Ribosomal protein methylation in Escherichia coli: the gene prmA, encoding the ribosomal protein L11 methyltransferase, is dispensable.
Molecular microbiology | 1994-12-01 | PMID 7715456
Vanet A, Plumbridge J A, Guérin M F and 1 more
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 456 of 10600
The site-specific recombination system regulating expression of the type 1 fimbrial subunit gene of Escherichia coli is sensitive to changes in DNA supercoiling.
Molecular microbiology | 1994-12-01 | PMID 7715458
Dove S L, Dorman C J
Structural analysis of Tpn1, a transposable element isolated from Japanese morning glory bearing variegated flowers.
Molecular & general genetics : MGG | 1995-04-10 | PMID 7715598
Hoshino A, Inagaki Y, Iida S
The glucose repression and RAS-cAMP signal transduction pathways of Saccharomyces cerevisiae each affect RNA processing and the synthesis of a reporter protein.
Molecular & general genetics : MGG | 1995-04-10 | PMID 7715603
Tung K S, Hopper A K
Glycogen synthase kinase-3 and dorsoventral patterning in Xenopus embryos.
Nature | 1995-04-13 | PMID 7715701
He X, Saint-Jeannet J P, Woodgett J R and 2 more
Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development.
Nature | 1995-04-13 | PMID 7715703
Zhou Q Y, Quaife C J, Palmiter R D
The structure of trp RNA-binding attenuation protein.
Nature | 1995-04-20 | PMID 7715723
Antson A A, Otridge J, Brzozowski A M and 7 more
A protein related to extracellular matrix proteins deleted in the mouse mutant reeler.
Nature | 1995-04-20 | PMID 7715726
D'Arcangelo G, Miao G G, Chen S C and 3 more
The barley Hooded mutation caused by a duplication in a homeobox gene intron.
Nature | 1995-04-20 | PMID 7715728
Müller K J, Romano N, Gerstner O and 4 more
[Congenital diseases of neuromuscular transmission: congenital myasthenia syndromes].
Der Nervenarzt | 1995-02-01 | PMID 7715748
Sieb J P
Trophoblast differentiation during formation of anchoring villi in a model of the early human placenta in vitro.
Placenta | 1995-01-01 | PMID 7716127
Vićovac L, Jones C J, Aplin J D
Unique DNA repair property of an ultraviolet-sensitive (radC) mutant of Dictyostelium discoideum.
Photochemistry and photobiology | 1995-03-01 | PMID 7716189
Okaichi K, Mori T, Ihara M and 1 more
Genes: CPD
Sodium intake linked to amiloride-sensitive gustatory transduction in C57BL/6J and 129/J mice.
Physiology & behavior | 1995-02-01 | PMID 7716197
Gannon K S, Contreras R J
Phytochrome A overexpression in transgenic tobacco. Correlation of dwarf phenotype with high concentrations of phytochrome in vascular tissue and attenuated gibberellin levels.
Plant physiology | 1995-03-01 | PMID 7716243
Jordan E T, Hatfield P M, Hondred D and 3 more
Differential radiosensitising effect of the scid mutation among tissues, studied using high and low dose rates: implications for prognostic indicators in radiotherapy.
Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology | 1994-12-01 | PMID 7716261
Hendry J H, Jiang T N
Mixed populations of Trypanosoma brucei in wild Glossina palpalis palpalis.
Tropical medicine and parasitology : official organ of Deutsche Tropenmedizinische Gesellschaft and of Deutsche Gesellschaft fur Technische Zusammenarbeit (GTZ) | 1994-12-01 | PMID 7716394
Stevens J R, Mathieu-Daudé F, McNamara J J and 2 more
Silver as a probe of pore-forming residues in a potassium channel.
Science (New York, N.Y.) | 1995-04-14 | PMID 7716526
Lü Q, Miller C
Revealing the architecture of a K+ channel pore through mutant cycles with a peptide inhibitor.
Science (New York, N.Y.) | 1995-04-14 | PMID 7716527
Hidalgo P, MacKinnon R
The role of Ig beta in precursor B cell transition and allelic exclusion.
Science (New York, N.Y.) | 1995-04-21 | PMID 7716544
Papavasiliou F, Misulovin Z, Suh H and 1 more
Adaptive mutation in Escherichia coli: a role for conjugation.
Science (New York, N.Y.) | 1995-04-21 | PMID 7716545
Radicella J P, Park P U, Fox M S
Evidence that F plasmid transfer replication underlies apparent adaptive mutation.
Science (New York, N.Y.) | 1995-04-21 | PMID 7716546
Galitski T, Roth J R
Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy.
Science (New York, N.Y.) | 1995-04-21 | PMID 7716548
Thomas P M, Cote G J, Wohllk N and 6 more
Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease.
Surgery | 1995-04-01 | PMID 7716719
Borst M J, VanCamp J M, Peacock M L and 1 more
Genes: RET
[Immunogenicity of attenuated reassortants of influenza A virus /Leningrad/134/47/57 (H2N2) for mice, depending on their genome].
Voprosy virusologii | 2000-01-01 | PMID 7716900
Egorov A Iu, Garmashova L M, Nevedomskaia G N and 3 more
[The NS gene--a possible determinant of apathogenicity of a cold-adapted donor of attenuation A /Leningrad/134/47/57 and its reassortants].
Voprosy virusologii | 2000-01-01 | PMID 7716901
Egorov A Iu, Garmashova L M, Lukashok I V and 3 more
A panel of monoclonal antibodies to rat plectin: distinction by epitope mapping and immunoreactivity with different tissues and cell lines.
Acta histochemica | 1994-12-01 | PMID 7717046
Foisner R, Feldman B, Sander L and 3 more
Epidemiological evaluation of the use of genetics to improve the predictive value of disease risk factors.
American journal of human genetics | 1995-04-01 | PMID 7717394
Khoury M J, Wagener D K
Identification of polymorphisms and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene.
American journal of human genetics | 1995-04-01 | PMID 7717395
Liu J, Fujiwara T M, Buu N T and 7 more
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypes.
American journal of human genetics | 1995-04-01 | PMID 7717396
Braun A, Ambach H, Kammerer S and 6 more
Genes: AMN, ADO
Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathers.
American journal of human genetics | 1995-04-01 | PMID 7717397
Schmitt-Ney M, Thiele H, Kaltwasser P and 3 more
Genes: SRY
Leaky splicing mutation in the acid maltase gene is associated with delayed onset of glycogenosis type II.
American journal of human genetics | 1995-04-01 | PMID 7717400
Boerkoel C F, Exelbert R, Nicastri C and 4 more
Genes: GAA
Characterization of nine novel mutations in the CD40 ligand gene in patients with X-linked hyper IgM syndrome of various ancestry.
American journal of human genetics | 1995-04-01 | PMID 7717401
Macchi P, Villa A, Strina D and 7 more
Y chromosomal DNA variation and the peopling of Japan.
American journal of human genetics | 1995-04-01 | PMID 7717406
Hammer M F, Horai S
Human T-cell receptor V beta gene polymorphism and multiple sclerosis.
American journal of human genetics | 1995-04-01 | PMID 7717407
Wei S, Charmley P, Birchfield R I and 1 more
Variability of the genetic contribution of Quebec population founders associated to some deleterious genes.
American journal of human genetics | 1995-04-01 | PMID 7717408
Heyer E, Tremblay M
Demographic history of India and mtDNA-sequence diversity.
American journal of human genetics | 1995-04-01 | PMID 7717409
Mountain J L, Hebert J M, Bhattacharyya S and 4 more
Interstitial deletions 4q21.1q25 and 4q25q27: phenotypic variability and relation to Rieger anomaly.
American journal of medical genetics | 1995-01-16 | PMID 7717415
Kulharya A S, Maberry M, Kukolich M K and 4 more
Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
American journal of medical genetics | 1995-01-16 | PMID 7717418
Toriello H V, Higgins J V
Interstitial duplication of proximal 22q: phenotypic overlap with cat eye syndrome.
American journal of medical genetics | 1995-01-16 | PMID 7717422
Knoll J H, Asamoah A, Pletcher B A and 1 more
Trisomy 2p: analysis of unusual phenotypic findings.
American journal of medical genetics | 1995-01-16 | PMID 7717424
Lurie I W, Ilyina H G, Gurevich D B and 5 more
Developmental anomalies suggestive of the human homologue of the mouse mutant disorganization.
American journal of medical genetics | 1995-01-16 | PMID 7717426
Elliott A M, Chen M F, Azouz E M and 1 more
Analysis of the neurofibromatosis 2 gene reveals molecular variants of meningioma.
The American journal of pathology | 1995-04-01 | PMID 7717450
Wellenreuther R, Kraus J A, Lenartz D and 7 more
Cerebrospinal fluid levels of amyloid beta-protein in Alzheimer's disease: inverse correlation with severity of dementia and effect of apolipoprotein E genotype.
Annals of neurology | 1995-04-01 | PMID 7717688
Nitsch R M, Rebeck G W, Deng M and 7 more
Genes: APP
Genetic difference in HLA-DR phenotypes between coeliac disease and transitory gluten intolerance.
Archives of disease in childhood | 1995-01-01 | PMID 7717732
Meuli R, Pichler W J, Gaze H and 1 more
Flow cytogenetic analysis of whole cell clastogenicity of herbicides found in groundwater.
Archives of environmental contamination and toxicology | 1995-01-01 | PMID 7717760
Biradar D P, Rayburn A L
Immunologic analyses of peripheral leukocytes from workers at an ethical narcotics manufacturing facility.
Archives of environmental health | 2000-01-01 | PMID 7717772
Biagini R E, Henningsen G M, Klincewicz S L
The hr locus and the toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in newborn mice.
Archives of toxicology | 1994-01-01 | PMID 7717866
Connor M J, Puhvel S M, Sakamoto M and 1 more
Direct mutational analysis in a family with hereditary non-polyposis colorectal cancer.
Australian and New Zealand journal of medicine | 1994-12-01 | PMID 7717919
Van de Water N S, Jeevaratnam P, Browett P J and 3 more
Genes: MSH2
Increased proteoglycan synthesis in cartilage in experimental canine osteoarthritis does not reflect a permanent change in chondrocyte phenotype.
Arthritis and rheumatism | 1995-04-01 | PMID 7718006
Venn G, Billingham M E, Hardingham T E
Genes: TNF
Detection of a single base deletion in codon 424 of the low density lipoprotein receptor gene in a Danish family with familial hypercholesterolemia.
Atherosclerosis | 1994-12-01 | PMID 7718023
Nissen H, Hansen A B, Guldberg P and 5 more
Genes: LDLR
Phenotypic expression and frequency of familial defective apolipoprotein B-100 in Belgian hypercholesterolemics.
Atherosclerosis | 1994-12-01 | PMID 7718024
Kotze M J, Peeters A V, Langenhoven E and 2 more
Igf1 gene disruption results in reduced brain size, CNS hypomyelination, and loss of hippocampal granule and striatal parvalbumin-containing neurons.
Neuron | 1995-04-01 | PMID 7718235
Beck K D, Powell-Braxton L, Widmer H R and 2 more
Odorant-specific adaptation pathways generate olfactory plasticity in C. elegans.
Neuron | 1995-04-01 | PMID 7718242
Colbert H A, Bargmann C I
Serotonin modulates the voltage dependence of delayed rectifier and Shaker potassium channels in Drosophila photoreceptors.
Neuron | 1995-04-01 | PMID 7718246
Hevers W, Hardie R C
A mutated acetylcholine receptor subunit causes neuronal degeneration in C. elegans.
Neuron | 1995-04-01 | PMID 7718248
Treinin M, Chalfie M
Fanconi anaemia research: current status and prospects.
European journal of cancer (Oxford, England : 1990) | 1995-01-01 | PMID 7718336
Joenje H, Mathew C, Gluckman E
Response of heat shock element within the human HSP70 promoter to mutated p53 genes.
Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research | 1995-01-01 | PMID 7718482
Tsutsumi-Ishii Y, Tadokoro K, Hanaoka F and 1 more
The effect of oncogenes on the growth and differentiation of oligodendrocyte type 2 astrocyte progenitor cells.
Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research | 1995-01-01 | PMID 7718486
Barnett S C, Crouch D H
Superantigen-reactive T cells that display an anergic phenotype in vitro appear functional in vivo.
International immunology | 1995-01-01 | PMID 7718507
Heeg K, Gaus H, Griese D and 3 more
An SRY mutation causing human sex reversal resolves a general mechanism of structure-specific DNA recognition: application to the four-way DNA junction.
Biochemistry | 1995-04-11 | PMID 7718558
Peters R, King C Y, Ukiyama E and 3 more
Genes: SRY
Identification of sequences mediating guanylyl cyclase dimerization.
Biochemistry | 1995-04-11 | PMID 7718574
Wilson E M, Chinkers M
Cytokinins affect spore formation but not cell division in the yeast Saccharomyces cerevisiae.
Biochimica et biophysica acta | 1995-04-06 | PMID 7718620
Laten H M
Lactate dehydrogenase-release assay: a reliable, nonradioactive technique for analysis of cytotoxic lymphocyte-mediated lytic activity against blasts from acute myelocytic leukemia.
Annals of hematology | 1995-03-01 | PMID 7718644
Weidmann E, Brieger J, Jahn B and 3 more
Genetic differences between BCG substrains.
Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease | 1995-02-01 | PMID 7718847
Zhang Y, Wallace R J, Mazurek G H
Analysis of VH genes used by neoplastic B cells in endemic Burkitt's lymphoma shows somatic hypermutation and intraclonal heterogeneity.
Blood | 1995-04-15 | PMID 7718888
Chapman C J, Mockridge C I, Rowe M and 2 more
TP53 mutations emerge at early phase of myelodysplastic syndrome and are associated with complex chromosomal abnormalities.
Blood | 1995-04-15 | PMID 7718890
Kaneko H, Misawa S, Horiike S and 2 more
Four new mutations in the NADH-cytochrome b5 reductase gene from patients with recessive congenital methemoglobinemia type II.
Blood | 1995-04-15 | PMID 7718898
Vieira L M, Kaplan J C, Kahn A and 1 more
Variation of short tandem repeats within and between species belonging to the Canidae family.
Mammalian genome : official journal of the International Mammalian Genome Society | 1995-01-01 | PMID 7719020
Fredholm M, Winterø A K
Genetic map of rat chromosome 5 including the fatty (fa) locus.
Mammalian genome : official journal of the International Mammalian Genome Society | 1995-01-01 | PMID 7719022
Truett G E, Jacob H J, Miller J and 5 more
Genetic map of the region surrounding the retrovirus restriction locus, Fv1, on mouse chromosome 4.
Mammalian genome : official journal of the International Mammalian Genome Society | 1995-01-01 | PMID 7719023
Stoye J P, Kaushik N, Jeremiah S and 1 more
Basic fibroblast growth factor increases the number of excitatory neurons containing glutamate in the cerebral cortex.
Cerebral cortex (New York, N.Y. : 1991) | 2000-01-01 | PMID 7719131
Vaccarino F M, Schwartz M L, Hartigan D and 1 more
Genes: NGF
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegia.
Neuromuscular disorders : NMD | 1995-01-01 | PMID 7719135
Fontaine B, Rime C S, Hazan J and 7 more
Absence of mutations in the Mn superoxide dismutase or catalase genes in familial amyotrophic lateral sclerosis.
Neuromuscular disorders : NMD | 1995-01-01 | PMID 7719145
Parboosingh J S, Rouleau G A, Meninger V and 3 more
Genes: SOD2, SOD1
Immunophenotypic and DNA genotypic analysis of T-cell and NK-cell subpopulations in patients with B-cell chronic lymphocytic leukaemia (B-CLL).
Leukemia & lymphoma | 1995-01-01 | PMID 7719238
Frolova E A, Richards S J, Jones R A and 6 more
Sequential phenotyping of myeloma patients on chemotherapy: persistence of activated T-cells and natural killer cells.
Leukemia & lymphoma | 1995-01-01 | PMID 7719242
Kay N E, Oken M M, Kyle R and 4 more
Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders.
Nature genetics | 1995-02-01 | PMID 7719337
Dodt G, Braverman N, Wong C and 5 more
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.
Nature genetics | 1995-02-01 | PMID 7719340
Ouahchi K, Arita M, Kayden H and 7 more
Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population.
Nature genetics | 1995-02-01 | PMID 7719342
Risch N, de Leon D, Ozelius L and 6 more
Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene.
Nature genetics | 1995-02-01 | PMID 7719343
Kremer H, Kraaij R, Toledo S P and 7 more
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome.
Nature genetics | 1995-02-01 | PMID 7719344
Wilkie A O, Slaney S F, Oldridge M and 7 more
Genes: FGFR2
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes.
Nature genetics | 1995-02-01 | PMID 7719345
Rutland P, Pulleyn L J, Reardon W and 7 more
Genes: FGFR2, FGFR1
Detection of mutations by cleavage of DNA heteroduplexes with bacteriophage resolvases.
Nature genetics | 1995-02-01 | PMID 7719346
Mashal R D, Koontz J, Sklar J
Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice.
Nature genetics | 1995-02-01 | PMID 7719348
Bingham P M, Scott M O, Wang S and 5 more
Rescue of neurophysiological phenotype seen in PrP null mice by transgene encoding human prion protein.
Nature genetics | 1995-02-01 | PMID 7719349
Whittington M A, Sidle K C, Gowland I and 5 more
Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production.
Nature genetics | 1995-02-01 | PMID 7719350
Pollock J D, Williams D A, Gifford M A and 6 more
Application of capillary high-performance liquid chromatography to biotechnology, with reference to the analysis of recombinant DNA-derived human growth hormone.
Journal of chromatography. B, Biomedical applications | 1994-12-09 | PMID 7719487
Battersby J E, Guzzetta A W, Hancock W S
A linkage study with D5 dopamine and alpha 2C-adrenergic receptor genes in six multiplex bipolar pedigrees.
Psychiatric genetics | 1994-01-01 | PMID 7719697
Byerley W, Hoff M, Holik J and 1 more
Association and haplotype analysis at the tyrosine hydroxylase locus in a combined German-British sample of manic depressive patients and controls.
Psychiatric genetics | 1994-01-01 | PMID 7719703
Körner J, Rietschel M, Hunt N and 7 more
The identification of bacterial gene expression differences using mRNA-based isothermal subtractive hybridization.
Canadian journal of microbiology | 1995-02-01 | PMID 7720012
Utt E A, Brousal J P, Kikuta-Oshima L C and 1 more
The biological action of cDNAs from mutated estrogen receptors transfected into breast cancer cells.
Cancer letters | 1995-03-23 | PMID 7720041
Catherino W H, Jordan V C
Mutations in breast cancer.
Cancer letters | 1995-03-23 | PMID 7720043
Cropp C S
Genes: BRCA1
CREB as a memory modulator: induced expression of a dCREB2 activator isoform enhances long-term memory in Drosophila.
Cell | 1995-04-07 | PMID 7720066
Yin J C, Del Vecchio M, Zhou H and 1 more
Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A.
Cell | 1995-04-07 | PMID 7720071
Richard I, Broux O, Allamand V and 7 more
Hemostatic, inflammatory, and fibroblast responses are blunted in mice lacking gelsolin.
Cell | 1995-04-07 | PMID 7720072
Witke W, Sharpe A H, Hartwig J H and 3 more
The torso receptor tyrosine kinase can activate Raf in a Ras-independent pathway.
Cell | 1995-04-07 | PMID 7720074
Hou X S, Chou T B, Melnick M B and 1 more
Multiallelic recognition: nonself-dependent dimerization of the bE and bW homeodomain proteins in Ustilago maydis.
Cell | 1995-04-07 | PMID 7720075
Kämper J, Reichmann M, Romeis T and 2 more
Mutations in aurora prevent centrosome separation leading to the formation of monopolar spindles.
Cell | 1995-04-07 | PMID 7720077
Glover D M, Leibowitz M H, McLean D A and 1 more
High IL-4 production is a stable phenotype of CD8negCD45RAnegCD27neg T cells.
Cellular immunology | 1995-02-01 | PMID 7720093
Sunder-Plassmann R, Majdic O, Knapp W and 1 more
[The reversing effect of 4-hydroxycarbophenyl retiamide (R II) on the malignant phenotype of mouse forestomach carcinoma (MFC) cell line and the mechanism of its action].
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae | 1994-12-01 | PMID 7720139
Cao J, Gao J
Modulation of phenotypic expression of fibroblasts by alteration of the cytoskeleton.
Cell biochemistry and function | 1995-03-01 | PMID 7720189
Evangelisti R, Becchetti E, Baroni T and 5 more