Construction and transposon mutagenesis in Escherichia coli of a full-length infectious clone of pseudorabies virus, an alphaherpesvirus.
Journal of virology | 1999-08-01 | PMID 10400733
Smith G A, Enquist L W
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 1170 of 10600
Both memory and CD45RA+/CD62L+ naive CD4(+) T cells are infected in human immunodeficiency virus type 1-infected individuals.
Journal of virology | 1999-08-01 | PMID 10400736
Ostrowski M A, Chun T W, Justement S J and 7 more
Genes: CXCR4
Establishment of a seronegative human T-cell leukemia virus type 1 (HTLV-1) carrier state in rats inoculated with a syngeneic HTLV-1-immortalized T-cell line preferentially expressing Tax.
Journal of virology | 1999-08-01 | PMID 10400737
Koya Y, Ohashi T, Kato H and 7 more
A lysine-to-arginine change found in natural alleles of the human T-cell lymphotropic/leukemia virus type 1 p12(I) protein greatly influences its stability.
Journal of virology | 1999-08-01 | PMID 10400740
Trovato R, Mulloy J C, Johnson J M and 3 more
Evolution of the hepatitis C virus second envelope protein hypervariable region in chronically infected patients receiving alpha interferon therapy.
Journal of virology | 1999-08-01 | PMID 10400744
Pawlotsky J M, Germanidis G, Frainais P O and 4 more
Comparison of genetic variability at multiple loci across the genomes of the major subtypes of Kaposi's sarcoma-associated herpesvirus reveals evidence for recombination and for two distinct types of open reading frame K15 alleles at the right-hand end.
Journal of virology | 1999-08-01 | PMID 10400762
Poole L J, Zong J C, Ciufo D M and 6 more
Patterns of chemokine receptor fusion cofactor utilization by human immunodeficiency virus type 1 variants from the lungs and blood.
Journal of virology | 1999-08-01 | PMID 10400765
Singh A, Besson G, Mobasher A and 1 more
Genes: CCR5, CXCR4, CCR3, CCR8, GPR15
Long-term infection and transformation of dermal microvascular endothelial cells by human herpesvirus 8.
Journal of virology | 1999-08-01 | PMID 10400787
Moses A V, Fish K N, Ruhl R and 5 more
TNF-alpha and HLA-DR genotyping as potential prognostic markers in pulmonary sarcoidosis.
European cytokine network | 1999-06-01 | PMID 10400819
Swider C, Schnittger L, Bogunia-Kubik K and 4 more
Genes: TNF
Cytokines in Gaucher's disease.
European cytokine network | 1999-06-01 | PMID 10400826
Barak V, Acker M, Nisman B and 4 more
Genes: TNF
Total serum IgE and its association with asthma symptoms and allergic sensitization among children.
The Journal of allergy and clinical immunology | 1999-07-01 | PMID 10400836
Sherrill D L, Stein R, Halonen M and 3 more
Mouse model of a familial hypertrophic cardiomyopathy mutation in alpha-tropomyosin manifests cardiac dysfunction.
Circulation research | 1999-07-09 | PMID 10400910
Muthuchamy M, Pieples K, Rethinasamy P and 7 more
A view of modern human origins from Y chromosome microsatellite variation.
Genome research | 1999-06-01 | PMID 10400923
Seielstad M, Bekele E, Ibrahim M and 2 more
A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families.
Genome research | 1999-06-01 | PMID 10400925
van der Velden P A, Sandkuijl L A, Bergman W and 3 more
Improved DNA sequencing accuracy and detection of heterozygous alleles using manganese citrate and different fluorescent dye terminators.
Genome research | 1999-06-01 | PMID 10400927
Korch C, Drabkin H
A high-density integrated genetic linkage and radiation hybrid map of the laboratory rat.
Genome research | 1999-06-01 | PMID 10400928
Steen R G, Kwitek-Black A E, Glenn C and 22 more
Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome.
Human molecular genetics | 1999-08-01 | PMID 10400982
Tsai T F, Jiang Y H, Bressler J and 2 more
Genes: SNRPN
Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle.
Human molecular genetics | 1999-08-01 | PMID 10400985
Cainarca S, Messali S, Ballabio A and 1 more
Genes: MID1
Mild impairment of learning and memory in mice overexpressing the mSim2 gene located on chromosome 16: an animal model of Down's syndrome.
Human molecular genetics | 1999-08-01 | PMID 10400987
Ema M, Ikegami S, Hosoya T and 6 more
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene.
Human molecular genetics | 1999-08-01 | PMID 10400989
Fransen E, Verstreken M, Verhagen W I and 10 more
Genes: COCH
An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness.
Human molecular genetics | 1999-08-01 | PMID 10400990
Yajima I, Sato S, Kimura T and 4 more
Genes: MITF, RPE
A common functional polymorphism (C-->A substitution at position -863) in the promoter region of the tumour necrosis factor-alpha (TNF-alpha) gene associated with reduced circulating levels of TNF-alpha.
Human molecular genetics | 1999-08-01 | PMID 10400991
Skoog T, van't Hooft F M, Kallin B and 5 more
Genes: TNF, CAT
Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds.
Human molecular genetics | 1999-08-01 | PMID 10400992
Ratovitski T, Corson L B, Strain J and 4 more
Genes: SOD1
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
Human molecular genetics | 1999-08-01 | PMID 10400993
Marsh D J, Kum J B, Lunetta K L and 22 more
Genes: PTEN
Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization.
Human molecular genetics | 1999-08-01 | PMID 10400994
Goodyer I D, Jones E E, Monaco A P and 1 more
Myotonic dystrophy is associated with a reduced level of RNA from the DMWD allele adjacent to the expanded repeat.
Human molecular genetics | 1999-08-01 | PMID 10400997
Alwazzan M, Newman E, Hamshere M G and 1 more
Genes: SIX5, DMPK
Cellular dysfunction of LQT5-minK mutants: abnormalities of IKs, IKr and trafficking in long QT syndrome.
Human molecular genetics | 1999-08-01 | PMID 10400998
Bianchi L, Shen Z, Dennis A T and 6 more
Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyria.
Human molecular genetics | 1999-08-01 | PMID 10401000
de Villiers J N, Hillermann R, Loubser L and 1 more
Genes: HFE, PPOX
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Abeta42 secretion.
Human molecular genetics | 1999-08-01 | PMID 10401002
De Jonghe C, Cruts M, Rogaeva E A and 13 more
Genes: PSEN1
A nonsense mutation in a novel gene is associated with retinitis pigmentosa in a family linked to the RP1 locus.
Human molecular genetics | 1999-08-01 | PMID 10401003
Guillonneau X, Piriev N I, Danciger M and 4 more
Novel alternatively spliced isoforms of the neurofibromatosis type 2 tumor suppressor are targeted to the nucleus and cytoplasmic granules.
Human molecular genetics | 1999-08-01 | PMID 10401006
Schmucker B, Tang Y, Kressel M
RPGR transcription studies in mouse and human tissues reveal a retina-specific isoform that is disrupted in a patient with X-linked retinitis pigmentosa.
Human molecular genetics | 1999-08-01 | PMID 10401007
Kirschner R, Rosenberg T, Schultz-Heienbrok R and 6 more
Genes: RPGR
Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice.
Human molecular genetics | 1999-08-01 | PMID 10401008
Dixon M J, Gazzard J, Chaudhry S S and 3 more
Implications of certain genetic polymorphisms in scarring in vesicoureteric reflux: importance of ACE polymorphism.
American journal of kidney diseases : the official journal of the National Kidney Foundation | 1999-07-01 | PMID 10401028
Ozen S, Alikasifoglu M, Saatci U and 7 more
Genes: ACE
Radiological analysis of children with cystic fibrosis who are homozygous for cystic fibrosis transmembrane conductance regulator mutation S549R (T-->G).
Journal of tropical pediatrics | 1999-06-01 | PMID 10401194
Frossard P M, Bakalinova D, Hertecant J and 2 more
Genes: CFTR
Memory self-appraisal in middle-aged and older adults with the apolipoprotein E-4 allele.
The American journal of psychiatry | 1999-07-01 | PMID 10401448
Small G W, Chen S T, Komo S and 12 more
Genes: APOE
Common genetic vulnerability for nicotine and alcohol dependence in men.
Archives of general psychiatry | 1999-07-01 | PMID 10401514
True W R, Xian H, Scherrer J F and 7 more
Human P2Y2 receptor polymorphism: identification and pharmacological characterization of two allelic variants.
British journal of pharmacology | 1999-06-01 | PMID 10401562
Janssens R, Paindavoine P, Parmentier M and 1 more
Singlet oxygen is part of a hyperoxidant state generated during spore germination.
Free radical biology & medicine | 1999-06-01 | PMID 10401603
Lledías F, Rangel P, Hansberg W
Endogenous insulin-like growth factors regulate the proliferation of TSH-independent mutants derived from FRTL5 cells.
Biochimie | 1999-04-01 | PMID 10401671
Chieffi P, Picascia A, Stanzione R and 2 more
Different mutations of the RET gene cause different human tumoral diseases.
Biochimie | 1999-04-01 | PMID 10401675
Santoro M, Melillo R M, Carlomagno F and 5 more
Genes: RET
Benign infantile familial convulsions: natural history of a case and clinical characteristics of a large Italian family.
Neuropediatrics | 1999-04-01 | PMID 10401694
Giordano L, Accorsi P, Valseriati D and 5 more
Successful myoblast transplantation in fibrotic muscles: no increased impairment by the connective tissue.
Transplantation | 1999-06-27 | PMID 10401771
Brussee V, Tardif F, Roy B and 3 more
Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindred.
Annals of neurology | 1999-07-01 | PMID 10401778
Butinar D, Zidar J, Leonardis L and 6 more
A de novo splice donor site mutation causes in-frame deletion of 14 amino acids in the proteolipid protein in Pelizaeus-Merzbacher disease.
Annals of neurology | 1999-07-01 | PMID 10401787
Aoyagi Y, Kobayashi H, Tanaka K and 3 more
Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease.
Annals of neurology | 1999-07-01 | PMID 10401788
Blumen S C, Brais B, Korczyn A D and 9 more
Genes: GCG
A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy.
Journal of the neurological sciences | 1999-04-01 | PMID 10402027
Hadjigeorgiou G M, Kim S H, Fischbeck K H and 6 more
Prevalence of mixed infection by different hepatitis C virus genotypes in patients with hepatitis C virus-related chronic liver disease.
The Journal of laboratory and clinical medicine | 1999-07-01 | PMID 10402061
Giannini C, Giannelli F, Monti M and 5 more
Alternatively spliced isoforms of nerve- and muscle-derived agrin: their roles at the neuromuscular junction.
Neuron | 1999-05-01 | PMID 10402191
Burgess R W, Nguyen Q T, Son Y J and 2 more
latheo encodes a subunit of the origin recognition complex and disrupts neuronal proliferation and adult olfactory memory when mutant.
Neuron | 1999-05-01 | PMID 10402192
Pinto S, Quintana D G, Smith P and 11 more
Genes: LAT, ORC2, ORC3
Identification and mechanism of action of two histidine residues underlying high-affinity Zn2+ inhibition of the NMDA receptor.
Neuron | 1999-05-01 | PMID 10402203
Choi Y B, Lipton S A
A YAC mouse model for Huntington's disease with full-length mutant huntingtin, cytoplasmic toxicity, and selective striatal neurodegeneration.
Neuron | 1999-05-01 | PMID 10402204
Hodgson J G, Agopyan N, Gutekunst C A and 16 more
Light chain variable region diversity in Atlantic cod (Gadus morhua L.).
Developmental and comparative immunology | 1999-04-01 | PMID 10402210
Widholm H, Lundbäck A S, Daggfeldt A and 3 more
The association between a mutated ras gene and cyclooxygenase-2 expression in human breast cancer cell lines.
International journal of oncology | 1999-08-01 | PMID 10402236
Gilhooly E M, Rose D P
Lack of mutations in DNA polymerase beta of estradiol-induced hamster kidney tumors: sequence of hamster DNA polymerase beta cDNA.
International journal of oncology | 1999-08-01 | PMID 10402247
Kong L Y, Hodgson A V, Springer I N and 1 more
Microsatellite instability and allelic losses in neuroendocrine tumors of the gastro-entero-pancreatic system.
International journal of oncology | 1999-08-01 | PMID 10402248
Ghimenti C, Lonobile A, Campani D and 2 more
Genes: MEN1
Sampling technique influences the detection of K-ras mutations in normal appearing mucosa of colorectal cancer patients.
International journal of oncology | 1999-08-01 | PMID 10402253
Schimanski C C, Sutter C, Linnemann U and 1 more
Colonisation of the developing human brain and spinal cord by microglia: a review.
Microscopy research and technique | 1999-06-15 | PMID 10402264
Rezaie P, Male D
Human male infertility and Y chromosome deletions: role of the AZF-candidate genes DAZ, RBM and DFFRY.
Human reproduction (Oxford, England) | 1999-07-01 | PMID 10402373
Ferlin A, Moro E, Garolla A and 1 more
Acephalic spermatozoa and abnormal development of the head-neck attachment: a human syndrome of genetic origin.
Human reproduction (Oxford, England) | 1999-07-01 | PMID 10402395
Chemes H E, Puigdomenech E T, Carizza C and 3 more
Frequency of CFTR gene mutations in males participating in an ICSI programme.
Human reproduction (Oxford, England) | 1999-07-01 | PMID 10402399
Jakubiczka S, Bettecken T, Stumm M and 6 more
Genes: CFTR
A recessive Arabidopsis mutant that grows photoautotrophically under salt stress shows enhanced active oxygen detoxification.
The Plant cell | 1999-07-01 | PMID 10402422
Tsugane K, Kobayashi K, Niwa Y and 3 more
Gnarley1 is a dominant mutation in the knox4 homeobox gene affecting cell shape and identity.
The Plant cell | 1999-07-01 | PMID 10402426
Foster T, Yamaguchi J, Wong B C and 2 more
ANI1. A sex pheromone-induced gene in ceratopteris gametophytes and its possible role in sex determination.
The Plant cell | 1999-07-01 | PMID 10402431
Wen C K, Smith R, Banks J A
Genes: ACE
Epigenetic interactions among three dTph1 transposons in two homologous chromosomes activate a new excision-repair mechanism in petunia.
The Plant cell | 1999-07-01 | PMID 10402432
van Houwelingen A, Souer E, Mol J and 1 more
The TRANSPARENT TESTA GLABRA1 locus, which regulates trichome differentiation and anthocyanin biosynthesis in Arabidopsis, encodes a WD40 repeat protein.
The Plant cell | 1999-07-01 | PMID 10402433
Walker A R, Davison P A, Bolognesi-Winfield A C and 6 more
Molecular characterization of the maize Rp1-D rust resistance haplotype and its mutants.
The Plant cell | 1999-07-01 | PMID 10402435
Collins N, Drake J, Ayliffe M and 4 more
A visual screen of a GFP-fusion library identifies a new type of nuclear envelope membrane protein.
The Journal of cell biology | 1999-07-12 | PMID 10402458
Rolls M M, Stein P A, Taylor S S and 3 more
Pex22p of Pichia pastoris, essential for peroxisomal matrix protein import, anchors the ubiquitin-conjugating enzyme, Pex4p, on the peroxisomal membrane.
The Journal of cell biology | 1999-07-12 | PMID 10402463
Koller A, Snyder W B, Faber K N and 4 more
Intracellular localization of proteasomal degradation of a viral antigen.
The Journal of cell biology | 1999-07-12 | PMID 10402464
Antón L C, Schubert U, Bacík I and 8 more
Yeast homologues of tomosyn and lethal giant larvae function in exocytosis and are associated with the plasma membrane SNARE, Sec9.
The Journal of cell biology | 1999-07-12 | PMID 10402465
Lehman K, Rossi G, Adamo J E and 1 more
DAP-kinase participates in TNF-alpha- and Fas-induced apoptosis and its function requires the death domain.
The Journal of cell biology | 1999-07-12 | PMID 10402466
Cohen O, Inbal B, Kissil J L and 5 more
Genes: DAP, TNF, FADD
Myosin light chain kinase functions downstream of Ras/ERK to promote migration of urokinase-type plasminogen activator-stimulated cells in an integrin-selective manner.
The Journal of cell biology | 1999-07-12 | PMID 10402467
Nguyen D H, Catling A D, Webb D J and 5 more
Drosophila roadblock and Chlamydomonas LC7: a conserved family of dynein-associated proteins involved in axonal transport, flagellar motility, and mitosis.
The Journal of cell biology | 1999-07-12 | PMID 10402468
Bowman A B, Patel-King R S, Benashski S E and 3 more
Genomic organization, expression, and analysis of the troponin C gene pat-10 of Caenorhabditis elegans.
The Journal of cell biology | 1999-07-12 | PMID 10402470
Terami H, Williams B D, Kitamura S i and 5 more
Glypican-3-deficient mice exhibit developmental overgrowth and some of the abnormalities typical of Simpson-Golabi-Behmel syndrome.
The Journal of cell biology | 1999-07-12 | PMID 10402475
Cano-Gauci D F, Song H H, Yang H and 14 more
Genes: GPC3
Structure and function of the extracellular calcium-sensing receptor (Review).
International journal of molecular medicine | 1999-08-01 | PMID 10402476
Bai M
Influence of apolipoprotein E genotype on blood redox status of Alzheimer's disease patients.
International journal of molecular medicine | 1999-08-01 | PMID 10402486
Fernandes M A, Proenca M T, Nogueira A J and 6 more
Genes: COMT
Modulation of biological phenotypes for tumor growth and metastasis by target-specific biological inhibitors in gastric cancer.
International journal of molecular medicine | 1999-08-01 | PMID 10402490
Rha S Y, Noh S H, Kim T S and 4 more
Association study of a polymorphism of nonerythroid alpha-spectrin gene with schizophrenia.
American journal of medical genetics | 1999-08-20 | PMID 10402491
Murakami N, Kitamura N, Kajimoto Y and 8 more
Genes: SPTAN1
Dopamine D2 receptor gene not associated with symptomatology of mood disorders.
American journal of medical genetics | 1999-08-20 | PMID 10402492
Serretti A, Smeraldi E
Genes: DRD2
Association study of schizophrenia among Indian families.
American journal of medical genetics | 1999-08-20 | PMID 10402493
Prasad S, Deshpande S N, Bhatia T and 3 more
Genes: DRD3
Novel polymorphism in the promoter region of the tumor necrosis factor alpha gene: No association with narcolepsy.
American journal of medical genetics | 1999-08-20 | PMID 10402494
Kato T, Honda M, Kuwata S and 5 more
Genes: TNF
Association analysis of exonic variants of the gene encoding the GABAB receptor and idiopathic generalized epilepsy.
American journal of medical genetics | 1999-08-20 | PMID 10402495
Sander T, Peters C, Kämmer G and 8 more
DNA polymorphism-diet-cofactor-development hypothesis and the gene-teratogen model for schizophrenia and other developmental disorders.
American journal of medical genetics | 1999-08-20 | PMID 10402496
Johnson W G
Analysis of GNAZ gene polymorphism in bipolar affective disorder.
American journal of medical genetics | 1999-08-20 | PMID 10402497
Saito T, Papolos D F, Chernak D and 3 more
Genes: GNAZ
Follow-up study on a susceptibility locus for schizophrenia on chromosome 6q.
American journal of medical genetics | 1999-08-20 | PMID 10402499
Martinez M, Goldin L R, Cao Q and 16 more
Apo E genotypes and risk of dementia in Down syndrome.
American journal of medical genetics | 1999-08-20 | PMID 10402500
Rubinsztein D C, Hon J, Stevens F and 5 more
Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21.
American journal of medical genetics | 1999-08-20 | PMID 10402501
Antonarakis S E, Blouin J L, Lasseter V K and 11 more
Genes: KCNN3
Trend for an association between schizophrenia and D3S1310, a marker in proximity to the dopamine D3 receptor gene.
American journal of medical genetics | 1999-08-20 | PMID 10402502
Jönsson E G, Nimgaonkar V L, Zhang X R and 5 more
Genes: DRD3
Studies of the 48 bp repeat polymorphism of the DRD4 gene in impulsive, compulsive, addictive behaviors: Tourette syndrome, ADHD, pathological gambling, and substance abuse.
American journal of medical genetics | 1999-08-20 | PMID 10402503
Comings D E, Gonzalez N, Wu S and 10 more
Genes: DRD4
Linkage analysis of a large Swedish kindred provides further support for a susceptibility locus for schizophrenia on chromosome 6p23.
American journal of medical genetics | 1999-08-20 | PMID 10402504
Lindholm E, Ekholm B, Balciuniene J and 7 more
Heritability of event-related brain potentials in families with a history of alcoholism.
American journal of medical genetics | 1999-08-20 | PMID 10402506
Almasy L, Porjesz B, Blangero J and 8 more
-141 C del/ins polymorphism of the dopamine receptor 2 gene is associated with schizophrenia in a British population.
American journal of medical genetics | 1999-08-20 | PMID 10402509
Breen G, Brown J, Maude S and 6 more
Genes: DRD2
HLA and schizophrenia: refutation of reported associations with A9 (A23/A24), DR4, and DQbeta1*0602.
American journal of medical genetics | 1999-08-20 | PMID 10402511
Gibson S, Hawi Z, Straub R E and 3 more
Schizophrenia and HLA: No association with PCR-SSOP typed classical loci in a large Irish familial sample.
American journal of medical genetics | 1999-08-20 | PMID 10402512
Hawi Z, Gibson S, Straub R E and 3 more
No association between serotonin transporter gene polymorphisms and personality traits.
American journal of medical genetics | 1999-08-20 | PMID 10402513
Gustavsson J P, Nöthen M M, Jönsson E G and 7 more
Genome scan for linkage to Gilles de la Tourette syndrome.
American journal of medical genetics | 1999-08-20 | PMID 10402514
Barr C L, Wigg K G, Pakstis A J and 5 more
Proton MR spectroscopy in a child with pyruvate dehydrogenase complex deficiency.
Magnetic resonance imaging | 1999-07-01 | PMID 10402601
Rubio-Gozalbo M E, Heerschap A, Trijbels J M and 3 more
tip genes act in parallel pathways of early Dictyostelium development.
Developmental genetics | 1999-01-01 | PMID 10402673
Stege J T, Laub M T, Loomis W F