Erp1p and Erp2p, partners for Emp24p and Erv25p in a yeast p24 complex.
Molecular biology of the cell | 1999-06-01 | PMID 10359606
Marzioch M, Henthorn D C, Herrmann J M and 5 more
Genes: SEC13
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 1154 of 10600
The PDZ domain of the LIM protein enigma binds to beta-tropomyosin.
Molecular biology of the cell | 1999-06-01 | PMID 10359609
Guy P M, Kenny D A, Gill G N
Basolateral localization of the Caenorhabditis elegans epidermal growth factor receptor in epithelial cells by the PDZ protein LIN-10.
Molecular biology of the cell | 1999-06-01 | PMID 10359617
Whitfield C W, Bénard C, Barnes T and 2 more
Genes: EGF
H,K-ATPase alpha subunit C-terminal membrane topology: epitope tags in the insect cell expression system.
The Biochemical journal | 1999-06-15 | PMID 10359643
Smolka A J, Larsen K A, Schweinfest C W and 1 more
How aneuploidy affects metabolic control and causes cancer.
The Biochemical journal | 1999-06-15 | PMID 10359645
Rasnick D, Duesberg P H
Transcription factor GCN4 for control of amino acid biosynthesis also regulates the expression of the gene for lipoamide dehydrogenase.
The Biochemical journal | 1999-06-15 | PMID 10359673
Zaman Z, Bowman S B, Kornfeld G D and 2 more
T-786-->C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm.
Circulation | 1999-06-08 | PMID 10359729
Nakayama M, Yasue H, Yoshimura M and 8 more
Lipoprotein lipase mutations, plasma lipids and lipoproteins, and risk of ischemic heart disease. A meta-analysis.
Circulation | 1999-06-08 | PMID 10359734
Wittrup H H, Tybjaerg-Hansen A, Nordestgaard B G
Signaling via beta1 integrins and mitogen-activated protein kinase determines human epidermal stem cell fate in vitro.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359780
Zhu A J, Haase I, Watt F M
A dominant-negative pleiotrophin mutant introduced by homologous recombination leads to germ-cell apoptosis in male mice.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359781
Zhang N, Yeh H J, Zhong R and 2 more
Genes: PTN
The Rpd3 histone deacetylase is required for segmentation of the Drosophila embryo.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359792
Mannervik M, Levine M
An experimental solution for the Luria-Delbrück fluctuation problem in measuring hypermutation rates.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359801
Bachl J, Dessing M, Olsson C and 2 more
Different mutator phenotypes in Mlh1- versus Pms2-deficient mice.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359802
Yao X, Buermeyer A B, Narayanan L and 6 more
The role of transient hypermutators in adaptive mutation in Escherichia coli.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359804
Rosche W A, Foster P L
Paternal monoallelic expression of the paired immunoglobulin-like receptors PIR-A and PIR-B.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359805
Chen C C, Hurez V, Brockenbrough J S and 2 more
Genes: PIR
p53 gene mutations are not required for early dissemination of cancer cells.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359818
Offner S, Schmaus W, Witter K and 5 more
Proteolytic release and nuclear translocation of Notch-1 are induced by presenilin-1 and impaired by pathogenic presenilin-1 mutations.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359821
Song W, Nadeau P, Yuan M and 3 more
A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359825
Imbach T, Burda P, Kuhnert P and 4 more
Genes: ALG6, ALG5
Guanosine triphosphatase stimulation of oncogenic Ras mutants.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359839
Ahmadian M R, Zor T, Vogt D and 4 more
Identification of the gregarization-associated dark-pigmentotropin in locusts through an albino mutant.
Proceedings of the National Academy of Sciences of the United States of America | 1999-06-08 | PMID 10359842
Tawfik A I, Tanaka S, De Loof A and 7 more
[The relation between mitochondrial DNA mutation and aminogly- coside antibiotics-induced deafness].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359860
Zhang L, Lu M, Huang Y and 3 more
[Screening for mitochondrial 1555(G) mutation in patients with aminoglycoside antibiotic-induced deafness].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359861
Yuan H, Jiang S, Yang W and 3 more
[Molecular characterization of glucose-6-phosphate dehydrogenase variants in four ethnic groups in Yunnan province of China].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359863
Jiang W, Du C, Duan S and 5 more
[Computerized ribosomal RNA secondary structure modeling of mutants found in Rett syndrome patients and their mothers].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359864
Qi Y, Wu X, Tang J and 1 more
[Mutation in the promoter region of 21-hydroxylase gene of patients with congenital adrenal hyperplasia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359865
Zhao Y, Ye J, Yang X and 1 more
[Distribution of six STR loci in Bai ethnic group in Yunnan province of China].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359866
Zou P, Yang Y, Li D and 2 more
[Genetic polymorphism at FES locus in Chinese and German populations].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359868
Wu J, Hou Y, Li Y and 2 more
Genes: FES
[The mutation of deletion for glutathione S-transferase M1 gene in the tissue of hepatocellular carcinoma].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 1999-06-01 | PMID 10359869
Bian J, Shen F, Wang J and 3 more
Genes: GSTM1
Monocyte chemotactic proteins in allergen-induced inflammation in the nasal mucosa: effect of topical corticosteroids.
The Journal of allergy and clinical immunology | 1999-06-01 | PMID 10359883
Christodoulopoulos P, Wright E, Frenkiel S and 2 more
Causal relationship between stressful life events and the onset of major depression.
The American journal of psychiatry | 1999-06-01 | PMID 10360120
Kendler K S, Karkowski L M, Prescott C A
Reversible activation of c-Myc in skin: induction of a complex neoplastic phenotype by a single oncogenic lesion.
Molecular cell | 1999-05-01 | PMID 10360173
Pelengaris S, Littlewood T, Khan M and 2 more
DNA polymerase epsilon catalytic domains are dispensable for DNA replication, DNA repair, and cell viability.
Molecular cell | 1999-05-01 | PMID 10360184
Kesti T, Flick K, Keränen S and 2 more
Genomic analysis of the thymine-DNA glycosylase (TDG) gene on 12q22-q24.1 in human pancreatic ductal adenocarcinoma.
International journal of pancreatology : official journal of the International Association of Pancreatology | 1999-04-01 | PMID 10360221
Yatsuoka T, Furukawa T, Abe T and 5 more
Genes: TDG
The beta enolase subunit displays three different patterns of microheterogeneity in human striated muscle.
Journal of muscle research and cell motility | 1999-01-01 | PMID 10360234
Merkulova T, Thornell L E, Butler-Browne G and 5 more
North Carolina macular dystrophy: clinical features, genealogy, and genetic linkage analysis.
Transactions of the American Ophthalmological Society | 1998-01-01 | PMID 10360311
Small K W
Stability of hairpin ribozyme tertiary structure is governed by the interdomain junction.
Nature structural biology | 1999-06-01 | PMID 10360357
Walter N G, Burke J M, Millar D P
Acceleration of the refolding of Arc repressor by nucleic acids and other polyanions.
Nature structural biology | 1999-06-01 | PMID 10360363
Rentzeperis D, Jonsson T, Sauer R T
Deletions and losses in chromosomes 5 or 7 in adult acute lymphocytic leukemia: incidence, associations and implications.
Leukemia | 1999-06-01 | PMID 10360374
Dabaja B S, Faderl S, Thomas D and 8 more
Megakaryocytic differentiation of human progenitor cells is negatively influenced by direct contact with stroma.
Leukemia | 1999-06-01 | PMID 10360383
Zweegman S, Veenhof M A, Debili N and 3 more
Genes: TPO
Achondroplasia-hypochondroplasia complex in a newborn infant.
American journal of medical genetics | 1999-06-11 | PMID 10360392
Huggins M J, Smith J R, Chun K and 3 more
Genes: FGFR3
Compound heterozygosity for the Achondroplasia-hypochondroplasia FGFR3 mutations: prenatal diagnosis and postnatal outcome.
American journal of medical genetics | 1999-06-11 | PMID 10360393
Chitayat D, Fernandez B, Gardner A and 7 more
Genes: FGFR3
Fabry disease: comparison of enzymatic, linkage, and mutation analysis for carrier detection in a family with a novel mutation (30delG).
American journal of medical genetics | 1999-06-11 | PMID 10360396
Ashton-Prolla P, Ashley G A, Giugliani R and 3 more
An efficient, robust and unified method for mapping complex traits (III): combined linkage/linkage-disequilibrium analysis.
American journal of medical genetics | 1999-06-11 | PMID 10360398
Zhao L P, Quiaoit F, Aragaki C and 1 more
RhD status of a fetus at risk for haemolytic disease with a discrepant maternal DNA-based RhD genotype.
Prenatal diagnosis | 1999-05-01 | PMID 10360510
Denomme G A, Akoury H, Sermer M and 1 more
Genes: RHD
Signals from the reproductive system regulate the lifespan of C. elegans.
Nature | 1999-05-27 | PMID 10360574
Hsin H, Kenyon C
Genetic and nongenetic factors influencing plasma homocysteine levels in patients with ischemic cerebrovascular disease and in healthy control subjects.
The Journal of laboratory and clinical medicine | 1999-06-01 | PMID 10360632
Lalouschek W, Aull S, Serles W and 5 more
Genes: MTHFR
Biosynthesis of HLA-C heavy chains in melanoma cells with multiple defects in the expression of HLA-A, -B, -C molecules.
British journal of cancer | 1999-05-01 | PMID 10360639
Martayan A, Fraioli R, Giorda E and 5 more
Rodent fibroblast model for studies of response of malignant cells to exogenous 5-aminolevulinic acid.
British journal of cancer | 1999-05-01 | PMID 10360643
Li G, Szewczuk M R, Raptis L and 4 more
Prognostic significance of loss of heterozygosity at loci on chromosome 17p13.3-ter in sporadic breast cancer is evidence for a putative tumour suppressor gene.
British journal of cancer | 1999-05-01 | PMID 10360661
Liscia D S, Morizio R, Venesio T and 3 more
Genes: ABR
Deletion mapping of chromosome 16q in hepatocellular carcinoma.
British journal of cancer | 1999-05-01 | PMID 10360665
Piao Z, Park C, Kim J J and 1 more
Somatic mutation of PTEN in bladder carcinoma.
British journal of cancer | 1999-05-01 | PMID 10360673
Aveyard J S, Skilleter A, Habuchi T and 1 more
Genes: PTEN
Clonality analysis suggests that early-onset acute lymphoblastic leukaemia is of single-cell origin and implies no major role for germ cell mutations in parents.
British journal of cancer | 1999-05-01 | PMID 10360674
Rinaldi F, Mairs R J, Wheldon T E and 3 more
Genes: MAOA
Implications of presenilin 1 mutations in Alzheimer's disease.
Mechanisms of ageing and development | 1999-03-15 | PMID 10360683
Komano H, Sudoh S, Kawamura Y and 2 more
From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.
Annals of neurology | 1999-06-01 | PMID 10360762
Nasreddine Z S, Loginov M, Clark L N and 7 more
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotype.
Annals of neurology | 1999-06-01 | PMID 10360767
Ricci E, Galluzzi G, Deidda G and 12 more
Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I.
Annals of neurology | 1999-06-01 | PMID 10360771
Triepels R H, van den Heuvel L P, Loeffen J L and 9 more
Genes: NDUFS7
Ataxia with isolated vitamin E deficiency: a Japanese family carrying a novel mutation in the alpha-tocopherol transfer protein gene.
Annals of neurology | 1999-06-01 | PMID 10360777
Hoshino M, Masuda N, Ito Y and 4 more
Genes: TTPA
A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.
Annals of neurology | 1999-06-01 | PMID 10360778
Hainfellner J A, Parchi P, Kitamoto T and 3 more
Genes: PRNP
Exercise intolerance due to a nonsense mutation in the mtDNA ND4 gene.
Annals of neurology | 1999-06-01 | PMID 10360780
Andreu A L, Tanji K, Bruno C and 7 more
Angiotensin II-induced modulation of rat mesangial cell phenotype.
Radiation research | 1999-06-01 | PMID 10360793
Zhang X, O'Malley Y, Robbins M E
Heterosexual transmission of HIV-1 is associated with high plasma viral load levels and a positive viral isolation in the infected partner.
Journal of acquired immune deficiency syndromes (1999) | 1999-06-01 | PMID 10360803
Pedraza M A, del Romero J, Roldán F and 4 more
Genes: CCR5
Structural alterations of transforming growth factor-beta receptor genes in human cervical carcinoma.
International journal of cancer | 1999-07-02 | PMID 10360819
Chen T, de Vries E G, Hollema H and 5 more
Halothane presynaptically depresses synaptic transmission in wild-type Drosophila larvae but not in halothane-resistant (har) mutants.
Anesthesiology | 1999-06-01 | PMID 10360868
Nishikawa K, Kidokoro Y
Hypercoagulable state mutation analysis in white patients with early first-trimester recurrent pregnancy loss.
Fertility and sterility | 1999-06-01 | PMID 10360908
Kutteh W H, Park V M, Deitcher S R
Genes: MTHFR
Functional analysis of LAT in TCR-mediated signaling pathways using a LAT-deficient Jurkat cell line.
International immunology | 1999-06-01 | PMID 10360968
Zhang W, Irvin B J, Trible R P and 2 more
Genes: LAT
Changes in the specificity of antibodies by site-specific mutagenesis followed by random mutagenesis.
Protein engineering | 1999-05-01 | PMID 10360981
Miyazaki C, Iba Y, Yamada Y and 3 more
sodVIC is an alpha-COP-related gene which is essential for establishing and maintaining polarized growth in Aspergillus nidulans.
Fungal genetics and biology : FG & B | 1999-04-01 | PMID 10361037
Whittaker S L, Lunness P, Milward K J and 2 more
Reactivation and persistence of human herpesvirus-8 infection in B cells and monocytes by Th-1 cytokines increased in Kaposi's sarcoma.
Blood | 1999-06-15 | PMID 10361101
Monini P, Colombini S, Stürzl M and 22 more
Altered multidrug resistance phenotype caused by anthracycline analogues and cytosine arabinoside in myeloid leukemia.
Blood | 1999-06-15 | PMID 10361105
Hu X F, Slater A, Kantharidis P and 6 more
Different effect of various mutant MITF encoded by mi, Mior, or Miwh allele on phenotype of murine mast cells.
Blood | 1999-06-15 | PMID 10361115
Kim D K, Morii E, Ogihara H and 6 more
Genes: MITF
Familial overexpression of beta antithrombin caused by an Asn135Thr substitution.
Blood | 1999-06-15 | PMID 10361121
Bayston T A, Tripodi A, Mannucci P M and 6 more
Variation at the von Willebrand factor (vWF) gene locus is associated with plasma vWF:Ag levels: identification of three novel single nucleotide polymorphisms in the vWF gene promoter.
Blood | 1999-06-15 | PMID 10361125
Keightley A M, Lam Y M, Brady J N and 2 more
Factor XII Tenri, a novel cross-reacting material negative factor XII deficiency, occurs through a proteasome-mediated degradation.
Blood | 1999-06-15 | PMID 10361128
Kondo S, Tokunaga F, Kawano S and 3 more
The expression of human blood group antigens during erythropoiesis in a cell culture system.
Blood | 1999-06-15 | PMID 10361141
Southcott M J, Tanner M J, Anstee D J
Characterization of phenotype and cytokine profiles of T cell lines derived from vitreous humour in ocular inflammation in man.
Clinical and experimental immunology | 1999-06-01 | PMID 10361227
Muhaya M, Calder V L, Towler H M and 3 more
Human B cells accumulate immunoglobulin V gene somatic mutations in a cell contact-dependent manner in cultures supported by activated T cells but not in cultures supported by CD40 ligand.
Clinical and experimental immunology | 1999-06-01 | PMID 10361232
Huang S C, Glas A M, Pinchuk G V and 4 more
Immunological changes in peripheral blood and in lymphoid tissue after treatment of HIV-infected subjects with highly active anti-retroviral therapy (HAART) or HAART + IL-2.
Clinical and experimental immunology | 1999-06-01 | PMID 10361239
Zanussi S, Simonelli C, Bortolin M T and 8 more
HLA class II homozygosity confers susceptibility to common variable immunodeficiency (CVID).
Clinical and experimental immunology | 1999-06-01 | PMID 10361244
De La Concha E G, Fernandez-Arquero M, Martinez A and 5 more
Rapid conversion of naive to effector T cell function counteracts diminished primary human newborn T cell responses.
Clinical and experimental immunology | 1999-06-01 | PMID 10361246
Early E, Reen D J
Bacterial secreted proteins are required for the internaliztion of Campylobacter jejuni into cultured mammalian cells.
Molecular microbiology | 1999-05-01 | PMID 10361274
Konkel M E, Kim B J, Rivera-Amill V and 1 more
Characterization of the dual start motif of a class II holin gene.
Molecular microbiology | 1999-05-01 | PMID 10361276
Barenboim M, Chang C Y, dib Hajj F and 1 more
Heat-induced cell cycle arrest of Saccharomyces cerevisiae: involvement of the RAD6/UBC2 and WSC2 genes in its reversal.
Molecular microbiology | 1999-05-01 | PMID 10361277
Raboy B, Marom A, Dor Y and 1 more
The product of the SNF2/SWI2 paralogue INO80 of Saccharomyces cerevisiae required for efficient expression of various yeast structural genes is part of a high-molecular-weight protein complex.
Molecular microbiology | 1999-05-01 | PMID 10361278
Ebbert R, Birkmann A, Schüller H J
Genes: INO80, CYC1
Poly(A) polymerase I of Escherichia coli: characterization of the catalytic domain, an RNA binding site and regions for the interaction with proteins involved in mRNA degradation.
Molecular microbiology | 1999-05-01 | PMID 10361280
Raynal L C, Carpousis A J
The role of the trehalose system in regulating the maltose regulon of Escherichia coli.
Molecular microbiology | 1999-05-01 | PMID 10361281
Decker K, Gerhardt F, Boos W
Genes: PTS
Mutational analysis of ComS: evidence for the interaction of ComS and MecA in the regulation of competence development in Bacillus subtilis.
Molecular microbiology | 1999-05-01 | PMID 10361283
Ogura M, Liu L, Lacelle M and 2 more
P-type ATPase spf1 mutants show a novel resistance mechanism for the killer toxin SMKT.
Molecular microbiology | 1999-05-01 | PMID 10361284
Suzuki C, Shimma Y I
ZapA, the IgA-degrading metalloprotease of Proteus mirabilis, is a virulence factor expressed specifically in swarmer cells.
Molecular microbiology | 1999-05-01 | PMID 10361285
Walker K E, Moghaddame-Jafari S, Lockatell C V and 2 more
Bacterial genes induced within the nodule during the Rhizobium-legume symbiosis.
Molecular microbiology | 1999-05-01 | PMID 10361286
Oke V, Long S R
In vivo and in vitro studies of major surface loop deletion mutants of the Escherichia coli K-12 maltoporin: contribution to maltose and maltooligosaccharide transport and binding.
Molecular microbiology | 1999-05-01 | PMID 10361287
Andersen C, Bachmeyer C, Täuber H and 6 more
The V-antigen of Yersinia is surface exposed before target cell contact and involved in virulence protein translocation.
Molecular microbiology | 1999-06-01 | PMID 10361299
Pettersson J, Holmström A, Hill J and 7 more
A Saccharomyces cerevisiae G-protein coupled receptor, Gpr1, is specifically required for glucose activation of the cAMP pathway during the transition to growth on glucose.
Molecular microbiology | 1999-06-01 | PMID 10361302
Kraakman L, Lemaire K, Ma P and 6 more
Evidence for a system of general protein glycosylation in Campylobacter jejuni.
Molecular microbiology | 1999-06-01 | PMID 10361304
Szymanski C M, Yao R, Ewing C P and 2 more
C-terminal interactions between the XerC and XerD site-specific recombinases.
Molecular microbiology | 1999-06-01 | PMID 10361305
Spiers A J, Sherratt D J
Aberrations in the primary T-cell receptor repertoire as a predisposition for synovial inflammation in rheumatoid arthritis.
Journal of investigative medicine : the official publication of the American Federation for Clinical Research | 1999-05-01 | PMID 10361384
Yang H, Rittner H, Weyand C M and 1 more
Construction and characterization of Escherichia coli disruptants defective in the yaeM gene.
Bioscience, biotechnology, and biochemistry | 1999-04-01 | PMID 10361694
Kuzuyama T, Takahashi S, Seto H
Several highly divergent histone H3 genes are present in the hypotrichous ciliate Stylonychia lemnae.
FEMS microbiology letters | 1999-06-01 | PMID 10361708
Bernhard D
A large subset of neutrophils expressing membrane proteinase 3 is a risk factor for vasculitis and rheumatoid arthritis.
Journal of the American Society of Nephrology : JASN | 1999-06-01 | PMID 10361860
Witko-Sarsat V, Lesavre P, Lopez S and 10 more
Association of human leukocyte antigen class II genes with autoantibody profiles, but not with disease susceptibility in Japanese patients with systemic sclerosis.
Internal medicine (Tokyo, Japan) | 1999-04-01 | PMID 10361906
Kuwana M, Inoko H, Kameda H and 9 more
Autosomal dominant cataracts and Peters anomaly in a large Australian family.
Clinical genetics | 1999-04-01 | PMID 10361984
Withers S J, Gole G A, Summers K M
Genes: PAX6