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 1052 of 10600

Cloning and sequence of a 3.835 kbp DNA fragment containing the HIS4 gene and a fragment of a PEX5-like gene from Candida albicans.
Yeast (Chichester, England) | 1998-09-15 | PMID 9778800
Navarro-García F, Pérez-Díaz R M, Negredo A I and 2 more
Genes: PEX5
[Association of the genetic variation of (MSX1-7) and non syndromic cleft lip palate in Chilean subjects].
Revista medica de Chile | 1998-06-01 | PMID 9778871
Blanco R, Jara L, Villaseca M C
Genes: MSX1
Resistance issues and treatment implications: pneumococcus, Staphylococcus aureus, and gram-negative rods.
Infectious disease clinics of North America | 1998-09-01 | PMID 9779381
Low D E
Advances in the macrolides and quinolones.
Infectious disease clinics of North America | 1998-09-01 | PMID 9779383
Boswell F J, Wise R
A study of the interactions between an IgG-binding domain based on the B domain of staphylococcal protein A and rabbit IgG.
Molecular biotechnology | 1998-08-01 | PMID 9779419
Brown N L, Bottomley S P, Scawen M D and 1 more
Pseudoangiomatous hyperplasia of the mammary stroma: true entity or phenotype?
Pathology, research and practice | 1998-01-01 | PMID 9779487
Zanella M, Falconieri G, Lamovec J and 1 more
Spontaneous programmed cell death in infiltrating duct carcinoma: association with p53, BCL-2, hormone receptors and tumor proliferation.
Pathology, research and practice | 1998-01-01 | PMID 9779489
Pillai M R, Kesari A L, Chellam V G and 3 more
Occurrence of monocytoid B-cells in reactive lymph node lesions.
Pathology, research and practice | 1998-01-01 | PMID 9779490
Kojima M, Nakamura S, Itoh H and 6 more
Studies on fetal hemoglobin and gamma globin gene triplication in newborns in Jordan.
Proceedings of the National Science Council, Republic of China. Part B, Life sciences | 1998-07-01 | PMID 9779599
Sadiq M F
p53 gene alternation in squamous cell carcinoma of the esophagus detected by PCR-cold SSCP analysis.
Proceedings of the National Science Council, Republic of China. Part B, Life sciences | 1998-07-01 | PMID 9779600
Wang L S, Chow K C, Liu C C and 1 more
Lactobacillus amylolyticus sp. nov., isolated from beer malt and beer wort.
Systematic and applied microbiology | 1998-08-01 | PMID 9779604
Bohak I, Back W, Richter L and 3 more
A procedure for detecting selection in highly variable viral genomes: evidence of positive selection in antigenic regions of capsid protein VP1 of foot-and-mouth disease virus.
Journal of virological methods | 1998-10-01 | PMID 9779622
Martín M J, Núñez J I, Sobrino F and 1 more
Dopamine receptor genetic variation, psychosis, and aggression in Alzheimer disease.
Archives of neurology | 1998-10-01 | PMID 9779662
Sweet R A, Nimgaonkar V L, Kamboh M I and 3 more
Genes: DRD1, DRD3, DRD2, DRD4
Oculomotor phenotypes in autosomal dominant ataxias.
Archives of neurology | 1998-10-01 | PMID 9779665
Buttner N, Geschwind D, Jen J C and 3 more
Genotype-environment correlations in late childhood and early adolescence: antisocial behavioral problems and coercive parenting.
Developmental psychology | 1998-09-01 | PMID 9779743
O'Connor T G, Deater-Deckard K, Fulker D and 2 more
Predicting structural effects in HIV-1 protease mutant complexes with flexible ligand docking and protein side-chain optimization.
Proteins | 1998-11-01 | PMID 9779795
Schaffer L, Verkhivker G M
Hereditary febrile seizures: phenotype and evidence for a chromosome 19p locus.
American journal of medical genetics | 1998-10-12 | PMID 9779801
Kugler S L, Stenroos E S, Mandelbaum D E and 7 more
Genes: DPT
Hearing loss due to the mitochondrial A1555G mutation in Italian families.
American journal of medical genetics | 1998-10-12 | PMID 9779807
Casano R A, Bykhovskaya Y, Johnson D F and 4 more
Predicting survival in malignant skin melanoma using Bayesian networks automatically induced by genetic algorithms. An empirical comparison between different approaches.
Artificial intelligence in medicine | 2000-01-01 | PMID 9779891
Sierra B, Larrañaga P
An anti-sense construct of full-length ATM cDNA imposes a radiosensitive phenotype on normal cells.
Oncogene | 1998-08-20 | PMID 9779997
Zhang N, Chen P, Gatei M and 3 more
Genes: ATM
Peptide containing the BCR oligomerization domain (AA 1-160) reverses the transformed phenotype of p210bcr-abl positive 32D myeloid leukemia cells.
Oncogene | 1998-08-20 | PMID 9779999
Guo X Y, Cuillerot J M, Wang T and 7 more
Genes: BCR
Expression of exon 5 deleted estrogen receptor variant messenger RNA in human uterine myometrium and leiomyoma.
The Journal of steroid biochemistry and molecular biology | 1998-10-01 | PMID 9780024
Mito K, Tamura T, Hosokawa K and 3 more
Translation efficiencies of the 5' untranslated region from representatives of the six major genotypes of hepatitis C virus using a novel bicistronic reporter assay system.
The Journal of general virology | 1998-10-01 | PMID 9780040
Collier A J, Tang S, Elliott R M
M protein correlates with the receptor-binding specificity of haemagglutinin protein of reassortant influenza A (H1N1) virus.
The Journal of general virology | 1998-10-01 | PMID 9780048
Tong N, Nobusawa E, Morishita M and 2 more
Human immunodeficiency virus type 1 in faeces and serum: evidence against independently evolving subpopulations.
The Journal of general virology | 1998-10-01 | PMID 9780051
van der Hoek L, Goudsmit J, Maas J and 1 more
Phylogenetic analysis of 22 complete genomes of the human polyomavirus JC virus.
The Journal of general virology | 1998-10-01 | PMID 9780056
Jobes D V, Chima S C, Ryschkewitsch C F and 1 more
Four geographically distinct genotypes of JC virus are prevalent in China and Mongolia: implications for the racial composition of modern China.
The Journal of general virology | 1998-10-01 | PMID 9780057
Guo J, Sugimoto C, Kitamura T and 10 more
A role for genetic predisposition in subglottic stenosis.
International journal of pediatric otorhinolaryngology | 1998-08-01 | PMID 9780075
Pizzuto M, Donaldson D, Brodsky L
Apolipoprotein E polymorphism influences the cerebral metabolic pattern in Alzheimer's disease.
Neuroscience letters | 1998-09-18 | PMID 9780089
Mielke R, Zerres K, Uhlhaas S and 2 more
Therapy with monoclonal antibodies. II. The contribution of Fc gamma receptor binding and the influence of C(H)1 and C(H)3 domains on in vivo effector function.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-15 | PMID 9780151
Isaacs J D, Greenwood J, Waldmann H
Functional analysis of peripheral blood B cells in patients with X-linked agammaglobulinemia.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-15 | PMID 9780159
Nonoyama S, Tsukada S, Yamadori T and 6 more
Comparisons of the ability of human IgG3 hinge mutants, IgM, IgE, and IgA2, to form small immune complexes: a role for flexibility and geometry.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-15 | PMID 9780179
Roux K H, Strelets L, Brekke O H and 2 more
A nontoxic adjuvant for mucosal immunity to pneumococcal surface protein A.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-15 | PMID 9780183
Yamamoto M, Briles D E, Yamamoto S and 3 more
Virus-induced immunoinflammatory lesions in the absence of viral antigen recognition.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-15 | PMID 9780205
Gangappa S, Babu J S, Thomas J and 2 more
Mutations in the activation loop tyrosines of protein tyrosine kinase Syk abrogate intracellular signaling but not kinase activity.
Journal of immunology (Baltimore, Md. : 1950) | 1998-10-15 | PMID 9780214
Zhang J, Kimura T, Siraganian R P
Evidence for zanamivir resistance in an immunocompromised child infected with influenza B virus.
The Journal of infectious diseases | 1998-11-01 | PMID 9780244
Gubareva L V, Matrosovich M N, Brenner M K and 2 more
Full-length sequence analysis of the vacA gene from cytotoxic and noncytotoxic Helicobacter pylori.
The Journal of infectious diseases | 1998-11-01 | PMID 9780260
Ito Y, Azuma T, Ito S and 5 more
Generation and testing of mutants of Enterococcus faecalis in a mouse peritonitis model.
The Journal of infectious diseases | 1998-11-01 | PMID 9780263
Singh K V, Qin X, Weinstock G M and 1 more
Direct human papillomavirus (HPV) sequencing method yields a novel HPV in a human immunodeficiency virus-positive Quebec woman and distinguishes a new HPV clade.
The Journal of infectious diseases | 1998-11-01 | PMID 9780273
Feoli-Fonseca J C, Oligny L L, Filion M and 3 more
Diversification of subtype E human immunodeficiency virus type 1 env in heterosexual seroconverters from Northern Thailand.
The Journal of infectious diseases | 1998-11-01 | PMID 9780276
Wang Z, Lyles C M, Beyrer C and 7 more
Effect of matching of class I HLA alleles on clinical outcome after transplantation of hematopoietic stem cells from an unrelated donor. Japan Marrow Donor Program.
The New England journal of medicine | 1998-10-22 | PMID 9780337
Sasazuki T, Juji T, Morishima Y and 9 more
Glycoproteins and their relationship to human disease.
Acta anatomica | 1998-01-01 | PMID 9780351
Brockhausen I, Schutzbach J, Kuhns W
Gender differences and age of onset in the catatonic subtypes of schizophrenia.
Psychopathology | 2000-01-01 | PMID 9780397
Stöber G, Franzek E, Haubitz I and 2 more
Factors affecting population variation in eastern Adriatic isolates (Croatia).
Human biology | 1998-10-01 | PMID 9780515
Waddle D M, Sokal R R, Rudan P
Allele frequencies of six highly polymorphic DNA loci in the Croatian population.
Human biology | 1998-10-01 | PMID 9780521
Drmić I, Schanfield M S, Andjelinović S and 6 more
Genes: APOB
Acetylator phenotypes: allele frequency in northwestern Argentina and review of acetylator distribution in the Americas.
Human biology | 1998-10-01 | PMID 9780522
Dipierri J E, Alfaro E, Bejarano I F and 1 more
Frequencies of the butyrylcholinesterase K mutation in Brazilian populations of European and African origin.
Human biology | 1998-10-01 | PMID 9780523
Souza R L, Castro R M, Pereira L and 3 more
HLA DQA1 genotyping of Chinese in Taiwan by PCR-RFLP.
The Kaohsiung journal of medical sciences | 1998-08-01 | PMID 9780594
Lo F S, Chang J G, Lee Y J and 2 more
[Mutations in the genes of the HNF-family cause maturity-onset diabetes of the young (MODY)].
Nihon rinsho. Japanese journal of clinical medicine | 1998-09-01 | PMID 9780731
Takeda J
Differential validity of informant-based diagnoses of dementia and depression in index subjects and in their first-degree relatives.
Social psychiatry and psychiatric epidemiology | 1998-10-01 | PMID 9780815
Heun R, Müller H, Papassotiropoulos A
Genetics of susceptibility to Theiler's virus infection.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1998-08-01 | PMID 9780837
Brahic M, Bureau J F
Neural cell adhesion molecule L1: relating disease to function.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1998-08-01 | PMID 9780841
Kenwrick S, Doherty P
From "magic bullet" to "specially engineered shotgun loads": the new genetics and the need for individualized pharmacotherapy.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1998-08-01 | PMID 9780843
Erickson R P
Average African American three-dimensional computed tomography skull images: the potential clinical importance of ethnicity and sex.
The Journal of craniofacial surgery | 1998-07-01 | PMID 9780930
Dean D, Bookstein F L, Koneru S and 5 more
Fine mapping of Noonan/cardio-facio cutaneous syndrome in a large family.
European journal of human genetics : EJHG | 1998-01-01 | PMID 9781012
Legius E, Schollen E, Matthijs G and 1 more
Short tandem repeat polymorphism evolution in humans.
European journal of human genetics : EJHG | 1998-01-01 | PMID 9781013
Calafell F, Shuster A, Speed W C and 2 more
Genes: FST
Concentrations of the atherogenic Lp(a) are elevated in FH.
European journal of human genetics : EJHG | 1998-01-01 | PMID 9781014
Lingenhel A, Kraft H G, Kotze M and 4 more
Genes: LDLR
Mutation at the phenylalanine hydroxylase gene (PAH) and its use to document population genetic variation: the Quebec experience.
European journal of human genetics : EJHG | 1998-01-01 | PMID 9781015
Carter K C, Byck S, Waters P J and 6 more
Genes: PAH
Modifier genes in humans: strategies for identification.
European journal of human genetics : EJHG | 1998-01-01 | PMID 9781018
Houlston R S, Tomlinson I P
Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF).
European journal of human genetics : EJHG | 1998-01-01 | PMID 9781020
Dewalle M, Domingo C, Rozenbaum M and 10 more
Genes: MEFV
Detection of an insertion deletion of region 8q13-q21.2 in a patient with Duane syndrome: implications for mapping and cloning a Duane gene.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781021
Calabrese G, Stuppia L, Morizio E and 8 more
A complete protein truncation test for BRCA1 and BRCA2.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781026
Garvin A M
Genes: BRCA1, BRCA2, SDS
Identical mutation in 55% of the ATM alleles in 11 Norwegian AT families: evidence for a founder effect.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781027
Laake K, Telatar M, Geitvik G A and 5 more
Genes: ATM
A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781028
Mustapha M, Chardenoux S, Nieder A and 5 more
Identification of four novel mutations in severe methylenetetrahydrofolate reductase deficiency.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781030
Kluijtmans L A, Wendel U, Stevens E M and 3 more
Genes: MTHFR
Linkage of AD HSP and cognitive impairment to chromosome 2p: haplotype and phenotype analysis indicates variable expression and low or delayed penetrance.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781032
Byrne P C, Webb S, McSweeney F and 3 more
Cloning and gene structure of the rod cGMP phosphodiesterase delta subunit gene (PDED) in man and mouse.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781033
Lorenz B, Migliaccio C, Lichtner P and 6 more
Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781034
Rozet J M, Gerber S, Souied E and 7 more
Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781035
Terwindt G M, Ophoff R A, Haan J and 3 more
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781036
Mornet E, Taillandier A, Peyramaure S and 15 more
Genetic diversity in northern Spain (Basque Country and Cantabria): GM and KM variation related to demographic histories.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781037
Esteban E, Dugoujon J M, Guitard E and 5 more
Absence of homozygosity for predominant mutations in PMM2 in Danish patients with carbohydrate-deficient glycoprotein syndrome type 1.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781039
Kjaergaard S, Skovby F, Schwartz M
Genes: PMM2
A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781041
Leal S M, Apaydin F, Barnwell C and 8 more
Asynchronous replication of allelic loci in Down syndrome.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781044
Amiel A, Avivi L, Gaber E and 1 more
mtDNA analysis of the Galician population: a genetic edge of European variation.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781045
Salas A, Comas D, Lareu M V and 2 more
Severe limb girdle muscular dystrophy in Spanish gypsies: further evidence for a founder mutation in the gamma-sarcoglycan gene.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781048
Lasa A, Piccolo F, de Diego C and 7 more
Genes: DMD
Prenatal diagnosis in CDG1 families: beware of heterogeneity.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781052
Matthijs G, Schollen E, Cassiman J J and 3 more
Genes: PMM2
A novel 25 bp tandem repeat within the human trefoil peptide gene TFF2 in 21q22.3: polymorphism and mammalian evolution.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781055
Kayademir T, Silva E dos S, Pusch C and 3 more
Genes: TFF2
Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781056
Neyroud N, Denjoy I, Donger C and 7 more
First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781060
Devoto M, Shimoya K, Caminis J and 12 more
Human EGFR, a candidate gene for the Silver-Russell syndrome, is biallelically expressed in a wide range of fetal tissues.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781061
Wakeling E L, Abu-Amero S N, Stanier P and 2 more
Genes: EGFR
Evaluation of CFTR gene mutation testing methods in 136 diagnostic laboratories: report of a large European external quality assessment.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781062
Dequeker E, Cassiman J J
Genes: CFTR
Germline mutational analysis of presenilin 1 and APP genes in Jewish-Israeli individuals with familial or early-onset Alzheimer disease using denaturing gradient gel electrophoresis (DGGE).
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781063
Reznik-Wolf H, Treves T A, Shabtai H and 8 more
Genes: APP
Screening of CFTR mutations in an isolated population: identification of carriers and patients.
European journal of human genetics : EJHG | 2000-01-01 | PMID 9781064
Chiba-Falek O, Nissim-Rafinia M, Argaman Z and 4 more
Genes: CFTR
[Primary hyperparathyroidism].
La Revue du praticien | 1998-06-01 | PMID 9781170
Paillard M
Haptoglobin genotyping by allele-specific polymerase chain reaction amplification.
Acta medica Okayama | 1998-08-01 | PMID 9781267
Yano A, Yamamoto Y, Miyaishi S and 1 more
Bacterial lactoferrin receptors.
Advances in experimental medicine and biology | 1998-01-01 | PMID 9781351
Schryvers A B, Bonnah R, Yu R H and 2 more
Polymerase chain reaction analysis of the Y chromosome long arm in azoospermic patients: lack of the Y chromosome recognition motif (YRRM1) gene.
International journal of urology : official journal of the Japanese Urological Association | 1998-09-01 | PMID 9781447
Baba K, Iwamoto T, Nakagome Y and 5 more
Characterization of a Pasteurella haemolytica A1 mutant deficient in production of three membrane lipoproteins.
American journal of veterinary research | 1998-10-01 | PMID 9781461
Murphy G L, Whitworth L C, Confer A W and 3 more
Biases associated with genotype and sex in prediction of fat-free lean mass and carcass value in hogs.
Journal of animal science | 1998-09-01 | PMID 9781476
Hicks C, Schinckel A P, Forrest J C and 3 more
Identification of quantitative trait loci affecting carcass composition in swine: I. Fat deposition traits.
Journal of animal science | 1998-09-01 | PMID 9781479
Rohrer G A, Keele J W
Identification of quantitative trait loci affecting carcass composition in swine: II. Muscling and wholesale product yield traits.
Journal of animal science | 1998-09-01 | PMID 9781480
Rohrer G A, Keele J W
A bootstrap approach to confidence regions for genetic parameters from Method R estimates.
Journal of animal science | 1998-09-01 | PMID 9781481
Reverter A, Kaiser C J, Mallinckrodt C H
Genetic parameters for sex-specific traits in beef cattle.
Journal of animal science | 1998-09-01 | PMID 9781482
Splan R K, Cundiff L V, Van Vleck L D
Effect of ignoring random sire and dam effects on estimates and standard errors of breed comparisons.
Journal of animal science | 1998-09-01 | PMID 9781483
Barkhouse K L, Van Vleck L D, Cundiff L V
Comparison of sire breed solutions for growth traits adjusted by mean expected progeny differences to a 1993 base.
Journal of animal science | 1998-09-01 | PMID 9781484
Barkhouse K L, Van Vleck L D, Cundiff L V and 2 more
Defining multiple-trait objectives for sustainable genetic improvement.
Journal of animal science | 1998-09-01 | PMID 9781486
Gibson J P, Wilton J W
The impact of genetic markers on selection.
Journal of animal science | 1998-09-01 | PMID 9781489
Davis G P, DeNise S K
Effects of preslaughter management on the quality of carcasses from porcine stress syndrome heterozygous market hogs.
Journal of animal science | 1998-09-01 | PMID 9781499
Stalder K J, Maya J, Christian L L and 2 more
Direct genetic evidence for involvement of tau in progressive supranuclear palsy. European Study Group on Atypical Parkinsonism Consortium.
Neurology | 1998-10-01 | PMID 9781517
Bennett P, Bonifati V, Bonuccelli U and 10 more