Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP390155.RAe0H0MWqdiJq7SnH7DToJuhjjZXCzRvgsVQAzX5SBsyk130_assertion description "[Comparative genomic hybridization (CGH) was performed on 32 UC-related and 42 stage-matched sporadic colorectal cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390155.RAe0H0MWqdiJq7SnH7DToJuhjjZXCzRvgsVQAzX5SBsyk130_provenance.
- NP390164.RAdRY4o-a0pO59mQG7m4HsV9_lsBWG0cLxZ9X90RPvlow130_assertion description "[This study evaluated the association of DNMT3A rs36012910 A>G with susceptibility to gastric cancer (GC) in a Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390164.RAdRY4o-a0pO59mQG7m4HsV9_lsBWG0cLxZ9X90RPvlow130_provenance.
- NP390170.RAYOLXHhRUv-jlZStiCCiPLcMQSGoXuz7FE5osH37GtZ4130_assertion description "[We performed mutation screenings of DAF and conducted a tag single-nucleotide polymorphisms (SNP) association analysis for 684 unrelated adult individuals with seasonal allergic rhinitis (SAR) with Japanese ceder pollen, 188 mite-sensitive adults with asthma, and 346 unrelated non-allergic healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390170.RAYOLXHhRUv-jlZStiCCiPLcMQSGoXuz7FE5osH37GtZ4130_provenance.
- NP390172.RAdGE85Fw3QywtXw_ObaenLNR8n0Jd5nD5iQA7zRL5ypE130_assertion description "[Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390172.RAdGE85Fw3QywtXw_ObaenLNR8n0Jd5nD5iQA7zRL5ypE130_provenance.
- NP390173.RATCWkxQulJ9GwKUSqU_igB6z9B-kj7iJz2LPHzlZMiFI130_assertion description "[Familial hypocalciuric hypercalcemia (FHH), neonatal severe hyperparathyroidism (NSHPT), and autosomal dominant hypocalcemia (ADH), in which calcium homeostasis is disordered, are associated with mutations in the calcium-sensing receptor (CASR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390173.RATCWkxQulJ9GwKUSqU_igB6z9B-kj7iJz2LPHzlZMiFI130_provenance.
- NP390184.RAVtYiOD5mztv6wEtuGmxO-nqDJUKadxb4RE3e5puCITk130_assertion description "[The patient was infused with G-CSF-primed peripheral blood cells (PBSC) from the original bone marrow donor and a full donor reconstitution, with no detectable molecular disease, was obtained within 4 months without clinical aplasia or GVHD, nor help from other forms of chemotherapy or use of biological response modifiers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390184.RAVtYiOD5mztv6wEtuGmxO-nqDJUKadxb4RE3e5puCITk130_provenance.
- NP390186.RAQe78JE9RizSSihHleHd4MTeNVFDc79xk6beROJTudnI130_assertion description "[PTEN gene (phosphatase and tensin homolog deleted on chromosome ten, MIM 601628) is a tumor suppressor gene implicated in PTEN hamartoma tumor syndromes (PHTS) including Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome and Proteus-like syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390186.RAQe78JE9RizSSihHleHd4MTeNVFDc79xk6beROJTudnI130_provenance.
- NP390187.RAb0zfeu2ThPfcshBYQQqcEhI2I4UefTccGBjEQ9RBGvI130_assertion description "[Homozygous carriers of the CRP 3' UTR +1444C>T polymorphism do not have a significantly increased risk of VTE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390187.RAb0zfeu2ThPfcshBYQQqcEhI2I4UefTccGBjEQ9RBGvI130_provenance.
- NP390195.RAZ4UJtNwKLraDJZNqDCnwG4dz6csTcWzOe9-OOlg8INg130_assertion description "[One of these genes, AML2, maps 200 kb distal to the UHG-NP breakpoint but is expressed only rarely in neuroblastoma and showed no mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390195.RAZ4UJtNwKLraDJZNqDCnwG4dz6csTcWzOe9-OOlg8INg130_provenance.
- NP390198.RAVaw_HmnmA4NQ0Eg6pVjqGbBSCCNyOILtFgmDDaVUTWk130_assertion description "[Hepatocyte growth factor/scatter factor is implicated in the mode of stromal invasion of uterine squamous cervical cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390198.RAVaw_HmnmA4NQ0Eg6pVjqGbBSCCNyOILtFgmDDaVUTWk130_provenance.
- NP390201.RAcMubnGNKlsnSv4LdL4IwXetjRq9vFuoIJMnGfH3kLLg130_assertion description "[To test this, we determined TK expression by immunohistochemistry in 74 archival thyroid tissue blocks (48 papillary thyroid carcinoma, PTC; 9 follicular thyroid carcinoma, FTC; 17 benign thyroid diseases) from children and young adults.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390201.RAcMubnGNKlsnSv4LdL4IwXetjRq9vFuoIJMnGfH3kLLg130_provenance.
- NP390202.RAaidTUFZOa1Mmb8thXyqWvvxhJqGzySsYSB-gihGmMTY130_assertion description "[High TRIB2 expression correlated with NOTCH1/FBXW7 mutations in a paediatric T-ALL cohort, strongly linking NOTCH1 activation and high TRIB2 expression in paediatric T-ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390202.RAaidTUFZOa1Mmb8thXyqWvvxhJqGzySsYSB-gihGmMTY130_provenance.
- NP390203.RAZdbDlUTJJtmIawtePKEBO-w0dS7NNL5vWUWHm5AdA8o130_assertion description "[Postpartum thyroiditis was also associated with frequency disturbances in BI and C4A allotypes but not C4B allotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390203.RAZdbDlUTJJtmIawtePKEBO-w0dS7NNL5vWUWHm5AdA8o130_provenance.
- NP390209.RAXR6JFbxBuhIgl9SV6Mnjq5StxELIImipCOuvGOu_FzQ130_assertion description "[Type 1 angiotensin II (Ang II) receptors transduce most of the known actions of Ang II, including steroidogenesis and trophic actions on the adrenal cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390209.RAXR6JFbxBuhIgl9SV6Mnjq5StxELIImipCOuvGOu_FzQ130_provenance.
- NP390212.RAYN88o7U-hLh-cbRxK-iuupFOck7K0cv1OYKVomLU5tA130_assertion description "[Risk alleles at genome loci containing phospholipase A2 receptor 1 (PLA2R1) and HLA-DQA1 closely associate with idiopathic membranous nephropathy (IMN) in the European population, but it is unknown whether a similar association exists in the Chinese population and whether high-risk alleles promote the development of anti-PLA2R antibodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390212.RAYN88o7U-hLh-cbRxK-iuupFOck7K0cv1OYKVomLU5tA130_provenance.
- NP390216.RAdjVdZyGTYZoOcbfBV0VboKQiTKSgrdosUf9qP9HM6Iw130_assertion description "[A mutation in CYP11B1 (Arg-448----His) associated with steroid 11 beta-hydroxylase deficiency in Jews of Moroccan origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390216.RAdjVdZyGTYZoOcbfBV0VboKQiTKSgrdosUf9qP9HM6Iw130_provenance.
- NP390219.RAaSKxDQAJAJEThfz2ptsYARTBgfhL7QXMgkr_vASkWkI130_assertion description "[Reverse transcription--polymerase chain reaction (RT-PCR) identified the expression of calcium-binding protein S100A5 in the noncancerous parts of resected samples from renal cell carcinoma (RCC) patients (n = 7) but not in the carcinoma lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390219.RAaSKxDQAJAJEThfz2ptsYARTBgfhL7QXMgkr_vASkWkI130_provenance.
- NP390222.RAdulVXeN0MsxonpXJF0UwaRTa2H_Pq6kjmXDEgu3MV6M130_assertion description "[Wnt and cyclooxygenase 2 (Cox2) are two pathways whose activation has been associated with BE and progression to EAC, but their role has not been tested experimentally.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390222.RAdulVXeN0MsxonpXJF0UwaRTa2H_Pq6kjmXDEgu3MV6M130_provenance.
- NP390225.RAe-siJs2cr7bdo01QNIGefMypVuLyMfdGQhBO1u-ZcSA130_assertion description "[The pathogenicity of the alpha 4(IV)NC1 antibodies establishes a conundrum because the pathogenic antibodies in patients are not targeted to the alpha 4(IV)NC1, but are targeted to the alpha 3(IV)NC1 domain in anti-GBM nephritis and to the alpha 3(IV)NC1 and alpha 5(IV)NC1 domains in Alport post-transplant anti-GBM nephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390225.RAe-siJs2cr7bdo01QNIGefMypVuLyMfdGQhBO1u-ZcSA130_provenance.
- NP390231.RAct0DTyDap86BUuQLkoNezyyClw8AkTvxpu2Sj7ZWajA130_assertion description "[Personalized synthetic lethality induced by targeting RAD52 in leukemias identified by gene mutation and expression profile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390231.RAct0DTyDap86BUuQLkoNezyyClw8AkTvxpu2Sj7ZWajA130_provenance.
- NP390239.RAbHcKCTE_ARE5r0lpi_WoNGIke-dM2KQoIgwUP-0aNLM130_assertion description "[Loss of FBW7, which encodes a tumour-suppressor protein, is frequently found in various types of human cancer, including breast cancer, colon cancer and T-cell acute lymphoblastic leukaemia (T-ALL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390239.RAbHcKCTE_ARE5r0lpi_WoNGIke-dM2KQoIgwUP-0aNLM130_provenance.
- NP390245.RAXBsnz6wxuMXyup8ErX13lUra0-PsettlQBvUD36scYY130_assertion description "[Transgenic TERT expression in mice induces marked upregulation of Wnt signaling and disrupts glomerular structure, resulting in a collapsing glomerulopathy resembling those in human disease, including HIV-associated nephropathy (HIVAN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390245.RAXBsnz6wxuMXyup8ErX13lUra0-PsettlQBvUD36scYY130_provenance.
- NP390251.RAY1_aXitUZDL6JYlFBizcYfNUixTA3r-9sffgV1MjopE130_assertion description "[This (DYT12) is a hereditary dystonia caused by mutations in the α₃ isoform of the sodium potassium adenosine triphosphatase (ATPase) pump (sodium pump), which partially hampers its physiological function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390251.RAY1_aXitUZDL6JYlFBizcYfNUixTA3r-9sffgV1MjopE130_provenance.
- NP390252.RARN8nxgY1vT6T458j2A_HRGVjm2WYDBP41XQb8DqoIx0130_assertion description "[We found no or reduced expression of KEPI in breast cancer cell lines, breast tumors and metastases in comparison to normal breast cell lines and tissues, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390252.RARN8nxgY1vT6T458j2A_HRGVjm2WYDBP41XQb8DqoIx0130_provenance.
- NP390264.RAfP3hm1hS_CjHYK3JyUCl35NNYq85uT5389ZLxLMzGy8130_assertion description "[Whereas at high doses, oCRF injected into the lateral intermediate septum containing predominantly CRF(2) increased anxiety-like behavior as CRF(2)-specific agonists do, cortagine did not.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390264.RAfP3hm1hS_CjHYK3JyUCl35NNYq85uT5389ZLxLMzGy8130_provenance.
- NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_assertion description "[Discovery of this new mutation confirms the association between fibrinogen A alpha chain variant and hereditary renal amyloidosis and establishes a new biochemical subtype of amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390265.RARXVM9fcGPOmm997tXc3xLTRV4Z_zPDgkiJDffuPpQok130_provenance.
- NP390274.RAe9wQqLEC4InGBtR1JSewf04C-ZJEl6_C9WEu8eU1zXw130_assertion description "[Our data suggest that the IL7R mutations may contribute to the development of diverse types of acute leukemias, and that possible therapies targeting the IL7R exon 6 mutation should include not only childhood T-ALL but also T-ALL, childhood precursor B-ALL, and adult AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390274.RAe9wQqLEC4InGBtR1JSewf04C-ZJEl6_C9WEu8eU1zXw130_provenance.
- NP390275.RAZW0pak_sFrux7DYrmWrC-Uyz0zK5PRe8XRe08dkaqqI130_assertion description "[Autosomal dominant polycystic kidney disease (ADPKD) is genetically heterogeneous, with at least three chromosomal loci (PKD1, PKD2, and PKD3) that account for the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390275.RAZW0pak_sFrux7DYrmWrC-Uyz0zK5PRe8XRe08dkaqqI130_provenance.
- NP390282.RAXlzgVkfOzdgx3j4xJHm1UhPWP4MxmVKFutGLRZcsFKI130_assertion description "[Similarly, in eMSC(PCOS) vs eMSC(Ctrl), the most up-regulated genes were related to inflammation and cancer (IL-8, ICAM1, SPRR3, LCN2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390282.RAXlzgVkfOzdgx3j4xJHm1UhPWP4MxmVKFutGLRZcsFKI130_provenance.
- NP390286.RAQtNv0kogq8zUibMdb_-yhf2_2j7J9n6g6We9sG1EZHQ130_assertion description "[β-Arrestin 1 modulates functions of autoimmune T cells from primary biliary cirrhosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390286.RAQtNv0kogq8zUibMdb_-yhf2_2j7J9n6g6We9sG1EZHQ130_provenance.
- NP390300.RAdv7aQ-k0ObgIGegch_LfPaDTRR2STN5trroa6BmWmdg130_assertion description "[Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390300.RAdv7aQ-k0ObgIGegch_LfPaDTRR2STN5trroa6BmWmdg130_provenance.
- NP390307.RAVWdiiXOaUTvCJyIvDPa5CUMDO4dpp9Mxk1oU07vw3fo130_assertion description "[Our results provide new evidence that genetic polymorphisms of PLA2R1 may be the underlying cause of IMN, and the polymorphisms revealed by this study warrant further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390307.RAVWdiiXOaUTvCJyIvDPa5CUMDO4dpp9Mxk1oU07vw3fo130_provenance.
- NP390319.RAY4us5C2y0r4PWM6HQkrxswk9LlQiA_sd-q32MhlEQw8130_assertion description "[Although activating mutations of Notch have been found in human T-ALL tumors, there is little evidence that the c-MYC locus is altered in this neoplasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390319.RAY4us5C2y0r4PWM6HQkrxswk9LlQiA_sd-q32MhlEQw8130_provenance.
- NP390330.RAUgAJo95-BHLKTSPVFbFYvzyyZPiXh14QH39o8CxeR_w130_assertion description "[FHIT gene LOH was found in 36% of CIN1 cases, 52% of CIN3 cases and 73% of microinvasive cases (p=0.029).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390330.RAUgAJo95-BHLKTSPVFbFYvzyyZPiXh14QH39o8CxeR_w130_provenance.
- NP390331.RAYuJ_bgLg9iO3UhnEtVcKdkZZcjoIRm3-hMfpl9rWpFA130_assertion description "[Since repression of pdyn transcription persists after inhibiting DREAM translation, DREAM appears to play no functional role in the kappa opioid receptor system in OA SFLCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390331.RAYuJ_bgLg9iO3UhnEtVcKdkZZcjoIRm3-hMfpl9rWpFA130_provenance.
- NP390333.RAbgFthNaJD4XSPkJZi2xcN9gvaZbCq-kD5wdpZo_dQlw130_assertion description "[NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390333.RAbgFthNaJD4XSPkJZi2xcN9gvaZbCq-kD5wdpZo_dQlw130_provenance.
- NP390335.RAUOcdRl2LemMMLGO8-9qCDJ6FIfAuIpHBxfqQ0QGXLjU130_assertion description "[Nuclear accumulation of the E3 ubiquitin ligase SIAH-1 supports different pro-tumorigenic cellular processes associated with tumor growth and tumor cell dissemination in human hepatocarcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390335.RAUOcdRl2LemMMLGO8-9qCDJ6FIfAuIpHBxfqQ0QGXLjU130_provenance.
- NP390338.RAZkEpnrRH3i9rexNNixSdXmWsZurz9H1eaNU4ynpdeWw130_assertion description "[Three patients initially treated with gefitinib and two with erlotinib discontinued epidermal growth factor receptor-tyrosine kinase inhibitor therapy because of severe non-hematologic toxicity (one because of gefitinib-induced interstitial lung disease, one because of erlotinib-induced lupus erythematosus-like eruption and three because of hepatotoxicity).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390338.RAZkEpnrRH3i9rexNNixSdXmWsZurz9H1eaNU4ynpdeWw130_provenance.
- NP390351.RARHdlqr5f_gn0GG3m-EW37TUvSwy2GTbLoGIrkU5HcV0130_assertion description "[As a result of testing for lipid and apolipoprotein(e) (apo E) phenotype status of an indigenous Australian community, an apo E variant associated with type III hyperlipoproteinaemia has been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390351.RARHdlqr5f_gn0GG3m-EW37TUvSwy2GTbLoGIrkU5HcV0130_provenance.
- NP390356.RAak8V6clGj4GasINcZbSShDRPW8dI8UTUlZRUf-IV-yc130_assertion description "[These results suggest that CDCP1 expression might play a crucial role in poor outcome of pancreatic cancer through promotion of invasion and metastasis and that molecules blocking the expression, phosphorylation, or the PKCdelta-binding site of CDCP1 are potential therapeutic candidates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390356.RAak8V6clGj4GasINcZbSShDRPW8dI8UTUlZRUf-IV-yc130_provenance.
- NP390360.RAYCit24TB-rfZFa0dfB2uUQJ18AFZlpsvfOZQ5nJbpD0130_assertion description "[To determine whether methylene tetrahydrofolate reductase (MTHFR) C677T mutation, factor II G20210A mutation and factor V Leiden are risk factors for retinal vein occlusion (RVO) in patients under fifty years of age.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390360.RAYCit24TB-rfZFa0dfB2uUQJ18AFZlpsvfOZQ5nJbpD0130_provenance.
- NP390361.RAXlr_j-gGmgY4A_HSabWVvxVH4g6tJFeYdC9MgWiF-D8130_assertion description "[The normal restriction pattern has not been altered by a t(3;8)(p14.2;q24.1) characteristic for a hereditary form of renal cell carcinoma, indicating that the breakpoint itself is not included in any of the mapped areas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390361.RAXlr_j-gGmgY4A_HSabWVvxVH4g6tJFeYdC9MgWiF-D8130_provenance.
- NP390363.RAYeHnUPQIoaYthZIXW_6RbVTzkQdyHrWe9E8Yszp_-eU130_assertion description "[Clinicopathological significance of KU70/KU80, a key DNA damage repair protein in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390363.RAYeHnUPQIoaYthZIXW_6RbVTzkQdyHrWe9E8Yszp_-eU130_provenance.
- NP390371.RAbjlrwteMhuhrC-jyaGW5rdpfCTFFhuCyJS6CmTUNj84130_assertion description "[In these specimens, we measured the expression of RRM1 and two other proteins that are relevant to non-small-cell lung cancer: the excision repair cross-complementation group 1 (ERCC1) protein and the phosphatase and tensin homologue (PTEN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390371.RAbjlrwteMhuhrC-jyaGW5rdpfCTFFhuCyJS6CmTUNj84130_provenance.
- NP390372.RAXSzNzA9BNp1212KZl5lMkKOr0PShswCtga2WdxjjGQQ130_assertion description "[Taken together, these data show that common variants in HACE1 and LIN28B influence neuroblastoma susceptibility and indicate that both genes likely have a role in disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390372.RAXSzNzA9BNp1212KZl5lMkKOr0PShswCtga2WdxjjGQQ130_provenance.
- NP390378.RAXDdzl3oCI8yzOIiSkxFKnlcG48VpwumQX2cAjliDfM4130_assertion description "[Genetic variation of human mononuclear leukocyte lysosomal acid lipase activity. Relationship to atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390378.RAXDdzl3oCI8yzOIiSkxFKnlcG48VpwumQX2cAjliDfM4130_provenance.
- NP390392.RAURZEOSaO0xdDIE2cnPKIffwfDroUh6hnzdnxu3xe0zw130_assertion description "[Post-UV DNA repair, cell survival and genetic complementation assigned these patients to the XP group C. All patients exhibited a new G→C homozygous substitution at 3'-end of XPC intron 12 (IVS 12-1G>C) leading to the abolition of an acceptor splicing site and the absence of the XPC protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390392.RAURZEOSaO0xdDIE2cnPKIffwfDroUh6hnzdnxu3xe0zw130_provenance.
- NP390395.RAeRh0ECwDlx4AR_dw6QFtIab8vlFiEBUZRkIleZHNEpQ130_assertion description "[The NEO analysis revealed that HTR2A and GRM2 are likely to regulate BDNF levels in the hippocampus and frontal cortex, respectively, whereas DRD2 and ADRA2A activity are likely to be regulated by BDNF in the frontal cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390395.RAeRh0ECwDlx4AR_dw6QFtIab8vlFiEBUZRkIleZHNEpQ130_provenance.
- NP390399.RATt1V4_60eg5PnxftkwY3z0z02DkkjwZlr-2DpdS7K90130_assertion description "[G6PD Gastonia disrupts dimerization of the enzyme and by itself causes chronic non-spherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390399.RATt1V4_60eg5PnxftkwY3z0z02DkkjwZlr-2DpdS7K90130_provenance.
- NP390405.RAdzij2Q8RdXb3J83L1qHKkOVXhV8YRHaFOhNYcd62QnU130_assertion description "[Huntington disease (HD) is an adult onset neurodegenerative disorder that predominantly affects the striatum and cortex despite ubiquitous expression of mutant huntingtin (htt).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390405.RAdzij2Q8RdXb3J83L1qHKkOVXhV8YRHaFOhNYcd62QnU130_provenance.
- NP390409.RAW3j03twABvWvg82rUY8LS9NkgpZybD_8_fCN_CMp0P0130_assertion description "[The relationship between Helicobacter pylori status and host tumor necrosis factor alpha (TNF-alpha) promoter susceptibility in ulcers inautoimmune pancreatitis (AIP) is unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390409.RAW3j03twABvWvg82rUY8LS9NkgpZybD_8_fCN_CMp0P0130_provenance.
- NP390413.RAUk0QekDtQZWz6ErWrrcSGwu1I0O3X7kVlvihfksHBec130_assertion description "[The aim of the present study was to compare the circulating concentrations of OPN and its mRNA expression in omental adipose tissue of lean, overweight, and obese individuals and to analyze the effect of weight loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390413.RAUk0QekDtQZWz6ErWrrcSGwu1I0O3X7kVlvihfksHBec130_provenance.
- NP390414.RAWv4Z-ramME7Lum01z6zzCLEacEHRasF8V2c5zz0drmI130_assertion description "[Mutations in PI3K or loss of Phosphatase and Tensin homolog (PTEN) in Smad4-defective tumors made CRC-SCs unresponsive to BMP4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390414.RAWv4Z-ramME7Lum01z6zzCLEacEHRasF8V2c5zz0drmI130_provenance.
- NP390415.RAa3NcPnstZQw1_rx9qxGjikgB-x3O3eS59LW_LpJck2A130_assertion description "[To report the clinical phenotype in patients with a retinal dystrophy associated with novel mutations in the MER tyrosine kinase (MERTK) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390415.RAa3NcPnstZQw1_rx9qxGjikgB-x3O3eS59LW_LpJck2A130_provenance.
- NP390425.RAWaBp404PBxEzxzWftkmsl1SWRNdyRQJGKDpmhmV3Yik130_assertion description "[Our findings demonstrate that GALNT3 inactivation in patients with TC leads to inadequate production of biologically active FGF23 as the most likely cause of the hyperphosphatemic phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390425.RAWaBp404PBxEzxzWftkmsl1SWRNdyRQJGKDpmhmV3Yik130_provenance.
- NP390426.RAU89y9tUGK8cLe7a0sOC4zYgSpS03Y0G7SPFHhmcVW34130_assertion description "[A KCR1 variant implicated in susceptibility to the long QT syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390426.RAU89y9tUGK8cLe7a0sOC4zYgSpS03Y0G7SPFHhmcVW34130_provenance.
- NP390432.RAZecDSPIhLMH1p5GrCAEkH6pQ_rLLijtiVXWAOWQ4p8A130_assertion description "[Programmed cell death 1 (PD-1) has been reported to have a genetic association in several autoimmune diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390432.RAZecDSPIhLMH1p5GrCAEkH6pQ_rLLijtiVXWAOWQ4p8A130_provenance.
- NP390433.RAQfFrKY4ZIc7LvGMLIYfqNh26RnUD_BVYb51w2i7yiAc130_assertion description "[While most studies, albeit on different enzymes, have tended to agree on the evidence for an increased PTP expression in breast cancer, any connection between PTP expression and the enzymes' role in cancer development and progression remains largely open to interpretation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390433.RAQfFrKY4ZIc7LvGMLIYfqNh26RnUD_BVYb51w2i7yiAc130_provenance.
- NP390434.RATLXgT1hTgxv15HppcS97H3Bk8uwY8Xvbh6lPyLk5JbM130_assertion description "[Notwithstanding the presence of high levels of IL-12Rβ2 mRNA in these patients elevated IFN-α expression could modulate their immune responses to Mycobacterium tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390434.RATLXgT1hTgxv15HppcS97H3Bk8uwY8Xvbh6lPyLk5JbM130_provenance.
- NP390443.RAduCkEQXiKr6sdALgbt2jZh0MszS43j_eghhw_keDoFA130_assertion description "[Although mutations in junctional EB have not been reported, findings of structural alterations in hemidesmosomes and immunohistochemical studies of kalinin (BM600 and epiligrin), and in junctional EB with pyloric atresia alterations in the integrin alpha 6 beta 4, indicate molecules involved in basal keratinocyte adhesion to the basement membrane that are candidate genes for junctional EB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390443.RAduCkEQXiKr6sdALgbt2jZh0MszS43j_eghhw_keDoFA130_provenance.
- NP390444.RAaEa4Uq4T1MV7eU-u99PBOBR6x0mbcE0QQWIskOIik_w130_assertion description "[There was a significant relationship between FPGS mRNA and enzyme activity in lymphoblasts from children with newly diagnosed ALL, and blast FPGS mRNA and activity increased after methotrexate treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390444.RAaEa4Uq4T1MV7eU-u99PBOBR6x0mbcE0QQWIskOIik_w130_provenance.
- NP390449.RAVVNlXvjnD_L-zR5mWhvTyHamaMWsM7ynBjuzbHhpkEo130_assertion description "[MYC rearrangement is a recurring genetic abnormality in several aggressive B-cell lymphomas including: Burkitt lymphoma, diffuse large B-cell lymphoma; B-cell lymphoma, unclassifiable with features intermediate between diffuse large B-cell lymphoma and Burkitt lymphoma; rare de novo acute lymphoblastic lymphoma/leukemia, transformed follicular lymphoma, and plasmablastic lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390449.RAVVNlXvjnD_L-zR5mWhvTyHamaMWsM7ynBjuzbHhpkEo130_provenance.
- NP390451.RARcwarQ4zKVvltZKc1wy0CDDfuvePRvOPJJtPOtCCQVU130_assertion description "[Of 261 cases of invasive breast cancer, high expression of the enhancer of zeste homolog 2 was detected in 87 (33%) cases, and it was strongly associated with a triple-negative breast cancer phenotype (P < .001) compared with all other non-triple-negative breast cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390451.RARcwarQ4zKVvltZKc1wy0CDDfuvePRvOPJJtPOtCCQVU130_provenance.
- NP390455.RAUOMIYkWFepIeAnNq_UQTTs9H6uDSZcHafiMYvoO8ixg130_assertion description "[A comparison between the efficacy of somatostatin receptor scintigraphy and that of in situ hybridization for somatostatin receptor subtype 2 messenger RNA to predict therapeutic outcome in carcinoid patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390455.RAUOMIYkWFepIeAnNq_UQTTs9H6uDSZcHafiMYvoO8ixg130_provenance.
- NP390456.RARvmok4U6f1CLPi1y194A1vrwHY253VRugBXlGEi8oWw130_assertion description "[Coding polymorphisms in Casp5, Casp8 and DR4 genes may play a role in predisposition to lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390456.RARvmok4U6f1CLPi1y194A1vrwHY253VRugBXlGEi8oWw130_provenance.
- NP390457.RAa_OmFGo_Spj5_EPgWHW8zb6URwbdlpoovHAQ79IqDcI130_assertion description "[Notch1 regulates the effects of matrix metalloproteinase-9 on colitis-associated cancer in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390457.RAa_OmFGo_Spj5_EPgWHW8zb6URwbdlpoovHAQ79IqDcI130_provenance.
- NP390458.RARiRwJ03S7hUah4m1NnWQEmCxc-AM0MeShJUhaf5LR_o130_assertion description "[We have shown that the new mutation L205P in Cx26 is strongly associated with congenital NSHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390458.RARiRwJ03S7hUah4m1NnWQEmCxc-AM0MeShJUhaf5LR_o130_provenance.
- NP390462.RAQPca_OZf3o6SSgNWPScU_TZ5nsmF6EssYty5PTO025Y130_assertion description "[Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390462.RAQPca_OZf3o6SSgNWPScU_TZ5nsmF6EssYty5PTO025Y130_provenance.
- NP390463.RATWq6n0JTJkzIeHpwCC-Bxc07CKXErBWEUuo-f7UWJOY130_assertion description "[Structure, stability and dynamics of the central domain of cardiac myosin binding protein C (MyBP-C): implications for multidomain assembly and causes for cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390463.RATWq6n0JTJkzIeHpwCC-Bxc07CKXErBWEUuo-f7UWJOY130_provenance.
- NP390464.RATs6yGmZhZUfDRx106xHdoARdpycDqdrpUCciv0jl1v8130_assertion description "[However, like the large non-structural protein NS1 of the human parvovirus B19, the ChpPV NS1 is a potent inducer of apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390464.RATs6yGmZhZUfDRx106xHdoARdpycDqdrpUCciv0jl1v8130_provenance.
- NP390483.RARfxtIUU9gzkUYhC45IqzGjjmBmPcDyQAH0xQfn7PE4U130_assertion description "[TAP1 and TAP2 polymorphisms associated with ankylosing spondylitis in genetically homogenous Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390483.RARfxtIUU9gzkUYhC45IqzGjjmBmPcDyQAH0xQfn7PE4U130_provenance.
- NP390487.RAVz-GSGCflcYJave7I0H99RTWqfkPtvgSf2oXgh84Bf0130_assertion description "[Moyamoya angiopathy can either be the sole manifestation of the disease (moyamoya disease) or be associated with various conditions, including neurofibromatosis, Down syndrome, TAAD (autosomal-dominant thoracic aortic aneurysm), and radiotherapy of head tumors (moyamoya syndromes).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390487.RAVz-GSGCflcYJave7I0H99RTWqfkPtvgSf2oXgh84Bf0130_provenance.
- NP390488.RAeMi7a4v8TkVQX2FWwbRxxvMkZA3RhnxVALvbT0fJsbw130_assertion description "[We have classified type III GBS by restriction digest patterns of chromosomal DNA and demonstrated that a subgroup of genetically related strains (RDP type III-3) causes the majority of type III GBS neonatal infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390488.RAeMi7a4v8TkVQX2FWwbRxxvMkZA3RhnxVALvbT0fJsbw130_provenance.
- NP390489.RAZbBfLB7fA8aPjycEK7CViF0SNAqPWgc52kBeAllGmow130_assertion description "[When either K14/bcl-2 mice or F(1) progeny of matings with mice expressing an activated Ha-ras oncogene (K14/bcl-2/ras) were treated with 9,10-dimethyl-1,2-benzanthracene/phorbol 12-myristate 13-acetate, the latency of first papilloma appearance was the same in transgenic mice and controls, but further papillomas developed more slowly in the mutant mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390489.RAZbBfLB7fA8aPjycEK7CViF0SNAqPWgc52kBeAllGmow130_provenance.
- NP390498.RAX6qku1K8RjRKXh2twA8YB4NBMT6cfp9Ai8TIGRbWbOo130_assertion description "[We identified a naturally processed, HLA-A*0201-restricted peptide epitope within the signal sequence region of KLK4 that induced CTL responses in vitro in most healthy donors and prostate cancer patients tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390498.RAX6qku1K8RjRKXh2twA8YB4NBMT6cfp9Ai8TIGRbWbOo130_provenance.
- NP390499.RAetUp1MgDrkWQNtU7ppbiJ59cNG_5lstnHCXXWaTOWlI130_assertion description "[We concluded that if the people lacking GSTm are smokers and have a cancer and/or lung cancer history among their relatives, they would challenge a greater risk of lung cancer than the individuals having GST mu isoenzyme.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390499.RAetUp1MgDrkWQNtU7ppbiJ59cNG_5lstnHCXXWaTOWlI130_provenance.
- NP390500.RATbN7aHeuA2f27-_QVIPk02RGEKFoNY8_6SWpHL6R1LI130_assertion description "[FCAS, MWS and CINCA could be different phenotype expressions of the same disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390500.RATbN7aHeuA2f27-_QVIPk02RGEKFoNY8_6SWpHL6R1LI130_provenance.
- NP390505.RAUPWZ5b0U3PxKmRBTdx6Z6hREeatcAxBlD2uITjeZgfI130_assertion description "[We genotyped 2 loss-of-function FLG mutations (R501X and 2282del4) in white children (age 5-12 years) with mild to moderate asthma in the Childhood Asthma Management Program.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390505.RAUPWZ5b0U3PxKmRBTdx6Z6hREeatcAxBlD2uITjeZgfI130_provenance.
- NP390515.RATt2IjJCNFgCGsKto82DM8k-bRw8f1O4YGXOpKgdGbMs130_assertion description "[Recently, the overexpression of DBC1 in cancer cells has been reported to be strongly related with unfavorable clinical outcome in several cancers, including breast and gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390515.RATt2IjJCNFgCGsKto82DM8k-bRw8f1O4YGXOpKgdGbMs130_provenance.
- NP390518.RATVchJwELuuxjDCw5LFrYJph70zFWZ4sBligyts-G1Co130_assertion description "[Even in the absence of virus infection, transiently expressed M013 protein alone inhibited cellular NF-kappaB-mediated reporter gene expression and nuclear translocation of NF-kappaB/p65.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390518.RATVchJwELuuxjDCw5LFrYJph70zFWZ4sBligyts-G1Co130_provenance.
- NP390529.RAZFIy-L0ZmCyUhOoKXQbOX6QuUJ4KRe_SwFQKPsmc0Z8130_assertion description "[When expressed on human cell lines, this molecule binds virus through direct interactions with the gp 120 viral envelope glycoprotein thus allowing virus infection to occur.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390529.RAZFIy-L0ZmCyUhOoKXQbOX6QuUJ4KRe_SwFQKPsmc0Z8130_provenance.
- NP390532.RAcDuGqVUU3_UuJ6F-lj5ABBeEpQeqM_l_5bJ7sKMcZrw130_assertion description "[Although several other mutations in the GR gene have been postulated as being relevant to the progression to type 2 diabetes and cardiovascular diseases, conflicting results makes it difficult to determine exactly what effect these GR variations have on metabolic syndrome incidence and progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390532.RAcDuGqVUU3_UuJ6F-lj5ABBeEpQeqM_l_5bJ7sKMcZrw130_provenance.
- NP390534.RAftL5hQ7OEhTtLlFSubBUj6onCTD7D38OEU-rV1RuITg130_assertion description "[This is the first report showing that p27 expression in malignant lymphomas has independent prognostic significance, which necessitates future studies regarding its more precise biological role in lymphoid tumorogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390534.RAftL5hQ7OEhTtLlFSubBUj6onCTD7D38OEU-rV1RuITg130_provenance.
- NP390535.RAd7459Z7H0N-1w8PgHY-Hoh7Hv_zTvBS4krdhIicASww130_assertion description "[Our work is the first to describe a role for WSTF in proper neural crest function, and suggests that neural crest defects resulting from WSTF haploinsufficiency may be a major contributor to the pathoembryology of WS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390535.RAd7459Z7H0N-1w8PgHY-Hoh7Hv_zTvBS4krdhIicASww130_provenance.
- NP390540.RAeOXfXLLl8ZkC0JjHr2NlF2KS3Obcl3WvcE98Ek8BbjE130_assertion description "[Investigations suggested Cushing's disease; there was suppression after high-dose dexamethasone (<20 nmol/liter) and a 950% increase in ACTH after stimulation with CRH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390540.RAeOXfXLLl8ZkC0JjHr2NlF2KS3Obcl3WvcE98Ek8BbjE130_provenance.
- NP390542.RATIdLqUVxIfAgHBynjZlJS32GZpllrzmVUo1iO2Qv_jg130_assertion description "[The genotypes and allele frequencies of SNPs S2 and ST+5 of the ADAM33 gene were significantly associated with asthma risk (P = 0.020 - < 0.001), whereas F+1, ST+4, V4 homozygous mutant genotypes and mutant alleles were significantly associated with increased asthma risk (P = 0.031 - < 0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390542.RATIdLqUVxIfAgHBynjZlJS32GZpllrzmVUo1iO2Qv_jg130_provenance.
- NP390545.RAT7JVFfR51jzWOIeBkZKhBsRSnoCR1Ua9qt5mTPQs2bE130_assertion description "[Taken together, we concluded that UCA1 regulated cell cycle through CREB via PI3K-AKT dependent pathway in bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390545.RAT7JVFfR51jzWOIeBkZKhBsRSnoCR1Ua9qt5mTPQs2bE130_provenance.
- NP390556.RASIviZJ6drsc7LLF5l9OUWCjkx52mZ6AfjtzVC7uULqc130_assertion description "[Using the mean percentage of nuclear p57KIP2 expression (25%) as the cut-off value, we divided our cases into those with high expression (n = 44, 40%) and low expression (n = 66, 60%) of p57KIP2 among 110 colorectal cancer cases tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390556.RASIviZJ6drsc7LLF5l9OUWCjkx52mZ6AfjtzVC7uULqc130_provenance.
- NP390559.RAWW5BXFyz1VvQm_p_kJh6wA7ujMTX2yCuPItZrXyaz4I130_assertion description "[Results showed that H19 overexpression promotes tumour progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390559.RAWW5BXFyz1VvQm_p_kJh6wA7ujMTX2yCuPItZrXyaz4I130_provenance.
- NP390565.RAS95etTkGaDZsQW_ZyhXdfdNMzcGHEYvzLw6Rw6l_lrI130_assertion description "[Besides genes that were already known to be highly expressed in CCSST, like S100A11 (S100 protein) or MITF (microphthalmia-associated transcription factor), this group shows an obvious portion of genes that are involved in cyclic AMP response or regulation, in pigmentation processes, or in neuronal structure and signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390565.RAS95etTkGaDZsQW_ZyhXdfdNMzcGHEYvzLw6Rw6l_lrI130_provenance.
- NP390569.RAZqfQ3YWqgBI2IYIGNETtWMbgRGe4MMivItftguiZQIs130_assertion description "[MTX significantly suppresses expression of NURR1 in vivo in patients with active psoriatic arthritis (n = 10; p < 0.002) who were prescribed low-dose MTX for management of peripheral arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390569.RAZqfQ3YWqgBI2IYIGNETtWMbgRGe4MMivItftguiZQIs130_provenance.
- NP390577.RAdauaLlPc5ycw9WV0lub-aeqQdkcWSqbTRtIegtPrjmM130_assertion description "[Two adenoviral vectors (AD) were compared in the study: AD5, that utilizes the CAR receptor, demonstrated poor infectivity to both normal and carcinoma tissues, while a capsid-modified-AD, recognizing haparan-sulfate receptor, demonstrated efficient infectivity of both tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390577.RAdauaLlPc5ycw9WV0lub-aeqQdkcWSqbTRtIegtPrjmM130_provenance.
- NP390582.RAWWvTYCzn08l1SmJsGHw1fA18QU7_z1daqZcauu6zrK8130_assertion description "[Serum C-reactive protein (CRP) elevation is associated with poor clinical outcome in patients with heart failure (HF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390582.RAWWvTYCzn08l1SmJsGHw1fA18QU7_z1daqZcauu6zrK8130_provenance.
- NP390584.RAWM4cuGI8Le3ghRTzMGdA19KI1LnC4pXps1mkLRQaA1g130_assertion description "[We point out common themes and features, that allow to speculate on the possible role of p63 downstream events and their potential exploitation in future attempts to correct the congenital defect in preclinical studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390584.RAWM4cuGI8Le3ghRTzMGdA19KI1LnC4pXps1mkLRQaA1g130_provenance.
- NP390588.RAVKztusQ2eP3LSESdvXF-Hsv9zrCbBmtnz8kWc8HU-mU130_assertion description "[Inactivation of the cell cycle regulator, p16 (CDKN2A), has recently been observed in a small subset of atypical and the majority of anaplastic meningiomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390588.RAVKztusQ2eP3LSESdvXF-Hsv9zrCbBmtnz8kWc8HU-mU130_provenance.
- NP390591.RAaTGmJ-JO7NJ6OC246fhQOBP5_SBF5D3q8P4SH8XH-mo130_assertion description "[In two of these specimens, an invasive cancer contained a c-Ki-ras mutation identical to that found in adjacent dysplastic epithelium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390591.RAaTGmJ-JO7NJ6OC246fhQOBP5_SBF5D3q8P4SH8XH-mo130_provenance.
- NP390596.RAbZ-Z2hToR9_iYjzLNX8g7KEL7WaqJ5NxdqNOEFP9kE0130_assertion description "[These results indicate that this PDB-associated p62 mutation is not sufficient to induce PDB and suggest that additional factors acting together with p62 mutation are necessary for the development of PDB in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390596.RAbZ-Z2hToR9_iYjzLNX8g7KEL7WaqJ5NxdqNOEFP9kE0130_provenance.
- NP390600.RAdytqrhc5rbiSG2bmSU2GdR7Aar_CxA5DEPHrvUTPkUA130_assertion description "[However, the demonstration that LCH cells are clonal, along with the recent discovery of activating BRAF mutations in LCH cells, strongly suggests that LCH is a neoplastic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390600.RAdytqrhc5rbiSG2bmSU2GdR7Aar_CxA5DEPHrvUTPkUA130_provenance.
- NP390601.RAXCsw784CTDlEcUyZ8FisocHO0PQpGA4s_TWXtiMKAzw130_assertion description "[Significantly increased levels of antibodies to beta-casein were found in patients with Type 1 diabetes, coeliac disease and in LADA compared to age-matched controls (p = 0.01, p = 0.02 and p = 0.01, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390601.RAXCsw784CTDlEcUyZ8FisocHO0PQpGA4s_TWXtiMKAzw130_provenance.
- NP390603.RAeYOpTwQ3GXVrzScjBDr74mgBAXuZ478aQBzdQ9iw0WA130_assertion description "[Only 62% patients with de novo ALL had significant decrease of MDR1 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390603.RAeYOpTwQ3GXVrzScjBDr74mgBAXuZ478aQBzdQ9iw0WA130_provenance.