The Arabidopsis FILAMENTOUS FLOWER gene is required for flower formation.
Development (Cambridge, England) | 1999-06-01 | PMID 10331982
Chen Q, Atkinson A, Otsuga D and 3 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 1146 of 10600
The zebrafish detour gene is essential for cranial but not spinal motor neuron induction.
Development (Cambridge, England) | 1999-06-01 | PMID 10331983
Chandrasekhar A, Schauerte H E, Haffter P and 1 more
Targeted inactivation of the EGF and amphiregulin genes reveals distinct roles for EGF receptor ligands in mouse mammary gland development.
Development (Cambridge, England) | 1999-06-01 | PMID 10331984
Luetteke N C, Qiu T H, Fenton S E and 4 more
Genes: EGF, EGFR
Cell division genes promote asymmetric interaction between Numb and Notch in the Drosophila CNS.
Development (Cambridge, England) | 1999-06-01 | PMID 10331986
Wai P, Truong B, Bhat K M
Signalling by the RET receptor tyrosine kinase and its role in the development of the mammalian enteric nervous system.
Development (Cambridge, England) | 1999-06-01 | PMID 10331988
Taraviras S, Marcos-Gutierrez C V, Durbec P and 7 more
Genes: RET, GDNF
Different sequence requirements for expression in erythroid and megakaryocytic cells within a regulatory element upstream of the GATA-1 gene.
Development (Cambridge, England) | 1999-06-01 | PMID 10331989
Vyas P, McDevitt M A, Cantor A B and 3 more
A myb-related protein required for culmination in Dictyostelium.
Development (Cambridge, England) | 1999-06-01 | PMID 10331990
Guo K, Anjard C, Harwood A and 3 more
Adenovirus-mediated expression of mutant DRPLA proteins with expanded polyglutamine stretches in neuronally differentiated PC12 cells. Preferential intranuclear aggregate formation and apoptosis.
Human molecular genetics | 1999-06-01 | PMID 10332031
Sato A, Shimohata T, Koide R and 8 more
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression.
Human molecular genetics | 1999-06-01 | PMID 10332033
Korade-Mirnics Z, Tarleton J, Servidei S and 5 more
Genes: SIX5, DMPK
Correlations of genotype and phenotype in hypophosphatasia.
Human molecular genetics | 1999-06-01 | PMID 10332035
Zurutuza L, Muller F, Gibrat J F and 4 more
Genes: GPI
Gene shifting: a novel therapy for mitochondrial myopathy.
Human molecular genetics | 1999-06-01 | PMID 10332036
Taivassalo T, Fu K, Johns T and 3 more
Cis-acting modifiers of expanded CAG/CTG triplet repeat expandability: associations with flanking GC content and proximity to CpG islands.
Human molecular genetics | 1999-06-01 | PMID 10332038
Brock G J, Anderson N H, Monckton D G
Intracellular localization and loss of copper responsiveness of Mnk, the murine homologue of the Menkes protein, in cells from blotchy (Mo blo) and brindled (Mo br) mouse mutants.
Human molecular genetics | 1999-06-01 | PMID 10332039
La Fontaine S, Firth S D, Lockhart P J and 3 more
Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
Human molecular genetics | 1999-06-01 | PMID 10332040
Shimozawa N, Suzuki Y, Zhang Z and 9 more
Genes: PEX13
The timing of XIST replication: dominance of the domain.
Human molecular genetics | 1999-06-01 | PMID 10332041
Gartler S M, Goldstein L, Tyler-Freer S E and 1 more
Defective intracellular transport of CLN3 is the molecular basis of Batten disease (JNCL)
Human molecular genetics | 1999-06-01 | PMID 10332042
Järvelä I, Lehtovirta M, Tikkanen R and 2 more
Genes: CLN3
Mitochondrial intermediate peptidase and the yeast frataxin homolog together maintain mitochondrial iron homeostasis in Saccharomyces cerevisiae.
Human molecular genetics | 1999-06-01 | PMID 10332043
Branda S S, Yang Z Y, Chew A and 1 more
Genes: MIP
Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background.
Human molecular genetics | 1999-06-01 | PMID 10332045
Hao H, Morrison L E, Moraes C T
The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypes.
Human molecular genetics | 1999-06-01 | PMID 10332046
Riou L, Zeng L, Chevallier-Lagente O and 6 more
Novel genetic association between the corneodesmosin (MHC S) gene and susceptibility to psoriasis.
Human molecular genetics | 1999-06-01 | PMID 10332047
Tazi Ahnini R, Camp N J, Cork M J and 4 more
Current modulation and membrane targeting of the calcium channel alpha1C subunit are independent functions of the beta subunit.
The Journal of physiology | 1999-06-01 | PMID 10332087
Gerster U, Neuhuber B, Groschner K and 2 more
Properties of C1 and other ventrolateral medullary neurones with hypothalamic projections in the rat.
The Journal of physiology | 1999-06-01 | PMID 10332096
Verberne A J, Stornetta R L, Guyenet P G
Selective detection of inactivating mutations of the tumor suppressor gene p53 in bladder tumors.
The Journal of urology | 1999-06-01 | PMID 10332483
Pfister C, Flaman J M, Martin C and 2 more
Indirect modulation of dopamine D2 receptors as potential pharmacotherapy for schizophrenia: I. Adenosine agonists.
The Annals of pharmacotherapy | 1999-04-01 | PMID 10332540
Dixon D A, Fenix L A, Kim D M and 1 more
Molecular genetics of gynoecium development in Arabidopsis.
Current topics in developmental biology | 1999-01-01 | PMID 10332605
Bowman J L, Baum S F, Eshed Y and 2 more
Apolipoprotein(B) identifies dyslipidemic phenotypes associated with cardiovascular risk in normocholesterolemic type 2 diabetic patients.
Diabetes care | 1999-05-01 | PMID 10332687
Wägner A M, Pérez A, Calvo F and 3 more
Several different clones present during the penetration phase of resistant Streptococcus pneumoniae in the city of Malmö, Sweden.
Microbial drug resistance (Larchmont, N.Y.) | 1999-01-01 | PMID 10332720
Nilsson P, Laurell M H
The role of the chemokine receptor CXCR4 in infection with feline immunodeficiency virus.
Molecular membrane biology | 2000-01-01 | PMID 10332739
Willett B J, Hosie M J
Genes: CXCR4
On the homology of structures and Hox genes: the vertebral column.
Novartis Foundation symposium | 1999-01-01 | PMID 10332754
Galis F
Homology and homoplasy: the retention of genetic programmes.
Novartis Foundation symposium | 1999-01-01 | PMID 10332758
Meyer A
Evolutionary dissociations between homologous genes and homologous structures.
Novartis Foundation symposium | 1999-01-01 | PMID 10332761
Wray G A
Genetic analysis of ossification of the posterior longitudinal ligament.
Spine | 1999-05-15 | PMID 10332781
Matsunaga S, Yamaguchi M, Hayashi K and 1 more
The Emerging Importance of Genetics in Epidemiologic Research III. Bioinformatics and statistical genetic methods.
Annals of epidemiology | 1999-05-01 | PMID 10332927
Ellsworth D L, Manolio T A
Blood pressure and the T174M and M235T polymorphisms of the angiotensinogen gene.
Annals of epidemiology | 1999-05-01 | PMID 10332930
Niu T, Chen C, Yang J and 5 more
Genes: AGT, DBP
Myogenin, MyoD, and myosin heavy chain isoform expression following hindlimb suspension.
Aviation, space, and environmental medicine | 1999-05-01 | PMID 10332949
Mozdziak P E, Greaser M L, Schultz E
Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population.
Teratology | 1999-05-01 | PMID 10332959
Trembath D, Sherbondy A L, Vandyke D C and 7 more
Genes: MTHFR, PAX3, FOLR1, FOLR2
HLA-DRB1 genotype influences risk for and severity of rheumatoid arthritis.
The Journal of rheumatology | 1999-05-01 | PMID 10332964
Meyer J M, Evans T I, Small R E and 4 more
Genes: TNF
The -308.1 polymorphism in the promoter region of the tumor necrosis factor gene is associated with ankylosing spondylitis independent of HLA-B27.
The Journal of rheumatology | 1999-05-01 | PMID 10332976
McGarry F, Walker R, Sturrock R and 1 more
Genes: TNF
Genetic heterogeneity of autoimmune diabetes: age of presentation in adults is influenced by HLA DRB1 and DQB1 genotypes (UKPDS 43). UK Prospective Diabetes Study (UKPDS) Group.
Diabetologia | 1999-05-01 | PMID 10333055
Horton V, Stratton I, Bottazzo G F and 6 more
Variants in the sulphonylurea receptor gene: association of the exon 16-3t variant with Type II diabetes mellitus in Dutch Caucasians.
Diabetologia | 1999-05-01 | PMID 10333056
Hart L M, de Knijff P, Dekker J M and 7 more
Three new mutations in the hepatocyte nuclear factor-1alpha gene in Japanese subjects with diabetes mellitus: clinical features and functional characterization.
Diabetologia | 1999-05-01 | PMID 10333057
Yoshiuchi I, Yamagata K, Yang Q and 16 more
Hyperinsulinaemic hypoglycaemia associated with persistent hyperammonaemia.
European journal of pediatrics | 1999-05-01 | PMID 10333126
Kitaura J, Miki Y, Kato H and 2 more
Resistance mutations selected in vivo under therapy with anti-HIV drug HBY 097 differ from resistance pattern selected in vitro.
Antiviral research | 1999-05-01 | PMID 10333139
Rübsamen-Waigmann H, Huguenel E, Shah A and 6 more
Multiple lymphomatous polyposis of the gastrointestinal tract is a heterogenous group that includes mantle cell lymphoma and follicular lymphoma: analysis of somatic mutation of immunoglobulin heavy chain gene variable region.
Human pathology | 1999-05-01 | PMID 10333231
Hashimoto Y, Nakamura N, Kuze T and 2 more
Genetic epidemiology of essential hypertension.
Journal of human hypertension | 1999-04-01 | PMID 10333339
Gavras I, Manolis A, Gavras H
Mutations in the promoter region of the androgen receptor gene are not common in males with idiopathic infertility.
Molecular human reproduction | 1999-03-01 | PMID 10333364
Ghadessy F J, Liow S L, Yong E L
Behavioral effects of tryptophan depletion in seasonal affective disorder associated with the serotonin transporter gene?
Psychiatry research | 1999-03-22 | PMID 10333377
Lenzinger E, Neumeister A, Praschak-Rieder N and 7 more
Genes: HTT
Development, evolution, and corroboration.
The Anatomical record | 1999-02-15 | PMID 10333399
Janies D, DeSalle R
Homeobox genes, fossils, and the origin of species.
The Anatomical record | 1999-02-15 | PMID 10333400
Schwartz J H
A genome-wide search for linkage to asthma. German Asthma Genetics Group.
Genomics | 1999-05-15 | PMID 10333435
Wjst M, Fischer G, Immervoll T and 22 more
Stable expression of protective protein/cathepsin A-green fluorescent protein fusion genes in a fibroblastic cell line from a galactosialidosis patient. Model system for revealing the intracellular transport of normal and mutated lysosomal enzymes.
The Biochemical journal | 1999-06-01 | PMID 10333491
Naganawa Y, Itoh K, Shimmoto M and 4 more
Characterization of the biotin biosynthesis pathway in Saccharomyces cerevisiae and evidence for a cluster containing BIO5, a novel gene involved in vitamer uptake.
Gene | 1999-05-17 | PMID 10333520
Phalip V, Kuhn I, Lemoine Y and 1 more
Micronuclei in blood lymphocytes and genetic polymorphism for GSTM1, GSTT1 and NAT2 in pesticide-exposed greenhouse workers.
Mutation research | 1999-05-17 | PMID 10333536
Falck G C, Hirvonen A, Scarpato R and 3 more
Genes: GSTM1, NAT2, GSTT1
Simultaneous production of catalase, glucose oxidase and gluconic acid by Aspergillus niger mutant.
Acta microbiologica Polonica | 1998-01-01 | PMID 10333558
Fiedurek J, Gromada A, Pielecki J
Isolation and characterization of the yeast las21 mutants, which are sensitive to a local anestheticum, tetracaine.
Genes & genetic systems | 1998-12-01 | PMID 10333567
Tohe A, Oguchi T
Control of hypocotyl elongation in Arabidopsis thaliana by photoreceptor interaction.
Planta | 1999-04-01 | PMID 10333589
Hennig L, Poppe C, Unger S and 1 more
Genes: ABO
WT1: what has the last decade told us?
BioEssays : news and reviews in molecular, cellular and developmental biology | 1999-03-01 | PMID 10333728
Little M, Holmes G, Walsh P
Oxidative DNA damage, antioxidants, and cancer.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1999-03-01 | PMID 10333733
Collins A R
Origin, genetic diversity, and genome structure of the domestic dog.
BioEssays : news and reviews in molecular, cellular and developmental biology | 1999-03-01 | PMID 10333734
Wayne R K, Ostrander E A
Clinical, immunological, and genetic heterogeneity of diabetes in an Italian population-based cohort of lean newly diagnosed patients aged 30-54 years. Piedmont Study Group for Diabetes Epidemiology.
Diabetes care | 1999-01-01 | PMID 10333903
Bruno G, De Salvia A, Arcari R and 6 more
Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes.
Diabetes care | 1999-02-01 | PMID 10333942
Doria A, Yang Y, Malecki M and 6 more
Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia.
The American journal of the medical sciences | 1999-05-01 | PMID 10334122
Rhodes S L, Plonczynski M, Harrell A and 4 more
B-cell pulmonary lymphoma: gene rearrangement analysis of bronchoalveolar lymphocytes by polymerase chain reaction.
Chest | 1999-05-01 | PMID 10334134
Philippe B, Delfau-Larue M H, Epardeau B and 4 more
Glutathione S-transferase M1 and T1 null genotypes as risk factors for oral leukoplakia in ethnic Indian betel quid/tobacco chewers.
Carcinogenesis | 1999-05-01 | PMID 10334189
Nair U J, Nair J, Mathew B and 1 more
Genes: GSTM1, GSTT1
Influence of p53 tumor suppressor protein on bias of DNA repair and apoptotic response in human cells.
Carcinogenesis | 1999-05-01 | PMID 10334192
Wani M A, Zhu Q Z, El-Mahdy M and 1 more
Carcinogen and dietary lipid regulate ras expression and localization in rat colon without affecting farnesylation kinetics.
Carcinogenesis | 1999-05-01 | PMID 10334194
Davidson L A, Lupton J R, Jiang Y H and 1 more
Combined mismatch and nucleotide excision repair defects in a human cell line: mismatch repair processes methylation but not UV- or ionizing radiation-induced DNA damage.
Carcinogenesis | 1999-05-01 | PMID 10334196
O'Driscoll M, Martinelli S, Ciotta C and 1 more
Intestinal tumorigenesis in the Apc1638N mouse treated with aspirin and resistant starch for up to 5 months.
Carcinogenesis | 1999-05-01 | PMID 10334197
Williamson S L, Kartheuser A, Coaker J and 4 more
Genes: APC
Clinical evidence for dystrophin dysfunction as a cause of hearing loss in locus DFN4.
The Laryngoscope | 1999-05-01 | PMID 10334222
Pfister M H, Apaydin F, Turan O and 6 more
Genes: DMD, ERG
Functional properties of leptin receptor isoforms: internalization and degradation of leptin and ligand-induced receptor downregulation.
Diabetes | 1999-02-01 | PMID 10334302
Uotani S, Bjørbaek C, Tornøe J and 1 more
Hyperglycemia-induced embryonic dysmorphogenesis correlates with genomic DNA mutation frequency in vitro and in vivo.
Diabetes | 1999-02-01 | PMID 10334316
Lee A T, Reis D, Eriksson U J
Mutational analysis of the coding regions of the genes encoding protein kinase B-alpha and -beta, phosphoinositide-dependent protein kinase-1, phosphatase targeting to glycogen, protein phosphatase inhibitor-1, and glycogenin: lessons from a search for genetic variability of the insulin-stimulated glycogen synthesis pathway of skeletal muscle in NIDDM patients.
Diabetes | 1999-02-01 | PMID 10334321
Hansen L, Fjordvang H, Rasmussen S K and 8 more
A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.
Diabetes | 1999-02-01 | PMID 10334322
Otonkoski T, Ammälä C, Huopio H and 10 more
Association of polymorphism in the NeuroD/BETA2 gene with type 1 diabetes in the Japanese.
Diabetes | 1999-02-01 | PMID 10334323
Iwata I, Nagafuchi S, Nakashima H and 12 more
Parental history of premature coronary heart disease mortality and signs of ischemia on the resting electrocardiogram.
Journal of the American College of Cardiology | 1999-05-01 | PMID 10334413
De Bacquer D, De Backer G, Kornitzer M and 1 more
Maternally inherited cardiomyopathy: clinical and molecular characterization of a large kindred harboring the A4300G point mutation in mitochondrial deoxyribonucleic acid.
Journal of the American College of Cardiology | 1999-05-01 | PMID 10334428
Casali C, d'Amati G, Bernucci P and 5 more
Survival after cardiac arrest or sustained ventricular tachycardia in patients with hypertrophic cardiomyopathy.
Journal of the American College of Cardiology | 1999-05-01 | PMID 10334430
Elliott P M, Sharma S, Varnava A and 3 more
Familial predisposition of left ventricular hypertrophy.
Journal of the American College of Cardiology | 1999-05-01 | PMID 10334443
Schunkert H, Bröckel U, Hengstenberg C and 7 more
Additive effect of three noradrenergic genes (ADRA2a, ADRA2C, DBH) on attention-deficit hyperactivity disorder and learning disabilities in Tourette syndrome subjects.
Clinical genetics | 1999-03-01 | PMID 10334470
Comings D E, Gade-Andavolu R, Gonzalez N and 3 more
Genes: DBH
Confirmation of linkage in X-linked infantile spasms (West syndrome) and refinement of the disease locus to Xp21.3-Xp22.1.
Clinical genetics | 1999-03-01 | PMID 10334471
Bruyere H, Lewis S, Wood S and 2 more
Accurate determination of the number of CAG repeats in the Huntington disease gene using a sequence-specific internal DNA standard.
Clinical genetics | 1999-03-01 | PMID 10334474
Bruland O, Almqvist E W, Goldberg Y P and 3 more
Genes: POP4
A threonine residue in the M2 region of the beta1 subunit is needed for expression of functional alpha1beta1 GABA(A) receptors.
European journal of pharmacology | 1999-04-16 | PMID 10334512
Dalziel J E, Birnir B, Everitt A B and 3 more
Neighboring glycine residues are essential for P2X2 receptor/channel function.
European journal of pharmacology | 1999-04-16 | PMID 10334514
Nakazawa K, Ohno Y
Moral concerns of different types of patients in clinical BRCA1/2 gene mutation testing.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology | 1999-05-01 | PMID 10334549
Goelen G, Rigo A, Bonduelle M and 1 more
Genes: BRCA1
Genomic DNA restriction site heterogeneity in bovine Pasteurella multocida serogroup A isolates detected with an rRNA probe.
Journal of medical microbiology | 1999-03-01 | PMID 10334595
Dabo S M, Debey B M, Montelongo M and 1 more
Genes: OMP, SDS
Genotypic and phenotypic similarity of multiresistant Acinetobacter baumannii isolates in the Czech Republic.
Journal of medical microbiology | 1999-03-01 | PMID 10334596
Nemec A, Janda L, Melter O and 1 more
Mutation spectrum in Salmonella induced by environmental tobacco smoke.
Environmental and molecular mutagenesis | 1999-01-01 | PMID 10334620
Zhou R, Yu G, Zhou Y and 1 more
Combinations of chlorocatechols and heavy metals cause DNA degradation in vitro but must not result in increased mutation rates in vivo.
Environmental and molecular mutagenesis | 1999-01-01 | PMID 10334622
Schweigert N, Belkin S, Leong-Morgenthaler P and 2 more
Nickel subsulfide is similar to potassium dichromate in protecting normal human fibroblasts from the mutagenic effects of benzo[a]pyrene diolepoxide.
Environmental and molecular mutagenesis | 1999-01-01 | PMID 10334623
Hamdan S, Morse B, Reinhold D
Genetic polymorphism of glutathione S-transferase P1 gene and lung cancer risk.
Cancer causes & control : CCC | 1999-02-01 | PMID 10334644
To-Figueras J, Gené M, Gómez-Catalán J and 5 more
Genes: GSTP1, GSTM1, GSTT1
The therapeutic response to D-penicillamine in rheumatoid arthritis: influence of glutathione S-transferase polymorphisms.
Rheumatology (Oxford, England) | 1999-01-01 | PMID 10334681
Layton M A, Jones P W, Alldersea J E and 4 more
Genes: GSTM1, GSTM3
DD angiotensin-converting enzyme gene polymorphism is associated with endothelial dysfunction in normal humans.
Hypertension (Dallas, Tex. : 1979) | 1999-05-01 | PMID 10334805
Butler R, Morris A D, Burchell B and 1 more
Genes: ACE
The Lys198Asn polymorphism in the endothelin-1 gene is associated with blood pressure in overweight people.
Hypertension (Dallas, Tex. : 1979) | 1999-05-01 | PMID 10334806
Tiret L, Poirier O, Hallet V and 9 more
The 825C/T polymorphism of the G-protein subunit beta3 is not related to hypertension.
Hypertension (Dallas, Tex. : 1979) | 1999-05-01 | PMID 10334807
Brand E, Herrmann S M, Nicaud V and 7 more
Genes: GNB3
Tyrosine modifications and inactivation of active site manganese superoxide dismutase mutant (Y34F) by peroxynitrite.
Archives of biochemistry and biophysics | 1999-06-01 | PMID 10334867
MacMillan-Crow L A, Thompson J A
Differential catalytic efficiency of allelic variants of human glutathione S-transferase Pi in catalyzing the glutathione conjugation of thiotepa.
Archives of biochemistry and biophysics | 1999-06-01 | PMID 10334868
Srivastava S K, Singhal S S, Hu X and 3 more
Multidrug-resistant phenotype influences the differentiation of a human colon carcinoma cell line.
Biochemical and biophysical research communications | 1999-05-27 | PMID 10334913
Rimet O, Mirrione A, Barra Y
Molecular and histological evaluation of pancreata from patients with a mitochondrial gene mutation associated with impaired insulin secretion.
Biochemical and biophysical research communications | 1999-05-27 | PMID 10334931
Otabe S, Yasuda K, Mori Y and 7 more
Interindividual differences in hepatic expression of CYP3A4: relationship to genetic polymorphism in the 5'-upstream regulatory region.
Biochemical and biophysical research communications | 1999-05-27 | PMID 10334940
Westlind A, Löfberg L, Tindberg N and 2 more
Overexpression of wild-type and catalytically inactive forms of GRK2 and GRK6 fails to alter the agonist-induced phosphorylation of the C5a receptor (CD88): evidence that GRK6 is autophosphorylated in COS-7 cells.
Biochemical and biophysical research communications | 1999-05-27 | PMID 10334944
Milcent M D, Christophe T, Rabiet M J and 2 more
Genes: GRK6, GRK2, GRK1