Patterns of phenotypic resistance to the macrolide-lincosamide-ketolide-streptogramin group of antibiotics in staphylococci.
The Journal of antimicrobial chemotherapy | 2000-12-01 | PMID 11102413
Hamilton-Miller J M, Shah S
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 1445 of 10600
Short-term infection with Helicobacter pylori and 1 week exposure to metronidazole does not enhance gastric mutation frequency in transgenic mice.
The Journal of antimicrobial chemotherapy | 2000-12-01 | PMID 11102419
Touati E, Hofnung M, Thiberge J M and 3 more
Regulation of the aldehyde dehydrogenase gene (aldA) and its role in the control of the coinducer level necessary for induction of the ethanol utilization pathway in Aspergillus nidulans.
The Journal of biological chemistry | 2001-03-09 | PMID 11102439
Flipphi M, Mathieu M, Cirpus I and 2 more
Calpain mutants with increased Ca2+ sensitivity and implications for the role of the C(2)-like domain.
The Journal of biological chemistry | 2001-03-09 | PMID 11102442
Hosfield C M, Moldoveanu T, Davies P L and 2 more
Molecular mechanism for functional interaction between DnaA protein and acidic phospholipids: identification of important amino acids.
The Journal of biological chemistry | 2001-03-09 | PMID 11102450
Makise M, Mima S, Tsuchiya T and 1 more
Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation.
The Journal of biological chemistry | 2001-03-09 | PMID 11102452
Szczesna D, Ghosh D, Li Q and 6 more
Ligand- and coactivator-mediated transactivation function (AF2) of the androgen receptor ligand-binding domain is inhibited by the cognate hinge region.
The Journal of biological chemistry | 2001-03-09 | PMID 11102454
Wang Q, Lu J, Yong E L
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2000-12-01 | PMID 11102465
Struyk A F, Scoggan K A, Bulman D E and 1 more
Adult spinal cord stem cells generate neurons after transplantation in the adult dentate gyrus.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2000-12-01 | PMID 11102479
Shihabuddin L S, Horner P J, Ray J and 1 more
Reliability of a fly motion-sensitive neuron depends on stimulus parameters.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2000-12-01 | PMID 11102498
Warzecha A K, Kretzberg J, Egelhaaf M
A snc1 endocytosis mutant: phenotypic analysis and suppression by overproduction of dihydrosphingosine phosphate lyase.
Molecular biology of the cell | 2000-12-01 | PMID 11102507
Grote E, Vlacich G, Pypaert M and 1 more
Distinct FTDP-17 missense mutations in tau produce tau aggregates and other pathological phenotypes in transfected CHO cells.
Molecular biology of the cell | 2000-12-01 | PMID 11102510
Vogelsberg-Ragaglia V, Bruce J, Richter-Landsberg C and 4 more
Mutation of cyclin/cdk phosphorylation sites in HsCdc6 disrupts a late step in initiation of DNA replication in human cells.
Molecular biology of the cell | 2000-12-01 | PMID 11102512
Herbig U, Griffith J W, Fanning E
Complex phenotype of mice lacking occludin, a component of tight junction strands.
Molecular biology of the cell | 2000-12-01 | PMID 11102513
Saitou M, Furuse M, Sasaki H and 5 more
Self-association of coilin reveals a common theme in nuclear body localization.
Molecular biology of the cell | 2000-12-01 | PMID 11102515
Hebert M D, Matera A G
Genes: PML
The sodium/proton exchanger Nhx1p is required for endosomal protein trafficking in the yeast Saccharomyces cerevisiae.
Molecular biology of the cell | 2000-12-01 | PMID 11102523
Bowers K, Levi B P, Patel F I and 1 more
New components of a system for phosphate accumulation and polyphosphate metabolism in Saccharomyces cerevisiae revealed by genomic expression analysis.
Molecular biology of the cell | 2000-12-01 | PMID 11102525
Ogawa N, DeRisi J, Brown P O
Apoptosis induced by Rac GTPase correlates with induction of FasL and ceramides production.
Molecular biology of the cell | 2000-12-01 | PMID 11102528
Embade N, Valerón P F, Aznar S and 2 more
Dual requirement for rho and protein kinase C in direct activation of phospholipase D1 through G protein-coupled receptor signaling.
Molecular biology of the cell | 2000-12-01 | PMID 11102529
Du G, Altshuller Y M, Kim Y and 4 more
Genes: PLD1
Identification of a novel transcription factor binding element involved in the regulation by differentiation of the human telomerase (hTERT) promoter.
Molecular biology of the cell | 2000-12-01 | PMID 11102531
Tzukerman M, Shachaf C, Ravel Y and 4 more
Genes: TERT
The TRAPP complex is a nucleotide exchanger for Ypt1 and Ypt31/32.
Molecular biology of the cell | 2000-12-01 | PMID 11102533
Jones S, Newman C, Liu F and 1 more
Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype.
Pediatric research | 2000-12-01 | PMID 11102542
Jeck N, Konrad M, Peters M and 3 more
Genes: CLCNKB
Evidence for autosomal recessive inheritance of infantile dilated cardiomyopathy: studies from the Eastern Province of Saudi Arabia.
Pediatric research | 2000-12-01 | PMID 11102545
Seliem M A, Mansara K B, Palileo M and 3 more
Asymptomatic CTG expansion at the SCA8 locus is associated with cerebellar atrophy on MRI.
Journal of the neurological sciences | 2000-12-15 | PMID 11102643
Ikeda Y, Shizuka-Ikeda M, Watanabe M and 3 more
Retinoic acid treatment enhances the acetylcholine contents in the human teratocarcinoma cell line NTera-2.
Regulatory peptides | 2000-12-22 | PMID 11102653
Fischer H S, Berti I, Schatz D S and 2 more
Genes: NPY, VIP
A new study challenges the current belief of a high human male:female mutation ratio.
Trends in genetics : TIG | 2000-12-01 | PMID 11102696
Crow J F
Tenascin-C in development and disease: gene regulation and cell function.
Matrix biology : journal of the International Society for Matrix Biology | 2000-12-01 | PMID 11102748
Jones P L, Jones F S
Revised genomic structure of the human MAGP1 gene and identification of alternate transcripts in human and mouse tissues.
Matrix biology : journal of the International Society for Matrix Biology | 2000-12-01 | PMID 11102756
Segade F, Broekelmann T J, Pierce R A and 1 more
Genes: MFAP2
Human autoimmunity genes in mice.
Current opinion in immunology | 2000-12-01 | PMID 11102775
Fugger L
Apoptosis genes and autoimmunity.
Current opinion in immunology | 2000-12-01 | PMID 11102778
Vaux D L, Flavell R A
Applied genomics: integration of the technology within pharmaceutical research and development.
Current opinion in biotechnology | 2000-12-01 | PMID 11102797
Cockett M, Dracopoli N, Sigal E
K-ras oncogene subtype mutations are associated with survival but not expression of p53, p16(INK4A), p21(WAF-1), cyclin D1, erbB-2 and erbB-3 in resected pancreatic ductal adenocarcinoma.
International journal of cancer | 2000-11-20 | PMID 11102889
Kawesha A, Ghaneh P, Andrén-Sandberg A and 7 more
Phenotypic overlap of McKusick-Kaufman syndrome with bardet-biedl syndrome: a literature review.
American journal of medical genetics | 2000-11-27 | PMID 11102925
Slavotinek A M, Biesecker L G
Folate pathway gene alterations in patients with neural tube defects.
American journal of medical genetics | 2000-11-27 | PMID 11102926
De Marco P, Moroni A, Merello E and 6 more
Genes: GPI, MTHFR
Plasma levels of amyloid beta 40 and 42 are independent from ApoE genotype and mental retardation in Down syndrome.
American journal of medical genetics | 2000-11-27 | PMID 11102927
Cavani S, Tamaoka A, Moretti A and 12 more
Genes: APP
Phenotypic features in a boy with monosomy 18 mosaicism.
American journal of medical genetics | 2000-11-27 | PMID 11102928
Jackson K E, Tsien F, Marble M
Clinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndrome.
American journal of medical genetics | 2000-11-27 | PMID 11102929
Faivre L, Prieur A M, Le Merrer M and 8 more
Unbalanced 4;6 translocation and progressive renal disease.
American journal of medical genetics | 2000-11-27 | PMID 11102935
Pierpont M E, Hentges A S, Gears L J and 2 more
Mutations in the LMNA gene encoding lamin A/C.
Human mutation | 2000-12-01 | PMID 11102973
Genschel J, Schmidt H H
Genes: LMNA
SALL1 mutations in Townes-Brocks syndrome and related disorders.
Human mutation | 2000-12-01 | PMID 11102974
Kohlhase J
Genes: SALL1
Identification of two functionally deficient plasma alpha 3-fucosyltransferase (FUT6) alleles.
Human mutation | 2000-12-01 | PMID 11102976
Elmgren A, Börjeson C, Mollicone R and 3 more
Genes: FUT6
High frequency of recurrent mutations in BRCA1 and BRCA2 genes in Polish families with breast and ovarian cancer.
Human mutation | 2000-12-01 | PMID 11102977
Grzybowska E, Zientek H, Jasinska A and 11 more
Genes: BRCA1, BRCA2
Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
Human mutation | 2000-12-01 | PMID 11102979
Prasad S, Cucci R A, Green G E and 1 more
Genes: GJB2
Genetic variation in ICF syndrome: evidence for genetic heterogeneity.
Human mutation | 2000-12-01 | PMID 11102980
Wijmenga C, Hansen R S, Gimelli G and 11 more
Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content.
Human mutation | 2000-12-01 | PMID 11102981
Escary J L, Cécillon M, Maciazek J and 3 more
Novel thymidylate synthase enhancer region alleles in African populations.
Human mutation | 2000-12-01 | PMID 11102983
Marsh S, Ameyaw M M, Githang'a J and 3 more
BTK mutations in patients with X-linked agammaglobulinemia: lack of correlation between presence of peripheral B lymphocytes and specific mutations.
Human mutation | 2000-12-01 | PMID 11102984
Tao L, Boyd M, Gonye G and 2 more
Genes: BTK
Frameshift mutations with severe and moderate clinical phenotypes in Thai hemophilia A patients.
Human mutation | 2000-12-01 | PMID 11102988
Akkarapatumwong V, Intorasoot S, Oranwiroon S and 6 more
[A comprehensive form for the standardized characterization of transgenic rodents: genotype, phenotype, welfare assessment, recommendations for refinement].
ALTEX | 2000-01-01 | PMID 11103109
Mertens C, Rülicke T
[The heartache of muscular dystrophy].
Nederlands tijdschrift voor geneeskunde | 2000-11-11 | PMID 11103252
Hoogerwaard E M, Ginjaar H B, Wilde A A and 3 more
[From gene to disease; from p16 to melanoma].
Nederlands tijdschrift voor geneeskunde | 2000-10-28 | PMID 11103670
Gruis N A, Bergman W
[Cerebrospinal fluid protein tau levels in the differential diagnosis of Alzheimer's disease].
Fortschritte der Neurologie-Psychiatrie | 2000-10-01 | PMID 11103680
Schonknecht P, Pantel J, Werle E and 5 more
Variability in centred house-of-cards mutation models.
IMA journal of mathematics applied in medicine and biology | 2000-09-01 | PMID 11103717
Mahdi S, Lessard S
Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomas.
Cancer research | 2000-11-15 | PMID 11103773
Huang S C, Koch C A, Vortmeyer A O and 8 more
Genes: RET
Frequent association of beta-catenin and WT1 mutations in Wilms tumors.
Cancer research | 2000-11-15 | PMID 11103785
Maiti S, Alam R, Amos C I and 1 more
Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome.
Cancer research | 2000-11-15 | PMID 11103790
Miyaki M, Iijima T, Hosono K and 11 more
Genes: APC
Functional analysis of human ornithine decarboxylase alleles.
Cancer research | 2000-11-15 | PMID 11103791
Guo Y, Harris R B, Rosson D and 2 more
Genes: MYC
The RB1 gene is the target of chromosome 13 deletions in malignant fibrous histiocytoma.
Cancer research | 2000-11-15 | PMID 11103795
Chibon F, Mairal A, Fréneaux P and 4 more
Selective replication and oncolysis in p53 mutant tumors with ONYX-015, an E1B-55kD gene-deleted adenovirus, in patients with advanced head and neck cancer: a phase II trial.
Cancer research | 2000-11-15 | PMID 11103798
Nemunaitis J, Ganly I, Khuri F and 10 more
Glutathione peroxidase codon 198 polymorphism variant increases lung cancer risk.
Cancer research | 2000-11-15 | PMID 11103801
Ratnasinghe D, Tangrea J A, Andersen M R and 4 more
Prognostic value of genetically diagnosed lymph node micrometastasis in non-small cell lung carcinoma cases.
Cancer research | 2000-11-15 | PMID 11103815
Hashimoto T, Kobayashi Y, Ishikawa Y and 9 more
A cancer modifier role for parathyroid hormone-related protein.
Oncogene | 2000-11-09 | PMID 11103933
Manenti G, Peissel B, Gariboldi M and 8 more
Loss of heterozygosity, allele silencing and decreased expression of p73 gene in breast cancers: prevalence of alterations in inflammatory breast cancers.
Oncogene | 2000-11-09 | PMID 11103943
Ahomadegbe J C, Tourpin S, Kaghad M and 9 more
Pattern formation in the cerebellar cortex.
Biochemistry and cell biology = Biochimie et biologie cellulaire | 2000-01-01 | PMID 11103945
Armstrong C L, Hawkes R
Genetic and biochemical diversity in the Pax gene family.
Biochemistry and cell biology = Biochimie et biologie cellulaire | 2000-01-01 | PMID 11103953
Underhill D A
E-cadherin mutation-based genetic counseling and hereditary diffuse gastric carcinoma.
Cancer genetics and cytogenetics | 2000-10-01 | PMID 11104024
Lynch H T, Grady W, Lynch J F and 3 more
HSNF5/INI1 gene mutations in lymphoid malignancy.
Cancer genetics and cytogenetics | 2000-10-01 | PMID 11104031
Yuge M, Nagai H, Uchida T and 5 more
Microdissection, DOP-PCR, and comparative genomic hybridization of paraffin-embedded familial prostate cancers.
Cancer genetics and cytogenetics | 2000-10-01 | PMID 11104032
Verhagen P C, Zhu X L, Rohr L R and 4 more
Differences in the susceptibility of some penaeid prawn species to gill-associated virus (GAV) infection.
Diseases of aquatic organisms | 2000-09-28 | PMID 11104074
Spann K M, Donaldson R A, Cowley J A and 1 more
No sex and age influence on the expression pattern and activities of human gastric alcohol and aldehyde dehydrogenases.
Alcoholism, clinical and experimental research | 2000-11-01 | PMID 11104109
Lai C L, Chao Y C, Chen Y C and 4 more
Contemporary diagnostic approach in Alport's syndrome.
Renal failure | 2000-11-01 | PMID 11104163
Grünfeld J P
Allelic association between the DRD2 TaqI A polymorphism and Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society | 2000-11-01 | PMID 11104188
Grevle L, Güzey C, Hadidi H and 3 more
Genes: DRD2
Linkage exclusion in French families with probable Parkinson' s disease.
Movement disorders : official journal of the Movement Disorder Society | 2000-11-01 | PMID 11104189
Farrer M, Destée T, Becquet E and 8 more
The DYT1 GAG deletion is infrequent in sporadic and familial writer' s cramp.
Movement disorders : official journal of the Movement Disorder Society | 2000-11-01 | PMID 11104212
Kamm C, Naumann M, Mueller J and 4 more
Genetic variation of susceptibility to Mycobacterium avium subsp. paratuberculosis infection in dairy cattle.
Journal of dairy science | 2000-11-01 | PMID 11104291
Koets A P, Adugna G, Janss L L and 5 more
Familial aggregation of ADHD characteristics.
Journal of abnormal child psychology | 2000-12-01 | PMID 11104319
Epstein J N, Conners C K, Erhardt D and 7 more
Demystifying two common genetic predispositions to venous thrombosis.
Cleveland Clinic journal of medicine | 2000-11-01 | PMID 11104333
Deitcher S R, Caiola E, Jaffer A
Monozygotic boys with fragile X syndrome.
Developmental medicine and child neurology | 2000-11-01 | PMID 11104350
Sheldon L, Turk J
Is mammography indicated for women with defective BRCA genes? Implications of recent scientific advances for the diagnosis, treatment, and prevention of hereditary breast cancer.
MedGenMed : Medscape general medicine | 2000-03-09 | PMID 11104455
Friedenson B
Phylogenetic variation and polymorphism at the toll-like receptor 4 locus (TLR4).
Genome biology | 2000-01-01 | PMID 11104518
Smirnova I, Poltorak A, Chan E K and 2 more
Genes: TLR4
Population carrier frequency of hMSH2 and hMLH1 mutations.
British journal of cancer | 2000-12-01 | PMID 11104559
Dunlop M G, Farrington S M, Nicholl I and 4 more
Most microsatellite unstable sporadic colorectal carcinomas carry MBD4 mutations.
British journal of cancer | 2000-12-01 | PMID 11104560
Bader S, Walker M, Harrison D
Genes: MBD4
Screening breast cancer patients for Norwegian ATM mutations.
British journal of cancer | 2000-12-01 | PMID 11104561
Laake K, Vu P, Andersen T I and 5 more
Genes: ATM
No evidence of linkage to chromosome 1q42.2-43 in 131 prostate cancer families from the ACTANE consortium. Anglo, Canada, Texas, Australia, Norway, EU Biomed.
British journal of cancer | 2000-12-01 | PMID 11104562
Singh R
Genes: NPL
Prognostic value of genomic alterations in minimal residual cancer cells purified from the blood of breast cancer patients.
British journal of cancer | 2000-12-01 | PMID 11104564
Austrup F, Uciechowski P, Eder C and 7 more
Genes: DCC
Glycerol restores p53-dependent radiosensitivity of human head and neck cancer cells bearing mutant p53.
British journal of cancer | 2000-12-01 | PMID 11104574
Ohnishi K, Ota I, Takahashi A and 1 more
Effects of active and negative mutants of Ras on rat arterial neointima formation.
The Journal of surgical research | 2000-12-01 | PMID 11104652
Jin G, Chieh-Hsi Wu J, Li Y S and 3 more
Worldwide genetic analysis of the CFTR region.
American journal of human genetics | 2001-01-01 | PMID 11104661
Mateu E, Calafell F, Lao O and 5 more
Genes: CFTR
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.
American journal of human genetics | 2001-01-01 | PMID 11104662
Phillips H A, Favre I, Kirkpatrick M and 8 more
Genes: CHRNB2
The C-terminus of NIPP1 (nuclear inhibitor of protein phosphatase-1) contains a novel binding site for protein phosphatase-1 that is controlled by tyrosine phosphorylation and RNA binding.
The Biochemical journal | 2000-12-15 | PMID 11104670
Beullens M, Vulsteke V, Van Eynde A and 3 more
Kinetic alteration of a human dihydrodiol/3alpha-hydroxysteroid dehydrogenase isoenzyme, AKR1C4, by replacement of histidine-216 with tyrosine or phenylalanine.
The Biochemical journal | 2000-12-15 | PMID 11104674
Ohta T, Ishikura S, Shintani S and 2 more
Conversion of Escherichia coli pyruvate oxidase to an 'alpha-ketobutyrate oxidase'.
The Biochemical journal | 2000-12-15 | PMID 11104678
Chang Y Y, Cronan J E
Inverse regulation of F1-ATPase activity by a mutation at the regulatory region on the gamma subunit of chloroplast ATP synthase.
The Biochemical journal | 2000-12-15 | PMID 11104686
Konno H, Yodogawa M, Stumpp M T and 5 more
Dynamic palmitoylation of lymphoma proprotein convertase prolongs its half-life, but is not essential for trans-Golgi network localization.
The Biochemical journal | 2000-12-15 | PMID 11104692
van de Loo J W, Teuchert M, Pauli I and 3 more
A carbon-source-responsive element is required for regulation of the hypoxic ADP/ATP carrier (AAC3) isoform in Saccharomyces cerevisiae.
The Biochemical journal | 2000-12-15 | PMID 11104700
Sokolíková B, Sabová L, Kissová I and 1 more
Cross-talk between interleukin 1beta (IL-1beta) and IL-6 signalling pathways: IL-1beta selectively inhibits IL-6-activated signal transducer and activator of transcription factor 1 (STAT1) by a proteasome-dependent mechanism.
The Biochemical journal | 2000-12-15 | PMID 11104703
Shen X, Tian Z, Holtzman M J and 1 more
Genes: STAT1, STAT3, JAK1, JAK2
Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes.
Circulation | 2000-12-05 | PMID 11104743
Zhang L, Timothy K W, Vincent G M and 18 more
Substitution of a glycogen synthase kinase-3beta phosphorylation site in presenilin 1 separates presenilin function from beta-catenin signaling.
The Journal of biological chemistry | 2001-03-09 | PMID 11104755
Kirschenbaum F, Hsu S C, Cordell B and 1 more
Predicted Michaelis-Menten complexes of cocaine-butyrylcholinesterase. Engineering effective butyrylcholinesterase mutants for cocaine detoxication.
The Journal of biological chemistry | 2001-03-23 | PMID 11104759
Sun H, El Yazal J, Lockridge O and 3 more
Pseudo-T-even bacteriophage RB49 encodes CocO, a cochaperonin for GroEL, which can substitute for Escherichia coli's GroES and bacteriophage T4's Gp31.
The Journal of biological chemistry | 2001-03-23 | PMID 11104767
Ang D, Richardson A, Mayer M P and 3 more