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 1546 of 10600

p53 gene mutation and protein accumulation during neoplastic progression in Barrett's esophagus.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | 2001-05-01 | PMID 11353048
Bian Y S, Osterheld M C, Bosman F T and 2 more
Mutational analysis of the 5' noncoding region of the bcl-6 gene in primary gastric lymphomas.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | 2001-05-01 | PMID 11353050
Go J H, Yang W I, Ree H J
Abnormal expression of MDM2 in prostate carcinoma.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | 2001-05-01 | PMID 11353053
Leite K R, Franco M F, Srougi M and 8 more
Genes: MDM2
Adenosquamous carcinoma of the pancreas: a clinicopathologic series of 25 cases.
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc | 2001-05-01 | PMID 11353055
Kardon D E, Thompson L D, Przygodzki R M and 1 more
UV induces nucleolar translocation of ING1 through two distinct nucleolar targeting sequences.
Nucleic acids research | 2001-05-15 | PMID 11353074
Scott M, Boisvert F M, Vieyra D and 3 more
Genes: ING1, NTS
Incoming nucleotide binds to Klenow ternary complex leading to stable physical sequestration of preceding dNTP on DNA.
Nucleic acids research | 2001-05-15 | PMID 11353079
Ramanathan S, Chary K V, Rao B J
Role of the ITS2-proximal stem and evidence for indirect recognition of processing sites in pre-rRNA processing in yeast.
Nucleic acids research | 2001-05-15 | PMID 11353080
Côté C A, Peculis B A
Two Arabidopsis methylation-deficiency mutations confer only partial effects on a methylated endogenous gene family.
Nucleic acids research | 2001-05-15 | PMID 11353082
Bartee L, Bender J
The complete genome sequence of the murine respiratory pathogen Mycoplasma pulmonis.
Nucleic acids research | 2001-05-15 | PMID 11353084
Chambaud I, Heilig R, Ferris S and 9 more
Phenotypic analysis of genes encoding yeast zinc cluster proteins.
Nucleic acids research | 2001-05-15 | PMID 11353088
Akache B, Wu K, Turcotte B
New variants of inducible Cre recombinase: a novel mutant of Cre-PR fusion protein exhibits enhanced sensitivity and an expanded range of inducibility.
Nucleic acids research | 2001-05-15 | PMID 11353092
Wunderlich F T, Wildner H, Rajewsky K and 1 more
Evidence for functionally significant polymorphism of human glutamate cysteine ligase catalytic subunit: association with glutathione levels and drug resistance in the National Cancer Institute tumor cell line panel.
Toxicological sciences : an official journal of the Society of Toxicology | 2001-06-01 | PMID 11353130
Walsh A C, Feulner J A, Reilly A
Progressive formation of inclusions in the striatum and hippocampus of mice transgenic for the human Huntington's disease mutation.
Journal of neurocytology | 2000-09-01 | PMID 11353291
Morton A J, Lagan M A, Skepper J N and 1 more
Apolipoproteins C-I and C-III as important modulators of lipoprotein metabolism.
Current opinion in lipidology | 2001-06-01 | PMID 11353333
Shachter N S
Unravelling the complex genetics of cleft lip in the mouse model.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-06-01 | PMID 11353389
Juriloff D M, Harris M J, Brown C J
Integration of the feline radiation hybrid and linkage maps.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-06-01 | PMID 11353390
Sun S, Murphy W J, Menotti-Raymond M and 1 more
Mutations in the agouti (ASIP), the extension (MC1R), and the brown (TYRP1) loci and their association to coat color phenotypes in horses (Equus caballus).
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-06-01 | PMID 11353392
Rieder S, Taourit S, Mariat D and 2 more
Genes: ASIP, TYRP1
DQX1, an RNA-dependent ATPase homolog with a novel DEAQ box: expression pattern and genomic sequence comparison of the human and mouse genes.
Mammalian genome : official journal of the International Mammalian Genome Society | 2001-06-01 | PMID 11353393
Ji W, Chen F, Do T and 3 more
Genes: DQX1, AUP1
Evidence for a susceptibility gene for autism on chromosome 2 and for genetic heterogeneity.
American journal of human genetics | 2001-06-01 | PMID 11353400
Buxbaum J D, Silverman J M, Smith C J and 7 more
Genes: NPL, PSD
Equivalence between Haseman-Elston and variance-components linkage analyses for sib pairs.
American journal of human genetics | 2001-06-01 | PMID 11353401
Sham P C, Purcell S
Genetic differentiation in South Amerindians is related to environmental and cultural diversity: evidence from the Y chromosome.
American journal of human genetics | 2001-06-01 | PMID 11353402
Tarazona-Santos E, Carvalho-Silva D R, Pettener D and 7 more
Evaluation of candidate genes in case-control studies: a statistical method to account for related subjects.
American journal of human genetics | 2001-06-01 | PMID 11353403
Slager S L, Schaid D J
Rippling muscle disease: evidence for phenotypic and genetic heterogeneity.
Muscle & nerve | 2001-03-01 | PMID 11353417
So Y T, Zu L, Barraza C and 2 more
Metabolic enzymes and phenotypic expression among human locomotor muscles.
Muscle & nerve | 2001-03-01 | PMID 11353424
Gregory C M, Vandenborne K, Dudley G A
Association study between cannabinoid receptor gene (CNR1) and pathogenesis and psychotic symptoms of mood disorders.
American journal of medical genetics | 2001-04-08 | PMID 11353438
Tsai S J, Wang Y C, Hong C J
Genes: CNR1
Genetic association analysis of behavioral inhibition using candidate loci from mouse models.
American journal of medical genetics | 2001-04-08 | PMID 11353440
Smoller J W, Rosenbaum J F, Biederman J and 9 more
Family-based association study of serotonin transporter promoter in suicidal adolescents: no association with suicidality but possible role in violence traits.
American journal of medical genetics | 2001-04-08 | PMID 11353442
Zalsman G, Frisch A, Bromberg M and 7 more
Lack of association between schizophrenia and the phospholipase-A(2) genes cPLA2 and sPLA2.
American journal of medical genetics | 2001-04-08 | PMID 11353443
Frieboes R M, Moises H W, Gattaz W F and 7 more
Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder.
American journal of medical genetics | 2001-04-08 | PMID 11353444
Barr C L, Shulman R, Wigg K and 5 more
Genes: MOG
An association study of DRD5 with smoking initiation and progression to nicotine dependence.
American journal of medical genetics | 2001-04-08 | PMID 11353446
Sullivan P F, Neale M C, Silverman M A and 7 more
Genes: DRD5
Relationship between Taq1 A dopamine D2 receptor (DRD2) polymorphism and prolactin response to bromperidol.
American journal of medical genetics | 2001-04-08 | PMID 11353448
Mihara K, Suzuki A, Kondo T and 5 more
Genes: DRD2
Systematic search for mutations in the human tissue inhibitor of metalloproteinases-3 (TIMP-3) gene on chromosome 22 and association study with schizophrenia.
American journal of medical genetics | 2001-04-08 | PMID 11353449
Hung C C, Chen Y H, Tsai M T and 1 more
Additional evidence that genetic variation of MAO-A gene supports a gender subtype in obsessive-compulsive disorder.
American journal of medical genetics | 2001-04-08 | PMID 11353450
Camarena B, Rinetti G, Cruz C and 3 more
DRD4 exon 3 variants associated with delusional symptomatology in major psychoses: a study on 2,011 affected subjects.
American journal of medical genetics | 2001-04-08 | PMID 11353451
Serretti A, Lilli R, Lorenzi C and 2 more
Genes: DRD4
Absence of a significant linkage between Na(+),K(+)-ATPase subunit (ATP1A3 and ATP1B3) genotypes and bipolar affective disorder in the old-order Amish.
American journal of medical genetics | 2001-04-08 | PMID 11353452
Philibert R A, Cheung D, Welsh N and 4 more
CUX2, a potential regulator of NCAM expression: genomic characterization and analysis as a positional candidate susceptibility gene for bipolar disorder.
American journal of medical genetics | 2001-04-08 | PMID 11353453
Jacobsen N J, Elvidge G, Franks E K and 3 more
Genes: CUX2
Identification of three polymorphisms in the translated region of PLC-gamma1 and their investigation in lithium responsive bipolar disorder.
American journal of medical genetics | 2001-04-08 | PMID 11353454
Ftouhi-Paquin N, Alda M, Grof P and 3 more
Direct removal in the mouse of a floxed neo gene from a three-loxP conditional knockout allele by two novel approaches.
Genesis (New York, N.Y. : 2000) | 2001-05-01 | PMID 11353511
Xu X, Li C, Garrett-Beal L and 3 more
Molecular characterization of Cephalothorax, the Tribolium ortholog of Sex combs reduced.
Genesis (New York, N.Y. : 2000) | 2001-05-01 | PMID 11353513
Curtis C D, Brisson J A, DeCamillis M A and 3 more
Variegated expression and delayed retinal pigmentation during development in transgenic mice with a deletion in the locus control region of the tyrosinase gene.
Genesis (New York, N.Y. : 2000) | 2001-05-01 | PMID 11353514
Giménez E, Giraldo P, Jeffery G and 1 more
Genes: RPE
A transgenic insertion causing cryptorchidism in mice.
Genesis (New York, N.Y. : 2000) | 2001-05-01 | PMID 11353515
Overbeek P A, Gorlov I P, Sutherland R W and 5 more
Characterization of a novel EGFP reporter mouse to monitor Cre recombination as demonstrated by a Tie2 Cre mouse line.
Genesis (New York, N.Y. : 2000) | 2001-05-01 | PMID 11353516
Constien R, Forde A, Liliensiek B and 4 more
Seasonal distribution of births in patients with Alzheimer's disease and elderly depressive patients.
European psychiatry : the journal of the Association of European Psychiatrists | 2001-04-01 | PMID 11353593
Ptok U, Papassotiropoulos A, Maier W and 1 more
Oxacillinase-mediated resistance to cefepime and susceptibility to ceftazidime in Pseudomonas aeruginosa.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353602
Aubert D, Poirel L, Chevalier J and 3 more
Selection and characterization of varicella-zoster virus variants resistant to (R)-9-[4-hydroxy-2-(hydroxymethy)butyl]guanine.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353604
Ng T I, Shi Y, Huffaker H J and 7 more
Molecular basis of rifampin and isoniazid resistance in Mycobacterium bovis strains isolated in Sardinia, Italy.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353606
Sechi L A, Zanetti S, Sanguinetti M and 7 more
Contributions of the 8-methoxy group of gatifloxacin to resistance selectivity, target preference, and antibacterial activity against Streptococcus pneumoniae.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353607
Fukuda H, Kishii R, Takei M and 1 more
Teicoplanin stress-selected mutations increasing sigma(B) activity in Staphylococcus aureus.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353616
Bischoff M, Berger-Bächi B
Real-time PCR and melting curve analysis for reliable and rapid detection of SHV extended-spectrum beta-lactamases.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353618
Randegger C C, Hächler H
Multidrug efflux pumps: expression patterns and contribution to antibiotic resistance in Pseudomonas aeruginosa biofilms.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353623
De Kievit T R, Parkins M D, Gillis R J and 5 more
Resistance studies with daptomycin.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353628
Silverman J A, Oliver N, Andrew T and 1 more
Genotypic and phenotypic resistance patterns of human immunodeficiency virus type 1 variants with insertions or deletions in the reverse transcriptase (RT): multicenter study of patients treated with RT inhibitors.
Antimicrobial agents and chemotherapy | 2001-06-01 | PMID 11353634
Masquelier B, Race E, Tamalet C and 11 more
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
Brain : a journal of neurology | 2001-06-01 | PMID 11353725
Sternberg D, Maisonobe T, Jurkat-Rott K and 7 more
DNA repair excision nuclease attacks undamaged DNA. A potential source of spontaneous mutations.
The Journal of biological chemistry | 2001-07-06 | PMID 11353769
Branum M E, Reardon J T, Sancar A
Rapid, local adaptation of zooplankton behavior to changes in predation pressure in the absence of neutral genetic changes.
Proceedings of the National Academy of Sciences of the United States of America | 2001-05-22 | PMID 11353872
Cousyn C, De Meester L, Colbourne J K and 3 more
Tamoxifen-induced hypertriglyceridemia in association with diabetes mellitus.
Diabetes & metabolism | 2001-04-01 | PMID 11353883
Milionis H J, Liberopoulos E N, Elisaf M S
Hereditary glucocorticoid resistance.
Annales d'endocrinologie | 2001-04-01 | PMID 11353888
Lamberts S W
[Involvement of the IGF system in the pathogenesis of adrenocortical tumors].
Annales d'endocrinologie | 2001-04-01 | PMID 11353893
Gicquel C, Boulle N, Logié A and 3 more
Congenital adrenal hypoplasia and DAX-1 gene mutations.
Annales d'endocrinologie | 2001-04-01 | PMID 11353895
Tabarin A
The molecular pathogenesis of ACTH insensitivity syndromes.
Annales d'endocrinologie | 2001-04-01 | PMID 11353896
Clark A J, Metherell L, Swords F M and 1 more
Calcitonin receptor gene polymorphism in japanese women: correlation with body mass and bone mineral density.
Calcified tissue international | 2001-04-01 | PMID 11353946
Nakamura M, Morimoto S, Zhang Z and 4 more
Genes: VDR
Involvement of nuclear factor-1 (NF1) binding motif in the regucalcin gene expression of rat kidney cortex: the expression is suppressed by cisplatin administration.
Molecular and cellular biochemistry | 2001-03-01 | PMID 11354250
Misawa H, Yamaguchi M
Expression of B-type natriuretic peptide in atrial natriuretic peptide gene disrupted mice.
Molecular and cellular biochemistry | 2001-03-01 | PMID 11354260
Tse M Y, Watson J D, Sarda I R and 2 more
Effect of multiple mutations in the core promoter and pre-core/core region of hepatitis B virus genome on the response to interferon in e antigen-positive chronic hepatitis B.
Journal of gastroenterology and hepatology | 2001-04-01 | PMID 11354277
Zhang X, Han Y, Lu Z and 3 more
Synthesis and evaluation of efavirenz (Sustiva) analogues as HIV-1 reverse transcriptase inhibitors: replacement of the cyclopropylacetylene side chain.
Bioorganic & medicinal chemistry letters | 2001-05-07 | PMID 11354371
Cocuzza A J, Chidester D R, Cordova B C and 6 more
A WbpL mutant of Pseudomonas putida DOT-T1E strain, which lacks the O-antigenic side chain of lipopolysaccharides, is tolerant to organic solvent shocks.
Extremophiles : life under extreme conditions | 2001-04-01 | PMID 11354460
Junker F, Rodríguez-Herva J J, Duque E and 3 more
Electrospray ionization mass spectrometry-based genotyping: an approach for identification of single nucleotide polymorphisms.
Analytical chemistry | 2001-05-01 | PMID 11354499
Zhang S, Van Pelt C K, Schultz G A
Biomarker monitoring for health risk based on sensitivity to environmental mutagens.
Reviews on environmental health | 2000-01-01 | PMID 11354541
Au W W, Oberheitmann B, Heo M Y and 2 more
Calprotectin expression and mononuclear phagocyte subpopulations in peripheral blood and bronchoalveolar lavage.
Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG | 2001-03-01 | PMID 11354548
Striz I, Pokorná-Sochurkova H, Zheng L and 3 more
Lysine metabolism in higher plants.
Amino acids | 2001-01-01 | PMID 11354603
Azevedo R A, Lea P J
The missense Glu298Asp variant of the endothelial nitric oxide synthase gene is strongly associated with placental abruption.
Human genetics | 2001-03-01 | PMID 11354626
Yoshimura T, Yoshimura M, Tabata A and 2 more
Analysis of the CC chemokine receptor 5 (CCR5) delta-32 polymorphism in inflammatory bowel disease.
Human genetics | 2001-03-01 | PMID 11354628
Rector A, Vermeire S, Thoelen I and 5 more
Genes: CCR5
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease.
Human genetics | 2001-03-01 | PMID 11354629
Carrieri G, Bonafè M, De Luca M and 12 more
Genes: APOE
Carrier rate of APC I1307K is not increased in inflammatory bowel disease patients of Ashkenazi Jewish origin.
Human genetics | 2001-03-01 | PMID 11354631
Silverberg M S, Clelland C, Murphy J E and 5 more
Genes: APC
CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease.
Human genetics | 2001-03-01 | PMID 11354633
Tzetis M, Efthymiadou A, Strofalis S and 5 more
Genes: CFTR
Characterisation of SMN hybrid genes in Spanish SMA patients: de novo, homozygous and compound heterozygous cases.
Human genetics | 2001-03-01 | PMID 11354634
Cuscó I, Barceló M J, del Rio E and 5 more
Genes: SMN2, SMN1, NAIP
Elite swimmers and the D allele of the ACE I/D polymorphism.
Human genetics | 2001-03-01 | PMID 11354635
Woods D, Hickman M, Jamshidi Y and 5 more
Genes: ACE
A single nucleotide polymorphism (SNP) in the leptin receptor is associated with BMI, fat mass and leptin levels in postmenopausal Caucasian women.
Human genetics | 2001-03-01 | PMID 11354636
Quinton N D, Lee A J, Ross R J and 2 more
Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes.
Human genetics | 2001-03-01 | PMID 11354637
Neerman-Arbez M, de Moerloose P, Honsberger A and 13 more
Genes: FGA, FGG, FGB
Cross-sectional study on cytokine polymorphisms, cytokine production after T-cell stimulation and clinical parameters in a random sample of a German population.
Human genetics | 2001-03-01 | PMID 11354638
Nieters A, Brems S, Becker N
Genes: IFNG, TNF
Increased reproductive success of MHC class II heterozygous males among free-ranging rhesus macaques.
Human genetics | 2001-03-01 | PMID 11354639
Sauermann U, Nürnberg P, Bercovitch F B and 6 more
SMN gene duplication and the emergence of the SMN2 gene occurred in distinct hominids: SMN2 is unique to Homo sapiens.
Human genetics | 2001-03-01 | PMID 11354640
Rochette C F, Gilbert N, Simard L R
Genes: SMN2, SMN1
De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss.
Human genetics | 2001-03-01 | PMID 11354642
Janecke A R, Nekahm D, Löffler J and 3 more
Evidence for the transmission of scrapie to sheep and goats from a vaccine against Mycoplasma agalactiae.
The Veterinary record | 2001-04-28 | PMID 11354646
Caramelli M, Ru G, Casalone C and 4 more
Clinical spectrum of Denys-Drash and Frasier syndrome.
Pediatric nephrology (Berlin, Germany) | 2001-04-01 | PMID 11354777
McTaggart S J, Algar E, Chow C W and 2 more
Polymorphisms of renin-angiotensin system genes in childhood IgA nephropathy.
Pediatric nephrology (Berlin, Germany) | 2001-04-01 | PMID 11354780
Maruyama K, Yoshida M, Nishio H and 6 more
Genes: ACE, AGT
Impact of ACE I/D gene polymorphism on congenital renal malformations.
Pediatric nephrology (Berlin, Germany) | 2001-04-01 | PMID 11354781
Hohenfellner K, Wingen A M, Nauroth O and 3 more
Genes: ACE
Anhidrotic Ectodermal Dysplasia (Christ-Seimens-Touraine syndrome)--case report with a review.
Indian journal of medical sciences | 2000-12-01 | PMID 11354819
Ali G, Kumar M, Verma R and 2 more
Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy.
Neurogenetics | 2001-03-01 | PMID 11354824
Bolino A, Lonie L J, Zimmer M and 4 more
Genes: MTMR2
Autism: evidence of association with adenosine deaminase genetic polymorphism.
Neurogenetics | 2001-03-01 | PMID 11354825
Bottini N, De Luca D, Saccucci P and 5 more
Genes: ADA
Hereditary demyelinating neuropathies: from gene to disease.
Neurogenetics | 2001-03-01 | PMID 11354826
Hanemann C O
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonates.
Neurogenetics | 2001-03-01 | PMID 11354829
De Luca A, Rizzardi M, Torrente I and 5 more
Genes: DRD4
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia.
Neurogenetics | 2001-03-01 | PMID 11354831
Ashley-Koch A, Bonner E R, Gaskell P C and 12 more
Molecular genetic analysis and mutation screening of the VHL gene in a Japanese family with von Hippel-Lindau disease.
The Kobe journal of medical sciences | 2000-08-01 | PMID 11354926
Wu Y, Nishio H, Lee M J and 5 more
Genes: VHL
[Lafora disease and founder effect in a small neotropical locality].
Revista de biologia tropical | 2000-01-01 | PMID 11354978
Solís M V
A nucleotide variant in the promoter region of the interleukin-6 gene associated with decreased bone mineral density.
Journal of human genetics | 2001-01-01 | PMID 11355017
Ota N, Nakajima T, Nakazawa I and 6 more
Risk factor-gene interaction in carotid atherosclerosis: effect of gene polymorphisms of renin-angiotensin system.
Journal of human genetics | 2001-01-01 | PMID 11355019
Tabara Y, Kohara K, Nakura J and 1 more
Genes: ACE, AGT
Identification of three missense mutations in the peroxisome proliferator-activated receptor alpha gene in Japanese subjects with maturity-onset diabetes of the young.
Journal of human genetics | 2001-01-01 | PMID 11355020
Hara M, Wang X, Paz V P and 4 more
Genes: PPARA
Analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene mutations in Japanese patients with chronic pancreatitis.
Journal of human genetics | 2001-01-01 | PMID 11355022
Kaneko K, Nagasaki Y, Furukawa T and 5 more
Genes: CFTR, PRSS1
Association of vitamin D receptor and estrogen receptor gene polymorphisms with bone mass in postmenopausal Korean women.
Menopause (New York, N.Y.) | 2000-01-01 | PMID 11355046
Kim J G, Lim K S, Kim E K and 2 more
Genes: VDR