Nanopublications

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NP311310.RAexY8d07vtH3wJZkYzK2BFbOW1Uspx87AoTkuRzvmjd4130_assertion description "[Effects of two Gbetagamma-binding proteins--N-terminally truncated phosducin and beta-adrenergic receptor kinase C terminus (betaARKct)--in heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311310.RAexY8d07vtH3wJZkYzK2BFbOW1Uspx87AoTkuRzvmjd4130_provenance.
NP311312.RARCuGIt8gvx3w2z50BfI0HGiPI_TAURaIFvgWx4N3TWY130_assertion description "[Similar to colorectal adenomas, they harbor APC and KRAS mutations; but BRAF mutations, p53 alterations, and DNA mismatch repair abnormalities are rare.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311312.RARCuGIt8gvx3w2z50BfI0HGiPI_TAURaIFvgWx4N3TWY130_provenance.
NP311313.RASNqImkHtIKXSIUeQF4Ga7b2SbKCZ_1OOSbEX0fvEfPg130_assertion description "[The distribution pattern and mean DEFB4 CN did not differ significantly in combined ChP cases vs. the controls; however, the mean DEFB4 CN in the severe ChP group differed significantly from those for the control and slight-to-moderate ChP groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311313.RASNqImkHtIKXSIUeQF4Ga7b2SbKCZ_1OOSbEX0fvEfPg130_provenance.
NP311314.RAbTAkfVgexARLBdvdH6ROn9vVa9DE6oVgLCZHvOR4u2A130_assertion description "[Our results show a significant over-expression of TARBP2, DICER, and DROSHA in the carcinomas compared with adenomas or adrenal cortices (P<0.001 for all comparisons).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311314.RAbTAkfVgexARLBdvdH6ROn9vVa9DE6oVgLCZHvOR4u2A130_provenance.
NP311315.RAUhMT24DSg8zb1HQueqdd9O2f4gW2iffLD-4NqtrO7VY130_assertion description "[Wolfram syndrome (WS) or diabetes insipidus, diabetes mellitus, optic atrophy, and deafness (DIDMOAD) (OMIM 222300) is an inherited neurodegenerative disease characterized by diabetes mellitus and optic atrophy as the 2 major criteria, followed later in life by deafness, diabetes insipidus, and various signs of neurologic impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311315.RAUhMT24DSg8zb1HQueqdd9O2f4gW2iffLD-4NqtrO7VY130_provenance.
NP311321.RAWGoTovuOxN_ARrArQMJa_ZqUzUl30D8OzWBSFS6uAHk130_assertion description "[These findings identified HOXC9 as a key regulator of neuroblastoma differentiation and suggested a therapeutic strategy for RA-resistant neuroblastomas through epigenetic activation of HOXC9 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311321.RAWGoTovuOxN_ARrArQMJa_ZqUzUl30D8OzWBSFS6uAHk130_provenance.
NP311325.RAUkRToRP48lkNOUb2UZKLYxIv-ReHJX0AMCE7khpvCFw130_assertion description "[Six of 12 patients diagnosed with hemifacial microsomia exhibited a novel insertion mutation 4127 ins G (frameshift) in exon 24 in the TCOF1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311325.RAUkRToRP48lkNOUb2UZKLYxIv-ReHJX0AMCE7khpvCFw130_provenance.
NP311331.RAcB3bsgRV2kS6fTDLoEvGNq_yAGyGh7gzqGuRC53-jFc130_assertion description "[Four of nine informative fetal rhabdomyomas and embryonal rhabdomyosarcomas showed loss of heterozygosity (LOH) in the PTCH region with two of these (one fetal rhabdomyoma and one embryonal rhabdomyosarcoma) also showing LOH in the SUFU region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311331.RAcB3bsgRV2kS6fTDLoEvGNq_yAGyGh7gzqGuRC53-jFc130_provenance.
NP311338.RAUylX8nqCfaqmGMWNy2xIEFBzkJvSSfOgZf0Zz8rx1-Y130_assertion description "[In cardiac failure, endothelial apelin expression correlates with other hypoxia-responsive genes, and in healthy animals both apelin and APJ are markedly upregulated in various tissues following systemic hypoxic exposure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311338.RAUylX8nqCfaqmGMWNy2xIEFBzkJvSSfOgZf0Zz8rx1-Y130_provenance.
NP311340.RAabpsLtv9Ggt2t7C9FS1HFQcs9G47dELwt4zIx13jgv0130_assertion description "[Association of apolipoprotein M gene polymorphisms with ischemic stroke in a Han Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311340.RAabpsLtv9Ggt2t7C9FS1HFQcs9G47dELwt4zIx13jgv0130_provenance.
NP311344.RATroNno3mCDzEMcYnUXsiQaSRkB71ehxHTGjLg3vIr7Y130_assertion description "[Mice lacking Mertk suffer from impaired apoptotic cell clearance and develop a lupus-like autoimmune syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311344.RATroNno3mCDzEMcYnUXsiQaSRkB71ehxHTGjLg3vIr7Y130_provenance.
NP311352.RAfN6MpmAxhBWOnm3xyQjKt9F6nHyHTc0vJkdWQYN_1FA130_assertion description "[The IVS8 TG(11)TG(12) genotype appears to provide some protection from acquiring enteric fever: having this protective genotype or a variation that is known to affect CFTR protein expression provides modest protection from enteric fever (odds ratio, 0.57; 95% confidence interval, 0.37-0.87; P<.01).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311352.RAfN6MpmAxhBWOnm3xyQjKt9F6nHyHTc0vJkdWQYN_1FA130_provenance.
NP311354.RATwD0_NMdNQkILjmP5fIFt9KAEKNyvP7A7_NGQHDVCjc130_assertion description "[Patients with FGFR3-associated craniosynostosis demonstrate a sexual dimorphism, with a male preponderance for unicoronal synostosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311354.RATwD0_NMdNQkILjmP5fIFt9KAEKNyvP7A7_NGQHDVCjc130_provenance.
NP311362.RAfCKQ9ARox6RmAzbN_ZXn4hHP-lCKgTm3k_dlwcpAIw0130_assertion description "[Also, of 100 CSF samples from suspected cases of meningococcal meningitis submitted for meningococcal PCR testing, 59 (59%) were enterovirus and 2 (2%) parechovirus 1 and 2 were positive by RT-PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311362.RAfCKQ9ARox6RmAzbN_ZXn4hHP-lCKgTm3k_dlwcpAIw0130_provenance.
NP311363.RAU6xJ_WC6jrknHE9UXy635vXJxqeIQ5Z2S7E-qk9tkYw130_assertion description "[Western blot analysis revealed activation of caspase-8 and caspase-3 within the first 6 to 12 hours of treatment with doxazosin in both PC-3 and BPH-1 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311363.RAU6xJ_WC6jrknHE9UXy635vXJxqeIQ5Z2S7E-qk9tkYw130_provenance.
NP311364.RAesyzqoZTZV6m0dQs2_d69LTNZjpKTLsC2Eodd9XOMEE130_assertion description "[CD44 variant exon 6 expressions in colon cancer assessed by quantitative analysis using real time reverse transcriptase-polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311364.RAesyzqoZTZV6m0dQs2_d69LTNZjpKTLsC2Eodd9XOMEE130_provenance.
NP311365.RAQjuCD9u2zdI3gaWTf08JfSdxtLLdiBIocbSYSU5Uh7Y130_assertion description "[Here we report on 3 cases of IL-6 transgenic mouse plasmacytomas (PCT) that harbor T(12;15) translocations that had been modified by frustrated switch attempts that result in C(H) deletions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311365.RAQjuCD9u2zdI3gaWTf08JfSdxtLLdiBIocbSYSU5Uh7Y130_provenance.
NP311368.RAWFZbA5CFM25q_nOvz9tym30XZ49KVZDaRmvEOLrwuN8130_assertion description "[HIF-1 alpha signaling is augmented during intermittent hypoxia by induction of the Nrf2 pathway in NOX1-expressing adenocarcinoma A549 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311368.RAWFZbA5CFM25q_nOvz9tym30XZ49KVZDaRmvEOLrwuN8130_provenance.
NP311376.RAWvG1TYqB7IwwxgX9qi-9d3X9zzUSFAXiqWqbjh-FihI130_assertion description "[Despite this broad interest the nucleotide sequence encoding ACTH and its precursor proopiomelanocortin (POMC) is not known, nor is it clear whether there are differences in POMC mRNA from the anterior lobe or the intermediate lobe of the normal pituitary or from pituitary tumours causing ACTH excess.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311376.RAWvG1TYqB7IwwxgX9qi-9d3X9zzUSFAXiqWqbjh-FihI130_provenance.
NP311382.RASJ_WrdHMtr4GE8opoAKZX4Uzoj6LezEzI2ZJRiUty5Q130_assertion description "[We developed new Drosophila transgenic models expressing different variants of full-length human TDP-43 proteins presenting different subcellular localizations: a wild-type form of hTDP-43 and two mutants forms of the protein, hTDP-43mutNLS and hTDP43mutNES, which lack nuclear localization signals (NLS) and nuclear export signals (NES), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311382.RASJ_WrdHMtr4GE8opoAKZX4Uzoj6LezEzI2ZJRiUty5Q130_provenance.
NP311384.RASHPjVclCM2OUWYkYJvbACbxZyqdpbbbNe5GVIxbBuao130_assertion description "[Pontocerebellar hypoplasia type 6 (PCH6) (MIM #611523) is a recently described disorder caused by mutations in RARS2 (MIM *611524), the gene encoding mitochondrial arginyl-transfer RNA (tRNA) synthetase, a protein essential for translation of all mitochondrially synthesised proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311384.RASHPjVclCM2OUWYkYJvbACbxZyqdpbbbNe5GVIxbBuao130_provenance.
NP311386.RAfHdV3Gy4kC1CGHWBQSr7lg6pbPHdqUtcnOUunwxgmC4130_assertion description "[Although there is an apparent association between VEGF C-2578A and the development of coronary atherosclerosis, this association is not independent of conventional cardiovascular risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311386.RAfHdV3Gy4kC1CGHWBQSr7lg6pbPHdqUtcnOUunwxgmC4130_provenance.
NP311388.RAV2yM0NQDNZhKC9Z_9JOt1C9CFYKfzCnREXAiZ2s-yQY130_assertion description "[All genotyping (IFN-gamma, TGF-beta1, TNF-alpha, IL-6 and IL-10) experiments were performed using sequence-specific primers (SSP)-PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311388.RAV2yM0NQDNZhKC9Z_9JOt1C9CFYKfzCnREXAiZ2s-yQY130_provenance.
NP311391.RAV1Z-7QkT4ZslkhctH4kjy_tH5fEdTuPkxFEpKbdjChU130_assertion description "[Methylation-mediated repression of GADD45A and GADD45G expression in gastric cardia adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311391.RAV1Z-7QkT4ZslkhctH4kjy_tH5fEdTuPkxFEpKbdjChU130_provenance.
NP311392.RASOukP82K3SPc_XLlAWimZzdEnV7ebZRjiogc_EOHR7U130_assertion description "[RT-PCR analysis showed the presence of DAN and PAX7 transcript fragments of the expected size in all of 8 chordoma samples, whereas the CASP9-specific fragment was observed in only 3 and EPH2A was absent in one.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311392.RASOukP82K3SPc_XLlAWimZzdEnV7ebZRjiogc_EOHR7U130_provenance.
NP311395.RAUU70XAPIA3ictHCXWWqwTdBvy6qMQIctRLZEtyL2ee0130_assertion description "[Consistent with this observation, TCEAL7-downregulated clones showed higher levels of NF-kappaB targets, such as pro-proliferative (cyclin-D1 and cMyc), pro-angiogenic (interleukin (IL)-6, IL-8 and vascular endothelial growth factor (VEGF)), inflammatory (intercellular adhesion molecule 1 (ICAM-1) and cyclooxygenase-2 (Cox-2)) and anti-apoptotic (B-cell lymphoma-extra large (Bcl-xl)) genes when compared with vector controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311395.RAUU70XAPIA3ictHCXWWqwTdBvy6qMQIctRLZEtyL2ee0130_provenance.
NP311396.RASsTXNKhhlyj_IzPaxgnHpbyeTYLc4DyW91oDEDZ21Hc130_assertion description "[MULTIMERIN2 impairs tumor angiogenesis and growth by interfering with VEGF-A/VEGFR2 pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311396.RASsTXNKhhlyj_IzPaxgnHpbyeTYLc4DyW91oDEDZ21Hc130_provenance.
NP311407.RAbLd9ibHUtuJdjnn8-o1s4ExPlK8bUePQt3HDCjzhBcA130_assertion description "[A causal relationship does not seem to exist between GATA4 and ANGPT2 haploinsufficiency and CHDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311407.RAbLd9ibHUtuJdjnn8-o1s4ExPlK8bUePQt3HDCjzhBcA130_provenance.
NP311409.RAXeuoW7QN0lpTckL2LC3fP2dqk0pZFDVi8j0pAsTBcG8130_assertion description "[Mutational analysis of the genes MYH3, TNNI2, TNNT3 and TPM2, known to cause DA2B revealed no apparent disease causing mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311409.RAXeuoW7QN0lpTckL2LC3fP2dqk0pZFDVi8j0pAsTBcG8130_provenance.
NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_assertion description "[Only three cases with neurological disorders have been reported, although more than 50 mutations of the ADAR1 gene causing DSH have been reported and none of them had any neurological symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311412.RAedtYsIe8v9EEO-mDKj866noSw0a-jNuErTF09L7Yegg130_provenance.
NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_assertion description "[Genetic linkage analysis and mutation studies have identified CYP1B1 as a causative gene in PCG, as a modifier gene in POAG, and, on rare occasions, as causative gene in POAG as well as in several ASD disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311414.RAdWzPv89LT035qRXCM4X7c9H1RumYrSO13n1Km3qEg3M130_provenance.
NP311420.RAV1TlE-5gOoGwZzbv5Rn9qNoBObWbr4qbzgIgcsU4W8o130_assertion description "[Because of the high level of LD within the extended CC2/CFB region, variation within SKIV2L may exert a functional effect in AMD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311420.RAV1TlE-5gOoGwZzbv5Rn9qNoBObWbr4qbzgIgcsU4W8o130_provenance.
NP311421.RAb1-I-6Uarg7L84rkY1Edugz2iMppTq26WHKhUQWoIbU130_assertion description "[The ability to demonstrate MSI in heterogeneous endometrial samples suggests potential for the development of a novel EC screening tool for women in HNPCC kindreds.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311421.RAb1-I-6Uarg7L84rkY1Edugz2iMppTq26WHKhUQWoIbU130_provenance.
NP311434.RAfzgK_8KheiHpjbJHFr-Ear08SI5kuSE8ZJSQFqkP8Gg130_assertion description "[The discovery of human ICOS deficiency showed that a monogenic disorder could account for the full spectrum of manifestations seen in childhood and adulthood-onset CVID, including autoimmune, inflammatory, and malignant disease complications, as well as recurrent infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311434.RAfzgK_8KheiHpjbJHFr-Ear08SI5kuSE8ZJSQFqkP8Gg130_provenance.
NP311436.RAa3sq-QhjvM4cgUlOriN1ioqU42BNY-t0D5IiGAEALr0130_assertion description "[High CD24 expression significantly correlated with lymph node metastasis and positive surgical margins in cholangiocarcinoma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311436.RAa3sq-QhjvM4cgUlOriN1ioqU42BNY-t0D5IiGAEALr0130_provenance.
NP311439.RAX3jjmmPcLj6c4X6JoktwOWBTjg3_wSJ_s--6-Zh1A3U130_assertion description "[In this study, we identify the BDV P protein as microbial gene product that associates with and inhibits the principal regulatory kinase of IRF3, Traf family member-associated NF-kappaB activator (TANK)-binding kinase 1 (TBK-1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311439.RAX3jjmmPcLj6c4X6JoktwOWBTjg3_wSJ_s--6-Zh1A3U130_provenance.
NP311443.RAZRJ00TY5K4BwyPUAp6dWpsG8szq3RrmCGOFKuGOR808130_assertion description "[Therefore, we tested the hypothesis that functional variants in IL2 and IL4 were associated with risk of gastric cancer by genotyping two promoter polymorphisms in IL2 G-330T (rs2069762) and IL4 T-168C (rs2070874) in a case-control study of 1045 patients with incident gastric cancer and 1100 cancer-free controls in a high-risk Han Chinese population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311443.RAZRJ00TY5K4BwyPUAp6dWpsG8szq3RrmCGOFKuGOR808130_provenance.
NP311447.RAWgTh5UzJDKcqTKjFRbTQYPtyMB7np78FdsJOHBLGZG0130_assertion description "[However, no significant evidence of biochemical or histological deterioration of the liver was observed in TTV positive cases amongst FHF, CAH and cirrhosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311447.RAWgTh5UzJDKcqTKjFRbTQYPtyMB7np78FdsJOHBLGZG0130_provenance.
NP311455.RAfyOG2JWMH1cTWAyww56sLMxIPh8o7yVauwfEzq3RArY130_assertion description "[To examine the presence of an ATXN2 mutation in patients with parkinsonism in the Korean population and to find the difference in the ATXN2 mutation between ataxic and parkinsonian phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311455.RAfyOG2JWMH1cTWAyww56sLMxIPh8o7yVauwfEzq3RArY130_provenance.
NP311457.RAdEpncR7MIAfDR578nkeJ7SBRu1gBxRT3HR3Qz26tvbs130_assertion description "[TFII-I gene family during tooth development: candidate genes for tooth anomalies in Williams syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311457.RAdEpncR7MIAfDR578nkeJ7SBRu1gBxRT3HR3Qz26tvbs130_provenance.
NP311459.RAepgugJ1Nwj3AbewBELrRB-ZWBZR_mw1HEqsoyjU3RUg130_assertion description "[To identify which of these factors may contribute to the modification of childhood homozygous, high-hemoglobin A2 (HbA2) beta-thalassemia in Greece, the interaction of alpha-thalassemia, types of beta-thalassemia mutations, and the presence of a polymorphic site 5' to the G gamma-globin gene, which has been described as associated with increased gamma-globin chain production in some cases, was assessed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311459.RAepgugJ1Nwj3AbewBELrRB-ZWBZR_mw1HEqsoyjU3RUg130_provenance.
NP311461.RAY2YrJ6QB3-cFCj5Wxf6jtA_HGlIrL9hOzTElGwQ2cAE130_assertion description "[The goal of the Familial Dilated Cardiomyopathy (FDC) Research Project, initiated in 1993, has been to identify and characterize FDC genetic cause.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311461.RAY2YrJ6QB3-cFCj5Wxf6jtA_HGlIrL9hOzTElGwQ2cAE130_provenance.
NP311463.RAUV_KkuAVwAd7rd5Q1DBUDhN5padMvFi3M8PPMdiTpSo130_assertion description "[Although the first English-language report of melanoma in 1820 contained a description of a melanoma-prone family, seminal studies by investigators at the National Cancer Institute and the University of Pennsylvania identified dysplastic nevi (DN) as an important melanoma precursor, suggested an autosomal dominant mode of inheritance for both melanoma and DN, and proposed that a melanoma-susceptibility gene (CMM1) was located on chromosome 1p36.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311463.RAUV_KkuAVwAd7rd5Q1DBUDhN5padMvFi3M8PPMdiTpSo130_provenance.
NP311478.RAYTd_JHvEX0LOAL4DqiglW5UdoQH3JUfdczZwIuJTEN8130_assertion description "[SSH was performed between messenger RNA (mRNA) from normal rat HSC and mRNA from HSC, isolated from rats with acute D-galactosamine (Gal)-induced hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311478.RAYTd_JHvEX0LOAL4DqiglW5UdoQH3JUfdczZwIuJTEN8130_provenance.
NP311481.RAVDYWivIN08Zaq9GVDkc7h3pPTgT3yG2kvqf5TNrGROI130_assertion description "[A single clone, GBS ST-17, is strongly associated with a deadly form of the infection called late-onset disease (LOD), which is characterized by meningitis in infants after the first week of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311481.RAVDYWivIN08Zaq9GVDkc7h3pPTgT3yG2kvqf5TNrGROI130_provenance.
NP311482.RAQJ3DrhXsMIiBAkON3KbusyKG9u-ygErWoTHhjOcR4Yo130_assertion description "[Our aim was to study the association of ADIPOR1 gene variations with body size and risk of type 2 diabetes in subjects with impaired glucose tolerance, who participated in the Finnish Diabetes Prevention Study (DPS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311482.RAQJ3DrhXsMIiBAkON3KbusyKG9u-ygErWoTHhjOcR4Yo130_provenance.
NP311487.RASpQqIrp-OrCSNiExd9XxaF8hRdsYqAFAgwLnhm8IGuE130_assertion description "[TSC1 or TSC2 gene mutations in TSC lead to mTOR pathway activation and p70S6kinase (phospho-S6K) and ribosomal S6 (phospho-S6) protein phosphorylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311487.RASpQqIrp-OrCSNiExd9XxaF8hRdsYqAFAgwLnhm8IGuE130_provenance.
NP311488.RAXn2UyCZLBio7uNqIZQQROtPF6FOtaCFoNElUJuURft8130_assertion description "[Association of familial colorectal cancer with variants in the E-cadherin (CDH1) and cyclin D1 (CCND1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311488.RAXn2UyCZLBio7uNqIZQQROtPF6FOtaCFoNElUJuURft8130_provenance.
NP311491.RAXURD9gX4j2Vw3fQBDPW_jkGviIinw6WdcxuCczvcHm0130_assertion description "[The roles of sphingosine kinases SK1 and SK2 in ischemia-reperfusion injury have not been fully elucidated since studies have found beneficial effects of SK1 while others showed no role in this injury.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311491.RAXURD9gX4j2Vw3fQBDPW_jkGviIinw6WdcxuCczvcHm0130_provenance.
NP311502.RAYdCZlHlmmm6UfPcbtyijmbNQ27-u_WMuu3giDCkEwcg130_assertion description "[These results suggest that M protein mutant vesicular stomatitis virus is a good candidate oncolytic virus for the treatment of selected metastatic colorectal cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311502.RAYdCZlHlmmm6UfPcbtyijmbNQ27-u_WMuu3giDCkEwcg130_provenance.
NP311507.RAXHr6wfbHZwT8K3o0ioBFzUbvhtWA80SBCqeADXEKw2U130_assertion description "[Diabetes-induced deficits in retrograde transport of nerve growth factor and sciatic-nerve levels of calcitonin gene-related product and neuropeptide Y were also ameliorated by treatment with the sonic hedgehog-IgG fusion protein, as was thermal hypoalgesia in the paw.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311507.RAXHr6wfbHZwT8K3o0ioBFzUbvhtWA80SBCqeADXEKw2U130_provenance.
NP311508.RASKXzChNR421Y3wZVKERRHnmF9d3Y7XrMGGAqh65FQhQ130_assertion description "[In contrast, the percentage of T cells producing IL-4 and IL-5 was small among PB T cells in both RA patients and normal controls and among SF T cells in RA patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311508.RASKXzChNR421Y3wZVKERRHnmF9d3Y7XrMGGAqh65FQhQ130_provenance.
NP311510.RAW7iWn1j5dIsx0moiL5FsQJ_qPhxztaIiOrLc6A1vni8130_assertion description "[One patient had a cleft palate, and another a congenital rigid spine phenotype-findings not previously described in the literature in patients with early-onset RYR1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311510.RAW7iWn1j5dIsx0moiL5FsQJ_qPhxztaIiOrLc6A1vni8130_provenance.
NP311511.RAe0e7wxVk6oX0hYzX2IVyDP15le3FLlbtmBcuxQVHOhs130_assertion description "[We investigated 31 variants located in PXR, SLCO1A2, SLCO1B1, SLCO1B3, and SLCO2B1 for an association with breast cancer risk and/or histo-pathological tumor characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311511.RAe0e7wxVk6oX0hYzX2IVyDP15le3FLlbtmBcuxQVHOhs130_provenance.
NP311512.RAfgNyxPgM3swKY7D9_jETXAG0WLIRoEp7ul_aBlf15fg130_assertion description "[IL-5 alone was able to generate significant numbers of eos in TG5 but not FVB mice, whereas a combination of IL-5 and IL-9 induced marked eosinophilia in both strains indicating a synergism between these 2 cytokines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311512.RAfgNyxPgM3swKY7D9_jETXAG0WLIRoEp7ul_aBlf15fg130_provenance.
NP311525.RAaq_3BVh4K94PM_-bS1Re7rnrc01SDEf1MsuM_jANAUw130_assertion description "[Quantitative results showed that the levels of CXCR7 mRNA in brain tissues from patients with neurilemmoma or meningioma were significantly higher than those with pituitary adenoma or hemangioblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311525.RAaq_3BVh4K94PM_-bS1Re7rnrc01SDEf1MsuM_jANAUw130_provenance.
NP311527.RAd7dJyNktLTMUhkXKRJj_y_klEv3EjmRDdkFivGgrVNs130_assertion description "[Statistically significant association between genotype at 7p12.2 (IKZF1), 10q21.2 (ARID5B) and the NBS associated locus, 8q21.3 (NBN) and ALL risk was found; odds ratios (ORs), 1.34 (P=0.002), 1.33 (P=0.003), and 1325.21 (P=0.0028), respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311527.RAd7dJyNktLTMUhkXKRJj_y_klEv3EjmRDdkFivGgrVNs130_provenance.
NP311529.RAQ4Rw1tTGMUCOqL0A46olJLcV42EpPK8h5J1a5i4B-YY130_assertion description "[The CGG triplet repeat found within the 5'UTR of the FMR1 gene is involved in the pathogenesis of both fragile X syndrome and fragile X-associated tremor/ataxia syndrome (FXTAS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311529.RAQ4Rw1tTGMUCOqL0A46olJLcV42EpPK8h5J1a5i4B-YY130_provenance.
NP311539.RAdDtvd7fOQLZhSFF3lf3DS3Om0s9NIdeg51iVydBE8NY130_assertion description "[When comparing the two-dimensional maps, 53 differentially expressed spots were found, four of which were identified by MALDI-TOF (matrix-assisted laser-desorption ionization-time-of-flight) MS as calreticulin, nucleophosmin, phosphoglycerate kinase and pyruvate kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311539.RAdDtvd7fOQLZhSFF3lf3DS3Om0s9NIdeg51iVydBE8NY130_provenance.
NP311540.RAQ31x83n87gZvkJvl7597S3HK0N69fsgu3NkYpEIiy8s130_assertion description "[DIM could effectively stimulate the expression of BRCA1 in vitro and in vivo and reduce ROS generation, leading to the inhibition of VCAM-1 expression and leukocyte-endothelial cell adhesion, and finally resulted in an alleviation of experimental colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311540.RAQ31x83n87gZvkJvl7597S3HK0N69fsgu3NkYpEIiy8s130_provenance.
NP311542.RAcwfqdDTAN6o9EsC9gssoQzoCqNWW4zdeoEDXcBnMCNo130_assertion description "[Glutathione S-transferase homozygous deletions and relapse in childhood acute lymphoblastic leukemia: a novel study design in a large Italian AIEOP cohort.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311542.RAcwfqdDTAN6o9EsC9gssoQzoCqNWW4zdeoEDXcBnMCNo130_provenance.
NP311559.RAT8aUiyYBPnEvQqYAthbgCWSK_XtD5OTyFFoW3IaMDtw130_assertion description "[The data suggest that somatic MEN1 gene mutations and deletions play a causative role in the development of a subgroup of sporadic pituitary adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311559.RAT8aUiyYBPnEvQqYAthbgCWSK_XtD5OTyFFoW3IaMDtw130_provenance.
NP311560.RAZdY_JLQHXiwF2qPCRYxk_zBLBwJCi29bEVp_XrR9e4M130_assertion description "[TcR V beta 5 gene products were represented in three cases of lymphoblastic malignancy (V beta 5.1, V beta 5.2) and two cases of peripheral T-cell lymphoma (PTCL) (V beta 5.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311560.RAZdY_JLQHXiwF2qPCRYxk_zBLBwJCi29bEVp_XrR9e4M130_provenance.
NP311561.RAQNmGu0xC6HAfMD6fuVSnI9l_uFqpvBaSE1-jkfIsNCY130_assertion description "[As the activation of PI3K/AKT signaling may be associated with alterations of the PTEN gene located at 10q23.3, a chromosomal region subject to frequent allelic losses in medulloblastoma, we screened PTEN for mutations and mRNA expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311561.RAQNmGu0xC6HAfMD6fuVSnI9l_uFqpvBaSE1-jkfIsNCY130_provenance.
NP311567.RAW8ZLSCxjuzGe6m4CUtHi7vBQZQ1FTQJAQJUGVakEBCE130_assertion description "[The possibility of gene-gene interactions was assessed, focusing on 11 polymorphisms in nine genes (DC-SIGN, IFN-γ, IFNGR1, IL-8, IL-1Ra, MBL, NRAMP1, RANTES, and SP-D) that have been associated with TB, some repeatedly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311567.RAW8ZLSCxjuzGe6m4CUtHi7vBQZQ1FTQJAQJUGVakEBCE130_provenance.
NP311574.RAUOcoFmsZCz3nQLtXpZjhXXN2ivoamPpy51J9RKhlkdk130_assertion description "[Polymorphisms of human paraoxonase 1 gene (PON1) and susceptibility to diabetic nephropathy in type I diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311574.RAUOcoFmsZCz3nQLtXpZjhXXN2ivoamPpy51J9RKhlkdk130_provenance.
NP311584.RAVHvtgo4_N0wPEhttbplQI_mHr903_kbpXrDh9hGtvfI130_assertion description "[Differential requirement for CD80 and CD80/CD86-dependent costimulation in the lung immune response to an influenza virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311584.RAVHvtgo4_N0wPEhttbplQI_mHr903_kbpXrDh9hGtvfI130_provenance.
NP311596.RAes9GS_Ap-aYeEcx9LwDR0nnWfFWY4X_OJghlIY5m_BA130_assertion description "[The unmethylated arginine-glycine-glycine domain preceding the PY-NLS interacts with TRN and arginine methylation in this domain reduces TRN binding.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311596.RAes9GS_Ap-aYeEcx9LwDR0nnWfFWY4X_OJghlIY5m_BA130_provenance.
NP311600.RAbsJ5ujJ9hoXgxI8ekJYb0RwlEuYfO_UgR6c1mUxCSEE130_assertion description "[In addition, other genes also implicated in other autoimmune diseases are linked to Addison's disease, such as cytotoxic T lymphocyte antigen 4 (CTLA-4), protein tyrosine phosphatase non-receptor type 22 (PTPN22), major histocompatibility complex class II transactivator (CIITA), and most recently the C-lectin type gene (CLEC16A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311600.RAbsJ5ujJ9hoXgxI8ekJYb0RwlEuYfO_UgR6c1mUxCSEE130_provenance.
NP311609.RAT2EDeQzHyOM73bkIIaPKQjZM_6PLjG9M4IrWRYhgXnQ130_assertion description "[In 2 of 4 cases, the expression of LBP mRNA (1.2 kilobases) was higher in carcinoma than in normal tissue.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311609.RAT2EDeQzHyOM73bkIIaPKQjZM_6PLjG9M4IrWRYhgXnQ130_provenance.
NP311610.RARDCbocDP1C2JtjdmAMXYwJ0LM9k6CpxtH7pTue0kZhw130_assertion description "[The only chromosome aberration restricted to a certain high-grade PTL was t(2;5)(p23;q35) in large-cell anaplastic lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311610.RARDCbocDP1C2JtjdmAMXYwJ0LM9k6CpxtH7pTue0kZhw130_provenance.
NP311617.RAWINEGq4XejrlWoSSwPc32YAxh9hj4ceoq_AsQeu8K3A130_assertion description "[Furthermore, chelation with EDTA stabilizes the structure of both wild-type rhodopsin and the most prevalent rhodopsin RP mutation, P(23)H. These interactions suggest that homeostatic regulation of trace metal concentrations in the rod outer segment of the retina may be important both physiologically and for an important cluster of RP mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311617.RAWINEGq4XejrlWoSSwPc32YAxh9hj4ceoq_AsQeu8K3A130_provenance.
NP311622.RAerI_vPSy0ytbM_xDYJPkZtBRKjwFk18JexGKKkiHOPE130_assertion description "[Deficiency of plasma protein S, protein C, or antithrombin III and arterial thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311622.RAerI_vPSy0ytbM_xDYJPkZtBRKjwFk18JexGKKkiHOPE130_provenance.
NP311625.RAd0R7w8A-eZTD6fNt_WAbZ5AjUWMSAq14mS-5o5hXIeg130_assertion description "[Furthermore, molecular classification based on matrix CGH data closely paralleled histological classification and was able to distinguish with few exceptions between diffuse astrocytomas and oligodendrogliomas, anaplastic astrocytomas and anaplastic oligodendrogliomas, anaplastic oligodendrogliomas and glioblastomas, as well as primary and secondary glioblastomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311625.RAd0R7w8A-eZTD6fNt_WAbZ5AjUWMSAq14mS-5o5hXIeg130_provenance.
NP311627.RAW_n8NWcgbIFFJMNmGvfYodnqk7VUUy7-DEhyDpqi2PE130_assertion description "[Identification of a novel factor X deletion in combination with a missense mutation in the F10 gene - Genotype-phenotype correlation in a girl with severe factor X deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311627.RAW_n8NWcgbIFFJMNmGvfYodnqk7VUUy7-DEhyDpqi2PE130_provenance.
NP311631.RARPyVXJtISwJ0NoMFEMouFOloCKBPpOwblpdx5L4egRI130_assertion description "[The present case-control study aimed to examine the associations between breast cancer risk and three functional polymorphisms (Interleukin (IL) -1A C-889T, IL-1B C-31T and IL-1RN 86-bp variable number tandem repeat) related to expression of IL-1beta, which combines estrogen receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311631.RARPyVXJtISwJ0NoMFEMouFOloCKBPpOwblpdx5L4egRI130_provenance.
NP311636.RAYOPBXXH13se5eQlqu3tWSYK7rfxkdI47COTxWxa44A8130_assertion description "[We therefore tested the polymerase chain reaction (PCR) for the detection of borrelial sequences in CSF and urine samples of consecutive children with neuroborreliosis seen in a single summer season.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311636.RAYOPBXXH13se5eQlqu3tWSYK7rfxkdI47COTxWxa44A8130_provenance.
NP311638.RAfIpwFezMxMXEYLnmxjGdy9LExyZnTrGh2c84xVFXnFU130_assertion description "[Addition of the p57 immunostain improved sensitivity of a diagnosis of CHM to a range of 93% to 96% for individual pathologists and 96% by consensus; specificity was improved from a range of 96% to 98% for individual pathologists and 96% by consensus; there was no substantial impact on diagnosis of PHMs and NMs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311638.RAfIpwFezMxMXEYLnmxjGdy9LExyZnTrGh2c84xVFXnFU130_provenance.
NP311643.RARS2mS6L-L40veDj_SBjNV3ahToXysnTEouWBtHryofk130_assertion description "[Eight SNPs in six genes were significantly associated with the PTDM development: TCF7L2 rs7903146 (odds ratio [OR]=2.20, P =0.016), SLC30A8 rs13266634 (OR=1.52, P =0.003), HHEX rs1111875 (OR=1.47, P =0.007), HHEX rs7923837 (OR=2.32, P =0.014), HHEX rs5015480 (OR=1.59, P =0.003), CDKAL1 rs10946398 (OR=1.43, P =0.008), CDKN2A/B rs10811661 (OR=1.33, P =0.039), and KCNQ1 rs2237892 (OR=1.46, P =0.009).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311643.RARS2mS6L-L40veDj_SBjNV3ahToXysnTEouWBtHryofk130_provenance.
NP311650.RAcvhxORD1w7i4uPc81ZZ_mTjCO2aUa_wN6nNGPMWR1uI130_assertion description "[Recent genetic studies have suggested that variations in the gene encoding LTA, which affect its expression and biological function, may contribute to the development of vascular diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311650.RAcvhxORD1w7i4uPc81ZZ_mTjCO2aUa_wN6nNGPMWR1uI130_provenance.
NP311655.RAWn9c0Ih0p2I5Ia3DGSokVf6CGhODMIJsSC5BQcVGMwU130_assertion description "[Prolactin in schizophrenia is considered in the context of antipsychotic drug-induced hyperprolactinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311655.RAWn9c0Ih0p2I5Ia3DGSokVf6CGhODMIJsSC5BQcVGMwU130_provenance.
NP311656.RAX0VNZ06PL0_bmFk0HUNDsz5FAcoJ0nvyJonA4lmxTl8130_assertion description "[Mechanisms of cytokine cascade activation in patients with sepsis: normal cytokine transcription despite reduced CD14 receptor expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311656.RAX0VNZ06PL0_bmFk0HUNDsz5FAcoJ0nvyJonA4lmxTl8130_provenance.
NP311657.RAWszE618KHKA4A5SDpz_GOhIxtQosyQ5K_d5e5aTevMg130_assertion description "[Mutations that activate the mitogen activated protein kinase (MAPK) pathway via BRAF or NRAS are present in the majority of melanomas arising on skin intermittently exposed to the sun.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311657.RAWszE618KHKA4A5SDpz_GOhIxtQosyQ5K_d5e5aTevMg130_provenance.
NP311679.RAWWt4VeyWFUan6w5RVA085IYsMBRyuB0BxPVW94WzMl0130_assertion description "[Resistance to TGF-beta-mediated tumour suppressor function in human lung cancer may occur through the loss of type II receptor (TbetaRII) expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311679.RAWWt4VeyWFUan6w5RVA085IYsMBRyuB0BxPVW94WzMl0130_provenance.
NP311680.RAWi1q82GwHTOmUrXfNGTP43U3QaPvru2XUNn4TV4SWOE130_assertion description "[Genes linked to rare cases of familial ALS and/or FTD, like FUS, TARDBP, OPTN, and UBQLN2 may converge onto a unifying pathogenic pathway and thereby provide novel therapeutic targets common to a spectrum of etiologically diverse forms of ALS and ALS-FTD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311680.RAWi1q82GwHTOmUrXfNGTP43U3QaPvru2XUNn4TV4SWOE130_provenance.
NP311681.RAbwwBcJKvZlQvHCzA23zc52M3PX890tBpUtDwuv_zLac130_assertion description "[Quantitative RT-PCR analysis revealed mRNA expression of all four Tensin genes to be significantly downregulated in human kidney tumors (50-100% reduction versus normal kidney cortex; P<0.001).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311681.RAbwwBcJKvZlQvHCzA23zc52M3PX890tBpUtDwuv_zLac130_provenance.
NP311684.RAceZrzAeW8Pteb195HWLwQnitpx4wWWcoypJSHCJF4p4130_assertion description "[All P-selectin polymorphisms as well as a common E-selectin polymorphism, Ser128Arg which has been reported as being associated with an increased risk of premature coronary heart disease (CHD), and is in tight linkage disequilibrium with several P-selectin polymorphisms, were investigated in 647 patients with MI and 758 control subjects from four regions of France and Northern Ireland (the ECTIM study).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311684.RAceZrzAeW8Pteb195HWLwQnitpx4wWWcoypJSHCJF4p4130_provenance.
NP311686.RAWwhnICHz9LQ63wpnIjDs-RAxFvV1k6SjT9gccjCLqCI130_assertion description "[The distribution of these novel and previously reported RP1 mutations makes it challenging to describe a unifying mutational mechanism for dominant versus recessive RP1-related RP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311686.RAWwhnICHz9LQ63wpnIjDs-RAxFvV1k6SjT9gccjCLqCI130_provenance.
NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_assertion description "[For those under treatment with LTG, UGT1A4 and UGT2B7 genotyping might be of clinical use and could contribute to the interindividual variability in LTG concentration to dose ratio in epileptic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311691.RAV0OgI3ejRSkT94CgXuVEzSmIKADNellQbDv9sp7K4yA130_provenance.
NP311698.RActhEyFfXojY-LLXtk2BRdryMQ-68K_fDTFG3glQlpyk130_assertion description "[To understand the effects of nitric oxide on cholangiocyte secretion and biliary tract pathophysiology we have investigated: (1) the effects of proinflammatory cytokines on NO production and expression of the inducible nitric oxide synthase (NOS2), (2) the effects of NO on cAMP-dependent secretory mechanisms, and (3) the immunohistochemical expression of NOS2 in a number of human chronic liver diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311698.RActhEyFfXojY-LLXtk2BRdryMQ-68K_fDTFG3glQlpyk130_provenance.
NP311699.RAfdp-Qa2qzPEvzvTEOJ8SnoHBxugU55qRwPZ1KFLaI6o130_assertion description "[Telomeric-repeat-amplification-protocol (TRAP) assay revealed that more than 80% of RCC tumor tissue exhibited telomerase activity, while none of the adjacent normal tissue did.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311699.RAfdp-Qa2qzPEvzvTEOJ8SnoHBxugU55qRwPZ1KFLaI6o130_provenance.
NP311709.RAfaYHaQa4rPJ6BJZh6Z5Dm5woC4tBqL2H4_mFgzMJlQ0130_assertion description "[We tested this hypothesis by examining the contribution of functional polymorphisms in MSH5 C85T and MLH3 C2531T to the risk of male infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311709.RAfaYHaQa4rPJ6BJZh6Z5Dm5woC4tBqL2H4_mFgzMJlQ0130_provenance.
NP311710.RAXCKiTCTvvep5vssZtONujk_xy5oPn47X42opS9gl5cY130_assertion description "[DEP-1/PTPRJ is a transmembrane protein-tyrosine phosphatase which has been proposed as a suppressor of epithelial tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311710.RAXCKiTCTvvep5vssZtONujk_xy5oPn47X42opS9gl5cY130_provenance.
NP311712.RAbyCouHqsff9c91yxMdOqiSlsCYLx_r9Mk1zETxamX9U130_assertion description "[A genetic deficiency of lysosomal alpha-mannosidase causes the lysosomal storage disease alpha-mannosidosis (AMD), in which oligosaccharide accumulation occurs in neurons and glia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311712.RAbyCouHqsff9c91yxMdOqiSlsCYLx_r9Mk1zETxamX9U130_provenance.
NP311720.RAfbLT1kyA114AFjIHOvDYYhUqEBmyGTtlBbUgGs7yzEU130_assertion description "[A significantly higher prevalence of DRB1*08 was observed in Mexican patients with juvenile onset disease (44.9%) and especially those with undifferentiated spondyloarthropathy (55.6%) compared to normal unrelated Mexican Mestizo (25.4%) (p < 0.01 for both) and in patients with undifferentiated spondyloarthropathy versus B27 controls (11.1%) (p = 0.03), although no significant differences were observed in within patient group comparisons based on phenotypic features of disease such as AAU and age at onset.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311720.RAfbLT1kyA114AFjIHOvDYYhUqEBmyGTtlBbUgGs7yzEU130_provenance.
NP311730.RAQ5vZUGN7PRqYxmBwTkdRNHdDD01Bi9_jEF8MxE0wVyQ130_assertion description "[High levels of pro-angiogenic factors, leptin, IL-1, Notch and VEGF (ligands and receptors), are found in breast cancer, which is commonly correlated with metastasis and lower survival of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311730.RAQ5vZUGN7PRqYxmBwTkdRNHdDD01Bi9_jEF8MxE0wVyQ130_provenance.
NP311733.RAZjyCnobYMuza4yWMraBlm888_0HSbktiIfGgTsytBYY130_assertion description "[Carcinoembryonic antigen (CEA, CEACAM5) is expressed on several human carcinomas including colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311733.RAZjyCnobYMuza4yWMraBlm888_0HSbktiIfGgTsytBYY130_provenance.
NP311734.RAVJw6BOQbiYtBsWpM-Yxsr1XuqOWuNyX5ADbsozpDkhs130_assertion description "[For this, IL-23p19(-/-), IL-17RA(-/-) and IL-22(-/-) mice were intravaginally inoculated with Candida, and vaginal lavage fluids were evaluated for fungal burden, PMN infiltration, the presence of S100 alarmins and inflammatory cytokines and chemokines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311734.RAVJw6BOQbiYtBsWpM-Yxsr1XuqOWuNyX5ADbsozpDkhs130_provenance.
NP311736.RAX126WsiQtdvM0Ti8C1BRATEU_WOBVtCseU5Rt8lFn3M130_assertion description "[Immunohistochemical staining for FHIT and PCNA proteins was carried out in 451 breast lesions showing nonproliferative benign breast disease (BBD) (n=263), proliferative BBD without atypia (n=128), proliferative BBD with atypia (n=11), carcinoma in situ (n=15) or invasive carcinoma (n=34) and for EGFR protein in a subset of 71 of these cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311736.RAX126WsiQtdvM0Ti8C1BRATEU_WOBVtCseU5Rt8lFn3M130_provenance.
NP311739.RASgjACEoKA1H4fPUghLbTdnrQTWKqofZziTlTLS4E43I130_assertion description "[Clinical, molecular, and cellular immunologic findings in patients with SP110-associated veno-occlusive disease with immunodeficiency syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311739.RASgjACEoKA1H4fPUghLbTdnrQTWKqofZziTlTLS4E43I130_provenance.

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