Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP132773.RAeEezv4HyzyNT8fj0ve1OXZ70oyTAJCy4tcw0p1wdUjI130_assertion description "[Results suggest that ADH1B polymorphisms play a pivotal role on esophageal cancer and that the effect of these polymorphisms was modified by the amount of alcohol consumed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132773.RAeEezv4HyzyNT8fj0ve1OXZ70oyTAJCy4tcw0p1wdUjI130_provenance.
- NP132780.RAY-mbHnmZb7r5Eqj-qtuwuvk0LR4veZUDQua97h59BLg130_assertion description "[elevated expression of Shh and its target genes is quite common in esophageal cancers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132780.RAY-mbHnmZb7r5Eqj-qtuwuvk0LR4veZUDQua97h59BLg130_provenance.
- NP132782.RASU3mhX9gwG_mJo0C0fiiR2gazkQOFR3trIurMLf7pO0130_assertion description "[In exon 9, a somatic mutation was found in two patients (2.2%) and in two cell lines; mutations included three E545K (G1633A) mutations and one E545Q (G1633C) mutation, in exon 20, no mutation was observed in our esophageal cancer patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132782.RASU3mhX9gwG_mJo0C0fiiR2gazkQOFR3trIurMLf7pO0130_provenance.
- NP132788.RAV72rXJReMlSbW2ZII1JHlSyBB_cVaMj2O7O7F9A8HWk130_assertion description "[The expression of the tumor suppressor gene connexin 26 is not mediated by methylation in human esophageal cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132788.RAV72rXJReMlSbW2ZII1JHlSyBB_cVaMj2O7O7F9A8HWk130_provenance.
- NP132791.RAYsJGCDtJHCppUMn0DRB4qw2xdBaR47MzBeV0vC8m5tc130_assertion description "[Elevated serum IGF-1 levels may be an important predictor of risk for esophageal cancer/related to the progression of esophageal cancer may depend on an autocrine function of IGF-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132791.RAYsJGCDtJHCppUMn0DRB4qw2xdBaR47MzBeV0vC8m5tc130_provenance.
- NP132802.RAc7WDh-3Q19YS5YJiEAN0IqOtmsB83yZCIgBQZPyU8g8130_assertion description "[MnSOD was overexpressed in ESCC and its up-regulation in esophageal cancer cells was associated with apoptosis resistance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132802.RAc7WDh-3Q19YS5YJiEAN0IqOtmsB83yZCIgBQZPyU8g8130_provenance.
- NP132803.RAfnzwwqPf-ilsZcl_7klOEZf6wCdk6O4FaN2Sv7OYP1s130_assertion description "[There is a genetic predisposition for the pulmonary complications following esophagectomy for esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132803.RAfnzwwqPf-ilsZcl_7klOEZf6wCdk6O4FaN2Sv7OYP1s130_provenance.
- NP132808.RAdkgHPcP0O3FnHiS4zY_TTz_irLGthLqwHnbcFuXXWh8130_assertion description "[Codon 31 polymorphism in p21 may be associated with the development of esophageal cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132808.RAdkgHPcP0O3FnHiS4zY_TTz_irLGthLqwHnbcFuXXWh8130_provenance.
- NP132812.RAbLGqJEBATWT0CWGGSgoA1tphEJb-9GHpAkjwLehYD-M130_assertion description "[Increased midkine expression is associated with superficial esophageal cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132812.RAbLGqJEBATWT0CWGGSgoA1tphEJb-9GHpAkjwLehYD-M130_provenance.
- NP132821.RATYlAsaeXrEkXyldnTJNa65MIlNC6jcTvTt2ZVByNaqY130_assertion description "[FAK, mTOR and IGF-IR are inhibited by TAE226 in esophageal cancer cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132821.RATYlAsaeXrEkXyldnTJNa65MIlNC6jcTvTt2ZVByNaqY130_provenance.
- NP132823.RAQUsl_iQ0Jg_7jIHDtc-3ZGj2uT26pgDgbUPm7jijlkw130_assertion description "[Genetic variation in both the promoter region and intron 1 of the SLC11A1 gene is associated with esophageal cancer susceptibility ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132823.RAQUsl_iQ0Jg_7jIHDtc-3ZGj2uT26pgDgbUPm7jijlkw130_provenance.
- NP132829.RAVb7A54dnQU2W8qYi08sLIw4tRGxGE4RDP4oP4ZTf0Oc130_assertion description "[ZNRD1 was down-regulated in esophageal cancer tissues compared to adjacent non-neoplastic tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132829.RAVb7A54dnQU2W8qYi08sLIw4tRGxGE4RDP4oP4ZTf0Oc130_provenance.
- NP132830.RAYtDddsMow5oUgrdY6HrdRwIHDvLQ5_o8rwK3HQsv6zk130_assertion description "[REG1A enhances chemo- and radiosensitivity in squamous cell esophageal cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132830.RAYtDddsMow5oUgrdY6HrdRwIHDvLQ5_o8rwK3HQsv6zk130_provenance.
- NP132834.RARHH_hBcIWR18cvPDckyoU83n9lDwklHdG4NZv1Lteo0130_assertion description "[preoperative chemoradiotherapy (CRT) reduced Bcl-X (L) expression, and this decrease closely correlated with the prolonged survival of advanced esophageal cancer patients treated with preoperative CRT ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132834.RARHH_hBcIWR18cvPDckyoU83n9lDwklHdG4NZv1Lteo0130_provenance.
- NP132841.RAby_uwmx3DXxTTwWSYfwyLfxC6qF7C9QJe5txyk69lwk130_assertion description "[In the CYP2E1 gene 5'-flanking region polymorphism, patients with esophageal cancer showed significantly higher frequency of the A4/A4 genotype compared with the control subjects (p = 0.02), but no difference was found in patients with lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132841.RAby_uwmx3DXxTTwWSYfwyLfxC6qF7C9QJe5txyk69lwk130_provenance.
- NP132852.RAQJrdqhcuaAhRmVnwWrfzC61ZAUQsjaFE5VagziKhx5c130_assertion description "[Sphingosine kinases and sphingosine-1-phosphate are critical for transforming growth factor beta-induced ERK1 and ERK2 activation and promotion of migration and invasion of esophageal cancer cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132852.RAQJrdqhcuaAhRmVnwWrfzC61ZAUQsjaFE5VagziKhx5c130_provenance.
- NP132853.RAYPfrsPR3ndu6VFXHEjbze-SsmkALfUG-ir3v9rtQJJI130_assertion description "[blood TGF-beta 1 has a role in preventing progression of esophageal neoplasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132853.RAYPfrsPR3ndu6VFXHEjbze-SsmkALfUG-ir3v9rtQJJI130_provenance.
- NP132863.RAQ8xSi13KcVX2KDSZVc9IXrVCo4oght6JRvlN55Xwv_E130_assertion description "[The high expression frequency of NY-ESO-1 mRNA and protein indicates NY-ESO-1 as a feasible vaccine target in esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132863.RAQ8xSi13KcVX2KDSZVc9IXrVCo4oght6JRvlN55Xwv_E130_provenance.
- NP132865.RASfOx4Pil2m7f7WhRZGJUIurF7F-f00Ro8hH8vaPIS6A130_assertion description "[Results indicate that loss of RAR-beta expression and accumulation of p 53 and Ki67 proteins may serve as biomarkers for early identification of esophageal cancer in the high-risk populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132865.RASfOx4Pil2m7f7WhRZGJUIurF7F-f00Ro8hH8vaPIS6A130_provenance.
- NP132867.RASpX6kFN05bykqNiYOYCTSSMNTXI_mjtrh8SF8CL91sQ130_assertion description "[High TS1 gene expression is associated with chemotherapy resistance in esophageal cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132867.RASpX6kFN05bykqNiYOYCTSSMNTXI_mjtrh8SF8CL91sQ130_provenance.
- NP132871.RATn85CTL7SCKx_WPZsT_-Dyc6wziSPCzHabMM3vkZIu0130_assertion description "[FGF-2 has a role in esophageal cancer recurrence and mortality ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132871.RATn85CTL7SCKx_WPZsT_-Dyc6wziSPCzHabMM3vkZIu0130_provenance.
- NP132877.RAXYfzoBgUCWjlHGOwIAgjCV433vjfQyDx6hnUFtswtOw130_assertion description "[As the TRAG-3 gene is located on Xq28, which is the same locus as the MAGE gene family, we found a frequent synchronous expression pattern with TRAG-3 and MAGE-3 in esophageal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132877.RAXYfzoBgUCWjlHGOwIAgjCV433vjfQyDx6hnUFtswtOw130_provenance.
- NP132885.RAbgbX8k6jPf01gDegEP_sPaoUsKtqY671-EBLHDhWLaM130_assertion description "[Prox1 plays an important, previously unanticipated role in mediating the aggressive behavior of vascular neoplasms such as Kaposi's sarcoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132885.RAbgbX8k6jPf01gDegEP_sPaoUsKtqY671-EBLHDhWLaM130_provenance.
- NP132887.RARmWdx56PaSOueYPY15fZ6_CEqXRS5phd_CRMaDknIL8130_assertion description "[Data show that beta-catenin is overexpressed in Kaposi sarcoma and primary effusion lymphoma, and that this overexpression is regulated by the Kaposi's sarcoma-associated herpesvirus (KSHV) latency-associated nuclear antigen LANA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132887.RARmWdx56PaSOueYPY15fZ6_CEqXRS5phd_CRMaDknIL8130_provenance.
- NP132888.RAePsYxgjt2mXwfrfkxopKLyx7c0TXFpoQ28uCDAuFjXI130_assertion description "[K15M may contribute to Kaposi's sarcoma associated herpesvirus-mediated tumor metastasis and angiogenesis via regulation of miR-21 and miR-31, which we show here for the first time to be a specific regulator of cell migration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132888.RAePsYxgjt2mXwfrfkxopKLyx7c0TXFpoQ28uCDAuFjXI130_provenance.
- NP132896.RAUCHXLo3IkNy59skFn1NkRxR0e7Hu8vb7AcZKqCwEGD4130_assertion description "[identifies Src and MMP-2 as potential therapeutic targets in human herpesvirus 8 associated Kaposi Sarcoma and idiopathic pulmonary arterial hypertension ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132896.RAUCHXLo3IkNy59skFn1NkRxR0e7Hu8vb7AcZKqCwEGD4130_provenance.
- NP132897.RAS9Woi1SnPPwg3NmCqgdh4pfHd9Fxe-l5bTof8UfOk0U130_assertion description "[Proliferative activity of 13 biopsy specimens of Kaposi sarcoma was assessed immunohistochemically using the monoclonal antibody to KI-67.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132897.RAS9Woi1SnPPwg3NmCqgdh4pfHd9Fxe-l5bTof8UfOk0U130_provenance.
- NP132906.RAaGHpjQM_DxR9Hdv3vulwSUPT2-ZAF0t4dRSegMe9YeA130_assertion description "[Monitoring P70 (S6K) phosphorylation can help predict and monitor the biological effectiveness of rapamycin in renal transplant recipients with Kaposi sarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132906.RAaGHpjQM_DxR9Hdv3vulwSUPT2-ZAF0t4dRSegMe9YeA130_provenance.
- NP132907.RAf5g5RTpYQjtDqGfa5AFolzL6p2gSzW2pHgxRhKGbwzQ130_assertion description "[Dramatic decrease of podocin expression was found in children with nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132907.RAf5g5RTpYQjtDqGfa5AFolzL6p2gSzW2pHgxRhKGbwzQ130_provenance.
- NP132913.RATIlUzh4zmfyh6248PcF7Bp2SmY_wOVRw-3Wy6Lakgco130_assertion description "[re-evaluated cclinical fils and echocardiography of 12 patients with NPHS2 mutation and sporadic nephrotic syndrome and failed to confirm association with cardiac defects ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132913.RATIlUzh4zmfyh6248PcF7Bp2SmY_wOVRw-3Wy6Lakgco130_provenance.
- NP132914.RAfRoZJfOqwfSulvXR1JsDhGmVEib8NwKFfclw1OuV3PU130_assertion description "[study suggests mutations in NPHS2 & WT1 are not a cause of uncomplicated steroid sensitive nephrotic syndrome or frequently relapsing & steroid-dependent nephrotic syndrome (FRNS/SDNS) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132914.RAfRoZJfOqwfSulvXR1JsDhGmVEib8NwKFfclw1OuV3PU130_provenance.
- NP132915.RASORZc14GdnQKjjFoH0VmEgdGO45GZuGvR560ErN6Dis130_assertion description "[Mutations may play pathogenetic roles in some patients with sporadic steroid resistant nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132915.RASORZc14GdnQKjjFoH0VmEgdGO45GZuGvR560ErN6Dis130_provenance.
- NP132917.RAeiUFv61FgreLoqGmWuNdek4rfss7f7NtCX_Q8TmcHOs130_assertion description "[Mutation of NPHS2 can be responsible for congenital nephrotic syndrome in Japanese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132917.RAeiUFv61FgreLoqGmWuNdek4rfss7f7NtCX_Q8TmcHOs130_provenance.
- NP132919.RARqWaf-_Q2NGqVlYem-BLDtxcYOAeMkOzV7mFXzt1lmQ130_assertion description "[A striking finding in this study is the lack of contribution of NPHS1, NPHS2, and NEPH1 genes in 15 Asian families with steroid-resistant nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132919.RARqWaf-_Q2NGqVlYem-BLDtxcYOAeMkOzV7mFXzt1lmQ130_provenance.
- NP132923.RAT9RIg2ytpgXCY9Zw8dIbbA6EjE26AyoiQ9GbF-zd3wU130_assertion description "[Thirteen novel NPHS1 mutations have been analyzed in a large cohort of children with congenital nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132923.RAT9RIg2ytpgXCY9Zw8dIbbA6EjE26AyoiQ9GbF-zd3wU130_provenance.
- NP132927.RARE-vZdhETFDvQXxAIue9j_S8QcLPnzom-erTM22aJYs130_assertion description "[A missense mutation of the nephrin gene (GAC-to-GTC transversion leading to Asp819Val) impairs targeting of the protein to the cell membrane and causes congenital nephrotic syndrome of the Finnish type (CNF).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132927.RARE-vZdhETFDvQXxAIue9j_S8QcLPnzom-erTM22aJYs130_provenance.
- NP132928.RAZ6ZJ4BNOai6mLg6zH_SQJCX2HvZlAv4HKiVgmf-AwgE130_assertion description "[Adenosine deaminase activity was abnormal in active nephrotic syndrome, and lymphocyte ADA demonstrated change both in active as well as remission stage of the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132928.RAZ6ZJ4BNOai6mLg6zH_SQJCX2HvZlAv4HKiVgmf-AwgE130_provenance.
- NP132934.RAcdvJJ48B5NO0P02eyR_U-9ge2v2WGSrw11RK42Q8xHg130_assertion description "[dysregulated heparanase expression may play a significant role in the pathogenesis of steroid-sensitive nephrotic syndrome, possibly through an abnormality in post-translational control of latent heparanase activation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132934.RAcdvJJ48B5NO0P02eyR_U-9ge2v2WGSrw11RK42Q8xHg130_provenance.
- NP132935.RAQ6mYlSr4UZK5MeJSLl2viHY17auQrodz378NW5MPEMQ130_assertion description "[Heparanase mRNA may be important to the loss of glomerular negative charge in GBM and lead to proteinuria in steroid responsive nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132935.RAQ6mYlSr4UZK5MeJSLl2viHY17auQrodz378NW5MPEMQ130_provenance.
- NP132942.RAV2ooLeBtMRiOf85L5iPr49_D0vbfRbA7Aoy9Dz5B0mA130_assertion description "[Increased serum and urine IL-18 levels were observed during relapse of idiopathic nephrotic syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132942.RAV2ooLeBtMRiOf85L5iPr49_D0vbfRbA7Aoy9Dz5B0mA130_provenance.
- NP132943.RAepEn48JnFlv5zwKfZsHL2jSK1lQM7Pk8mp_8t9oeRXs130_assertion description "[Results suggest that interleukin-8/CXCL8 and TGF-beta1 are involved in the pathogenesis of idiopathic nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132943.RAepEn48JnFlv5zwKfZsHL2jSK1lQM7Pk8mp_8t9oeRXs130_provenance.
- NP132958.RAdTnBuqBm83aMeBhohCjCJAl-WLpaLDsHfA3iyslj1u4130_assertion description "[The results demonstrate that the decreased serum albumin level might be a main determinant of the increased CETP concentration in pediatric nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132958.RAdTnBuqBm83aMeBhohCjCJAl-WLpaLDsHfA3iyslj1u4130_provenance.
- NP132959.RARIWEStD6gtdFDDzoUXtwQ4yfSSrMDB79OljRgj4xvZM130_assertion description "[Polymorphisms in the IL12B promoter region associate with two different clinical courses of steroid-sensitive childhood nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132959.RARIWEStD6gtdFDDzoUXtwQ4yfSSrMDB79OljRgj4xvZM130_provenance.
- NP132963.RAU2nCiOQBKeN8TUkUermt4v7au1sQ1ELDndhJmo2Wat8130_assertion description "[A striking finding in this study is the lack of contribution of NEPH1, NPHS1, and NPHS2 genes in 15 Asian families with steroid-resistant nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132963.RAU2nCiOQBKeN8TUkUermt4v7au1sQ1ELDndhJmo2Wat8130_provenance.
- NP132975.RAblTkym0Gpuj-pXSJWh5NJ99lxd4savZboRbyMStWNcU130_assertion description "[genetic variations of NR3C1 in children with sporadic steroid-resistant nephrotic syndrome & sporadic steroid-sensitive NS; no causative mutations were found; 6 previously identified & 6 novel polymorphisms were detected & 2 novel haplotypes identified ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132975.RAblTkym0Gpuj-pXSJWh5NJ99lxd4savZboRbyMStWNcU130_provenance.
- NP132976.RASZTTRF57TXGKdhnB5zDICA_UnBXe2pgoEg8SjvrZ9Zc130_assertion description "[Twelve polymorphisms in the NR3C1 gene were detected, two types of newly found haplotypes were associated with steroid-resistant idiopathic nephrotic syndrome, which might be responsible for steroid-resistance in partial idiopathic nephrotic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132976.RASZTTRF57TXGKdhnB5zDICA_UnBXe2pgoEg8SjvrZ9Zc130_provenance.
- NP132990.RAWeGjkndISHj4qI99qiNu_sTFzAJQAhKvhPjP9tq6u2A130_assertion description "[Functional effects of nemaline myopathy mutations on human skeletal alpha-actin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132990.RAWeGjkndISHj4qI99qiNu_sTFzAJQAhKvhPjP9tq6u2A130_provenance.
- NP132996.RAfhIjQvyZcDEKcOAIa-pHrzAvw8Smmwu2RzWUjA1KUfo130_assertion description "[Results describe clinical and pathological features associated with 29 alpha-actin (ACTA1) mutations found in 38 individuals with nemaline myopathy from 28 families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132996.RAfhIjQvyZcDEKcOAIa-pHrzAvw8Smmwu2RzWUjA1KUfo130_provenance.
- NP132999.RAWGqfO3dS7lp5QAEDj4uuRQXcyKnMioh7mJeO_B_mlbo130_assertion description "[Nemaline myopathy with exclusively intranuclear rods and a novel mutation in ACTA1 (Q139H).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP132999.RAWGqfO3dS7lp5QAEDj4uuRQXcyKnMioh7mJeO_B_mlbo130_provenance.
- NP133004.RASgqN7A2jPBwXCpz9eoIT-j4l-seiXcM99-sUy7eICQg130_assertion description "[Common mutations in the BLM gene were studied in 4 Japanese Bloom Syndrome kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133004.RASgqN7A2jPBwXCpz9eoIT-j4l-seiXcM99-sUy7eICQg130_provenance.
- NP133007.RAeNNFbjn7zNOHS6-IL7HV7C6g_AhzckeklpoA7pIpIBg130_assertion description "[Somatic frameshift mutations in the Bloom syndrome BLM gene are frequent in sporadic gastric carcinomas with microsatellite mutator phenotype ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133007.RAeNNFbjn7zNOHS6-IL7HV7C6g_AhzckeklpoA7pIpIBg130_provenance.
- NP133008.RAckxnGsf_HduWDNFS3-hJ3WjrYbmBHzSIaE2LmEJxd2s130_assertion description "[The presence of widespread founder mutations in persons with Bloom syndrome points to population genetic processes that repeatedly and pervasively generate mutations that recur in unrelated persons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133008.RAckxnGsf_HduWDNFS3-hJ3WjrYbmBHzSIaE2LmEJxd2s130_provenance.
- NP133009.RASJzwwBR91xUqH7gJ3BCOjou-LaivnH3Ch3REFJhNTB0130_assertion description "[Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133009.RASJzwwBR91xUqH7gJ3BCOjou-LaivnH3Ch3REFJhNTB0130_provenance.
- NP133012.RAcVxd7ynyvkyrfbf2HZJG6Y7dEbFn348Z-HGxB8rclb4130_assertion description "[binds Bloom syndrome protein; nuclear localization ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133012.RAcVxd7ynyvkyrfbf2HZJG6Y7dEbFn348Z-HGxB8rclb4130_provenance.
- NP133015.RAfUxwi5izWw2FZWCsANmd16yxKBF28nHHrp44P9F0Cw8130_assertion description "[This is the first report of high ATM-Chk2 kinase activation and its linkage to replication defects in a Bloom syndrome model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133015.RAfUxwi5izWw2FZWCsANmd16yxKBF28nHHrp44P9F0Cw8130_provenance.
- NP133019.RATR3FBOV8Zf8mId6BO_d-ZJ689m19g9dKCuG0qM_4rIs130_assertion description "[This is the first report of high ATM-Chk2 kinase activation and its linkage to replication defects in a Bloom syndrome model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133019.RATR3FBOV8Zf8mId6BO_d-ZJ689m19g9dKCuG0qM_4rIs130_provenance.
- NP133023.RAZD2siMziltAtzOTwc9YIrd8hpCCidWRRjF6F14uPv9c130_assertion description "[CRTC1/MAML2 translocation and fusion transcript is asscociated with Warthin's tumor and mucoepidermoid carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133023.RAZD2siMziltAtzOTwc9YIrd8hpCCidWRRjF6F14uPv9c130_provenance.
- NP133025.RAdrQRLPRu77fgRS1UEth1XPLW1iP1hzsmIZaJRp77pyw130_assertion description "[mucoepidermoid carcinoma of the thyroid (MECT) displays consistent neoexpression of P-cadherin and major alterations in the expression of E-cadherin and the three catenins ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133025.RAdrQRLPRu77fgRS1UEth1XPLW1iP1hzsmIZaJRp77pyw130_provenance.
- NP133027.RAcLDdvmNrt15_cmw9SeC3J8pz0P6U_GWU4Ig9K1sur1I130_assertion description "[MUC4 expression is related to a better prognosis in mucoepidermoid carcinomas of the salivary glands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133027.RAcLDdvmNrt15_cmw9SeC3J8pz0P6U_GWU4Ig9K1sur1I130_provenance.
- NP133028.RAV3h5Sf-Rv2lx1SWnHgxRRzOeDexPiH55WYDJ2zxnWZY130_assertion description "[cloning and functional analyses of the t (11; 19) fusion oncogene t (11; 19) (q21; p13) translocation in mucoepidermoid carcinoma creates a novel fusion product that disrupts a Notch signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133028.RAV3h5Sf-Rv2lx1SWnHgxRRzOeDexPiH55WYDJ2zxnWZY130_provenance.
- NP133036.RAT5ewWZzxu5x5FlWpufXLFOyxA2bMJ3_DK7eOtHuSVCg130_assertion description "[cloning of a novel fusion gene in mucoepidermoid carcinomas & benign Warthin's tumors; the fusion, which results from a translocation, creates a chimeric gene in which exon 1 of a novel gene designated WAMTP1 is linked to exons 2-5 of MAML2 [WAMPT1]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133036.RAT5ewWZzxu5x5FlWpufXLFOyxA2bMJ3_DK7eOtHuSVCg130_provenance.
- NP133037.RAXMK-f-YkwmSE-YPhd6gQKu2jFmuQSXh09opU3aSEfqo130_assertion description "[The presence of the t (11; 19) (q21; p13) rearrangement favors a diagnosis of mucoepidermoid carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133037.RAXMK-f-YkwmSE-YPhd6gQKu2jFmuQSXh09opU3aSEfqo130_provenance.
- NP133046.RAWxCFMkQZxgOkjimgJz_UF4n38rMy6XdGPrOTDNlVdPg130_assertion description "[Abnormal immunoexpression of Dicer in aggressive mucoepidermoid carcinoma suggests a role for microRNA and microRNA machinery in tumor progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133046.RAWxCFMkQZxgOkjimgJz_UF4n38rMy6XdGPrOTDNlVdPg130_provenance.
- NP133047.RAVWBSJ9ANREE3HtUW-NYHO9rVxSQ2GERBuU1d9ozifQA130_assertion description "[study reports for the first time a CRTC3-MAML2 fusion gene in a mucoepidermoid carcinoma, as determined by RT-PCR and sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133047.RAVWBSJ9ANREE3HtUW-NYHO9rVxSQ2GERBuU1d9ozifQA130_provenance.
- NP133052.RAVUCVcakLOc5wYkZsBNlbAR0EuH1Z6eZv0P6j7KX1uh0130_assertion description "[The authors describe four members of a family with a novel P284S presenilin 1 mutation presenting a clinical phenotype characterized by early-onset dementia, paratetraparesis, dysarthria, dysphagia, and marked involvement of brain white matter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133052.RAVUCVcakLOc5wYkZsBNlbAR0EuH1Z6eZv0P6j7KX1uh0130_provenance.
- NP133063.RASQLtbWJaeJkc3iHZ0V01yaB8Bxy7nUJ--sNSSb_Vz_U130_assertion description "[Data suggest that the microcephaly observed in patients with MCPH1 deficiencies is due to disruption of the ATR-BRCA1-Chk1 signaling pathway that is also disrupted in Seckel syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133063.RASQLtbWJaeJkc3iHZ0V01yaB8Bxy7nUJ--sNSSb_Vz_U130_provenance.
- NP133068.RAcvQxyZbD1yWJKy-di4jcaBIVmoG2ljfdYXs0x6MuBco130_assertion description "[Primary microcephaly is an autosomal-recessive congenital disorder characterized by smaller brain size and mental retardation, in which homozygote mutations in STIL proteins are found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133068.RAcvQxyZbD1yWJKy-di4jcaBIVmoG2ljfdYXs0x6MuBco130_provenance.
- NP133074.RAVlgelxtDIqu-Kv-6BEGk-JPLSpISx_aIq1mTk3aTSA0130_assertion description "[This report on a South African family that presented with progressive dementia and a movement disorder affecting numerous family members/of the JPH3 CTG repeat revealed pathogenic expansions in three affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133074.RAVlgelxtDIqu-Kv-6BEGk-JPLSpISx_aIq1mTk3aTSA0130_provenance.
- NP133078.RARziTzzsRdJLrPNWWe85cHZH5E-dl9rqAk_zg2mqddkU130_assertion description "[This study report an case of ombination of infantile spasms, non-epileptic seizures and complex movement disorder on the electroclinical features of a 4-year-old boy with an expansion of the trinucleotide repeat in the ARX gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133078.RARziTzzsRdJLrPNWWe85cHZH5E-dl9rqAk_zg2mqddkU130_provenance.
- NP133082.RAQg96MY_X3F_Im2eoKwmBliakKFpZAITeOSos-1DrdZQ130_assertion description "[IL-18 activates both intrinsic and extrinsic proapoptotic signaling pathways, induces endothelial cell death, and thereby may play a role in myocardial inflammation and injury ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133082.RAQg96MY_X3F_Im2eoKwmBliakKFpZAITeOSos-1DrdZQ130_provenance.
- NP133086.RAQdfsnCL1A0jUoC4SjJM0RRDM811RmGzeXDk28YdgOx8130_assertion description "[overproduction of AT1-autoantibody is a novel risk factor in pregnant women and may play a causative role in the development of hypertension and vascular injury in preeclamptic patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133086.RAQdfsnCL1A0jUoC4SjJM0RRDM811RmGzeXDk28YdgOx8130_provenance.
- NP133102.RAUNlraLd0U_yvk04gvdK_3gCxUIYcWSqt7gmvIIwK4ZY130_assertion description "[blockade of an NKG2D-ligand interaction completely prevents the HBV- and CD1d-dependent, nonclassical NKT cell-mediated acute hepatitis and liver injury ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133102.RAUNlraLd0U_yvk04gvdK_3gCxUIYcWSqt7gmvIIwK4ZY130_provenance.
- NP133124.RAYb3v-GlD6fy1j5F2fo0glHR1nXP65szmpptsdNC5k94130_assertion description "[Catalytically inactive mutant, HO-2H45A, overexpressed in HEK293 cell lines was more sensitive to hemin as compared to control/was also able to protect cells against oxidative stress injury.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133124.RAYb3v-GlD6fy1j5F2fo0glHR1nXP65szmpptsdNC5k94130_provenance.
- NP133128.RAWx4x1C-z2hrkcYUpoQRl57N8Oh6FLkFdc8u21YpS7e4130_assertion description "[IGF-1 may protect from hyperglycemia-induced oxidative stress and neuronal injuries by regulating mitochondrial membrane potential, possibly by the involvement of UCP3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133128.RAWx4x1C-z2hrkcYUpoQRl57N8Oh6FLkFdc8u21YpS7e4130_provenance.
- NP133129.RAQPhZpLpcbwZiFh3q4iFijrwZ0_WQZ77JEES-jDpF2HY130_assertion description "[Transgenic interferon-gamma induces alveolar epithelial cell DNA injury and apoptosis via a novel murine cathepsin S-dependent pathway, a critical event in the pathogenesis of alveolar remodeling, emphysema and inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133129.RAQPhZpLpcbwZiFh3q4iFijrwZ0_WQZ77JEES-jDpF2HY130_provenance.
- NP133136.RAR2ZZIPHuarG_VLjX1-u6SplpeS7pkBjNtjD6zyo_JSQ130_assertion description "[Intracellular localization of OPG in HUVEC, in association with vWF, together with its rapid and sustained secretory response to inflammatory stimuli, strongly support a modulatory role in vascular injury, inflammation and hemostasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133136.RAR2ZZIPHuarG_VLjX1-u6SplpeS7pkBjNtjD6zyo_JSQ130_provenance.
- NP133138.RAcDPltErFepZDCDdOP8OGgLC7L9yn2XwJaxOKI4hoNHE130_assertion description "[fas Receptors are up-regulated in acute lung injury and the acute respiratory distress syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133138.RAcDPltErFepZDCDdOP8OGgLC7L9yn2XwJaxOKI4hoNHE130_provenance.
- NP133140.RAdh6UFY6HVAAL_Wr154vG1AjCutXPNH-r3pEUmrgjF0c130_assertion description "[Results suggest that irrespective of the underlying disease, lung injury that causes extensive fibrosis induces wide expression of COX-2 in the regenerating metaplastic epithelium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133140.RAdh6UFY6HVAAL_Wr154vG1AjCutXPNH-r3pEUmrgjF0c130_provenance.
- NP133141.RAc313P_v_h-50YkmbHArIJXobDt9zDsHcyLroj4GSTuQ130_assertion description "[Rac1-dependent Noxs play a critical role in activating c-Src following hypoxia/reoxygenation injury [NADPH oxidase 2]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133141.RAc313P_v_h-50YkmbHArIJXobDt9zDsHcyLroj4GSTuQ130_provenance.
- NP133161.RAYYaK5TPeOscayunRE0sCwx7uVQx15rXFWJ-0cXcqPMo130_assertion description "[findings show that COL4A1 mutations segregate with porencephaly in human families; propose that Col4a1 mutations conspire with environmental trauma in causing the disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133161.RAYYaK5TPeOscayunRE0sCwx7uVQx15rXFWJ-0cXcqPMo130_provenance.
- NP133165.RAfn7b_zcJnZ8ek25ry-2EY1qpKzWHQ2VO77eBCMfcFz4130_assertion description "[LECT2 participates in liver regeneration and injury following hepatectomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133165.RAfn7b_zcJnZ8ek25ry-2EY1qpKzWHQ2VO77eBCMfcFz4130_provenance.
- NP133168.RARXTEsPThCAJhqDj3q-R_DriM7k0zk0Ar4n7H0EAyi_w130_assertion description "[Somatic mutations of EGFR or KIT of the thymomas and thymic carcinomas are presented in a small number of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133168.RARXTEsPThCAJhqDj3q-R_DriM7k0zk0Ar4n7H0EAyi_w130_provenance.
- NP133169.RAXiQHrOSVxvgTxn5Vci1k6wNTc-ZRxhKQPJoBDqIxgnI130_assertion description "[The greater abundance of mRNA for AChR epsilon-subunit than for other subunits suggests that the AChR epsilon-subunit may play a distinctive role in autosensitization in MG-associated thymomas, particularly those of type A or AB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133169.RAXiQHrOSVxvgTxn5Vci1k6wNTc-ZRxhKQPJoBDqIxgnI130_provenance.
- NP133170.RAeR_A4QR_iERl-JT8jOy3_nqDieLqnay6KlYijRjqxCE130_assertion description "[High levels of serum CYFRA21-1 were correlated with the progression of thymic carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133170.RAeR_A4QR_iERl-JT8jOy3_nqDieLqnay6KlYijRjqxCE130_provenance.
- NP133171.RARSu5NGPh7_0MynhlgXod7B_zUz1UofArlFK9ehPCoVA130_assertion description "[The 620W risk allele was increased in 293 nonthymoma patients without anti-titin antibodies (odds ratio, 1.97; 95% confidence interval, 1.32-2.97, p = 0.00059) but not in nonthymoma patients with anti-titin antibodies or in thymoma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133171.RARSu5NGPh7_0MynhlgXod7B_zUz1UofArlFK9ehPCoVA130_provenance.
- NP133176.RAYCXjA0EUIAMfH0ILUHQUnbyW1XWMdTEbL8szWVtC-Ds130_assertion description "[GAPDH mRNA expression was correlated with evidence of tumor progression in thymoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133176.RAYCXjA0EUIAMfH0ILUHQUnbyW1XWMdTEbL8szWVtC-Ds130_provenance.
- NP133186.RAe7BXyLnR53RMz801QQw-C7tN-Xi69HkV2QuzYK5W2Es130_assertion description "[in T-cell prolymphocytic leukemia, TCL1 represents a highly regulated, targetable modulator of T cell receptor-mediated AKT growth signaling ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133186.RAe7BXyLnR53RMz801QQw-C7tN-Xi69HkV2QuzYK5W2Es130_provenance.
- NP133189.RAc2hb2Z7D7EFNEFYWnBOQk-JFgfXvWR_Aw3OFI2711yI130_assertion description "[increased plasma concentration in patients with idiopathic thrombocytopenic purpura ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133189.RAc2hb2Z7D7EFNEFYWnBOQk-JFgfXvWR_Aw3OFI2711yI130_provenance.
- NP133193.RATUg9WIAFcBc_tC1TNjWAvl0GOIVGwdaH_UKHFD5WlTc130_assertion description "[Decreased mRNA expression in peripheral blood mononuclear cells in patients with idiopathic thrombocytopenic purpura ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133193.RATUg9WIAFcBc_tC1TNjWAvl0GOIVGwdaH_UKHFD5WlTc130_provenance.
- NP133199.RAX5NSIDIY5ovP2lp_W8rRrpEFRCyIw2_5H-EqFk0BxQs130_assertion description "[CD20, a trans-membrane B-cell-specific antigen, is a potential target for treatment of certain malignant and nonmalignant plasma cell disorders including refractory idiopathic thrombocytopenic purpura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133199.RAX5NSIDIY5ovP2lp_W8rRrpEFRCyIw2_5H-EqFk0BxQs130_provenance.
- NP133211.RAYzMBF3INAsRKG-wGs91Q-WgkC_koI4SDJLaVWhu8WGM130_assertion description "[A CpG island proximal to ONECUT2 is frequently methylated in diffuse large B-cell lymphoma (DLBCL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133211.RAYzMBF3INAsRKG-wGs91Q-WgkC_koI4SDJLaVWhu8WGM130_provenance.
- NP133216.RAZKJVBHhHkx31eZkPP1QrRaCGez6-54f-LKQo-d6UZ78130_assertion description "[a polymorphism in the promoter region of il-10 does not have a role in response to drug therapy in diffuse large B-cell lymphoma [letter]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133216.RAZKJVBHhHkx31eZkPP1QrRaCGez6-54f-LKQo-d6UZ78130_provenance.
- NP133218.RAcyiw-ttztloHUfx_SZUNuGwRYvboq8NjrQokWHk9qFc130_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." NP133218.RAcyiw-ttztloHUfx_SZUNuGwRYvboq8NjrQokWHk9qFc130_provenance.
- NP133222.RAT4CMy79F0I2QOl_WnZwbCXni903imHTn-UjkdiV_mqo130_assertion description "[HGF/MET signaling and aberrant HGF-activator expression is associated with diffuse large B-cell lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133222.RAT4CMy79F0I2QOl_WnZwbCXni903imHTn-UjkdiV_mqo130_provenance.
- NP133225.RAb0bDKWWCrGcWD9II_xV9s5MfcrWYpJC8Z8iCbecQnrA130_assertion description "[Translocations involving the MYC locus were detected in six cases of B-cell lymphoma, five of them derived from a MYC/IGH juxtaposition and one from a translocation involving a non-IG gene partner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133225.RAb0bDKWWCrGcWD9II_xV9s5MfcrWYpJC8Z8iCbecQnrA130_provenance.
- NP133231.RAUStejKh1g-gk9UQnmTQqgsw9axWA_JZy3YOokLuXedc130_assertion description "[There is a somatic hypermutation of this gene in B-cell lymphoma and multiple myeloma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133231.RAUStejKh1g-gk9UQnmTQqgsw9axWA_JZy3YOokLuXedc130_provenance.
- NP133232.RAYNcSmZTI2-MNGCOWUMIXtBf83hSRErvmTiFYBwfiQog130_assertion description "[review of role of the NFKB pathway in treatment outcome in diffuse large B-cell lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133232.RAYNcSmZTI2-MNGCOWUMIXtBf83hSRErvmTiFYBwfiQog130_provenance.
- NP133235.RAZrqmGmVylBW--5MbqT_ad1DHKInfUZ2foNXYq3IJ2Gs130_assertion description "[Abnormal FHIT mRNA expression is noted frequently in NHL cell lines and a certain proportion of NHL patients, and decreased FHIT protein expression indicates a significantly worse prognosis in diffuse large B-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133235.RAZrqmGmVylBW--5MbqT_ad1DHKInfUZ2foNXYq3IJ2Gs130_provenance.
- NP133236.RATdTlAzXrr26cMULGto1YlN9UqPScSeGOHpJ5T92apok130_assertion description "[MTHFR variants were not related to FHIT hypermethylation in diffuse large B-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133236.RATdTlAzXrr26cMULGto1YlN9UqPScSeGOHpJ5T92apok130_provenance.
- NP133238.RAdYeoUHJPRilrhqy8djqNESZXTrv8IWy53_Pwqop0Cd0130_assertion description "[CD117 expression can be detected sporadically in DLBCL (diffuse large B-cell lymphoma) of follicle center-cell origin and a subset of plasmablastic lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133238.RAdYeoUHJPRilrhqy8djqNESZXTrv8IWy53_Pwqop0Cd0130_provenance.