Crkl enhances leukemogenesis in BCR/ABL P190 transgenic mice.
Cancer research | 2001-02-15 | PMID 11245441
Hemmeryckx B, van Wijk A, Reichert A and 6 more
Genes: BCR, CRKL
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 1503 of 10600
The pharmacological phenotype of combined multidrug-resistance mdr1a/1b- and mrp1-deficient mice.
Cancer research | 2001-02-15 | PMID 11245453
Johnson D R, Finch R A, Lin Z P and 2 more
Gene expression patterns associated with the metastatic phenotype in rodent and human tumors.
Cancer research | 2001-02-15 | PMID 11245467
Nestl A, Von Stein O D, Zatloukal K and 4 more
End-joining deficiency and radiosensitization induced by gemcitabine.
Cancer research | 2001-02-15 | PMID 11245469
van Putten JWG, Groen HJM, Smid K and 2 more
MSH6 and MSH3 are rarely involved in genetic predisposition to nonpolypotic colon cancer.
Cancer research | 2001-02-15 | PMID 11245474
Huang J, Kuismanen S A, Liu T and 13 more
Genes: MSH6, MSH3, MLH1, MSH2
Anoikis and metastatic potential of cloudman S91 melanoma cells.
Cancer research | 2001-02-15 | PMID 11245487
Zhu Z, Sanchez-Sweatman O, Huang X and 4 more
Inhibition of fibroblast growth factor/fibroblast growth factor receptor activity in glioma cells impedes tumor growth by both angiogenesis-dependent and -independent mechanisms.
Cancer research | 2001-02-15 | PMID 11245488
Auguste P, Gürsel D B, Lemière S and 5 more
Genes: FGFR1, FGFR2
Mechanism of functional inactivation of a Li-Fraumeni syndrome p53 that has a mutation outside of the DNA-binding domain.
Cancer research | 2001-02-15 | PMID 11245491
Gu J, Kawai H, Wiederschain D and 1 more
Influence of the vitamin D receptor alleles on human osteoblast-like cells.
The Journal of bone and joint surgery. British volume | 2001-01-01 | PMID 11245522
Ohtera K, Ishii S, Matsuyama T
Genes: VDR
A single histone H1 isoform (H1.1) is essential for chromatin silencing and germline development in Caenorhabditis elegans.
Development (Cambridge, England) | 2001-04-01 | PMID 11245572
Jedrusik M A, Schulze E
Establishment and maintenance of parasegmental compartments.
Development (Cambridge, England) | 2001-04-01 | PMID 11245576
Hughes S C, Krause H M
Differential global gene expression in red and white skeletal muscle.
American journal of physiology. Cell physiology | 2001-04-01 | PMID 11245591
Campbell W G, Gordon S E, Carlson C J and 3 more
Agouti regulates adipocyte transcription factors.
American journal of physiology. Cell physiology | 2001-04-01 | PMID 11245612
Mynatt R L, Stephens J M
Genes: STAT3
Ontogenetic, gravity-dependent development of rat soleus muscle.
American journal of physiology. Cell physiology | 2001-04-01 | PMID 11245617
Ohira Y, Tanaka T, Yoshinaga T and 6 more
Thrombomodulin Ala455Val polymorphism and risk of coronary heart disease.
Circulation | 2001-03-13 | PMID 11245641
Wu K K, Aleksic N, Ahn C and 3 more
Regulation of neurotransmitter vesicles by the homeodomain protein UNC-4 and its transcriptional corepressor UNC-37/groucho in Caenorhabditis elegans cholinergic motor neurons.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2001-03-15 | PMID 11245684
Lickteig K M, Duerr J S, Frisby D L and 3 more
The primate amygdala mediates acute fear but not the behavioral and physiological components of anxious temperament.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2001-03-15 | PMID 11245690
Kalin N H, Shelton S E, Davidson R J and 1 more
GABA(A) receptors containing (alpha)5 subunits in the CA1 and CA3 hippocampal fields regulate ethanol-motivated behaviors: an extended ethanol reward circuitry.
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2001-03-15 | PMID 11245701
June H L, Harvey S C, Foster K L and 11 more
MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features.
Neurology | 2001-03-13 | PMID 11245712
Auranen M, Vanhala R, Vosman M and 6 more
Genes: MECP2
Aldosterone synthase (CYP11B2) gene polymorphism and cerebral white matter hyperintensities.
Neurology | 2001-03-13 | PMID 11245725
Verpillat P, Alpérovitch A, Cambien F and 3 more
The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome.
Neurology | 2001-03-13 | PMID 11245730
Carrozzo R, Tessa A, Vázquez-Memije M E and 10 more
Genetic renal tubular disorders of renal ion channels and transporters.
Seminars in nephrology | 2001-03-01 | PMID 11245772
Meneton P, Oh Y S, Warnock D G
The genetics and physiology of polycystic kidney disease.
Seminars in nephrology | 2001-03-01 | PMID 11245774
Calvet J P, Grantham J J
Genes: PKD1, PKD2
Modification of inhibitor binding sites in the cytochrome bf complex by directed mutagenesis of cytochrome b(6) in Synechococcus sp. PCC 7002.
Biochimica et biophysica acta | 2001-04-02 | PMID 11245788
Lee T, Metzger S U, Cho Y S and 2 more
Two functionally distinct manganese clusters formed by introducing a mutation in the carboxyl terminus of a photosystem II reaction center polypeptide, D1, of the green alga Chlamydomonas reinhardtii.
Biochimica et biophysica acta | 2001-04-02 | PMID 11245793
Hatano-Iwasaki A, Minagawa J, Inoue Y and 1 more
Dynamic changes in glucose metabolism accompanying the expression of the neural phenotype after differentiation in PC12 cells.
Brain research | 2001-03-09 | PMID 11245818
Waki A, Yano R, Yoshimoto M and 3 more
The genomic basis of K(V)3.4 potassium channel mRNA diversity in mice.
Gene | 2001-02-07 | PMID 11245975
Vullhorst D, Jockusch H, Bartsch J W
Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locus.
Gene | 2001-02-07 | PMID 11245985
Kasai N, Fukushima K, Ueki Y and 7 more
Genes: STS
The structure and function of tenascins in the nervous system.
Matrix biology : journal of the International Society for Matrix Biology | 2001-02-01 | PMID 11246000
Joester A, Faissner A
Substrate assisted catalysis -- application to G proteins.
Trends in biochemical sciences | 2001-03-01 | PMID 11246021
Kosloff M, Selinger Z
Phenotypic flexibility in digestive system structure and function in migratory birds and its ecological significance.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology | 2001-03-01 | PMID 11246046
McWilliams S R, Karasov W H
Genetic and environmental interactions on oral cancer in Southern Thailand.
Environmental and molecular mutagenesis | 2001-01-01 | PMID 11246217
Kietthubthew S, Sriplung H, Au W W
Genes: GSTM1, GSTT1
Spontaneous mutation of the lacI transgene in rodents: absence of species, strain, and insertion-site influence.
Environmental and molecular mutagenesis | 2001-01-01 | PMID 11246220
Zhang S, Glickman B W, de Boer J G
Computer simulations for biological aging and sexual reproduction.
Anais da Academia Brasileira de Ciencias | 2001-03-01 | PMID 11246266
Stauffer D, de Oliveira P M, de Oliveira S M and 2 more
Multidrug resistance in tumour cells: characterization of the multidrug resistant cell line K562-Lucena 1.
Anais da Academia Brasileira de Ciencias | 2001-03-01 | PMID 11246270
Rumjanek V M, Trindade G S, Wagner-Souza K and 4 more
Molecular scanning for mutations in the melanocortin-4 receptor gene in obese/diabetic Japanese.
Annals of human genetics | 1999-11-01 | PMID 11246450
Ohshiro Y, Sanke T, Ueda K and 7 more
Molecular instability of the mitochondrial haplogroup T sequences at nucleotide positions 16292 and 16296.
Annals of human genetics | 1999-11-01 | PMID 11246451
Malyarchuk B A, Derenko M V
Analysis of lipoprotein lipase haplotypes reveals associations not apparent from analysis of the constituent loci.
Annals of human genetics | 1999-11-01 | PMID 11246452
Hallman D M, Groenemeijer B E, Jukema J W and 2 more
Genes: LPL
Linking genotype to aorto-coronary atherosclerosis: a model using familial hypercholesterolemia and aorto-coronary calcification.
Annals of human genetics | 1999-11-01 | PMID 11246453
Jensen J M, Kruse T A, Brorholt-Petersen J U and 4 more
Hardy-Weinberg quality control.
Annals of human genetics | 1999-11-01 | PMID 11246455
Gomes I, Collins A, Lonjou C and 4 more
A genome-based study of consanguinity in three co-resident endogamous Pakistan communities.
Annals of human genetics | 2000-01-01 | PMID 11246460
Wang W, Sullivan S G, Ahmed S and 3 more
Equivalence by descent: pedigree analysis with inbreeding and gametic phase disequilibrium.
Annals of human genetics | 2000-01-01 | PMID 11246462
Denniston C
The FMR2 gene, FRAXE and non-specific X-linked mental retardation: clinical and molecular aspects.
Annals of human genetics | 2000-03-01 | PMID 11246464
Gecz J
Microsatellite evolution in modern humans: a comparison of two data sets from the same populations.
Annals of human genetics | 2000-03-01 | PMID 11246466
Jin L, Baskett M L, Cavalli-Sforza L L and 3 more
Beta2-adrenergic receptor allele frequencies in the Quechua, a high altitude native population.
Annals of human genetics | 2000-03-01 | PMID 11246467
Rupert J L, Monsalve M V, Devine D V and 1 more
Adaptation of the extended transmission/disequilibrium test to distinguish disease associations of multiple loci: the Conditional Extended Transmission/Disequilibrium Test.
Annals of human genetics | 2000-05-01 | PMID 11246472
Koeleman B P, Dudbridge F, Cordell H J and 1 more
Conditional ETDT analysis of the human leukocyte antigen region in type 1 diabetes.
Annals of human genetics | 2000-05-01 | PMID 11246473
Koeleman B P, Herr M H, Zavattari P and 10 more
Genes: TNF
Fine scale association mapping of disease loci using simplex families.
Annals of human genetics | 2000-05-01 | PMID 11246474
Morris A P, Whittaker J C
An EM algorithm for obtaining maximum likelihood estimates in the multi-phenotype variance components linkage model.
Annals of human genetics | 2000-07-01 | PMID 11246476
Iturria S J, Blangero J
Plasma tumor necrosis factor alpha levels and the -238*A promoter polymorphism in patients with antiphospholipid syndrome.
Thrombosis and haemostasis | 2001-02-01 | PMID 11246532
Bertolaccini M L, Atsumi T, Lanchbury J S and 7 more
Genes: TNF
Lack of association between the platelet glycoprotein Ia C807T gene polymorphism and myocardial infarction in Japanese. An approach entailing melting curve analysis with specific fluorescent hybridization probes.
Thrombosis and haemostasis | 2001-02-01 | PMID 11246537
Morita H, Kurihara H, Imai Y and 5 more
The E27 beta2-adrenergic receptor polymorphism reduces the risk of myocardial infarction in dyslipidemic young males.
Thrombosis and haemostasis | 2001-02-01 | PMID 11246538
Sala G, Di Castelnuovo A, Cuomo L and 4 more
F X Nottingham and F X Taunton. Two novel mutations in factor X resulting in loss of functional activity and an interpretation using molecular modelling.
Thrombosis and haemostasis | 2001-02-01 | PMID 11246545
Deam S, Srinivasan N, Westby J and 2 more
Family history of coronary heart disease, a strong risk factor for myocardial infarction interacting with other cardiovascular risk factors: results from the Stockholm Heart Epidemiology Program (SHEEP).
Epidemiology (Cambridge, Mass.) | 2001-03-01 | PMID 11246583
Leander K, Hallqvist J, Reuterwall C and 2 more
Treatment with interferon-alpha2b of naive non-cirrhotic patients with chronic hepatitis C according to viraemia and genotype. Results of a randomized multicentre study. The North West Italian Hepatological Group.
European journal of gastroenterology & hepatology | 2001-02-01 | PMID 11246614
Saracco G, Ciancio A, Ghisetti V and 17 more
HLA-DRB1 alleles encoding an aspartic acid at position 70 protect against development of rheumatoid arthritis.
The Journal of rheumatology | 2001-02-01 | PMID 11246655
Mattey D L, Dawes P T, Gonzalez-Gay M A and 4 more
Effects of inherited thrombophilic mutations in an adolescent with antiphospholipid syndrome and systemic lupus erythematosus.
The Journal of rheumatology | 2001-02-01 | PMID 11246680
Higginbotham E A, Zimmerman S A, Howard T A and 3 more
Defective function of Fas in patients with type 1 diabetes associated with other autoimmune diseases.
Diabetes | 2001-03-01 | PMID 11246866
DeFranco S, Bonissoni S, Cerutti F and 10 more
Genes: TYR
Multipotential nestin-positive stem cells isolated from adult pancreatic islets differentiate ex vivo into pancreatic endocrine, exocrine, and hepatic phenotypes.
Diabetes | 2001-03-01 | PMID 11246871
Zulewski H, Abraham E J, Gerlach M J and 6 more
A genome-wide scan for abdominal fat assessed by computed tomography in the Québec Family Study.
Diabetes | 2001-03-01 | PMID 11246882
Pérusse L, Rice T, Chagnon Y C and 9 more
Glucokinase gene locus transgenic mice are resistant to the development of obesity-induced type 2 diabetes.
Diabetes | 2001-03-01 | PMID 11246883
Shiota M, Postic C, Fujimoto Y and 7 more
A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarction.
Diabetes | 2001-03-01 | PMID 11246885
Vaessen N, Heutink P, Janssen J A and 7 more
A gene conferring susceptibility to type 2 diabetes in conjunction with obesity is located on chromosome 18p11.
Diabetes | 2001-03-01 | PMID 11246890
Parker A, Meyer J, Lewitzky S and 10 more
A genome scan for type 2 diabetes susceptibility loci in a genetically isolated population.
Diabetes | 2001-03-01 | PMID 11246891
Permutt M A, Wasson J C, Suarez B K and 10 more
Evidence for gene-nutrient interaction at the PPARgamma locus.
Diabetes | 2001-03-01 | PMID 11246892
Luan J, Browne P O, Harding A H and 4 more
In vitro and in vivo studies of a naturally occurring variant of the human p85alpha regulatory subunit of the phosphoinositide 3-kinase: inhibition of protein kinase B and relationships with type 2 diabetes, insulin secretion, glucose disappearance constant, and insulin sensitivity.
Diabetes | 2001-03-01 | PMID 11246893
Hansen L, Zethelius B, Berglund L and 6 more
Mutations in the coding region of the neurogenin 3 gene (NEUROG3) are not a common cause of maturity-onset diabetes of the young in Japanese subjects.
Diabetes | 2001-03-01 | PMID 11246894
del Bosque-Plata L, Lin J, Horikawa Y and 7 more
Genes: NEUROG3
Decreased fasting and oral glucose stimulated C-peptide in nondiabetic subjects with sequence variants in the sulfonylurea receptor 1 gene.
Diabetes | 2001-03-01 | PMID 11246895
Weisnagel S J, Rankinen T, Nadeau A and 4 more
Genes: INS
Functional status, medical impairments, and rehabilitation resources in 84 females with Rett syndrome: a snapshot across the world from the parental perspective.
Disability and rehabilitation | 2000-01-01 | PMID 11247006
Leonard H, Fyfe S, Leonard S and 1 more
Rett syndrome: clinical characteristics and recent genetic advances.
Disability and rehabilitation | 2000-01-01 | PMID 11247014
Ellaway C, Christodoulou J
Genes: MECP2
Cadmium biosorption by a cadmium resistant strain of Bacillus thuringiensis: regulation and optimization of cell surface affinity for metal cations.
Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine | 2000-12-01 | PMID 11247032
El-Helow E R, Sabry S A, Amer R M
New synthetic catecholate-type siderophores based on amino acids and dipeptides.
Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine | 2000-12-01 | PMID 11247040
Schnabelrauch M, Wittmann S, Rahn K and 3 more
[The human genome project as a scientific background of preventive medicine].
Vestnik Rossiiskoi akademii meditsinskikh nauk | 2000-01-01 | PMID 11247123
Baranov V S
[Identification of mutation and polymorphic changes in the CFTR gene of patients with obstructive azoospermia].
Wiadomosci lekarskie (Warsaw, Poland : 1960) | 2000-01-01 | PMID 11247407
Sobczyńska-Tomaszewska A, Wolski J K, Bal J
Genes: CFTR
Protein phosphatase 2A: identification in Oryza sativa of the gene encoding the regulatory A subunit.
Plant molecular biology | 2001-01-01 | PMID 11247601
Yu S, Lei H, Chang W and 2 more
Genes: RPA1
The brassica MIP-MOD gene encodes a functional water channel that is expressed in the stigma epidermis.
Plant molecular biology | 2001-01-01 | PMID 11247606
Dixit R, Rizzo C, Nasrallah M and 1 more
Genes: MIP
Polymorphisms/mutations of TCR-zeta-chain promoter and 3' untranslated region and selective expression of TCR zeta-chain with an alternatively spliced 3' untranslated region in patients with systemic lupus erythematosus.
Journal of autoimmunity | 2001-03-01 | PMID 11247639
Nambiar M P, Enyedy E J, Warke V G and 4 more
Genetic diversity of the human serotonin receptor 1B (HTR1B) gene.
Genomics | 2001-02-15 | PMID 11247661
Sanders A R, Cao Q, Taylor J and 13 more
Linkage and allelic association of chromosome 5 cytokine cluster genetic markers with atopy and asthma associated traits.
Genomics | 2001-02-15 | PMID 11247662
Walley A J, Wiltshire S, Ellis C M and 1 more
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia.
Genomics | 2001-02-15 | PMID 11247663
Bartoloni L, Blouin J L, Maiti A K and 14 more
Genes: DNAH9
Cloning and characterization of SLC26A6, a novel member of the solute carrier 26 gene family.
Genomics | 2001-02-15 | PMID 11247665
Waldegger S, Moschen I, Ramirez A and 4 more
High-resolution mapping of the blood pressure QTL on chromosome 7 using Dahl rat congenic strains.
Genomics | 2001-02-15 | PMID 11247666
Cicila G T, Garrett M R, Lee S J and 3 more
A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice.
Genomics | 2001-02-15 | PMID 11247667
Rieger D K, Reichenberger E, McLean W and 2 more
A chromosome 15 quantitative trait locus controls levels of radiation-induced jejunal crypt cell apoptosis in mice.
Genomics | 2001-02-15 | PMID 11247668
Weil M M, Xia C, Xia X and 3 more
Disruption of Apc10/Doc1 in three alleles of oligosyndactylism.
Genomics | 2001-02-15 | PMID 11247669
Pravtcheva D D, Wise T L
Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysis.
Genomics | 2001-02-15 | PMID 11247670
Wines M E, Lee L, Katari M S and 7 more
Molecular cloning of a novel member of the GLUT family of transporters, SLC2a10 (GLUT10), localized on chromosome 20q13.1: a candidate gene for NIDDM susceptibility.
Genomics | 2001-02-15 | PMID 11247674
McVie-Wylie A J, Lamson D R, Chen Y T
Investigation of aciclovir-resistant herpes simplex virus I infection in a bone marrow transplantation unit: genotyping shows that different strains are involved.
The Journal of hospital infection | 2001-03-01 | PMID 11247677
Venard V, Dauendorffer J N, Carret A S and 4 more
Genetic and diurnal variation in the juvenile hormone titer in a wing-polymorphic cricket: implications for the evolution of life histories and dispersal.
Physiological and biochemical zoology : PBZ | 2000-01-01 | PMID 11247748
Zera A J, Cisper G
Enhanced central response to dehydration in mice lacking angiotensin AT(1a) receptors.
American journal of physiology. Regulatory, integrative and comparative physiology | 2001-04-01 | PMID 11247842
Morris M, Means S, Oliverio M I and 1 more
Genes: ANG
Skeletal muscle calcineurin: influence of phenotype adaptation and atrophy.
American journal of physiology. Regulatory, integrative and comparative physiology | 2001-04-01 | PMID 11247852
Spangenburg E E, Williams J H, Roy R R and 1 more
Differences between female and male patients with familial rheumatoid arthritis.
Annals of the rheumatic diseases | 2001-04-01 | PMID 11247876
Laivoranta-Nyman S, Luukkainen R, Hakala M and 5 more
Association of the interleukin 1 receptor antagonist gene with ulcerative colitis in Northern European Caucasians.
Gut | 2001-04-01 | PMID 11247888
Carter M J, di Giovine F S, Jones S and 4 more
Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneity.
Gut | 2001-04-01 | PMID 11247895
Scott R J, Meldrum C, Crooks R and 4 more
Genes: FAP, APC
Can APC mutation analysis contribute to therapeutic decisions in familial adenomatous polyposis? Experience from 680 FAP families.
Gut | 2001-04-01 | PMID 11247896
Friedl W, Caspari R, Sengteller M and 10 more
Genes: APC, FAP
Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins.
Gut | 2001-04-01 | PMID 11247900
Amann S T, Gates L K, Aston C E and 2 more
CNTF genotype is associated with muscular strength and quality in humans across the adult age span.
Journal of applied physiology (Bethesda, Md. : 1985) | 2001-04-01 | PMID 11247915
Roth S M, Schrager M A, Ferrell R E and 5 more
Genes: CNTF
Angiogenin gene-race interaction for resting and exercise BP phenotypes: the HERITAGE Family Study.
Journal of applied physiology (Bethesda, Md. : 1985) | 2001-04-01 | PMID 11247919
Rivera M A, Echegaray M, Rankinen T and 8 more
Selected contribution: variation in acute hypoxic ventilatory response is linked to mouse chromosome 9.
Journal of applied physiology (Bethesda, Md. : 1985) | 2001-04-01 | PMID 11247969
Tankersley C G
Male fertility defects in mice lacking the serine protease inhibitor protease nexin-1.
Proceedings of the National Academy of Sciences of the United States of America | 2001-03-13 | PMID 11248026
Murer V, Spetz J F, Hengst U and 3 more