Nanopublications LDF server

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

• NP144052.RAUXqdH3Imn7XcaudhPWwdEUdLC3hD82Q_xlbJttInEbU130_assertion description "[elevated neutral endopeptidase activity in the skin and chronic ulcers of subjects with diabetes combined with peripheral neuropathy may contribute to deficient neuroinflammatory signaling and may impair wound healing in subjects with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144052.RAUXqdH3Imn7XcaudhPWwdEUdLC3hD82Q_xlbJttInEbU130_provenance.
• NP144053.RAQ371s3mFE2TcGa8UGOEwnLAScffWpc1Q0w7K_Y8sAb0130_assertion description "[Insufficient upregulation of hBD2 in both diabetic foot and venous calf ulcers may suggest the pathological role of this protein in the chronicity of ulcers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144053.RAQ371s3mFE2TcGa8UGOEwnLAScffWpc1Q0w7K_Y8sAb0130_provenance.
• NP144055.RAQ9EC7vK-vUpzGtrQlNR_CEK_8XE8CsHCXoEqYHTXICw130_assertion description "[induction of MxA expression in some patients with systemic sclerosis, correlating with the presence of ischemic ulcers and other signs of worse disease, suggests a potential role of Type I IFN in the pathogenesis of this disease and/or its complications ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144055.RAQ9EC7vK-vUpzGtrQlNR_CEK_8XE8CsHCXoEqYHTXICw130_provenance.
• NP144058.RAe6OMH3eD1KHzyJn-40X2190LtehHQoX7lfR8hgmdArY130_assertion description "[data show that host genetic variants at the IL-1beta locus predispose to bacterial vaginosis among Caucasian non-pregnant women ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144058.RAe6OMH3eD1KHzyJn-40X2190LtehHQoX7lfR8hgmdArY130_provenance.
• NP144064.RAQQpaIEQX--USFAXPEGySC__CN8VHnIlWn7ppCAf1Wvc130_assertion description "[In African Americans, midpregnancy human neutrophil peptide 1-3 levels were more informative to preterm delivery risk than was bacterial vaginosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144064.RAQQpaIEQX--USFAXPEGySC__CN8VHnIlWn7ppCAf1Wvc130_provenance.
• NP144077.RAbsRZfJBS5G8jyHDIkjBJG_hjA7G5NpXah-ospoH573s130_assertion description "[Lack of activation KIR2DS5 may play an important role in the development of bronchiolitis obliterans but not in the control of cytomegalovirus reactivation after lung transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144077.RAbsRZfJBS5G8jyHDIkjBJG_hjA7G5NpXah-ospoH573s130_provenance.
• NP144084.RAadD9qTcOvxZ2qe1jjZIwmsn2nI_WMF6uPTq0dVjAyjw130_assertion description "[Significantly elevated tissue inhibitor of metalloproteinase 1 in broncho-alveolar lavage fluid is associated with Bronchiolitis obliterans ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144084.RAadD9qTcOvxZ2qe1jjZIwmsn2nI_WMF6uPTq0dVjAyjw130_provenance.
• NP144085.RAff8GptdiqGn3b3RPhEzPfL-JB-zk0gCeo3ew2YOjgCM130_assertion description "[Peroxiredoxin II (PRXII) exclusively expressed in bronchiolitis obliterans syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144085.RAff8GptdiqGn3b3RPhEzPfL-JB-zk0gCeo3ew2YOjgCM130_provenance.
• NP144086.RAaaW36Dgp56fG9cS1rZIJIWDk94jdBH5_PLNDkkaclhc130_assertion description "[Serum measurement has the potential to serve as a noninvasive diagnostic test for the detection of bronchiolitis obliterans syndrome in lung transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144086.RAaaW36Dgp56fG9cS1rZIJIWDk94jdBH5_PLNDkkaclhc130_provenance.
• NP144089.RARaMJGakBREVuCgVZAvFB0j9Llg2I8J6cuwpkY-0I89Y130_assertion description "[results strongly suggest sCD30 levels of lung transplant patients increase several months prior to clinical evidence of Bronchiolitis Obliterans Syndrome (BOS); rise in serum sCD30 levels can be used as a marker to detect patients at risk to develop BOS ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144089.RARaMJGakBREVuCgVZAvFB0j9Llg2I8J6cuwpkY-0I89Y130_provenance.
• NP144091.RAZZ__EHd0twXCuUDnNOSLf1L8zUdSJDXPj19y4kMfuNc130_assertion description "[Surfactant protein A (SP-A), expressed consistently less in bronchiolitis obliterans syndrome patients than in stable lung transplant recipients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144091.RAZZ__EHd0twXCuUDnNOSLf1L8zUdSJDXPj19y4kMfuNc130_provenance.
• NP144093.RASwtknSo7BEbwpngfNOq6as1eLlKxKNk9spd6LTQk8w8130_assertion description "[p16INK4a and p14ARF aberrations are common in oral verrucous leukoplakia/of heterozygosity occured in 45% of PVL patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144093.RASwtknSo7BEbwpngfNOq6as1eLlKxKNk9spd6LTQk8w8130_provenance.
• NP144097.RAQMzG2D-3injIgchtBNl48b6KlsOu_9844bA6FuVht9Y130_assertion description "[Type IV collagen expression changed in candidal leukoplakia with epithelial dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144097.RAQMzG2D-3injIgchtBNl48b6KlsOu_9844bA6FuVht9Y130_provenance.
• NP144098.RAXMbV20dFG5bXf1aDwbzDDv1sZC_ZBlYsvvIXae71JBU130_assertion description "[Genetic variants of IL4 could contribute to the development of chronic disseminated candidiasis in adult patients with acute leukemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144098.RAXMbV20dFG5bXf1aDwbzDDv1sZC_ZBlYsvvIXae71JBU130_provenance.
• NP144102.RAVRdguUA410boJCn3zvYqj9twGYPpVVpCjBcE7LKnaqc130_assertion description "[SLC25A3 protein deficiency is associated with lactic acidosis, hypertrophic cardiomyopathy, and muscular hypotonia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144102.RAVRdguUA410boJCn3zvYqj9twGYPpVVpCjBcE7LKnaqc130_provenance.
• NP144105.RAQBsqghBEtnGiRPXuZcutBEx2EdocA1UsQUiaq_mJUmE130_assertion description "[clinical features & electroencephalographic findings of 2 patients affected by a previously unreported CDKL5 mutation; both manifest Hanefeld variant Rett syndrome & had early-onset seizures, hand stereotypies, congenital psychomotor delay & hypotonia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144105.RAQBsqghBEtnGiRPXuZcutBEx2EdocA1UsQUiaq_mJUmE130_provenance.
• NP144111.RATssYC9bq6bD1w9Q2kTRXg6d0uQ-ovsupew4Z16-YoDs130_assertion description "[The glycogen-storage cardiomyopathy produced by LAMP2 or PRKAG2 mutations resembles hypertrophic cardiomyopathy but is distinguished by electrophysiological abnormalities ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144111.RATssYC9bq6bD1w9Q2kTRXg6d0uQ-ovsupew4Z16-YoDs130_provenance.
• NP144115.RARauECoDrzBVQ04KJEmnbBPtmRrT8G9-R8RSMOHGffdo130_assertion description "[The EDN2 A985 allele, which is considered to be protective in cardiovascular disease, may be a risk factor for atrial fibrillation in patients with hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144115.RARauECoDrzBVQ04KJEmnbBPtmRrT8G9-R8RSMOHGffdo130_provenance.
• NP144117.RAcyXPGUQFOwjEy1BqEL8P_ICbQyXODajVgs3jLkiqmkM130_assertion description "[Genetic variation in angiotensin-converting enzyme 2 gene is associated with extent of left ventricular hypertrophy in hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144117.RAcyXPGUQFOwjEy1BqEL8P_ICbQyXODajVgs3jLkiqmkM130_provenance.
• NP144118.RAVdGYrgZG-vh0L80NEZIZLqSlfHj5YmQTiOlkJazSQOU130_assertion description "[mutation causes early onset hypertrophic cardiomyopathy and encephalopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144118.RAVdGYrgZG-vh0L80NEZIZLqSlfHj5YmQTiOlkJazSQOU130_provenance.
• NP144122.RAUqbMEh6JEDyr3e_Zdu47_j1mh_Esr9YA3C0nEDvfIMQ130_assertion description "[the missense MYBPC3 mutation E334K destabilizes its protein and may contribute to cardiac dysfunction in hypertrophic cardiomyopathy through impairment of the ubiquitin-proteasome system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144122.RAUqbMEh6JEDyr3e_Zdu47_j1mh_Esr9YA3C0nEDvfIMQ130_provenance.
• NP144125.RAVq0Ig_zzFRIi7UwfdQKpswAok9lv3HvPyQSwRbpz2ec130_assertion description "[Screening of the exons in hypertrophic cardiomyopathy revealed two variations - one novel frame shift mutation in exon 19 at the nucleotide position 11577-11578 and one novel single nucleotide polymorphism (SNP) in codon 1093 of exon 31.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144125.RAVq0Ig_zzFRIi7UwfdQKpswAok9lv3HvPyQSwRbpz2ec130_provenance.
• NP144126.RAcUDnA2RlB4L6YpwjzVXLNXTr3LhTgyRH837CL_CFJZk130_assertion description "[Results suggest that the cardiac myosin-binding protein C gene (MYBPC3) is the predominant gene for hypertrophic cardiomyopathy in eastern Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144126.RAcUDnA2RlB4L6YpwjzVXLNXTr3LhTgyRH837CL_CFJZk130_provenance.
• NP144128.RAdEmukRdYsjKKvSFo2r1pQWHOI90CN4ixn4qS9lW-GU0130_assertion description "[Troponin T mutations have distinct cardiac functional effects in hypertrophic cardiomyopathy patients without hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144128.RAdEmukRdYsjKKvSFo2r1pQWHOI90CN4ixn4qS9lW-GU0130_provenance.
• NP144131.RAVvf3zAkuU3K300NPFjK4pn9GaGDQF7y8cPmGwE5zpns130_assertion description "[Left ventricular end systolic diameter increased and ejection fraction reduction was noted in the majority of R403W (MYH7) mutations in progression to hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144131.RAVvf3zAkuU3K300NPFjK4pn9GaGDQF7y8cPmGwE5zpns130_provenance.
• NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_assertion description "[hypertrophic cardiomyopathy, left ventricular non-compaction (HCM and LVNC) may appear as overlapping entities/ACTC E101K mutation should be considered in the genetic diagnosis of LVNC, apical HCM, and septal defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144134.RAYcExd-1bQcEMXaAw_osM7vLEePtoY8rmCeyCPspRxnM130_provenance.
• NP144138.RAcnEuxdiw29goX23UbudkHicyjJ1BHrhFH1mTZgNgvyA130_assertion description "[This is th e first study to show that serum CA 125 is related to the presence and severity of heart failure and diastolic dysfunction in hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144138.RAcnEuxdiw29goX23UbudkHicyjJ1BHrhFH1mTZgNgvyA130_provenance.
• NP144144.RAcXC7cR_JoqCUA494tH3zWJsL_ZuXmXBbfySzcJVFghg130_assertion description "[Studies suggest that the obscurin abnormality may be involved in the pathogenesis of hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144144.RAcXC7cR_JoqCUA494tH3zWJsL_ZuXmXBbfySzcJVFghg130_provenance.
• NP144149.RAeawGowKqJIvc7nHjL9m944sUfzsRlVHJ3aIWQH2Z1SI130_assertion description "[One novel SCO2 mutation has been identified in a patient with hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144149.RAeawGowKqJIvc7nHjL9m944sUfzsRlVHJ3aIWQH2Z1SI130_provenance.
• NP144150.RASwGUTXEOrzoNU6ed8b5p-aQep3XkpI4Q4BOduFFz5Zo130_assertion description "[CT genotype of CYP11B2 gene may be one of factors responsible for the pathogenesis of hypertrophic cardiomyopathy HCM in a proportion of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144150.RASwGUTXEOrzoNU6ed8b5p-aQep3XkpI4Q4BOduFFz5Zo130_provenance.
• NP144153.RAZC3P7HZQiCgkxOrkZ_jmuAznLH81SF6psx89mMh9rPc130_assertion description "[this is the first report on JPH2 mutation associated with hypertrophic cardiomyopathy ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144153.RAZC3P7HZQiCgkxOrkZ_jmuAznLH81SF6psx89mMh9rPc130_provenance.
• NP144162.RAZxfarGvGCBaIZCihgXKYYLgjutPNTjrCZnP0YPS6dpU130_assertion description "[Polymorphism A1166C contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy/mutated receptor has changed sensitivity to Angiotensine II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144162.RAZxfarGvGCBaIZCihgXKYYLgjutPNTjrCZnP0YPS6dpU130_provenance.
• NP144163.RAW0ENTngKmxT0v4sjr4KlUUWv5JVxwvftQh7iYuX5QRc130_assertion description "[Screening patients with dilated cardiomyopathy, as well as hypertrophic cardiomyopathy, for this mutation is of signifiant importance with this mutation diagnosing dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144163.RAW0ENTngKmxT0v4sjr4KlUUWv5JVxwvftQh7iYuX5QRc130_provenance.
• NP144164.RAThocSjP8vD6JXdd00-SAe3hEsFcFj7Hw7sUM6PKbZrw130_assertion description "[Identification of interactions between domains of Myosin binding protein-C that are modulated by hypertrophic cardiomyopathy missense mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144164.RAThocSjP8vD6JXdd00-SAe3hEsFcFj7Hw7sUM6PKbZrw130_provenance.
• NP144166.RAQq3LfGJphNE3mGJLa57nO1QURTUj6LW79eDsGiXfF9Y130_assertion description "[Two mutations in troponin I that cause hypertrophic cardiomyopathy have contrasting effects on cardiac muscle contractility ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144166.RAQq3LfGJphNE3mGJLa57nO1QURTUj6LW79eDsGiXfF9Y130_provenance.
• NP144173.RAZP8TJLgeAP9EGzM7FU_7ExgiBDHN_nXozAOnjOaFmME130_assertion description "[the expression of the human Hypertrophic Cardiomyopathy Mutant Tropomyosin in transgenic Mice results in myocardial contractile dysfunction ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144173.RAZP8TJLgeAP9EGzM7FU_7ExgiBDHN_nXozAOnjOaFmME130_provenance.
• NP144176.RARhmsnxLe6bdI69PaYC4faLfJn2ZGdlD9MT115gVAFY4130_assertion description "[Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144176.RARhmsnxLe6bdI69PaYC4faLfJn2ZGdlD9MT115gVAFY4130_provenance.
• NP144178.RAdiGV0a0szfq0teBsVZoJf1v4dmHojGFNIgBy_DQy8HM130_assertion description "[Polymorphism I/D for the eNOS gene is described as modyfying for the gene ACE, worsening the hypertrophic cardiomyopathy condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144178.RAdiGV0a0szfq0teBsVZoJf1v4dmHojGFNIgBy_DQy8HM130_provenance.
• NP144180.RAb-2ZQdOXi48CBTLqZLn3zYdxUuVT5UK3PC7BQdMvtuA130_assertion description "[Mutations in the CRP3/MLP gene can cause hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144180.RAb-2ZQdOXi48CBTLqZLn3zYdxUuVT5UK3PC7BQdMvtuA130_provenance.
• NP144185.RAQJCRuQ_LS4kZSw4rXbRahUKHiULFwILeu_fP7dPDO6o130_assertion description "[our data reveal a novel function of p110alpha in medulloblastoma growth and survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144185.RAQJCRuQ_LS4kZSw4rXbRahUKHiULFwILeu_fP7dPDO6o130_provenance.
• NP144187.RAezrx2SP4Gb2PgqrpL4HUBXqYfFH2pVeAaV2W8TeinIY130_assertion description "[Msi1 may promote cancer cell proliferation and survival as its loss seems to have a detrimental effect in the maintenance of medulloblastoma cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144187.RAezrx2SP4Gb2PgqrpL4HUBXqYfFH2pVeAaV2W8TeinIY130_provenance.
• NP144189.RAQh98RbYwFffIXKM9bd1zewUtOzl3PWiDi2hGc4FoSvY130_assertion description "[Gain of 8q-mapped EF-1 delta is associated with adverse outcome in Medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144189.RAQh98RbYwFffIXKM9bd1zewUtOzl3PWiDi2hGc4FoSvY130_provenance.
• NP144190.RAZmncGubT1ENWaTUiufC5-E7ctI5MZxS4fmTpR9AhtpI130_assertion description "[protein levels of translational, splicing, processing, chaperone, protein handling, and metabolism machineries were shown to depend on neurotrophin-3-induced TrkC activation in the medulloblastoma cell line DAOY ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144190.RAZmncGubT1ENWaTUiufC5-E7ctI5MZxS4fmTpR9AhtpI130_provenance.
• NP144191.RARDC3GIsAY7Ugl0Nvx6vhwXvWZdPkEJjv9yzRafWXNpU130_assertion description "[overexpression of survivin mRNA is a common feature in medulloblastoma, may contribute to their anti-apoptosis properties and clinical behaviours ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144191.RARDC3GIsAY7Ugl0Nvx6vhwXvWZdPkEJjv9yzRafWXNpU130_provenance.
• NP144192.RAf_TtnoR7Tjt459yrkxB35hagoq955FsnixCV7JLxAwg130_assertion description "[MYC, LDHB, and CCNB1 may have roles in progression of medulloblastoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144192.RAf_TtnoR7Tjt459yrkxB35hagoq955FsnixCV7JLxAwg130_provenance.
• NP144194.RAaMTZ1mcDKqryF8NnqNB2eBwN_DcTwP7uI2kpGOUGfyY130_assertion description "[c-myc seems to play a causal role in inducing anaplasia in medulloblastoma; it is proposed that c-myc dysregulation is involved in the progression of these malignant embryonal neoplasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144194.RAaMTZ1mcDKqryF8NnqNB2eBwN_DcTwP7uI2kpGOUGfyY130_provenance.
• NP144200.RAcjtEPL2LFoIGVvzyMOE-uOL-7AqmM0B8iT-0fSfF3Mo130_assertion description "[Amino acid substitutions in the Cxcr4 is associated with the pathogenesis of medulloblastomas ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144200.RAcjtEPL2LFoIGVvzyMOE-uOL-7AqmM0B8iT-0fSfF3Mo130_provenance.
• NP144214.RAf4YziDAdJblpSjhsWz86wffowE4Yn67QN-ff_x1PSm4130_assertion description "[Overexpression of CDK6 correlated significantly with poor prognosis and represented an independent prognostic marker of overall survival in medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144214.RAf4YziDAdJblpSjhsWz86wffowE4Yn67QN-ff_x1PSm4130_provenance.
• NP144215.RAR1g42zo-ThpQh0bVm8Acl1rE5Ivuf7Vvs4N79RbNrDc130_assertion description "[CDK6 is regulated by microRNA 124 in medulloblastoma and that miR 124 modulates medulloblastoma cell growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144215.RAR1g42zo-ThpQh0bVm8Acl1rE5Ivuf7Vvs4N79RbNrDc130_provenance.
• NP144218.RAVZNqhm8qDyiDz616LinLGU8oHrVTi6zAMFPtmdmUHNA130_assertion description "[OTX2 functions to specify the fate of neuroectoderm in various regions of the developing brain/developmental role is consistent with the evidence suggesting that OTX2 is a medulloblastoma oncogene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144218.RAVZNqhm8qDyiDz616LinLGU8oHrVTi6zAMFPtmdmUHNA130_provenance.
• NP144224.RATPb3Y0UHrym3rKbr_TWoDfbwcyF-SFC9T-RPCO9iGRI130_assertion description "[CDK6 is regulated by microRNA 124 in medulloblastoma and that miR 124 modulates medulloblastoma cell growth ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144224.RATPb3Y0UHrym3rKbr_TWoDfbwcyF-SFC9T-RPCO9iGRI130_provenance.
• NP144225.RAXtbYDoaiDbrZyH8OzL9-VgrrEKQBOXgnl-3xQ7qm0SA130_assertion description "[The importance of STAT3 signaling in maintenance and survival of medulloblastoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144225.RAXtbYDoaiDbrZyH8OzL9-VgrrEKQBOXgnl-3xQ7qm0SA130_provenance.
• NP144231.RAQwwc3lDMZWM2nkUu2zx4NGdPAyy6L4IO3cexgemn4Ak130_assertion description "[alpha dystroglycan glycosylation & laminin binding to alpha dystroglycan are altered in certain pediatric solid tumors and suggest that aberrant dystroglycan glycosylation may contribute to tumor cell biology in patients with RMS, medulloblastoma, & NBL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144231.RAQwwc3lDMZWM2nkUu2zx4NGdPAyy6L4IO3cexgemn4Ak130_provenance.
• NP144239.RAcDQf6ZayRGRA6Y9zKxxsr1tamz93ZHduEQSmdWBpx2w130_assertion description "[These data suggest that mGlu4 receptor enhancers are promising drugs for the treatment of medulloblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144239.RAcDQf6ZayRGRA6Y9zKxxsr1tamz93ZHduEQSmdWBpx2w130_provenance.
• NP144241.RAQnFyRKgMeHvDY_OLrTCgrH74gPTzRShllZ4PKCPnNtU130_assertion description "[Study identified inherited loss-of-function KIF1Bbeta missense mutations in neuroblastomas and pheochromocytomas and an acquired loss-of-function mutation in a medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144241.RAQnFyRKgMeHvDY_OLrTCgrH74gPTzRShllZ4PKCPnNtU130_provenance.
• NP144249.RAURlTo5nzuQijchNJhp_FfofgC79Lk7oiIJhniwvd7mw130_assertion description "[The gene encoding the alpha 2 subunit of type I collagen, COL1A2, was overexpressed in medulloblastoma and supratentorial PNET specimens, and confirmed in three gene expression datasets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144249.RAURlTo5nzuQijchNJhp_FfofgC79Lk7oiIJhniwvd7mw130_provenance.
• NP144250.RAXRLRERuvqaeWl8AimBiWgKddsO_NEzJiDEP9gy4TAgw130_assertion description "[data support the role of SPINT2 as a putative tumor suppressor gene in medulloblastoma and further implicate dysregulation of the HGF/MET signaling pathway in the pathogenesis of medulloblastoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144250.RAXRLRERuvqaeWl8AimBiWgKddsO_NEzJiDEP9gy4TAgw130_provenance.
• NP144251.RAb3G1NkxRa8syYUwlddUwb-Vd319ilhu3a1uTMFQUpXU130_assertion description "[Gain of 8q-mapped RPS20 is associated with adverse outcome in Medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144251.RAb3G1NkxRa8syYUwlddUwb-Vd319ilhu3a1uTMFQUpXU130_provenance.
• NP144252.RATqZiJ1ku5hl5pSnL4FvgPb9jn4KBqYYmTLr3qH-MMCA130_assertion description "[In medulloblastoma, HGF induces cell cycle progression, cell proliferation, apoptosis and increase in cell size in a c-Myc-dependent manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144252.RATqZiJ1ku5hl5pSnL4FvgPb9jn4KBqYYmTLr3qH-MMCA130_provenance.
• NP144256.RAclWyotDSp1kPrMPlxcU79amK8utVAnWadjg_EsXd1QE130_assertion description "[up-regulates S100A4 and several other prometastatic genes in medulloblastoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144256.RAclWyotDSp1kPrMPlxcU79amK8utVAnWadjg_EsXd1QE130_provenance.
• NP144257.RAYDu1LFuZ98C-GPcd8YSzuiBngsyrgCkad_IRKvXCVyk130_assertion description "[Role of Wnt pathway in medulloblastoma oncogenesis: accumulation of beta-catenin in tumor cells was immunohistochemically proven in 5 cases; 2 cases showed positive immunoreactivity for Wnt-1 and another 2 showed mutation of either CTNNB1 or AXIN1 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144257.RAYDu1LFuZ98C-GPcd8YSzuiBngsyrgCkad_IRKvXCVyk130_provenance.
• NP144258.RAVfa4d0lYD_XHr4IhQRJoJnRmpIqkKastNJgscLevFxg130_assertion description "[S100A4 is a direct target of ERBB2 signaling in medulloblastoma cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144258.RAVfa4d0lYD_XHr4IhQRJoJnRmpIqkKastNJgscLevFxg130_provenance.
• NP144259.RAb_xqaQrPc0dJ1tIdVs5rXQVgCHKHa_aERE-UcrJhlOI130_assertion description "[The expression of FOXG1 showed an inverse relationship/copy gain was seen in 55/59 of a validating set of tumors and showed a positive correlation with protein expression representing the first report of FOXG1 dysregulation in medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144259.RAb_xqaQrPc0dJ1tIdVs5rXQVgCHKHa_aERE-UcrJhlOI130_provenance.
• NP144272.RASNjmWTP1fVISPVHYZ51mU0Spnist4FF5J4YU7ehUhm4130_assertion description "[Translocation in chromosome 3 and 12 involves fusion of this protein with HMGA2 in pulmonary chondroid hamartoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144272.RASNjmWTP1fVISPVHYZ51mU0Spnist4FF5J4YU7ehUhm4130_provenance.
• NP144275.RAUlrm_mY1PRWKgBR1b0C7OgxRu0e_5EpcxrZLV_fqy3U130_assertion description "[Expression of the HMGA2-LPP fusion transcript in only 1 of 61 karyotypically normal pulmonary chondroid hamartomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144275.RAUlrm_mY1PRWKgBR1b0C7OgxRu0e_5EpcxrZLV_fqy3U130_provenance.
• NP144278.RAX1E3w0Ahm3Tji56Ivh9Sn1rUU15f89ZJ_4abLXwjy5E130_assertion description "[IL-10 gene expression in esophageal squamous cell cancer specimens was significantly correlated with VEGF121 gene expression/results suggested that IL-10 stimulates angiogenic factor gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144278.RAX1E3w0Ahm3Tji56Ivh9Sn1rUU15f89ZJ_4abLXwjy5E130_provenance.
• NP144279.RARVj02XPJpusSORrRUiT2We--5xCrlJSS9xCnKq6dYGw130_assertion description "[CYP2E1 wild type (c1/c1) increased the susceptibility to esophageal squamous cell cancer risk in Kazakh individuals with GSTM1 presence genotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144279.RARVj02XPJpusSORrRUiT2We--5xCrlJSS9xCnKq6dYGw130_provenance.
• NP144281.RAUJGzoL8d1JONqSkYcIwKcKxu4eOwn8oBfTkpuDqo8RI130_assertion description "[data suggest that this tumor suppressor gene plays a critical role in the multistep carcinogenesis process for esophageal squamous cell cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144281.RAUJGzoL8d1JONqSkYcIwKcKxu4eOwn8oBfTkpuDqo8RI130_provenance.
• NP144287.RARsid_bHGluXheYevGCOlBqf-0LvfqCnha5wWgbUiISc130_assertion description "[IL-10 gene expression in esophageal squamous cell cancer specimens was significantly correlated with VEGF121 gene expression/results suggested that IL-10 stimulates angiogenic factor gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144287.RARsid_bHGluXheYevGCOlBqf-0LvfqCnha5wWgbUiISc130_provenance.
• NP144291.RAQTxEYNteHZLuqzzFWIKNuk8B0ayIiJj54RPGQKknDDA130_assertion description "[the determination of nuclear survivin expression could be used to individualise therapeutic strategies in oesophageal squamous cell cancer in the future.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144291.RAQTxEYNteHZLuqzzFWIKNuk8B0ayIiJj54RPGQKknDDA130_provenance.
• NP144297.RAax3UYtDW91GBR1hjwPDzx6chLQ8IeO3KnlLocR3E1Vs130_assertion description "[A novel mutation in helix 12 of this receptor impairs coactivator interaction and causes hereditary 1, 25-dihydroxyvitamin D-resistant rickets without alopecia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144297.RAax3UYtDW91GBR1hjwPDzx6chLQ8IeO3KnlLocR3E1Vs130_provenance.
• NP144302.RAYgTScdv24Af1N8IPtzO9NH-g6TLZOj6LPWNW22rNJUo130_assertion description "[IL-10 significantly decreased RANKL+ Th1-associated alveolar bone loss and expression of IFN gamma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144302.RAYgTScdv24Af1N8IPtzO9NH-g6TLZOj6LPWNW22rNJUo130_provenance.
• NP144303.RATSzcdqHp4xLxvnjRJBrF-s-wfXlBfOJK4Ht1u0RHtO4130_assertion description "[A negative association is noted for alveolar bone loss and salivary osteonectin in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144303.RATSzcdqHp4xLxvnjRJBrF-s-wfXlBfOJK4Ht1u0RHtO4130_provenance.
• NP144306.RAZiJK-SnaKYkUWtHi9SlgGh57u7_JZEEvju0z4eBZVAA130_assertion description "[Salivary HGF measured at baseline may predict future alveolar bone loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144306.RAZiJK-SnaKYkUWtHi9SlgGh57u7_JZEEvju0z4eBZVAA130_provenance.
• NP144313.RARbhHdNN6eefiFUdG3rI9roI3GeRtpGczJbG7g4JfjKg130_assertion description "[MMP-3 and IL-6 promoter polymorphisms constitute important factors for the genetic predisposition to scoliosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144313.RARbhHdNN6eefiFUdG3rI9roI3GeRtpGczJbG7g4JfjKg130_provenance.
• NP144316.RAURT_P4CpUD5XkxoFteRofBfdpeDHIkrW_gLISiK1Nio130_assertion description "[The major clinical characteristics of patients with mutated ROBO3 were horizontal gaze palsy, progressive scoliosis, and brainstem malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144316.RAURT_P4CpUD5XkxoFteRofBfdpeDHIkrW_gLISiK1Nio130_provenance.
• NP144325.RAW_qT54IBVlPdHz5GTnuCJxjMUIlaZ7n1MtwsDQzthrE130_assertion description "[Despite the negative association reported here, further investigation of the gene and its potential association to familial idiopathic scoliosis is required.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144325.RAW_qT54IBVlPdHz5GTnuCJxjMUIlaZ7n1MtwsDQzthrE130_provenance.
• NP144328.RAY4-R0rHTNMrwivTw3uIOfBQikRemwMO7n3oRdiBkwx4130_assertion description "[A novel mutation affecting the OSTM1 locus responsible for ARO/addition to common clinical features of osteopetrosis, the patient developed a unique neuronal pathology that provided evidence for the role of OSTM1 in normal neuronal cell development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144328.RAY4-R0rHTNMrwivTw3uIOfBQikRemwMO7n3oRdiBkwx4130_provenance.
• NP144329.RAcvDf9Lrs5dq7LUn83PxL5EiQN8wvdOoM0LzR3FOaHkI130_assertion description "[mutations in OSTM1 such as the C-terminal deletion mutant studied herein provoke dysregulation of the canonical Wnt/beta-catenin signaling pathway, providing a molecular basis for severe autosomal recessive osteopetrosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144329.RAcvDf9Lrs5dq7LUn83PxL5EiQN8wvdOoM0LzR3FOaHkI130_provenance.
• NP144330.RAVGjfWIRd0syBimVRkMu9bUH-DuuX3Cm7jP6lObeuTbU130_assertion description "[This study reports on a 12-month-old female with recessive OSMT1 mutations and neuroimaging findings suggesting a malignant infantile osteopetrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144330.RAVGjfWIRd0syBimVRkMu9bUH-DuuX3Cm7jP6lObeuTbU130_provenance.
• NP144334.RAa6gDrkMN99BZxNG675Vfh6a-TmOHadf_q5oEgBmBGaY130_assertion description "[ClC-7 has a role in causing autosomal dominant osteopetrosis type II ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144334.RAa6gDrkMN99BZxNG675Vfh6a-TmOHadf_q5oEgBmBGaY130_provenance.
• NP144335.RARoE1DE0SC6T9joDkwTEX-xFB6nMUb4nVFlLNNkNQeKY130_assertion description "[Significant association of CLCN7 polymorphisms with the variance of bone density in postmenopausal women with osteopetrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144335.RARoE1DE0SC6T9joDkwTEX-xFB6nMUb4nVFlLNNkNQeKY130_provenance.
• NP144339.RAXfKF-3ZNbezu9gaLitgfmhiv9k6tkowJvtpypcSGdPI130_assertion description "[Osteopetrosis, with unusual clinical manifestations, was caused by a mutation in CLCN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144339.RAXfKF-3ZNbezu9gaLitgfmhiv9k6tkowJvtpypcSGdPI130_provenance.
• NP144343.RAUPoiZUurWwcwxxIvJ3TyA8S26vbXVwpj8ydZZcr_NkY130_assertion description "[localization to chromosome 11q12-13 in autosomal dominant osteopetrosis type I ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144343.RAUPoiZUurWwcwxxIvJ3TyA8S26vbXVwpj8ydZZcr_NkY130_provenance.
• NP144349.RAZ4TQMriQrJaofW4ZgTcp8rbTkfhlw9Kgp69BjRgwSB0130_assertion description "[There is more frequent p16 hypermethylation in mantle cell lymphoma and p15 or Rb1 hypermethylation in follicular lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144349.RAZ4TQMriQrJaofW4ZgTcp8rbTkfhlw9Kgp69BjRgwSB0130_provenance.
• NP144360.RAas1zWmWr0-_xmu2iWzM1AX-r-nhwdoy7-6viy80ohAY130_assertion description "[Follicular lymphoma cells showed exceptionally high IL-21R expression/induced apoptosis in follicular lymphoma cells expressing high levels of IL-21 receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144360.RAas1zWmWr0-_xmu2iWzM1AX-r-nhwdoy7-6viy80ohAY130_provenance.
• NP144362.RAe-k5qBCw_p6wdZNT7FZvFt1_wFAvywi6M5kHuteiVGk130_assertion description "[Diffuse large B-cell lymphoma and follicular lymphoma grade 3 is more influenced by expression of B-cell differentiation stage genes than by tumor cells growth pattern, BCL2 and BCL6 abnormalities, and International Prognostic Index.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144362.RAe-k5qBCw_p6wdZNT7FZvFt1_wFAvywi6M5kHuteiVGk130_provenance.
• NP144363.RAf9CBdkZ5_LELIqnYpiJkhZyGhyfQvNHSQM3oVuY2JEM130_assertion description "[MUM1 expression dichotomises follicular lymphoma (FL) into low-grade FL of CD10+/Bcl-6+/MUM1-/Ki-67low phenotype, and high-grade FL of CD10+/-/Bcl-6+/weak/MUM1+/Ki-67high phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144363.RAf9CBdkZ5_LELIqnYpiJkhZyGhyfQvNHSQM3oVuY2JEM130_provenance.
• NP144365.RAfhS1qSg7V2izeYklq39Ae4_hULNOmV5w7-8Gt6Zyx10130_assertion description "[In humans, BNIP3 is strongly expressed in most follicular lymphomas, especially those that are Bcl-2 negative.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144365.RAfhS1qSg7V2izeYklq39Ae4_hULNOmV5w7-8Gt6Zyx10130_provenance.
• NP144374.RAV52TZigIyAcI_hOwMrYhHrZnDUNVX1frKgJcgpswnRI130_assertion description "[beta2M level was an independent prognostic marker in patients with follicular lymphoma treated with anthracycline ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144374.RAV52TZigIyAcI_hOwMrYhHrZnDUNVX1frKgJcgpswnRI130_provenance.
• NP144375.RAWzX40EJxSP4Rf_GaC4Pc6WArOV8__qfD8psvxAeqx_8130_assertion description "[SOX5 is upregulated by promoter swapping with the P2RY8 gene in primary splenic follicular lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144375.RAWzX40EJxSP4Rf_GaC4Pc6WArOV8__qfD8psvxAeqx_8130_provenance.
• NP144383.RAfrdhC13CBlSW0TOA8upn4RdLxdn24v_hkxExMY_lvPg130_assertion description "[findings not only illustrate MCL1 as an aberrantly expressed reprogramming oncoprotein in follicular lymphomas but also highlight MCL1 as key therapeutic target ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144383.RAfrdhC13CBlSW0TOA8upn4RdLxdn24v_hkxExMY_lvPg130_provenance.
• NP144385.RAZ29is_CS_e5ME-Fu6N-rqEbR-uxVxbxnK0RB1xxBAps130_assertion description "[Dysregulated bcl-2 expression does not play a significant pathogenetic role in most pediatric follicular lymphomas, but does identify a subset of patients in whom disease is often disseminated and more refractory to combination chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144385.RAZ29is_CS_e5ME-Fu6N-rqEbR-uxVxbxnK0RB1xxBAps130_provenance.
• NP144386.RAZiZi7OTLfu2XeXgSqVKJ8CgVp8P-XGGNF5khrqLxfBo130_assertion description "[Bcl-2 overexpression leads to the induction of activated signal transducer and activator of transcription 3 (STAT3) and to the induction of SOCS3, which may contribute to the pathogenesis of follicular lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144386.RAZiZi7OTLfu2XeXgSqVKJ8CgVp8P-XGGNF5khrqLxfBo130_provenance.
• NP144388.RAejvgldiWHKaRREXn5xcHYZG3Rt0-UFtVbOi2u5uoBtQ130_assertion description "[The low frequency of BCL-2/IgH translocation in healthy Chinese individuals of Han nationality located in Zhejiang area may be one of the reasons for the difference in the incidence of follicular lymphoma between China and Western countries.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144388.RAejvgldiWHKaRREXn5xcHYZG3Rt0-UFtVbOi2u5uoBtQ130_provenance.
• NP144392.RAfg6WJ944a4h4Msxp3wvxo6vvx63pzJ4xqQphclNKpfo130_assertion description "[FVT1 is significantly underexpressed by germinal center-type diffuse large B-cell lymphoma compared with non-germinal center-type DLBCL, follicular lymphoma, & normal tonsil control samples/expression of FVT1 correlated with decreased survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144392.RAfg6WJ944a4h4Msxp3wvxo6vvx63pzJ4xqQphclNKpfo130_provenance.
• NP144397.RAWgc7-3VTMy40pEVtFdX8H4CPPPa1TMUnUlb0v3m0mdY130_assertion description "[Levels of BLyS protein were, on average, threefold higher in patients with follicular lymphoma compared to normal donors ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144397.RAWgc7-3VTMy40pEVtFdX8H4CPPPa1TMUnUlb0v3m0mdY130_provenance.
• NP144398.RAQkMexZMPuGTBHP0wToxT1HfLlYWY5t-zgCqHcfNBHOc130_assertion description "[IL-21 induced apoptosis in follicular lymphoma cells expressing high levels of IL-21 receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144398.RAQkMexZMPuGTBHP0wToxT1HfLlYWY5t-zgCqHcfNBHOc130_provenance.
• NP144400.RAQnryKkpM6WJVLMkGewkZd6Cd-ChmRG-TkKoeuznLqkw130_assertion description "[Gemin3 and Gemin4 function in Sm core assembly and correlate the activity of this pathway with Spinal Muscular Atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144400.RAQnryKkpM6WJVLMkGewkZd6Cd-ChmRG-TkKoeuznLqkw130_provenance.
• NP144405.RARiXVZF7c8tNJKCorNfnyNL9DrfgiIKVrMv_ZvVS6Ubk130_assertion description "[Data demonstrate that hnRNP Q is a splicing modulator of SMN2, further underscoring the potential of hnRNP Q as a therapeutic target for spinal muscular atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP144405.RARiXVZF7c8tNJKCorNfnyNL9DrfgiIKVrMv_ZvVS6Ubk130_provenance.

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