallucinations in patients with idiopathic Parkinson's disease.
Pharmacogenetics | 2000-02-01 | PMID 10739171
Makoff A J, Graham J M, Arranz M J and 5 more
Genes: DRD2, DRD3
Phenotypes of flavin-containing monooxygenase activity determined by ranitidine N-oxidation are positively correlated with genotypes of linked FM03 gene mutations in a Korean population.
Pharmacogenetics | 2000-02-01 | PMID 10739174
Kang J H, Chung W G, Lee K H and 7 more
Genes: FMO3
Arylamine N-acetyltransferase 1 (NAT1) genotypes in a Lebanese population.
Pharmacogenetics | 2000-02-01 | PMID 10739175
Dhaini H R, Levy G N
Genes: NAT1, NAT2
Myotonic dystrophy CTG repeats in an Italian population sample: evaluation of the polymorphism for forensic applications.
The American journal of forensic medicine and pathology | 2000-03-01 | PMID 10739235
D'Apote L, Pelotti S, Bini C and 4 more
Interaction with magnesium and ADP stabilizes both components of nitrogenase from Klebsiella pneumoniae against urea denaturation.
Protein science : a publication of the Protein Society | 2000-01-01 | PMID 10739254
Zou L, Baguinon M C, Guo X and 3 more
A step toward the prediction of the fluorescence lifetimes of tryptophan residues in proteins based on structural and spectral data.
Protein science : a publication of the Protein Society | 2000-01-01 | PMID 10739258
Sillen A, Díaz J F, Engelborghs Y
Heritable variation for latent inhibition and its correlation with reversal learning in honeybees (Apis mellifera).
Journal of comparative psychology (Washington, D.C. : 1983) | 2000-03-01 | PMID 10739314
Chandra S B, Hosler J S, Smith B H
Peripheral blood and intrathyroidal T cell clones from patients with thyroid autoimmune diseases.
Autoimmunity | 1999-01-01 | PMID 10739333
Massart C, Caroff G, Maugendre D and 2 more
Genes: TNF
Use of gel electrophoresis for the study of enzymatic activities of cold-adapted bacteria.
Journal of microbiological methods | 2000-03-01 | PMID 10739349
Berchet V, Boulanger D, Gounot A M
Blood coagulation factor X deficiency causes partial embryonic lethality and fatal neonatal bleeding in mice.
Thrombosis and haemostasis | 2000-02-01 | PMID 10739370
Dewerchin M, Liang Z, Moons L and 4 more
The factor V R2 allele: risk of venous thromboembolism, factor V levels and resistance to activated protein C.
Thrombosis and haemostasis | 2000-02-01 | PMID 10739373
Luddington R, Jackson A, Pannerselvam S and 2 more
Genes: APC
Genetic polymorphisms and coronary artery disease in the south of France.
Thrombosis and haemostasis | 2000-02-01 | PMID 10739375
Canavy I, Henry M, Morange P E and 5 more
Genes: ACE, CAD
Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults.
Thrombosis and haemostasis | 2000-02-01 | PMID 10739378
Voetsch B, Damasceno B P, Camargo E C and 5 more
Genes: MTHFR
The impact of Glu102Lys on the factor X function in a patient with a doubly homozygous factor X deficiency (Gla14Lys and Glu102Lys).
Thrombosis and haemostasis | 2000-02-01 | PMID 10739379
Forberg E, Huhmann I, Jimenez-Boj E and 1 more
Role of gender and genetic variance in plasminogen activator inhibitor-1 secretion from human adipose tissue.
Thrombosis and haemostasis | 2000-02-01 | PMID 10739390
van Harmelen V, Wahrenberg H, Eriksson P and 1 more
Monitoring of aspirin (ASA) pharmacodynamics with the platelet function analyzer PFA-100.
Thrombosis and haemostasis | 2000-02-01 | PMID 10739392
Homoncik M, Jilma B, Hergovich N and 3 more