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.

Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.

Publications

Page 753 of 10600

Genotyping may provide rapid identification of Escherichia coli K1 organisms that cause neonatal meningitis.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America | 1996-01-01 | PMID 8824985
Bingen E, Denamur E, Brahimi N and 1 more
Diagnosis of malignant hyperthermia: a comparison of the in vitro contracture test with the molecular genetic diagnosis in a large pedigree.
Journal of medical genetics | 1996-01-01 | PMID 8825043
Healy J M, Quane K A, Keating K E and 3 more
Genes: RYR1
Variation of phenotype in patients with glucocorticoid remediable aldosteronism.
Journal of medical genetics | 1996-01-01 | PMID 8825044
Gates L J, MacConnachie A A, Lifton R P and 2 more
Haplotype analysis in prenatal diagnosis and carrier identification of Salla disease.
Journal of medical genetics | 1996-01-01 | PMID 8825046
Schleutker J, Sistonen P, Aula P
X linked hydrocephalus and MASA syndrome.
Journal of medical genetics | 1996-01-01 | PMID 8825051
Kenwrick S, Jouet M, Donnai D
Clinical features of cystic fibrosis patients with rare genotypes.
Journal of medical genetics | 1996-01-01 | PMID 8825054
Castaldo G, Rippa E, Raia V and 4 more
Locus-dependent profiles of the rescue of nonexcitable behavioral mutants during conjugation in Paramecium caudatum.
Cell structure and function | 1995-12-01 | PMID 8825064
Takahashi M
Genetic heterogeneity in familial dilated cardiomyopathy.
Biochemical and molecular medicine | 1995-12-01 | PMID 8825069
Schultz K R, Gajarski R J, Pignatelli R and 4 more
Characterization of the N314D allele of human galactose-1-phosphate uridylyltransferase using a yeast expression system.
Biochemical and molecular medicine | 1995-12-01 | PMID 8825075
Fridovich-Keil J L, Quimby B B, Wells L and 2 more
Genes: GALT
In vivo oxidation of [13C]galactose in patients with galactose-1-phosphate uridyltransferase deficiency.
Biochemical and molecular medicine | 1995-12-01 | PMID 8825079
Berry G T, Nissim I, Mazur A T and 6 more
Genes: GALT
Modulation of DNA topology by flaR, a new gene from Listeria monocytogenes.
Molecular microbiology | 1995-12-01 | PMID 8825084
Sanchez-Campillo M, Dramsi S, Gómez-Gómez J M and 5 more
Helicobacter pylori picB, a homologue of the Bordetella pertussis toxin secretion protein, is required for induction of IL-8 in gastric epithelial cells.
Molecular microbiology | 1995-12-01 | PMID 8825091
Tummuru M K, Sharma S A, Blaser M J
A missense mutation in rpoD results in an A-signalling defect in Myxococcus xanthus.
Molecular microbiology | 1995-12-01 | PMID 8825098
Davis J M, Mayor J, Plamann L
Osmoregulation of fission yeast: cloning of two distinct genes encoding glycerol-3-phosphate dehydrogenase, one of which is responsible for osmotolerance for growth.
Molecular microbiology | 1995-12-01 | PMID 8825100
Ohmiya R, Yamada H, Nakashima K and 2 more
Genes: GPD1
The product of the pilQ gene is essential for the biogenesis of type IV pili in Neisseria gonorrhoeae.
Molecular microbiology | 1995-12-01 | PMID 8825101
Drake S L, Koomey M
Evaluation of different amplification protocols for use in primer-extension preamplification.
BioTechniques | 1996-02-01 | PMID 8825151
Casas E, Kirkpatrick B W
General approach to analysis of polymorphic short tandem repeat loci.
BioTechniques | 1996-02-01 | PMID 8825157
Sprecher C J, Puers C, Lins A M and 1 more
Clinical features and natural history of spinocerebellar ataxia type 1.
Acta neurologica Scandinavica | 1996-01-01 | PMID 8825276
Sasaki H, Fukazawa T, Yanagihara T and 7 more
Role of the common cytokine receptor gamma chain in cytokine signaling and lymphoid development.
Immunological reviews | 1995-12-01 | PMID 8825284
Leonard W J, Shores E W, Love P E
Genes: TSLP
Comparative studies of the efficacy of a recombinant feline leukaemia virus vaccine.
The Veterinary record | 1996-01-06 | PMID 8825325
Jarrett O, Ganière J P
The CDC6 gene is required for centromeric, episomal, and 2-microns plasmid stability in the yeast Saccharomyces cerevisiae.
Plasmid | 1995-11-01 | PMID 8825371
Storici F, Oberto J, Bruschi C V
Genes: CDC6
Postnatal differentiation of rabbit collecting duct intercalated cells.
Pediatric research | 1996-01-01 | PMID 8825379
Matsumoto T, Fejes-Toth G, Schwartz G J
Host genotype controls the ability of the ISGF3 complex to activate transcription of IFN-inducible genes.
Journal of cellular biochemistry | 1996-01-01 | PMID 8825418
Gariglio M, Foresta P, Ying G G and 3 more
Genes: CAT, BLK
Malic dehydrogenase isoenzymatic pattern in lung-nematode parasite species.
Parasitology research | 1996-01-01 | PMID 8825454
Cutillas C, Arias P, Spakulova M
Detection of the plasma cholinesterase K variant by PCR using an amplification-created restriction site.
Human heredity | 2000-01-01 | PMID 8825459
Jensen F S, Nielsen L R, Schwartz M
Genetic epidemiology of the Mitsuda reaction in leprosy.
Human heredity | 2000-01-01 | PMID 8825460
Feitosa M, Krieger H, Borecki I and 2 more
p53 polymorphisms and haplotypes show distinct differences between major ethnic groups.
Human heredity | 2000-01-01 | PMID 8825462
Själander A, Birgander R, Saha N and 2 more
p53 polymorphisms and haplotypes in nasopharyngeal cancer.
Human heredity | 2000-01-01 | PMID 8825463
Birgander R, Själander A, Zhou Z and 3 more
BalI and MspI polymorphisms of the dopamine D3 receptor gene in African Blacks and Caucasians.
Human heredity | 2000-01-01 | PMID 8825465
Crocq M A, Buguet A, Bisser S and 6 more
Membrane protein assembly: genetic, evolutionary and medical perspectives.
Annual review of genetics | 1995-01-01 | PMID 8825471
Manoil C, Traxler B
Molecular genetic aspects of human mitochondrial disorders.
Annual review of genetics | 1995-01-01 | PMID 8825472
Larsson N G, Clayton D A
Conservation genetics.
Annual review of genetics | 1995-01-01 | PMID 8825477
Frankham R
Genetics of hereditary colon cancer.
Annual review of genetics | 1995-01-01 | PMID 8825478
de la Chapelle A, Peltomäki P
Genetic variation and aging.
Annual review of genetics | 1995-01-01 | PMID 8825486
Curtsinger J W, Fukui H H, Khazaeli A A and 4 more
Genetic analysis of the multidrug transporter.
Annual review of genetics | 1995-01-01 | PMID 8825488
Gottesman M M, Hrycyna C A, Schoenlein P V and 2 more
Inherited hearing defects in mice.
Annual review of genetics | 1995-01-01 | PMID 8825490
Steel K P
Cystic fibrosis: genotypic and phenotypic variations.
Annual review of genetics | 1995-01-01 | PMID 8825494
Zielenski J, Tsui L C
Genes: CFTR
Genetic differentiation of Aedes aegypti, the vector of dengue virus in French Polynesia.
Journal of the American Mosquito Control Association | 1995-12-01 | PMID 8825508
Failloux A B, Darius H, Pasteur N
Mutations of neighboring polar residues on the second transmembrane helix disrupt signaling by the parathyroid hormone receptor.
Molecular endocrinology (Baltimore, Md.) | 1996-02-01 | PMID 8825553
Turner P R, Bambino T, Nissenson R A
Genes: PTH
Chronological difference in walking impairment among Japanese group A xeroderma pigmentosum (XP-A) patients with various combinations of mutation sites.
Clinical genetics | 1995-11-01 | PMID 8825598
Maeda T, Sato K, Minami H and 2 more
Genes: XPA
Muscle expression of glucose-6-phosphate dehydrogenase deficiency in different variants.
Clinical genetics | 1995-11-01 | PMID 8825599
Ninfali P, Baronciani L, Bardoni A and 1 more
Mitochondrial gene mutations in familial non-insulin-dependent diabetes mellitus in Taiwan.
Clinical genetics | 1995-11-01 | PMID 8825603
Chuang L M, Wu H P, Chiu K C and 3 more
A novel missense mutation in exon 3 of the COL4A5 gene associated with late-onset Alport syndrome.
Clinical genetics | 1995-11-01 | PMID 8825605
Turco A E, Rossetti S, Biasi M O and 6 more
Identification of neurofibromatosis 1 (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids.
Genomics | 1995-12-10 | PMID 8825634
Purandare S M, Huntsman Breidenbach H, Li Y and 7 more
A precise meiotic map in the class I region of the human major histocompatibility complex.
Genomics | 1995-12-10 | PMID 8825635
Bouissou C, Pontarotti P, Crouau-Roy B
Ultrarapid mutation detection by multiplex, solid-phase chemical cleavage.
Genomics | 1995-12-10 | PMID 8825645
Rowley G, Saad S, Giannelli F and 1 more
Increased frequency of HLA DR13 in hepatitis C virus carriers with persistently normal ALT levels.
Journal of medical virology | 1996-01-01 | PMID 8825703
Kuzushita N, Hayashi N, Katayama K and 10 more
Analysis of hepatitis B virus genotypes and pre-core region variability during interferon treatment of HBe antigen negative chronic hepatitis B.
Journal of medical virology | 1996-01-01 | PMID 8825704
Zhang X, Zoulim F, Habersetzer F and 2 more
Evidence in Gabon for an intrafamilial clustering with mother-to-child and sexual transmission of a new molecular variant of human T-lymphotropic virus type-II subtype B.
Journal of medical virology | 1996-01-01 | PMID 8825706
Tuppin P, Gessain A, Kazanji M and 6 more
Gradual accumulation of mutations in precore core region of HBV in patients with chronic active hepatitis: implications of clustering changes in a small region of the HBV core region.
Journal of medical virology | 1996-01-01 | PMID 8825708
Hur G M, Lee Y I, Suh D J and 2 more
Genital papillomavirus in Greek women with high-grade cervical intraepithelial neoplasia and cervical carcinoma.
Journal of medical virology | 1996-01-01 | PMID 8825715
Labropoulou V, Diakomanolis E, Dailianas S and 5 more
Genotypes of human polyomaviruses in urine samples of pregnant women in Taiwan.
Journal of medical virology | 1996-01-01 | PMID 8825717
Chang D, Wang M, Ou W C and 3 more
Detection of a nuclear antigen 2 (EBNA2)-variant Epstein-Barr virus strain in two siblings with fatal lymphoproliferative disease.
Journal of medical virology | 1996-01-01 | PMID 8825720
Schuster V, Seidenspinner S, Kreth H W
Molecular dynamics simulations indicate that F87W,T185F-cytochrome P450cam may reductively dehalogenate 1,1,1-trichloroethane.
Journal of biomolecular structure & dynamics | 1995-12-01 | PMID 8825721
Manchester J I, Ornstein R L
Cloning and characterization of the white gene from Anopheles gambiae.
Insect molecular biology | 1995-11-01 | PMID 8825759
Besansky N J, Bedell J A, Benedict M Q and 3 more
The effect of the stringent response on mutation rates in Escherichia coli K-12.
Molecular microbiology | 1996-01-01 | PMID 8825767
Wright B E
A dual role for the Bacillus subtilis glpD leader and the GlpP protein in the regulated expression of glpD: antitermination and control of mRNA stability.
Molecular microbiology | 1996-01-01 | PMID 8825777
Glatz E, Nilsson R P, Rutberg L and 1 more
Identification and characterization of genes required for post-translational modification of Campylobacter coli VC167 flagellin.
Molecular microbiology | 1996-01-01 | PMID 8825781
Guerry P, Doig P, Alm R A and 3 more
Genes: SDS
Characterization of a post-translational modification of Campylobacter flagellin: identification of a sero-specific glycosyl moiety.
Molecular microbiology | 1996-01-01 | PMID 8825782
Doig P, Kinsella N, Guerry P and 1 more
Hepatitis C viral infection in thalassemic children: clinical and molecular studies.
Pediatric research | 1996-02-01 | PMID 8825807
Ni Y H, Chang M H, Lin K H and 4 more
Sequence analysis of the 5' untranslated region of pestivirus RNA demonstrated in interferons for human use.
Biologicals : journal of the International Association of Biological Standardization | 1995-12-01 | PMID 8825854
Harasawa R, Sasaki T
Family patterns of developmental dyslexia, part II: behavioral phenotypes.
American journal of medical genetics | 1995-12-18 | PMID 8825885
Wolff P H, Melngailis I, Obregon M and 1 more
Analysis of clozapine response and polymorphisms of the dopamine D4 receptor gene (DRD4) in schizophrenic patients.
American journal of medical genetics | 1995-12-18 | PMID 8825892
Shaikh S, Collier D A, Sham P and 6 more
Genes: DRD4
Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives.
American journal of medical genetics | 1995-12-18 | PMID 8825894
Pérez-Tur J, Campion D, Martinez M and 7 more
Genes: APOE
Association study of dopamine D3 receptor gene and schizophrenia.
American journal of medical genetics | 1995-12-18 | PMID 8825896
Kennedy J L, Billett E A, Macciardi F M and 5 more
Genes: DRD3
Allele doses of apolipoprotein E type epsilon 4 in sporadic late-onset Alzheimer's disease.
American journal of medical genetics | 1995-12-18 | PMID 8825898
Lucotte G, Aouizérate A, Gérard N and 2 more
Association analysis of a polymorphism of the monoamine oxidase B gene with Parkinson's disease in a Japanese population.
American journal of medical genetics | 1995-12-18 | PMID 8825899
Morimoto Y, Murayama N, Kuwano A and 3 more
Lack of association between dopamine D4 receptor gene and schizophrenia.
American journal of medical genetics | 1995-12-18 | PMID 8825901
Tanaka T, Igarashi S, Onodera O and 5 more
Induction of the phoE promoter upon invasion of Salmonella typhimurium into eukaryotic cells.
Microbial pathogenesis | 1995-10-01 | PMID 8825907
Janssen R, Verjans G M, Kusters J G and 1 more
Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.
Journal of medical genetics | 1995-12-01 | PMID 8825918
Eng C, Crossey P A, Mulligan L M and 7 more
Genes: VHL, RET
An extended Li-Fraumeni kindred with gastric carcinoma and a codon 175 mutation in TP53.
Journal of medical genetics | 1995-12-01 | PMID 8825920
Varley J M, McGown G, Thorncroft M and 6 more
The Irish cystic fibrosis database.
Journal of medical genetics | 1995-12-01 | PMID 8825927
Cashman S M, Patino A, Delgado M G and 3 more
Genes: CFTR
Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria.
Journal of medical genetics | 1995-12-01 | PMID 8825929
Lundin G, Hashemi J, Floderus Y and 6 more
Genes: AIP
Familial café au lait spots: a variant of neurofibromatosis type 1.
Journal of medical genetics | 1995-12-01 | PMID 8825931
Abeliovich D, Gelman-Kohan Z, Silverstein S and 4 more
Partial disomy of Xp and the presence of SRY in a phenotypic female.
Journal of medical genetics | 1995-12-01 | PMID 8825932
Bajalica S, Blennow E, Tşezou A and 4 more
Genes: SRY, DMD, ZFY
Del(3) (p25.3) without phenotypic effect.
Journal of medical genetics | 1995-12-01 | PMID 8825934
Knight L A, Yong M H, Tan M and 1 more
Phylogeny of Muntiacus (Cervidae) based on mitochondrial DNA restriction maps.
Biochemical genetics | 1995-12-01 | PMID 8825938
Lan H, Wang W, Shi L
Differential alcohol dehydrogenase and malate dehydrogenase isozyme expression in long-term callus tissue cultures of Cereus peruvianus (Cactaceae).
Biochemical genetics | 1995-12-01 | PMID 8825939
Torquato E F, Prioli A J, Machado M F
Attempts to find phenotypic markers of the virulence plasmid of Rhodococcus equi.
Canadian journal of veterinary research = Revue canadienne de recherche veterinaire | 1996-01-01 | PMID 8825990
De La Peña-Moctezuma A, Prescott J F, Goodfellow M
Prevalence of various phenotypes of Streptococcus suis isolated from swine in the U.S.A. based on the presence of muraminidase-released protein and extracellular factor.
Canadian journal of veterinary research = Revue canadienne de recherche veterinaire | 1996-01-01 | PMID 8825999
Galina L, Vecht U, Wisselink H J and 1 more
Inherited predisposition to colorectal neoplasia.
British journal of hospital medicine | 2000-01-01 | PMID 8826039
Stephenson B M, Hall N R, Finan P J and 1 more
Tel Aviv-Heidelberg three-generation offspring study: genetic determinants of plasma fibrinogen level.
American journal of medical genetics | 1996-06-28 | PMID 8826427
Livshits G, Schettler G, Graff E and 3 more
Aprosencephaly and cerebellar dysgenesis in sibs.
American journal of medical genetics | 1996-06-28 | PMID 8826432
Florell S R, Townsend J J, Klatt E C and 4 more
Heteroallelic missense mutations of the galactosamine-6-sulfate sulfatase (GALNS) gene in a mild form of Morquio disease (MPS IVA).
American journal of medical genetics | 1996-06-28 | PMID 8826435
Cole D E, Fukuda S, Gordon B A and 7 more
Genes: GALNS
Molecular analysis of chromosome 21 in a patient with a phenotype of Down syndrome and apparently normal karyotype.
American journal of medical genetics | 1996-06-28 | PMID 8826436
Ahlbom B E, Goetz P, Korenberg J R and 5 more
Genes: ERG
Congenital central hypoventilation syndrome: mutation analysis of the receptor tyrosine kinase RET.
American journal of medical genetics | 1996-06-28 | PMID 8826440
Bolk S, Angrist M, Schwartz S and 3 more
Genes: RET
5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects.
American journal of medical genetics | 1996-06-28 | PMID 8826441
Ou C Y, Stevenson R E, Brown V K and 6 more
Genes: MTHFR
X chromosome inactivation and X-linked mental retardation.
American journal of medical genetics | 1996-07-12 | PMID 8826443
Willard H F
An assay for X inactivation based on differential methylation at the fragile X locus, FMR1.
American journal of medical genetics | 1996-07-12 | PMID 8826444
Carrel L, Willard H F
Genes: FMR1
X-linked neurodegenerative syndrome with congenital ataxia, late-onset progressive myoclonic encephalopathy and selective macular degeneration, linked to Xp22.33-pter.
American journal of medical genetics | 1996-07-12 | PMID 8826451
des Portes V, Bachner L, Brüls T and 11 more
The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule.
American journal of medical genetics | 1996-07-12 | PMID 8826452
Fransen E, Vits L, Van Camp G and 1 more
Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region.
American journal of medical genetics | 1996-07-12 | PMID 8826459
Robledo R, Melis P, Laficara F and 4 more
Genes: MAOB
Frequency of Fra X syndrome among institutionalized mentally retarded males in Poland.
American journal of medical genetics | 1996-07-12 | PMID 8826472
Mazurczak T, Bocian E, Milewski M and 5 more
Prenatal diagnosis and carrier screening for fragile X by PCR.
American journal of medical genetics | 1996-07-12 | PMID 8826474
Brown W T, Nolin S, Houck G and 8 more
Genes: FMR1
Prevalence of fragile X syndrome.
American journal of medical genetics | 1996-07-12 | PMID 8826475
Turner G, Webb T, Wake S and 1 more
Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity.
American journal of medical genetics | 1996-07-12 | PMID 8826478
Chiurazzi P, Genuardi M, Kozak L and 9 more
Genes: FMR1
Extended gene diversity at the FMR1 locus and neighbouring CA repeats in a sub-Saharan population.
American journal of medical genetics | 1996-07-12 | PMID 8826479
Chiurazzi P, Destro-Bisol G, Genuardi M and 3 more
Genes: FMR1
Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populations.
American journal of medical genetics | 1996-07-12 | PMID 8826480
Eichler E E, Nelson D L
Genes: FMR1
Fragile X founder effects and new mutations in Finland.
American journal of medical genetics | 1996-07-12 | PMID 8826481
Zhong N, Kajanoja E, Smits B and 8 more
Genes: FMR1
Genes involved in cell cycle G1 checkpoint control are frequently mutated in human melanoma metastases.
British journal of cancer | 1996-09-01 | PMID 8826861
Platz A, Sevigny P, Norberg T and 3 more