Complete genome sequence of Neisseria meningitidis serogroup B strain MC58.
Science (New York, N.Y.) | 2000-03-10 | PMID 10710307
Tettelin H, Saunders N J, Heidelberg J and 39 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 1292 of 10600
gridlock, an HLH gene required for assembly of the aorta in zebrafish.
Science (New York, N.Y.) | 2000-03-10 | PMID 10710309
Zhong T P, Rosenberg M, Mohideen M A and 2 more
Correlates of sleep and waking in Drosophila melanogaster.
Science (New York, N.Y.) | 2000-03-10 | PMID 10710313
Shaw P J, Cirelli C, Greenspan R J and 1 more
Genetic suppression of polyglutamine toxicity in Drosophila.
Science (New York, N.Y.) | 2000-03-10 | PMID 10710314
Kazemi-Esfarjani P, Benzer S
Myofibrillar or mitochondrial creatine kinase deficiency alone does not impair mouse diaphragm isotonic function.
Journal of applied physiology (Bethesda, Md. : 1985) | 2000-03-01 | PMID 10710393
Watchko J F, Daood M J, Wieringa B and 1 more
Angiotensin-converting enzyme ID polymorphism and fitness phenotype in the HERITAGE Family Study.
Journal of applied physiology (Bethesda, Md. : 1985) | 2000-03-01 | PMID 10710400
Rankinen T, Pérusse L, Gagnon J and 6 more
Genes: ACE
Characterization of an unusual tRNA-like sequence found inserted in a Neurospora retroplasmid.
Nucleic acids research | 2000-04-01 | PMID 10710417
Mohr S, Wanner L A, Bertrand H and 1 more
Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures.
Nucleic acids research | 2000-04-01 | PMID 10710419
Weisman-Shomer P, Cohen E, Fry M
Genes: FMR1
A missense mutation in the nuclear gene coding for the mitochondrial aspartyl-tRNA synthetase suppresses a mitochondrial tRNA(Asp) mutation.
Nucleic acids research | 2000-04-01 | PMID 10710420
Chiang C S, Liaw G J
Positive and negative mutant selection in the human histone hairpin-binding protein using the yeast three-hybrid system.
Nucleic acids research | 2000-04-01 | PMID 10710426
Martin F, Michel F, Zenklusen D and 2 more
2-Hydroxy-dATP is incorporated opposite G by Escherichia coli DNA polymerase III resulting in high mutagenicity.
Nucleic acids research | 2000-04-01 | PMID 10710431
Kamiya H, Kasai H
Human RecQ5beta, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3alpha and 3beta.
Nucleic acids research | 2000-04-01 | PMID 10710432
Shimamoto A, Nishikawa K, Kitao S and 1 more
Genes: BLM, WRN
Rapid, high fidelity analysis of simple sequence repeats on an electronically active DNA microchip.
Nucleic acids research | 2000-04-01 | PMID 10710434
Radtkey R, Feng L, Muralhidar M and 8 more
Interstrain variation in murine susceptibility to inhaled acid-coated particles.
American journal of physiology. Lung cellular and molecular physiology | 2000-03-01 | PMID 10710518
Ohtsuka Y, Clarke R W, Mitzner W and 3 more
Mutations in sixth transmembrane domain of AQP2 inhibit its translocation induced by vasopression.
American journal of physiology. Renal physiology | 2000-03-01 | PMID 10710544
Yamashita Y, Hirai K, Katayama Y and 3 more
Genes: AQP2
Single-chain 434 repressors with altered DNA-binding specificities. Isolation of mutant single-chain repressors by phenotypic screening of combinatorial mutant libraries.
Genetica | 1999-01-01 | PMID 10710713
Simoncsits A, Tjörnhammar M L, Wang S and 1 more
An identical neo-mutation in the thyroid hormone receptor beta gene (A317T) in 2 unrelated Thai families with resistance to thyroid hormone.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet | 2000-02-01 | PMID 10710882
Sunthornthepvarakul T, Jaruratanasirikul S, Likitmaskul S and 2 more
Genes: TRH
[Effect of hydroxylation polymorphism on the concentration of propranolol in the blood of humans with hyperlipidemia].
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego | 1999-12-01 | PMID 10710948
Sulzyc-Bielicka V, Droździk M, Gawrońska-Szklarz B and 4 more
Screening for hereditary cancer and genetic testing, epitomized by breast cancer.
European journal of cancer (Oxford, England : 1990) | 1999-12-01 | PMID 10711238
Eeles R A
Genetic pathways in colorectal and other cancers.
European journal of cancer (Oxford, England : 1990) | 1999-12-01 | PMID 10711241
Ilyas M, Straub J, Tomlinson I P and 1 more
The genetic aspects of adult-onset glaucoma: a perspective from the Greater Toronto area.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie | 2000-02-01 | PMID 10711378
Williams-Lyn D, Flanagan J, Buys Y and 4 more
Genetic polymorphisms in ethanol metabolism: issues and goals for physiologically based pharmacokinetic modeling.
Drug and chemical toxicology | 2000-02-01 | PMID 10711397
Pastino G M, Flynn E J, Sultatos L G
Allelic imbalance on 16q in small, unifocal hepatocellular carcinoma: correlation with HBV and HCV infections and cellular proliferation rate.
Digestive diseases and sciences | 2000-02-01 | PMID 10711443
Gramantieri L, Trerè D, Pession A and 5 more
Mutations of p53 tumor suppressor gene, apoptosis, and proliferation in intrahepatic cholangiocellular carcinoma of the liver.
Digestive diseases and sciences | 2000-02-01 | PMID 10711445
Tannapfel A, Weinans L, Geissler F and 5 more
Genes: PCNA
Molecular basis of androgen receptor diseases.
Annals of medicine | 2000-02-01 | PMID 10711573
Yong E L, Lim J, Qi W and 2 more
Interleukin-1 genetic association with periodontitis in clinical practice.
Journal of periodontology | 2000-02-01 | PMID 10711605
McDevitt M J, Wang H Y, Knobelman C and 5 more
Peptostreptococcus micros smooth and rough genotypes in periodontitis and gingivitis.
Journal of periodontology | 2000-02-01 | PMID 10711611
Kremer B H, Loos B G, van der Velden U and 6 more
Intellectual characteristics of Prader-Willi syndrome: comparison of genetic subtypes.
Journal of intellectual disability research : JIDR | 2000-02-01 | PMID 10711647
Roof E, Stone W, MacLean W and 3 more
A case of mosaic trisomy 21 with Down's syndrome signs and normal intellectual development.
Journal of intellectual disability research : JIDR | 2000-02-01 | PMID 10711655
de A Moreira L M, San Juan A, Pereira P S and 1 more
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.
Investigative ophthalmology & visual science | 2000-03-01 | PMID 10711710
Simonelli F, Testa F, de Crecchio G and 6 more
TIMP-3, collagen, and elastin immunohistochemistry and histopathology of Sorsby's fundus dystrophy.
Investigative ophthalmology & visual science | 2000-03-01 | PMID 10711711
Chong N H, Alexander R A, Gin T and 2 more
Genes: RPE
Genome mapping in ruminants and map locations for genes influencing reproduction.
Reviews of reproduction | 2000-01-01 | PMID 10711733
Montgomery G W
Heritability and molecular genetic studies of endometriosis.
Human reproduction update | 2000-01-01 | PMID 10711828
Bischoff F Z, Simpson J L
Genes: PTEN
Clinical diversity of hereditary Duane's retraction syndrome.
Ophthalmology | 2000-03-01 | PMID 10711888
Chung M, Stout J T, Borchert M S
Visual acuity in children with coloboma: clinical features and a new phenotypic classification system.
Ophthalmology | 2000-03-01 | PMID 10711890
Hornby S J, Adolph S, Gilbert C E and 2 more
Illicit psychoactive substance use, heavy use, abuse, and dependence in a US population-based sample of male twins.
Archives of general psychiatry | 2000-03-01 | PMID 10711912
Kendler K S, Karkowski L M, Neale M C and 1 more
Thalassaemia in Sri Lanka: implications for the future health burden of Asian populations. Sri Lanka Thalassaemia Study Group.
Lancet (London, England) | 2000-03-04 | PMID 10711926
de Silva S, Fisher C A, Premawardhena A and 7 more
Muscular dystrophy: historical overview and classification in the genetic era.
Seminars in neurology | 1999-01-01 | PMID 10711984
Kissel J T, Mendell J R
The myotonic dystrophies.
Seminars in neurology | 1999-01-01 | PMID 10711986
Thornton C
Genes: DMPK
Facioscapulohumeral dystrophy.
Seminars in neurology | 1999-01-01 | PMID 10711987
Kissel J T
Distal myopathies.
Seminars in neurology | 1999-01-01 | PMID 10711988
Barohn R J, Amato A A
Oculopharyngeal muscular dystrophy.
Seminars in neurology | 1999-01-01 | PMID 10711989
Brais B, Rouleau G A, Bouchard J P and 2 more
Genes: GCG
Emery-Dreifuss muscular dystrophy.
Seminars in neurology | 1999-01-01 | PMID 10711990
Zacharias A S, Wagener M E, Warren S T and 1 more
Nucleolus organizer regions in Physalaemus cuvievi (Anura, Leptodactylidae), with evidence of a unique case of Ag-NOR variability.
Hereditas | 1999-01-01 | PMID 10712096
Silva A P, Haddad C F, Kasahara S
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome.
American journal of human genetics | 2000-03-01 | PMID 10712195
Glaser R L, Jiang W, Boyadjiev S A and 9 more
Genes: FGFR2, FGFR3
Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain.
American journal of human genetics | 2000-03-01 | PMID 10712197
Fahsold R, Hoffmeyer S, Mischung C and 10 more
High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal alleles.
American journal of human genetics | 2000-03-01 | PMID 10712199
Silveira I, Alonso I, Guimarães L and 11 more
Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes.
American journal of human genetics | 2000-03-01 | PMID 10712200
Sperandeo M P, Ungaro P, Vernucci M and 9 more
Genes: IGF2
Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
American journal of human genetics | 2000-03-01 | PMID 10712201
Lee S, Wevrick R
Genes: SNRPN
Functional analysis of the neurofibromatosis type 2 protein by means of disease-causing point mutations.
American journal of human genetics | 2000-03-01 | PMID 10712203
Stokowski R P, Cox D R
Genes: EBP
A locus for brachydactyly type A-1 maps to chromosome 2q35-q36.
American journal of human genetics | 2000-03-01 | PMID 10712204
Yang X, She C, Guo J and 5 more
Fine mapping of the chromosome 12 late-onset Alzheimer disease locus: potential genetic and phenotypic heterogeneity.
American journal of human genetics | 2000-03-01 | PMID 10712207
Scott W K, Grubber J M, Conneally P M and 7 more
Genes: APOE
A genome screen of multiplex sibships with prostate cancer.
American journal of human genetics | 2000-03-01 | PMID 10712208
Suarez B K, Lin J, Burmester J K and 7 more
Combined analysis of hereditary prostate cancer linkage to 1q24-25: results from 772 hereditary prostate cancer families from the International Consortium for Prostate Cancer Genetics.
American journal of human genetics | 2000-03-01 | PMID 10712209
Xu J
Multipoint estimation of genetic maps for human trisomies with one parent or other partial data.
American journal of human genetics | 2000-03-01 | PMID 10712210
Feingold E, Brown A S, Sherman S L
Significant admixture linkage disequilibrium across 30 cM around the FY locus in African Americans.
American journal of human genetics | 2000-03-01 | PMID 10712211
Lautenberger J A, Stephens J C, O'Brien S J and 1 more
Genes: SPTA1
The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data.
American journal of human genetics | 2000-03-01 | PMID 10712212
Jorde L B, Watkins W S, Bamshad M J and 4 more
mtDNA affinities of the peoples of North-Central Mexico.
American journal of human genetics | 2000-03-01 | PMID 10712213
Green L D, Derr J N, Knight A
mtDNA and the origin of the Icelanders: deciphering signals of recent population history.
American journal of human genetics | 2000-03-01 | PMID 10712214
Helgason A, Sigureth ardóttir S, Gulcher J R and 2 more
Phylogenetic network of the mtDNA haplogroup U in Northern Finland based on sequence analysis of the complete coding region by conformation-sensitive gel electrophoresis.
American journal of human genetics | 2000-03-01 | PMID 10712215
Finnilä S, Hassinen I E, Ala-Kokko L and 1 more
QTL fine mapping by measuring and testing for Hardy-Weinberg and linkage disequilibrium at a series of linked marker loci in extreme samples of populations.
American journal of human genetics | 2000-03-01 | PMID 10712216
Deng H W, Chen W M, Recker R R
A two-stage variable-stringency semiparametric method for mapping quantitative-trait loci with the use of genomewide-scan data on sib pairs.
American journal of human genetics | 2000-03-01 | PMID 10712217
Ghosh S, Majumder P P
The trimmed-haplotype test for linkage disequilibrium.
American journal of human genetics | 2000-03-01 | PMID 10712218
MacLean C J, Martin R B, Sham P C and 3 more
Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes.
American journal of human genetics | 2000-03-01 | PMID 10712220
Göring H H, Terwilliger J D
Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions.
American journal of human genetics | 2000-03-01 | PMID 10712221
Göring H H, Terwilliger J D
Bias and efficiency in family-based gene-characterization studies: conditional, prospective, retrospective, and joint likelihoods.
American journal of human genetics | 2000-03-01 | PMID 10712222
Kraft P, Thomas D C
A recurrent expansion of a maternal allele with 36 CAG repeats causes Huntington disease in two sisters.
American journal of human genetics | 2000-03-01 | PMID 10712225
Laccone F, Christian W
Analysis of aneuploidy frequencies in sperm from patients with hereditary nonpolyposis colon cancer and an hMSH2 mutation.
American journal of human genetics | 2000-03-01 | PMID 10712226
Martin R H, Green J, Ko E and 2 more
Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components.
American journal of human genetics | 2000-03-01 | PMID 10712227
Pratt S C, Daly M J, Kruglyak L
The transmission/disequilibrium test for linkage on the X chromosome.
American journal of human genetics | 2000-03-01 | PMID 10712228
Ho G Y, Bailey-Wilson J E
The transmission/disequilibrium test and parental-genotype reconstruction for X-chromosomal markers.
American journal of human genetics | 2000-03-01 | PMID 10712229
Horvath S, Laird N M, Knapp M
Gamete-competition models.
American journal of human genetics | 2000-03-01 | PMID 10712230
Sinsheimer J S, Blangero J, Lange K
A myosin phosphatase targeting subunit isoform transition defines a smooth muscle developmental phenotypic switch.
American journal of physiology. Cell physiology | 2000-03-01 | PMID 10712248
Dirksen W P, Vladic F, Fisher S A
Characterization of inducible nature of MRP3 in rat liver.
American journal of physiology. Gastrointestinal and liver physiology | 2000-03-01 | PMID 10712264
Ogawa K, Suzuki H, Hirohashi T and 6 more
Association study of the chromosomal region containing the FCER2 gene suggests it has a regulatory role in atopic disorders.
American journal of respiratory and critical care medicine | 2000-03-01 | PMID 10712310
Laitinen T, Ollikainen V, Lázaro C and 8 more
Genes: FCER2
Lung T-helper cells expressing T-cell receptor AV2S3 associate with clinical features of pulmonary sarcoidosis.
American journal of respiratory and critical care medicine | 2000-03-01 | PMID 10712327
Grunewald J, Berlin M, Olerup O and 1 more
Bronchial responsiveness among inbred mouse strains. Role of airway smooth-muscle shortening velocity.
American journal of respiratory and critical care medicine | 2000-03-01 | PMID 10712331
Duguet A, Biyah K, Minshall E and 5 more
A pilot study of the effect of gentamicin on nasal potential difference measurements in cystic fibrosis patients carrying stop mutations.
American journal of respiratory and critical care medicine | 2000-03-01 | PMID 10712334
Wilschanski M, Famini C, Blau H and 5 more
Genes: CFTR
Allelic heterogeneity in hereditary surfactant protein B (SP-B) deficiency.
American journal of respiratory and critical care medicine | 2000-03-01 | PMID 10712351
Nogee L M, Wert S E, Proffit S A and 2 more
Fine mapping of PPH1, a gene for familial primary pulmonary hypertension, to a 3-cM region on chromosome 2q33.
American journal of respiratory and critical care medicine | 2000-03-01 | PMID 10712363
Deng Z, Haghighi F, Helleby L and 6 more
p53, p21(WAF1/CIP1), and MDM2 involvement in proliferation and apoptosis in an in vitro model of conditionally immortalized human vascular smooth muscle cells.
Arteriosclerosis, thrombosis, and vascular biology | 2000-03-01 | PMID 10712385
Hsieh J K, Kletsas D, Clunn G and 3 more
Genes: MDM2
Plasma levels of extracellular superoxide dismutase in an Australian population: genetic contribution to normal variation and correlations with plasma nitric oxide and apolipoprotein A-I levels.
Arteriosclerosis, thrombosis, and vascular biology | 2000-03-01 | PMID 10712391
Mahaney M C, Czerwinski S A, Adachi T and 2 more
Association of the C-514T polymorphism in the hepatic lipase gene with variations in lipoprotein subclass profiles: The Framingham Offspring Study.
Arteriosclerosis, thrombosis, and vascular biology | 2000-03-01 | PMID 10712408
Couture P, Otvos J D, Cupples L A and 4 more
Atherosclerosis progression in LDL receptor-deficient and apolipoprotein E-deficient mice is independent of genetic alterations in plasminogen activator inhibitor-1.
Arteriosclerosis, thrombosis, and vascular biology | 2000-03-01 | PMID 10712412
Sjöland H, Eitzman D T, Gordon D and 3 more
Genes: LDLR
Polymorphisms in the 5' regulatory region of the tissue factor gene and the risk of myocardial infarction and venous thromboembolism: the ECTIM and PATHROS studies. Etude Cas-Témoins de l'Infarctus du Myocarde. Paris Thrombosis case-control Study.
Arteriosclerosis, thrombosis, and vascular biology | 2000-03-01 | PMID 10712418
Arnaud E, Barbalat V, Nicaud V and 9 more
The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients.
The Journal of clinical investigation | 2000-03-01 | PMID 10712431
Joutel A, Andreux F, Gaulis S and 7 more
Genes: EGF
Osteoclasts expressing the measles virus nucleocapsid gene display a pagetic phenotype.
The Journal of clinical investigation | 2000-03-01 | PMID 10712432
Kurihara N, Reddy S V, Menaa C and 2 more
Paternal versus maternal transmission of a stimulatory G-protein alpha subunit knockout produces opposite effects on energy metabolism.
The Journal of clinical investigation | 2000-03-01 | PMID 10712433
Yu S, Gavrilova O, Chen H and 7 more
Use of autoantigen-knockout mice in developing an active autoimmune disease model for pemphigus.
The Journal of clinical investigation | 2000-03-01 | PMID 10712434
Amagai M, Tsunoda K, Suzuki H and 3 more
CD28-B7 blockade prevents the development of experimental autoimmune glomerulonephritis.
The Journal of clinical investigation | 2000-03-01 | PMID 10712436
Reynolds J, Tam F W, Chandraker A and 6 more
Genes: CTLA4
Gene dosage affects the cardiac and brain phenotype in nonmuscle myosin II-B-depleted mice.
The Journal of clinical investigation | 2000-03-01 | PMID 10712438
Uren D, Hwang H K, Hara Y and 9 more
Discontinuous actin hexagon, a protein essential for cortical furrow formation in Drosophila, is membrane associated and hyperphosphorylated.
Molecular biology of the cell | 2000-03-01 | PMID 10712516
Zhang C X, Rothwell W F, Sullivan W and 1 more
Expression of AtPRP3, a proline-rich structural cell wall protein from Arabidopsis, is regulated by cell-type-specific developmental pathways involved in root hair formation.
Plant physiology | 2000-03-01 | PMID 10712533
Bernhardt C, Tierney M L
Hormone autotrophic growth and differentiation identifies mutant lines of Arabidopsis with altered cytokinin and auxin content or signaling.
Plant physiology | 2000-03-01 | PMID 10712535
Frank M, Rupp H M, Prinsen E and 3 more
Characterization of XET-related genes of rice.
Plant physiology | 2000-03-01 | PMID 10712549
Uozu S, Tanaka-Ueguchi M, Kitano H and 2 more
Analysis of reductant supply systems for ferredoxin-dependent sulfite reductase in photosynthetic and nonphotosynthetic organs of maize.
Plant physiology | 2000-03-01 | PMID 10712553
Yonekura-Sakakibara K, Onda Y, Ashikari T and 3 more
Molecular cloning and characterization of ATP-phosphoribosyl transferase from Arabidopsis, a key enzyme in the histidine biosynthetic pathway.
Plant physiology | 2000-03-01 | PMID 10712555
Ohta D, Fujimori K, Mizutani M and 4 more
Expression of tryptophan decarboxylase and tyrosine decarboxylase genes in tobacco results in altered biochemical and physiological phenotypes.
Plant physiology | 2000-03-01 | PMID 10712558
Guillet G, Poupart J, Basurco J and 1 more
Genotypical differences in aluminum resistance of maize are expressed in the distal part of the transition zone. Is reduced basipetal auxin flow involved in inhibition of root elongation by aluminum?
Plant physiology | 2000-03-01 | PMID 10712559
Kollmeier M, Felle H H, Horst W J
Abscisic acid accumulation maintains maize primary root elongation at low water potentials by restricting ethylene production.
Plant physiology | 2000-03-01 | PMID 10712561
Spollen W G, LeNoble M E, Samuels T D and 2 more