Hepatic lymphoid aggregates in chronic hepatitis C and mixed cryoglobulinemia.
Springer seminars in immunopathology | 1997-01-01 | PMID 9266634
Monteverde A, Ballarè M, Pileri S
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 884 of 10600
The etiology and pathophysiology of mixed cryoglobulinemia secondary to hepatitis C virus infection.
Springer seminars in immunopathology | 1997-01-01 | PMID 9266635
Agnello V
Genes: LDLR
Structural characterization of four genetic variants of human serum albumin associated with alloalbuminemia in Italy.
European journal of biochemistry | 1997-07-15 | PMID 9266687
Minchiotti L, Watkins S, Madison J and 6 more
The solution structure and activity of caerin 1.1, an antimicrobial peptide from the Australian green tree frog, Litoria splendida.
European journal of biochemistry | 1997-07-15 | PMID 9266696
Wong H, Bowie J H, Carver J A
Dimerization of Cdc25p, the guanine-nucleotide exchange factor for Ras from Saccharomyces cerevisiae, and its interaction with Sdc25p.
European journal of biochemistry | 1997-07-15 | PMID 9266716
Camus C, Geymonat M, Garreau H and 2 more
Familial spongiform encephalopathy associated with a novel prion protein gene mutation.
Annals of neurology | 1997-08-01 | PMID 9266722
Nitrini R, Rosemberg S, Passos-Bueno M R and 8 more
A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey.
Annals of neurology | 1997-08-01 | PMID 9266733
Dinçer P, Leturcq F, Richard I and 16 more
Origin of pleural cells after lung transplantation: from donor or recipient?
Chest | 1997-08-01 | PMID 9266879
Judson M A, Sahn S A, Hahn A B
A variant of the EPB3 gene of the anti-Lepore type in hereditary spherocytosis.
British journal of haematology | 1997-08-01 | PMID 9266920
Bianchi P, Zanella A, Alloisio N and 8 more
Genes: SDS
Paroxysmal nocturnal haemoglobinuria due to an 88 bp direct tandem repeat insertion in the PIG-A gene.
British journal of haematology | 1997-08-01 | PMID 9266921
Pavlu J, Mortazavi Y, Tooze J and 3 more
Structural analysis of a missense mutation (Val414Phe) in the catalytic core domain of the factor XIII(A) subunit.
British journal of haematology | 1997-08-01 | PMID 9266932
Aslam S, Yee V C, Narayanan S and 2 more
Specificity and sensitivity of RHD genotyping methods by PCR-based DNA amplification.
British journal of haematology | 1997-08-01 | PMID 9266934
Aubin J T, Le Van Kim C, Mouro I and 4 more
Genes: RHD, RHCE
A human monoclonal anti-D antibody which detects a nonconformation-dependent epitope on the RhD protein by immunoblot.
British journal of haematology | 1997-08-01 | PMID 9266935
Apoil P A, Reid M E, Halverson G and 5 more
Genes: RHD, RHCE
Increased frequency of somatic mutations at glycophorin A loci in patients with aplastic anaemia, myelodysplastic syndrome and paroxysmal nocturnal haemoglobinuria.
British journal of haematology | 1997-08-01 | PMID 9266937
Hattori H, Machii T, Ueda E and 3 more
Mutations of thyrotropin receptor isolated from thyroid autonomous functioning adenomas confer TSH-independent growth to thyroid cells.
Oncogene | 1997-08-14 | PMID 9266964
Porcellini A, Ruggiano G, Pannain S and 4 more
Biochemical characterization of C3G: an exchange factor that discriminates between Rap1 and Rap2 and is not inhibited by Rap1A(S17N).
Oncogene | 1997-08-14 | PMID 9266971
van den Berghe N, Cool R H, Horn G and 1 more
Random selection: a model for poliovirus infection of the central nervous system.
The Journal of general virology | 1997-08-01 | PMID 9266975
Georgescu M M, Balanant J, Ozden S and 1 more
Human immunodeficiency virus type 1 Rev- and Tat-specific cytotoxic T lymphocyte frequencies inversely correlate with rapid progression to AIDS.
The Journal of general virology | 1997-08-01 | PMID 9266987
van Baalen C A, Pontesilli O, Huisman R C and 6 more
PHYL acts to down-regulate TTK88, a transcriptional repressor of neuronal cell fates, by a SINA-dependent mechanism.
Cell | 1997-08-08 | PMID 9267026
Tang A H, Neufeld T P, Kwan E and 1 more
Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) in a Donegal kindred--clinical features and molecular genetic analysis.
Irish medical journal | 2000-01-01 | PMID 9267093
McEntagart M, Droogan O, Burke M and 3 more
Strains of Drosophila melanogaster differ in alcohol tolerance.
Hereditas | 1997-01-01 | PMID 9267180
Bokor K, Pecsenye K
Apolipoprotein E genotyping by capillary electrophoretic analysis of restriction fragments.
Clinical chemistry | 1997-08-01 | PMID 9267308
de Bellis G, Salani G, Panigone S and 3 more
A homogeneous method for genotyping with fluorescence polarization.
Clinical chemistry | 1997-08-01 | PMID 9267310
Gibson N J, Gillard H L, Whitcombe D and 3 more
Study by ribosomal DNA ITS 2 sequencing and RAPD analysis on the systematics of four Metastrongylus species (Nematoda:Metastrongyloidea).
The Journal of parasitology | 1997-08-01 | PMID 9267399
Leignel V, Humbert J F, Elard L
A suicide vector for allelic recombination involving the gene for glutamate 1-semialdehyde aminotransferase in the cyanobacterium Synechococcus PCC 7942.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9267435
Allison G, Gough K, Rogers L and 1 more
The MBR1 gene from Saccharomyces cerevisiae is activated by and required for growth under sub-optimal conditions.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9267436
Reisdorf P, Boy-Marcotte E, Bolotin-Fukuhara M
Mutational analysis of the Streptomyces lividans recA gene suggests that only mutants with residual activity remain viable.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9267438
Muth G, Frese D, Kleber A and 1 more
Use of allele specificity of comigrating AFLP markers to align genetic maps from different potato genotypes.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9267440
Rouppe van der Voort J N, van Zandvoort P, van Eck H J and 7 more
Genetic variation in the VP7 gene of human rotavirus serotype 3 (G3 type) isolated in China and Japan.
Archives of virology | 1997-01-01 | PMID 9267457
Wen L, Nakayama M, Yamanishi Y and 8 more
Quick method for confirmation of quantitative trait loci.
Alcoholism, clinical and experimental research | 1997-08-01 | PMID 9267523
Bennett B, Beeson M, Gordon L and 1 more
Fear-potentiated startle in two strains of inbred mice.
Behavioral neuroscience | 1997-08-01 | PMID 9267664
Falls W A, Carlson S, Turner J G and 1 more
The impact of T-cell depletion on the effects of HLA DR beta 1 and DQ beta allele matching in HLA serologically identical unrelated donor bone marrow transplantation.
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation | 1997-06-01 | PMID 9267667
Gajewski J, Gjertson D, Cecka M and 20 more
Polymerase chain reaction-based technique for the selective enrichment and analysis of mosaic arg201 mutations in G alpha s from patients with fibrous dysplasia of bone.
Bone | 1997-08-01 | PMID 9267696
Candeliere G A, Roughley P J, Glorieux F H
Fast 5-hour determination of angiotensin-converting enzyme genotypes from blood by SDS-PAGE using PhastSystem.
Clinica chimica acta; international journal of clinical chemistry | 1997-08-08 | PMID 9267703
Huang X H, Koivula T, Ilveskoski E and 5 more
Genes: ACE, SDS
Changes in phenotypes of apolipoprotein E and apolipoprotein(a) in liver transplant recipients.
Clinical transplantation | 1997-08-01 | PMID 9267723
Fernández-Miranda C, Cancelas P, de la Calle A and 4 more
Prevalence of hepatitis C virus antibodies and evaluation of hepatitis C virus genotypes in patients with lichen planus.
Dermatology (Basel, Switzerland) | 1997-01-01 | PMID 9267728
Imhof M, Popal H, Lee J H and 2 more
Cancer proneness of linear porokeratosis may be explained by allelic loss.
Dermatology (Basel, Switzerland) | 1997-01-01 | PMID 9267731
Happle R
Acetylator phenotype in patients with p-phenylenediamine allergy.
Dermatology (Basel, Switzerland) | 1997-01-01 | PMID 9267736
Kawakubo Y, Nakamori M, Schöpf E and 1 more
Epidermolysis bullosa pruriginosa.
Dermatology (Basel, Switzerland) | 1997-01-01 | PMID 9267744
Cambiaghi S, Brusasco A, Restano L and 2 more
Steatocystoma multiplex and oligosymptomatic pachyonychia congenita of the Jackson-Sertoli type.
Dermatology (Basel, Switzerland) | 1997-01-01 | PMID 9267753
Hohl D
Prostate cancer: indicators of aggressiveness.
European urology | 1997-01-01 | PMID 9267782
Sakr W A, Grignon D J
Serum-free culture of mouse tracheal epithelial cells.
Experimental lung research | 2000-01-01 | PMID 9267797
Kumar R K, Maronese S E, O'Grady R
High-resolution physical and transcriptional mapping of the autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy locus on chromosome 21q22.3 by FISH.
Genome research | 1997-08-01 | PMID 9267805
Aaltonen J, Horelli-Kuitunen N, Fan J B and 5 more
Genes: PGD
Problems and potential for gene therapy in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD | 1997-07-01 | PMID 9267845
Kakulas B A
Genes: DMD
Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?
Neuromuscular disorders : NMD | 1997-07-01 | PMID 9267847
Wilton S D, Dye D E, Blechynden L M and 1 more
Genes: DMD
A splice-site mutation causing ovine McArdle's disease.
Neuromuscular disorders : NMD | 1997-07-01 | PMID 9267848
Tan P, Allen J G, Wilton S D and 3 more
Positive association between the GABRA5 gene and unipolar recurrent major depression.
Neuropsychobiology | 1997-01-01 | PMID 9267853
Oruc L, Verheyen G R, Furac I and 4 more
Genes: GABRA5
Chromosomal mapping and mutational analysis of the coding region of the glycogen synthase kinase-3alpha and beta isoforms in patients with NIDDM.
Diabetologia | 1997-08-01 | PMID 9267989
Hansen L, Arden K C, Rasmussen S B and 6 more
A missense mutation of the muscle glycogen synthase gene (M416V) is associated with insulin resistance in the Japanese population.
Diabetologia | 1997-08-01 | PMID 9267990
Shimomura H, Sanke T, Ueda K and 3 more
Genes: GYS1
The beta cell glucokinase promoter variant is an unlikely risk factor for diabetes mellitus. Diabetes Incidence Study in Sweden (DISS).
Diabetologia | 1997-08-01 | PMID 9267992
Lotfi K, Sund G, Lowe R and 5 more
Allelic variation in the vitamin D receptor influences susceptibility to IDDM in Indian Asians.
Diabetologia | 1997-08-01 | PMID 9267994
McDermott M F, Ramachandran A, Ogunkolade B W and 5 more
Molecular screening of the human melanocortin-4 receptor gene: identification of a missense variant showing no association with obesity, plasma glucose, or insulin.
Diabetologia | 1997-08-01 | PMID 9267995
Gotoda T, Scott J, Aitman T J
Studies of the genetic variability of the coding region of the hepatocyte nuclear factor-4alpha in Caucasians with maturity onset NIDDM.
Diabetologia | 1997-08-01 | PMID 9267996
Møller A M, Urhammer S A, Dalgaard L T and 6 more
The Aspergillus nidulans lysF gene encodes homoaconitase, an enzyme involved in the fungus-specific lysine biosynthesis pathway.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9268014
Weidner G, Steffan B, Brakhage A A
Double-strand breaks increase the incidence of genetic deletion associated with intermolecular recombination in bacteriophage T7.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9268018
Yang Y, Masker W
Heat stress transcription factors from tomato can functionally replace HSF1 in the yeast Saccharomyces cerevisiae.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9268023
Boscheinen O, Lyck R, Queitsch C and 3 more
Genes: HSF1
Characterisation of the Schizosaccharomyces pombe rad4/cut5 mutant phenotypes: dissection of DNA replication and G2 checkpoint control function.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9268024
McFarlane R J, Carr A M, Price C
Genes: ATM
Cloning and characterization of the lipoyl-protein ligase gene LIPB from the yeast Kluyveromyces lactis: synergistic respiratory deficiency due to mutations in LIPB and mitochondrial F1-ATPase subunits.
Molecular & general genetics : MGG | 1997-07-01 | PMID 9268025
Chen X J
Genes: LIPB
Mutagenicity of cyclopenta-fused polynuclear aromatic hydrocarbons and a non-polar fraction from a fuel combustion sample in a Salmonella forward mutation assay without exogenous metabolic activation.
Mutation research | 1997-07-14 | PMID 9268036
Busby W F, Smith H, Plummer E F and 5 more
Genes: PAH
Metabolic activation of meta-phenylenediamine by the alga Chlamydomonas reinhardtii.
Mutation research | 1997-07-14 | PMID 9268039
Vlcek D, Miadoková E, Vlckova V and 2 more
Assessment of the in vivo mutagenicity of ethylene oxide in the tissues of B6C3F1 lacI transgenic mice following inhalation exposure.
Mutation research | 1997-07-14 | PMID 9268040
Sisk S C, Pluta L J, Meyer K G and 2 more
MODED: microcephaly-oculo-digito-esophageal-duodenal syndrome.
American journal of medical genetics | 1997-08-22 | PMID 9268091
Frydman M, Katz M, Cabot S G and 3 more
Novel case of del(17)(q23.1q23.3) further highlights a recognizable phenotype involving deletions of chromosome (17)(q21q24).
American journal of medical genetics | 1997-08-22 | PMID 9268095
Mickelson E C, Robinson W P, Hrynchak M A and 1 more
Exclusion of BMP6 as a candidate gene for cleidocranial dysplasia.
American journal of medical genetics | 1997-08-22 | PMID 9268099
Innis J W, Asher J H, Liang Y and 7 more
Genes: BMP6
Intersitial deletion of 20p: new candidate region for Hirschsprung disease and autism?
American journal of medical genetics | 1997-08-22 | PMID 9268100
Michaelis R C, Skinner S A, Deason R and 3 more
Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1.
American journal of medical genetics | 1997-08-22 | PMID 9268104
Caggana M, Ashley G A, Desnick R J and 1 more
Molecular analysis of the L1CAM gene in patients with X-linked hydrocephalus demonstrates eight novel mutations and suggests non-allelic heterogeneity of the trait.
American journal of medical genetics | 1997-08-22 | PMID 9268105
Gu S M, Orth U, Zankl M and 2 more
Are Melnick-Needles syndrome and oto-palato-digital syndrome type II allelic? Observations in a four-generation kindred.
American journal of medical genetics | 1997-08-22 | PMID 9268106
Robertson S, Gunn T, Allen B and 2 more
Progressive diaphyseal dysplasia: a three-generation family with markedly variable expressivity.
American journal of medical genetics | 1997-08-22 | PMID 9268107
Saraiva J M
Proximal interstitial 6q deletion: a recognizable syndrome.
American journal of medical genetics | 1997-08-22 | PMID 9268108
Kumar R, Riordan D, Dawson A J and 1 more
Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted region.
American journal of medical genetics | 1997-08-22 | PMID 9268110
Robin N H, Harari-Shacham A, Schwartz S and 1 more
Mutation producing alternative splicing of exon 26 in the COL1A2 gene causes type IV osteogenesis imperfecta with intrafamilial clinical variability.
American journal of medical genetics | 1997-08-22 | PMID 9268111
Zolezzi F, Valli M, Clementi M and 4 more
Mutational analyses support a model for the HRV2 2A proteinase.
Virology | 1997-08-04 | PMID 9268151
Sommergruber W, Seipelt J, Fessl F and 3 more
Persistence and evolution of feline coronavirus in a closed cat-breeding colony.
Virology | 1997-08-04 | PMID 9268167
Herrewegh A A, Mähler M, Hedrich H J and 5 more
Double-stranded RNA-dependent protein kinase (PKR) is regulated by reovirus structural proteins.
Virology | 1997-08-04 | PMID 9268168
Yue Z, Shatkin A J
The VITA project: phenotypic resistance to activated protein C and FV Leiden mutation in the general population. Vicenza Thrombophilia and Atherosclerosis.
Thrombosis and haemostasis | 1997-08-01 | PMID 9268185
Tosetto A, Missiaglia E, Gatto E and 1 more
Genes: APC, ABO
Detection of three transthyretin gene mutations in familial amyloidotic polyneuropathy by analysis of DNA extracted from formalin-fixed and paraffin-embedded tissues.
Journal of the neurological sciences | 1997-09-10 | PMID 9268242
Date Y, Nakazato M, Kangawa K and 3 more
Genes: TTR, FAP
Significance of individual point mutations, T202C and C314T, in the human Lewis (FUT3) gene for expression of Lewis antigens by the human alpha(1,3/1,4)-fucosyltransferase, Fuc-TIII.
The Journal of biological chemistry | 1997-08-29 | PMID 9268337
Elmgren A, Mollicone R, Costache M and 4 more
Genes: FUT3
Axon tracts correlate with netrin-1a expression in the zebrafish embryo.
Molecular and cellular neurosciences | 1997-01-01 | PMID 9268507
Lauderdale J D, Davis N M, Kuwada J Y
Model systems for the study of kidney development: use of the pronephros in the analysis of organ induction and patterning.
Developmental biology | 1997-08-15 | PMID 9268568
Vize P D, Seufert D W, Carroll T J and 1 more
Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4.
Developmental biology | 1997-08-15 | PMID 9268572
Dunn N R, Winnier G E, Hargett L K and 3 more
Different MRF4 knockout alleles differentially disrupt Myf-5 expression: cis-regulatory interactions at the MRF4/Myf-5 locus.
Developmental biology | 1997-08-15 | PMID 9268580
Yoon J K, Olson E N, Arnold H H and 1 more
Evaluation of the rhodopsin kinase gene in patients with retinitis pigmentosa.
Experimental eye research | 1997-08-01 | PMID 9268593
Yamamoto S, Khani S C, Berson E L and 1 more
Obesity QTLs on mouse chromosomes 2 and 17.
Genomics | 1997-08-01 | PMID 9268627
Taylor B A, Phillips S J
Characterization of the C3 YAC contig from proximal mouse chromosome 17 and analysis of allelic expression of genes flanking the imprinted Igf2r gene.
Genomics | 1997-08-01 | PMID 9268631
Schweifer N, Valk P J, Delwel R and 5 more
Three modified nucleosides present in the anticodon stem and loop influence the in vivo aa-tRNA selection in a tRNA-dependent manner.
Journal of molecular biology | 1997-08-15 | PMID 9268653
Li J, Esberg B, Curran J F and 1 more
NMR structural studies of human cystatin C dimers and monomers.
Journal of molecular biology | 1997-08-15 | PMID 9268658
Ekiel I, Abrahamson M, Fulton D B and 9 more
Amide hydrogen exchange and internal dynamics in the chemotactic protein CheY from Escherichia coli.
Journal of molecular biology | 1997-08-22 | PMID 9268672
Lacroix E, Bruix M, López-Hernández E and 2 more
New diallelic markers in the HLA region of chromosome 6.
Blood cells, molecules & diseases | 1997-08-01 | PMID 9268673
Beutler E, West C
Selective interaction of a conformationally-constrained Arg-Gly-Asp (RGD) motif with the integrin receptor alphavbeta3 expressed on human tumor cells.
Blood cells, molecules & diseases | 1997-08-01 | PMID 9268674
Lanza P, Felding-Habermann B, Ruggeri Z M and 2 more
Infiltration of lung carcinomas with macrophages of the 27E10-positive phenotype.
Lung cancer (Amsterdam, Netherlands) | 1997-08-01 | PMID 9268946
Endress H, Freudenberg N, Fitzke E and 3 more
Familial determinants of moderate and intense physical activity: a twin study.
Medicine and science in sports and exercise | 1997-08-01 | PMID 9268964
Lauderdale D S, Fabsitz R, Meyer J M and 3 more
Distinct effects of various p53 mutants on differentiation and viability of human K562 leukemia cells.
Oncology research | 1997-01-01 | PMID 9268986
Kremenetskaya O S, Logacheva N P, Baryshnikov A Y and 2 more
Study of immunogenicity and virulence of bovine herpesvirus 1 mutants deficient in the UL49 homolog, UL49.5 homolog and dUTPase genes in cattle.
Vaccine | 1997-07-01 | PMID 9269047
Liang X, Chow B, Babiuk L A
Molecular basis of Kell blood group phenotypes.
Vox sanguinis | 1997-01-01 | PMID 9269063
Lee S
Genes: KEL
Abnormal skeletal growth in Kniest dysplasia caused by type II collagen mutations.
Clinical orthopaedics and related research | 1997-08-01 | PMID 9269170
Cole W G
Autosomal dominant Alport syndrome linked to the type IV collage alpha 3 and alpha 4 genes (COL4A3 and COL4A4).
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 1997-08-01 | PMID 9269635
Jefferson J A, Lemmink H H, Hughes A E and 4 more
The factor V Leiden mutation and risk of renal vein thrombosis in patients with nephrotic syndrome.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 1997-08-01 | PMID 9269648
Irish A B
Risk factors for development of diabetic nephropathy: a review.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 1997-01-01 | PMID 9269695
Strojek K, Grzeszczak W, Ritz E
Angiotensin I converting enzyme gene polymorphism and diabetic nephropathy in type II diabetes.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 1997-01-01 | PMID 9269698
Schmidt S, Ritz E
Genes: ACE