Nanopublications

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

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NP188264.RAYveSEaqJ1wixqPMaFXnLcN3VxpHH5089HCZzHq9SEpU130_assertion description "[Previous studies have discovered several mutations in the screening of GDF9 in premature ovarian failure but none in PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188264.RAYveSEaqJ1wixqPMaFXnLcN3VxpHH5089HCZzHq9SEpU130_provenance.
NP188273.RAceS2DzJfFGMclg1jFdOUIKR_-S-b2Ob92SWyrlgy3ic130_assertion description "[Neither was there any evidence of association between common TRPM6 and TRPM7 haplotypes and diabetes risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188273.RAceS2DzJfFGMclg1jFdOUIKR_-S-b2Ob92SWyrlgy3ic130_provenance.
NP188275.RAXUgAXpDUc2l7FGUrwwyKoayfxwyOB_yeHJ6BqJxQC88130_assertion description "[The oestrogen-progesterone receptor ratio: an indicator of breast cancer evolution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188275.RAXUgAXpDUc2l7FGUrwwyKoayfxwyOB_yeHJ6BqJxQC88130_provenance.
NP188277.RAcEvxXi9_L6u2P5KoshLriIg6W4ljByI1cnxW8Ua2jRQ130_assertion description "[A gene locus for HGF has been localized to a 37-cM genetic interval on chromosome 2p21-p22 (D2S1352, Zmax = 5.10, theta = 0.00) flanked by D2S1788 and D2S441.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188277.RAcEvxXi9_L6u2P5KoshLriIg6W4ljByI1cnxW8Ua2jRQ130_provenance.
NP188282.RASqoaAog__W3zGXxiBf30nyn92GGnpOgfPu4dAfmiOyE130_assertion description "[Targeting of MCL-1 kills MYC-driven mouse and human lymphomas even when they bear mutations in p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188282.RASqoaAog__W3zGXxiBf30nyn92GGnpOgfPu4dAfmiOyE130_provenance.
NP188283.RAYu3qGgW1kjUKC98fD2o-i9eC9gzGi3iB_50okl-8D-c130_assertion description "[When examined by Northern analysis, the mRNA hybridizing to AMN-22 is extremely polydisperse in cystic fibrosis (CF) trachea, with apparent message length varying from approximately 2 kb to greater than 10 kb.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188283.RAYu3qGgW1kjUKC98fD2o-i9eC9gzGi3iB_50okl-8D-c130_provenance.
NP188292.RARZ9P6GdaLrgaa0EOM5lia5r0IcEfQh0hfgrauf510rQ130_assertion description "[We undertook this study to analyze the expression of CXCR7 in RA synovium and the pathogenic role of the CXCL12/CXCR7 pathway in RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188292.RARZ9P6GdaLrgaa0EOM5lia5r0IcEfQh0hfgrauf510rQ130_provenance.
NP188304.RAUyC5egz-j9mBn42Zy6Sfe7BsMiQbdXeCsMoCaNYOtok130_assertion description "[The localization and functional characteristics of tumor necrosis factor(TNF) beta gene raise the possibility that it may be involved in the susceptibility to autoimmune thyroid diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188304.RAUyC5egz-j9mBn42Zy6Sfe7BsMiQbdXeCsMoCaNYOtok130_provenance.
NP188308.RAX0vRICVgSqzAzHGunJTOFjBQpDB2soTJV_8QN_o5toc130_assertion description "[Finally, E2F4 was found to be overexpressed, phosphorylated and nuclear localized in epithelial cells from human colorectal adenomas exhibiting mutations in APC and KRAS or BRAF genes, known to deregulate GSK3/β-catenin and MEK/ERK signaling, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188308.RAX0vRICVgSqzAzHGunJTOFjBQpDB2soTJV_8QN_o5toc130_provenance.
NP188309.RAfuPnAQNyL-FH5GGt5s0Os-rd0GMPYMqPZpDbIK6R0zg130_assertion description "[The mechanism by which Pak1 induces cancer metastasis may involve activation of JNK and phosphorylation of paxillin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188309.RAfuPnAQNyL-FH5GGt5s0Os-rd0GMPYMqPZpDbIK6R0zg130_provenance.
NP188314.RAa2wBeMP-SkCfbHsioSM-Nnfl9LmBiCH_tsyIek7A7s4130_assertion description "[We suggest that the 2G allele of the 1G/2G MMP-1 gene polymorphism may be associated with the lymph node metastasis in patients with breast cancer and therefore it can be considered as a progression marker in this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188314.RAa2wBeMP-SkCfbHsioSM-Nnfl9LmBiCH_tsyIek7A7s4130_provenance.
NP188320.RAdOMZGD-OlLDLPvvVZMZLYg7PSQ-xEN9qRyQopBESCb4130_assertion description "[Two genes, PARD3 (two SNPs) and MAGI2 (two SNPs), showed weak association with GSE in a Dutch cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188320.RAdOMZGD-OlLDLPvvVZMZLYg7PSQ-xEN9qRyQopBESCb4130_provenance.
NP188322.RARWypJ5O0AZxmaQyclFn_dwiJbrUJ_v2p75SqU-jjWUY130_assertion description "[A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188322.RARWypJ5O0AZxmaQyclFn_dwiJbrUJ_v2p75SqU-jjWUY130_provenance.
NP188323.RAbVaJQfL-BWFxgtObF5G9htX29b_8ANssDGoY6DmHBU8130_assertion description "[The aim of this study was to determine whether the common SNPs +49A/G on exon1 and CT60A/G in 3'UTR of the CTLA-4 gene are associated with susceptibility to SLE and GD in Thai population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188323.RAbVaJQfL-BWFxgtObF5G9htX29b_8ANssDGoY6DmHBU8130_provenance.
NP188330.RAarDZ9FKKDoJjoHedKsevRSm1eo_4QTlCji5prh-5RrU130_assertion description "[SDF-1 is a powerful chemokine that upregulates T-cell migration and activation, and the gene for SDF-1 is located near type 1 diabetes susceptibility locus IDDM10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188330.RAarDZ9FKKDoJjoHedKsevRSm1eo_4QTlCji5prh-5RrU130_provenance.
NP188332.RAa3SB4iXVQ9G-uD07jJPH62B8p3G4UIkkNne0ONoXLa4130_assertion description "[We studied frequencies of HLA A, B, DR and DQ in patients with nasal polyposis in order to determine a possible genetic component in the multifactorial pathogenesis of nasal polyps.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188332.RAa3SB4iXVQ9G-uD07jJPH62B8p3G4UIkkNne0ONoXLa4130_provenance.
NP188341.RAWzA8y4coJ1l_btQ6nymbLMLjjMDqwkpW0bzqSGSac0w130_assertion description "[Interestingly, MCT-1 in combination with AZA significantly induced the recently identified suppressor of leukemogenesis Nur77 and attenuated AZA-induced MMP-9 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188341.RAWzA8y4coJ1l_btQ6nymbLMLjjMDqwkpW0bzqSGSac0w130_provenance.
NP188343.RAcEsKE0NNsdChHHo7nisI6TiM8ToY2yGbQkyi9Scw2M4130_assertion description "[FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188343.RAcEsKE0NNsdChHHo7nisI6TiM8ToY2yGbQkyi9Scw2M4130_provenance.
NP188358.RAartPSfZP2MNFfCbiG69Ahsj3mxHk4IWjjmitiRnYuRM130_assertion description "[As a strategy to define the embryonic origin and neurochemical phenotype of cells in this disease, we probed specimens (n = 10) resected during epilepsy surgery with a panel of 13 antibodies recognizing proteins associated with (i) specific progenitor cell types including brain lipid binding protein (BLBP), collapsin response mediator protein 4 (CRMP4), Dlx1, Dlx2, GFAPdelta, MASH1, Otx1, Pax6, vimentin and phosphorylated vimentin and (ii) excitatory or inhibitory neurochemical phenotypes such as the vesicular glutamate transporters-1 and 2 (VGLUT-1, VGLUT-2), or the vesicular GABA transporter (VGAT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188358.RAartPSfZP2MNFfCbiG69Ahsj3mxHk4IWjjmitiRnYuRM130_provenance.
NP188364.RAWo9DtzaSDLJw6ODYea0vXsLGVO3q2GeKsgIriqmOg0A130_assertion description "[RQ-PCR analysis of the junctional regions of the rearranged immunoglobulin heavy-chain gene (IgH) serves as the most broadly applicable MRD target in B-NHL (∼80%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188364.RAWo9DtzaSDLJw6ODYea0vXsLGVO3q2GeKsgIriqmOg0A130_provenance.
NP188365.RATCR93_yOhS2IW1H_-n_OUjEpsQwgll8P-tk4IEhRfF4130_assertion description "[To describe a Japanese patient with lattice corneal dystrophy type I (LCD I) who lacked the typical lattice lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188365.RATCR93_yOhS2IW1H_-n_OUjEpsQwgll8P-tk4IEhRfF4130_provenance.
NP188372.RAbXEhiRqMnaYrGixdpzJ_xYMURd9VTmBEbxFAhh_IvY4130_assertion description "[Reverse transcriptase-polymerase chain reaction amplification (RT-PCR) and Southern blot analysis were used to evaluate ligand and receptor expression of interleukin 1 alpha (IL-1 alpha), interleukin 3 (IL-3), interleukin 6 (IL-6) and stem cell factor (SCF) in peripheral blood lymphocytes and monocytes and in several acute leukemia blast cell populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188372.RAbXEhiRqMnaYrGixdpzJ_xYMURd9VTmBEbxFAhh_IvY4130_provenance.
NP188373.RAb4FL_65cXWzdKiDfA5GNoeecBSF2EggqMzfgoMFt8M4130_assertion description "[Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188373.RAb4FL_65cXWzdKiDfA5GNoeecBSF2EggqMzfgoMFt8M4130_provenance.
NP188374.RAdurz6v4zbi4zvP4Y2zArz_MFnIIYBO17benbHSEKNp8130_assertion description "[Two independent MHC regions showed the main overlap, with several alleles in the human leukocyte antigen (HLA) class II region exhibiting an opposite risk effect for follicular lymphoma and type I diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188374.RAdurz6v4zbi4zvP4Y2zArz_MFnIIYBO17benbHSEKNp8130_provenance.
NP188378.RAfPo_t6YskDr_73pUOqWIhwvdxh087cDCBl_MztO9tOg130_assertion description "[No signal for 92-kDa type IV collagenase mRNA was detected in circulating eosinophils or in eosinophils associated with Hodgkin's lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188378.RAfPo_t6YskDr_73pUOqWIhwvdxh087cDCBl_MztO9tOg130_provenance.
NP188383.RAZPYw-nD5UGWTfmtrqanDOeXu_FuHxCRbOUa6Svp3xIU130_assertion description "[Our results showed that TLR7 is significantly down-regulated in neoplastic hepatocytes (P < .001), especially in the patients with hepatitis B (n = 52) or C (n = 24) virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188383.RAZPYw-nD5UGWTfmtrqanDOeXu_FuHxCRbOUa6Svp3xIU130_provenance.
NP188410.RATKy3QsfJG-wIF5UdDaeXjQbTnHKyGW28lmztFz5jEsQ130_assertion description "[MHC class I chain-related gene-A (MIC-A) has been shown to be associated with susceptibility to T1DM in different populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188410.RATKy3QsfJG-wIF5UdDaeXjQbTnHKyGW28lmztFz5jEsQ130_provenance.
NP188415.RASRVCIfIMa72SIunEG66Mhp-fMZWPCjaB3L3AZEO44JQ130_assertion description "[The bifunctional microRNA miR-9/miR-9* regulates REST and CoREST and is downregulated in Huntington's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188415.RASRVCIfIMa72SIunEG66Mhp-fMZWPCjaB3L3AZEO44JQ130_provenance.
NP188418.RAc_JjR33QsafaBf14crLAwEuy3pFVXHT8DhmAllMAFlc130_assertion description "[Expression of the C-kit receptor (CD117) is a feature of almost all subtypes of de novo acute myeloblastic leukemia (AML), including cytogenetically good-risk AML, and lacks prognostic significance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188418.RAc_JjR33QsafaBf14crLAwEuy3pFVXHT8DhmAllMAFlc130_provenance.
NP188425.RAZGHDQeRFVjuLHi4FecgDbEvoquLzeGTSdHm1HvbvXwc130_assertion description "[Lower expression levels of the programmed death 1 receptor on CD4+CD25+ T cells and correlation with the PD-1.3A genotype in patients with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188425.RAZGHDQeRFVjuLHi4FecgDbEvoquLzeGTSdHm1HvbvXwc130_provenance.
NP188426.RATQvldttDME7ecN31U9qs2Ia8da4o5tP_fY30woSwWeE130_assertion description "[Inclusion criteria were the presence of a PRSS1 mutation with pancreatic symptoms or chronic pancreatitis in at least two first-degree relatives or three second-degree relatives without another cause.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188426.RATQvldttDME7ecN31U9qs2Ia8da4o5tP_fY30woSwWeE130_provenance.
NP188427.RAYhf4ZlcKVpiYhyDdNFTS6Yzu9yEAqaIGMgHVyzr7aYY130_assertion description "[We conclude that mutations of the GSY gene are unlikely to play a major role in the predisposition to NIDDM in our families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188427.RAYhf4ZlcKVpiYhyDdNFTS6Yzu9yEAqaIGMgHVyzr7aYY130_provenance.
NP188431.RAajEPBk0y7CGwA4bpf0afHFH5hNW1ilnPsevs1qh7dtI130_assertion description "[The purpose of the current study was to quantify the expression of KLK6 in malignant and benign colorectal tissues and to statistically analyze whether KLK6 expression levels correlate with clinicopathologic variables and prognosis in patients with colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188431.RAajEPBk0y7CGwA4bpf0afHFH5hNW1ilnPsevs1qh7dtI130_provenance.
NP188434.RAT1gdTZVmVgf_FVajyYavY3cKBRcIZ0sN979gSA21ol4130_assertion description "[Mutations in the neurofibromatosis type 2 (NF2) gene predispose individuals to the development of nervous system tumors and ocular abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188434.RAT1gdTZVmVgf_FVajyYavY3cKBRcIZ0sN979gSA21ol4130_provenance.
NP188445.RAfeTyHryn35WfMMzFZ7H4vyD-KOuPokqoU3WMNHrdnuI130_assertion description "[The SNPs in the CD14, TLR4, IL-1beta, and TNF-alpha genes were not associated with the severity of appendicitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188445.RAfeTyHryn35WfMMzFZ7H4vyD-KOuPokqoU3WMNHrdnuI130_provenance.
NP188446.RAeofQpJPza473tRZSH-FQ0DXJumjoARX8SQo1AWohfjk130_assertion description "[Polymerase chain reaction (PCR) performed on cerebrospinal fluid (CSF) showed positivity for DNA of Cytomegalovirus (CMV) and Herpes-virus type 7 (HHV-7), whereas the same test applied on peripheral blood mononuclear cells gave negative result.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188446.RAeofQpJPza473tRZSH-FQ0DXJumjoARX8SQo1AWohfjk130_provenance.
NP188453.RAdbkXuKhimGvCx5UaHBvPMmDJdd7vjvHQtx-uWSg2uSw130_assertion description "[Mutations in the OTOF gene are frequent causes of AN in Brazil and our results confirm that they are spread worldwide.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188453.RAdbkXuKhimGvCx5UaHBvPMmDJdd7vjvHQtx-uWSg2uSw130_provenance.
NP188454.RAeaZ2NRHAswAvBgsgHjkUSMjeLrB9nxDvmPB5GEpcbmM130_assertion description "[Forty-three isolates harboring bla(CTX-M-14) or bla(CTX-M-15) were analyzed by pulsed-field gel electrophoresis (PFGE), and plasmids containing these genes were typed using PCR-based replicon typing (PBRT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188454.RAeaZ2NRHAswAvBgsgHjkUSMjeLrB9nxDvmPB5GEpcbmM130_provenance.
NP188455.RAfG19vjUikBB42fk7_drE0LTgla-tGi4ZHhUK7vl6WH8130_assertion description "[The mean serum levels of FSH in the groups with nonobstructive azoospermia (n = 9), obstructive azoospermia (n = 10), severe oligozoospermia (n = 9), and the normal donors (n = 6) were 17.5 +/- 8.2 (P<.05), 3.5 +/- 2.6, 14.6 +/- 3.5 (P<.05), and 3.1 +/- 0.4 IU/mL, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188455.RAfG19vjUikBB42fk7_drE0LTgla-tGi4ZHhUK7vl6WH8130_provenance.
NP188459.RAffej6AfqQw5Lyk4GjZKi39WqILiRrlxlrC5nwYOFqXU130_assertion description "[When the combined NAT2/CYP1A2 status was examined, women with slow NAT2 and rapid CYP1A2 activity were at highest risk (adjusted OR 6.9, 95% CI 1.3-37.6) relative to women with rapid NAT2 and slow CYP1A2 activity, for lung adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188459.RAffej6AfqQw5Lyk4GjZKi39WqILiRrlxlrC5nwYOFqXU130_provenance.
NP188461.RAbxAaRVu7dp2Ftl6YySZWMc8yifFr3qeNr2h4FV87Aok130_assertion description "[The LKB1/STK11 serine/threonine kinase is mutated in Peutz-Jeghers' syndrome and acts as a tumour suppressor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188461.RAbxAaRVu7dp2Ftl6YySZWMc8yifFr3qeNr2h4FV87Aok130_provenance.
NP188470.RAX27_RePSeQc5okk-SbpOC00FajLBmebh_zPIRKOHtbU130_assertion description "[Tests for mutant TP53 might be developed to improve the diagnosis of and screening for pancreatic cancer and high-grade dysplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188470.RAX27_RePSeQc5okk-SbpOC00FajLBmebh_zPIRKOHtbU130_provenance.
NP188471.RAb7NMtYJs8KPh70kTz4GJRlsYf-8qE438iblJZcItxyQ130_assertion description "[PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188471.RAb7NMtYJs8KPh70kTz4GJRlsYf-8qE438iblJZcItxyQ130_provenance.
NP188475.RAeQbeGaq9oYTVqJwP5MftHYcXUc73Zrh4pVyoml0aqJg130_assertion description "[Motor neuron disease-associated mutant vesicle-associated membrane protein-associated protein (VAP) B recruits wild-type VAPs into endoplasmic reticulum-derived tubular aggregates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188475.RAeQbeGaq9oYTVqJwP5MftHYcXUc73Zrh4pVyoml0aqJg130_provenance.
NP188476.RARe6ZgkjSATFZT2u2W7Vwfe2RuLvoBNUj2OBCrcJgLy4130_assertion description "[p16 gene methylation was detected in 6 of 55 patients (10.9%), who were 1 patient with M2a, 1 patient with M5a, 2 patients with chronic myelogenous leukemia (CML) in blast crisis, 1 patient with progressing multiple myeloma (MM), 1 with non-Hodgkin's lymphoma (NHL) accompanied by B-ALL, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188476.RARe6ZgkjSATFZT2u2W7Vwfe2RuLvoBNUj2OBCrcJgLy4130_provenance.
NP188477.RATkISC54o6BQPQGBt9VVy_Pz9p_fs6w4uu_6QLrqPsEk130_assertion description "[Neurofibromatosis type 2 (NF2) gene is somatically mutated in mesothelioma but not in lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188477.RATkISC54o6BQPQGBt9VVy_Pz9p_fs6w4uu_6QLrqPsEk130_provenance.
NP188478.RAfcGkV3_-AB280R_LK9BdxOgKjmkI7y9w50OL94P1sNA130_assertion description "[These results indicate that variation in the PDYN gene is associated with a dimensional trait or intermediate phenotype that reflects a preference for heavy drinking and engaging in related risky behaviors (e.g., drug use, sexual activity).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188478.RAfcGkV3_-AB280R_LK9BdxOgKjmkI7y9w50OL94P1sNA130_provenance.
NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_assertion description "[Although PPHP does not have the biochemical features of hypocalcemia and elevated parathyroid hormone levels as seen in pseudohypoparathyroidism, it seems from this case to share the potential for multiple endocrine neoplasia seen in a number of metabolic disorders in which pheochromocytoma may be a prominent manifestation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188481.RAbr4ncjVhn4o-G9MDrAxcD6GBrY0Mmm-opD7UQVHhFyk130_provenance.
NP188483.RAWXpKR-GLPaU3QjAILYcNisB-5gV8ryvSoHcPgME6WZA130_assertion description "[Of particular interest was the prognostic value of HBII-239 snoRNA, which was significantly over-expressed in cases of AITL and PTCL-NOS that had favorable outcomes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188483.RAWXpKR-GLPaU3QjAILYcNisB-5gV8ryvSoHcPgME6WZA130_provenance.
NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_assertion description "[The present results support the hypothesis that rare de novo mutations in GRIN2A or GRIN2B can be associated with cases of sporadic SCZ or ASD, just as it has recently been described for the related neurodevelopmental disease intellectual disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188484.RAa4ZxXSsx_4h6iEE6w8srL68hjhG6u51xwMdpwpdEpj0130_provenance.
NP188487.RAVPNCIdQnCis0LH8Vo1UAV4UQU9YL53b7hH_zNF15t6Q130_assertion description "[Stromal CXCR4 and CXCL12 expression is associated with distant recurrence and poor prognosis in rectal cancer after chemoradiotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188487.RAVPNCIdQnCis0LH8Vo1UAV4UQU9YL53b7hH_zNF15t6Q130_provenance.
NP188491.RAfiwLNBDqjbHD5xrG6PWHJp_M_AjuDHZtJ-aJtNzA1Ig130_assertion description "[The objectives of this study are to examine the effects of the histone deacetylase inhibitor FR901228 on the level of coxsackie and adenovirus receptor (CAR) expression and OBP-301-mediated oncolysis in human non-small cell lung cancer cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188491.RAfiwLNBDqjbHD5xrG6PWHJp_M_AjuDHZtJ-aJtNzA1Ig130_provenance.
NP188492.RAUWha4JK3_C7iw65mfyKIp8Ghyb8gwEjZqOh5dVg3yOA130_assertion description "[These results also indicate that the NAT2 in combination with CYP1A1*2C, CYP1A2*1C, or GSTM1 genotypes may strongly confer susceptibility to colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188492.RAUWha4JK3_C7iw65mfyKIp8Ghyb8gwEjZqOh5dVg3yOA130_provenance.
NP188496.RAUhcE7Qle-R9ZiYPQd2w7dZuaDqeMxssmfkv-qeWpySE130_assertion description "[Congenital erythropoietic porphyria (CEP) is a rare inborn error of metabolism that results from a deficient activity of uroporphyrinogen III synthase (URO-synthase).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188496.RAUhcE7Qle-R9ZiYPQd2w7dZuaDqeMxssmfkv-qeWpySE130_provenance.
NP188497.RAVLe9lSvlKI2TI6In_dBDUu84LGvo7hU2alMY0HWiXaI130_assertion description "[For the first time, we provide images of human prostate carcinoma metastasis precursor cells isolated from blood and shown to overexpress both BMI1 and Ezh2 oncoproteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188497.RAVLe9lSvlKI2TI6In_dBDUu84LGvo7hU2alMY0HWiXaI130_provenance.
NP188498.RAelUQaksaHtW1BLOUFADf2d5GkByvVvFaVbXZvvYI2wk130_assertion description "[When we analysed time to breast cancer progression adjusting for grade or hormone receptor status, presence of SBEM mRNA in BM defines distinct prognostic groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188498.RAelUQaksaHtW1BLOUFADf2d5GkByvVvFaVbXZvvYI2wk130_provenance.
NP188501.RAaGmVEsQjVLb0uBLWyYDN989n9wM8F_ig01_NkeIYcOM130_assertion description "[C57Bl/6J mice were injected subcutaneously with bone marrow derived dendritic cells (DCs) pulsed with a melanoma epitope (TRP2-P2/Agonist), melanoma epitope tyrosinase (TYR/Agonist), a nonfunctional reverse conformation C5a agonist bound to TYR(reverse peptide) or DMSO-PBS vehicle.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188501.RAaGmVEsQjVLb0uBLWyYDN989n9wM8F_ig01_NkeIYcOM130_provenance.
NP188514.RARrFh5UM8-4xRAD8a0xHLqJ-8ElpCQ_gL6R-azQeFZCE130_assertion description "[Sequencing was used to identify mutations in PIK3CA, a real-time PCR-based method to identify KRAS mutations, and immunohistochemical staining was used to evaluate the expression of PIK3CA, phosphorylated AKT and PTEN in 58 HNPCC-associated colorectal cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188514.RARrFh5UM8-4xRAD8a0xHLqJ-8ElpCQ_gL6R-azQeFZCE130_provenance.
NP188516.RAbM9j-nsutTNnK6RfIUeDS-TpaAzGe-deQOHbowExMPA130_assertion description "[B7-H4 expression promotes tumorigenesis in ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188516.RAbM9j-nsutTNnK6RfIUeDS-TpaAzGe-deQOHbowExMPA130_provenance.
NP188518.RAYd08OViYA2b_w2CQnin3VnVdB74T2EVUSWJafNoiOKE130_assertion description "[Mutational analysis revealed in the first patient the APC germline mutation 3183_87del ACAAA and in the second patient the del9-10 (del9080dup11) novel APC variant; the first mutation has been already reported in association with PTC; to our knowledge the second mutation has never been previously reported in association with FAP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188518.RAYd08OViYA2b_w2CQnin3VnVdB74T2EVUSWJafNoiOKE130_provenance.
NP188519.RARGkUK1WL2XwJIqnPH6D3T17obRgMuu6A-JLAkQ6U3mA130_assertion description "[In spite of this beneficial effect of LPL, Tg WHHL rabbits had two-fold greater aortic atherosclerosis than non-Tg WHHL rabbits.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188519.RARGkUK1WL2XwJIqnPH6D3T17obRgMuu6A-JLAkQ6U3mA130_provenance.
NP188523.RAYF_pfqVVUYPOIkP6QJ187j8mK_han1lPnjhSLnOPVDc130_assertion description "[Initial analysis indicated that Pin1 activity was decreased in parathyroid protein extracts from both hypocalcemic and CKD rats and that pharmacologic inhibition of Pin1 increased PTH mRNA levels posttranscriptionally in rat parathyroid and in transfected cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188523.RAYF_pfqVVUYPOIkP6QJ187j8mK_han1lPnjhSLnOPVDc130_provenance.
NP188524.RARZ8ECpe_9XaUc7mGQ3VCmglAqePzIfrB3d7KP3AmHiY130_assertion description "[FMR1 premutation alleles uniquely produce FMR1 transcripts with an elongated CGG repeat, leading to the hypothesis that premutant transcripts cause the neurodegenerative disease in carriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188524.RARZ8ECpe_9XaUc7mGQ3VCmglAqePzIfrB3d7KP3AmHiY130_provenance.
NP188525.RAVHC-iLJg7RprsswcZq5IopqVFcl_fauBrm3CSDt3YZc130_assertion description "[We tested the hypothesis that iNOS is deregulated in NPM-ALK(+) T-cell lymphoma and promotes the survival of this lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188525.RAVHC-iLJg7RprsswcZq5IopqVFcl_fauBrm3CSDt3YZc130_provenance.
NP188539.RAe0boopnkoCYYRggeBAWBfMe3-qhanLCw0LUPuEFGwRM130_assertion description "[Rare disorders of either chain of the IFN-γ receptor, but not of IFN-γ itself, have been shown to confer predisposition to mycobacterial disease in patients otherwise normally resistant to most viruses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188539.RAe0boopnkoCYYRggeBAWBfMe3-qhanLCw0LUPuEFGwRM130_provenance.
NP188547.RAQg-XpJMF_VVqvcIxDhYU0CsHQo4TYfJ450l9K89Gl7w130_assertion description "[Data on distant disease-free interval (DDFI) and the localization of the first distant metastasis (DM) in BRCA1- and BRCA2-associated breast cancer (BC) patients are as yet scarcely available.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188547.RAQg-XpJMF_VVqvcIxDhYU0CsHQo4TYfJ450l9K89Gl7w130_provenance.
NP188549.RATaFwbfoz7TXL1dSaCuthkrT-kqTtwuMhx4idTczwKk8130_assertion description "[Frequent copy number gains were seen at 1q25-41 (23%), 8q11.1-q21.1 (23%), 8q21.3-qter (21%); 28% of these tumors exhibited high-frequency MI (MSI-H); Methylation of the MLH1 promoter was observed in 92% of EACs with MSI-H. Southern blotting showed amplification of MYCN in one tumor, which has been documented for the first time in a primary human EAC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188549.RATaFwbfoz7TXL1dSaCuthkrT-kqTtwuMhx4idTczwKk8130_provenance.
NP188551.RAUA50NCwFlWS2AN3LzSPnH0Hl_hvkn-_I3rjcFnItNz0130_assertion description "[The pros and cons of targeting protein kinase C (PKC) in the management of cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188551.RAUA50NCwFlWS2AN3LzSPnH0Hl_hvkn-_I3rjcFnItNz0130_provenance.
NP188555.RAQ1uMX1pYBByPmoa6ccEhN9KoqDVxmxBhBHLxvwri1HI130_assertion description "[The 6.5-kB full-length cDNA of this RBP2-related gene, termed RBP2 homolog 1 (RBP2-H1), was obtained from a human teratocarcinoma cDNA library.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188555.RAQ1uMX1pYBByPmoa6ccEhN9KoqDVxmxBhBHLxvwri1HI130_provenance.
NP188556.RAVe2TEfQmrImC99UL7ZvbVPQ4x1W2ZfLv7igNe-wcDo0130_assertion description "[No correlation between A(-1438)G polymorphism in 5-HT2A receptor gene promoter and the density of frontal cortical 5-HT2A receptors in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188556.RAVe2TEfQmrImC99UL7ZvbVPQ4x1W2ZfLv7igNe-wcDo0130_provenance.
NP188560.RAVeE0Au-rCpr75R2ngq9rPpPmHUvl8lNZSU6_wx7kwK8130_assertion description "[Quantitative immunohistochemical determination showed that PMP22 protein expression relative to that of myelin protein zero and myelin basic protein was increased in all CMT1A patients and reduced in all HNPP patients, as compared with biopsy samples of patients with normal PMP22 gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188560.RAVeE0Au-rCpr75R2ngq9rPpPmHUvl8lNZSU6_wx7kwK8130_provenance.
NP188561.RAYoDWIS3xWno4lxf1V9vgwMfJ0Xrw4M14dAedwUh-UiM130_assertion description "[Taken together, these data demonstrate the role of AR in regulating iNOS expression induced by TNF-α in cultured HMC, indicating the novel function of AR in glomerulonephritis besides glucose metabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188561.RAYoDWIS3xWno4lxf1V9vgwMfJ0Xrw4M14dAedwUh-UiM130_provenance.
NP188565.RAVD_3OiLu2ugTEXIL-aE0XhwPhnW9QX0oIr9sqLHYjJ8130_assertion description "[In previous studies, we could show that point mutations in the gene for the granulocyte colony-stimulating factor (G-CSF) receptor CSF3R are a highly predictive marker for leukemic development in CN patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188565.RAVD_3OiLu2ugTEXIL-aE0XhwPhnW9QX0oIr9sqLHYjJ8130_provenance.
NP188567.RAaC0Val3Oveor7RmWSDcFRX65JpS0cKdeTN7pj6uB5-A130_assertion description "[BRCA1 disruptions were associated with the C2 (immunoreactive) molecular subtype of HGSC, characterized by intense intratumoral T-cell infiltration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188567.RAaC0Val3Oveor7RmWSDcFRX65JpS0cKdeTN7pj6uB5-A130_provenance.
NP188568.RASZgVa-sbe9NYkcxwQ32yvn4x2GtoemW7PWpu6_jQ4JY130_assertion description "[The increased expression of the ODC gene was noted in 86% of colorectal cancer tissues by RT-PCR, however, it was not due to point mutations in ODC coding exons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188568.RASZgVa-sbe9NYkcxwQ32yvn4x2GtoemW7PWpu6_jQ4JY130_provenance.
NP188576.RATpkBPNm2VIjcLv5e7Zth5hOOVEtpOUn0uepd2ChMOmM130_assertion description "[The findings that protein tyrosine phosphatases (PTPs) regulate cell proliferation, response to growth factors, and cellular adhesion and the discovery that mutations in PTP genes are associated with breast cancer suggest that altered expression of PTPs contributes to the breast cancer cell phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188576.RATpkBPNm2VIjcLv5e7Zth5hOOVEtpOUn0uepd2ChMOmM130_provenance.
NP188581.RAWjrS1EJkZWub9PuVjDi8CiN2jdU0EJWRjEIsKyAGv_Q130_assertion description "[However, unlike health care workers, the NRL allergy phenotype was not significantly associated with promoter polymorphisms in IL13 or IL18 when comparing NRL allergic SB and BE patients with nonsensitized patients and with atopic and nonatopic controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188581.RAWjrS1EJkZWub9PuVjDi8CiN2jdU0EJWRjEIsKyAGv_Q130_provenance.
NP188584.RAYdZXQZVCqKJr3kMPe-m8FRB2NlzNJ2hbWHSU4cYF53A130_assertion description "[NK cells derived from patients with Wiskott-Aldrich syndrome/X-linked thrombocytopenia (WAS/XLT), carrying different mutations in the WASP coding gene, displayed reduced migration through intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), or endothelial cells in response to CXCL12/stromal cell-derived factor-1 and CX3CL1/fractalkine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188584.RAYdZXQZVCqKJr3kMPe-m8FRB2NlzNJ2hbWHSU4cYF53A130_provenance.
NP188586.RAcB61___YzwaF3CMsdAJY5RSr1lhnnsY1p2svrCQpMnU130_assertion description "[Metachromatic leukodystrophy (MLD) is an autosomal recessive progressive demyelination disorder caused by the deficiency of arylsulfatase A (ASA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188586.RAcB61___YzwaF3CMsdAJY5RSr1lhnnsY1p2svrCQpMnU130_provenance.
NP188587.RAXaDdSXlWgb7XoHoLK5p3Vwxn3NIwzhpk2TAcOgn4CAc130_assertion description "[Here we evaluated whether the EOS is altered in brain areas involved in cognitive control of addiction including the dorsolateral prefrontal cortex (dl-PFC), orbitofrontal cortex (OFC) and hippocampus in human alcohol-dependent subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188587.RAXaDdSXlWgb7XoHoLK5p3Vwxn3NIwzhpk2TAcOgn4CAc130_provenance.
NP188589.RARdYLHXfL3AuSQhsA0f_otL-l92kIYpsqabyUeKvfN5M130_assertion description "[Cell surface phenotypic analysis for TAA revealed positive populations in 28/31 cell lines (90%) for Her-2/neu, 18/31 (58%) for CEA and 8/31 (26%) for GD-2, with gamma-IFN having no effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188589.RARdYLHXfL3AuSQhsA0f_otL-l92kIYpsqabyUeKvfN5M130_provenance.
NP188595.RAb1BVI-mO7i10Hmj8fd8NXaGv-Y1A1ZJqp6Hzz6mvICI130_assertion description "[rKSHV.219 infection was detected in human CD14+ and CD19+ cells recovered from NOD/SCID mouse bone marrow and spleen following reconstitution with rKSHV.219-infected CD34+ HPCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188595.RAb1BVI-mO7i10Hmj8fd8NXaGv-Y1A1ZJqp6Hzz6mvICI130_provenance.
NP188599.RAdbsHiRFQm309mq4fAX0f-XvTm5Pz9w1rvT5A1VvWQkg130_assertion description "[Structural requirements for VAP-B oligomerization and their implication in amyotrophic lateral sclerosis-associated VAP-B(P56S) neurotoxicity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188599.RAdbsHiRFQm309mq4fAX0f-XvTm5Pz9w1rvT5A1VvWQkg130_provenance.
NP188600.RAbIHlwTrmOGSZnh5xD-QsYJAw8WuNtR3LTN9JfdSnUXU130_assertion description "[The objective of this report is to evaluate the literature on the association of common glutathione S-transferase (GST) variants (GSTM1 null, GSTT1 null and GSTP1 Ile105Val polymorphism) and lung cancer, and to assess the credibility of the associations using the newly proposed cumulative evidence guidelines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188600.RAbIHlwTrmOGSZnh5xD-QsYJAw8WuNtR3LTN9JfdSnUXU130_provenance.
NP188604.RAUdVchDLcZOfcfM51mnkv2tFTWrgfpF6PJe-z6WC4KSo130_assertion description "[Thus, we studied the antiproliferative and apoptotic effects and the underlying mechanisms of gemcitabine combined with the β2-adrenoceptor blocker ICI 118551 (1-[2,3-(dihydro-7-methyl-1H-iden-4-yl)oxy]-3-[(1-methylethyl)amino]-2-butanol), in human pancreatic cancer BxPC-3 and MIA PaCa-2 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188604.RAUdVchDLcZOfcfM51mnkv2tFTWrgfpF6PJe-z6WC4KSo130_provenance.
NP188606.RAaBhmVaC_EuaZwGJnFsl0wxfp1qnR_n119HlEWahc7QE130_assertion description "[Because the DLBCL-associated `activating mutations` specifically target these exon 1 binding sites, and because the entire exon 1 is usually removed in the BCL-6-translocated tumors, this autoregulation is bypassed in 30-40% of all DLBCL cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188606.RAaBhmVaC_EuaZwGJnFsl0wxfp1qnR_n119HlEWahc7QE130_provenance.
NP188607.RAbPy0t3MrkKoYkL88iF8en93xIhYYNQSOrsh8pl60Go8130_assertion description "[The PIG-A gene is mutated in all patients with PNH reported to date.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188607.RAbPy0t3MrkKoYkL88iF8en93xIhYYNQSOrsh8pl60Go8130_provenance.
NP188617.RAUIwb5swvdyzN6ueIEnC8CoFlw9PrF_ZGQ1W_r6t0CfA130_assertion description "[Recently, homozygous mutations in the antiapoptotic gene HAX1 were found in patients with autosomal recessive severe congenital neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188617.RAUIwb5swvdyzN6ueIEnC8CoFlw9PrF_ZGQ1W_r6t0CfA130_provenance.
NP188619.RAUn3QZcUHm_wLCuNCmRZdFwNtYpzVdqOIl_6jIH__kJU130_assertion description "[Thus, CD8+IL-17+ T cells share some key features with Th17 cells and exhibit remarkable differential abilities attributable to the CD8+ lineage of T lymphocytes, adding new insights into the functional resources of IL-17-producing cells from human epidermis that could be of potential interest to our understanding of the pathogenesis of psoriasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188619.RAUn3QZcUHm_wLCuNCmRZdFwNtYpzVdqOIl_6jIH__kJU130_provenance.
NP188622.RAYIoIibgSa8d19l7wGrDzjcc7UEVpqSNUpBtKh9zrdoU130_assertion description "[Further understanding of the APC gene function may define a rational approach for early detection, prevention strategies, assessment of prognosis and treatment of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188622.RAYIoIibgSa8d19l7wGrDzjcc7UEVpqSNUpBtKh9zrdoU130_provenance.
NP188625.RAXeU3p9To6Vwi4AxNk7SxU9LnsK7j_uDBVOKuxTYfqvs130_assertion description "[Early-onset NIFID had similar inclusions that were positive with both commercial anti-FUS antibodies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188625.RAXeU3p9To6Vwi4AxNk7SxU9LnsK7j_uDBVOKuxTYfqvs130_provenance.
NP188629.RAcIduCBDoHjlziUn3NZ4wXaSNvxOK5w0pB-fpjaqWEYU130_assertion description "[In a nested case-control study of breast cancer in US radiologic technologists exposed to low levels of ionizing radiation (858 cases, 1,083 controls), we examined whether risk of breast cancer conferred by radiation was modified by nucleotide excision gene polymorphisms ERCC2 (XPD) rs13181, ERCC4 (XPF) rs1800067 and rs1800124, ERCC5 (XPG) rs1047769 and rs17655; and ERCC6 rs2228526.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188629.RAcIduCBDoHjlziUn3NZ4wXaSNvxOK5w0pB-fpjaqWEYU130_provenance.
NP188633.RAaDKWOm9qefKU_aR1Ji_lwvcAgyGQ5_1EgUvXFUtAIQQ130_assertion description "[PITX2 expression was significantly and strongly decreased in prostate cancer compared to benign tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188633.RAaDKWOm9qefKU_aR1Ji_lwvcAgyGQ5_1EgUvXFUtAIQQ130_provenance.
NP188638.RAV0vzkPgCynocnpMFFGBAsdSbgFJCsAIIF3Q8bqPHzgg130_assertion description "[We have identified a set of genes including NAD(P)H:quinone oxidoreductase-1 (NQO1), heme oxygenase-1 (HO-1), ferritin (heavy and light chains), microsomal epoxide hydrolase, glutathione S-transferase, and gamma-glutamylcysteine synthase, whose expression is induced by exposure to prolonged physiological levels of steady laminar flow (shear stress = 20 dyn/cm(2)) in endothelial cells (EC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188638.RAV0vzkPgCynocnpMFFGBAsdSbgFJCsAIIF3Q8bqPHzgg130_provenance.
NP188642.RASselRJARUaJqZwT28UBc_hP6V92DkZTHEcJhQz3Kzko130_assertion description "[A review of maternal-fetal genotype incompatibility studies suggests that schizophrenia susceptibility is increased by maternal-fetal genotype combinations at the RHD and HLA-B loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188642.RASselRJARUaJqZwT28UBc_hP6V92DkZTHEcJhQz3Kzko130_provenance.
NP188644.RAZ4inK_iDhRf8dO9JO4XJoA8rMAbAYBojHCdXXDJfjzU130_assertion description "[Our data suggest that the Taq1 B2 allelic variant of the CETP gene may be associated, as a protective factor, with occurrence of ischaemic stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188644.RAZ4inK_iDhRf8dO9JO4XJoA8rMAbAYBojHCdXXDJfjzU130_provenance.
NP188645.RAW8XX98ofHH2xgwoWJXkd0JHhBdAsHxOzIkSwnn15v3g130_assertion description "[The overexpression of gankyrin was associated with extensive intraductal carcinoma and ErbB2 expression in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188645.RAW8XX98ofHH2xgwoWJXkd0JHhBdAsHxOzIkSwnn15v3g130_provenance.
NP188646.RAWDeSPyANVdQg0FI7XPdSKWp9grgatO9UJ-OoWBo83ag130_assertion description "[A rare case of Turner's syndrome with 45,X/46,X,Dic (X) (qter----p11.1::p11.4----qter).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188646.RAWDeSPyANVdQg0FI7XPdSKWp9grgatO9UJ-OoWBo83ag130_provenance.
NP188648.RAc08PMkJFSdtkTp-lq2vQmQCz9cjH_fTOA0KwTlTwYBw130_assertion description "[We investigated the immunohistochemical expression of EGFR and PCNA using the appropriate monoclonal antibodies in 40 cases of astrocytic tumors of which 21 cases were glioblastoma, eight cases were Grade III or anaplastic astrocytomas and six cases were Grade II or diffuse astrocytomas and five cases were Grade I or pilocytic astrocytomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188648.RAc08PMkJFSdtkTp-lq2vQmQCz9cjH_fTOA0KwTlTwYBw130_provenance.
NP188650.RAfWFVcPRr6j6ECbimX-UtWC9ebavxujwOmSFmkeipgHo130_assertion description "[The mean of the relative expression of the LGALS3 gene in non-small-cell lung cancer (3.065 +/- 3.976) was significantly higher than those of small-cell lung cancer (0.02 +/- 0.03) (P < 0.025).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP188650.RAfWFVcPRr6j6ECbimX-UtWC9ebavxujwOmSFmkeipgHo130_provenance.

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