The leuO gene product has a latent ability to relieve bgl silencing in Escherichia coli.
Journal of bacteriology | 1998-01-01 | PMID 9422614
Ueguchi C, Ohta T, Seto C and 2 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.
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Publications
Page 933 of 10600
Requirement for DCP-1 caspase during Drosophila oogenesis.
Science (New York, N.Y.) | 1998-01-09 | PMID 9422696
McCall K, Steller H
Electrophysiological and biochemical evidence that DEG/ENaC cation channels are composed of nine subunits.
The Journal of biological chemistry | 1998-01-09 | PMID 9422716
Snyder P M, Cheng C, Prince L S and 2 more
Genes: BNC1
Analysis of the mechanisms of action of the Saccharomyces cerevisiae dominant lethal cdc42G12V and dominant negative cdc42D118A mutations.
The Journal of biological chemistry | 1998-01-09 | PMID 9422741
Davis C R, Richman T J, Deliduka S B and 3 more
Adrenocortical lipid depletion gene (ald) in AKR mice is associated with an acyl-CoA:cholesterol acyltransferase (ACAT) mutation.
The Journal of biological chemistry | 1998-01-09 | PMID 9422770
Meiner V L, Welch C L, Cases S and 4 more
A debilitating mutation in transcription factor IIE with differential effects on gene expression in yeast.
The Journal of biological chemistry | 1998-01-09 | PMID 9422776
Tijerina P, Sayre M H
Towards the goal of cancer-specific imaging and therapy.
Nuclear medicine communications | 1997-11-01 | PMID 9423199
Britton K E
The inherited basis of venous thrombosis.
Pathology | 1997-11-01 | PMID 9423212
Appleby R D, Olds R J
Platelet antigen allele frequencies in Australian aboriginal and Caucasian populations.
Pathology | 1997-11-01 | PMID 9423221
Chen Z, Lester S, Boettcher B and 1 more
From genotypes to genes: doubling the sample size.
Biometrics | 1997-12-01 | PMID 9423247
Sasieni P D
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophilia.
Thrombosis and haemostasis | 1997-12-01 | PMID 9423788
Makris M, Preston F E, Beauchamp N J and 6 more
Prevalence of the prothrombin gene variant (nt20210A) in venous thrombosis and arterial disease.
Thrombosis and haemostasis | 1997-12-01 | PMID 9423789
Arruda V R, Annichino-Bizzacchi J M, Gonçalves M S and 1 more
Electrospray ionisation mass spectrometry facilitates detection of fibrinogen (Bbeta 14 Arg --> Cys) mutation in a family with thrombosis.
Thrombosis and haemostasis | 1997-12-01 | PMID 9423799
Brennan S O, Hammonds B, Spearing R and 1 more
Heterozygous beta-thalassemia with thalassemia intermedia phenotype.
American journal of hematology | 1998-01-01 | PMID 9423815
Gasperini D, Perseu L, Melis M A and 5 more
Role of the Haemophilus ducreyi Ton system in internalization of heme from hemoglobin.
Infection and immunity | 1998-01-01 | PMID 9423852
Elkins C, Totten P A, Olsen B and 1 more
Periplasmic superoxide dismutase in meningococcal pathogenicity.
Infection and immunity | 1998-01-01 | PMID 9423860
Wilks K E, Dunn K L, Farrant J L and 4 more
Temporal variation of the merozoite surface protein-2 gene of Plasmodium falciparum.
Infection and immunity | 1998-01-01 | PMID 9423864
Eisen D, Billman-Jacobe H, Marshall V F and 2 more
Abnormal transglutaminase 1 expression pattern in a subset of patients with erythrodermic autosomal recessive ichthyosis.
The Journal of investigative dermatology | 1998-01-01 | PMID 9424079
Choate K A, Williams M L, Khavari P A
Re-epithelialization of porcine skin by the sweat apparatus.
The Journal of investigative dermatology | 1998-01-01 | PMID 9424080
Miller S J, Burke E M, Rader M D and 2 more
Increased expression of TGF-beta receptors by scleroderma fibroblasts: evidence for contribution of autocrine TGF-beta signaling to scleroderma phenotype.
The Journal of investigative dermatology | 1998-01-01 | PMID 9424086
Kawakami T, Ihn H, Xu W and 3 more
Induction of squamous cell carcinoma in p53-deficient mice after ultraviolet irradiation.
The Journal of investigative dermatology | 1998-01-01 | PMID 9424091
Li G, Tron V, Ho V
[The efficacy of interferon alfa treatment in chronic hepatitis C in relation to the serum concentration of RNA-HCV and the viral genotype].
Anales de medicina interna (Madrid, Spain : 1984) | 1997-10-01 | PMID 9424139
Hermida M, Castro A, López S and 2 more
Genes: LIPA
[A new form of hereditary ataxia: X-linked congenital cerebellar hypoplasia (a clinical and molecular genetic analysis)].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova | 1997-01-01 | PMID 9424342
Illarioshkin S N, Ivanova-Smolenskaia I A, Markova E D and 2 more
New insights into risk factors of asthma.
Respirology (Carlton, Vic.) | 1996-09-01 | PMID 9424391
Zhong N S
[PNH--paroxysmal nocturnal hemoglobinuria. An old disease explained by new technology].
Lakartidningen | 1997-11-19 | PMID 9424527
Hast R
Genes: GPI
[Selection of Bvg- variants of Bordetella pertussis].
Revista Argentina de microbiologia | 2000-01-01 | PMID 9424628
Passerini de Rossi B N, Friedman L E, Darnaud S and 2 more
Genes: OMP
[The apolipoprotein E genotype and Down's syndrome].
Revista clinica espanola | 1997-10-01 | PMID 9424665
Rascón Trincado M V, González Sarmiento R, Salazar A-Villalobos V
[Prevalence of glucose-6-phosphate dehydrogenase deficiency in a student population on the island of Menorca].
Sangre | 1997-10-01 | PMID 9424735
Cladera Serra A, Oliva Berini E, Torrent Quetglas M and 1 more
Clarification of the risk for venous thrombosis associated with hereditary protein S deficiency by investigation of a large kindred with a characterized gene defect.
Annals of internal medicine | 1998-01-01 | PMID 9424998
Simmonds R E, Ireland H, Lane D A and 3 more
Overloaded endoplasmic reticulum-Golgi compartments, a possible pathomechanism of peripheral neuropathies caused by mutations of the peripheral myelin protein PMP22.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1998-01-15 | PMID 9425015
D'Urso D, Prior R, Greiner-Petter R and 2 more
Genes: PMP22
Deuterium exchange mass spectrometry as a probe of protein kinase activation. Analysis of wild-type and constitutively active mutants of MAP kinase kinase-1.
Biochemistry | 1998-01-13 | PMID 9425067
Resing K A, Ahn N G
Role of the C9 methyl group in rhodopsin activation: characterization of mutant opsins with the artificial chromophore 11-cis-9-demethylretinal.
Biochemistry | 1998-01-13 | PMID 9425074
Han M, Groesbeek M, Smith S O and 1 more
Topography of the yeast ATP synthase F0 sector by using cysteine substitution mutants. Cross-linkings between subunits 4, 6, and f.
Biochemistry | 1998-01-13 | PMID 9425084
Spannagel C, Vaillier J, Chaignepain S and 1 more
Characterization of Glu350 as a critical residue involved in the N-terminal amine binding site of aminopeptidase N (EC 3.4.11.2): insights into its mechanism of action.
Biochemistry | 1998-01-13 | PMID 9425092
Luciani N, Marie-Claire C, Ruffet E and 3 more
Thrombomodulin increases the rate of thrombin inhibition by BPTI.
Biochemistry | 1998-01-13 | PMID 9425093
Rezaie A R, He X, Esmon C T
Substituent effects on the binding of phenols to the D38N mutant of 3-oxo-delta5-steroid isomerase. A probe for the nature of hydrogen bonding to the intermediate.
Biochemistry | 1998-01-13 | PMID 9425094
Petrounia I P, Pollack R M
Sonic hedgehog is not required for polarising activity in the Doublefoot mutant mouse limb bud.
Development (Cambridge, England) | 1998-02-01 | PMID 9425131
Hayes C, Brown J M, Lyon M F and 1 more
Equivalence in the genetic control of hindbrain segmentation in fish and mouse.
Development (Cambridge, England) | 1998-02-01 | PMID 9425134
Moens C B, Cordes S P, Giorgianni M W and 2 more
Zebrafish hox genes: expression in the hindbrain region of wild-type and mutants of the segmentation gene, valentino.
Development (Cambridge, England) | 1998-02-01 | PMID 9425135
Prince V E, Moens C B, Kimmel C B and 1 more
Muscle and nerve-specific regulation of a novel NK-2 class homeodomain factor in Caenorhabditis elegans.
Development (Cambridge, England) | 1998-02-01 | PMID 9425137
Harfe B D, Fire A
Drosophila Rac1 controls motor axon guidance.
Development (Cambridge, England) | 1998-02-01 | PMID 9425140
Kaufmann N, Wills Z P, Van Vactor D
eagle is required for the specification of serotonin neurons and other neuroblast 7-3 progeny in the Drosophila CNS.
Development (Cambridge, England) | 1998-02-01 | PMID 9425141
Lundell M J, Hirsh J
The short-period mutant, toc1-1, alters circadian clock regulation of multiple outputs throughout development in Arabidopsis thaliana.
Development (Cambridge, England) | 1998-02-01 | PMID 9425143
Somers D E, Webb A A, Pearson M and 1 more
The HOBBIT gene is required for formation of the root meristem in the Arabidopsis embryo.
Development (Cambridge, England) | 1998-02-01 | PMID 9425146
Willemsen V, Wolkenfelt H, de Vrieze G and 2 more
Prospore membrane formation defines a developmentally regulated branch of the secretory pathway in yeast.
The Journal of cell biology | 1998-01-12 | PMID 9425151
Neiman A M
Genes: NSF
Pex17p of Saccharomyces cerevisiae is a novel peroxin and component of the peroxisomal protein translocation machinery.
The Journal of cell biology | 1998-01-12 | PMID 9425153
Huhse B, Rehling P, Albertini M and 3 more
Genes: PTS
Relocalization of phospholipase D activity mediates membrane formation during meiosis.
The Journal of cell biology | 1998-01-12 | PMID 9425156
Rudge S A, Morris A J, Engebrecht J
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
Human molecular genetics | 1998-02-01 | PMID 9425222
David G, Dürr A, Stevanin G and 13 more
Expanded CAG repeats in Swedish spinocerebellar ataxia type 7 (SCA7) patients: effect of CAG repeat length on the clinical manifestation.
Human molecular genetics | 1998-02-01 | PMID 9425223
Johansson J, Forsgren L, Sandgren O and 3 more
Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion.
Human molecular genetics | 1998-02-01 | PMID 9425224
Del-Favero J, Krols L, Michalik A and 10 more
HLA-DR alleles display sex-dependent effects on survival and discriminate between individual and familial longevity.
Human molecular genetics | 1998-02-01 | PMID 9425225
Ivanova R, Hénon N, Lepage V and 3 more
Mutations in the BRCA1-associated RING domain (BARD1) gene in primary breast, ovarian and uterine cancers.
Human molecular genetics | 1998-02-01 | PMID 9425226
Thai T H, Du F, Tsan J T and 11 more
Genes: BARD1, BRCA1
Mutations of the alpha2(V) chain of type V collagen impair matrix assembly and produce ehlers-danlos syndrome type I.
Human molecular genetics | 1998-02-01 | PMID 9425231
Michalickova K, Susic M, Willing M C and 2 more
Significant impact of the +93 C/T polymorphism in the apolipoprotein(a) gene on Lp(a) concentrations in Africans but not in Caucasians: confounding effect of linkage disequilibrium.
Human molecular genetics | 1998-02-01 | PMID 9425232
Kraft H G, Windegger M, Menzel H J and 1 more
Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients.
Human molecular genetics | 1998-02-01 | PMID 9425233
Jalanko A, Tenhunen K, McKinney C E and 10 more
Genes: AGA
Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits.
Human molecular genetics | 1998-02-01 | PMID 9425237
Mitchison H M, Hofmann S L, Becerra C H and 14 more
Genes: NCL
Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients.
Human molecular genetics | 1998-02-01 | PMID 9425239
Martorell L, Monckton D G, Gamez J and 4 more
A point mutation in the neu-1 locus causes the neuraminidase defect in the SM/J mouse.
Human molecular genetics | 1998-02-01 | PMID 9425240
Rottier R J, Bonten E, d'Azzo A
Relationship of K+-uptaking system with H+-translocating ATPase in Enterococcus hirae, grown at a high or low alkaline pH.
Current microbiology | 1998-02-01 | PMID 9425250
Trchounian A, Kobayashi H
Stability of mutant superoxide dismutase-1 associated with familial amyotrophic lateral sclerosis determines the manner of copper release and induction of thioredoxin in erythrocytes.
Biochemical and biophysical research communications | 1997-12-18 | PMID 9425258
Ogawa Y, Kosaka H, Nakanishi T and 5 more
Molecular scanning of the human peroxisome proliferator activated receptor gamma (hPPAR gamma) gene in diabetic Caucasians: identification of a Pro12Ala PPAR gamma 2 missense mutation.
Biochemical and biophysical research communications | 1997-12-18 | PMID 9425261
Yen C J, Beamer B A, Negri C and 6 more
Mutation detection in glycogen storage-disease type II by RT-PCR and automated sequencing.
Biochemical and biophysical research communications | 1997-12-18 | PMID 9425285
Hermans M M, van Leenen D, Kroos M A and 1 more
Genes: GAA
Overexpression of GML promotes radiation-induced cell cycle arrest and apoptosis.
Biochemical and biophysical research communications | 1997-12-18 | PMID 9425296
Kagawa K, Inoue T, Tokino T and 2 more
Genes: GML
Genetic diversity among Leishmania (Viannia) parasites.
Annals of tropical medicine and parasitology | 1997-09-01 | PMID 9425364
Cupolillo E, Grimaldi G, Momen H
Analysis of the retinoblastoma tumour suppressor gene in pancreatic endocrine tumours.
Clinical endocrinology | 1997-11-01 | PMID 9425391
Chung D C, Smith A P, Louis D N and 3 more
Inhibition of HIV-1 replication by a Tat transdominant negative mutant in human peripheral blood lymphocytes from healthy donors and HIV-1-infected patients.
Gene therapy | 1997-11-01 | PMID 9425451
Rossi C, Balboni P G, Betti M and 5 more
Bone dimensional change with age: interactions of genetic, hormonal, and body size variables.
Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA | 1997-01-01 | PMID 9425499
Heaney R P, Barger-Lux M J, Davies K M and 3 more
Genes: VDR
Leber hereditary optic neuropathy: mitochondrial mutations and degeneration of the optic nerve.
Vision research | 1997-12-01 | PMID 9425526
Howell N
Advances in the genetic mechanisms of mitochondrial disease.
Current opinion in neurology | 1997-12-01 | PMID 9425567
Vladutiu G D
Role of HOX genes in human development.
Current opinion in pediatrics | 1997-12-01 | PMID 9425595
Innis J W
Genetic analysis of dyslexia and other complex behavioral phenotypes.
Current opinion in pediatrics | 1997-12-01 | PMID 9425598
Pennington B F, Smith S D
Will genetics really revolutionize the drug discovery process?
Current opinion in biotechnology | 1997-12-01 | PMID 9425654
Gelbert L M, Gregg R E
The medical utility of genomics data in neuropsychiatry: mutational genetics versus association genetics.
Current opinion in biotechnology | 1997-12-01 | PMID 9425657
Peroutka S J
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.
Nature genetics | 1998-01-01 | PMID 9425895
Singh N A, Charlier C, Stauffer D and 13 more
Genes: KCNQ2
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase.
Nature genetics | 1998-01-01 | PMID 9425897
Jenne D E, Reimann H, Nezu J and 6 more
Genes: STK11
Association of a human G-protein beta3 subunit variant with hypertension.
Nature genetics | 1998-01-01 | PMID 9425898
Siffert W, Rosskopf D, Siffert G and 8 more
Genes: GNB3
An activating splice donor mutation in the thrombopoietin gene causes hereditary thrombocythaemia.
Nature genetics | 1998-01-01 | PMID 9425899
Wiestner A, Schlemper R J, van der Maas A P and 1 more
Genes: THPO, TPO
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.
Nature genetics | 1998-01-01 | PMID 9425900
Charlier C, Singh N A, Ryan S G and 4 more
Genes: KCNQ3, KCNQ2, KCNQ1
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model.
Nature genetics | 1998-01-01 | PMID 9425902
Southard-Smith E M, Kos L, Pavan W J
Genes: SOX10, SRY
A polymorphism in the regulatory region of APOE associated with risk for Alzheimer's dementia.
Nature genetics | 1998-01-01 | PMID 9425904
Bullido M J, Artiga M J, Recuero M and 10 more
Genes: APOE
Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome.
Nature genetics | 1998-01-01 | PMID 9425907
Kohlhase J, Wischermann A, Reichenbach H and 2 more
Genes: SALL1
Dysregulation of proteoglycan production by intrahepatic biliary epithelial cells bearing defective (delta-f508) cystic fibrosis transmembrane conductance regulator.
Hepatology (Baltimore, Md.) | 1998-01-01 | PMID 9425910
Bhaskar K R, Turner B S, Grubman S A and 2 more
Genes: CFTR
Control of mouse hepatocyte proliferation and ploidy by p53 and p53ser246 mutation in vivo.
Hepatology (Baltimore, Md.) | 1998-01-01 | PMID 9425920
Yin L, Ghebranious N, Chakraborty S and 3 more
High prevalence of the His63Asp HFE mutation in Italian patients with porphyria cutanea tarda.
Hepatology (Baltimore, Md.) | 1998-01-01 | PMID 9425935
Sampietro M, Piperno A, Lupica L and 9 more
Genes: HFE
Hepatitis B virus S mutants in liver transplant recipients who were reinfected despite hepatitis B immune globulin prophylaxis.
Hepatology (Baltimore, Md.) | 1998-01-01 | PMID 9425940
Ghany M G, Ayola B, Villamil F G and 4 more
Comparison of the rate of sequence variation in the hypervariable region of E2/NS1 region of hepatitis C virus in normal and hypogammaglobulinemic patients.
Hepatology (Baltimore, Md.) | 1998-01-01 | PMID 9425941
Booth J C, Kumar U, Webster D and 2 more
Influence of HLA haplotypes on the clinical courses of individuals infected with hepatitis C virus.
Hepatology (Baltimore, Md.) | 1998-01-01 | PMID 9425943
Kuzushita N, Hayashi N, Moribe T and 10 more
Hepatitis B virus with antigenically altered hepatitis B surface antigen is selected by high-dose hepatitis B immune globulin after liver transplantation.
Hepatology (Baltimore, Md.) | 1998-01-01 | PMID 9425945
Protzer-Knolle U, Naumann U, Bartenschlager R and 5 more
Frequency and phenotypes of familial dilated cardiomyopathy.
Journal of the American College of Cardiology | 1998-01-01 | PMID 9426039
Grünig E, Tasman J A, Kücherer H and 3 more
Precise microdissection of human prostate cancers reveals genotypic heterogeneity.
Cancer research | 1998-01-01 | PMID 9426051
Macintosh C A, Stower M, Reid N and 1 more
Breast cancer and CYPIA1, GSTM1, and GSTT1 polymorphisms: evidence of a lack of association in Caucasians and African Americans.
Cancer research | 1998-01-01 | PMID 9426059
Bailey L R, Roodi N, Verrier C S and 3 more
Genes: GSTM1, GSTT1
Specific phosphatidylethanolamine dependence of Serratia marcescens cytotoxin activity.
Molecular microbiology | 1997-12-01 | PMID 9426124
Hertle R, Brutsche S, Groeger W and 4 more
Genes: SDS
Requirement of topoisomerase IV parC and parE genes for cell cycle progression and developmental regulation in Caulobacter crescentus.
Molecular microbiology | 1997-12-01 | PMID 9426128
Ward D, Newton A
Discrimination between structurally related ligands nitrate and nitrite controls autokinase activity of the NarX transmembrane signal transducer of Escherichia coli K-12.
Molecular microbiology | 1997-12-01 | PMID 9426129
Williams S B, Stewart V
The Cryptococcus neoformans STE12alpha gene: a putative Saccharomyces cerevisiae STE12 homologue that is mating type specific.
Molecular microbiology | 1997-12-01 | PMID 9426132
Wickes B L, Edman U, Edman J C
Expression of gpsA encoding biosynthetic sn-glycerol 3-phosphate dehydrogenase suppresses both the LB- phenotype of a secB null mutant and the cold-sensitive phenotype of a secG null mutant.
Molecular microbiology | 1997-12-01 | PMID 9426138
Shimizu H, Nishiyama K, Tokuda H
Evidence for two chemosensory pathways in Rhodobacter sphaeroides.
Molecular microbiology | 1997-12-01 | PMID 9426144
Hamblin P A, Maguire B A, Grishanin R N and 1 more
Genes: PTS
The consequence of translesional replication of unique UV-induced photoproducts.
Biological chemistry | 1997-11-01 | PMID 9426188
Gentil A, Le Page F, Sarasin A
Genomic targeting of a bicistronic DNA fragment by Cre-mediated site-specific recombination.
Gene | 1997-12-12 | PMID 9426252
Kolb A F, Siddell S G
A truncated SV40 large T antigen lacking the p53 binding domain overcomes p53-induced growth arrest and immortalizes primary mesencephalic cells.
Cell and tissue research | 1998-02-01 | PMID 9426306
Truckenmiller M E, Tornatore C, Wright R D and 4 more