Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP130769.RATjSUaqo15gkGUqjgDdbSXq2z4vcZYb0_a8g5bo8wOb8130_assertion description "[mutations in genes encoding ADH1C (G78Stop) as genetic risk factors for Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130769.RATjSUaqo15gkGUqjgDdbSXq2z4vcZYb0_a8g5bo8wOb8130_provenance.
- NP130771.RAcnDmN4aBvgYPHR2k14uRBzzfBvuEOzPqdcVPJzfNLfY130_assertion description "[Quinone reductase 2 is a catechol quinone reductase.quinone reductase 2 could play important roles in the regulation of catecholamine oxidation processes that may be involved in the etiology of Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130771.RAcnDmN4aBvgYPHR2k14uRBzzfBvuEOzPqdcVPJzfNLfY130_provenance.
- NP130772.RATuyEteQgPfBcT6BxRYp39G-eok2zhBlbVnrIkQT7EUk130_assertion description "[Novel mitochondrial DNA mutations in Parkinson's disease.we report novel homoplasmic base changes/were unable to detect heteroplasmic base changes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130772.RATuyEteQgPfBcT6BxRYp39G-eok2zhBlbVnrIkQT7EUk130_provenance.
- NP130773.RASzQPSnU21BBHEnMWfSUs0BusegwB1Zk9nL8M7AhlZ1M130_assertion description "[Beta-scorpion toxin enhance channel activation, which could make it a model drug to replace deep brain stimulation of the subthalamic nucleus in patients with Parkinson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130773.RASzQPSnU21BBHEnMWfSUs0BusegwB1Zk9nL8M7AhlZ1M130_provenance.
- NP130774.RATjXRd1wflhdZiG0gfnJn6u4TDvyxSLPmOuWGY6Qsz_A130_assertion description "[Results suggest that tuberin dysfunction may represent a mechanism for neuronal damage in Alzheimer's disease (AD), Parkinson's disease with dementia (PD/DLB), and a mouse model of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130774.RATjXRd1wflhdZiG0gfnJn6u4TDvyxSLPmOuWGY6Qsz_A130_provenance.
- NP130776.RASAiFSjOiU8GcGW7gWbeiQBS1aUMuNnsPLgYcGgCVceo130_assertion description "[common genetic variants in the IGF2-INS-TH cluster modify susceptibility to idiopathic Parkinson's disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130776.RASAiFSjOiU8GcGW7gWbeiQBS1aUMuNnsPLgYcGgCVceo130_provenance.
- NP130782.RAcUZPlH-nEZoNtQl3nPfXfQVp9CRYw2I2jpAe_2u4oOo130_assertion description "[germline mutations with familial hyperparathyroidism associated with 80% recurrence/persistence rate, increasingly difficult re-operations and risk of parathyroid carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130782.RAcUZPlH-nEZoNtQl3nPfXfQVp9CRYw2I2jpAe_2u4oOo130_provenance.
- NP130792.RAa6bVIu-2nnj2Sd7kMBkYmq65hZOPJaK1bpk2MONlaBY130_assertion description "[genotype phenotype analysis in familial isolated hyperparathyroidism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130792.RAa6bVIu-2nnj2Sd7kMBkYmq65hZOPJaK1bpk2MONlaBY130_provenance.
- NP130795.RAXn3tfbKS1dw99X8qTFbByNeCCG3iYwEKa7fo7M9MYAo130_assertion description "[conclude that the altered MEN1 gene function is of importance in the development of familial isolated hyperparathyroidism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130795.RAXn3tfbKS1dw99X8qTFbByNeCCG3iYwEKa7fo7M9MYAo130_provenance.
- NP130796.RAbFVwh6uJlDunm69YSG4GP1uxu2jILWF6fvthbgAYsc4130_assertion description "[genotype phenotype analysis in familial isolated hyperparathyroidism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130796.RAbFVwh6uJlDunm69YSG4GP1uxu2jILWF6fvthbgAYsc4130_provenance.
- NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_assertion description "[The glial cell missing gene, GCMB, encodes a transcription factor, which is a master regulator of parathyroid development/expression is upregulated in abnormal parathyroid glands of hyperparathyroidism and decreases in response to hypocalcemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130805.RAQVzWCmj_MN442zqzc3C4jCtPGPhZ0MLsq6SAlhJi-Ko130_provenance.
- NP130807.RAaFW0AXpPPJqZ855SX1cZpwyBXGYTmY0LTFnhRDyIPvs130_assertion description "[A woman with a mutation of the KCNQ1 gene was found to have long QT syndrome and primary hyperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130807.RAaFW0AXpPPJqZ855SX1cZpwyBXGYTmY0LTFnhRDyIPvs130_provenance.
- NP130808.RAcoid6r_iLsBFWOPXaWamWjMrQfyHQUJ-IqbPZ57gckI130_assertion description "[A non-consensus (non-canonical) donor splice site within exon 1 of the HRPT2 gene is associated with familial isolated primary hyperparathyroidism (FIHP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130808.RAcoid6r_iLsBFWOPXaWamWjMrQfyHQUJ-IqbPZ57gckI130_provenance.
- NP130814.RAXrSx1fxPWaruDRO2B8rtRhtxwjD4GgapTN1i5GkhXAI130_assertion description "[Erythropoietin receptor is present in normal parathyroid, parathyroid adenoma, and hyperplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130814.RAXrSx1fxPWaruDRO2B8rtRhtxwjD4GgapTN1i5GkhXAI130_provenance.
- NP130824.RAacK9HNTlUNeYqtufQOJxm4Qu7RGz1BIocepQTjXAb5g130_assertion description "[The weak immunoreactive expression of p53, combined with a relatively strong expression of bcl-2 contributes to the characteristic slow progression of parathyroid adenoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130824.RAacK9HNTlUNeYqtufQOJxm4Qu7RGz1BIocepQTjXAb5g130_provenance.
- NP130831.RATtMidQjKcKPlgPUjg0WTSvCSl_Os7zfyxBBwlkhdQGo130_assertion description "[Because PTHrP contributes to hypercalcemia and bone metastases, switching of G-protein usage by the CaR may contribute to the pathogenesis of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130831.RATtMidQjKcKPlgPUjg0WTSvCSl_Os7zfyxBBwlkhdQGo130_provenance.
- NP130832.RAY6CVes3PZjPadxbUpjiNrb9_2lzNm6AmGyJ6r9DVCDQ130_assertion description "[functional characterization of seven novel mutations of the CaSR found in familial hypocalciuric hypercalcemia patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130832.RAY6CVes3PZjPadxbUpjiNrb9_2lzNm6AmGyJ6r9DVCDQ130_provenance.
- NP130837.RAUUYLKIyQxUVS5m6pYUN7nh09-ZL_tc0J6WUchYIef44130_assertion description "[A cytosine-to-guanine mutation at 1772 caused a new serine-to-cysteine substitution of the calcium-sensing receptor gene, causing severe neonatal hyperparathyroidism, a variant of hypocalciuric hypercalcemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130837.RAUUYLKIyQxUVS5m6pYUN7nh09-ZL_tc0J6WUchYIef44130_provenance.
- NP130840.RAbaKmNAWkUuzqGCuJsTfyxecRMugRKR8g5xM7AD3J0Vk130_assertion description "[Impaired cotranslational processing of the calcium-sensing receptor due to signal peptide missense mutations is associated with familial hypocalciuric hypercalcemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130840.RAbaKmNAWkUuzqGCuJsTfyxecRMugRKR8g5xM7AD3J0Vk130_provenance.
- NP130841.RAR028UDO1UiiPVLPBeQLZbl71esKICn1B_mPtG6tMe-E130_assertion description "[Direct sequence analysis of exon 4 of her CASR gene identified a heterozygous R227Q mutation in the extracellular domain of the receptor in familial (benign) hypocalciuric hypercalcemia or neonatal yperparathyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130841.RAR028UDO1UiiPVLPBeQLZbl71esKICn1B_mPtG6tMe-E130_provenance.
- NP130843.RATO9MrDiRpaPJzXjvvQjMAXNS3jQcqX8SZU9eVwmh0Rc130_assertion description "[In childhood acute lymphoblastic leukemia and hypercalcemia, translocation was observed in E2A-HLF fusion protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130843.RATO9MrDiRpaPJzXjvvQjMAXNS3jQcqX8SZU9eVwmh0Rc130_provenance.
- NP130852.RAanVSVm8yIPeqSzHcAozU01Q9iBZ1U5VDff8TWBRXtFo130_assertion description "[Missense mutations in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130852.RAanVSVm8yIPeqSzHcAozU01Q9iBZ1U5VDff8TWBRXtFo130_provenance.
- NP130856.RAaB69w7Gg8mEntPJx3_s-rMjhuDtEkHCQKjLPik9Cc7U130_assertion description "[Direct evidence relating to the molecular pathogenesis of pure hair-nail ectodermal dysplasias with KRTHB5 gene mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130856.RAaB69w7Gg8mEntPJx3_s-rMjhuDtEkHCQKjLPik9Cc7U130_provenance.
- NP130862.RAdiXGpMX1KR0sVtUVdw1sMq34K0Uv5A1hQLLTnHr5gBs130_assertion description "[Mutation of the gene encoding NEMO can result in immunodeficiency without ectodermal dysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130862.RAdiXGpMX1KR0sVtUVdw1sMq34K0Uv5A1hQLLTnHr5gBs130_provenance.
- NP130868.RAadeeyPMFDdVHFcJaWEz3rLOlqH7XpIlxbZlZK32X3uE130_assertion description "[point mutation (G1149A) in exon 8 changes codon 291 from glycine to arginine causing X-linked hypohidrotic ectodermal dysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130868.RAadeeyPMFDdVHFcJaWEz3rLOlqH7XpIlxbZlZK32X3uE130_provenance.
- NP130869.RAbD2HHPWnt3fkCx-iG72c4tf3_rCWXUF7jK9H4q9GR24130_assertion description "[data confirm that mutations could cause both X-linked hipohydrotic ectodermal dysplasia and isolated hypodontia and provide evidence that EDA is a strong candidate gene for tooth genesis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130869.RAbD2HHPWnt3fkCx-iG72c4tf3_rCWXUF7jK9H4q9GR24130_provenance.
- NP130870.RARWE9kkrqT6w9TQqPNwvi9nIiyzPFJUnPqCN7Hn_5nTc130_assertion description "[Screening of EDA1 gene in X-linked anhiderotic ectodermal dysplasia using DHPLC: identification of 14 novel mutations in Italian patients is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130870.RARWE9kkrqT6w9TQqPNwvi9nIiyzPFJUnPqCN7Hn_5nTc130_provenance.
- NP130876.RAV8O5UhBU-OYqwQt7BhVjRmfyxEPrHkyKQ6TsQfrpPPs130_assertion description "[p63 and Dlx play central roles in embryonic patterning and regulation of different developmental processes, and their mutations have been associated with ectodermal dysplasias [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130876.RAV8O5UhBU-OYqwQt7BhVjRmfyxEPrHkyKQ6TsQfrpPPs130_provenance.
- NP130877.RASz9QaZ7Ik0k3rX0y0b1Rg11GXBPBs-Re8t4XtKsvnxw130_assertion description "[NF-kappaB is necessary for CYBB and NCF1 gene expression and activation of the phagocyte NADPH oxidase normal and anhidrotic ectodermal dysplasia leukocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130877.RASz9QaZ7Ik0k3rX0y0b1Rg11GXBPBs-Re8t4XtKsvnxw130_provenance.
- NP130885.RATvRhUWDUSnt21NicGHu_RiSg5C1tOYvb95jAP7HPFCQ130_assertion description "[Involvement of the TAB2/TRAF6/TAK1 signalling complex in the Edar signal transduction pathway has important implications for understanding of NF-kappaB activation and anhidrotic ectodermal dysplasia in human.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130885.RATvRhUWDUSnt21NicGHu_RiSg5C1tOYvb95jAP7HPFCQ130_provenance.
- NP130888.RAS6QCWW_kmlbb1MrexR9LU-tCEk53_F616ReqXp-HIIg130_assertion description "[Familial T-cell non-Hodgkin lymphoma caused by biallelic MSH2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130888.RAS6QCWW_kmlbb1MrexR9LU-tCEk53_F616ReqXp-HIIg130_provenance.
- NP130892.RASmLuqS0Tl7Mi6OtMR_-YQwKQgEk2STyeNMoNxilWxHw130_assertion description "[P-gp is expressed before treatment of non-Hodgkin's lymphoma of HIV patients, and is related to poor response to treatment and overall survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130892.RASmLuqS0Tl7Mi6OtMR_-YQwKQgEk2STyeNMoNxilWxHw130_provenance.
- NP130893.RAYXsvCBeLv9BHOIO61XRSEW7HlH8fj_E21_8hAKV6mtQ130_assertion description "[the ATA haplotype was identified as a favourable prognostic factor for T-cell non-Hodgkin lymphoma compared to non-ATA haplotype (P = 0.037, hazard ratio 2.1); IL10 polymorphism may affect the survival of T-cell non-Hodgkin lymphoma patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130893.RAYXsvCBeLv9BHOIO61XRSEW7HlH8fj_E21_8hAKV6mtQ130_provenance.
- NP130895.RAb6pEv2rfr5xv-B2fhII4MZmHfC-6igETI9F6NSJ4rIA130_assertion description "[IL-10 gene variations could be associated to the clinical course of aggressive non-hodgkin's lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130895.RAb6pEv2rfr5xv-B2fhII4MZmHfC-6igETI9F6NSJ4rIA130_provenance.
- NP130900.RARclo5hpO8mBAAPIxSJiliS1ADuwuzsz-xl7Ifu8mOxo130_assertion description "[Increased levels of IL-6 were found in the whole group of untreated patients with B non-Hodgkins lymphoma in comparison with normal controls: IL-6 levels were lower in complete responders ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130900.RARclo5hpO8mBAAPIxSJiliS1ADuwuzsz-xl7Ifu8mOxo130_provenance.
- NP130911.RAf5tfaaW8i9SuPJnWGpVUWUv9GOum_X5sRjYu5gjIVUY130_assertion description "[expression associated with poor outcome in non-Hodgkin lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130911.RAf5tfaaW8i9SuPJnWGpVUWUv9GOum_X5sRjYu5gjIVUY130_provenance.
- NP130919.RAcpRuor2_WcK-0TqLGCp_d8VgVbxXDPJ6fWM7A8_VNOQ130_assertion description "[Genetic variation may affect the degree of association between pre-1980 hair dye use and the risk of non-Hodgkin lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130919.RAcpRuor2_WcK-0TqLGCp_d8VgVbxXDPJ6fWM7A8_VNOQ130_provenance.
- NP130921.RARxfx0g01lMiwLZ7DaHEbTLUkN-3V4BwOB5jSayHd-Vo130_assertion description "[Increased circulating levels of interleukin 1 receptor, type II is associated with Hepatitis C virus positive patients and with those affected also by non-Hodgkin's lymphoma and cryoglobulinemia syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130921.RARxfx0g01lMiwLZ7DaHEbTLUkN-3V4BwOB5jSayHd-Vo130_provenance.
- NP130924.RAVhGwMan_cW-zz04IpVZSwqafx9_26-dz-lJA4uMWdJU130_assertion description "[lower mutational frequencies & decreased BCL-6 mRNA expression in vivo suggest no major role of aberrant somatic hypermutation in HCV-associated mixed cryoglobulinaemia & B-cell non-Hodgkin lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130924.RAVhGwMan_cW-zz04IpVZSwqafx9_26-dz-lJA4uMWdJU130_provenance.
- NP130925.RAbwUzxUoWbmyhMCKbGNBAPxv_zs4mEHg0CKfmamPFHAQ130_assertion description "[BCL6 translocation has a pathogenic in B-cell non-Hodgkin's lymphoma (review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130925.RAbwUzxUoWbmyhMCKbGNBAPxv_zs4mEHg0CKfmamPFHAQ130_provenance.
- NP130927.RASZABwN09NikEYC2sS3fFURuPsF84oEtnm0xxy586q9M130_assertion description "[GM-CSF-driven apoptosis, but not TNF-driven apoptosis was reversibly associated with bcl-2-expression (bcl-2-dependent mechanism) in acute lymphoblastic leukaemia and non-Hodgkin's lymphoma in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130927.RASZABwN09NikEYC2sS3fFURuPsF84oEtnm0xxy586q9M130_provenance.
- NP130936.RAWZu3Abzbzkp23eRKgB7FeHlnDhsEaVqKTFGc7sQ0CzE130_assertion description "[sIL-2R and IL-6, but not IL-2, IL-4, or IL-10, may have a role in preventing progression of aggressive non-Hodgkin's lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130936.RAWZu3Abzbzkp23eRKgB7FeHlnDhsEaVqKTFGc7sQ0CzE130_provenance.
- NP130938.RAfs3hNvb6EQpFg6heSTxRbl__ANJfd253ycP3cn3mux4130_assertion description "[reveal a novel role for non-Hodgkin lymphoma B cells in the development of intratumoral regulatory T cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130938.RAfs3hNvb6EQpFg6heSTxRbl__ANJfd253ycP3cn3mux4130_provenance.
- NP130939.RAef-nnvSj9zAt35CpXZjqRI_0E23l3nzfIhn95sWZQE4130_assertion description "[For T-cell non-Hodgkins Lymphoma, homozygosis for the IL1RN rs454078 T-allele was associated with a 4.5-fold elevated risk ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130939.RAef-nnvSj9zAt35CpXZjqRI_0E23l3nzfIhn95sWZQE4130_provenance.
- NP130943.RAY6r153XIBZIYhHAVpMpjYdBZwM0o5lgvdO9hjOap85c130_assertion description "[Strong expression of vascular endothelial growth factor protein is associated with non-Hodgkin's lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130943.RAY6r153XIBZIYhHAVpMpjYdBZwM0o5lgvdO9hjOap85c130_provenance.
- NP130947.RATnD5bp3Ho8rUxZZFZdaXLWjIV4oLH_nF8UywFGBgDvA130_assertion description "[These observations document a high prevalence of ataxia telangiectasia mutated (ATM) gene and protein expression alterations, suggesting that ATM is involved in childhood non-Hodgkin lymphoma (NHL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130947.RATnD5bp3Ho8rUxZZFZdaXLWjIV4oLH_nF8UywFGBgDvA130_provenance.
- NP130948.RAVz_rFzaf_tU0s-gIl68ImjJ1Jr9bbxr2PrYiz6wa3yo130_assertion description "[expression of the transcription factor DP-1 and its heterodimeric partner E2F-1 in non-Hodgkin lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130948.RAVz_rFzaf_tU0s-gIl68ImjJ1Jr9bbxr2PrYiz6wa3yo130_provenance.
- NP130952.RAVLhpr_yAoJS8nk6D64_ERr-Q2YEhNF3PDkFy_5s5pgA130_assertion description "[non-Hodgkin's lymphoma is not associated with increased expression of VEGF-C ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130952.RAVLhpr_yAoJS8nk6D64_ERr-Q2YEhNF3PDkFy_5s5pgA130_provenance.
- NP130963.RAQ564HTshuEMe1AtgLH3s70Nh09iNtZi7YU5Jepf_MjA130_assertion description "[a marker of follicular B-cell non-Hodgkin's lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130963.RAQ564HTshuEMe1AtgLH3s70Nh09iNtZi7YU5Jepf_MjA130_provenance.
- NP130966.RAR6j6IUi8azv024Q1s0Ks-KsS1BC4_uvOK66iboDh8S4130_assertion description "[analyses of statistical interactions between polymorphisms (p73 G4A, p53 Arg72Pro and p21 Ser31Arg polymorphisms) revealed the marginally significant risk of non-Hodgkin's lymphoma for interaction between p53 Arg72Pro and p73 G4A polymorphisms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130966.RAR6j6IUi8azv024Q1s0Ks-KsS1BC4_uvOK66iboDh8S4130_provenance.
- NP130967.RAQMrjQZsiLEz9iKtgzKCijiEcTeV1QdmFMjyelog-uG4130_assertion description "[Patients with non-Hodgkin's lymphoma presented a high level of survivin expression, it was more pronounced in aggressive than in indolent nHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130967.RAQMrjQZsiLEz9iKtgzKCijiEcTeV1QdmFMjyelog-uG4130_provenance.
- NP130970.RAXgnu-t2Da5-piQkpqQwGuBLAjoK7oMK8Z-Qy2Zejhr8130_assertion description "[expression values for TGF 1 and its receptors I, II, and III were twice as high in the group of patients with a diagnosis of high-grade lymphomas as in the group of patients diagnosed with low-grade lymphomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130970.RAXgnu-t2Da5-piQkpqQwGuBLAjoK7oMK8Z-Qy2Zejhr8130_provenance.
- NP130974.RAZtqQukTXCRe7-9rGIW9rHItlXzrJovDtpcMPgxvXL8Q130_assertion description "[Increased levels of HGF in circulating blood is associated with non-Hodgkin's lymphoma or Hodgkin's lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130974.RAZtqQukTXCRe7-9rGIW9rHItlXzrJovDtpcMPgxvXL8Q130_provenance.
- NP130979.RAfYmx19R-AkcpHaavWBTloF24REY0NDIdlhedLl80mBQ130_assertion description "[CD40L expressed on adjacent non tumoral cells induces multidrug resistance to cytotoxic agents and ceramides in both breast carcinoma and non Hodgkin's lymphoma cell lines, albeit through a caspase independent and dependent pathway respectively ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130979.RAfYmx19R-AkcpHaavWBTloF24REY0NDIdlhedLl80mBQ130_provenance.
- NP130985.RAdAcCqHP52n00O3zI3dRLL57b6p_PIwNbVt8fRQR6fG0130_assertion description "[6 additional carriers of the 657del5 mutation and 2 carriers of the pathogenic NBS1 R215W mutation were identified among 186 non-Hodgkin lymphoma patients from Central Poland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130985.RAdAcCqHP52n00O3zI3dRLL57b6p_PIwNbVt8fRQR6fG0130_provenance.
- NP130987.RAZqS_QtoZLph76ibgd7DFghZehdOB5ZsQD-DMEZWGgc0130_assertion description "[GM-CSF-driven apoptosis, but not TNF-driven apoptosis was reversibly associated with bcl-2-expression (bcl-2-dependent mechanism) in acute lymphoblastic leukaemia and non-Hodgkin's lymphoma in children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130987.RAZqS_QtoZLph76ibgd7DFghZehdOB5ZsQD-DMEZWGgc0130_provenance.
- NP130989.RAVM7LniTw5TeG0I8ZRV2H5y7NuE8ZttPPmUwe2ysgIBg130_assertion description "[data support the hypothesis that genetic variation in the H2AFX gene influences genetic susceptibility or resistance to some subtypes of non-Hodgkin lymphoma by contributing to the maintenance of genome stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130989.RAVM7LniTw5TeG0I8ZRV2H5y7NuE8ZttPPmUwe2ysgIBg130_provenance.
- NP130993.RAS-lgbfpCp6P2TblcBx8j5BAklxBbBBiZaeJ_dik64cQ130_assertion description "[A novel SIX1 mutation suggests a slightly different clinical profile compared to EYA1-related branchio-oto-renal syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP130993.RAS-lgbfpCp6P2TblcBx8j5BAklxBbBBiZaeJ_dik64cQ130_provenance.
- NP131004.RAQoOHvm9fEM_YxkSC_ya_QCGRD_sL1FNvIYqkg0wZGjg130_assertion description "[Elevated CD30 expression is considered one of the causes of constitutive NF-kappaB activation in adult T-cell Leukemia (ATL) cells, and may be involved in ATL development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131004.RAQoOHvm9fEM_YxkSC_ya_QCGRD_sL1FNvIYqkg0wZGjg130_provenance.
- NP131009.RAT_gnWdnfPANok9oTsz3FvKV6LflM9l18k4HG_MXYu4Y130_assertion description "[Up-regulation of cytokine inducible SH2-containing protein is associated with adult T-cell leukemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131009.RAT_gnWdnfPANok9oTsz3FvKV6LflM9l18k4HG_MXYu4Y130_provenance.
- NP131011.RAf2K1U95iGSEC1I2u7oSGVxSMNokOcVqnf8KTfZVY9Ck130_assertion description "[Possible involvement of aryl hydrocarbon receptor (AhR) in adult T-cell leukemia (ATL) leukemogenesis: constitutive activation of AhR in ATL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131011.RAf2K1U95iGSEC1I2u7oSGVxSMNokOcVqnf8KTfZVY9Ck130_provenance.
- NP131015.RAUGup7krGrUPzUgMLCiQFSL7dtrFRtuL5gAIZfH5rN0U130_assertion description "[Down-regulation of TCF8 expression in ATLL cells was associated with resistance to TGF-beta1, a well-known characteristic of ATLL cells, suggesting that escape from TGF-beta1-mediated growth inhibition is important in the pathogenesis of ATLL ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131015.RAUGup7krGrUPzUgMLCiQFSL7dtrFRtuL5gAIZfH5rN0U130_provenance.
- NP131022.RAdFcFYpUEGmW6HIk71_3lA5SPqtre2UiKUoJJTkMPY2o130_assertion description "[PD-1/PD-L1 expression on cells from asymptomatic HTLV-1 carriers and ATLL patients in comparison with cells from healthy donors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131022.RAdFcFYpUEGmW6HIk71_3lA5SPqtre2UiKUoJJTkMPY2o130_provenance.
- NP131024.RAZW22EZ7unOiQfB40CGQTROIQuggrMpA-8q2KZjmZ5ZU130_assertion description "[Upregulation of CCL18 expression and downregulation of CX3CR1 expression play a role in immune responses against the adult t-cell leukemia cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131024.RAZW22EZ7unOiQfB40CGQTROIQuggrMpA-8q2KZjmZ5ZU130_provenance.
- NP131025.RAdSPVJEkFo4vCRXSQxBaI_KsBTDVCYYcJ9UxG_Tt7kQ8130_assertion description "[ASY/Nogo gene may act as a suppressor against adult T-cell leukemia/lymphoma progression, independent of Tax expression ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131025.RAdSPVJEkFo4vCRXSQxBaI_KsBTDVCYYcJ9UxG_Tt7kQ8130_provenance.
- NP131026.RAZucG75t3DwPIvO66tG7PDQ-UKMwIa2Po75Ly_aL5iDU130_assertion description "[LRP was highly expressed and is associated with adult T-cell leukemia/lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131026.RAZucG75t3DwPIvO66tG7PDQ-UKMwIa2Po75Ly_aL5iDU130_provenance.
- NP131038.RAW-5KaF-hFk1eoXWgmpPbbxVcNUmpM5tx95TVWWsZ6pM130_assertion description "[Correction opf X-linked chronic granulomatous disease by gene therapy was augmented by insertional activation of PRDM16.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131038.RAW-5KaF-hFk1eoXWgmpPbbxVcNUmpM5tx95TVWWsZ6pM130_provenance.
- NP131039.RAZ5HGRSazr_f58gV3xvJbzc3r_PmpbGnFoFk4XWPYBew130_assertion description "[Chronic granulomatous disease (CGD) is a genetic disease caused by structural mutations in the enzyme NADPH oxidase that results in severe immunodeficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131039.RAZ5HGRSazr_f58gV3xvJbzc3r_PmpbGnFoFk4XWPYBew130_provenance.
- NP131040.RAVqSgkDXMtvAbP3ZnfeiFbjUCuBAjVdqmeHhE7FRMeVw130_assertion description "[17% of patients, proven to have chronic granulomatous disease, have p47 (phox) deficiency ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131040.RAVqSgkDXMtvAbP3ZnfeiFbjUCuBAjVdqmeHhE7FRMeVw130_provenance.
- NP131044.RAc90nlip-8bAGXdzo5z4-JZ4UC4KnK2NOna37eTOQsIo130_assertion description "[A child with chronic granulomatous disease (CGD) who developed acute lymphoblastic leukemia who was found to have a mutation om the MLL gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131044.RAc90nlip-8bAGXdzo5z4-JZ4UC4KnK2NOna37eTOQsIo130_provenance.
- NP131045.RAcAunDVrxGQ_ODH5flBw1wuhLy_scXbOwITFA5hTCR5M130_assertion description "[gp91 (phox) protein with a Y41D mutation and modest superoxide activity in chronic granulomatous disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131045.RAcAunDVrxGQ_ODH5flBw1wuhLy_scXbOwITFA5hTCR5M130_provenance.
- NP131048.RATeT1J5o7sQTa56eZlXM_RG6IYha4CauAAOaNnuuqdzQ130_assertion description "[monoclonal antibody CL5 was used to probe for the presence of gp91phox in membrane preparations from neutrophils of patients with nine genetically distinct forms of X-linked chronic granulomatous disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131048.RATeT1J5o7sQTa56eZlXM_RG6IYha4CauAAOaNnuuqdzQ130_provenance.
- NP131050.RAR-U3lRNZ3-NcjkGfrth5ghA5u7dkpvr1iGSh-JShALs130_assertion description "[A novel and unusual case of chronic granulomatous disease in a child with a homozygous 36-bp deletion in the CYBA gene (A22 (0)) leading to the activation of a cryptic splice site in intron 4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131050.RAR-U3lRNZ3-NcjkGfrth5ghA5u7dkpvr1iGSh-JShALs130_provenance.
- NP131051.RAbPE0EZ_u6u4x1Rho87Z-GBVdJ6BYCC115zEt-_qCaBc130_assertion description "[a heterozygous alteration in the PRF1 gene may have made the patient more susceptible for hemophagocytic lymphohistiocytosis under the circumstances of ongoing infection associated with X-linked chronic granulomatous disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131051.RAbPE0EZ_u6u4x1Rho87Z-GBVdJ6BYCC115zEt-_qCaBc130_provenance.
- NP131056.RATcozuarHA_InLawyls1jDMnNwYPG_V6B6YBXF82qP48130_assertion description "[Significant cross-talk between calcium and retinoic acid signaling pathways regulates the differentiation of myeloid leukemia cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131056.RATcozuarHA_InLawyls1jDMnNwYPG_V6B6YBXF82qP48130_provenance.
- NP131057.RAf_zoHPqQZQt7v0FOWAU5B_pll-EY0IzhXi8UdZCY-SU130_assertion description "[neoplastic cells in myeloid leukemias frequently express VEGFR including NRP-1 and NRP-2 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131057.RAf_zoHPqQZQt7v0FOWAU5B_pll-EY0IzhXi8UdZCY-SU130_provenance.
- NP131073.RAd53VnZIcTPynvyiHgCgMSTkdhhdlfiLl9sLenc7FGeY130_assertion description "[AML1-ETO may facilitate accumulation of genetic alterations by suppressing endogenous DNA repair in acutet myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131073.RAd53VnZIcTPynvyiHgCgMSTkdhhdlfiLl9sLenc7FGeY130_provenance.
- NP131075.RATvND-S0AsNCv4wVGvr7qjX8VFBXQmZCpG_B4qd5P5WU130_assertion description "[L3MBTL may have a role in myeloid leukemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131075.RATvND-S0AsNCv4wVGvr7qjX8VFBXQmZCpG_B4qd5P5WU130_provenance.
- NP131078.RAXOaPPwZALvNlfW3Ry-6W5GQ9KwVFl64fY3DNqRr7EHM130_assertion description "[Data show that Bcr-Abl-induced activation of the nuclear factor kappaB cascade in myeloid leukemia cells is largely mediated by tyrosine-phosphorylated PKD2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131078.RAXOaPPwZALvNlfW3Ry-6W5GQ9KwVFl64fY3DNqRr7EHM130_provenance.
- NP131083.RAdSVaspDTVaYMd12ALMYdgNQJght-CL8cz4_d2OBBQM8130_assertion description "[A new fusion gene NUP98-IQCG identified in an acute T-lymphoid/myeloid leukemia with a t (3; 11) (q29q13; p15) del (3) (q29) translocation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131083.RAdSVaspDTVaYMd12ALMYdgNQJght-CL8cz4_d2OBBQM8130_provenance.
- NP131087.RAXxUhPUbVt6X9OSZrGL2czvXHJTqgdaScMNkB4MMdQIM130_assertion description "[High incidence of t (7; 12) (q36; p13) in infant myeloid leukemia is associated with ectopic expression of HLXB9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131087.RAXxUhPUbVt6X9OSZrGL2czvXHJTqgdaScMNkB4MMdQIM130_provenance.
- NP131094.RAbcwH-JwmUO-n-K-JtoGDdY0KTWExilTrkG_oo3joPVQ130_assertion description "[Activation of clg, a novel dbl family guanine nucleotide exchange factor gene, by proviral insertion at evi24, a common integration site in B cell and myeloid leukemias ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131094.RAbcwH-JwmUO-n-K-JtoGDdY0KTWExilTrkG_oo3joPVQ130_provenance.
- NP131100.RAdJObQpfrNsPuUektUcCC808lc4AdVrUT5N6PW1c_H9U130_assertion description "[MTHFR C677T polymorphism displays a similar distribution pattern in lymphoid and myeloid leukemias and that the frequency of the homozygote variant genotype (677TT) is lower in all leukemia types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131100.RAdJObQpfrNsPuUektUcCC808lc4AdVrUT5N6PW1c_H9U130_provenance.
- NP131106.RAdL_uPVXsoJ9zwzq_umdnOVtGMtaiZzOMXwDLd6T9r3A130_assertion description "[c-Jun has an important functional role in the induction of cell cycle arrest and proliferation arrest of myeloid leukemia cells because of the ligation of the cell surface adhesion receptor CD44 by anti-CD44 antibody.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131106.RAdL_uPVXsoJ9zwzq_umdnOVtGMtaiZzOMXwDLd6T9r3A130_provenance.
- NP131107.RAQ1RZQ9PkH6AhEHeUaiMjHQrQl8sFEP6BQ8OvxEZIpKE130_assertion description "[MLL5 is a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131107.RAQ1RZQ9PkH6AhEHeUaiMjHQrQl8sFEP6BQ8OvxEZIpKE130_provenance.
- NP131117.RAXNxkLkHYsowjUuXVmvxpESIi_9uWXsdCAMHO5RCTzx4130_assertion description "[Eight novel mutations were identified in CFTR in Indian Cystic fibrosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131117.RAXNxkLkHYsowjUuXVmvxpESIi_9uWXsdCAMHO5RCTzx4130_provenance.
- NP131121.RASEfU9n0sej1enIpiT-6XKw3SmxWEqUZHAHsVlLJtkW0130_assertion description "[An analysis of 143 unrelated Belgian patients with a positive diagnosis of cystic fibrosis for mutations in the cystic fibrosis transmembrane conductance regulator gene is presented.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131121.RASEfU9n0sej1enIpiT-6XKw3SmxWEqUZHAHsVlLJtkW0130_provenance.
- NP131131.RAefRyLrgohzAx_3PAVgE9jRw1Hvh9rdshmhgVQMHOwBw130_assertion description "[annexin A1 downregulation in cystic fibrosis knock-out mice and patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131131.RAefRyLrgohzAx_3PAVgE9jRw1Hvh9rdshmhgVQMHOwBw130_provenance.
- NP131135.RAbgYTneAFxZZ6S5cErWzpMWIqDmMF8F2IvJgPIdONLas130_assertion description "[gene therapy target for cystic fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131135.RAbgYTneAFxZZ6S5cErWzpMWIqDmMF8F2IvJgPIdONLas130_provenance.
- NP131140.RAU2qLir9wX-ICp4iih-0dJw_opXSK4j_jcA8ow-wuT8E130_assertion description "[CTFR gene transfer to human cystic fibrosis pancreatic duct cells using a Sendai virus vector.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131140.RAU2qLir9wX-ICp4iih-0dJw_opXSK4j_jcA8ow-wuT8E130_provenance.
- NP131142.RATKNkItjSc9bxpW9AbLCSOH3G0GfQfZuZd_L_bx7DeBA130_assertion description "[Improved maturation of CFTR mediated by a valine signal may be of potential use in gene therapy of cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131142.RATKNkItjSc9bxpW9AbLCSOH3G0GfQfZuZd_L_bx7DeBA130_provenance.
- NP131145.RAfJuPN9z2F1izX74FF919623eJsjrWopfl9CCYZXPdAU130_assertion description "[Induced-sputum innate immune factor levels discriminate inflammatory changes in cystic fibrosis, COPD, and asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131145.RAfJuPN9z2F1izX74FF919623eJsjrWopfl9CCYZXPdAU130_provenance.
- NP131147.RAbeN6G5SkjIs5jMgyeVyCeOc047iXiiHl8QPTEmLpLLY130_assertion description "[CXCR1 cleavage on neutrophils disables bacterial killing in cystic fibrosis lung disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131147.RAbeN6G5SkjIs5jMgyeVyCeOc047iXiiHl8QPTEmLpLLY130_provenance.
- NP131148.RAaMwvkYoKxCgcSfrtGc0S_R77hPCoen2KD01ovT2Q6CQ130_assertion description "[spontaneous release of IL-8 and IL-1ra by airway neutrophils was significantly higher than that from blood neutrophils in cystic fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131148.RAaMwvkYoKxCgcSfrtGc0S_R77hPCoen2KD01ovT2Q6CQ130_provenance.
- NP131149.RAX9WFixW-pM8NDvRmZv1UN1Zl_jqmeB-lxdc9w-d-i6c130_assertion description "[confirmed the regulation of IL-8 promoter by CHOP in cystic fibrosis cells using the IL-8 reporter assay ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131149.RAX9WFixW-pM8NDvRmZv1UN1Zl_jqmeB-lxdc9w-d-i6c130_provenance.
- NP131164.RASxYVbLit3iUF4rx4wCJCGu1m8Nf1w-c05mMAFYsQQ9Y130_assertion description "[Tyrosine kinase c-Src constitutes a bridge between cystic fibrosis transmembrane regulator channel failure and MUC1 overexpression in cystic fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131164.RASxYVbLit3iUF4rx4wCJCGu1m8Nf1w-c05mMAFYsQQ9Y130_provenance.
- NP131169.RAVKMjhQybwEA-_ThdMTPtwS8HHefH9TZbSSnDH5ltjWU130_assertion description "[Protein kinase C epsilon-dependent regulation of cystic fibrosis transmembrane regulator involves binding to a receptor for activated C kinase (RACK1) and RACK1 binding to Na+/H+ exchange regulatory factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131169.RAVKMjhQybwEA-_ThdMTPtwS8HHefH9TZbSSnDH5ltjWU130_provenance.
- NP131172.RAUEHjXnTe-24H1dYL96uVBDvIJBuJGzBJgDvXge7MdU0130_assertion description "[Synthesized locally at mucosal sites/inhibit target enzymes released into interstitium/be important in controlling excessive neutrophil elastase release in chronic obstructive pulmonary disease and cystic fibrosis.(review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131172.RAUEHjXnTe-24H1dYL96uVBDvIJBuJGzBJgDvXge7MdU0130_provenance.
- NP131188.RAbPVDODYtQqLGYA1TtW3bKNTWLns7cTyvHsACbwzN97M130_assertion description "[spontaneous release of IL-8 and IL-1ra by airway neutrophils was significantly higher than that from blood neutrophils in cystic fibrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131188.RAbPVDODYtQqLGYA1TtW3bKNTWLns7cTyvHsACbwzN97M130_provenance.
- NP131194.RAQU_ITmD_P2j2HV5cRboPGGfroMCzhgB9tYyTUqXsGuA130_assertion description "[FXYD5 is upregulated in cystic fibrosis epithelia which may exacerbate the Na (+) hyperabsorption and surface liquid dehydration observed in cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131194.RAQU_ITmD_P2j2HV5cRboPGGfroMCzhgB9tYyTUqXsGuA130_provenance.