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 1045 of 10600

Childhood absence epilepsy with tonic-clonic seizures and electroencephalogram 3-4-Hz spike and multispike-slow wave complexes: linkage to chromosome 8q24.
American journal of human genetics | 1998-10-01 | PMID 9758624
Fong G C, Shah P U, Gee M N and 11 more
Deletions in HOXD13 segregate with an identical, novel foot malformation in two unrelated families.
American journal of human genetics | 1998-10-01 | PMID 9758628
Goodman F, Giovannucci-Uzielli M L, Hall C and 3 more
Genes: HOXD13
Linkage disequilibrium mapping of the gene for Margarita Island ectodermal dysplasia (ED4) to 11q23.
American journal of human genetics | 1998-10-01 | PMID 9758630
Suzuki K, Bustos T, Spritz R A
Scale-up and optimization of the low-temperature inducible cspA promoter system.
Biotechnology progress | 2000-01-01 | PMID 9758660
Vasina J A, Peterson M S, Baneyx F
N-cadherin/catenin-mediated morphoregulation of somite formation.
Developmental biology | 1998-10-01 | PMID 9758705
Linask K K, Ludwig C, Han M D and 3 more
Identification of gametophytic mutations affecting female gametophyte development in Arabidopsis.
Developmental biology | 1998-10-01 | PMID 9758709
Christensen C A, Subramanian S, Drews G N
Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency.
Molecular genetics and metabolism | 1998-08-01 | PMID 9758712
Yang B Z, Ding J H, Dewese T and 8 more
Molecular basis of hyperargininemia: structure-function consequences of mutations in human liver arginase.
Molecular genetics and metabolism | 1998-08-01 | PMID 9758714
Ash D E, Scolnick L R, Kanyo Z F and 3 more
Genetic heterogeneity of adrenocorticotropin (ACTH) resistance syndromes: identification of a novel mutation of the ACTH receptor gene in hereditary glucocorticoid deficiency.
Molecular genetics and metabolism | 1998-08-01 | PMID 9758716
Wu S M, Stratakis C A, Chan C H and 4 more
Genes: HGD
PCR-based methods for identifying genetic variations in human alpha1B- and beta2-adrenergic receptors.
Molecular genetics and metabolism | 1998-08-01 | PMID 9758717
Büscher R, Herrmann V, Insel P A
Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population.
Molecular genetics and metabolism | 1998-08-01 | PMID 9758720
Li L, Eng C, Desnick R J and 2 more
Alteration of the intestinal intraepithelial lymphocytes during total parenteral nutrition.
The Journal of surgical research | 1998-10-01 | PMID 9758721
Kiristioglu I, Teitelbaum D H
Coexpression of G-CSF with an unglycosylated G-CSF receptor mutant results in secretion of a stable complex.
Protein expression and purification | 1998-10-01 | PMID 9758750
Horan T P, Simonet L, Jacobsen R and 6 more
Genes: CRH
The transcriptional activator XlnR regulates both xylanolytic and endoglucanase gene expression in Aspergillus niger.
Applied and environmental microbiology | 1998-10-01 | PMID 9758775
van Peij N N, Gielkens M M, de Vries R P and 2 more
Phenotypic and phylogenetic characterization of ruminal tannin-tolerant bacteria.
Applied and environmental microbiology | 1998-10-01 | PMID 9758806
Nelson K E, Thonney M L, Woolston T K and 2 more
New hybrids between Saccharomyces sensu stricto yeast species found among wine and cider production strains.
Applied and environmental microbiology | 1998-10-01 | PMID 9758815
Masneuf I, Hansen J, Groth C and 2 more
Isolation and identification of Helicobacter spp. from canine and feline gastric mucosa.
Applied and environmental microbiology | 1998-10-01 | PMID 9758832
Jalava K, On S L, Vandamme P A and 3 more
Resistance to tellurite as a selection marker for genetic manipulations of Pseudomonas strains.
Applied and environmental microbiology | 1998-10-01 | PMID 9758838
Sanchez-Romero J M, Diaz-Orejas R, De Lorenzo V
[Val384Asp in hMLH1 gene in Chinese, Japanese and German and its etiological role in colorectal cancer].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1998-10-10 | PMID 9758868
Wang Y, Friedl W, Propping P and 3 more
[Association between the debrisoquine hydroxylase gene polymorphism and the genetic susceptibility of Parkinson's disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1998-10-10 | PMID 9758873
Tao E, Liu Z, Chen B and 2 more
[Identification of a mutation hotspot in exon 8 of Wilson's disease gene by cycle sequencing].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1998-10-10 | PMID 9758874
Xu Y, Fan Y, Yu L and 6 more
[A study of correlation between essential hypertension and HLA-DQA1 alleles].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1998-10-10 | PMID 9758875
Sun N, Yan W, Yan Z and 3 more
[Comparison of genotype and intellectual phenotype in untreated phenylketonuric children].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1998-10-10 | PMID 9758878
Yuan L, Fang B, Wang M and 4 more
Genes: PAH
[Relationship between methylenetetrahydrofolate reductase gene polymorphism and coronary heart disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1998-10-10 | PMID 9758879
Chen B, Wang X, Yu J and 7 more
Genes: MTHFR
[PCR in combination with silver as a method for the determination of apolipoprotein E alleles].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1998-10-10 | PMID 9758882
Zhang A, Han Z, Wang L and 1 more
[Genetic basis of Prader-Willi and Angelman syndromes: implications for the biologic diagnosis].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie | 1998-04-01 | PMID 9759164
Dupont J M, Cuisset L
Atypical microtubule organization in undifferentiated human colon cancer cells.
Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie | 1998-01-01 | PMID 9759353
Chazaud B, Muriel M P, Aubery M and 1 more
[Physiopathology of calcium channels: identification of calcium channelopathies].
Comptes rendus des seances de la Societe de biologie et de ses filiales | 1998-01-01 | PMID 9759359
Lory P, Monteil A
[Culture of human keratocytes. Influence of culture conditions and ultrastructural aspects].
Journal francais d'ophtalmologie | 1998-02-01 | PMID 9759390
Borderie V, Sabolic V, Laroche L
A splicing mutation of the RHAG gene associated with the Rhnull phenotype.
Annals of human genetics | 1998-03-01 | PMID 9759472
Kawano M, Iwamoto S, Okuda H and 3 more
Genes: RHAG, RHD
Age-related changes of the 3'APOB-VNTR genotype pool in ageing cohorts.
Annals of human genetics | 1998-03-01 | PMID 9759473
De Benedictis G, Carotenuto L, Carrieri G and 6 more
Genes: APOB
HLA evidence for the lack of genetic heterogeneity in Basques.
Annals of human genetics | 1998-03-01 | PMID 9759474
Comas D, Calafell F, Mateu E and 2 more
Genes: FST
Diversity in protein, nuclear DNA, and mtDNA in South Amerinds--agreement or discrepancy?
Annals of human genetics | 1998-03-01 | PMID 9759475
Bortolini M C, Baptista C, Callegari-Jacques S M and 2 more
Hidden linkage: a comparison of the affected sib pair (ASP) test and transmission/disequilibrium test (TDT).
Annals of human genetics | 1998-03-01 | PMID 9759477
McGinnis R E
Characterization of polymorphisms at the 11 beta-hydroxylase (CYP11B1) locus.
Annals of human genetics | 1998-03-01 | PMID 9759478
Skinner C A, Yousaf N, Honour J W and 1 more
Selection of EPS-deficient mutants (Exo-) from Rhizobiun huakuii 107 by region-directed Tn5 mutagenesis.
Chinese journal of biotechnology | 1998-01-01 | PMID 9759544
Zhou B, Huang J, Su W and 1 more
What is a cystic fibrosis diagnosis?
Clinics in chest medicine | 1998-09-01 | PMID 9759547
Rosenstein B J
Clinical implications of cystic fibrosis transmembrane conductance regulator mutations.
Clinics in chest medicine | 1998-09-01 | PMID 9759548
Mickle J E, Cutting G R
Genes: CFTR
What we know and what we do not know about cystic fibrosis transmembrane conductance regulator.
Clinics in chest medicine | 1998-09-01 | PMID 9759549
Ma J, Davis P B
Genes: CFTR
Therapies directed at the basic defect in cystic fibrosis.
Clinics in chest medicine | 1998-09-01 | PMID 9759553
Zeitlin P L
The prothrombin 20210A allele is the most prevalent genetic risk factor for venous thromboembolism in the Spanish population.
Thrombosis and haemostasis | 1998-09-01 | PMID 9759610
Souto J C, Coll I, Llobet D and 5 more
A mutation in plasma platelet-activating factor acetylhydrolase (Val279Phe) is a genetic risk factor for cerebral hemorrhage but not for hypertension.
Thrombosis and haemostasis | 1998-09-01 | PMID 9759612
Yoshida H, Imaizumi T, Fujimoto K and 5 more
Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasma.
Thrombosis and haemostasis | 1998-09-01 | PMID 9759618
Castoldi E, Kalafatis M, Lunghi B and 6 more
Genes: APC
Analysis of platelet glycoprotein Ia (alpha2 integrin) allele frequencies in three North American populations reveals genetic association between nucleotide 807C/T and amino acid 505 Glu/Lys (HPA-5) dimorphisms.
Thrombosis and haemostasis | 1998-09-01 | PMID 9759626
Reiner A P, Aramaki K M, Teramura G and 1 more
Altered protein localization in melanocytes from Hermansky-Pudlak syndrome: support for the role of the HPS gene product in intracellular trafficking.
Laboratory investigation; a journal of technical methods and pathology | 1998-09-01 | PMID 9759648
Boissy R E, Zhao Y, Gahl W A
Cell cycle-related gene abnormalities and product expression in esophageal carcinoma.
Laboratory investigation; a journal of technical methods and pathology | 1998-09-01 | PMID 9759649
Roncalli M, Bosari S, Marchetti A and 7 more
Permanent skin replacement using engineered epidermis containing fewer than 5% syngeneic keratinocytes.
Laboratory investigation; a journal of technical methods and pathology | 1998-09-01 | PMID 9759653
Larochelle F, Ross G, Rouabhia M
Acquired resistance of a mammalian cell line to hypoxia-reoxygenation through cotransfection of Kir6.2 and SUR1 clones.
Laboratory investigation; a journal of technical methods and pathology | 1998-09-01 | PMID 9759654
Jovanovic A, Jovanovic S, Carrasco A J and 1 more
Down-regulation of E-cadherin in mouse skin carcinoma cells enhances a migratory and invasive phenotype linked to matrix metalloproteinase-9 gelatinase expression.
Laboratory investigation; a journal of technical methods and pathology | 1998-09-01 | PMID 9759657
Llorens A, Rodrigo I, López-Barcons L and 6 more
Drosophila oocyte localization is mediated by differential cadherin-based adhesion.
Nature | 1998-09-24 | PMID 9759729
Godt D, Tepass U
Position and orientation of the globular domain of linker histone H5 on the nucleosome.
Nature | 1998-09-24 | PMID 9759733
Zhou Y B, Gerchman S E, Ramakrishnan V and 2 more
Fine specificity of the myelin-reactive T cell repertoire: implications for TCR antagonism in autoimmunity.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-01 | PMID 9759852
Anderton S M, Manickasingham S P, Burkhart C and 4 more
C4d DNA sequences of two infrequent human allotypes (C4A13 and C4B12) and the presence of signal sequences enhancing recombination.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-01 | PMID 9759862
Martínez-Quiles N, Paz-Artal E, Moreno-Pelayo M A and 4 more
Structural basis of specificity and degeneracy of T cell recognition: pluriallelic restriction of T cell responses to a peptide antigen involves both specific and promiscuous interactions between the T cell receptor, peptide, and HLA-DR.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-01 | PMID 9759873
Doherty D G, Penzotti J E, Koelle D M and 4 more
CYP2E1 genotyping in renal cell/urothelial cancer patients in comparison with control populations.
International journal of clinical pharmacology and therapeutics | 1998-09-01 | PMID 9760005
Farker K, Lehmann M H, Kästner R and 5 more
Abnormal mushroom body plasticity in the Drosophila memory mutant amnesiac.
Neuroreport | 1998-08-24 | PMID 9760108
Hitier R, Heisenberg M, Préat T
Molecular analysis of Chs3p participation in chitin synthase III activity.
European journal of biochemistry | 1998-09-01 | PMID 9760183
Cos T, Ford R A, Trilla J A and 3 more
Biochemical characterization and crystal structure of a recombinant hen avidin and its acidic mutant expressed in Escherichia coli.
European journal of biochemistry | 1998-09-01 | PMID 9760187
Nardone E, Rosano C, Santambrogio P and 10 more
Japanese juvenile retinoschisis is caused by mutations of the XLRS1 gene.
Human genetics | 1998-08-01 | PMID 9760195
Hotta Y, Fujiki K, Hayakawa M and 9 more
Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B).
Human genetics | 1998-08-01 | PMID 9760196
Svensson P J, Anvret M, Molander M L and 1 more
Genes: RET, EDNRB, GDNF, EDN3
A high proportion of mutations in the BRCA1 gene in German breast/ovarian cancer families with clustering of mutations in the 3' third of the gene.
Human genetics | 1998-08-01 | PMID 9760198
Dong J, Chang-Claude J, Wu Y and 4 more
Genes: BRCA1
Mutations in the pterin-4alpha-carbinolamine dehydratase (PCBD) gene cause a benign form of hyperphenylalaninemia.
Human genetics | 1998-08-01 | PMID 9760199
Thöny B, Neuheiser F, Kierat L and 9 more
A novel splice site mutation in the tissue inhibitor of the metalloproteinases-3 gene in Sorsby's fundus dystrophy with unusual clinical features.
Human genetics | 1998-08-01 | PMID 9760202
Tabata Y, Isashiki Y, Kamimura K and 2 more
Genes: TIMP3
Linkage disequilibrium and linkage analysis of the glucose-6-phosphatase gene.
Human genetics | 1998-08-01 | PMID 9760206
Wong L J, Liang M H, Hwu W L and 1 more
Extensive polymorphism of the FUT2 gene in an African (Xhosa) population of South Africa.
Human genetics | 1998-08-01 | PMID 9760207
Liu Y, Koda Y, Soejima M and 4 more
Genes: FUT2
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus.
Human genetics | 1998-08-01 | PMID 9760208
Kidd K K, Morar B, Castiglione C M and 11 more
Genes: DRD2
Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNA.
Human genetics | 1998-08-01 | PMID 9760209
Millar D S, Krawczak M, Cooper D N
An ecological study of association between coronary heart disease mortality rates in men and the relative frequencies of common allelic variations in the gene coding for apolipoprotein E.
Human genetics | 1998-08-01 | PMID 9760210
Stengård J H, Weiss K M, Sing C F
Genotype/phenotype correlation in affected individuals of a family with a deletion of the entire coding sequence of the connexin 32 gene.
Human genetics | 1998-08-01 | PMID 9760211
Ainsworth P J, Bolton C F, Murphy B C and 2 more
Genetic and other determinants of AMP deaminase activity in healthy adult skeletal muscle.
Journal of applied physiology (Bethesda, Md. : 1985) | 1998-10-01 | PMID 9760316
Norman B, Mahnke-Zizelman D K, Vallis A and 1 more
Genes: AMPD1, AMPD3
[Polymorphism of the ACE gene and left ventricular morphology and function in patients with borderline, mild and moderate hypertension].
Polskie Archiwum Medycyny Wewnetrznej | 1998-03-01 | PMID 9760806
Swierblewska E, Chrostowska M, Dudziak M and 5 more
Genes: ACE
[Combined hemostatic defects in family members of symptomatic carriers of Leiden mutations of factor V].
Polskie Archiwum Medycyny Wewnetrznej | 1998-03-01 | PMID 9760807
Lewandowski K, Rozek M, Turowiecka Z and 2 more
[Association of bone mineral density with vitamin D receptor gene polymorphism--changes in radial bone mineral density with long-term follow-up: longitudinal study].
Rinsho byori. The Japanese journal of clinical pathology | 1998-08-01 | PMID 9760828
Murakami F, Hagino H, Shimomura T and 4 more
Genes: VDR
[The examination of apoE phenotypes in diabetic patients with peripheral neuropathy].
Rinsho byori. The Japanese journal of clinical pathology | 1998-08-01 | PMID 9760837
Tsuzuki S, Murano T, Watanabe H and 3 more
Genetics of the febrile seizure susceptibility trait.
Brain & development | 1998-08-01 | PMID 9760995
Kugler S L, Johnson W G
Fatal cyst formation after fetal mesencephalic allograft transplant for Parkinson's disease.
Journal of neurosurgery | 1998-10-01 | PMID 9761053
Mamelak A N, Eggerding F A, Oh D S and 5 more
CFTR deltaF508 carrier status, risk of breast cancer before the age of 40 and histological grading in a population-based case-control study.
International journal of cancer | 1998-10-23 | PMID 9761117
Southey M C, Batten L, Andersen C R and 5 more
Genes: CFTR
Association between genetic polymorphisms of glutathione S-transferase P1 and N-acetyltransferase 2 and susceptibility to squamous-cell carcinoma of the esophagus.
International journal of cancer | 1998-10-23 | PMID 9761122
Morita S, Yano M, Tsujinaka T and 7 more
Genes: GSTP1, NAT2
Carcinomas of the renal pelvis associated with smoking and phenacetin abuse: p53 mutations and polymorphism of carcinogen-metabolising enzymes.
International journal of cancer | 1998-10-23 | PMID 9761125
Bringuier P P, McCredie M, Sauter G and 5 more
Genes: GSTM1, GSTT1, NAT1
Plasma concentration, kinetic constants, and gene polymorphism of angiotensin I-converting enzyme in centenarians.
Clinical chemistry | 1998-10-01 | PMID 9761238
Faure-Delanef L, Baudin B, Bénéteau-Burnat B and 3 more
Genes: ACE
Myofibroblast transformation of cat corneal endothelium by transforming growth factor-beta1, -beta2, and -beta3.
Investigative ophthalmology & visual science | 1998-10-01 | PMID 9761280
Petroll W M, Jester J V, Bean J J and 1 more
Vitreous treatment of retinal pigment epithelial cells results in decreased expression of FGF-2.
Investigative ophthalmology & visual science | 1998-10-01 | PMID 9761290
Hunt D M, Chen W H, Hunt R C
Genes: RPE
Glutamate receptor mechanisms in human epileptic dysplastic cortex.
Epilepsy research | 1998-09-01 | PMID 9761306
Babb T L, Ying Z, Hadam J and 1 more
Bacteriocin production and competitiveness of Lactobacillus plantarum LPCO10 in olive juice broth, a culture medium obtained from olives.
International journal of food microbiology | 1998-08-18 | PMID 9761347
Leal M V, Baras M, Ruiz-Barba J L and 2 more
Establishment and characterization of pro-B cell lines from motheaten mutant mouse defective in SHP-1 protein tyrosine phosphatase.
Immunology letters | 1998-09-01 | PMID 9761368
Miyamoto A, Kunisada T, Yamazaki H and 5 more
Activation of CD4+ and CD8+ parasite -specific T-cells by macrophages infected with live T. cruzi amastigotes.
Immunology letters | 1998-09-01 | PMID 9761371
Caulada-Benedetti Z, Vecchio L C, Pardi C C and 3 more
Molecular analysis of the BRCA2 gene in 16 breast/ovarian cancer Spanish families.
Clinical genetics | 1998-08-01 | PMID 9761393
Osorio A, Robledo M, Martínez B and 5 more
Genes: BRCA2
Class-directed structure determination: foundation for a protein structure initiative.
Protein science : a publication of the Protein Society | 1998-09-01 | PMID 9761466
Terwilliger T C, Waldo G, Peat T S and 3 more
Conversion of a beta-strand to an alpha-helix induced by a single-site mutation observed in the crystal structure of Fis mutant Pro26Ala.
Protein science : a publication of the Protein Society | 1998-09-01 | PMID 9761469
Yang W Z, Ko T P, Corselli L and 2 more
Effects of salt bridges on protein structure and design.
Protein science : a publication of the Protein Society | 1998-09-01 | PMID 9761471
Sindelar C V, Hendsch Z S, Tidor B
The structure of serine hydroxymethyltransferase as modeled by homology and validated by site-directed mutagenesis.
Protein science : a publication of the Protein Society | 1998-09-01 | PMID 9761478
Pascarella S, Angelaccio S, Contestabile R and 3 more
Methylenetetrahydrofolate-reductase gene C677T variant and kidney-transplant survival.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association | 1998-09-01 | PMID 9761522
Liangos O, Kreutz R, Beige J and 3 more
Genes: MTHFR
Sequence-dependent extrusion of a small DNA hairpin at the N4 virion RNA polymerase promoters.
Journal of molecular biology | 1998-01-01 | PMID 9761672
Dai X, Kloster M, Rothman-Denes L B
Towards the design of rare cutting restriction endonucleases: using directed evolution to generate variants of EcoRV differing in their substrate specificity by two orders of magnitude.
Journal of molecular biology | 1998-01-01 | PMID 9761673
Lanio T, Jeltsch A, Pingoud A
HIV-1 rev nuclear export signal binding peptides isolated by phage display.
Journal of molecular biology | 1998-01-01 | PMID 9761687
Jensen A, Jensen T H, Kjems J
The cysteine-string domain of the secretory vesicle cysteine-string protein is required for membrane targeting.
The Biochemical journal | 1998-10-15 | PMID 9761715
Chamberlain L H, Burgoyne R D
Stimulation of gene expression in neonatal rat ventricular myocytes by Ras is mediated by Ral guanine nucleotide dissociation stimulator (Ral.GDS) and phosphatidylinositol 3-kinase in addition to Raf.
The Biochemical journal | 1998-10-15 | PMID 9761720
Fuller S J, Finn S G, Downward J and 1 more
Atypical protein kinase Clambda binds and regulates p70 S6 kinase.
The Biochemical journal | 1998-10-15 | PMID 9761742
Akimoto K, Nakaya M, Yamanaka T and 5 more
Molecular mimicry and immune-mediated diseases.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 1998-10-01 | PMID 9761770
Oldstone M B
Putative susceptibility markers of coronary artery disease: association between VDR genotype, smoking, and aromatic DNA adduct levels in human right atrial tissue.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology | 1998-10-01 | PMID 9761785
Van Schooten F J, Hirvonen A, Maas L M and 4 more
Genes: CAD, VDR, GSTM1, GSTT1