p53 exon 5 mutations as a prognostic indicator of shortened survival in non-small-cell lung cancer.
British journal of cancer | 1997-01-01 | PMID 9218731
Vega F J, Iniesta P, Caldés T and 7 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 869 of 10600
DNA binding of Escherichia coli arginine repressor mutants altered in oligomeric state.
Molecular microbiology | 1997-06-01 | PMID 9218764
Chen S H, Merican A F, Sherratt D J
Isolation of a dnaE mutation which enhances RecA-independent homologous recombination in the Escherichia coli chromosome.
Molecular microbiology | 1997-06-01 | PMID 9218771
Bierne H, Vilette D, Ehrlich S D and 1 more
ftsW is an essential cell-division gene in Escherichia coli.
Molecular microbiology | 1997-06-01 | PMID 9218774
Boyle D S, Khattar M M, Addinall S G and 2 more
Genes: BAD
Structure of the PH domain and Btk motif from Bruton's tyrosine kinase: molecular explanations for X-linked agammaglobulinaemia.
The EMBO journal | 1997-06-16 | PMID 9218782
Hyvönen M, Saraste M
Identification of a motor protein required for filamentous growth in Ustilago maydis.
The EMBO journal | 1997-06-16 | PMID 9218789
Lehmler C, Steinberg G, Snetselaar K M and 3 more
The Aspergillus nidulans sepA gene encodes an FH1/2 protein involved in cytokinesis and the maintenance of cellular polarity.
The EMBO journal | 1997-06-16 | PMID 9218790
Harris S D, Hamer L, Sharpless K E and 1 more
Alternative lipid remodelling pathways for glycosylphosphatidylinositol membrane anchors in Saccharomyces cerevisiae.
The EMBO journal | 1997-06-16 | PMID 9218792
Sipos G, Reggiori F, Vionnet C and 1 more
Genes: GPI
A role for the divergent actin gene, ACT2, in nuclear pore structure and function.
The EMBO journal | 1997-06-16 | PMID 9218799
Yan C, Leibowitz N, Mélèse T
High level transcription of a member of a repeated gene family confers dehydration tolerance to callus tissue of Craterostigma plantagineum.
The EMBO journal | 1997-06-16 | PMID 9218801
Furini A, Koncz C, Salamini F and 1 more
Evidence for genetic heterogeneity in inflammatory bowel disease (IBD); HLA genes in the predisposition to suffer from ulcerative colitis (UC) and Crohn's disease (CD).
Clinical and experimental immunology | 1997-07-01 | PMID 9218841
Bouma G, Oudkerk Pool M, Crusius J B and 7 more
The normally expressed kappa immunoglobulin light chain gene repertoire and somatic mutations studied by single-sided specific polymerase chain reaction (PCR); frequent occurrence of features often assigned to autoimmunity.
Clinical and experimental immunology | 1997-07-01 | PMID 9218844
Juul L, Hougs L, Andersen V and 2 more
Cyclin-dependent kinase activation and S-phase induction of the cyclin B1 gene are linked through the CCAAT elements.
Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research | 1997-07-01 | PMID 9218875
Katula K S, Wright K L, Paul H and 6 more
Improving contact predictions by the combination of correlated mutations and other sources of sequence information.
Folding & design | 1997-01-01 | PMID 9218963
Olmea O, Valencia A
Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes.
Genes, chromosomes & cancer | 1997-07-01 | PMID 9218993
Pensotti V, Radice P, Presciuttini S and 10 more
Genes: MSH2
Two discrete regions of deletion at 7q in uterine leiomyomas.
Genes, chromosomes & cancer | 1997-07-01 | PMID 9218996
Ishwad C S, Ferrell R E, Hanley K and 4 more
Regenerative lesions in ulcerative colitis are characterized by microsatellite mutation.
Genes, chromosomes & cancer | 1997-07-01 | PMID 9218998
Heinen C D, Noffsinger A E, Belli J and 4 more
Loss of heterozygosity on chromosome arm 16q in breast cancer metastases.
Genes, chromosomes & cancer | 1997-07-01 | PMID 9219000
Driouch K, Dorion-Bonnet F, Briffod M and 3 more
Patterns of meiotic variability of the (CAG)n repeat in the Huntington disease gene.
Genetic counseling (Geneva, Switzerland) | 1997-01-01 | PMID 9219003
Lucotte G, Gérard N, Aouizérate A and 2 more
Hereditary multiple benign cystic epithelioma (multiple trichoepithelioma) with onset at early age.
Genetic counseling (Geneva, Switzerland) | 1997-01-01 | PMID 9219004
Correa-Cerro L S, García-Cruz D, Sarralde A and 3 more
Penetrance of familial hypertrophic cardiomyopathy.
Genetic counseling (Geneva, Switzerland) | 1997-01-01 | PMID 9219008
Charron P, Carrier L, Dubourg O and 11 more
Brachydactyly and short stature in a mother and her daughter with a fragile site at 16q22.
Genetic counseling (Geneva, Switzerland) | 1997-01-01 | PMID 9219009
Stoll C, Roy-Doray B, Dott B and 1 more
Hyperacusis in Williams syndrome: a sample survey study.
Genetic counseling (Geneva, Switzerland) | 1997-01-01 | PMID 9219010
Van Borsel J, Curfs L M, Fryns J P
Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?
Genetic counseling (Geneva, Switzerland) | 1997-01-01 | PMID 9219011
Mégarbané A, Abi Moussa M
On the phenotypic overlap between "severe" oto-palato digital type II syndrome and Larsen syndrome. Variable manifestation of a single autosomal dominant gene.
Genetic counseling (Geneva, Switzerland) | 1997-01-01 | PMID 9219012
Alembik Y, Stoll C, Messer J
Molecular diagnosis of pancreas carcinoma.
Journal of clinical laboratory analysis | 1997-01-01 | PMID 9219065
Chu T M
Genes: CDK4
Suppressive action of docosahexaenoic acid enriched-Euglena on reduction of endothelium-dependent relaxation in stroke-prone spontaneously hypertensive rats (SHRSP).
Journal of nutritional science and vitaminology | 1997-04-01 | PMID 9219094
Murakami T, Ogawa H, Hayashi M and 1 more
Prenatal determination of genotypes Kell and Cellano in at-risk pregnancies.
The Journal of reproductive medicine | 1997-06-01 | PMID 9219123
Spence W C, Maddalena A, Demers D B and 1 more
Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease.
Journal of the American Society of Nephrology : JASN | 1997-07-01 | PMID 9219161
Jansen J J, Maassen J A, van der Woude F J and 6 more
Deregulation of CLN1 and CLN2 in the Saccharomyces cerevisiae whi2 mutant.
Yeast (Chichester, England) | 1997-06-30 | PMID 9219335
Radcliffe P, Trevethick J, Tyers M and 1 more
Genes: CLN3
Cloning of the multicopy suppressor gene SUR7: evidence for a functional relationship between the yeast actin-binding protein Rvs167 and a putative membranous protein.
Yeast (Chichester, England) | 1997-06-30 | PMID 9219339
Sivadon P, Peypouquet M F, Doignon F and 2 more
Infrared fluorescent detection of D1S80 alleles.
Forensic science international | 1997-05-23 | PMID 9219360
Roy R
Methods for predicting carcinogenic hazards: new opportunities coming from recent developments in molecular oncology and SAR studies.
Mutation research | 1997-06-13 | PMID 9219545
Taningher M, Malacarne D, Mancuso T and 3 more
Arsenic methylation capacity, body retention, and null genotypes of glutathione S-transferase M1 and T1 among current arsenic-exposed residents in Taiwan.
Mutation research | 1997-06-01 | PMID 9219558
Chiou H Y, Hsueh Y M, Hsieh L L and 11 more
Mutant frequency of lacI in transgenic mice following benzo[a]pyrene treatment and partial hepatectomy.
Mutation research | 1997-06-09 | PMID 9219573
Shane B S, Lockhart A M, Winston G W and 1 more
Types of mutations induced by glyoxal, a major oxidative DNA-damage product, in Salmonella typhimurium.
Mutation research | 1997-06-09 | PMID 9219574
Murata-Kamiya N, Kaji H, Kasai H
Isolation of an APRT heterozygote from TK6 human lymphoblasts: predominance of multi-locus loss of heterozygosity among spontaneous APRT-mutants.
Mutation research | 1997-06-09 | PMID 9219576
Pongsaensook P, Smith L E, Grosovsky A J
Genes: APRT
Dichotomous relationship between DNA reactivity and the induction of sister chromatid exchanges in vivo and in vitro.
Mutation research | 1997-06-09 | PMID 9219577
Labbauf A, Klopman G, Rosenkranz H S
Mutation load and human longevity.
Mutation research | 1997-06-09 | PMID 9219579
Gavrilov L A, Gavrilova N S, Kroutko V N and 6 more
The effects of maternal cigarette smoke exposure on somatic mutant frequencies at the hprt locus in healthy newborns.
Mutation research | 1997-06-09 | PMID 9219586
Finette B A, Poseno T, Vacek P M and 1 more
In vivo antioxidant status, DNA damage, mutation and DNA repair capacity in cultured lymphocytes from healthy 75- to 80-year-old humans.
Mutation research | 1997-06-09 | PMID 9219588
King C M, Bristow-Craig H E, Gillespie E S and 1 more
Genes: CAT
Mutation rates as adaptations.
Journal of theoretical biology | 1997-06-07 | PMID 9219670
Maley C
Activation of fibrillar collagen synthesis and phenotypic modulation of chondrocytes in early human osteoarthritic cartilage lesions.
Osteoarthritis and cartilage | 1997-05-01 | PMID 9219681
Aigner T, Glückert K, von der Mark K
The Ras-RasGAP complex: structural basis for GTPase activation and its loss in oncogenic Ras mutants.
Science (New York, N.Y.) | 1997-07-18 | PMID 9219684
Scheffzek K, Ahmadian M R, Kabsch W and 4 more
Alternative cleavage of Alzheimer-associated presenilins during apoptosis by a caspase-3 family protease.
Science (New York, N.Y.) | 1997-07-18 | PMID 9219695
Kim T W, Pettingell W H, Jung Y K and 2 more
In vitro propagation of the prion-like state of yeast Sup35 protein.
Science (New York, N.Y.) | 1997-07-18 | PMID 9219697
Paushkin S V, Kushnirov V V, Smirnov V N and 1 more
Mating type switching in yeast controlled by asymmetric localization of ASH1 mRNA.
Science (New York, N.Y.) | 1997-07-18 | PMID 9219698
Long R M, Singer R H, Meng X and 3 more
Mutilating neuropathic ulcerations in a chromosome 3q13-q22 linked Charcot-Marie-Tooth disease type 2B family.
Journal of neurology, neurosurgery, and psychiatry | 1997-06-01 | PMID 9219740
De Jonghe P, Timmerman V, FitzPatrick D and 3 more
Influence of hepatitis C virus genotypes and HIV infection on histological severity of chronic hepatitis C. The Hepatitis/HIV Spanish Study Group.
The American journal of gastroenterology | 1997-07-01 | PMID 9219784
García-Samaniego J, Soriano V, Castilla J and 6 more
Significance of interleukin-1beta and interleukin-1 receptor antagonist genetic polymorphism in inflammatory bowel diseases.
The American journal of gastroenterology | 1997-07-01 | PMID 9219791
Heresbach D, Alizadeh M, Dabadie A and 5 more
Mutation analysis and loss of heterozygosity of PEDF in central nervous system primitive neuroectodermal tumors.
International journal of cancer | 1997-07-17 | PMID 9219833
Slavc I, Rodriguez I R, Mazuruk K and 2 more
Deletion of chromosome 11p15, p12, q22, q23-24 loci in human prostate cancer.
International journal of cancer | 1997-07-17 | PMID 9219834
Dahiya R, McCarville J, Lee C and 4 more
Lack of phospholipase A2 mutations in neuroblastoma, melanoma and colon-cancer cell lines.
International journal of cancer | 1997-07-17 | PMID 9219842
Haluska F G, Thiele C, Goldstein A and 3 more
Characterization of a cAMP-dependent protein kinase mutant resistant to cisplatin.
International journal of cancer | 1997-07-17 | PMID 9219844
Cvijic M E, Chin K V
Genetic association between susceptibility to Parkinson's disease and alpha1-antichymotrypsin polymorphism.
Brain research | 1997-06-06 | PMID 9219874
Yamamoto M, Kondo I, Ogawa N and 3 more
Estrogenic activity is increased for an antiestrogen by a natural mutation of the estrogen receptor.
The Journal of steroid biochemistry and molecular biology | 1997-03-01 | PMID 9219916
Levenson A S, Catherino W H, Jordan V C
Expression and distribution of cortical type aromatase mRNA variant in the adult rat brain.
The Journal of steroid biochemistry and molecular biology | 1997-03-01 | PMID 9219924
Yamada-Mouri N, Hirata S, Kato J and 1 more
Mutations in the terminase genes of bacteriophage lambda that bypass the necessity for FI.
Molecular microbiology | 1997-06-01 | PMID 9220002
Murialdo H, Tzamtzis D, Berrú M and 2 more
Paracoccus denitrificans CcmG is a periplasmic protein-disulphide oxidoreductase required for c- and aa3-type cytochrome biogenesis; evidence for a reductase role in vivo.
Molecular microbiology | 1997-06-01 | PMID 9220005
Page M D, Ferguson S J
The Neisseria type 2 IgA1 protease cleaves LAMP1 and promotes survival of bacteria within epithelial cells.
Molecular microbiology | 1997-06-01 | PMID 9220014
Lin L, Ayala P, Larson J and 5 more
Genes: LAMP1
Oct-1, silencer sequence, and GC box regulate thyroid hormone receptor beta1 promoter.
Molecular and cellular endocrinology | 1997-06-20 | PMID 9220031
Nagasawa T, Takeda T, Minemura K and 1 more
Analysis of primate major histocompatibility complex (MHC)-DQA1 locus by PCR-single strand conformation polymorphism (SSCP).
Cellular and molecular biology (Noisy-le-Grand, France) | 1997-06-01 | PMID 9220140
Mwenda J M, Hashiba K, Bambra C S and 1 more
Non-haematological traits associated with congenital dyserythropoietic anaemia type 1: a new entity emerging.
Clinical dysmorphology | 1997-07-01 | PMID 9220189
Sabry M A, Zaki M, al Awadi S A and 2 more
Exclusion of the p75 neurotrophin receptor gene as a candidate gene for Meckel syndrome.
Clinical dysmorphology | 1997-07-01 | PMID 9220190
Wartiovaara K, Paavola P, Suvanto P and 4 more
Genes: NGFR
A syndrome of leukonychia totalis and multiple sebaceous cysts.
Clinical dysmorphology | 1997-07-01 | PMID 9220192
Slee J J, Wallman I S, Goldblatt J
The syndrome of hypoparathyroidism, severe growth failure, developmental delay and distinctive facies.
Clinical dysmorphology | 1997-07-01 | PMID 9220193
al-Gazali L I, Dawodu A
Human leukocyte antigen class II associations in patients with idiopathic dilated cardiomyopathy. Myocarditis Treatment Trial Investigators.
Journal of cardiac failure | 1997-06-01 | PMID 9220309
Lozano M D, Rubocki R J, Wilson J E and 2 more
Epicardial temperature is a major predictor of myocardial infarct size in dogs.
Journal of molecular and cellular cardiology | 1997-06-01 | PMID 9220343
Schwartz L M, Verbinski S G, Vander Heide R S and 1 more
Detection of HHV-6 genotypes by in situ hybridization with variant-specific oligonucleotide probes.
Journal of virological methods | 1997-06-01 | PMID 9220385
Arivananthan M, Yadav M, Kumar S
Ehlers-Danlos syndrome type VI results from a nonsense mutation and a splice site-mediated exon-skipping mutation in the lysyl hydroxylase gene.
Proceedings of the Association of American Physicians | 1997-07-01 | PMID 9220536
Yeowell H N, Walker L C
Variation in open reading frames 3, 4 and 7 among porcine reproductive and respiratory syndrome virus isolates in the UK.
Veterinary microbiology | 1997-04-01 | PMID 9220616
Drew T W, Lowings J P, Yapp F
Population genetic structure of Ixodes pacificus (Acari:Ixodidae) using allozymes.
Journal of medical entomology | 1997-07-01 | PMID 9220679
Kain D E, Sperling F A, Lane R S
The role of phenylalanine 31 in maintaining the conformational stability of ribonuclease P2 from Sulfolobus solfataricus under extreme conditions of temperature and pressure.
Biochemistry | 1997-07-22 | PMID 9220960
Mombelli E, Afshar M, Fusi P and 4 more
[The induction of mutations in Streptomyces aureofaciens by UV rays and nitrosoguanidine and the identification of the mutants obtained].
Mikrobiolohichnyi zhurnal (Kiev, Ukraine : 1993) | 2000-01-01 | PMID 9221058
Lavrinchuk V Ia, Stryzhkova H M, Matseliukh B P
[Clinical value of the CA 19-9 tumor marker with special reference to the Lewis phenotype].
Medizinische Klinik (Munich, Germany : 1983) | 1997-04-15 | PMID 9221306
Kolb G, Safi F, Beckh K and 1 more
[Chronic hepatitis C: virologic and immunologic aspects and questions of therapy].
Orvosi hetilap | 1997-06-01 | PMID 9221376
Pár A
Genes: GPT
[The role of the outer-membrane antigens of Yersinia pseudotuberculosis in the pathogenesis and diagnosis of pseudotuberculosis].
Zhurnal mikrobiologii, epidemiologii i immunobiologii | 2000-01-01 | PMID 9221648
Kuliashova L B, Tseneva G Ia, Buĭnevich Iu B
[The isolation and characteristics of mutants of the Saccharopolyspora erythraea strain resistant to thiostrepton].
Antibiotiki i khimioterapiia = Antibiotics and chemoterapy [sic] | 1997-01-01 | PMID 9221705
Nastasiak I N, Fedorenko V A, Danilenko V N
Slow-channel myasthenic syndrome caused by enhanced activation, desensitization, and agonist binding affinity attributable to mutation in the M2 domain of the acetylcholine receptor alpha subunit.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1997-08-01 | PMID 9221765
Milone M, Wang H L, Ohno K and 5 more
Caenorhabditis elegans levamisole resistance genes lev-1, unc-29, and unc-38 encode functional nicotinic acetylcholine receptor subunits.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1997-08-01 | PMID 9221782
Fleming J T, Squire M D, Barnes T M and 8 more
Mammalian homolog of Drosophila retinal degeneration B rescues the mutant fly phenotype.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 1997-08-01 | PMID 9221785
Chang J T, Milligan S, Li Y and 7 more
Renal cell regeneration following oxidant exposure: inhibition by TGF-beta1 and stimulation by ascorbic acid.
Toxicology and applied pharmacology | 1997-07-01 | PMID 9221835
Nowak G, Schnellmann R G
Genes: EGF
Proteolytical processing of mutated human amyloid precursor protein in transgenic mice.
Brain research. Molecular brain research | 1997-07-01 | PMID 9221907
Czech C, Delaère P, Macq A F and 11 more
Genes: APP
Arginine-481 mutation abolishes ligand-binding of the AMPA-selective glutamate receptor channel alpha1-subunit.
Brain research. Molecular brain research | 1997-07-01 | PMID 9221933
Kawamoto S, Uchino S, Xin K Q and 5 more
X linked adrenoleukodystrophy: clinical presentation, diagnosis, and therapy.
Journal of neurology, neurosurgery, and psychiatry | 1997-07-01 | PMID 9221959
van Geel B M, Assies J, Wanders R J and 1 more
Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six families.
Journal of neurology, neurosurgery, and psychiatry | 1997-07-01 | PMID 9221962
Uziel G, Moroni I, Lamantea E and 4 more
No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry | 1997-07-01 | PMID 9221977
Didierjean O, Martinez M, Campion D and 13 more
Emergence of resistant variants of HIV in vivo during monotherapy with the proteinase inhibitor saquinavir.
The Journal of antimicrobial chemotherapy | 1997-06-01 | PMID 9222047
Ives K J, Jacobsen H, Galpin S A and 5 more
Abnormal naive and memory T lymphocyte subsets in the peripheral blood of patients with uveitis.
Current eye research | 1997-07-01 | PMID 9222081
Ohta K, Norose K, Wang X C and 2 more
Apolipoprotein E genotypes in primary progressive aphasia.
Neurology | 1997-07-01 | PMID 9222169
Mesulam M M, Johnson N, Grujic Z and 1 more
Genetic association of the low-density lipoprotein receptor-related protein gene (LRP), an apolipoprotein E receptor, with late-onset Alzheimer's disease.
Neurology | 1997-07-01 | PMID 9222170
Kang D E, Saitoh T, Chen X and 6 more
Genes: APOE
Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles.
Neurology | 1997-07-01 | PMID 9222191
Peroutka S J, Wilhoit T, Jones K
Genes: DRD2
Heterogeneous clinical presentation of the mtDNA NARP/T8993G mutation.
Neurology | 1997-07-01 | PMID 9222207
Santorelli F M, Tanji K, Shanske S and 1 more
Phenotypes in three Swedish families with X-linked retinitis pigmentosa caused by different mutations in the RPGR gene.
American journal of ophthalmology | 1997-07-01 | PMID 9222238
Andréasson S, Ponjavic V, Abrahamson M and 5 more
Genes: RPGR
Maximal gamma-globin expression in the compound heterozygous state for -175G gamma HPFH and beta degree 39 nonsense thalassaemia: a case study.
European journal of haematology | 1997-05-01 | PMID 9222287
Pistidda P, Frogheri L, Guiso L and 4 more
Dominant-negative mutations of the Wilms' tumour predisposing gene (WT1) are infrequent in CML blast crisis and de novo acute leukaemia.
European journal of haematology | 1997-05-01 | PMID 9222290
Carapeti M, Goldman J M, Cross N C
The effect of Theiler's murine encephalomyelitis virus (TMEV) VP1 carboxyl region on the virus-induced central nervous system disease.
Journal of neurovirology | 1995-03-01 | PMID 9222346
Senkowski A, Shim B, Roos R P
Mutation of a major histocompatibility class I locus, H-2D, leads to an increased virus burden and disease susceptibility in Theiler's virus-induced demyelinating disease.
Journal of neurovirology | 1995-06-01 | PMID 9222352
Lipton H L, Melvold R, Miller S D and 1 more
Frequent mutation in pX region of HTLV-1 is observed in HAM/TSP patients, but is not specifically associated with the central nervous system lesions.
Journal of neurovirology | 1995-09-01 | PMID 9222367
Saito M, Furukawa Y, Kubota R and 5 more
Isolation and characterization of intranuclear ribonucleoprotein complexes associated with double-stranded RNA adenosine deaminase from brain cells: implications for RNA-editing and hypermutation of viral RNA in the CNS.
Journal of neurovirology | 1995-09-01 | PMID 9222368
Chen Z, Hirano A, Wong T C