Publication catalog

Biomedical publications with connected research

Browse 110,000 source-attributed publications. Each article page includes bibliographic context, indexed concepts and a SPECTER2 semantic neighborhood of 8 to 12 related publications.

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Publications

Page 1098 of 1100

[Long-term results after restorative proctocolectomy and ileoanal pouch in children with familial adenomatous polyps].
Langenbecks Archiv fur Chirurgie. Supplement. Kongressband. Deutsche Gesellschaft fur Chirurgie. Kongress | 1998-01-01 | PMID 9931824
Kadmon M, Tandara A, Herfarth C
Genes: FAP
Post-transcriptional contribution of a cAMP-dependent pathway to the formation of alpha- and beta/gamma-secretases-derived products of beta APP maturation in human cells expressing wild-type and Swedish mutated beta APP.
Molecular medicine (Cambridge, Mass.) | 1998-11-01 | PMID 9932109
Marambaud P, Chevallier N, Ancolio K and 1 more
Genes: APP
Functional analysis of a human tumor necrosis factor alpha (TNF-alpha) promoter polymorphism related to joint damage in rheumatoid arthritis.
Molecular medicine (Cambridge, Mass.) | 1998-11-01 | PMID 9932110
Kaijzel E L, van Krugten M V, Brinkman B M and 7 more
Genes: TNF
The preserved speech variant: a subgroup of the Rett complex: a clinical report of 30 cases.
Journal of autism and developmental disorders | 1998-12-01 | PMID 9932238
Zappella M, Gillberg C, Ehlers S
Cataract mutations and lens development.
Progress in retinal and eye research | 1999-03-01 | PMID 9932285
Graw J
Reduced neuronal activity and reactivation in Alzheimer's disease.
Progress in brain research | 1998-01-01 | PMID 9932420
Swaab D F, Lucassen P J, Salehi A and 3 more
Genes: APOE
Association between nm23-H1 expression, proliferation and apoptosis in non-small cell lung carcinomas.
Clinical & experimental metastasis | 1998-10-01 | PMID 9932606
Volm M, Mattern J, Koomägi R
Neo-angiogenesis in locally advanced squamous cell head and neck cancer correlates with thymidine phosphorylase expression and p53 nuclear oncoprotein accumulation.
Clinical & experimental metastasis | 1998-10-01 | PMID 9932613
Giatromanolaki A, Fountzilas G, Koukourakis M I and 6 more
Reliable genotyping of short tandem repeat loci without an allelic ladder using time-of-flight mass spectrometry.
International journal of legal medicine | 1998-01-01 | PMID 9932742
Butler J M, Li J, Shaler T A and 2 more
Genetic variation and sequence studies of a highly variable short tandem repeat at the D17S976 locus.
International journal of legal medicine | 1998-01-01 | PMID 9932743
Klintschar M, Glock B, Dauber E M and 1 more
Validation studies and characterization of variant alleles at the short tandem repeat locus D12S391.
International journal of legal medicine | 1998-01-01 | PMID 9932747
Junge A, Madea B
A Spanish population study of the STR loci HumLPL, D5S818, D7S820 and D13S317.
International journal of legal medicine | 1998-01-01 | PMID 9932748
Martín P, García O, Albarrán C and 2 more
Population genetic data on four STR loci in a Hungarian Romany population.
International journal of legal medicine | 1998-01-01 | PMID 9932749
Füredi S, Kozma Z, Woller J and 4 more
Catalonian population study of the tetranucleotide repeat loci D3S1358, D8S1179, D18S51 and D19S253.
International journal of legal medicine | 1998-01-01 | PMID 9932750
Gené M, Piqué E, Borrego N and 3 more
Y-chromosome STR haplotypes in an Italian population sample.
International journal of legal medicine | 1998-01-01 | PMID 9932751
Rossi E, Rolf B, Schürenkamp M and 1 more
Polymerase chain reaction-single strand conformation polymorphism or how to detect reliably and efficiently each sequence variation in many samples and many genes.
Electrophoresis | 1998-12-01 | PMID 9932793
Jaeckel S, Epplen J T, Kauth M and 3 more
Symptomatic colonic polyps in childhood: not so benign.
Journal of pediatric gastroenterology and nutrition | 1999-02-01 | PMID 9932851
Hoffenberg E J, Sauaia A, Maltzman T and 2 more
Apolipoprotein E-epsilon4 genotype predicts a poor outcome in survivors of traumatic brain injury.
Neurology | 1999-01-15 | PMID 9932938
Friedman G, Froom P, Sazbon L and 6 more
Genes: APOE
Alpha1-antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease.
Neurology | 1999-01-15 | PMID 9932947
Muñoz E, Obach V, Oliva R and 5 more
Natural killer cells in relapsing-remitting MS: effect of treatment with interferon beta-1B.
Neurology | 1999-01-15 | PMID 9932956
Kastrukoff L F, Morgan N G, Zecchini D and 4 more
Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis.
Neurology | 1999-01-15 | PMID 9932957
Lauronen L, Munroe P B, Järvelä I and 9 more
Genes: CLN3
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy.
Neurology | 1999-01-15 | PMID 9932958
Tein I, Haslam R H, Rhead W J and 3 more
GM2 gangliosidosis AB variant: clinical and biochemical studies of a Japanese patient.
Neurology | 1999-01-15 | PMID 9932959
Sakuraba H, Itoh K, Shimmoto M and 10 more
Analysis of a very large trinucleotide repeat in a patient with juvenile Huntington's disease.
Neurology | 1999-01-15 | PMID 9932964
Nance M A, Mathias-Hagen V, Breningstall G and 2 more
A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration.
Neurology | 1999-01-15 | PMID 9932968
Higgins J J, Litvan I, Nee L E and 1 more
Studies on the phenotype of migrant thymic stem cells.
European journal of immunology | 1999-01-01 | PMID 9933088
Suniara R K, Jenkinson E J, Owen J J
Activation of gp130 signaling in vivo by the IL-6 super-agonist K-7/D-6 accelerates repopulation of lymphoid organs after irradiation.
European journal of immunology | 1999-01-01 | PMID 9933112
Frasca D, Doria G, Barattini P and 4 more
CD40 ligand expression deficiency in a female carrier of the X-linked hyper-IgM syndrome as a result of X chromosome lyonization.
European journal of immunology | 1999-01-01 | PMID 9933119
de Saint Basile G, Tabone M D, Durandy A and 3 more
Different tachykinin receptors mediate chloride secretion in the distal colon through activation of submucosal neurones.
Naunyn-Schmiedeberg's archives of pharmacology | 1999-01-01 | PMID 9933154
Frieling T, Dobreva G, Weber E and 4 more
Genes: VIP
HIRA, a DiGeorge syndrome candidate gene, is required for cardiac outflow tract septation.
Circulation research | 1999-02-05 | PMID 9933243
Farrell M J, Stadt H, Wallis K T and 5 more
Genes: HIRA
Brain stem MRI signal abnormalities in CADASIL.
Stroke | 1999-02-01 | PMID 9933287
Chabriat H, Mrissa R, Levy C and 6 more
Fine localization of the CMT4A locus using a PAC contig and haplotype analysis.
Neurogenetics | 1998-12-01 | PMID 9933296
Ben Othmane K, Rochelle J M, Ben Hamida M and 5 more
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis.
Neurogenetics | 1998-12-01 | PMID 9933299
Fuchs C, Liehr T, Ozbey S and 3 more
GRC5 and NMD3 function in translational control of gene expression and interact genetically.
Current genetics | 1999-01-01 | PMID 9933353
Karl T, Onder K, Kodzius R and 9 more
Genes: NMD3
The influence of mutation rad57-1 on the fidelity of DNA double-strand gap repair in Saccharomyces cerevisiae.
Current genetics | 1999-01-01 | PMID 9933354
Glasunov A V, Glaser V M
YNT20, a bypass suppressor of yme1 yme2, encodes a putative 3'-5' exonuclease localized in mitochondria of Saccharomyces cerevisiae.
Current genetics | 1999-01-01 | PMID 9933355
Hanekamp T, Thorsness P E
The Aspergillus nidulans gltA gene encoding glutamate synthase is required for ammonium assimilation in the absence of NADP-glutamate dehydrogenase.
Current genetics | 1999-01-01 | PMID 9933358
Macheda M L, Hynes M J, Davis M A
Functional characterization of SOR1, a gene required for resistance to photosensitizing toxins in the fungus Cercospora nicotianae.
Current genetics | 1999-01-01 | PMID 9933360
Ehrenshaft M, Chung K R, Jenns A E and 1 more
Identification of incompatibility alleles and characterisation of molecular markers genetically linked to the A incompatibility locus in the white rot fungus Pleurotus ostreatus.
Current genetics | 1999-01-01 | PMID 9933361
Larraya L, Peñas M M, Pérez G and 4 more
Drosophila virilis has atypical kinds and arrangements of histone repeats.
Chromosoma | 1998-12-01 | PMID 9933406
Schienman J E, Lozovskaya E R, Strausbaugh L D
Experimental melanin-induced uveitis in the Fischer 344 rat is inhibited by anti-CD4 monoclonal antibody, but not by mannose-6-phosphate.
Clinical and experimental immunology | 1999-01-01 | PMID 9933421
Smith J R, Hart P H, Parish C R and 3 more
Circulating soluble factor-inhibiting natural killer (NK) activity of fresh peripheral blood mononuclear cells (PBMC) from inflammatory bowel disease (IBD) patients.
Clinical and experimental immunology | 1999-01-01 | PMID 9933422
Giacomelli R, Passacantando A, Frieri G and 8 more
Expression of CD30 mRNA, CD30L mRNA and a variant form of CD30 mRNA in restimulated peripheral blood mononuclear cells (PBMC) of patients with helminthic infections resembling a Th2 disease.
Clinical and experimental immunology | 1999-01-01 | PMID 9933429
Kilwinski J, Berger T, Mpalaskas J and 3 more
Genes: TNF
Molecular analysis of rheumatoid factor (RF)-negative B cell hybridomas from rheumatoid synovial tissue: evidence for an antigen-induced stimulation with selection of high mutated IgVH and low mutated IgVL/lambda genes.
Clinical and experimental immunology | 1999-01-01 | PMID 9933438
Krenn V, König A, Hensel F and 6 more
Genetic markers in clinically well defined patients with ulcerative colitis (UC).
Clinical and experimental immunology | 1999-02-01 | PMID 9933456
Bouma G, Crusius J B, García-González M A and 7 more
Genes: TNF
Alterations in the number of circulating leucocytes, phenotype of monocyte and cytokine production in patients undergoing cardiothoracic surgery.
Clinical and experimental immunology | 1999-02-01 | PMID 9933459
Hiesmayr M J, Spittler A, Lassnigg A and 6 more
Role of peripheral blood mononuclear cell (PBMC) phenotype changes in the pathogenesis of haemorrhagic fever with renal syndrome (HFRS).
Clinical and experimental immunology | 1999-02-01 | PMID 9933461
Markotić A, Dasić G, Gagro A and 8 more
TNFalpha*2 marks high risk of severe disease during Plasmodium falciparum malaria and other infections in Sri Lankans.
Clinical and experimental immunology | 1999-02-01 | PMID 9933464
Wattavidanage J, Carter R, Perera K L and 7 more
Genes: TNF
A novel mutant gammac chain from a patient with typical phenotype of X-linked severe combined immunodeficiency (SCID) has partial signalling function for mediating IL-2 and IL-4 receptor action.
Clinical and experimental immunology | 1999-02-01 | PMID 9933465
Kumaki S, Ochs H D, Kuropatwinski K K and 4 more
Mapping the gene causing hereditary primary hyperparathyroidism in a Portuguese kindred to chromosome 1q22-q31.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 1999-02-01 | PMID 9933477
Williamson C, Cavaco B M, Jauch A and 12 more
The material basis for reduced mechanical properties in oim mice bones.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research | 1999-02-01 | PMID 9933481
Camacho N P, Hou L, Toledano T R and 5 more
NMR-Observed phosphate trafficking and polyphosphate dynamics in wild-type and vph1-1 mutant Saccharomyces cerevisae in response to stresses.
Biotechnology progress | 2000-01-01 | PMID 9933515
Castrol C D, Koretsky A P, Domach M M
Genetic analysis of susceptibility to dextran sulfate sodium-induced colitis in mice.
Genomics | 1999-01-15 | PMID 9933561
Mähler M, Bristol I J, Sundberg J P and 4 more
Physical delineation of a 700-kb region overlapping the Looptail mutation on mouse chromosome 1.
Genomics | 1999-01-15 | PMID 9933565
Underhill D A, Mullick A, Groulx N and 2 more
Genes: STS
A PstI polymorphism detects the mutation of serine128 to arginine in CD 62E gene - a risk factor for coronary artery disease.
Journal of biomedical science | 1999-01-01 | PMID 9933738
Ye S Q, Usher D, Virgil D and 3 more
Genes: CAD
Activation of a cryptic splice donor in human immunodeficiency virus type-1.
Journal of biomedical science | 1999-01-01 | PMID 9933742
Borg K T, Favaro J P, Arrigo S J and 1 more
Association between HLA-DRB1*15 and Japanese patients with rheumatoid arthritis complicated by renal involvement.
Nephron | 1999-02-01 | PMID 9933752
Tokunaga N K, Noda R, Kaneoka H and 5 more
Long-term effect on blood pressure of early brief treatment by different antihypertensive agents: a study in the prague hypertensive rat.
Kidney & blood pressure research | 1998-01-01 | PMID 9933830
Heller J, Hellerová S
Genes: ACE
Monoclonal antibodies to 2,4-dichlorophenol hydroxylase as probes for the 2,4-D-degradative phenotype.
Canadian journal of microbiology | 1998-10-01 | PMID 9933912
Farhana L, Fulthorpe R R, Harbour C and 1 more
RecA-dependent viral burst in bacterial colonies during the entry into stationary phase.
FEMS microbiology letters | 1999-01-15 | PMID 9933926
Ramírez E, Schmidt M, Rinas U and 1 more
Characterisation of Listeria ivanovii isolates from the UK using pulsed-field gel electrophoresis.
FEMS microbiology letters | 1999-01-15 | PMID 9933929
Ramage C P, Low J C, McLauchlin J and 1 more
Contribution of the regulatory gene lasR to the pathogenesis of Pseudomonas aeruginosa infection of burned mice.
The Journal of burn care & rehabilitation | 2000-01-01 | PMID 9934636
Rumbaugh K P, Griswold J A, Hamood A N
Evolutionary pattern of the G glycoprotein of human respiratory syncytial viruses from antigenic group B: the use of alternative termination codons and lineage diversification.
The Journal of general virology | 1999-01-01 | PMID 9934694
Mart Nez I, Vald S O, Delfraro A and 3 more
A divergent genotype of hepatitis E virus in Chinese patients with acute hepatitis.
The Journal of general virology | 1999-01-01 | PMID 9934699
Wang Y, Ling R, Erker J C and 5 more
Sequence analysis and genetic classification of tick-borne encephalitis viruses from Europe and Asia.
The Journal of general virology | 1999-01-01 | PMID 9934700
Ecker M, Allison S L, Meixner T and 1 more
Diversity of human endogenous retrovirus class II-like sequences.
The Journal of general virology | 1999-01-01 | PMID 9934709
Andersson M L, Lindeskog M, Medstrand P and 3 more
Randomized controlled trial of lymphoblastoid interferon alpha for chronic hepatitis C (comparison of 9-MU and 6-MU doses). IFN Treatment Group of Affiliated Hospitals of the Third Department of Internal Medicine at Nagoya University School of Medicine.
The American journal of gastroenterology | 1999-01-01 | PMID 9934749
Yoshioka K, Yano M, Kusakabe A and 7 more
Peutz-Jeghers syndrome: molecular analysis of a three-generation kindred with a novel defect in the serine threonine kinase gene STK11.
The American journal of gastroenterology | 1999-01-01 | PMID 9934767
Trojan J, Brieger A, Raedle J and 2 more
Genes: STK11
238Pu alpha-particle-induced C3H10T1/2 transformants are less tumorigenic than the X-ray-induced equivalent.
Carcinogenesis | 1999-01-01 | PMID 9934847
Lehane M M, Bryant P E, Riches A C and 4 more
Chemoprevention of intestinal adenomas in the ApcMin mouse by piroxicam: kinetics, strain effects and resistance to chemosuppression.
Carcinogenesis | 1999-01-01 | PMID 9934849
Ritland S R, Gendler S J
Aberrant methylation of p16INK4a and deletion of p15INK4b are frequent events in human esophageal cancer in Linxian, China.
Carcinogenesis | 1999-01-01 | PMID 9934853
Xing E P, Nie Y, Wang L D and 2 more
Strain differences in Blastocystis isolates as detected by a single set of polymerase chain reaction primers.
Parasitology research | 1999-02-01 | PMID 9934962
Init I, Mak J W, Lokman Hakim S and 1 more
1p microdeletion in sibs with minimal phenotypic manifestations.
American journal of medical genetics | 1999-01-15 | PMID 9934971
Martínez J E, Tuck-Muller C M, Gasparrini W and 2 more
Different mutations in the same codon of the proteolipid protein gene, PLP, may help in correlating genotype with phenotype in Pelizaeus-Merzbacher disease/X-linked spastic paraplegia (PMD/SPG2).
American journal of medical genetics | 1999-01-15 | PMID 9934976
Hodes M E, Zimmerman A W, Aydanian A and 7 more
Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory.
American journal of medical genetics | 1999-01-15 | PMID 9934980
Caron L, Tihy F, Dallaire L
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndrome.
American journal of medical genetics | 1999-01-15 | PMID 9934984
Gripp K W, Stolle C A, Celle L and 3 more
Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews.
American journal of medical genetics | 1999-01-15 | PMID 9934985
Shaag A, Saada A, Berger I and 4 more
Association between apolipoprotein(a) phenotypes and coronary heart disease at a young age.
Journal of the American College of Cardiology | 1999-01-01 | PMID 9935023
Gazzaruso C, Garzaniti A, Buscaglia P and 5 more
A MAGE-1-encoded HLA-A24-binding synthetic peptide induces specific anti-tumor cytotoxic T lymphocytes.
International journal of cancer | 1999-01-18 | PMID 9935194
Fujie T, Tahara K, Tanaka F and 3 more
Genes: APC
Identification of two distinct deletion targets at 11q23 in cutaneous malignant melanoma.
International journal of cancer | 1999-01-18 | PMID 9935201
Herbst R A, Gutzmer R, Matiaske F and 4 more
Genes: APOC3
N-acetyl transferase 2 genotypes, meat intake and breast cancer risk.
International journal of cancer | 1999-01-05 | PMID 9935222
Gertig D M, Hankinson S E, Hough H and 5 more
Genes: NAT2
New DNA polymorphisms of human MMH/OGG1 gene: prevalence of one polymorphism among lung-adenocarcinoma patients in Japanese.
International journal of cancer | 1999-01-05 | PMID 9935223
Ishida T, Takashima R, Fukayama M and 11 more
Genes: OGG1
Inhibitory effect of the transcription factor encoded by the mi mutant allele in cultured mast cells of mice.
Blood | 1999-02-15 | PMID 9949161
Ito A, Morii E, Kim D K and 5 more
Genes: MITF
Characterization of two naturally occurring mutations in the second epidermal growth factor-like domain of factor VII.
Blood | 1999-02-15 | PMID 9949166
Hunault M, Arbini A A, Carew J A and 2 more
Activating mutation in the catalytic domain of c-kit elicits hematopoietic transformation by receptor self-association not at the ligand-induced dimerization site.
Blood | 1999-02-15 | PMID 9949175
Tsujimura T, Hashimoto K, Kitayama H and 7 more
Genes: KIT
GCKR links the Bcr-Abl oncogene and Ras to the stress-activated protein kinase pathway.
Blood | 1999-02-15 | PMID 9949177
Shi C S, Tuscano J M, Witte O N and 1 more
Genes: GCKR
Protein glycosylation mutants of procyclic Trypanosoma brucei: defects in the asparagine-glycosylation pathway.
Glycobiology | 1999-02-01 | PMID 9949195
Hwa K Y, Acosta-Serrano A, Khoo K H and 2 more
Truncated CBP protein leads to classical Rubinstein-Taybi syndrome phenotypes in mice: implications for a dominant-negative mechanism.
Human molecular genetics | 1999-03-01 | PMID 9949198
Oike Y, Hata A, Mamiya T and 7 more
Intranuclear inclusions and neuritic aggregates in transgenic mice expressing a mutant N-terminal fragment of huntingtin.
Human molecular genetics | 1999-03-01 | PMID 9949199
Schilling G, Becher M W, Sharp A H and 11 more
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.
Human molecular genetics | 1999-03-01 | PMID 9949200
Mustapha M, Weil D, Chardenoux S and 5 more
Genes: TECTA
The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis.
Human molecular genetics | 1999-03-01 | PMID 9949201
Wong A, Yang J, Cavadini P and 4 more
Genes: GAA
Allele-specific late replication and fragility of the most active common fragile site, FRA3B.
Human molecular genetics | 1999-03-01 | PMID 9949202
Wang L, Darling J, Zhang J S and 3 more
Single sperm analysis of the CAG repeats in the gene for dentatorubral-pallidoluysian atrophy (DRPLA): the instability of the CAG repeats in the DRPLA gene is prominent among the CAG repeat diseases.
Human molecular genetics | 1999-03-01 | PMID 9949204
Takiyama Y, Sakoe K, Amaike M and 4 more
Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3.
Human molecular genetics | 1999-03-01 | PMID 9949206
Sprunger L K, Escayg A, Tallaksen-Greene S and 2 more
Genes: SCNM1
Characterization of the expression of DMPK and SIX5 in the human eye and implications for pathogenesis in myotonic dystrophy.
Human molecular genetics | 1999-03-01 | PMID 9949207
Winchester C L, Ferrier R K, Sermoni A and 2 more
Genes: DMPK, SIX5
Germinal and somatic mutations in the PKD2 gene of renal cysts in autosomal dominant polycystic kidney disease.
Human molecular genetics | 1999-03-01 | PMID 9949210
Koptides M, Hadjimichael C, Koupepidou P and 2 more
Genes: PKD2, PKD1
Distinct mutation patterns of breast cancer-associated alleles of the HRAS1 minisatellite locus.
Human molecular genetics | 1999-03-01 | PMID 9949211
Ding S, Larson G P, Foldenauer K and 2 more
Abnormalities in central nervous system development in osteogenesis imperfecta type II.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society | 2000-01-01 | PMID 9949218
Emery S C, Karpinski N C, Hansen L and 1 more
Variant EWS-WT1 chimeric product in the desmoplastic small round cell tumor.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society | 2000-01-01 | PMID 9949226
Chan A S, MacNeill S, Thorner P and 2 more
[Identification of mutations in the phenylalanine hydroxylase gene and exon 5 novel mutation Y166X(C-->G) in Yunnan].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-02-10 | PMID 9949232
Wang N, Zhu Y, Xu K and 3 more
Genes: PAH