Schirrous invasive ductal carcinoma of the breast overexpress p53 oncoprotein.
Sao Paulo medical journal = Revista paulista de medicina | 2001-01-04 | PMID 11175617
Ferrini F S, Rossi M A, Neto M M and 1 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 1480 of 10600
Analysis of 2 antiapoptotic factors in gliomas: bcl-2 overexpression and p53 mutations.
Archives of pathology & laboratory medicine | 2001-02-01 | PMID 11175638
Rodriguez-Pereira C, Suarez-Peñaranda J M, Barros F and 3 more
Repeated exposure of C3H/HeJ mice to ultra-wideband electromagnetic pulses: lack of effects on mammary tumors.
Radiation research | 2001-02-01 | PMID 11175673
Jauchem J R, Ryan K L, Frei M R and 3 more
Imaging FRET between spectrally similar GFP molecules in single cells.
Nature biotechnology | 2001-02-01 | PMID 11175733
Harpur A G, Wouters F S, Bastiaens P I
Cofilin/ADF is required for cell motility during Drosophila ovary development and oogenesis.
Nature cell biology | 2001-02-01 | PMID 11175754
Chen J, Godt D, Gunsalus K and 3 more
Interleukin 12 and autoimmune diabetes.
Nature genetics | 2001-02-01 | PMID 11175771
Adorini L
Prostate cancer: simplicity to complexity.
Nature genetics | 2001-02-01 | PMID 11175773
Peters M E, Ostrander E A
Genes: ELAC2
Modifying with mitochondria.
Nature genetics | 2001-02-01 | PMID 11175774
Avraham K B
DSPP mutation in dentinogenesis imperfecta Shields type II.
Nature genetics | 2001-02-01 | PMID 11175779
Zhang X, Zhao J, Li C and 7 more
Genes: DSPP
Great ape DNA sequences reveal a reduced diversity and an expansion in humans.
Nature genetics | 2001-02-01 | PMID 11175781
Kaessmann H, Wiebe V, Weiss G and 1 more
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome.
Nature genetics | 2001-02-01 | PMID 11175783
Crisponi L, Deiana M, Loi A and 19 more
Genes: FOXL2
A candidate prostate cancer susceptibility gene at chromosome 17p.
Nature genetics | 2001-02-01 | PMID 11175785
Tavtigian S V, Simard J, Teng D H and 40 more
Genes: ELAC2
Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.
Nature genetics | 2001-02-01 | PMID 11175790
Xiao S, Yu C, Chou X and 15 more
Genes: DSPP
Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects.
Nature genetics | 2001-02-01 | PMID 11175793
Joosten P H, Toepoel M, Mariman E C and 1 more
Genes: PDGFRA
Linkage disequilibrium of a type 1 diabetes susceptibility locus with a regulatory IL12B allele.
Nature genetics | 2001-02-01 | PMID 11175794
Morahan G, Huang D, Ymer S I and 7 more
Inhibition of lymphangiogenesis with resulting lymphedema in transgenic mice expressing soluble VEGF receptor-3.
Nature medicine | 2001-02-01 | PMID 11175851
Mäkinen T, Jussila L, Veikkola T and 9 more
Deficiency or inhibition of Gas6 causes platelet dysfunction and protects mice against thrombosis.
Nature medicine | 2001-02-01 | PMID 11175853
Angelillo-Scherrer A, de Frutos P, Aparicio C and 10 more
The 2.0 A structure of human ferrochelatase, the terminal enzyme of heme biosynthesis.
Nature structural biology | 2001-02-01 | PMID 11175906
Wu C K, Dailey H A, Rose J P and 3 more
Crystal structure of the retaining galactosyltransferase LgtC from Neisseria meningitidis in complex with donor and acceptor sugar analogs.
Nature structural biology | 2001-02-01 | PMID 11175908
Persson K, Ly H D, Dieckelmann M and 3 more
The structure of Sky1p reveals a novel mechanism for constitutive activity.
Nature structural biology | 2001-02-01 | PMID 11175909
Nolen B, Yun C Y, Wong C F and 3 more
Hyperplastic polyposis: association with colorectal cancer.
The American journal of surgical pathology | 2001-02-01 | PMID 11176066
Leggett B A, Devereaux B, Biden K and 3 more
Synthetic and modified glycerides: effects on plasma lipids.
Current opinion in lipidology | 2001-02-01 | PMID 11176204
Hayes K C
Silent stroke: pathogenesis, genetic factors and clinical implications as a risk factor.
Current opinion in neurology | 2001-02-01 | PMID 11176221
Masuda J, Nabika T, Notsu Y
Current status of prophylactic surgery for hereditary breast and gynecologic cancers.
Current opinion in obstetrics & gynecology | 2001-02-01 | PMID 11176229
Lynch H T, Casey M J
Diamond-Blackfan anemia.
Current opinion in pediatrics | 2001-02-01 | PMID 11176237
Da Costa L, Willig T N, Fixler J and 2 more
Genes: RPS19
Sickle cell disease: no longer a single gene disorder.
Current opinion in pediatrics | 2001-02-01 | PMID 11176239
Chui D H, Dover G J
Influence of preassay and sequence variations on viral load determination by a multiplex real-time reverse transcriptase-polymerase chain reaction for feline immunodeficiency virus.
Journal of acquired immune deficiency syndromes (1999) | 2001-01-01 | PMID 11176264
Klein D, Leutenegger C M, Bahula C and 5 more
Patterns of resistance mutations to antiretroviral drugs in extensively treated HIV-1-infected patients with failure of highly active antiretroviral therapy.
Journal of acquired immune deficiency syndromes (1999) | 2001-01-01 | PMID 11176267
Rousseau M N, Vergne L, Montes B and 4 more
Pilot study of a combination of highly active antiretroviral therapy and cytokines to induce HIV-1 remission.
Journal of acquired immune deficiency syndromes (1999) | 2001-01-01 | PMID 11176268
Lafeuillade A, Poggi C, Chadapaud S and 4 more
Interferon-alpha treatment of chronic hepatitis C in children with hemophilia.
Journal of pediatric gastroenterology and nutrition | 2001-01-01 | PMID 11176323
Ko J S, Choe Y H, Kim E J and 3 more
Tumor necrosis factor-alpha gene mutations and genotype changes in renal cell carcinoma.
The Journal of urology | 2001-02-01 | PMID 11176446
Nakajima K, Sasaki M, Nojima D and 4 more
Genes: TNF
Contractile protein expression in bladder smooth muscle is a marker of phenotypic modulation after outlet obstruction in the rabbit model.
The Journal of urology | 2001-03-01 | PMID 11176523
Burkhard F C, Lemack G E, Zimmern P E and 2 more
Classification, clinical manifestations, and immunopathological mechanisms of the epithelial variant of paraneoplastic autoimmune multiorgan syndrome: a reappraisal of paraneoplastic pemphigus.
Archives of dermatology | 2001-02-01 | PMID 11176692
Nguyen V T, Ndoye A, Bassler K D and 7 more
Genes: PNP, DSG3, DSG1
Genetic testing in spinocerebellar ataxias: defining a clinical role.
Archives of neurology | 2001-02-01 | PMID 11176956
Tan E K, Ashizawa T
Genetic variation analysis in parkinson disease patients with and without hallucinations: case-control study.
Archives of neurology | 2001-02-01 | PMID 11176958
Goetz C G, Burke P F, Leurgans S and 4 more
Genes: APOE, DRD3, DRD1, DRD2, DRD4
Missense CACNA1A mutation causing episodic ataxia type 2.
Archives of neurology | 2001-02-01 | PMID 11176968
Denier C, Ducros A, Durr A and 3 more
Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family.
Archives of neurology | 2001-02-01 | PMID 11176969
Gwinn-Hardy K, Singleton A, O'Suilleabhain P and 7 more
Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene.
Archives of ophthalmology (Chicago, Ill. : 1960) | 2001-02-01 | PMID 11176989
Burstedt M S, Forsman-Semb K, Golovleva I and 3 more
Genes: RLBP1
Autosomal dominant inherited hearing impairment caused by a missense mutation in COL11A2 (DFNA13).
Archives of otolaryngology--head & neck surgery | 2001-01-01 | PMID 11177008
De Leenheer E M, Kunst H H, McGuirt W T and 5 more
A family study of Alzheimer disease and early- and late-onset depression in elderly patients.
Archives of general psychiatry | 2001-02-01 | PMID 11177121
Heun R, Papassotiropoulos A, Jessen F and 2 more
Gene-nutrient interactions: dietary behaviour associated with high coronary heart disease risk particularly affects serum LDL cholesterol in apolipoprotein E epsilon4-carrying free-living individuals.
The British journal of nutrition | 2000-12-01 | PMID 11177205
Loktionov A, Scollen S, McKeown N and 1 more
5,10-methylenetetrahydrofolate reductase common mutations, folate status and plasma homocysteine in healthy French adults of the Supplementation en Vitamines et Mineraux Antioxydants (SU.VI.MAX) cohort.
The British journal of nutrition | 2000-12-01 | PMID 11177206
Chango A, Potier De Courcy G, Boisson F and 9 more
Genes: MTHFR, MAX
Biological functions of ceruloplasmin and their deficiency caused by mutation in genes regulating copper and iron metabolism.
Bulletin of experimental biology and medicine | 2000-08-01 | PMID 11177225
Mzhel'skaya T I
Emotional state and one-trial learning in OXYS rats with hereditarily elevated production of oxygen radicals.
Bulletin of experimental biology and medicine | 2000-08-01 | PMID 11177232
Loskutova L V, Kolosova N G
Pleomorphic adenoma and myotonic dystrophy: an association?
The Journal of laryngology and otology | 2000-12-01 | PMID 11177377
Draper M R, Pickles J M
Efficacy, tolerance, and pharmacokinetics of the combination of stavudine, nevirapine, nelfinavir, and saquinavir as salvage regimen after ritonavir or indinavir failure.
AIDS research and human retroviruses | 2001-01-20 | PMID 11177388
Casado J L, Dronda F, Hertogs K and 5 more
Stable expression of human immunodeficiency virus type 1 Nef confers resistance against Fas-mediated apoptosis.
AIDS research and human retroviruses | 2001-01-20 | PMID 11177389
Yoon K, Jeong J G, Kim S
HIV type 2 Vpx interaction with Gag and incorporation into virus-like particles.
AIDS research and human retroviruses | 2001-01-20 | PMID 11177390
Jin L, Zhou Y, Ratner L
Comparison of Vif sequences from diverse geographical isolates of HIV type 1 and SIV(cpz) identifies substitutions common to subtype C isolates and extensive variation in a proposed nuclear transport inhibition signal.
AIDS research and human retroviruses | 2001-01-20 | PMID 11177396
Stephens E B, Singh D K, Pacyniak E and 1 more
Phenotypic cross-resistance to nelfinavir: the role of prior antiretroviral therapy and the number of mutations in the protease gene.
AIDS research and human retroviruses | 2001-02-10 | PMID 11177403
Dronda F, Casado J L, Moreno S and 6 more
Follow-up study of intrahost HIV type 2 variability reveals discontinuous evolution of C2V3 sequences.
AIDS research and human retroviruses | 2001-02-10 | PMID 11177408
Esteves A, Piedade J, Santos C and 3 more
An HIV type 1 subtype A strain of low genetic diversity continues to spread among injecting drug users in Russia: study of the new local outbreaks in Moscow and Irkutsk.
AIDS research and human retroviruses | 2001-02-10 | PMID 11177409
Bobkov A, Kazennova E, Khanina T and 5 more
Genetic analysis of hiv type 1 strains in bujumbura (burundi): predominance of subtype c variant.
AIDS research and human retroviruses | 2001-02-10 | PMID 11177411
Koch N, Ndihokubwayo J B, Yahi N and 3 more
Serological approaches to subtyping of HIV-1 in injecting drug users in Russia: evidence of subtype homogeneity at the main sites of the epidemic.
International journal of STD & AIDS | 2001-01-01 | PMID 11177480
Bobkova M R, Kazennova E V, Selimova L M and 6 more
Phenotypic correction of lipid storage and growth arrest in wolman disease fibroblasts by gene transfer of lysosomal acid lipase.
Human gene therapy | 2001-02-10 | PMID 11177564
Tietge U J, Sun G, Czarnecki S and 6 more
Optimization of retroviral gene transfer protocol to maintain the lymphoid potential of progenitor cells.
Human gene therapy | 2001-02-10 | PMID 11177565
Hacein-Bey S, Gross F, Nusbaum P and 4 more
The renin angiotensin system as a risk factor for coronary artery disease.
Current atherosclerosis reports | 2001-03-01 | PMID 11177655
Farmer J A, Torre-Amione G
Racial differences and the genetics of hypertension.
Current hypertension reports | 2001-02-01 | PMID 11177703
Cooper R S, Zhu X
Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice.
BMC genetics | 2001-01-01 | PMID 11178107
Anderson M G, Smith R S, Savinova O V and 7 more
The genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genes.
Arthritis research | 2001-01-01 | PMID 11178115
Jirholt J, Lindqvist A B, Holmdahl R
The sequence of human chromosome 21 and implications for research into Down syndrome.
Genome biology | 2000-01-01 | PMID 11178230
Gardiner K, Davisson M
From lymphocytes to sharks: V(D)J recombinase moves to the germline.
Genome biology | 2000-01-01 | PMID 11178236
Roth D B
Secret sharers in the immune system: a novel RNA editing activity links switch recombination and somatic hypermutation.
Genome biology | 2000-01-01 | PMID 11178252
Maizels N
Higher plant cellulose synthases.
Genome biology | 2000-01-01 | PMID 11178255
Richmond T
Human genomic variation.
Genome biology | 2000-01-01 | PMID 11178257
Disotell T R
Polymorphism in regulatory gene sequences.
Genome biology | 2001-01-01 | PMID 11178274
Mitchison N A
Effectiveness of specific RNA-mediated interference through ingested double-stranded RNA in Caenorhabditis elegans.
Genome biology | 2001-01-01 | PMID 11178279
Kamath R S, Martinez-Campos M, Zipperlen P and 2 more
[Advances in research on the molecular pathogenesis of the malignant tumours and implications for their early diagnosis and treatment].
Medycyna wieku rozwojowego | 2000-01-01 | PMID 11178325
Steffen J
Congenital erythropoietic porphyria: prenatal diagnosis and autopsy findings in two sibling fetuses.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society | 2000-01-01 | PMID 11178635
Daïkha-Dahmane F, Dommergues M, Narcy F and 7 more
Phenotypic and phylogenetic characterization of Burkholderia (Pseudomonas) sp. strain LB400.
Current microbiology | 2001-04-01 | PMID 11178728
Fain M G, Haddock J D
Genetic architecture of adiposity in the cross of LG/J and SM/J inbred mice.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-01-01 | PMID 11178736
Cheverud J M, Vaughn T T, Pletscher L S and 4 more
Genome-wide linkage analysis of inherited hydrocephalus in the H-Tx rat.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-01-01 | PMID 11178739
Jones H C, Depelteau J S, Carter B J and 2 more
Detection of QTL for milk production on Chromosomes 1 and 6 of Holstein cattle.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-01-01 | PMID 11178740
Nadesalingam J, Plante Y, Gibson J P
Estimation of DNA sequence diversity in bovine cytokine genes.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-01-01 | PMID 11178741
Heaton M P, Grosse W M, Kappes S M and 6 more
Genetic analysis of testis weight and fertility in an interspecies hybrid congenic strain for Chromosome X.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-01-01 | PMID 11178743
Elliott R W, Miller D R, Pearsall R S and 5 more
Complex genetic interactions among four receptor tyrosine phosphatases regulate axon guidance in Drosophila.
Molecular and cellular neurosciences | 2001-02-01 | PMID 11178866
Sun Q, Schindelholz B, Knirr M and 2 more
Expression of QKI proteins and MAP1B identifies actively myelinating oligodendrocytes in adult rat brain.
Molecular and cellular neurosciences | 2001-02-01 | PMID 11178867
Wu H Y, Dawson M R, Reynolds R and 1 more
Genes: QKI
A nonsense mutation in the alpha1 subunit of the inhibitory glycine receptor associated with bovine myoclonus.
Molecular and cellular neurosciences | 2001-02-01 | PMID 11178872
Pierce K D, Handford C A, Morris R and 4 more
Immunogenetic analysis reveals that epitope shifting occurs during B-cell affinity maturation in primary biliary cirrhosis.
Journal of molecular biology | 2001-02-09 | PMID 11178892
Potter K N, Thomson R K, Hamblin A and 3 more
Genes: PDC
Structural basis of diverse sequence-dependent target recognition by the 8 kDa dynein light chain.
Journal of molecular biology | 2001-02-09 | PMID 11178896
Fan J, Zhang Q, Tochio H and 2 more
Subunit assembly and mode of DNA cleavage of the type III restriction endonucleases EcoP1I and EcoP15I.
Journal of molecular biology | 2001-02-23 | PMID 11178902
Janscak P, Sandmeier U, Szczelkun M D and 1 more
Solution structure of Grb2 reveals extensive flexibility necessary for target recognition.
Journal of molecular biology | 2001-02-23 | PMID 11178911
Yuzawa S, Yokochi M, Hatanaka H and 6 more
Point mutations in alpha-subunit of human cardiac Na+ channels alter Na+ current kinetics.
Biochemical and biophysical research communications | 2001-02-16 | PMID 11178958
Xiao Y F, Ke Q, Wang S Y and 4 more
A novel host cell reactivation assay to assess homologous recombination capacity in human cancer cell lines.
Biochemical and biophysical research communications | 2001-02-16 | PMID 11178982
Slebos R J, Taylor J A
Genes: BRCA1
Differentially expressed cDNAs in PLCbeta3-induced tumor suppression in a human endocrine pancreatic tumor cell line: activation of the human mismatch repair protein 3 gene.
Biochemical and biophysical research communications | 2001-02-16 | PMID 11178984
Stålberg P, Lopez-Egido J R, Wang S and 3 more
Genes: PLCB3, MEN1
MDM2 enhances the function of estrogen receptor alpha in human breast cancer cells.
Biochemical and biophysical research communications | 2001-02-16 | PMID 11178989
Saji S, Okumura N, Eguchi H and 6 more
Genes: MDM2
Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis.
American journal of human genetics | 2001-03-01 | PMID 11179007
Göransdotter Ericson K, Fadeel B, Nilsson-Ardnor S and 15 more
Genetic and mutational analyses of a large multiethnic Bardet-Biedl cohort reveal a minor involvement of BBS6 and delineate the critical intervals of other loci.
American journal of human genetics | 2001-03-01 | PMID 11179009
Beales P L, Katsanis N, Lewis R A and 8 more
Genes: BBS2, BBS5, MKKS
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effects.
American journal of human genetics | 2001-03-01 | PMID 11179010
Periquet M, Lücking C, Vaughan J and 16 more
Compound heterozygosity for a recurrent 16.5-kb Alu-mediated deletion mutation and single-base-pair substitutions in the ABCC6 gene results in pseudoxanthoma elasticum.
American journal of human genetics | 2001-03-01 | PMID 11179012
Ringpfeil F, Nakano A, Uitto J and 1 more
Genes: ABCC6
Use of homozygosity mapping to identify a region on chromosome 1 bearing a defective gene that causes autosomal recessive homozygous hypercholesterolemia in two unrelated families.
American journal of human genetics | 2001-03-01 | PMID 11179013
Eden E R, Naoumova R P, Burden J J and 2 more
Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.
American journal of human genetics | 2001-03-01 | PMID 11179014
Gurling H M, Kalsi G, Brynjolfson J and 9 more
Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease.
American journal of human genetics | 2001-03-01 | PMID 11179015
Yamada R, Tanaka T, Unoki M and 11 more
Complex HLA-DR and -DQ interactions confer risk of narcolepsy-cataplexy in three ethnic groups.
American journal of human genetics | 2001-03-01 | PMID 11179016
Mignot E, Lin L, Rogers W and 12 more
Patterns of ancestral human diversity: an analysis of Alu-insertion and restriction-site polymorphisms.
American journal of human genetics | 2001-03-01 | PMID 11179020
Watkins W S, Ricker C E, Bamshad M J and 6 more
Familial dysautonomia is caused by mutations of the IKAP gene.
American journal of human genetics | 2001-03-01 | PMID 11179021
Anderson S L, Coli R, Daly I W and 5 more
Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma).
American journal of human genetics | 2001-03-01 | PMID 11179023
Aradhya S, Courtois G, Rajkovic A and 4 more
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.
American journal of human genetics | 2001-03-01 | PMID 11179024
Héon E, Paterson A D, Fraser M and 7 more
A new locus for autosomal dominant familial exudative vitreoretinopathy maps to chromosome 11p12-13.
American journal of human genetics | 2001-03-01 | PMID 11179025
Downey L M, Keen T J, Roberts E and 3 more
Analysis of the prostate cancer-susceptibility locus HPC20 in 172 families affected by prostate cancer.
American journal of human genetics | 2001-03-01 | PMID 11179028
Bock C H, Cunningham J M, McDonnell S K and 10 more