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 1185 of 10600

Switch recombination in a transfected plasmid occurs preferentially in a B cell line that undergoes switch recombination of its chromosomal Ig heavy chain genes.
Journal of immunology (Baltimore, Md. : 1950) | 1999-08-15 | PMID 10438941
Stavnezer J, Bradley S P, Rousseau N and 5 more
A null mutation in the inflammation-associated S100 protein S100A8 causes early resorption of the mouse embryo.
Journal of immunology (Baltimore, Md. : 1950) | 1999-08-15 | PMID 10438963
Passey R J, Williams E, Lichanska A M and 5 more
A putative susceptibility locus on chromosome 18 is not a major contributor to human selective IgA deficiency: evidence from meiotic mapping of 83 multiple-case families.
Journal of immunology (Baltimore, Md. : 1950) | 1999-08-15 | PMID 10438966
Vorechovský I, Blennow E, Nordenskjöld M and 2 more
Sequence polymorphisms in the chemokines Scya1 (TCA-3), Scya2 (monocyte chemoattractant protein (MCP)-1), and Scya12 (MCP-5) are candidates for eae7, a locus controlling susceptibility to monophasic remitting/nonrelapsing experimental allergic encephalomyelitis.
Journal of immunology (Baltimore, Md. : 1950) | 1999-08-15 | PMID 10438970
Teuscher C, Butterfield R J, Ma R Z and 3 more
High T cell epitope sharing between two HLA-B27 subtypes (B*2705 and B*2709) differentially associated to ankylosing spondylitis.
Journal of immunology (Baltimore, Md. : 1950) | 1999-08-15 | PMID 10438975
García-Peydró M, Martí M, López de Castro J A
Haptoglobin genotype and natural fertility in humans.
Fertility and sterility | 1999-08-01 | PMID 10438998
Bottini N, Gimelfarb A, Gloria-Bottini F and 3 more
Recycling of a single human blastomere fixed on a microscopic slide for sexing and diagnosis of specific mutations by various types of polymerase chain reaction.
Fertility and sterility | 1999-08-01 | PMID 10439008
He Z Y, Liu H C, Mele C A and 3 more
Tumour-associated E-cadherin mutations alter cellular morphology, decrease cellular adhesion and increase cellular motility.
Oncogene | 1999-07-29 | PMID 10439038
Handschuh G, Candidus S, Luber B and 8 more
PAX3 and PAX7 exhibit conserved cis-acting transcription repression domains and utilize a common gain of function mechanism in alveolar rhabdomyosarcoma.
Oncogene | 1999-07-29 | PMID 10439042
Bennicelli J L, Advani S, Schäfer B W and 1 more
Genes: PAX7, PAX3
Mice defective in the DNA mismatch gene PMS2 are hypersensitive to MNU induced thymic lymphoma and are partially protected by transgenic expression of human MGMT.
Oncogene | 1999-07-29 | PMID 10439048
Qin X, Liu L, Gerson S L
Genes: PMS2, MGMT
A new transthyretin variant--ATTR Arg104Cys.
Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis | 1999-06-01 | PMID 10439123
Saraiva M J, Torres M de F, Serra J and 1 more
Genetic causes of rickets.
Current opinion in pediatrics | 1999-08-01 | PMID 10439207
Miller W L, Portale A A
Genes: PHEX
Diabetic embryopathy.
Current opinion in pediatrics | 1999-08-01 | PMID 10439209
Kousseff B G
RSH (so-called Smith-Lemli-Opitz) syndrome.
Current opinion in pediatrics | 1999-08-01 | PMID 10439210
Opitz J M
CD4+ and CD8+ T-cell clones from congenital rubella syndrome patients with IDDM recognize overlapping GAD65 protein epitopes. Implications for HLA class I and II allelic linkage to disease susceptibility.
Human immunology | 1999-08-01 | PMID 10439311
Ou D, Jonsen L A, Metzger D L and 1 more
Mutation in the beta 2m gene is not a frequent event in head and neck squamous cell carcinomas.
Human immunology | 1999-08-01 | PMID 10439315
Feenstra M, Rozemuller E, Duran K and 5 more
Homozygous deletion of the CYP21A-TNXA-RP2-C4B gene region conferring C4B deficiency associated with recurrent respiratory infections.
Human immunology | 1999-08-01 | PMID 10439316
Jaatinen T, Ruuskanen O, Truedsson L and 1 more
Genes: TNXB
The DRB1 Val86/Val86 genotype associates with multiple sclerosis in Australian patients.
Human immunology | 1999-08-01 | PMID 10439317
Teutsch S M, Bennetts B H, Buhler M M and 2 more
Molecular analysis of HLA class II polymorphisms among different ethnic groups in Israel.
Human immunology | 1999-08-01 | PMID 10439318
Amar A, Kwon O J, Motro U and 4 more
HLA-B22 diversity including a novel B54 variant (B*5507) in the Korean population.
Human immunology | 1999-08-01 | PMID 10439319
Lee K W, Yang S Y
Determination of Duffy genotypes in three populations of African descent using PCR and sequence-specific oligonucleotides.
Human immunology | 1999-08-01 | PMID 10439320
Nickel R G, Willadsen S A, Freidhoff L R and 10 more
Dapsone resistance does not appear to be associated with a mutation in the dihydropteroate synthase-2 gene of Mycobacterium leprae.
Indian journal of leprosy | 2000-01-01 | PMID 10439322
Gillis T P, Williams D L
Genes: DHPS
Trilineage phenotypic compromise in acute leukemia.
Leukemia & lymphoma | 1999-07-01 | PMID 10439377
Scolnik M P, Palacios M F, Ramirez F R and 3 more
The nuclear rDNA intergenic spacer of the ectomycorrhizal basidiomycete Laccaria bicolor: structural analysis and allelic polymorphism.
Microbiology (Reading, England) | 1999-07-01 | PMID 10439399
Martin Francis, Selosse Marc-André, Tacon Francois Le
The Candida albicans CHS4 gene complements a Saccharomyces cerevisiae skt5/chs4 mutation and is involved in chitin biosynthesis.
Microbiology (Reading, England) | 1999-07-01 | PMID 10439400
Sudoh Masayuki, Tatsuno Kenji, Ono Naomi and 4 more
A presenilin-1 Thr116Asn substitution in a family with early-onset Alzheimer's disease.
Neuroreport | 1999-08-02 | PMID 10439444
Romero I, Jørgensen P, Bolwig G and 5 more
Association of the enkephalinase gene with low amplitude P300 waves.
Neuroreport | 1999-08-02 | PMID 10439449
Comings D E, Dietz G, Johnson J P and 1 more
Genes: MME
Neuron-targeted gene transfer by adenovirus carrying neural-restrictive silencer element.
Neuroreport | 1999-08-02 | PMID 10439462
Miyaguchi K, Maeda Y, Kojima T and 2 more
[D/D genotype of the gene for angiotensin converting enzyme as a risk factor for post-stent coronary restenosis].
Revista espanola de cardiologia | 1999-07-01 | PMID 10439670
Guarda E, Fajuri A, Marchant E and 9 more
Genes: ACE
[The effect of bromantane on the behavior of inbred mouse strains with different phenotypes of emotional stress reaction].
Eksperimental'naia i klinicheskaia farmakologiia | 2000-01-01 | PMID 10439937
Seredenin S B, Miramedova A G, Kozlovskaia M M
Analysis of mutations in the tudor domain of the survival motor neuron protein SMN.
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439956
Mohaghegh P, Rodrigues N R, Owen N and 4 more
Genetic basis of transferase-deficient galactosaemia in Ireland and the population history of the Irish Travellers.
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439960
Murphy M, McHugh B, Tighe O and 4 more
Genes: GALT
Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter.
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439962
Angelicheva D, Turnev I, Dye D and 3 more
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus--a GISC study.
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439963
Annese V, Latiano A, Bovio P and 14 more
Genes: NPL
Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease.
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439967
Liechti-Gallati S, Schneider V, Neeser D and 1 more
Genes: CFTR, DMD, OTC
Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439968
Aguirre T, Matthijs G, Robberecht W and 2 more
Genes: SOD1
Marfan-like habitus and familial adenomatous polyposis in two unrelated males: a significant association?
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439970
Calin G, Wijnen J, van der Klift H and 10 more
Genes: APC, FAP, FBN2
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues.
European journal of human genetics : EJHG | 1999-07-01 | PMID 10439971
Filisetti D, Ostermann G, von Bredow M and 11 more
Genes: PHEX
Handedness and lexical skills in undergraduates.
Cortex; a journal devoted to the study of the nervous system and behavior | 1999-06-01 | PMID 10440074
Annett M
Earedness and handedness: distribution in a German sample with some family data.
Cortex; a journal devoted to the study of the nervous system and behavior | 1999-06-01 | PMID 10440077
Reiss M, Reiss G
Pharmacological properties of TRK-820 on cloned mu-, delta- and kappa-opioid receptors and nociceptin receptor.
European journal of pharmacology | 1999-07-02 | PMID 10440101
Seki T, Awamura S, Kimura C and 5 more
Overexpression of dominant negative mutant hepatocyte nuclear factor (HNF)-1alpha inhibits arginine-induced insulin secretion in MIN6 cells.
Diabetologia | 1999-07-01 | PMID 10440133
Tanizawa Y, Ohta Y, Nomiyama J and 6 more
Homozygosity of the Pro12Ala variant of the peroxisome proliferation-activated receptor-gamma2 (PPAR-gamma2): divergent modulating effects on body mass index in obese and lean Caucasian men.
Diabetologia | 1999-07-01 | PMID 10440134
Ek J, Urhammer S A, Sørensen T I and 3 more
Angiotensinogen gene M235T polymorphism predicts left ventricular hypertrophy in endurance athletes.
Journal of the American College of Cardiology | 1999-08-01 | PMID 10440164
Karjalainen J, Kujala U M, Stolt A and 4 more
Genes: AGT, ACE
High-dose natural interferon-alpha therapy for chronic hepatitis C with a high viral load: predictors of efficacy. The Aomori, Akita and Iwate Areas Viral Hepatitis Research Group.
Journal of gastroenterology and hepatology | 1999-07-01 | PMID 10440212
Komatsu M, Suto T, Ishikawa K and 1 more
Association of MICA gene and HLA-B*5101 with Behçet's disease in Greece.
Investigative ophthalmology & visual science | 1999-08-01 | PMID 10440244
Yabuki K, Mizuki N, Ota M and 10 more
Genes: MICA
Cohesin Rec8 is required for reductional chromosome segregation at meiosis.
Nature | 1999-07-29 | PMID 10440376
Watanabe Y, Nurse P
The humoral immune response against an HLA class I allodeterminant correlates with the HLA-DR phenotype of the responder.
Transplantation | 1999-07-27 | PMID 10440383
Fuller T C, Fuller A
Fast lymphoid reconstitution after vascularized bone marrow transplantation in lethally irradiated rats.
Transplantation | 1999-07-27 | PMID 10440388
Janczewska S, Ziolkowska A, Durlik M and 2 more
Genes: MLN
High-throughput genotyping method for glutathione S-transferase T1 and M1 gene deletions using TaqMan probes.
Research communications in molecular pathology and pharmacology | 1999-01-01 | PMID 10440566
Shi M M, Myrand S P, Bleavins M R and 1 more
Genes: GSTM1, GSTT1
The relationship between the interleukin-1 periodontal genotype and implant loss. Initial data.
Journal of periodontology | 1999-07-01 | PMID 10440632
Wilson T G, Nunn M
Cometabolism of chlorinated solvents and binary chlorinated solvent mixtures using M. trichosporium OB3b PP358.
Biotechnology and bioengineering | 1999-10-05 | PMID 10440676
Aziz C E, Georgiou G, Speitel G E
Intratumoral heterogeneity of DNA content in renal cell carcinoma and its prognostic significance.
Cancer | 1999-08-15 | PMID 10440695
Ruiz-Cerdá J L, Hernández M, Sempere A and 3 more
Having children after cancer. A pilot survey of survivors' attitudes and experiences.
Cancer | 1999-08-15 | PMID 10440699
Schover L R, Rybicki L A, Martin B A and 1 more
Is Hsp90 a regulator of evolvability?
The Journal of experimental zoology | 1999-08-15 | PMID 10440722
Wagner G P, Chiu C H, Hansen T F
Viral RNA and evolved mutational robustness.
The Journal of experimental zoology | 1999-08-15 | PMID 10440723
Wagner A, Stadler P F
Evolution of the HOXB6 intergenic region: motif conservation at the lateral plate mesoderm (LPM) enhancer element.
The Journal of experimental zoology | 1999-08-15 | PMID 10440728
Deinard A, Dorit R, Castiglione C and 5 more
Genes: HOXB6, HOXB7
BMP-4 inhibits neural differentiation of murine embryonic stem cells.
Journal of neurobiology | 1999-09-05 | PMID 10440729
Finley M F, Devata S, Huettner J E
Nested transcripts of gap junction gene have distinct expression patterns.
Journal of neurobiology | 1999-09-05 | PMID 10440730
Zhang Z, Curtin K D, Sun Y A and 1 more
Anxiety and increased 5-HT1A receptor response in NCAM null mutant mice.
Journal of neurobiology | 1999-09-05 | PMID 10440734
Stork O, Welzl H, Wotjak C T and 4 more
Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation).
The Journal of pathology | 1999-08-01 | PMID 10440752
Zimmer K P, le Coutre P, Aerts H M and 4 more
Evolution of wild-type and precore mutant HBV infection after liver transplantation.
Journal of medical virology | 1999-09-01 | PMID 10440801
Torre F, Wong P Y, Macartney M and 2 more
Prevalence of precore mutants in anti-HBe-positive hepatitis B virus carriers in Germany.
Journal of medical virology | 1999-09-01 | PMID 10440802
Knöll A, Rohrhofer A, Kochanowski B and 2 more
Immunoassay detection of hepatitis B surface antigen mutants.
Journal of medical virology | 1999-09-01 | PMID 10440803
Coleman P F, Chen Y C, Mushahwar I K
Hypervariable region diversity of hepatitis C virus and humoral response: comparison between patients with or without cirrhosis.
Journal of medical virology | 1999-09-01 | PMID 10440804
Allain J P, Zhai W, Shang D and 2 more
Molecular characterization of the 5' non-coding region of South African GBV-C/HGV isolates: major deletion and evidence for a fourth genotype.
Journal of medical virology | 1999-09-01 | PMID 10440808
Tucker T J, Smuts H, Eickhaus P and 2 more
Four new genotypes of adenovirus type 3 isolated from patients with conjunctivitis in Japan.
Journal of medical virology | 1999-09-01 | PMID 10440811
Itoh N, Tanaka K, Aoki K and 6 more
Human cytomegalovirus glycoprotein B genotypes in blood of AIDS patients: lack of association with either the viral DNA load in leukocytes or presence of retinitis.
Journal of medical virology | 1999-09-01 | PMID 10440815
Gilbert C, Handfield J, Toma E and 3 more
Partial monosomy of distal 10q: three new cases and a review.
American journal of medical genetics | 1999-09-03 | PMID 10440820
Waggoner D J, Chow C K, Dowton S B and 1 more
Congenital cholesteatoma and malformations of the facial nerve: rare manifestations of the BOR syndrome.
American journal of medical genetics | 1999-09-03 | PMID 10440824
Graham G E, Allanson J E
Patient with a 22q11.2 deletion with no overlap of the minimal DiGeorge syndrome critical region (MDGCR).
American journal of medical genetics | 1999-09-03 | PMID 10440825
McQuade L, Christodoulou J, Budarf M and 4 more
Genes: COMT, TBX1
Molecular and clinical correlation study of Williams-Beuren syndrome: No evidence of molecular factors in the deletion region or imprinting affecting clinical outcome.
American journal of medical genetics | 1999-09-03 | PMID 10440826
Wang M S, Schinzel A, Kotzot D and 7 more
Genes: ELN, LIMK1
Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literature.
American journal of medical genetics | 1999-09-03 | PMID 10440827
Matsuo M, Muroya K, Kosaki K and 4 more
Partial duplication of 4q12q13 leads to a mild phenotype.
American journal of medical genetics | 1999-09-03 | PMID 10440828
Shashi V, Berry M N, Santos C and 1 more
Autosomal dominant inheritance of Barber-Say syndrome.
American journal of medical genetics | 1999-09-03 | PMID 10440829
Dinulos M B, Pagon R A
Relationship of the C242T p22phox gene polymorphism to angiographic coronary artery disease and endothelial function.
American journal of medical genetics | 1999-09-03 | PMID 10440830
Li A, Prasad A, Mincemoyer R and 4 more
Genes: CAD
Molecular genetic diagnosis of the familial myxoma syndrome (Carney complex).
American journal of medical genetics | 1999-09-03 | PMID 10440831
Goldstein M M, Casey M, Carney J A and 1 more
Methylenetetrahydrofolate reductase thermolabile variant and oral clefts.
American journal of medical genetics | 1999-09-03 | PMID 10440833
Mills J L, Kirke P N, Molloy A M and 6 more
Genes: MTHFR
Two cases with interstitial deletions of chromosome 2 and sex reversal in one.
American journal of medical genetics | 1999-09-03 | PMID 10440834
Slavotinek A, Schwarz C, Getty J F and 3 more
Genes: DLX1, DLX2, EVX2
Enhancer of split [E(spl)(D)] is a gro-independent, hypermorphic mutation in Drosophila.
Developmental genetics | 1999-01-01 | PMID 10440851
Nagel A C, Yu Y, Preiss A
Nijmegen breakage syndrome: consequences of defective DNA double strand break repair.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1999-08-01 | PMID 10440861
Digweed M, Reis A, Sperling K
Should we kill the messenger? The role of the surveillance complex in translation termination and mRNA turnover.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1999-08-01 | PMID 10440865
Czaplinski K, Ruiz-Echevarria M J, González C I and 1 more
Isochromosome 8q formation is associated with 8p loss of heterozygosity in a prostate cancer cell line.
The Prostate | 1999-09-15 | PMID 10440875
Virgin J B, Hurley P M, Nahhas F A and 5 more
A mouse gene knockout model for juvenile ceroid-lipofuscinosis (Batten disease).
Journal of neuroscience research | 1999-08-15 | PMID 10440905
Katz M L, Shibuya H, Liu P C and 3 more
Genes: CLN3
Paroxysmal nocturnal hemoglobinuria: analysis of the effects of mutant PIG-A on gene expression.
American journal of hematology | 1999-08-01 | PMID 10440907
Kanai N, Vreeke T M, Parker C J
Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors.
American journal of hematology | 1999-08-01 | PMID 10440914
Antoniadi T, Hatzis T, Kroupis C and 2 more
Genes: MTHFR
Molecular genetic basis of pancreatic adenocarcinoma.
Genes, chromosomes & cancer | 1999-09-01 | PMID 10440999
Hilgers W, Kern S E
Genomic organization and chromosomal localization of the human CUL2 gene and the role of von Hippel-Lindau tumor suppressor-binding protein (CUL2 and VBP1) mutation and loss in renal-cell carcinoma development.
Genes, chromosomes & cancer | 1999-09-01 | PMID 10441001
Clifford S C, Walsh S, Hewson K and 6 more
Genes: VHL, CUL2, VBP1
Sporadic follicular thyroid tumors show loss of a 200-kb region in 11q13 without evidence for mutations in the MEN1 gene.
Genes, chromosomes & cancer | 1999-09-01 | PMID 10441003
Nord B, Larsson C, Wong F K and 3 more
Genes: MEN1
Malignant transformation of human diploid fibroblasts and suppression of their anchorage independence by introduction of chromosome 13.
Genes, chromosomes & cancer | 1999-09-01 | PMID 10441005
Oka K, Tomonaga Y, Nakazawa T and 7 more
SMAD genes in juvenile polyposis.
Genes, chromosomes & cancer | 1999-09-01 | PMID 10441006
Roth S, Sistonen P, Salovaara R and 12 more
Genes: SMAD2, SMAD3, SMAD4, SMAD7
Loss of heteroplasmy in the displacement loop of brain mitochondrial DNA in astrocytic tumors.
Genes, chromosomes & cancer | 1999-09-01 | PMID 10441009
Kirches E, Michael M, Woy C and 6 more
Molecular scanning of the beta-3-adrenergic receptor gene in Pima Indians and Caucasians.
Diabetes/metabolism research and reviews | 2000-01-01 | PMID 10441039
Silver K, Walston J, Yang Y and 4 more
Cellular memory of transcriptional states by Polycomb-group proteins.
Seminars in cell & developmental biology | 1999-04-01 | PMID 10441076
Jacobs J J, van Lohuizen M
Age-dependent association of apolipoprotein E genotype with coronary and aortic atherosclerosis in middle-aged men: an autopsy study.
Circulation | 1999-08-10 | PMID 10441097
Ilveskoski E, Perola M, Lehtimäki T and 9 more
Structure of the extended-spectrum class C beta-lactamase of Enterobacter cloacae GC1, a natural mutant with a tandem tripeptide insertion.
Biochemistry | 1999-08-10 | PMID 10441119
Crichlow G V, Kuzin A P, Nukaga M and 3 more
Effect of the bm12 class II mutation on proliferative and cytokine responses of encephalitogenic T cells in myelin oligodendrocyte glycoprotein (MOG)-induced experimental autoimmune encephalomyelitis.
Journal of autoimmunity | 1999-08-01 | PMID 10441162
Gur H, Mendel I, Kerlero de Rosbo N and 1 more
Genes: MOG
A duplex PCR assay for detection and genotyping of Herpes simplex virus in cerebrospinal fluid.
Molecular and cellular probes | 1999-08-01 | PMID 10441204
González-Villaseñor L I
A frequent polymorphism in the coding exon of the human cannabinoid receptor (CNR1) gene.
Molecular and cellular probes | 1999-08-01 | PMID 10441206
Gadzicki D, Müller-Vahl K, Stuhrmann M
Genes: CNR1
Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.
Human molecular genetics | 1999-09-01 | PMID 10441321
Araishi K, Sasaoka T, Imamura M and 6 more
Genes: BSG