Aspergillus fumigatusConidia Induce a Th1‐Type Cytokine Response
1997-12-01 | PMID 9395370
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 9865 of 10600
Mutations in<i>Plasmodium falciparum</i>Dihydrofolate Reductase and Dihydropteroate Synthase and Epidemiologic Patterns of Pyrimethamine‐Sulfadoxine Use and Resistance
1997-12-01 | PMID 9395372
An Outbreak of Foodborne Illness Caused by<i>Escherichia coli</i>O39:NM, an Agent Not Fitting into the Existing Scheme for Classifying Diarrheogenic<i>E. coli</i>
1997-12-01 | PMID 9395379
DNA methylation directs a time-dependent repression of transcription initiation
1997-03-01 | PMID 9395433
Two NFAT Transcription Factor Binding Sites Participate in the Regulation of CD95 (Fas) Ligand Expression in Activated Human T Cells
1997-12-01 | PMID 9395475
Structural Analysis of the Human BIN1 Gene
1997-12-01 | PMID 9395479
Cloning and Targeted Deletion of the Mouse Fetuin Gene
1997-12-01 | PMID 9395485
Diagnostic molecular genetics.
Advances in veterinary medicine | 1997-01-01 | PMID 9395730
Sack G H
Overexpression of Protein Tyrosine Kinases in Human Esophageal Cancer
2008-10-08 | PMID 9396043
Abundance and Location of the Small Heat Shock Proteins HSP25 and αB-Crystallin in Rat and Human Heart
1997-11-18 | PMID 9396443
Chinese hamster ovary cells lacking GM1 and GD1a synthesize gangliosides upon transfection with human GM2 synthase
1997-11-01 | PMID 9396632
Mechanisms of Action of Anti‐GM<sub>1</sub>and Anti‐GQ<sub>1b</sub>Ganglioside Antibodies in Guillain‐Barré Syndrome
1997-12-01 | PMID 9396699
Molecular Mimicry between Gangliosides and Lipopolysaccharides of<i>Campylobacter jejuni</i>Isolated from Patients with Guillain‐Barré Syndrome and Miller Fisher Syndrome
1997-12-01 | PMID 9396700
The Role of Cytokines in Schwann Cell Damage, Protection, and Repair
1997-12-01 | PMID 9396706
Key Role of the <i>Cdx2</i> Homeobox Gene in Extracellular Matrix–mediated Intestinal Cell Differentiation
1997-12-15 | PMID 9396760
Heredity and prostate cancer: A study of World War II veteran twins
1997-12-01 | PMID 9397195
HpaII-polymorphism of the atrial-natriuretic-peptide gene and essential hypertension in whites.
American journal of hypertension | 1997-11-01 | PMID 9397256
Beige J, Ringel J, Hohenbleicher H and 3 more
Detection of tumour DNA in serum of colorectal cancer patients
1997-01-01 | PMID 9397491
Multiple levels of control of insulin-like growth factor gene expression
1994-05-01 | PMID 9397969
Up-regulation of Fas (CD95) in human p53wild-type cancer cells treated with ionizing radiation
1997-11-27 | PMID 9398058
Altered Ligand Binding Properties and Enhanced Stability of a Constitutively Active Estrogen Receptor: Evidence That an Open Pocket Conformation Is Required for Ligand Interaction
1997-12-01 | PMID 9398213
Cloning of cDNAs Encoding G Protein-Coupled Receptor Expressed in Human Endothelial Cells Exposed to Fluid Shear Stress
1997-11-01 | PMID 9398636
Inhibin B as a Serum Marker of Spermatogenesis: Correlation to Differences in Sperm Concentration and Follicle-Stimulating Hormone Levels. A Study of 349 Danish Men<sup>1</sup>
1997-12-01 | PMID 9398713
Sporadic Pheochromocytomas Are Rarely Associated with Germline Mutations in the<i>vhl</i>Tumor Suppressor Gene or the<i>ret</i>Protooncogene<sup>1</sup>
1997-12-01 | PMID 9398721
A Novel Point Mutation in the Intracellular Domain of the<i>ret</i>Protooncogene in a Family with Medullary Thyroid Carcinoma<sup>1</sup>
1997-12-01 | PMID 9398735
Identification of a New Thyrotropin Receptor Germline Mutation (Leu629Phe) in a Family with Neonatal Onset of Autosomal Dominant Nonautoimmune Hyperthyroidism
1997-12-01 | PMID 9398746
Human Estrogen Receptor β-Gene Structure, Chromosomal Localization, and Expression Pattern1
1997-12-01 | PMID 9398750
Genetic control of blood parasitaemia in mouse malaria maps to chromosome 8
1997-12-01 | PMID 9398835
Mutation in hepatocyte nuclear factor-1 beta gene (TCF2) associated with MODY.
Nature genetics | 1997-12-01 | PMID 9398836
Horikawa Y, Iwasaki N, Hara M and 11 more
An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains.
Nature genetics | 1997-12-01 | PMID 9398840
Genes: AIRE
Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation
1997-12-01 | PMID 9398843
Urokinase-generated plasmin activates matrix metalloproteinases during aneurysm formation
1997-12-01 | PMID 9398846
EWS/FLI1-induced manic fringe renders NIH 3T3 cells tumorigenic
1997-12-01 | PMID 9398859
Hereditary kidney diseases. Introduction.
Contributions to nephrology | 1997-01-01 | PMID 9399028
Sessa A, Conte F, Meroni M and 1 more
Pathogenesis of autosomal dominant polycystic kidney disease: recent developments.
Contributions to nephrology | 1997-01-01 | PMID 9399029
Grantham J J
Autosomal recessive polycystic kidney disease.
Contributions to nephrology | 1997-01-01 | PMID 9399030
Zerres K, Becker J, Mücher G and 1 more
Prevalence of hypertension according to phenotype and gender in autosomal-dominant polycystic kidney disease.
Contributions to nephrology | 1997-01-01 | PMID 9399031
Boulahrouz R, Mazeau P, Charasse C and 4 more
Mutations and intragenic polymorphisms in the diagnosis of autosomal dominant polycystic kidney disease type 1.
Contributions to nephrology | 1997-01-01 | PMID 9399037
Badenas C, Torra R, Darnell A and 1 more
Molecular genetic investigations in autosomal dominant polycystic kidney disease. Gene Mutation detection, linkage analysis, and preliminary ACE gene I/D polymorphism association studies: an update.
Contributions to nephrology | 1997-01-01 | PMID 9399039
Turco A E, Bresin E, Rossetti S and 10 more
Genes: ACE
The TSC2/PKD1 contiguous gene syndrome.
Contributions to nephrology | 1997-01-01 | PMID 9399043
Harris P C
Genes: PKD1, TSC2
A tuberous sclerosis patient with a large TSC2 and PKD1 gene deletion shows extrarenal signs of autosomal dominant polycystic kidney disease.
Contributions to nephrology | 1997-01-01 | PMID 9399046
Longa L, Brusco A, Carbonara C and 6 more
Genes: PKD1, TSC2
Tuberous sclerosis complex and early-onset autosomal dominant polycystic kidney disease as a 'contiguous gene' syndrome: report of a case.
Contributions to nephrology | 1997-01-01 | PMID 9399047
Mancino C, Balducci A
The kidney and von Hippel-Lindau disease: impact of molecular genetic analysis of the VHL gene for clinical management.
Contributions to nephrology | 1997-01-01 | PMID 9399049
Neumann H P, Bender B U, Schultze-Seemann W and 8 more
Genes: VHL
Von Hippel-Lindau (VHL) gene analysis in Italian families with VHL disease.
Contributions to nephrology | 1997-01-01 | PMID 9399050
Montera M, Bellone E, Ajmar F and 1 more
Genes: VHL
Alport syndrome: clinical and genetic correlation in a type-IV collagen disease.
Contributions to nephrology | 1997-01-01 | PMID 9399052
Netzer K O, Gross O, Jung C and 4 more
Clinical and molecular diagnosis in inherited kidney diseases: three examples.
Contributions to nephrology | 1997-01-01 | PMID 9399053
Grünfeld J P, Lesavre P, Richard S
Expression of alpha (IV) chains in Alport's syndrome and its correlation with ultrastructural and genetic data.
Contributions to nephrology | 1997-01-01 | PMID 9399054
Mazzucco G, Barsotti P, Onetti Muda A and 4 more
Molecular diagnosis of Alport syndrome: the experience in Siena.
Contributions to nephrology | 1997-01-01 | PMID 9399055
Renieri A, Bruttini M, Piccini M and 8 more
Kidney transplantation in Alport's syndrome.
Contributions to nephrology | 1997-01-01 | PMID 9399057
Scolari F, Valzorio B, Fasciolo F and 7 more
Primary hyperoxaluria.
Contributions to nephrology | 1997-01-01 | PMID 9399058
Watts R W
Cystinuria: recent advances in pathophysiology and genetics.
Contributions to nephrology | 1997-01-01 | PMID 9399061
Bruno M, Marangella M
Kidney involvement in Anderson-Fabry disease.
Contributions to nephrology | 1997-01-01 | PMID 9399062
Meroni M, Sessa A, Battini G and 2 more
Frequency of familial inheritance among 488 index patients with idiopathic focal dystonia and clinical variability in a large family
1997-11-01 | PMID 9399227
Molecular tracking of Candida albicans in a neonatal intensive care unit: long-term colonizations versus catheter-related infections
1997-12-01 | PMID 9399489
Racial tropism of a highly toxic clone of Actinobacillus actinomycetemcomitans associated with juvenile periodontitis
1997-12-01 | PMID 9399490
Multicenter evaluation of the updated and extended API (RAPID) Coryne database 2.0
1997-12-01 | PMID 9399506
Specific identification of Mycobacterium tuberculosis with the luciferase reporter mycobacteriophage: use of p-nitro-alpha-acetylamino-beta-hydroxy propiophenone
1997-12-01 | PMID 9399524
Coexistence of Ehrlichia phagocytophila and Borrelia burgdorferi sensu lato in Ixodes ricinus ticks from Italy as determined by 16S rRNA gene sequencing
1997-12-01 | PMID 9399564
Factor V Leiden mutation presenting as repeated massive GI hemorrhages secondary to venous thrombosis.
The American journal of gastroenterology | 1997-12-01 | PMID 9399782
Lynch J P, Rosato E F, Kochman M L
The factor VIII Structure and Mutation Resource Site: HAMSTeRS version 4
1998-01-01 | PMID 9399839
Cloning of the Human Carnitine-Acylcarnitine Carrier cDNA and Identification of the Molecular Defect in a Patient
1997-12-01 | PMID 9399886
Identification of an interstitial deletion in an adult female with schizophrenia, mental retardation, and dysmorphic features: further support for a putative schizophrenia-susceptibility locus at 5q21-23.1.
American journal of human genetics | 1997-12-01 | PMID 9399892
Bennett R L, Karayiorgou M, Sobin C A and 2 more
Localization of the Gene for Thiamine-Responsive Megaloblastic Anemia Syndrome, on the Long Arm of Chromosome 1, by Homozygosity Mapping
1997-12-01 | PMID 9399900
Skewed X-Chromosome Inactivation Is Common in Fetuses or Newborns Associated with Confined Placental Mosaicism
1997-12-01 | PMID 9399909
Genomic imprinting: a chromatin connection.
American journal of human genetics | 1997-12-01 | PMID 9399913
Feil R, Kelsey G
Dynamic interrelationships between DNA replication, methylation, and repair.
American journal of human genetics | 1997-12-01 | PMID 9399916
Robertson K D, Jones P A
Aberrant nuclear factor-kappaB/Rel expression and the pathogenesis of breast cancer.
1997-12-15 | PMID 9399940
Constitutive nuclear factor-kappaB-RelA activation is required for proliferation and survival of Hodgkin's disease tumor cells.
1997-12-15 | PMID 9399941
Lung disease in mice with cystic fibrosis.
1997-12-15 | PMID 9399953
TERATOMA WITH MALIGNANT TRANSFORMATION: DIVERSE MALIGNANT HISTOLOGIES ARISING IN MEN WITH GERM CELL TUMORS
1998-01-01 | PMID 9400455
POLYMERASE CHAIN REACTION AMPLIFICATION OF BACTERIAL 16S rRNA GENES IN INTERSTITIAL CYSTITIS AND CONTROL PATIENT BLADDER BIOPSIES
1998-01-01 | PMID 9400495
Human herpesvirus 8 variants in sarcoid tissues
1997-12-01 | PMID 9400509
Lymphocyte Phenotyping in Infants: Maturation of Lymphocyte Subpopulations and the Effects of HIV Infection
1997-12-01 | PMID 9400627
ErbB kinases and NDF signaling in human prostate cancer cells
1997-11-27 | PMID 9400997
Cloning of the RHO1 gene from Candida albicans and its regulation of beta-1,3-glucan synthesis
1997-12-01 | PMID 9401032
Physiological function of receptor-SH2 interactions.
Current topics in microbiology and immunology | 1998-01-01 | PMID 9401206
Ponzetto C
Influence of a secondary genetic factor in cystic fibrosis genotype-phenotype correlations.
Monaldi archives for chest disease = Archivio Monaldi per le malattie del torace | 1997-08-01 | PMID 9401373
Luisetti M
Stage‐specific degeneration of germ cells in the seminiferous tubules of non‐obese diabetic mice
1997-08-01 | PMID 9401828
Congenital nephrogenic diabetes insipidus.
Journal of the American Society of Nephrology : JASN | 1997-12-01 | PMID 9402099
Bichet D G, Oksche A, Rosenthal W
t(11;18)(q21;q21) is the most common translocation in MALT lymphomas
1997-10-01 | PMID 9402171
Utilization of retrieved oocytes as an index of the efficiency of superovulation strategies for in-vitro fertilization treatment
1997-10-01 | PMID 9402267
Immunomodulation by human seminal plasma: a benefit for spermatozoon and pathogen?
1997-10-01 | PMID 9402282
Apoptosis of germ cells during human prenatal oogenesis
1997-10-01 | PMID 9402287
The chromosomal constitution of multipronuclear zygotes resulting from in-vitro fertilization
1997-10-01 | PMID 9402291
Mitotic chromosomal anomalies among infertile men
1997-10-01 | PMID 9402306
Recovery of small colony variants of Staphylococcus aureus following gentamicin bead placement for osteomyelitis.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | 1997-11-01 | PMID 9402396
von Eiff C, Bettin D, Proctor R A and 4 more
Identification by polymerase chain reaction fingerprinting ofCryptococcus neoformansserotype AD
1997-01-01 | PMID 9402529
Detection of plasma (1 → 3)-β- d -glucan in patients withFusarium, Trichosporon, SaccharomycesandAcremoniumfungaemias
1997-01-01 | PMID 9402532
To be a mutator, or how pathogenic and commensal bacteria can evolve rapidly.
Trends in microbiology | 1997-11-01 | PMID 9402695
Taddei F, Matic I, Godelle B and 1 more
Automated capillary electrophoresis in the genotyping of apolipoprotein E.
Genomics | 1997-11-15 | PMID 9403075
Sell S M, Ren K
[The metabolic syndrome].
Der Internist | 1995-05-01 | PMID 9403089
Effect of CCR2 and CCR5 variants on HIV disease: abstract and commentary.
JAMA | 1997-12-17 | PMID 9403430
Collman R G
Genes: CCR2, CCR5
Spinocerebellar ataxia type 6: CAG repeat expansion in α<sub>1a</sub> voltage‐dependent calcium channel gene and clinical variations in japanese population
1997-12-01 | PMID 9403480
Mapping of a second locus for familial hemiplegic migraine to 1q21–q23 and evidence of further heterogeneity
1997-12-01 | PMID 9403481
Modulation of Growth Factor Action
1997-12-02 | PMID 9403634
Neuroblastoma and related tumors in Turner’s syndrome
1997-11-01 | PMID 9403643
Heavy prenatal alcohol exposure with or without physical features of fetal alcohol syndrome leads to IQ deficits
1997-11-01 | PMID 9403652
Genetic polymorphism of plasminogen in dairy cattle.
The Journal of dairy research | 1997-11-01 | PMID 9403775
Wang W, Turner J D, Robitaille G
Antirotaviral activity of milk proteins: lactoferrin prevents rotavirus infection in the enterocyte-like cell line HT-29
1997-10-30 | PMID 9403835
The transmission dynamics of antibiotic–resistant bacteria: the relationship between resistance in commensal organisms and antibiotic consumption
1997-11-22 | PMID 9404026