Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP215957.RAmLQWxls-PtB1pMPr2gwTJMJE2OsWE3g2M0ACVwgb3YE130_assertion description "[Here the expression of mRNA of IGFBP-3 and uPA in tissue biopsies from eutopic endometrium and endometriotic lesions obtained at laparoscopy from women with endometriosis have been analyzed, and it is documented that both IGFBP-3 and uPA mRNA expression are increased from 3- to 10-fold in endometriotic lesions versus eutopic endometrium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215957.RAmLQWxls-PtB1pMPr2gwTJMJE2OsWE3g2M0ACVwgb3YE130_provenance.
- NP215962.RAhE3UidaYjuPMIx042uukGQzuIM1MJjLGCd4sR1_471A130_assertion description "[Hereditary Vitamin D Resistant Rickets (HVDRR) is a rare disease caused by mutations in the vitamin D receptor (VDR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215962.RAhE3UidaYjuPMIx042uukGQzuIM1MJjLGCd4sR1_471A130_provenance.
- NP215966.RAmpe0NY59Y0d6tnUvsfZq-t2ThnMk44M5YXH1bSz_A_M130_assertion description "[CHOP was also elevated in the hippocampus from epileptic mice and patients with pharmacoresistant epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215966.RAmpe0NY59Y0d6tnUvsfZq-t2ThnMk44M5YXH1bSz_A_M130_provenance.
- NP215969.RArFKBwgys7hW41q4uh70RtUtmvWU9Xe9APruEQSHFU-4130_assertion description "[Decreased expression of cytochromes P450 1A2, 2E1, and 3A4 and drug transporters Na+-taurocholate-cotransporting polypeptide, organic cation transporter 1, and organic anion-transporting peptide-C correlates with the progression of liver fibrosis in chronic hepatitis C patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215969.RArFKBwgys7hW41q4uh70RtUtmvWU9Xe9APruEQSHFU-4130_provenance.
- NP215975.RAi2QAfu7aYpdy_xoOhPRGSB3VdUjnLv1oLTdc8GkbZNQ130_assertion description "[Mutation of mitochondrial DNA (mtDNA) G13513A, encoding the ND5 subunit of respiratory chain complex I, can cause mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and Leigh syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215975.RAi2QAfu7aYpdy_xoOhPRGSB3VdUjnLv1oLTdc8GkbZNQ130_provenance.
- NP215983.RAlds3bqf49TybOL2rAQDBH6qLIuapMGlrPd3e4JQVxYw130_assertion description "[To determine the clinical relevance of p53R2 induction, we measured p53R2 expression in bone marrow samples from 15 myelodysplastic syndrome/acute myelogenous leukemia (MDS/AML) patients undergoing decitabine therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215983.RAlds3bqf49TybOL2rAQDBH6qLIuapMGlrPd3e4JQVxYw130_provenance.
- NP215986.RAlTj8FNquYQYYJx-U6ddzhzeRZhPfnLVTRJhroMMFCwI130_assertion description "[Somatic mutations affecting histone methyltransferases such as enhancer of zeste 2 and mixed lineage leukemia 2, histone demethylases including ubiquitously transcribed X chromosome tetratricopeptide repeat and Jumonji domain-containing 2C, and histone acetyltransferases including CBP and p300 are recurrent and common in lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215986.RAlTj8FNquYQYYJx-U6ddzhzeRZhPfnLVTRJhroMMFCwI130_provenance.
- NP215992.RAjqOM2drDQEBPU4bVd2HrGih_xFE5M1eV865mpNB5CLc130_assertion description "[The purpose of this work was to the hypothesis that MHC encoded susceptibility factors for SLE lie in the TNF region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215992.RAjqOM2drDQEBPU4bVd2HrGih_xFE5M1eV865mpNB5CLc130_provenance.
- NP215996.RAmgamXLFlYengruSItgwONGiXPKHC1mm6WRKfTuVuyTc130_assertion description "[A trend for association between depression severity and PDYN variation was detected.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP215996.RAmgamXLFlYengruSItgwONGiXPKHC1mm6WRKfTuVuyTc130_provenance.
- NP216002.RAvoiYj0BpqzfpLSaVraUE0RGymttzsQUntL7vbZqBZ0A130_assertion description "[High-grade carcinomas had a variable p16(INK4A) expression pattern.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216002.RAvoiYj0BpqzfpLSaVraUE0RGymttzsQUntL7vbZqBZ0A130_provenance.
- NP216009.RApingKAFH3vEmejjcbekdhh-tmPLmyCuiVH9kTd99PxQ130_assertion description "[In bladder tumor cell lines derived from aggressive carcinomas, there were significant alterations in the relative expression of isoforms including an overall decrease in the proportion of FGFR3 Delta8-10 and predominant expression of FGFR3 IIIc in some cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216009.RApingKAFH3vEmejjcbekdhh-tmPLmyCuiVH9kTd99PxQ130_provenance.
- NP216013.RAiv9RSAv3Va1pg70tKScm-ksp7yaxNb9gCmRmuDq7ET0130_assertion description "[The NUP98 gene on chromosome band 11p15 is involved in several different chromosomal aberrations that have been associated with t-MDS/AML.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216013.RAiv9RSAv3Va1pg70tKScm-ksp7yaxNb9gCmRmuDq7ET0130_provenance.
- NP216019.RAgpMXwyd0JuHWrQL-dHPEXT7uG7XAocM37cTMMChJotY130_assertion description "[An additional band indicating an anomalous molecular form of AChE was present in CSF from 19 of 23 patients with a histological diagnosis of Alzheimer's disease and no other central nervous system disorder but in none of the 19 non-demented patients (without a histological diagnosis of Alzheimer's disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216019.RAgpMXwyd0JuHWrQL-dHPEXT7uG7XAocM37cTMMChJotY130_provenance.
- NP216022.RAkNh3Yg2ZF_IzXIg7F71_xm_J9i4xDyOApY04415_pZI130_assertion description "[The tissue-specific translation elongation factor eEF1A2 was recently shown to be a potential oncogene that is overexpressed in ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216022.RAkNh3Yg2ZF_IzXIg7F71_xm_J9i4xDyOApY04415_pZI130_provenance.
- NP216032.RAhVZ5zczgQ1Mp63If_X69cTh5AuZzp90_sCZuIAyyk3I130_assertion description "[In addition, cervical squamous cell carcinoma and adenocarcinoma have distinct molecular profiles, suggesting that clinical outcomes may be improved with the use of more tailored treatment strategies, including PI3K and MEK inhibitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216032.RAhVZ5zczgQ1Mp63If_X69cTh5AuZzp90_sCZuIAyyk3I130_provenance.
- NP216036.RAiV6T5HC-ZuY1Xervnzy1gMyBn9hsiiM6YVgGjtvUDgQ130_assertion description "[Given the potential importance of IL-6 in the pathogenesis of colorectal tumors, we tested the hypothesis that butyrate acts by inhibiting IL-6-induced signaling events in colorectal carcinoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216036.RAiV6T5HC-ZuY1Xervnzy1gMyBn9hsiiM6YVgGjtvUDgQ130_provenance.
- NP216039.RAgiBrh3IWE4QpQr1RuqxwQUi8darYJ8wVlQklGGAMYEY130_assertion description "[In familial hyperaldosteronism type I (FH-I), inheritance of a hybrid 11beta-hydroxylase/aldosterone synthase gene causes ACTH-regulated aldosterone overproduction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216039.RAgiBrh3IWE4QpQr1RuqxwQUi8darYJ8wVlQklGGAMYEY130_provenance.
- NP216042.RAqw2e3dGTEMFxXehX35fvgV99fzfeRofYU0u3ID4DPIc130_assertion description "[Monocyte chemoattractant protein-1 (MCP-1) seems to be involved in the pathogenesis of multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216042.RAqw2e3dGTEMFxXehX35fvgV99fzfeRofYU0u3ID4DPIc130_provenance.
- NP216043.RApVZLQlke8oc8F8K0zpv08zflFZ3REBiUDbdje2gWfSM130_assertion description "[To examine the possible association of adiponectin (ADIPOQ), adiponectin receptor (ADIPOR1/2) gene polymorphisms with polycystic ovary syndrome (PCOS) and their influence on insulin resistance in Japanese women with PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216043.RApVZLQlke8oc8F8K0zpv08zflFZ3REBiUDbdje2gWfSM130_provenance.
- NP216056.RAgtxio6foMcLlq7OssHn0i4opHTOhqi9ovan7_QXX6qs130_assertion description "[For the study, 321 cases of venous thrombosis in the splanchnic and nonsplanchnic regions (cerebral venous thrombosis [CVT], 70; deep venous thrombosis [DVT], 36; Budd-Chiari syndrome [BCS], 137; portal venous thrombosis [PVT], 78) were studied for the presence of JAK2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216056.RAgtxio6foMcLlq7OssHn0i4opHTOhqi9ovan7_QXX6qs130_provenance.
- NP216057.RAljjJex1PGCfqoB5kb0qR6KLh06x44txgL8OiM3vb_0k130_assertion description "[In this study, we utilised the serial analysis of gene expression (SAGE) and expressed sequence tag (EST) databases of the Cancer Genome Anatomy Project (CGAP) to perform in silico analyses of the expression pattern of the 15 human kallikrein genes in normal and cancerous breast tissues and cell lines using different analytical tools such as Virtual Northern blotting, Digital Differential Display and X-profiler.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216057.RAljjJex1PGCfqoB5kb0qR6KLh06x44txgL8OiM3vb_0k130_provenance.
- NP216068.RAsEuL9iiJXRa-bP3wknR7hUpUpHxbPFnDq5Vu__-W3Io130_assertion description "[Altogether, our results indicate that MAL expression is recurrent in PMBLs, providing further evidence that PMBL represents a distinct entity among DLBLs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216068.RAsEuL9iiJXRa-bP3wknR7hUpUpHxbPFnDq5Vu__-W3Io130_provenance.
- NP216069.RAgo-r1UfkA_0fnvTlCHoJkhmKeMMJzHXA3Giaa9a0TV4130_assertion description "[Deficiency of dihydropteridine reductase causes a variant form of phenylketonuria associated with a devastating neurological disease characterized by mental retardation, hypokinesis and other features relating to basal ganglia disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216069.RAgo-r1UfkA_0fnvTlCHoJkhmKeMMJzHXA3Giaa9a0TV4130_provenance.
- NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_assertion description "[Since the identification of the first SCN5A mutation associated with long QT syndrome in 1995, several mutations in this gene for the alpha subunit of the cardiac sodium channel have been identified in a heterogeneous subset of cardiac rhythm syndromes, including Brugada syndrome, progressive cardiac conduction defect, sick sinus node syndrome, atrial fibrillation and dilated cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216070.RAvayK0q9jlx-AAvH3yZlH6qW5qlLv35bPxwtGUoBfB_Q130_provenance.
- NP216089.RAqF7pnejWsH4cwGNRFqp_ISB-N0kmu3IGZzJS1Ri8NZ8130_assertion description "[By siRNA knockdown and stable overexpression, we demonstrated that human p29 is involved in DNA damage response and Fanconi anemia pathway in cultured cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216089.RAqF7pnejWsH4cwGNRFqp_ISB-N0kmu3IGZzJS1Ri8NZ8130_provenance.
- NP216098.RAoyzNytDCnVNs5kN1h1mcj2PtiP5iBZYdUZm3vQX1Pt0130_assertion description "[The distributions of the five FAB subtypes were comparable in both groups of patients, except for a higher percentage of refractory anemia with ringed sideroblasts in older patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216098.RAoyzNytDCnVNs5kN1h1mcj2PtiP5iBZYdUZm3vQX1Pt0130_provenance.
- NP216100.RAqbq79LiL2H9-WkEbS4x1fV4KA0CeP3lYKMR8F_I3IGI130_assertion description "[Cutting edge: transgenic expression of human MUC1 in IL-10-/- mice accelerates inflammatory bowel disease and progression to colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216100.RAqbq79LiL2H9-WkEbS4x1fV4KA0CeP3lYKMR8F_I3IGI130_provenance.
- NP216108.RAlHHe_dyQD-9B7sY--qiuDwiorl6A26hh3XlKHgyYUZ0130_assertion description "[Sera from individuals with pulmonary and extrapulmonary TB, human immunodeficiency virus (HIV)-TB coinfections, and purified protein derivative (PPD)-positive and PPD-negative status with no evidence of disease were tested.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216108.RAlHHe_dyQD-9B7sY--qiuDwiorl6A26hh3XlKHgyYUZ0130_provenance.
- NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_assertion description "[The first congenital defect of hypoxia-sensing homozygosity for VHL 598C>T mutation was recently identified in Chuvash polycythemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216113.RAuBSWbegZCif_IeApsZh8BALARlL-v9xDlxExWedqHDA130_provenance.
- NP216124.RAqTQ0p4oGWIKU0dwKoOOuLQ9q3OLRT5EN7BAj0p452-4130_assertion description "[The mechanisms for osteoclast expression and the expression of RANKL, RANK, OPG and VEGF merit further prospective analysis, particularly in the context of BP treatment and progressive bone metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216124.RAqTQ0p4oGWIKU0dwKoOOuLQ9q3OLRT5EN7BAj0p452-4130_provenance.
- NP216127.RAhQ48oDst2AJvox8CxsfqU1-XGUsO-zZaWSMJcOTAipo130_assertion description "[Evidence for defective Rab GTPase-dependent cargo traffic in immune disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216127.RAhQ48oDst2AJvox8CxsfqU1-XGUsO-zZaWSMJcOTAipo130_provenance.
- NP216135.RAmYOJI-acI-CZjJqsQg9crGsSK59qw63bg2vEdsl-Kqo130_assertion description "[Identification of a novel and recurrent mutation in the SERPING1 gene in patients with hereditary angioedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216135.RAmYOJI-acI-CZjJqsQg9crGsSK59qw63bg2vEdsl-Kqo130_provenance.
- NP216151.RAhdha1ewG7sSwIRvbJnwSPz24Br28JLx08Goy0CKPaQg130_assertion description "[Therefore, deficiency in a weak intracellular inhibitor of NE results in an acute inflammatory response that protects from P. aeruginosa but does not cause lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216151.RAhdha1ewG7sSwIRvbJnwSPz24Br28JLx08Goy0CKPaQg130_provenance.
- NP216153.RAjSosRhS_Im9r2y4XNGJuLPqZ1kClMPm0_A_WObYFYKk130_assertion description "[No correlations, however, were observed between mRNA levels of TIMPs and prognostic factors such as patient age, tumor size, grade of anaplasia, or steroid receptor status; neither were any correlations found between these clinicopathological characteristics and the mRNA expression of the collagenolytic enzymes matrix metalloproteinase-2 and matrix metalloproteinase-9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216153.RAjSosRhS_Im9r2y4XNGJuLPqZ1kClMPm0_A_WObYFYKk130_provenance.
- NP216154.RAn6KfXQTT-YadVP0aPS3Z58bMxWqya6U1yii1EwKpccQ130_assertion description "[Genetic variants in MYLK are significantly associated with both asthma and sepsis in populations of African ancestry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216154.RAn6KfXQTT-YadVP0aPS3Z58bMxWqya6U1yii1EwKpccQ130_provenance.
- NP216170.RAhg0yPXv1G0p3a8D9N2OUcxI32m1FAI0GTtHQPIBVZOE130_assertion description "[Fabry disease is an X-linked inherited metabolic disorder caused by a deficiency of alpha-galactosidase (alpha-gal), resulting in the accumulation of ceramide trihexoside (CTH) in body fluids and in many organs and tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216170.RAhg0yPXv1G0p3a8D9N2OUcxI32m1FAI0GTtHQPIBVZOE130_provenance.
- NP216171.RAm5GEHw_DpBCvySCXFuAaT9jgMfQlNI10bp5xjL7BNdA130_assertion description "[The present study provided evidence of a potential role for XRCC1 codon 194 and 399 polymorphisms in genetic predisposition to glioma among the Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216171.RAm5GEHw_DpBCvySCXFuAaT9jgMfQlNI10bp5xjL7BNdA130_provenance.
- NP216172.RApFX9ce_KuIcXbHNdTE3FBIvRP26rNEOp8faSBMlSfSI130_assertion description "[Further, our results signify a critical role for PI3K/p110γ in pancreatic cancer, and we hypothesize that PI3K/p110γ overexpression is a key event in the disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216172.RApFX9ce_KuIcXbHNdTE3FBIvRP26rNEOp8faSBMlSfSI130_provenance.
- NP216179.RArXzqt4zukmAK5mv6fJje1u81Hi1_iQ2ejrim2bJVSbk130_assertion description "[HGF has been implicated to play an important role in invasion and metastasis of various human cancers through tumor-stromal interactions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216179.RArXzqt4zukmAK5mv6fJje1u81Hi1_iQ2ejrim2bJVSbk130_provenance.
- NP216180.RAtFjxdeZoMsOtxg3YoGzij2ok_ZkOPVROQLOvZ7lGmt4130_assertion description "[Regulation of urokinase-type plasminogen activator expression in squamous-cell carcinoma of the oral cavity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216180.RAtFjxdeZoMsOtxg3YoGzij2ok_ZkOPVROQLOvZ7lGmt4130_provenance.
- NP216188.RAjratPMLuHISh7dOAp4dkJHvbaTGktfqPg6LzlEXCyG8130_assertion description "[However, fixed-effects model showed significant risk of AML in the presence of null genotypes of GSTM1 and GSTT1(p < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216188.RAjratPMLuHISh7dOAp4dkJHvbaTGktfqPg6LzlEXCyG8130_provenance.
- NP216193.RAu4-kMgWZTy3jZykIzsGdFBShR3rIagER2a-5FrlpP-M130_assertion description "[The present study suggests that p53 gene mutation frequently occurs in recurrent ovarian cancer and that alteration of p53 gene status affects salvage chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216193.RAu4-kMgWZTy3jZykIzsGdFBShR3rIagER2a-5FrlpP-M130_provenance.
- NP216196.RAjmtQepkRz3BvCmOL1BaZOho-4AJ4B30_YZC4JF_VczA130_assertion description "[Impaired natural and CD16-mediated NK cell cytotoxicity in patients with WAS and XLT: ability of IL-2 to correct NK cell functional defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216196.RAjmtQepkRz3BvCmOL1BaZOho-4AJ4B30_YZC4JF_VczA130_provenance.
- NP216205.RAk0rKml1TIlvet7haj3YmC2__9OA8GMdR56h84nrfBT8130_assertion description "[These functions may underlie the correlation between altered MET regulation and autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216205.RAk0rKml1TIlvet7haj3YmC2__9OA8GMdR56h84nrfBT8130_provenance.
- NP216206.RAqKJPQCKiJN6xyVcLCXwmbk1v_PzEa6iUrD0umjd7VmQ130_assertion description "[Specifically, CLDC-based intravenous delivery of the p53 and GM-CSF genes were each as effective as the potent antiangiogenic gene, angiostatin, in reducing both tumor metastasis and tumor angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216206.RAqKJPQCKiJN6xyVcLCXwmbk1v_PzEa6iUrD0umjd7VmQ130_provenance.
- NP216209.RAqiOw7sU-Bhap6bp3FEhFQuXwRUnTLwdxFulirkyJNk4130_assertion description "[The autosomal dominant form of Emery-Dreifuss muscular dystrophy (AD-EDMD) is caused by mutations in the gene encoding for the lamins A and C (LMNA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216209.RAqiOw7sU-Bhap6bp3FEhFQuXwRUnTLwdxFulirkyJNk4130_provenance.
- NP216210.RAsyd5By8BEgmDAB_TrsoUN0r8DSnMlAiei-iNMc0FiRE130_assertion description "[Interaction of nephrocystin-4 and RPGRIP1 is disrupted by nephronophthisis or Leber congenital amaurosis-associated mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216210.RAsyd5By8BEgmDAB_TrsoUN0r8DSnMlAiei-iNMc0FiRE130_provenance.
- NP216211.RAhBP8z9_uOZuJ86isMwFfvBSsG4pLE6DJAeoZwufvE64130_assertion description "[Mutations in MECP2 gene, located in Xq28, have been reported as being the major cause of Rett syndrome and are also associated with some cases of X-linked mental retardation in both males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216211.RAhBP8z9_uOZuJ86isMwFfvBSsG4pLE6DJAeoZwufvE64130_provenance.
- NP216213.RArkqLHh-kShXjdp2sFOZTuUuS20yrlMTUZtvdij-IN8I130_assertion description "[Although the underlying mechanism of action requires further investigation, this study provides new insight into the interaction between S100 proteins and CacyBP/SIP, which might enrich our knowledge of S100 proteins and be helpful for our understanding of the development of gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216213.RArkqLHh-kShXjdp2sFOZTuUuS20yrlMTUZtvdij-IN8I130_provenance.
- NP216214.RAq1BawQrYBtfIVFuaJIZqhQnPGTR68uJ0oUWMp4QRilg130_assertion description "[POAG and PCAG patients recruited from different areas of Pakistan were diagnosed on the basis of clinical history, raised intraocular pressure (IOP), cup-to-disc ratio (CDR) and visual field defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216214.RAq1BawQrYBtfIVFuaJIZqhQnPGTR68uJ0oUWMp4QRilg130_provenance.
- NP216219.RAvEnWXocv9fcYvE_Vtr39R_bk4-qENGgSZNH86M1V3-Q130_assertion description "[The butyrylcholinesterase knockout mouse a research tool in the study of drug sensitivity, bio-distribution, obesity and Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216219.RAvEnWXocv9fcYvE_Vtr39R_bk4-qENGgSZNH86M1V3-Q130_provenance.
- NP216230.RAkfoeGTA55jrWUPp5frcYT7ZMPKswp_ZCXQTk0Hzt4Fg130_assertion description "[Immunoblot analyses with a specific antiserum for CYP4Z1 clearly demonstrated protein expression in mammary gland and breast carcinoma tissue specimens as well as in CYP4Z1-transduced cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216230.RAkfoeGTA55jrWUPp5frcYT7ZMPKswp_ZCXQTk0Hzt4Fg130_provenance.
- NP216235.RAqxu7QgU5XhpDsgSdVKOynlLbREJ-1EkMl5k0pu2RH2I130_assertion description "[The results were substantially the same when a preterm spontaneous labour group (PTL) (n=26), exclusive of deliveries complicated by pre-eclampsia (n=1) or intrauterine growth restriction (n=3), was compared to the CST and SLT groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216235.RAqxu7QgU5XhpDsgSdVKOynlLbREJ-1EkMl5k0pu2RH2I130_provenance.
- NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_assertion description "[In a case-control study, including 210 Caucasoid migraine patients and 210 controls, we examined association between three single nucleotide polymorphisms in the coding region of ESR1, rs2077642, rs1801132, and rs2228480, and an Alu insertion in PGR, and migraine, migraine without aura or migraine with aura.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216241.RAhS2mocn9OdRjS3ifU78hHSeDoCfrJeYzf7eeH-CwLFI130_provenance.
- NP216242.RAiTjVIV0r-eLi1dyyXZzPOG7-SrQCRwgRuFQmrwy9DRA130_assertion description "[Although we had at least 89% power to detect a relative risk of 1.5 (alpha=0.05) in all subgroups, we did not find any association between ESR1 haplotype carriership and risk of stroke and ischemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216242.RAiTjVIV0r-eLi1dyyXZzPOG7-SrQCRwgRuFQmrwy9DRA130_provenance.
- NP216244.RAgF_OeF64Z7voUEe0P01NhdtQMZlo7geq54YcfI5-ZDs130_assertion description "[Targeting MDM2 could be a new approach in colon cancer therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216244.RAgF_OeF64Z7voUEe0P01NhdtQMZlo7geq54YcfI5-ZDs130_provenance.
- NP216245.RAoa49XAyoMMDYqQ0-Na4IMgyHflOFCl_rslgugQRsbCc130_assertion description "[RECK mRNA is lowest in RA synovial membranes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216245.RAoa49XAyoMMDYqQ0-Na4IMgyHflOFCl_rslgugQRsbCc130_provenance.
- NP216247.RAoJUE_0wZTpaDPKqBPhU5O7UFVMpQH3OXQflDlCJS-dw130_assertion description "[Human leukocyte antigen alleles in patients with bipolar disorder in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216247.RAoJUE_0wZTpaDPKqBPhU5O7UFVMpQH3OXQflDlCJS-dw130_provenance.
- NP216248.RAljnFkkEwJiP_KfH4SkAShSCv-biy5uUsCnqA_J1vH5I130_assertion description "[Myocardial cells isolated from 9 patients with end-stage heart failure and 18 donor nonfailing hearts were infected with adenoviruses encoding for either the antisense of phospholamban (Ad.asPL), the SERCA2a gene (Ad.SERCA2a), or the reporter genes beta-galactosidase and green fluorescent protein (Ad.betagal-GFP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216248.RAljnFkkEwJiP_KfH4SkAShSCv-biy5uUsCnqA_J1vH5I130_provenance.
- NP216249.RAnvTvw7HfEFGxkypvvsMzemzPDYgIodjEt_ihsz4KSLs130_assertion description "[By topographical dissection of surgical specimens, we found no differences in cell proliferation or density but significant differences with regard to MMP-2 mRNA expression between central and peripheral regions, being highest at the center of malignant gliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216249.RAnvTvw7HfEFGxkypvvsMzemzPDYgIodjEt_ihsz4KSLs130_provenance.
- NP216252.RAqaJOFl1v16dk9bIbntS99e4P7R6X1bFv-5xqJfYEfnk130_assertion description "[Cytological atypia, bronchial metaplasia, protein (hnRNP A2/B1) overexpression, ras oncogene activation and tumour-suppressor gene deletion, genomic instability (loss of heterozygosity, microsatellite alterations), abnormal methylation, helical CT detection of atypical adenomatous hyperplasia and fluorescent bronchoscopic detection of angiogenic squamous dysplasia offer great promise for molecular diagnosis of lung cancer far in advance of clinical presentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216252.RAqaJOFl1v16dk9bIbntS99e4P7R6X1bFv-5xqJfYEfnk130_provenance.
- NP216255.RAhzf8GWicAgQdlgMLOxA7cnXGyK_ipM_kB2nq9Gvsyog130_assertion description "[Detailed analysis of myeloma cell lines has shown that myeloma is characterized by frequent chromosome translocations involving the switch regions of the immunoglobulin heavy-chain (IgH) locus on 14q32.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216255.RAhzf8GWicAgQdlgMLOxA7cnXGyK_ipM_kB2nq9Gvsyog130_provenance.
- NP216258.RAoac4-jB54zJsZSmGhfWayHlXGhKfadMsu_F94pcfTN4130_assertion description "[The association with major depression, suicide, and panic disorder of a new functional 5-HT1A polymorphism at C(-1019)G that selectively blocks repression of the 5-HT1A autoreceptor by NUDR further suggests a causative role for altered regulation of this receptor in predisposition to mental illness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216258.RAoac4-jB54zJsZSmGhfWayHlXGhKfadMsu_F94pcfTN4130_provenance.
- NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_assertion description "[Twenty-one unrelated children with persistent familial hematuria as well as their families were studied for segregation of hematuria with haplotypes at the COL4A3/COL4A4 locus for benign familial hematuria and at the COL4A5 locus for X-linked Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216259.RApt9uTdXem0Bt0VDGw7W7nVKS7yPTnn7Je7fQdYoI8cc130_provenance.
- NP216261.RAi0hgbQv3DWLDQTXyFKoaT5SKfZ8hLVtAgHZEB0WA85M130_assertion description "[Calreticulin promotes cell motility and enhances resistance to anoikis through STAT3-CTTN-Akt pathway in esophageal squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216261.RAi0hgbQv3DWLDQTXyFKoaT5SKfZ8hLVtAgHZEB0WA85M130_provenance.
- NP216263.RAiyExt0R3L5bxuHpx7R8idWPmyuEZ5SF0ukZKIm5t6Hs130_assertion description "[The t(12;21)(p13;q22) translocation, fusing the ETV6 and AML1 genes, is the most frequent chromosomal translocation associated with pediatric B-cell precursor acute lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216263.RAiyExt0R3L5bxuHpx7R8idWPmyuEZ5SF0ukZKIm5t6Hs130_provenance.
- NP216268.RAqqTYNRwg0-fnK1ToULtjHCbEh23s8aBNDqnWgI4MEAM130_assertion description "[Individuals heterozygous for an IP variant, IP(R212C), displayed exaggerated loss of platelet IP responsiveness and accelerated cardiovascular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216268.RAqqTYNRwg0-fnK1ToULtjHCbEh23s8aBNDqnWgI4MEAM130_provenance.
- NP216271.RAuPgEfTpabG8YDexD1LZZrAbmiasN1XMJ6YlWCfF5s_A130_assertion description "[Pseudohypoparathyroidism type Ib (PHP-Ib) is characterized by hypocalcemia and hyperphosphatemia due to proximal renal tubular resistance to PTH but without evidence for Albright's hereditary osteodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216271.RAuPgEfTpabG8YDexD1LZZrAbmiasN1XMJ6YlWCfF5s_A130_provenance.
- NP216280.RAhOn9NmnJZOUPRV8EVcxj9avP3KeoAzcC70KGJ7PMuRQ130_assertion description "[Osteopontin, which was identified as a lead gene in the signature, was over-expressed in metastatic HCC; an osteopontin-specific antibody effectively blocked HCC cell invasion in vitro and inhibited pulmonary metastasis of HCC cells in nude mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216280.RAhOn9NmnJZOUPRV8EVcxj9avP3KeoAzcC70KGJ7PMuRQ130_provenance.
- NP216285.RAgMtcUBiizhJoVqMNqtnor9qQpuqSNZtBWoWYUqYjI4E130_assertion description "[Programmed cell death 1 (PD-1) has recently been reported to have a genetic association in several autoimmune diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216285.RAgMtcUBiizhJoVqMNqtnor9qQpuqSNZtBWoWYUqYjI4E130_provenance.
- NP216295.RAtSzFNIqHCXNMbcSKtELgzxLgpJG4TbPbQ-T1Id_Jjn4130_assertion description "[It is also attenuated by PD 98059, an inhibitor of the MAPK/extracellular-regulated kinase kinase MEK1/2, SP 600125, an inhibitor of c-Jun N-terminal kinase (JNK), and SB 202190, an inhibitor of p38 MAPK.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216295.RAtSzFNIqHCXNMbcSKtELgzxLgpJG4TbPbQ-T1Id_Jjn4130_provenance.
- NP216298.RAtNCiWCz1-8KfP2Es_ir_wgQnXU3csSWjjXUCkB-4WVU130_assertion description "[We investigated the relationship between the CYP2D6-predicted phenotype and tamoxifen response in a nested case-control study among women from the International Breast cancer Intervention Study (IBIS-I), which evaluated tamoxifen in the preventive setting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216298.RAtNCiWCz1-8KfP2Es_ir_wgQnXU3csSWjjXUCkB-4WVU130_provenance.
- NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_assertion description "[The major recommendations are to use testing for EGFR mutations and ALK fusions to guide patient selection for therapy with an epidermal growth factor receptor (EGFR) or anaplastic lymphoma kinase (ALK) inhibitor, respectively, in all patients with advanced-stage adenocarcinoma, regardless of sex, race, smoking history, or other clinical risk factors, and to prioritize EGFR and ALK testing over other molecular predictive tests.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216303.RAkdu7Ui33PjLxrWK4xyj2k1KKEMLPhADM6Kwk9ljwYNM130_provenance.
- NP216315.RAkzl35kVN2KxiToQkB9rO0DHCJ--VCn-UqB-G63fd6Eo130_assertion description "[Efficacy of low-dose proton pump inhibitor (PPI) in the eradication of Helicobacter pylori following combination PPI/AC therapy in Japan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216315.RAkzl35kVN2KxiToQkB9rO0DHCJ--VCn-UqB-G63fd6Eo130_provenance.
- NP216318.RApdCjXFwEIPCLvzRQCXWOwRyMDXP_0NFFCwdcXNUGtq4130_assertion description "[Endostatin- and interleukin-2-expressing retroviral bicistronic vector for gene therapy of metastatic renal cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216318.RApdCjXFwEIPCLvzRQCXWOwRyMDXP_0NFFCwdcXNUGtq4130_provenance.
- NP216323.RAkJ7NR4H3S_A4h7zyA5vlaH1vaCmnPnRlKp_7QXB56lA130_assertion description "[Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216323.RAkJ7NR4H3S_A4h7zyA5vlaH1vaCmnPnRlKp_7QXB56lA130_provenance.
- NP216325.RAkjYLg0EdSPvx6un0zlV1zf_CtV3DQfbgejcdmkh8cC8130_assertion description "[The SYT-SSX1 fusion type of synovial sarcoma is associated with increased expression of cyclin A and D1. A link between t(X;18)(p11.2; q11.2) and the cell cycle machinery.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216325.RAkjYLg0EdSPvx6un0zlV1zf_CtV3DQfbgejcdmkh8cC8130_provenance.
- NP216326.RAuAgvZ88vd7Opn3dSzn27_a60lAIc_megiJPpNdJxnpI130_assertion description "[There was no significant difference in the pulmonary function, nutritional status, and in the prevalence of meconium ileus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216326.RAuAgvZ88vd7Opn3dSzn27_a60lAIc_megiJPpNdJxnpI130_provenance.
- NP216332.RAs3iaGxYFz7cU5242Ad3L9-Fhjk850KQd_S2qG4rAjss130_assertion description "[Concomitant PI3K-AKT and p53 alterations in endometrial carcinomas are associated with poor prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216332.RAs3iaGxYFz7cU5242Ad3L9-Fhjk850KQd_S2qG4rAjss130_provenance.
- NP216334.RAjoAVMXI_HZUbcnN4We-9jL7tzQbTCdvSXYce1eWunEE130_assertion description "[In invasive tumours, FCM offers quantitative prognostic information in terms of pelvic lymph-node metastasis and metastasis to distant sites.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216334.RAjoAVMXI_HZUbcnN4We-9jL7tzQbTCdvSXYce1eWunEE130_provenance.
- NP216337.RAl0Y0JMi2KMER4o2tWtp336xWVyYgJpbvvrZlIGVjCX4130_assertion description "[Mouse models of mammary neoplasia have confirmed the role of EphA2 as mice carrying a knockout allele of EphA2 were resistant to breast cancer, a phenotype that was associated with interactions between EphA2 and ErbB2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216337.RAl0Y0JMi2KMER4o2tWtp336xWVyYgJpbvvrZlIGVjCX4130_provenance.
- NP216339.RAo_2GYl_Qmlv6alB-J_NJQYriIBb-onS6fTcUj9whSKE130_assertion description "[Neutralizing antibody to TGF-beta normalized lymphocyte proliferation in response to PPD, partially restored blastogenesis to candidal antigen, and significantly increased PPD-stimulated production of IFN-gamma in TB patients but not in contacts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216339.RAo_2GYl_Qmlv6alB-J_NJQYriIBb-onS6fTcUj9whSKE130_provenance.
- NP216344.RAncRJcR3P-PqfT_DvBPZhg5LhjElIE4rNl1y7LVjNaHc130_assertion description "[Allelic mutations in each of these genes can result in a wide spectrum of clinical conditions, ranging from severe congenital onset with associated structural brain malformations (Walker Warburg syndrome; muscle-eye-brain disease; Fukuyama muscular dystrophy; congenital muscular dystrophy type 1D) to a relatively milder congenital variant with no brain involvement (congenital muscular dystrophy type 1C), and to limb-girdle muscular dystrophy (LGMD) type 2 variants with onset in childhood or adult life (LGMD2I, LGMD2L, and LGMD2N).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216344.RAncRJcR3P-PqfT_DvBPZhg5LhjElIE4rNl1y7LVjNaHc130_provenance.
- NP216345.RArWa_Uy3T9-jCSV7HN9DEHAELYvubzG9GUoiqvp6WtyE130_assertion description "[Intracortical inhibition of the motor cortex in Segawa disease (DYT5).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216345.RArWa_Uy3T9-jCSV7HN9DEHAELYvubzG9GUoiqvp6WtyE130_provenance.
- NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_assertion description "[Missense germline mutations of the RET proto-oncogene have recently been identified in the hereditary cancer syndromes MEN2A, MEN2B, and FMTC, all characterized by medullary carcinoma, but also including phaeochromocytoma in MEN2A and MEN2B and parathyroid disease in MEN2A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_provenance.
- NP216367.RAs5ikmEg0ABYhC7U_UVd-LF8byxxFcPnoWYQ54odu49I130_assertion description "[Laron Syndrome, first described in Israel, is a form of dwarfism similar to isolated growth hormone deficiency caused by molecular defects in the GH receptor gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216367.RAs5ikmEg0ABYhC7U_UVd-LF8byxxFcPnoWYQ54odu49I130_provenance.
- NP216368.RAqLzMBP0uSzRmSohptOIRIU3Nbcx8M26J5o-wWCIjbvQ130_assertion description "[We detected the expression of the H(4)R on pDC in the blood and in lesional psoriasis skin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216368.RAqLzMBP0uSzRmSohptOIRIU3Nbcx8M26J5o-wWCIjbvQ130_provenance.
- NP216369.RAk2_ivDZ7gQCcI708Be-2ih0Y4ZrNOyJH11dMZOwnPr4130_assertion description "[We observed promoter methylation for CDKN2A in 21% (26/123) of tumours, for CDKN2B in 32% (23/71) and p14 ARF in 21% (23/108).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216369.RAk2_ivDZ7gQCcI708Be-2ih0Y4ZrNOyJH11dMZOwnPr4130_provenance.
- NP216375.RAg86FGS61V3cEIKiUEldm34Qcty9meXbj4b3YmDO6I2o130_assertion description "[AD patients who possessed the CYP2D6B mutant allele, in comparison with those without the CYP2D6B allele, were found to have a smaller decline in two synaptic markers, choline acetyltransferase and synaptophysin, in the frontal cortex relative to normal control values.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216375.RAg86FGS61V3cEIKiUEldm34Qcty9meXbj4b3YmDO6I2o130_provenance.
- NP216379.RAj5iQ3_JGcSLRcwHsn5q9JtThhHFP3WABxNH7DHrZmtw130_assertion description "[Chimeric JAZF1-JJAZ1 mRNA transcribed from DNA spanning the site of recombination in the (7;17)(p15;q21) chromosomal translocation found in half of endometrial stromal sarcomas and most cases of benign stromal nodules is one such example.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216379.RAj5iQ3_JGcSLRcwHsn5q9JtThhHFP3WABxNH7DHrZmtw130_provenance.
- NP216381.RAvGDSSQOr4msPBjqXU_Ywk-GjuSXegu-4sX6qzw3CH9k130_assertion description "[In the liver, deficient prohibitin activity participates in the progression of non-alcoholic steatohepatitis and obesity, according to mechanisms that still must be elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216381.RAvGDSSQOr4msPBjqXU_Ywk-GjuSXegu-4sX6qzw3CH9k130_provenance.
- NP216383.RAqfoiWuZHIOYs8q5-zMa5XwamhtG436byehdqJZNp-lY130_assertion description "[Two of the three affected family members, 9- and 7-year-old brothers, showed the unique features of BCM in their color vision and ERG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216383.RAqfoiWuZHIOYs8q5-zMa5XwamhtG436byehdqJZNp-lY130_provenance.
- NP216386.RAvp9_SRPTzy_OAC2qKnvOV6yCtaYG2BnhkALESEdZ3fc130_assertion description "[We have examined how disease progression correlates with changes in expression of the p14ARF (ARF) tumour suppressor, a key regulator of the p53 tumour suppressor pathway that is silenced in some 30% of cancers overall, but for which a role in oesophageal cancer is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216386.RAvp9_SRPTzy_OAC2qKnvOV6yCtaYG2BnhkALESEdZ3fc130_provenance.
- NP216389.RAtrET9Q6Cw8ZoEi1n_YDKFTrLoCV9Lne3XYHd4Xxy0v4130_assertion description "[The results revealed that caspase-2 plays an important role in TSA-induced apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216389.RAtrET9Q6Cw8ZoEi1n_YDKFTrLoCV9Lne3XYHd4Xxy0v4130_provenance.
- NP216390.RAsylkAukwFVS4kRy-XmxluK9NC_GRdDGQd1O1dHuor8c130_assertion description "[The melanocortin 1 receptor, a G protein-coupled receptor positively coupled to adenylyl cyclase, is a key regulator of epidermal melanocyte proliferation and differentiation and a determinant of human skin phototype and skin cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216390.RAsylkAukwFVS4kRy-XmxluK9NC_GRdDGQd1O1dHuor8c130_provenance.
- NP216391.RAlEDYhlzCdl7KiDPW_BZmYcen44KcKV2KhhfRx9bva_8130_assertion description "[We previously showed that synthetic peroxisome proliferator-activated receptor gamma (PPARgamma) ligands inhibit non-small cell lung carcinoma (NSCLC) cell growth through multiple signaling pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216391.RAlEDYhlzCdl7KiDPW_BZmYcen44KcKV2KhhfRx9bva_8130_provenance.
- NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_assertion description "[Our data confirm that fibroblast growth factor signalling pathways are involved in craniofacial development and suggest that some human malformation pedigrees or sporadic craniosynostosis may be caused by mutations that deregulate expression of the Fgf ligands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_provenance.
- NP216412.RAgAKiADD9ko3rhrko8K4NsBN2MUnQ-iuoeYDisEb3yd4130_assertion description "[Molecular studies have revealed the preponderance of the RAS-RAF-MAPK signaling pathway in the pathogenesis of OvLGSCa, thereby representing an attractive therapeutic target for patients affected by this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216412.RAgAKiADD9ko3rhrko8K4NsBN2MUnQ-iuoeYDisEb3yd4130_provenance.
- NP216418.RAmvt7KKmNTEiR6_9wkZioYh2Cj39SJ9m1IQZAeeyKXGQ130_assertion description "[The study in the validation cohort of the significant methylated sites from the discovery cohort found that hypermethylation of five genes was significantly associated with shorter RFS in stage I NSCLC: HIST1H4F, PCDHGB6, NPBWR1, ALX1, and HOXA9.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216418.RAmvt7KKmNTEiR6_9wkZioYh2Cj39SJ9m1IQZAeeyKXGQ130_provenance.
- NP216419.RAiZOVEJiJm8QdLm8QU1TaTB6qvHszIrSjNz_OSRchkRI130_assertion description "[We speculate that a complex pattern of regulation requiring interaction between a proximal CRE/AP-1-like motif and other upstream control elements play an important role in the high-level constitutive expression of NT/N in the human endocrine cell line BON.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP216419.RAiZOVEJiJm8QdLm8QU1TaTB6qvHszIrSjNz_OSRchkRI130_provenance.