Nanopublications

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

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NP347405.RAZAmTr2mLZ9L8f-a6_j8QRsSH7-8PW8CQl0T4YyunfAw130_assertion description "[A heterozygous TGC to CGC mutation of codon 634 (cysteine to arginine) was found in the PHAEO and medullary thyroid cancer from the MEN 2A patient.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347405.RAZAmTr2mLZ9L8f-a6_j8QRsSH7-8PW8CQl0T4YyunfAw130_provenance.
NP347407.RAc3jxjyFAR7mW0qVxekuWpO8-cT7eEnp5tNrRLpeMKkk130_assertion description "[CTLA-4 and autoimmune thyroid disease: lack of influence of the A49G signal peptide polymorphism on functional recombinant human CTLA-4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347407.RAc3jxjyFAR7mW0qVxekuWpO8-cT7eEnp5tNrRLpeMKkk130_provenance.
NP347413.RAUZ1mAkT1Ltt1io-G1BL4yHzkk5PbJlsq3WJ2dxRpcsA130_assertion description "[Activation of p38 MAPK is a key pathway for cell proliferation and differentiation in breast cancer and thyroid cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347413.RAUZ1mAkT1Ltt1io-G1BL4yHzkk5PbJlsq3WJ2dxRpcsA130_provenance.
NP347417.RAeYex3UraaDQyrU69lHeEHtNzdR98z7JuGo6WsoYMObM130_assertion description "[Associations of the ATP-binding cassette transporter A1 R219K polymorphism with HDL-C level and coronary artery disease risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347417.RAeYex3UraaDQyrU69lHeEHtNzdR98z7JuGo6WsoYMObM130_provenance.
NP347424.RAa2GcR2er4AxWfRxBb3pqsFv58lOrHX5Qe7m0uNbY_GE130_assertion description "[Sp1 is regulated by oxidative stress, and Sp1 mRNA was found to be upregulated in AD cortex and hippocampus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347424.RAa2GcR2er4AxWfRxBb3pqsFv58lOrHX5Qe7m0uNbY_GE130_provenance.
NP347426.RAYuE7u5lFNfON7X2t2SMrWpB04SvTbznZcBHCklZUKMQ130_assertion description "[The aryl hydrocarbon receptor as a target for estrogen receptor-negative breast cancer chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347426.RAYuE7u5lFNfON7X2t2SMrWpB04SvTbznZcBHCklZUKMQ130_provenance.
NP347433.RATO1q49VhD3angwe-_XqIJPndhUaEOhsV39wSuomQ3iQ130_assertion description "[We report a child whose hypothyroidism was recognized clinically at age 6 weeks, and subsequently found to have GH and Prl as well as TSH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347433.RATO1q49VhD3angwe-_XqIJPndhUaEOhsV39wSuomQ3iQ130_provenance.
NP347434.RATerFzA6z6TDM6Ujopvhr5eC7aUnY15kAoE8NTeXsTOg130_assertion description "[Recent data indicate that the up-regulation of coxsackievirus and adenovirus receptor (CAR) in viral cardiomyopathy contributes to viral infection as a key factor in the pathogenesis of this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347434.RATerFzA6z6TDM6Ujopvhr5eC7aUnY15kAoE8NTeXsTOg130_provenance.
NP347435.RAX5pGIevlEyyTY-Lij5wYsPQwfIzMnYE9nudn8NiFMsY130_assertion description "[We screened CANT1 and CHST3 in 38 DD cases (6 type 1 patients, 1 Kim variant, and 31 type 2 patients) and found CANT1 mutations in all DD type 1 cases, the Kim variant and in one atypical DD type 2 expanding the clinical spectrum of hand anomalies observed with CANT1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347435.RAX5pGIevlEyyTY-Lij5wYsPQwfIzMnYE9nudn8NiFMsY130_provenance.
NP347437.RAULVHG0irA7Iw65s93OaYaJ_ti-o4msHmuV70Rtb15pc130_assertion description "[Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347437.RAULVHG0irA7Iw65s93OaYaJ_ti-o4msHmuV70Rtb15pc130_provenance.
NP347446.RAdw9_-0UhP3KjsrQkZDqDE44dqyli93eL4WcrNTiyXG4130_assertion description "[We conclude that thiamine deficiency was commonly present in the alcoholic patients, and that a subgroup of patients may be predisposed to more severe brain damage as a consequence of abnormalities in the transketolase protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347446.RAdw9_-0UhP3KjsrQkZDqDE44dqyli93eL4WcrNTiyXG4130_provenance.
NP347449.RAZkU532yH6cYQqlN7DMEVhf5oD-N_yQq-cwP0GjO4VR0130_assertion description "[Contrariwise, DNA methylation prevents CTCF binding to FXS alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347449.RAZkU532yH6cYQqlN7DMEVhf5oD-N_yQq-cwP0GjO4VR0130_provenance.
NP347450.RAbhbQyIVw6ddw3La1Je5AcAbS6piRK0fPnp-5phdve54130_assertion description "[GeXP assay permitted measurement of changes in gene expression of cytokines in response to insulin and adiponectin, indicating the potential for insulin and adiponectin regulation of mediators of inflammation associated with early events in colon carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347450.RAbhbQyIVw6ddw3La1Je5AcAbS6piRK0fPnp-5phdve54130_provenance.
NP347455.RAUfpE2GWL8QXhAYTrYRFf0gIz5xCO_CbY9aE4xXgNhF8130_assertion description "[It is speculated that 15d-PGJ(2), once effluxed through MRP, liberates from the GSH conjugate, and the free 15d-PGJ(2) re-enters the cell and forms the GSH conjugate again.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347455.RAUfpE2GWL8QXhAYTrYRFf0gIz5xCO_CbY9aE4xXgNhF8130_provenance.
NP347462.RAWW30NIR2ntJEbAjK1qOqT1REFfaW05t9L_VF1YbXnDc130_assertion description "[The contribution of the BACH1 gene to the pathophysiology of trisomy or monosomy 21 is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347462.RAWW30NIR2ntJEbAjK1qOqT1REFfaW05t9L_VF1YbXnDc130_provenance.
NP347464.RARVu6yEbtyjRnsvJVpuxdIvui0rh8z33zW0xIMSTUNOk130_assertion description "[In this study, the synergistic effect of XAF1 and TRAIL on colon cancer growth was investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347464.RARVu6yEbtyjRnsvJVpuxdIvui0rh8z33zW0xIMSTUNOk130_provenance.
NP347474.RAeOA5PS5UB3ZmVooDLxd-CxcTAK133n0VSeFg4dBMYS8130_assertion description "[We have recently mapped this sex reversal locus, DSS, to a 160-kb region of Xp21 that includes the adrenal hypoplasia congenita locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347474.RAeOA5PS5UB3ZmVooDLxd-CxcTAK133n0VSeFg4dBMYS8130_provenance.
NP347480.RAZA0447AQe4x2uXUEx344vE7xukfGP4Esv1WhTC5-uPQ130_assertion description "[These findings provide evidence that Sema4D/Plexin-B1-mediated NF-κB activation and IL-8 production is critical in the generation a pro-angiogenic phenotype in endothelial cells and suggests a new therapeutic target for the anti-angiogenic treatment of some cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347480.RAZA0447AQe4x2uXUEx344vE7xukfGP4Esv1WhTC5-uPQ130_provenance.
NP347487.RAQVMWN5es_zfZyT-BCxBYP1NcM5e6SmnJnKAJHKHDoiM130_assertion description "[BACE was expressed in specific areas in the cortex, hippocampus, cerebellum, pons, and spinal cord.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347487.RAQVMWN5es_zfZyT-BCxBYP1NcM5e6SmnJnKAJHKHDoiM130_provenance.
NP347489.RAQWv1J730c_7WNNIT-T4uzuPEFkFViHKcfvg9OgVQmHo130_assertion description "[Cytogenetic studies on a 17-year-old phenotypic male, with short stature and clinical and hormonal features of hypogonadism similar to those of an XX male, revealed an X;Y translocation, karyotype, 46,Xt(X;Y)(p22;?p11?q11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347489.RAQWv1J730c_7WNNIT-T4uzuPEFkFViHKcfvg9OgVQmHo130_provenance.
NP347492.RAYNui1IONgNq198iS9-TlU4QSswqEKRqWA6pShKfeAlY130_assertion description "[The results suggest that IAP overexpression may be associated with Fe-NTA-induced renal cortical tubular damage and regeneration that lead to a polycystic state, and with tumor progression and metastasis of the induced RCCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347492.RAYNui1IONgNq198iS9-TlU4QSswqEKRqWA6pShKfeAlY130_provenance.
NP347495.RAS0liJu_gCGTsUQLAEeawOu57gbW0VRlfqpI8hz4b0wk130_assertion description "[The role of enoyl-CoA hydratase short chain 1 and peroxiredoxin 3 in PP2-induced apoptosis in human breast cancer MCF-7 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347495.RAS0liJu_gCGTsUQLAEeawOu57gbW0VRlfqpI8hz4b0wk130_provenance.
NP347503.RAdUmwAFzqQSiu7Y_zqWXpCx5ZjaSCflSYtaItP9KLVZk130_assertion description "[The association of COMT genotype with psychological distress may be of importance as identifying subgroups is a challenge in the diagnosis and treatment of fibromyalgia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347503.RAdUmwAFzqQSiu7Y_zqWXpCx5ZjaSCflSYtaItP9KLVZk130_provenance.
NP347505.RAaK-TEvgDylA6mhTSOWtt5xwRSp3wADswNOR6eld4IPM130_assertion description "[C-terminal deletions in the ALAS2 gene lead to gain of function and cause X-linked dominant protoporphyria without anemia or iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347505.RAaK-TEvgDylA6mhTSOWtt5xwRSp3wADswNOR6eld4IPM130_provenance.
NP347508.RARYrsYWNMtFkZwoiaY67YhgFQLsAEQg43ct0iqd7Ts9M130_assertion description "[The main goal of the present study was to elucidate the functional implications of six homozygous mutations (G193R, A267S, G319R, A508T, del526N, and Y998X) in the bumetanide-sensitive Na-K-2Cl cotransporter (hNKCC2) identified in patients diagnosed with BS type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347508.RARYrsYWNMtFkZwoiaY67YhgFQLsAEQg43ct0iqd7Ts9M130_provenance.
NP347511.RAds1jJ4P4cLaAyfCPLb0hr0WOWtc5C0zihj1giE0o6QY130_assertion description "[New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of Siemens.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347511.RAds1jJ4P4cLaAyfCPLb0hr0WOWtc5C0zihj1giE0o6QY130_provenance.
NP347518.RAYYlqiMLHB9giokFzlcjQ7Z5fAOxi0Ug542sEN_qytqk130_assertion description "[The frequencies of seven NAT2 point mutations, namely G191A, C282T, T341C, C481T, G590A, A803G, and G857A, and genotypes were determined by PCR/RFLP in a total of 70 patients with allergic contact dermatitis to PPD and 100 control subjects with no history of allergy, atopy, lung disease, diabetes mellitus and cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347518.RAYYlqiMLHB9giokFzlcjQ7Z5fAOxi0Ug542sEN_qytqk130_provenance.
NP347522.RAXAsrMEwlvdTvh_z6yVe7_6kqvoaDWTOf0iy6kG6Rk10130_assertion description "[The discovery in 1986 of a plasma protein termed LPS binding protein (LBP) led to the discovery of unanticipated mechanisms of LPS-induced cell activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347522.RAXAsrMEwlvdTvh_z6yVe7_6kqvoaDWTOf0iy6kG6Rk10130_provenance.
NP347529.RAWpNtXqJoy3aiJcDlccMIJI-BAGDjersNXnTSLoewwbU130_assertion description "[Three other genes implicated for ARVC, plakoglobin (Naxos disease), desmoplakin (ARVC8) and plakophilin (ARVC9) have prompted the speculation that ARVC is primarily a disease of desmosomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347529.RAWpNtXqJoy3aiJcDlccMIJI-BAGDjersNXnTSLoewwbU130_provenance.
NP347533.RAbOlc1sP0nbU8VR9UnxfJPPHXQqDL9nJB91Q7mQ6O2fk130_assertion description "[The expression levels of spermine anabolic enzymes: ornithine decarboxylase (ODC1) and S-adenosylmethionine decarboxylase (AMD1) in benign epithelia surrounding cancer glands was logarithmically reduced with the increase of Vpsa (ODC1, p < 0.016; AMD1, p < 0.048), and antizyme (OAZ1) expression in cancer cells was increased with the increase of Vpsa (p < 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347533.RAbOlc1sP0nbU8VR9UnxfJPPHXQqDL9nJB91Q7mQ6O2fk130_provenance.
NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_assertion description "[To elucidate the specific role of the TT genotype of MTHFR in the development of cerebral infarction with and without cognitive impairment, we determined the prevalence of hyperhomocyst(e)inemia and the C677T genotypes of MTHFR in 143 patients with vascular dementia, 122 patients with cerebral infarction, and 217 healthy subjects matched for age and sex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347540.RAWet9LNQA5zLWffVWpY1RY3iNDcGVnQJW2R5T2YAkUKo130_provenance.
NP347549.RAVR5Q6sv1G4Lbex2jcOzPENRBbvbhon9yML_KmQBXd1g130_assertion description "[Inhibition of PKA activity by PKI(5-22) or H-89 failed to attenuate homologous desensitization of CRF1 receptors, and direct activation of PKA by forskolin or dibutyryl cAMP failed to desensitize CRF-induced cAMP accumulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347549.RAVR5Q6sv1G4Lbex2jcOzPENRBbvbhon9yML_KmQBXd1g130_provenance.
NP347551.RAeQtdzNFaRak30FUDHAqnfizhBMUQstU3Hq8ZGYv5ypo130_assertion description "[The associations with MICA and MICB cannot be accounted for by linkage disequilibrium with the HLA class II locus indicating a role in genetic susceptibility to leprosy that is independent of HLA-DRB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347551.RAeQtdzNFaRak30FUDHAqnfizhBMUQstU3Hq8ZGYv5ypo130_provenance.
NP347556.RAaw4taIeufTUMnYOJog57GptEaa52lmPvcMqegf87OyU130_assertion description "[We evaluated chromosome aberrations (CAs) in lymphocytes of 200 workers exposed to organic solvents and 200 referents and the influence of polymorphisms in xenobiotic-metabolism (CYP2E1, GSTM1 and GSTT1) and in DNA repair genes (XRCC1(194) Arg/Trp, XRCC1(280) Arg/His, XRCC1(399) Arg/Gln and XRCC3(241) Thr/Met).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347556.RAaw4taIeufTUMnYOJog57GptEaa52lmPvcMqegf87OyU130_provenance.
NP347559.RAXgMC_RculuPI859Y572aSt3D1fcOldDL8brXPdnVivM130_assertion description "[The super elongation complex (SEC) consists of the RNA polymerase II (Pol II) elongation factors eleven-nineteen Lys-rich leukaemia (ELL) proteins, positive transcription elongation factor b (P-TEFb) and several frequent mixed lineage leukaemia (MLL) translocation partners.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347559.RAXgMC_RculuPI859Y572aSt3D1fcOldDL8brXPdnVivM130_provenance.
NP347569.RAUYHecKjsAUcGesPQEVRxcIFFkXbFGcu1xwssl1opTqo130_assertion description "[To analyze the mechanisms responsible for inhibitor development in such patients, we characterized FVIII-specific CD4(+) T-cell clones derived from a mild hemophilia A patient carrying an Arg2150His substitution in the C1 domain and who presented with a high titer inhibitor toward normal but not self-FVIII.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347569.RAUYHecKjsAUcGesPQEVRxcIFFkXbFGcu1xwssl1opTqo130_provenance.
NP347572.RAdPG-Gld8VGixVdyjYKn7wFVQ9-SOyPm6KE_HIrwAzm4130_assertion description "[These results suggest that KDR, FLT-1, PlGF and TIE1 mRNAs are present in the mesenchymal cells of RCC, while VEGF and FGFR-4 genes are expressed in RCC cells themselves in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347572.RAdPG-Gld8VGixVdyjYKn7wFVQ9-SOyPm6KE_HIrwAzm4130_provenance.
NP347576.RAZIAYlwDavA_ldN47EGMLxT3VuoBbkL9YiLXjLtPFDqk130_assertion description "[The findings in this study unravel new ERG-directed molecular signals that may contribute to the resistance of current therapies in acute leukemia patients with poor prognosis characterized by high ERG mRNA expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347576.RAZIAYlwDavA_ldN47EGMLxT3VuoBbkL9YiLXjLtPFDqk130_provenance.
NP347580.RAZzYE4_QNPHFmxZrZyknzGd9LLr-MHMaYogMCVNO2H0Y130_assertion description "[Polymorphisms in key metabolizing enzymes modified DBP-associated bladder cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347580.RAZzYE4_QNPHFmxZrZyknzGd9LLr-MHMaYogMCVNO2H0Y130_provenance.
NP347584.RAU8gSwWJg8X_ysN0XuekDNv1SL2E4-2MoOn2PLDGF0to130_assertion description "[The X(+),D haplotype of APOB is associated with increased risk for development of GBC and the risk is not modified in the presence of gallstones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347584.RAU8gSwWJg8X_ysN0XuekDNv1SL2E4-2MoOn2PLDGF0to130_provenance.
NP347585.RAc1fd5G5J-jtyWahM_1kTL-rlu1I-czi_57fWJbWJWGk130_assertion description "[Biologic markers resulting from genetic lesions in lung cancer are grouped as follows: (a) oncogene amplification and overexpression (aberrant gene expression) and mutated tumor suppressor genes -- ras gene, myc gene, HER-2/neu and survivin gene, p53 and mutated beta-tubulin gene; (b) tumor biologic/radiobiologic factors -- tumor cell proliferation kinetics, hypoxia, intrinsic cellular radiosensitivity, gamma factor, and DNA content; (c) enzymes and hormones: neuron-specific enolase, serum lactate dehydrogenase, and enhanced glucose metabolic rate supported by increased glucose transporter protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347585.RAc1fd5G5J-jtyWahM_1kTL-rlu1I-czi_57fWJbWJWGk130_provenance.
NP347586.RAcgh7u3-n9bpGcJlZoB8c3V8_UdidUyUSp1LkFF032mc130_assertion description "[We have shown previously that metastatic tumors of human colorectal cancer in lung as compared to liver have high levels of thymidylate synthase (TS) mRNA expression that correlated with high levels of E2F-1 mRNA expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347586.RAcgh7u3-n9bpGcJlZoB8c3V8_UdidUyUSp1LkFF032mc130_provenance.
NP347588.RAY0ANETAtwm9noysGEqKUu4rS8C2s8nDe161gxFlVQDs130_assertion description "[bFGF, IL-8, and EGFR appear to be upregulated in early precursor lesions (CIS), whereas VEGF appears to be upregulated at later stages in the development of muscle-invasive TCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347588.RAY0ANETAtwm9noysGEqKUu4rS8C2s8nDe161gxFlVQDs130_provenance.
NP347591.RAaY93P8MSX5m-p2yK-3LA72WEKCzfnSeRG8cAINYqOOI130_assertion description "[Previous studies suggest that a single-nucleotide polymorphism (SNP) in the promoter of the ODC gene (rs2302615) may be associated with adenoma risk and/or response to aspirin chemoprevention.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347591.RAaY93P8MSX5m-p2yK-3LA72WEKCzfnSeRG8cAINYqOOI130_provenance.
NP347594.RAUD4oMK30timcpgNA1Om39mwl-1RzI5GgBUT8KMLqaio130_assertion description "[Up-regulation of activating transcription factor-5 suppresses SAP expression to activate T cells in hemophagocytic syndrome associated with Epstein-Barr virus infection and immune disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347594.RAUD4oMK30timcpgNA1Om39mwl-1RzI5GgBUT8KMLqaio130_provenance.
NP347595.RAQoazBqSwvvE8wIKwPAlAyvw467O6WN26o-Gefs1NLE8130_assertion description "[At present, it is unclear how the interaction between TF and FVIIa influences the development of metastasis in colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347595.RAQoazBqSwvvE8wIKwPAlAyvw467O6WN26o-Gefs1NLE8130_provenance.
NP347605.RAViewUKlg31CNdxfoMctBGzJD6hbF6s7z3lVPsEWka_g130_assertion description "[We studied the influence of the MTRR 66A>G polymorphism on CHD risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347605.RAViewUKlg31CNdxfoMctBGzJD6hbF6s7z3lVPsEWka_g130_provenance.
NP347615.RAStUccu6VCxS3nvA4C3LJRb7WYm3bS43igFpLcJmeKlI130_assertion description "[There were 407 patients in the study sample (TD = 252; non-TD = 155) and seven single nucleus polymorphisms (SNPs) in the RGS9 gene were genotyped for each subject.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347615.RAStUccu6VCxS3nvA4C3LJRb7WYm3bS43igFpLcJmeKlI130_provenance.
NP347621.RAWmS02rdgywW2iP6gD-IDlG4vz1-OMfTe-vvleANEPoo130_assertion description "[These findings suggest that an inherited or acquired genomic defect of m-GDH in lymphocytes, and possibly in pancreatic B-cells, may participate to the pathogenesis of non-insulin-dependent diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347621.RAWmS02rdgywW2iP6gD-IDlG4vz1-OMfTe-vvleANEPoo130_provenance.
NP347629.RAS7nALXBczuzvHSKJZEPQqezFi7y3vlmrTHPgI66zoxg130_assertion description "[The IKZF1 deletion also was identified in the progression of chronic myeloid leukemia to lymphoid blast crisis (66%) but never in myeloid blast crisis or chronic-phase chronic myeloid leukemia or in patients with acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347629.RAS7nALXBczuzvHSKJZEPQqezFi7y3vlmrTHPgI66zoxg130_provenance.
NP347632.RAeBkWnakk54SFWhtidx-ROiO41D5ZVlWo-BBEtOqe0sg130_assertion description "[Identification of a human mutation of DMT1 in a patient with microcytic anemia and iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347632.RAeBkWnakk54SFWhtidx-ROiO41D5ZVlWo-BBEtOqe0sg130_provenance.
NP347633.RATy6Fd59ZqWGbY-2qGzHACPGilwkaL3zV_tTSWGXNtVQ130_assertion description "[Expression of p63 (TA and deltaN isoforms) in human primary well differentiated buccal carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347633.RATy6Fd59ZqWGbY-2qGzHACPGilwkaL3zV_tTSWGXNtVQ130_provenance.
NP347635.RAUVfzPc2Rrp3LEqt_zPw9LBorHrVzPgzJTsXMxloyFTA130_assertion description "[Several studies in the last decade have highlighted the role of the type I interferon (IFN-I) pathway, and particularly interferon alpha (IFNα) in SLE pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347635.RAUVfzPc2Rrp3LEqt_zPw9LBorHrVzPgzJTsXMxloyFTA130_provenance.
NP347641.RATE96Evt5o8jyeXIDwStOHg1uyXSdBMa4g6MpPDKt45I130_assertion description "[Deletion of chromosome 11p15, p12, q22, q23-24 loci in human prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347641.RATE96Evt5o8jyeXIDwStOHg1uyXSdBMa4g6MpPDKt45I130_provenance.
NP347644.RAXjZFzlaPOOqMg0G9SYd-gRjUMwDFImfpt1jWCmFqf2Q130_assertion description "[In this study, we evaluate the value of identifying MAML2 rearrangement by fluorescence in situ hybridization (FISH) to distinguish TMEC from poorly differentiated squamous cell carcinoma and adenosquamous carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347644.RAXjZFzlaPOOqMg0G9SYd-gRjUMwDFImfpt1jWCmFqf2Q130_provenance.
NP347646.RAWHbYS9LZNIkIuIRXlM_8mF6YXRpfO9w91GYV_ecX9qk130_assertion description "[Familial adenomatous polyposis (FAP), which includes familial polyposis coli (FPC) and the Gardner syndrome (GS), is a genetically determined premalignant disease of the colon inherited by a locus (APC) mapping within 5q15-q22.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347646.RAWHbYS9LZNIkIuIRXlM_8mF6YXRpfO9w91GYV_ecX9qk130_provenance.
NP347657.RATK8IZmuPpUHBJ_TC9_cXlH1MRHe39zc6y9QkQ8bIrzk130_assertion description "[These results suggest that overexpression of enzymatically active PN1 may play a pathogenic role in the development of the scleroderma phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347657.RATK8IZmuPpUHBJ_TC9_cXlH1MRHe39zc6y9QkQ8bIrzk130_provenance.
NP347659.RAXfuB6hynpvo3Z9v4mvqjpSkOMq6v6DALv1w7w5jHVTY130_assertion description "[Analysis with quantitative real-time PCR and gene-specific assays showed higher expression of neuropilin-2 (NRP2) and VEGF-receptor-3 (VEGFR-3) mRNAs in vascular malformations (VascM) as compared to infantile hemangiomas (Hem).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347659.RAXfuB6hynpvo3Z9v4mvqjpSkOMq6v6DALv1w7w5jHVTY130_provenance.
NP347660.RAacP9heQLcOSHW0KU_M4ThfajGwg-9vwPw0LTZwCbOM0130_assertion description "[First, we survey the SNPs and genes identified as genetic markers that are correlated and associated with the drug efficacy of antidepressants in the Sequenced Treatment Alternatives for Depression (STAR*D) study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347660.RAacP9heQLcOSHW0KU_M4ThfajGwg-9vwPw0LTZwCbOM0130_provenance.
NP347661.RAW-iL4OvYmlkHkEcihW6sqK_rK-TPo2CUMMmJorWauYY130_assertion description "[Aquaporin 4, Kir4.1 and dystrophin 1 were also reduced in autopsied brain tissue from individuals with AD that also display moderate and severe CAA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347661.RAW-iL4OvYmlkHkEcihW6sqK_rK-TPo2CUMMmJorWauYY130_provenance.
NP347663.RAcm2X-kNCGMQXiCzOWxuOC5PewkmaDP5ZftR4XRX-B5o130_assertion description "[Two of these partners, ENL and AF9, code for proteins that are highly similar to each other and as fusions with HRX induce myeloid leukemias in mice as demonstrated by retroviral gene transfer and knock-in experiments, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347663.RAcm2X-kNCGMQXiCzOWxuOC5PewkmaDP5ZftR4XRX-B5o130_provenance.
NP347668.RASblT7vU0Vo6uParCnPM93VZCE5Epyu6nBtMX6IMpR3c130_assertion description "[These results indicate peptide cocktail-treated activated α-type-1 DC-based immunotherapy to be a potential therapeutic tool against recurrent high-grade glioma with mainly HLA-A*2402.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347668.RASblT7vU0Vo6uParCnPM93VZCE5Epyu6nBtMX6IMpR3c130_provenance.
NP347671.RAe88GlQ-2TIRyKEk7_2ergJhwoGHWZxrl6mzEcr7XVFo130_assertion description "[Mutations in the CLCN1 gene, encoding a muscle-specific chloride channel, can cause either recessive or dominant myotonia congenita (MC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347671.RAe88GlQ-2TIRyKEk7_2ergJhwoGHWZxrl6mzEcr7XVFo130_provenance.
NP347676.RAYGAByWL8_WPPY1mSprXLmbJ78tL8RzLJmWhIRW-uTJg130_assertion description "[The presence of the B14,DR1 supratype can be used to predict the presence of `abnormal` DR1 and the clinical status of individuals not previously known to be 21-OH-defL carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347676.RAYGAByWL8_WPPY1mSprXLmbJ78tL8RzLJmWhIRW-uTJg130_provenance.
NP347685.RAephGZhui0D_V4mKKu8S0dy1_qR-4vZuy6fF_ZRmlo2U130_assertion description "[The increased NIS expression and reduced PDS expression may make radioiodine therapy more effective in patients with thyroid cancer, especially when the tumors have no or low uptake of radioiodine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347685.RAephGZhui0D_V4mKKu8S0dy1_qR-4vZuy6fF_ZRmlo2U130_provenance.
NP347693.RAfCl6mtEkQ9I8HqMA3TNuiE7Fondy-m2RIkyPTiPbCCQ130_assertion description "[Association analysis of glutathione-S-transferase P1 (GSTP1) polymorphism with urothelial cancer susceptibility and myelosuppression after M-VAC chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347693.RAfCl6mtEkQ9I8HqMA3TNuiE7Fondy-m2RIkyPTiPbCCQ130_provenance.
NP347696.RAZ4e4G_6-ysqOm_z8sn2Rr8VGVhQshsU13qF2nS0wdXY130_assertion description "[These findings together with the observation that several of these genes have human leukocyte antigen (HLA) class I ligands, have led to a flurry of investigation into how KIR participate in viral infections, autoimmune diseases and malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347696.RAZ4e4G_6-ysqOm_z8sn2Rr8VGVhQshsU13qF2nS0wdXY130_provenance.
NP347699.RATpFlQ_ipwqEP60-0qEbYnzREblrCY7GULBMb8upGDDQ130_assertion description "[Non-syndromic isolated cleft lip with or without cleft palate (NCL/P) is a common congenital anomaly in humans, the aetiology of which is complex and associated with both genetic and environmental factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347699.RATpFlQ_ipwqEP60-0qEbYnzREblrCY7GULBMb8upGDDQ130_provenance.
NP347701.RAUfL3bnlSvn4tAprJ7LvabeO-NXrmsel5d6qzpUSd7IA130_assertion description "[The gene, CRTH2, encoding a receptor for prostaglandin D(2) (PGD(2)), is located within the peak linkage region for asthma on chromosome (Chr.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347701.RAUfL3bnlSvn4tAprJ7LvabeO-NXrmsel5d6qzpUSd7IA130_provenance.
NP347702.RAb-RNiu3AyZf4ekKIXLjjddtrVx6aXjKHlZFfqyPj4p0130_assertion description "[In this study we analyze the frequencies of Leiden Factor V polymorphism (G1691A), and G20210A of prothrombin (FII) in three cohorts of subjects: patients with Alzheimer's disease (unsuccessful aging), nonagenarians (successful aging) and young healthy controls, to assess whether allelic variants associated to the modification of haemostatic system function, may play a role in the protection or susceptibility to Alzheimer disease, as well as to reach a successful aging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347702.RAb-RNiu3AyZf4ekKIXLjjddtrVx6aXjKHlZFfqyPj4p0130_provenance.
NP347704.RASro88tH3eqsZ4QelDOv9f7v23WsryPDnziw2D7SAdT0130_assertion description "[The role of ubiquitin C-terminal hydrolase L1 in neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347704.RASro88tH3eqsZ4QelDOv9f7v23WsryPDnziw2D7SAdT0130_provenance.
NP347707.RAWES1PROx0AwbQY_iVwzsAi7bj4Exvr3YE0upaFFt0jE130_assertion description "[In 2002, The Hunter Family Cancer Service (HFCS) and the HCR developed a system to ensure at risk family members become informed of their risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347707.RAWES1PROx0AwbQY_iVwzsAi7bj4Exvr3YE0upaFFt0jE130_provenance.
NP347710.RASAIBd132V6A-2SlYsfIAlLZhh4EHjqckiUZSInRYUYE130_assertion description "[Loss of function of the G protein-coupled receptor of kisspeptins (GPR54) was recently described as a new cause of isolated hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347710.RASAIBd132V6A-2SlYsfIAlLZhh4EHjqckiUZSInRYUYE130_provenance.
NP347717.RAaoMGTNAy0poIEesb01qYK5HDaNK0RejT-JFs4oGzocU130_assertion description "[We studied duodenal biopsies and blood samples of patients with active CD (Cel) and controls in order to determine the regulatory role proposed for CD30(+) T cells in this Th1-driven disease and the potential influences of IL-15 on CD30 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347717.RAaoMGTNAy0poIEesb01qYK5HDaNK0RejT-JFs4oGzocU130_provenance.
NP347719.RAUp4bc11zsoVvqKbJy3zpUdwOBPpThbo_SB1HSPT9rSo130_assertion description "[Subsequently others have also shown that caspase-8 is silenced by methylation in neuroblastoma and peripheral neural ectodermal tumors, and that the caspase-9 regulator Apaf-1 is silenced by methylation in melanoma cell lines and patient samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347719.RAUp4bc11zsoVvqKbJy3zpUdwOBPpThbo_SB1HSPT9rSo130_provenance.
NP347722.RAZ1Lu2x9dx7PED0cJ4QSNrbe8cjmKv-Rn-lSpH23qelM130_assertion description "[Recently, basal cell carcinoma (BCC) susceptibility genes, human homolog of the Drosophila pathed gene (PTCH), and the xeroderma pigmentosa group A-complementing gene (XPA), have been cloned and localized on chromosome 9q22.3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347722.RAZ1Lu2x9dx7PED0cJ4QSNrbe8cjmKv-Rn-lSpH23qelM130_provenance.
NP347723.RAUGfFHTJ-6xRR6LTUkABXFgGk5oymn_5mr2GufnGHW74130_assertion description "[Low-grade leiomyosarcomas contained more IGF-II mRNAs than myometrium and leiomyoma, fewer type II IGF/mannose 6-phosphate receptors and less IGFBP-3 than myometrium and, in addition, fewer IGF-I mRNAs and type I IGF receptors than leiomyoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347723.RAUGfFHTJ-6xRR6LTUkABXFgGk5oymn_5mr2GufnGHW74130_provenance.
NP347724.RAXWXAo1-lYR8g7upIATPVVATm3PAFvD4HAnN8lN_aEKY130_assertion description "[Six of nine volunteers elicited anti-serovar Typhi lipopolysaccharide (LPS) immunoglobulin A (IgA) antibody-secreting cell (ASC) responses, with three of three vaccinees receiving 10(8) and two of three receiving 10(9) CFU which elicited high-titer LPS-specific serum IgG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347724.RAXWXAo1-lYR8g7upIATPVVATm3PAFvD4HAnN8lN_aEKY130_provenance.
NP347725.RAZdRxzLYkl2XClxyb1Z_2x_jJfcAC5RpV2IO9WKOYpEg130_assertion description "[In this study, we analyzed IGF-II mRNA and protein expression in a series of 80 cases of invasive breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347725.RAZdRxzLYkl2XClxyb1Z_2x_jJfcAC5RpV2IO9WKOYpEg130_provenance.
NP347726.RAcunp6UjUFGPM7YNrp4hmCe8tymTY-vsgYf2mMWSHmis130_assertion description "[The voltage-gated sodium channel Na(V)1.7 is preferentially expressed in peripheral somatic and visceral sensory neurons, olfactory sensory neurons and sympathetic ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347726.RAcunp6UjUFGPM7YNrp4hmCe8tymTY-vsgYf2mMWSHmis130_provenance.
NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_assertion description "[This group of conditions includes Fuchs' endothelial dystrophy of the cornea (FECD), one of the commonest indications for corneal transplantation performed in developed countries, posterior polymorphous dystrophy (PPCD) and the congenital hereditary endothelial dystrophies (CHED).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347738.RAaZumPL2KsdPX-NUdEPo1Z1InyZ7C9Usc9NllSobHSZA130_provenance.
NP347747.RAamb0ciYn3h5pqBtPWDEk5080XdI4SrPnGEDrnMBH7U4130_assertion description "[A total of 2 patients with trisomy 18p with PACAP overexpression and transgenic mice overexpressing PACAP in megakaryocytes have thrombopathy, a mild thrombocytopenia, and a reduced number of mature megakaryocytes in their bone marrow.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347747.RAamb0ciYn3h5pqBtPWDEk5080XdI4SrPnGEDrnMBH7U4130_provenance.
NP347749.RARf4wG45v1Y65fPW-OnlYm4mSnbAxiaX8yVP1NlKBq6A130_assertion description "[The translocation results in the fusion of two known genes, ETV6/TEL(12p13) and AML1(21q22), both of which have been shown to be involved in other hematological malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347749.RARf4wG45v1Y65fPW-OnlYm4mSnbAxiaX8yVP1NlKBq6A130_provenance.
NP347751.RAThUDpmhFmzc0FxikqX_PzHVkzAnDZw0m4fiWJbwMynw130_assertion description "[Evaluation of p53 gene mutation and loss of heterozygosity of 3p, 9p and 17p in precancerous lesions of 29 lung cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347751.RAThUDpmhFmzc0FxikqX_PzHVkzAnDZw0m4fiWJbwMynw130_provenance.
NP347752.RAZDwv5mx7jmniXNSksoFjx8k2Drs2sDS8Gjl-v9KaxYg130_assertion description "[The G-CSFR has also been implicated in the etiology of disease, with mutations/variants of G-CSFR implicated in neutropenia, myelodysplasia and leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347752.RAZDwv5mx7jmniXNSksoFjx8k2Drs2sDS8Gjl-v9KaxYg130_provenance.
NP347755.RAY931E_pklbCHvt0SliQvnnOg2ujud4aJGpcsVjc7X5g130_assertion description "[Neuropathogenic potential of a Southern African HIV-1C isolate (from Zambia; HIV-1C 1084i), a HIV-1C isolate (HIV-1 IndieC1) from Southeast Asia and a HIV-1B isolate (HIV-1 ADA) from the US were tested using in vitro assays to measure neurovirulence and a SCID mouse HIV encephalitis model to measure cognitive deficits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347755.RAY931E_pklbCHvt0SliQvnnOg2ujud4aJGpcsVjc7X5g130_provenance.
NP347757.RAZk9Xd70Kvt34oXE_QhPiLFNcWgKJYNROS4_EZW25aJc130_assertion description "[Chromosome abnormalities in chronic lymphocytic leukemia revealed by TPA as a mitogen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347757.RAZk9Xd70Kvt34oXE_QhPiLFNcWgKJYNROS4_EZW25aJc130_provenance.
NP347758.RAYo58zWoNDagLraiBYZ2DAzngtoYNsecmYTTwtmwjsEU130_assertion description "[Statistical associations with FAB subtypes were found: aCLL and trisomy 12 (P < 0.00001); mantle zone lymphoma (MZL) and t(11;14) (P < 0.00001) and del(6)(q) (P < 0.0001); CLL/mixed cell type and del(6)(q) (P < 0.002); follicular lymphoma and t(14;18) (P < 0.00001); splenic lymphoma with villous lymphocytes and del(7)(q) (P < 0.0004); leukemic lymphoma (LL) with rearrangements in chromosome 9q (P < 0.0001) and trisomy of 3 (P < 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347758.RAYo58zWoNDagLraiBYZ2DAzngtoYNsecmYTTwtmwjsEU130_provenance.
NP347760.RAdOhh3icpG7VZiYjsVQ4deQubQzF3AUgBUDVe-JcTZ0w130_assertion description "[Given the association between blood groups and both activated protein C resistance (APCR) and von Willebrand factor (VWF) levels, post hoc pilot studies on first-trimester APCR and VWF antigen levels and blood group genotypes were performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347760.RAdOhh3icpG7VZiYjsVQ4deQubQzF3AUgBUDVe-JcTZ0w130_provenance.
NP347770.RAYudcfvEAy3qVVtlGg1FnkdyEiBC8JEhGBnY8o8F-RBI130_assertion description "[In the prostate, EMT processes have been implicated in benign prostatic hyperplasia and prostate cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347770.RAYudcfvEAy3qVVtlGg1FnkdyEiBC8JEhGBnY8o8F-RBI130_provenance.
NP347776.RAeIRW7HpfcvytK2D9qsx7xJoSt5SqWueCVBKP2AoNSwY130_assertion description "[This data suggests that mutations in the CRX gene are associated with photoreceptor degeneration and that the Crx protein is necessary for the maintenance of normal cone and rod function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347776.RAeIRW7HpfcvytK2D9qsx7xJoSt5SqWueCVBKP2AoNSwY130_provenance.
NP347778.RAW6dj9RV6amzIm48XiTuvxk-ouSxrMu-lngHUYjWbhoI130_assertion description "[Mechanisms and techniques of reprogramming: using PDX-1 homeobox protein as a novel treatment of insulin dependent diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347778.RAW6dj9RV6amzIm48XiTuvxk-ouSxrMu-lngHUYjWbhoI130_provenance.
NP347785.RAeAl07S0B3pZXNOKHHjv9BDFKCwtRTzr-vLg5ww3cXLQ130_assertion description "[Polymorphism in CYP1A1, GSTMI, GSTT1 genes and organochlorine pesticides in the etiology of hypospadias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347785.RAeAl07S0B3pZXNOKHHjv9BDFKCwtRTzr-vLg5ww3cXLQ130_provenance.
NP347786.RAXTfKnNqhXPd-LGdta32Sic5PNrj7Drl4MfoMcWHahx4130_assertion description "[In this study, we analyzed whether PTCL, NOS with genomic aberrations also has multiple subclones as found in ATLL by means of high-resolution oligo-array comparative genomic hybridization (CGH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347786.RAXTfKnNqhXPd-LGdta32Sic5PNrj7Drl4MfoMcWHahx4130_provenance.
NP347790.RAXWUh7EIxMXWZ7y8ilF0G3z4WUUwT6uTfOx4AaT8_RIc130_assertion description "[The 46 signature genes for EHR included many cell adhesion-related genes (ITGA6, SPP1, DNMBP, CD44 and POSTN), which all showed higher expression in HCC with EHR than in HCC without EHR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347790.RAXWUh7EIxMXWZ7y8ilF0G3z4WUUwT6uTfOx4AaT8_RIc130_provenance.
NP347791.RAfDvdrHB9zhzFP1dqOWR3ELYPHTRi_m_yFT4cZvGzjoM130_assertion description "[Importance of the intracytoplasmic domain of the simian immunodeficiency virus (SIV) envelope glycoprotein for pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347791.RAfDvdrHB9zhzFP1dqOWR3ELYPHTRi_m_yFT4cZvGzjoM130_provenance.
NP347797.RAcBsDtCNVo8rbISmAWcA4yliK7iTwsq3gEqPdlgOSEvs130_assertion description "[Thus, inherited variation in IL1A and ALOX5 seems to affect ovarian cancer risk which, for IL1A, is limited to rarer subtypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347797.RAcBsDtCNVo8rbISmAWcA4yliK7iTwsq3gEqPdlgOSEvs130_provenance.
NP347798.RARixbuRQHmZOS8HaqmvHLb2QIUFunlxvUt81abPEfQ0c130_assertion description "[Severe congenital hypothyroidism (CH) due to a total iodide organification defect (TIOD) is usually due to mutations in the thyroid peroxidase (TPO) gene located at chromosome 2p25.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347798.RARixbuRQHmZOS8HaqmvHLb2QIUFunlxvUt81abPEfQ0c130_provenance.
NP347802.RAX0P05oe2E9IVfrII6FR2Sd-iiWBnpb8b_6RTutQy_h8130_assertion description "[Recent findings from rodent studies with chronic administration of antipsychotic drugs have indicated the role of neural nitric oxide synthase (NOS1) on the susceptibility of tardive dyskinesia (TD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347802.RAX0P05oe2E9IVfrII6FR2Sd-iiWBnpb8b_6RTutQy_h8130_provenance.
NP347811.RAe8qYOFhCyip7Yk8aNnsKyXiaDQA-h4UHsZ_CTvM3lBk130_assertion description "[The receptor tyrosine kinase FLT3 is an important regulatory molecule in hematopoiesis and is expressed on the blasts in most cases of acute leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP347811.RAe8qYOFhCyip7Yk8aNnsKyXiaDQA-h4UHsZ_CTvM3lBk130_provenance.

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