Nanopublications

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

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NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_assertion description "[Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency..]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187036.RAYrV7e_CHmftLvfPkaSuevyAmv7I7Vf8c6C1FCiIhAbc130_provenance.
NP187040.RAba5OCCFHwGfd3U9ycZd14jP7p2u9WX2x2t1wRnJLoOg130_assertion description "[In the glioblastomas with no alterations of CDKN2A, CDK4 or RB1, several other genes (CCND1, CCND2, CCND3, CDK6, E2F, CDK7, MYC and MYCN) whose products take part in cell cycle regulation were examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187040.RAba5OCCFHwGfd3U9ycZd14jP7p2u9WX2x2t1wRnJLoOg130_provenance.
NP187043.RAYRpLL4YG3U88haA_LX2xfPRD9V8T-CXznyzutuNOGMM130_assertion description "[Collectively, these data suggest that increased CYP4Z1 expression promotes tumor angiogenesis and growth in breast cancer partly via PI3K/Akt and ERK1/2 activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187043.RAYRpLL4YG3U88haA_LX2xfPRD9V8T-CXznyzutuNOGMM130_provenance.
NP187045.RAUbtJI2c5wGbfb3yuCbkjT7K9Wyyb4dhhE5R9Gc7nyPs130_assertion description "[N-pEGFR independently predicted worse DSS in both training (P = 0.0468, HR = 2.024) and test sets (P = 0.0223, HR = 5.573).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187045.RAUbtJI2c5wGbfb3yuCbkjT7K9Wyyb4dhhE5R9Gc7nyPs130_provenance.
NP187047.RAfyUXAdK2TrDRuMZjVeC8n9UcUipAWaqiklm5NXV7GEM130_assertion description "[Another emerging research topic is in the designation of genetic markers for specific cirrhosis-related complications, such as spontaneous bacterial peritonitis (NOD2) and hepatic encephalopathy (glutaminase), of potential future relevance in prioritizing patients for preemptive treatment strategies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187047.RAfyUXAdK2TrDRuMZjVeC8n9UcUipAWaqiklm5NXV7GEM130_provenance.
NP187052.RASAwoRoPMSP2ri2p0ctWMjMgUkQopzwNRwOCHvOSX9sc130_assertion description "[KIAA1509 is a novel PDGFRB fusion partner in imatinib-responsive myeloproliferative disease associated with a t(5;14)(q33;q32).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187052.RASAwoRoPMSP2ri2p0ctWMjMgUkQopzwNRwOCHvOSX9sc130_provenance.
NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_assertion description "[However, three further cell strains (TTD4VI and TTD6VI from two French siblings and TTD1BR from an English patient) showed restoration of normal UV-induced DNA repair synthesis after fusion with XP or TTD cells belonging to XP group D. These observations, which give the first indication that TTD is associated with repair defects behaving differently in the functional test of complementation, suggest some kind of causal connection between defective excision-repair factors and clinical features diagnostic for TTD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187060.RAb3wwYokV2z09TO4lsrMZWoe6QuEj6oqeFj9TvohppCE130_provenance.
NP187062.RAR_dKBBK6VDQxcMTNqgIDcUF4o1NPssFfsPbry_94SjY130_assertion description "[The aim of this study was to evaluate the frequency and predictive value of diabetes-associated autoantibodies, such as islet cell antibodies (ICA) and autoantibodies to insulin (IAA), GAD65 (GADA), and the IA-2 molecule (IA-2A) in genetically susceptible children from the general population during the first 2 yr of life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187062.RAR_dKBBK6VDQxcMTNqgIDcUF4o1NPssFfsPbry_94SjY130_provenance.
NP187067.RARIQCCAUA_1abaUF2OPPV82P4MC7aLRlYdD9A1TEm-iA130_assertion description "[All subjects who developed diabetes were positive for antibodies to GAD and expressed the HLA-DR3 or DR4 alleles, whereas only one of the non-progressors had these parameters (P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187067.RARIQCCAUA_1abaUF2OPPV82P4MC7aLRlYdD9A1TEm-iA130_provenance.
NP187068.RAYac2HjSZTD6_sSj5UKc_5eF7uSu32L2sdo6OyqpWKug130_assertion description "[In this work we report the genetic basis of C7 deficiency in a previously reported Spanish patient exhibiting a combined total deficiency of C7 and C4B associated with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187068.RAYac2HjSZTD6_sSj5UKc_5eF7uSu32L2sdo6OyqpWKug130_provenance.
NP187074.RAf_T6QY83Flz6q6rl4NHL3loIfdp07nCWwBNuCL_oeO0130_assertion description "[Galectin-3 is a galactoside binding protein found at elevated levels in a wide variety of neoplastic cells and thought to be involved in cognitive cellular interactions during transformation and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187074.RAf_T6QY83Flz6q6rl4NHL3loIfdp07nCWwBNuCL_oeO0130_provenance.
NP187076.RAQG_KpaqbbXwUvzYMcZhO_Qp2ZUZ_bCFwOgRJeL0l17Q130_assertion description "[Our results demonstrated that strain M was a weaker gamma interferon (IFN-gamma) inducer than H37Rv for group N. Strain M induced the highest interleukin-4 expression in CD4+ and CD8+ T cells from MDR- and S-TB patients, along with the lowest cytotoxic T-lymphocyte (CTL) activity in patients and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187076.RAQG_KpaqbbXwUvzYMcZhO_Qp2ZUZ_bCFwOgRJeL0l17Q130_provenance.
NP187079.RAdeTOOysjttVtsXPyPCfYt2_L3Xdt5b8h8f-dgUSqag8130_assertion description "[In addition, common variation in 3 genes (MAPT, LRRK2, and SNCA) and loss-of-function mutations in GBA have been well-validated as susceptibility factors for PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187079.RAdeTOOysjttVtsXPyPCfYt2_L3Xdt5b8h8f-dgUSqag8130_provenance.
NP187084.RAROxvTk-KsTbM8zufOqHp36fWKqID7AaOEW6G3mwFHI0130_assertion description "[Fragile-X syndrome, a frequent cause of inherited mental retardation, is characterised in almost all cases by a CGG-repeat expansion that is located within the FMR-1 gene and that prevents the expression of fragile-X mental retardation protein (FMRP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187084.RAROxvTk-KsTbM8zufOqHp36fWKqID7AaOEW6G3mwFHI0130_provenance.
NP187086.RAftsT_qiUc3xeXPgGtvDQQBRhmLgHRS92BXevCMHjCC0130_assertion description "[An additional syntenic cluster exists within a peak of linkage disequilibrium with the HFE gene and may define coding sequences that underlie the defect in genetic iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187086.RAftsT_qiUc3xeXPgGtvDQQBRhmLgHRS92BXevCMHjCC0130_provenance.
NP187087.RAWDHWRQg1fa7mdsD9CigG66lUWmbnEpXkv1KzE2p8ByI130_assertion description "[Five (45.5%) of the subjects at high risk for panic disorder, but none of the LR-C subjects (p = .007), nor any of the HR-AD subjects (p = .011), developed a panic attack following inhalation of the CO2 mixture.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187087.RAWDHWRQg1fa7mdsD9CigG66lUWmbnEpXkv1KzE2p8ByI130_provenance.
NP187089.RATT9k8D5cnvDQZKo6kz2fZortqIjlrXU29YDcLQSTQe8130_assertion description "[Full-length p43, but not p43(ARF) or endothelial monocyte activating polypeptide II, activated THP1 monocytes (upregulation of tumor necrosis factor alpha, interleukin 1 beta, interleukin 8, macrophage inflammatory protein (MIP)-1 alpha, MIP1 beta, MIP2 alpha) and endothelial cells (enhanced synthesis of E-selectin, vascular cell adhesion molecule-1, intercellular adhesion molecule-1, tissue factor).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187089.RATT9k8D5cnvDQZKo6kz2fZortqIjlrXU29YDcLQSTQe8130_provenance.
NP187105.RATgbDsQ5ZDLkjoh8IkkgpyVjdnoPCFt76T6vni16oMWw130_assertion description "[Decreased availability of GDP-L-fucose in a patient with LAD II with normal GDP-D-mannose dehydratase and FX protein activities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187105.RATgbDsQ5ZDLkjoh8IkkgpyVjdnoPCFt76T6vni16oMWw130_provenance.
NP187112.RAcyKtQWNtPqe9_KVUVQqbyNC9qqeQqj_L0IO67kTjyEk130_assertion description "[To investigate whether BLM was involved in cellular responses to DNA damage Bloom's syndrome fibroblasts were treated with either UV or ionizing radiation and the levels of p53 and two of its down stream effectors, p21waf1/cip1 and hdm2, were determined by western blot analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187112.RAcyKtQWNtPqe9_KVUVQqbyNC9qqeQqj_L0IO67kTjyEk130_provenance.
NP187115.RAfcjsedN1gg5WOExCKHRAmh9kz20vT2nZ3g5fm6sb7uw130_assertion description "[We therefore studied the relationship between the circulating levels of interleukin-1beta (IL-1beta) and interleukin-18 (IL-18), a new member of the IL-1 complex, as well as polymorphisms within the IL-1 cluster with the occurrence of anaemia in patients with AA amyloidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187115.RAfcjsedN1gg5WOExCKHRAmh9kz20vT2nZ3g5fm6sb7uw130_provenance.
NP187126.RAUxlb9kBDEFe_0SDuAK9J8kxJwuZMJPjjl-Pfpee0Sbc130_assertion description "[We conclude that quantitation of AHSP is not likely to be useful for detection of preclinical prion disease in man.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187126.RAUxlb9kBDEFe_0SDuAK9J8kxJwuZMJPjjl-Pfpee0Sbc130_provenance.
NP187128.RAembVHyTXmi3qRhgIyzPl6pG3GxCjHleUr7oWrJy7JvU130_assertion description "[Pepsinogen C is an aspartic proteinase mainly involved in the digestion of proteins in the stomach, which is also synthesized by certain human breast tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187128.RAembVHyTXmi3qRhgIyzPl6pG3GxCjHleUr7oWrJy7JvU130_provenance.
NP187132.RAdvM10b7fxAENThl9XyCtWz8dMM9HgnqvWVmVav9212g130_assertion description "[Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187132.RAdvM10b7fxAENThl9XyCtWz8dMM9HgnqvWVmVav9212g130_provenance.
NP187134.RAcFZ30HuZ_jycRYNOMob6efLC934PDZAhfVc5Sa-2VYg130_assertion description "[Rearrangement of the human ABL oncogene in a glioblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187134.RAcFZ30HuZ_jycRYNOMob6efLC934PDZAhfVc5Sa-2VYg130_provenance.
NP187135.RATCHtCIE3tN0Yaq9fA_bxdeHU5Qw2CVRgIhL8scNMeQs130_assertion description "[For ERCC2 Asp312Asn polymorphism, significantly elevated GC risk was associated with Asn/Asn genotype (AA vs. GG + GA: OR = 1.36, 95%CI = 1.04-1.77, P = 0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187135.RATCHtCIE3tN0Yaq9fA_bxdeHU5Qw2CVRgIhL8scNMeQs130_provenance.
NP187137.RAYc_HPv6qg9afEzdQzcUJX1trWV37ShTh7Wv60L89_ms130_assertion description "[Western immunoblotting experiments demonstrated high levels of p100 and p105 proteins not only in HPV16+ cervical carcinoma-derived keratinocytes but also in keratinocytes stably transfected by HPV16 E6 or E7 oncogenes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187137.RAYc_HPv6qg9afEzdQzcUJX1trWV37ShTh7Wv60L89_ms130_provenance.
NP187146.RAdWbycwS7q3_jNOcn-47hKhiKuP4HhExHvwrg-9t_c7Y130_assertion description "[Direct sequencing of segments of the factor VIII gene in 30 hemophiliacs with sporadic disease (32+ kb of sequence in total) revealed two missense transitions: glutamate 1704 to lysine (E1704----K) in a patient with severe hemophilia A and proline 2300 to serine (P2300----S) in a patient with mild hemophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187146.RAdWbycwS7q3_jNOcn-47hKhiKuP4HhExHvwrg-9t_c7Y130_provenance.
NP187150.RATNeYI-7QB6FBLOnjNYy_VRWrSxnksnhU-FsIVkEOtxw130_assertion description "[CFTR and/or SPINK1 gene mutations associate with IP (idiopathic CP and IRAP) independently of the presence of PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187150.RATNeYI-7QB6FBLOnjNYy_VRWrSxnksnhU-FsIVkEOtxw130_provenance.
NP187152.RAZgbqfQEm-x927No_N-F3ieAK11mYAPUhc5aOx5wXeJI130_assertion description "[These findings suggest that (i) MICB expression is related to temporary skin inflammation, and (ii) expression of MICB is not directly associated with BD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187152.RAZgbqfQEm-x927No_N-F3ieAK11mYAPUhc5aOx5wXeJI130_provenance.
NP187153.RAWG6zs-bIMayJpq5HuIxiQLs2tCgq27s-GgLLKwOS4G0130_assertion description "[Arg(184)His mutant GTP cyclohydrolase I, causing recessive hyperphenylalaninemia, is responsible for dopa-responsive dystonia with parkinsonism: a case report.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187153.RAWG6zs-bIMayJpq5HuIxiQLs2tCgq27s-GgLLKwOS4G0130_provenance.
NP187161.RAVFN_0VkyfxLy4HWrD9Se8YlkRh-xdnF28JHbGg6V000130_assertion description "[We predict that the long intracellular domain form of OB-R is crucial for initiating intracellular signal transduction, and as a corollary, the inability to produce this form of OB-R leads to the severe obese phenotype found in db/db mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187161.RAVFN_0VkyfxLy4HWrD9Se8YlkRh-xdnF28JHbGg6V000130_provenance.
NP187179.RAW_h1LxyO_rDPOQYPtKdqbXbibobh1UYV8Z_SoQBJmBg130_assertion description "[Important advances have been made within the past year in the area of glaucoma genetics, including the identification of the TIGR gene for adult as well as juvenile GLC1A glaucoma, a P450 gene for GLC3A congenital glaucoma, and a bicoidhomeobox transcription factor gene RIEG for developmental glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187179.RAW_h1LxyO_rDPOQYPtKdqbXbibobh1UYV8Z_SoQBJmBg130_provenance.
NP187180.RAVvBXA7XDiTEJ6vxe9Bv-KwiFiAD18z0jfPMA1e2xEKg130_assertion description "[Taken together, our data support that noncanonical NF-κB activation is the pathway through which extracellular TG2 promotes OC metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187180.RAVvBXA7XDiTEJ6vxe9Bv-KwiFiAD18z0jfPMA1e2xEKg130_provenance.
NP187181.RAU8SdS9tq-qRJnGsNwlYSUtcInnMjgI_ga4Y8gO2Gam8130_assertion description "[The results showed that there was no positive association between the genetic variations of DLG3 and NSMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187181.RAU8SdS9tq-qRJnGsNwlYSUtcInnMjgI_ga4Y8gO2Gam8130_provenance.
NP187182.RAZddBt7jG68TWFJwJTaF7W46WbPjB2ylruvosrXZkJ8U130_assertion description "[The 46 signature genes for EHR included many cell adhesion-related genes (ITGA6, SPP1, DNMBP, CD44 and POSTN), which all showed higher expression in HCC with EHR than in HCC without EHR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187182.RAZddBt7jG68TWFJwJTaF7W46WbPjB2ylruvosrXZkJ8U130_provenance.
NP187187.RAaEvtPANMqLPgYI7HubGihgN_c6OsBCrQgpt6xwAqYD8130_assertion description "[These data suggest that the HER2 FISH analysis may be an effective screening test in breast cancer metastases and G3 tumors, irrespective of the hormone receptor status or presence of lymphovascular invasion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187187.RAaEvtPANMqLPgYI7HubGihgN_c6OsBCrQgpt6xwAqYD8130_provenance.
NP187191.RAfevIxGWuhi2B-zMYcWWQ4N1jNhZuIxpsyZQ-nLNaZXI130_assertion description "[The CYP26 gene, which plays a key role in retinol metabolism, was examined to define any single-nucleotide polymorphisms (SNP) associations with AS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187191.RAfevIxGWuhi2B-zMYcWWQ4N1jNhZuIxpsyZQ-nLNaZXI130_provenance.
NP187192.RAX_Rusvnn4ircwIpI-rb1zEGgPfdMzvxdIQ2UoH1rNFM130_assertion description "[Our results indicate that p16INK4a promoter hypermethylation predicts a poor 5-year survival rates for patients with resectable non-small cell lung cancer, particularly for those with early stage tumors, whereas RASSF1A promoter hypermethylation is a profound prognostic predictor for patients with locally advanced non-small cell lung cancer, suggesting an important role of RASSF1A in non-small cell lung cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187192.RAX_Rusvnn4ircwIpI-rb1zEGgPfdMzvxdIQ2UoH1rNFM130_provenance.
NP187195.RAX97_lL6Gdn7pIENDqdBvxBLaNQYqMde22OpmGROKZ4k130_assertion description "[Semaphorin 5A and protein phosphatase 1F are the common genes represented as major hubs in both the smoking and cancer related network.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187195.RAX97_lL6Gdn7pIENDqdBvxBLaNQYqMde22OpmGROKZ4k130_provenance.
NP187198.RAWXzIi4QVl9yDUD4lNXpQ7Z1RdR6JPO9EqMY8cvwGa0o130_assertion description "[To investigate this hypothesis, adhesion, transendothelial penetration and NCAM (CD56) adhesion receptor expression of drug-resistant versus drug-sensitive NB tumor cells were evaluated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187198.RAWXzIi4QVl9yDUD4lNXpQ7Z1RdR6JPO9EqMY8cvwGa0o130_provenance.
NP187199.RAToTve9ZazA1hMUb6simWwPbtsh4ZsWj8LE6g-d3cPNc130_assertion description "[HBV viral loads, genotypes, precore and basal core promotor mutations, serum hepatitis B surface antigen (HBsAg) and interferon-gamma inducible protein 10 (IP-10) levels as well as four SNPs of IL28B were determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187199.RAToTve9ZazA1hMUb6simWwPbtsh4ZsWj8LE6g-d3cPNc130_provenance.
NP187206.RATWcAPDf65PR8KTukuofuXqIRizX0vu9xcZqJgFD8I5I130_assertion description "[Leptin exerts its physiological action through its receptor Ob-R. Overexpression of Ob-R has been implicated in the pathogenesis of a variety of malignancies; however, its role in DLBCL has not been investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187206.RATWcAPDf65PR8KTukuofuXqIRizX0vu9xcZqJgFD8I5I130_provenance.
NP187208.RAZA5IrVYHbN2D2E6kN4nGX-mmua3vF593AZzV4hut-jU130_assertion description "[In this review the authors discuss the efficacy of DBS in the treatment of dystonia and levodopa-induced dyskinesias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187208.RAZA5IrVYHbN2D2E6kN4nGX-mmua3vF593AZzV4hut-jU130_provenance.
NP187211.RAU8nVJduFsTI-01arx1jTqibzbHakiNg2lUsweQgMKWk130_assertion description "[From the resulting list of candidate genes, six were selected for protein-expression analysis based on the availability of antibodies applicable to paraffinised tissue: fatty acid synthase (FASN), MYC, beta-adrenergic receptor kinase 1 (BARK1, GRK2) the catalytic subunits of protein phosphatases PP1alpha (PPP1CA) and PP2A (PPP2CB) and metastasis suppressor NM23-H1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187211.RAU8nVJduFsTI-01arx1jTqibzbHakiNg2lUsweQgMKWk130_provenance.
NP187213.RAdylTR-ut9C-FDKhzi5mYtW87M9FkNMmiGquTqBVjtiw130_assertion description "[Together they contribute to approximately one-third of acute myelogenous leukemia (AML) and one-quarter of acute lymphoblastic leukemia (ALL) cases, making RUNX1 and CBFbeta the most frequently affected genes known in the pathogenesis of acute leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187213.RAdylTR-ut9C-FDKhzi5mYtW87M9FkNMmiGquTqBVjtiw130_provenance.
NP187224.RAeCyr2xpr4MvurxgSiQCEjrnLeogRS-WuCnX_rxQD0KA130_assertion description "[The speech perception in 9 children with GJB2 gene-related deafness fitted with CI was compared with those in matched 10 children who were diagnosed as having no genetic loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187224.RAeCyr2xpr4MvurxgSiQCEjrnLeogRS-WuCnX_rxQD0KA130_provenance.
NP187229.RAS1f2BMeeuSUfAE3oPxdZFQrFlsUhR_kb7c-Ovt0toQk130_assertion description "[The Trp64Arg variant of the beta3-adrenergic receptor gene is reported to be associated with abdominal obesity and resistance to insulin, and as a consequence, this variant may be a genetic factor in the development of atherosclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187229.RAS1f2BMeeuSUfAE3oPxdZFQrFlsUhR_kb7c-Ovt0toQk130_provenance.
NP187235.RAapecjp-EM1b7fXXEewENd1_ygqEKKdK-84_yGZz5zHA130_assertion description "[The preferred substrates for transglutaminase 2 in a complex wheat gluten digest are Peptide fragments harboring celiac disease T-cell epitopes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187235.RAapecjp-EM1b7fXXEewENd1_ygqEKKdK-84_yGZz5zHA130_provenance.
NP187237.RAQhRQcIwTSJ0J3RYbYesobZ2JZXTSmnvAy81EHGFhdBU130_assertion description "[A type 2C pVHL mutant (V188L), which is associated with a PHE only phenotype (and had been shown previously to retain the ability to promote HIF ubiquitylation), retained the ability to suppress CCND1expression suggesting that loss of pVHL-mediated suppression of cyclin D1 is not necessary for PHE development in VHL disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187237.RAQhRQcIwTSJ0J3RYbYesobZ2JZXTSmnvAy81EHGFhdBU130_provenance.
NP187238.RAZ8aR1nyuLjtXgptdOR7tHTsFgbU8QDwZY-nj4ltzYwU130_assertion description "[Mesenchymal transition and PDGFRA amplification/mutation are key distinct oncogenic events in pediatric diffuse intrinsic pontine gliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187238.RAZ8aR1nyuLjtXgptdOR7tHTsFgbU8QDwZY-nj4ltzYwU130_provenance.
NP187243.RAVPME1vmRTdtZfk566vEvn-C27700BrZosXNwUBw3piI130_assertion description "[In addition to NBs, lower levels of BCL2 protein were also found in a variety of other neural crest-derived tumors and tumor cell lines, including some neuroepitheliomas, Ewing's sarcomas, neurofibromas, and melanomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187243.RAVPME1vmRTdtZfk566vEvn-C27700BrZosXNwUBw3piI130_provenance.
NP187248.RATAURR-wpiJHkflUnphI21U_1khsOFW6veCJaSnlzuO0130_assertion description "[The Ser37Ala (T/G) SNP is associated with BMD and the rate of bone loss in osteoporosis and osteoporosis fractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187248.RATAURR-wpiJHkflUnphI21U_1khsOFW6veCJaSnlzuO0130_provenance.
NP187255.RAWnaIEyWUbhIyQ4Ix4eVl7Nwl17RfigjSLy6zx10vZFc130_assertion description "[Both clinical observations initially appeared to be very similar to WHIM syndrome (Warts, Hypogammaglobulinemia, Infection, Myelokathexis), a rare immunodeficiency disease correlated with CXC chemokine receptor 4 (CXCR4) mutation leading to an impaired internalization of the receptor upon its ligand CXCL12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187255.RAWnaIEyWUbhIyQ4Ix4eVl7Nwl17RfigjSLy6zx10vZFc130_provenance.
NP187261.RATdAcNhEwUQKV66ZrRphKdEKnLGr-OxiZPWuFUxGC2fs130_assertion description "[Fusion of the FUS and ATF1 genes in a large, deep-seated angiomatoid fibrous histiocytoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187261.RATdAcNhEwUQKV66ZrRphKdEKnLGr-OxiZPWuFUxGC2fs130_provenance.
NP187269.RAR7WLzbZIpSJZbiFB8166kO97rtuKWneEr4mCu9BYSLs130_assertion description "[These CD141(+) DDC-like cells can be generated in vitro and, once transferred in vivo, have the capacity to inhibit xeno-graft versus host disease and tumor alloimmunity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187269.RAR7WLzbZIpSJZbiFB8166kO97rtuKWneEr4mCu9BYSLs130_provenance.
NP187271.RAbBLqDnxIX5lqvzkoRlLBVNilSJFedi2b5yqofYlvs50130_assertion description "[Decreased XOR is associated with poorer prognosis in patients with serous ovarian cancer especially in those with an otherwise more favorable prognostic profile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187271.RAbBLqDnxIX5lqvzkoRlLBVNilSJFedi2b5yqofYlvs50130_provenance.
NP187274.RAa6VxZKUr2rcU9l2-WjA1blaP0DySVXuXJWW_yvniu9I130_assertion description "[The current controversy concerning optimal hemoglobin levels in chronic kidney disease patients treated with ESAs and the potential negative clinical outcomes of ESA treatment in cancer reinforces the need for cautious evaluation of the pleiotropic effects of ESAs in non-erythroid tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187274.RAa6VxZKUr2rcU9l2-WjA1blaP0DySVXuXJWW_yvniu9I130_provenance.
NP187277.RAWBYMMQCxelk1YqYlTqQmUo5KfB2J4TuR0zpT6J3HLQM130_assertion description "[Negative or diminished gene expression of DDX3Y, RBMY1, DAZ and TSPY in tissues samples with SCOS or focal SCOS reflects the absence or the lower number of germ cells, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187277.RAWBYMMQCxelk1YqYlTqQmUo5KfB2J4TuR0zpT6J3HLQM130_provenance.
NP187280.RAcz_rwG66eNB3c0_s7h3tvDroUWOt7og1mdN3npLlrZw130_assertion description "[Seventy-four male veterans entering an alcohol abuse treatment program were screened for additional psychiatric diagnoses using the Diagnostic Interview Schedule (DIS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187280.RAcz_rwG66eNB3c0_s7h3tvDroUWOt7og1mdN3npLlrZw130_provenance.
NP187288.RAQ_6Iz5fJsiG2XpQQwUvBrfcaH_ofZw2fa9ZFCbTA-Lk130_assertion description "[Among the most significantly differentially expressed genes between ALK+ and ALK- samples, we found BCL6, PTPN12, CEBPB, and SERPINA1 genes to be overexpressed in ALK+ ALCL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187288.RAQ_6Iz5fJsiG2XpQQwUvBrfcaH_ofZw2fa9ZFCbTA-Lk130_provenance.
NP187289.RAZW_JXZnMhY6rf9xA52XCqZr7P1SSJdIn_bsPpB3HplQ130_assertion description "[Involvement of transporter associated with antigen processing 2 (TAP2) gene polymorphisms in hepatitis C virus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187289.RAZW_JXZnMhY6rf9xA52XCqZr7P1SSJdIn_bsPpB3HplQ130_provenance.
NP187290.RARWVGm3ClXfgbjzw6uMo-JTy8mKjVT98BKLurOYYpEQU130_assertion description "[Treatment of Ptf1a(cre/+) ;LSL-Kras(G12D/+) ;Tgfbr2(flox/flox) mice with the JNK inhibitor decreased growth of murine pancreatic cancer and prolonged survival of the mice significantly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187290.RARWVGm3ClXfgbjzw6uMo-JTy8mKjVT98BKLurOYYpEQU130_provenance.
NP187294.RAbCk1GN6Ac6IDgnQ9WfZ6NCxronUnZurJWVMKs7I8Bbo130_assertion description "[This unusual alpha1 globin variant clearly causes alpha thalassemia, but the unexpectedly severe phenotype suggests that this mutation may have additional effects on red cell physiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187294.RAbCk1GN6Ac6IDgnQ9WfZ6NCxronUnZurJWVMKs7I8Bbo130_provenance.
NP187296.RAYp47LJiP0ODxvqrVMi_q1eZL2uylAoPSjfAoG3kRFew130_assertion description "[We found that TRIOBP, a cytoskeleton-associated protein mutated in human hereditary deafness DFNB28, is localized to rootlets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187296.RAYp47LJiP0ODxvqrVMi_q1eZL2uylAoPSjfAoG3kRFew130_provenance.
NP187297.RASBRifWL6Qr2_1NKRuD6KnGfqQtwkQMMylKhL7WLkans130_assertion description "[Some of its features, including choreic movements, peripheral neuropathy with areflexia, elevated serum creatine kinase levels and myopathy are shared by another form of neuroacanthocytosis, McLeod syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187297.RASBRifWL6Qr2_1NKRuD6KnGfqQtwkQMMylKhL7WLkans130_provenance.
NP187298.RAeIfnb7s9qVUIgDwpkTCi1XZGyVlf_RM2fmOF6c4l0PE130_assertion description "[We established two mouse models of human MCL by subcutaneous xenotransplantation of JEKO-1 and HBL-2 cell lines into immunodeficient mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187298.RAeIfnb7s9qVUIgDwpkTCi1XZGyVlf_RM2fmOF6c4l0PE130_provenance.
NP187300.RAUBOyfdSrySRhjW64WDpKEIZf8MtXzAhmr89IURvJqbc130_assertion description "[A novel PSEN1 gene mutation (L235R) associated with familial early-onset Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187300.RAUBOyfdSrySRhjW64WDpKEIZf8MtXzAhmr89IURvJqbc130_provenance.
NP187305.RASs31a_uES1iCIIx6M4gd3cLc6XnLb69qG6KjSqvbcok130_assertion description "[The -1,031C and -863A alleles, in the absence of the HLA B61 or the DRB1*0901 allele which is in linkage disequilibrium with these alleles, were associated with increased susceptibility to HU.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187305.RASs31a_uES1iCIIx6M4gd3cLc6XnLb69qG6KjSqvbcok130_provenance.
NP187311.RAbL4I_WT4Du8AN4oSCorLrZIEPx3NlTS5I-MuMpRzFPw130_assertion description "[The deletions of Rb, ARHI, and FAT, as well as amplification of N-myc, FASL, GITRL, and EGFR, may be the crucial factors for tumorigenesis and the aggressive biological behavior of PPNET.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187311.RAbL4I_WT4Du8AN4oSCorLrZIEPx3NlTS5I-MuMpRzFPw130_provenance.
NP187312.RARgVfpD2c11IVwn3Ecw3tyDg8z4GpsB2y_k_EnIfTYB4130_assertion description "[Vitamin D receptor (VDR) gene variants have been variably associated with risk of colon cancer in epidemiologic studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187312.RARgVfpD2c11IVwn3Ecw3tyDg8z4GpsB2y_k_EnIfTYB4130_provenance.
NP187322.RAXqTKPbOhn5MSbCdkhMpTnY4M6ry-2IfEz1uzYcHAsm8130_assertion description "[These data suggest that AM may act as a new member of adipokines, although its functional role, as well as its pathophysiological significance in obesity, remains to be determined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187322.RAXqTKPbOhn5MSbCdkhMpTnY4M6ry-2IfEz1uzYcHAsm8130_provenance.
NP187340.RAV-CnqWmqp2349FqTtqywQuDLhaq4YKNWAGodRGR8Fvw130_assertion description "[By using HBV-Alu PCR, we have now isolated, from nine hepatocellular carcinomas, nine HBV-DNA integration sites showing that the viral genome mutates key regulatory cellular genes: neurotropic tyrosin receptor kinase 2 (NTRK2) gene, IL-1R-associated kinase 2 (IRAK2) gene, p42 mitogen-activated protein kinase 1 (p42MAPK1) gene, inositol 1,4,5-triphosphate receptor type 2 (IP3R2) gene, inositol 1,4,5-triphosphate receptor (IP3R) type 1 (IP3R1) gene, alpha 2,3 sialyltransferase (ST3GAL VI or SITA) gene, thyroid hormone uncoupling protein (TRUP) gene, EMX2-like gene, and human telomerase reverse transcriptase (hTERT) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187340.RAV-CnqWmqp2349FqTtqywQuDLhaq4YKNWAGodRGR8Fvw130_provenance.
NP187341.RAYib3iB4TrUyC2IMLRK-_H_E4XhGJk7rOuPu2A8LP5J8130_assertion description "[Several mutations in presenilin 1 (PSEN1), presenilin 2 (PSEN2), and amyloid-beta precursor protein are involved in the etiology of familial AD (FAD); these mutations alter the Abeta(42/40) ratio and promote apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187341.RAYib3iB4TrUyC2IMLRK-_H_E4XhGJk7rOuPu2A8LP5J8130_provenance.
NP187350.RAWNvCBNnN5lS9caDE2O-RvYct9p0aAqOkT_LWZpFc8jU130_assertion description "[To examine the expression level and function of follistatin-related protein gene (FRP, also referred to as FSTL1) in rheumatoid arthritis (RA), and possible association of its polymorphisms with genetic susceptibility to RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187350.RAWNvCBNnN5lS9caDE2O-RvYct9p0aAqOkT_LWZpFc8jU130_provenance.
NP187352.RAU9vQD-mVrlBijtIXJqQsw0iyRQMCrQ3BK0RsM-N0DS8130_assertion description "[GSTT1 and CYP2E1 polymorphisms and trihalomethanes in drinking water: effect on childhood leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187352.RAU9vQD-mVrlBijtIXJqQsw0iyRQMCrQ3BK0RsM-N0DS8130_provenance.
NP187353.RAXTrwWzlw1fcOrqhcYMsfoVEELaE6znN-tZu_ACDwl8o130_assertion description "[Serum TNF-alpha was higher in unused (8.72+/-1.3 pg/mL, n=13) than in used (6.12+/-0.8 pg/mL, n=25, P:<0.05) donors and HF (4.0+/-0.4 pg/mL, n=17, P:<0.005).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187353.RAXTrwWzlw1fcOrqhcYMsfoVEELaE6znN-tZu_ACDwl8o130_provenance.
NP187358.RAR2brfC1HDu-X5ItwCbPDUXHywMvFi_fNLihtXgKjYxs130_assertion description "[Present data suggest that an insertion/deletion polymorphism in the promoter region of the NQO2 gene plays an important role in the pathogenesis of alcoholism and alcohol withdrawal symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187358.RAR2brfC1HDu-X5ItwCbPDUXHywMvFi_fNLihtXgKjYxs130_provenance.
NP187360.RAR0evCm502fuQfLn9fpjBiDrJ62ZgW95Dwz0S1I0gXpM130_assertion description "[The expression of AT2R mRNA in human CAKUT was established for the first time and was not affected by -1332A/G polymorphism in children with CAKUT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187360.RAR0evCm502fuQfLn9fpjBiDrJ62ZgW95Dwz0S1I0gXpM130_provenance.
NP187362.RATmfBJw2SPMfWq5UHyAuv-Ox4RQjyFBEsmJPCYK5B6yg130_assertion description "[Since heterozygote females might develop the symptoms of G6PD deficiency later, these results suggest that the G6PD neonatal screening may not be helpful in preventing disease in females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187362.RATmfBJw2SPMfWq5UHyAuv-Ox4RQjyFBEsmJPCYK5B6yg130_provenance.
NP187363.RAZC8QRK5aavBdcaiFclddPCzVlZ-0yKtkhcPlfYk7avc130_assertion description "[These findings suggest that E185Q polymorphism in NBS1 may be a genetic modifier for developing ALL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187363.RAZC8QRK5aavBdcaiFclddPCzVlZ-0yKtkhcPlfYk7avc130_provenance.
NP187366.RASa1brgXziKgpwgAeQX9Fj9S5z7-mpV9rCx8Ke7WXdCo130_assertion description "[More recently, additional mutations in the exon 12 of the JAK2 gene have been described in 5 to 10% of the patients with erythrocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187366.RASa1brgXziKgpwgAeQX9Fj9S5z7-mpV9rCx8Ke7WXdCo130_provenance.
NP187369.RAT-D16UOvPEIbD_qMhHhu92V-l_QrPfSklZTFWQA5Uw0130_assertion description "[Finally, PrpL cleaves casein, lactoferrin, transferrin, elastin, and decorin and contributes to PAO1's ability to persist in a rat chronic pulmonary infection model .]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187369.RAT-D16UOvPEIbD_qMhHhu92V-l_QrPfSklZTFWQA5Uw0130_provenance.
NP187370.RASwHv2kVC0hoEajsTId5wnOGUOeJ67cI0HWJXkUV7tZI130_assertion description "[Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy disease) results from the deficient activity of the lysosomal enzyme, arylsulfatase B (ASB; N-acetylgalactosamine-4-sulfatase E.C.3.1.6.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187370.RASwHv2kVC0hoEajsTId5wnOGUOeJ67cI0HWJXkUV7tZI130_provenance.
NP187371.RAZIode373m86IZHOHmCLM_ptU4eE77420h0aGCQF5FiA130_assertion description "[Whether inefficient fat digestion or another property of colipase contributes to the risk for developing diabetes remains to be clarified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187371.RAZIode373m86IZHOHmCLM_ptU4eE77420h0aGCQF5FiA130_provenance.
NP187378.RAegGj47Nqa7fn-7lx4Ikp8r4tWwmldUv7yUBWMKFEPNM130_assertion description "[Primary lung disease in children homoallelic for L444P mutation in GBA gene emerges as a significant clinical manifestation of GD with unclear response to ERT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187378.RAegGj47Nqa7fn-7lx4Ikp8r4tWwmldUv7yUBWMKFEPNM130_provenance.
NP187380.RAV-Ltm0hctDU8zlxo7Ljp0ZyPF0kA_Ad3kIBumGSTazw130_assertion description "[We investigated p53 and its downstream effectors p21WAF1/CIP1, BAX, and hMSH2 as well as the proliferation marker Ki-67 (mki-67/MIB-1) in patients undergoing preoperative radiochemotherapy for rectal carcinoma to identify prognostic and predictive factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187380.RAV-Ltm0hctDU8zlxo7Ljp0ZyPF0kA_Ad3kIBumGSTazw130_provenance.
NP187381.RAUEmBbrSugPfzyGqmnPegZjmAPOfOzArx6_snPEpZreA130_assertion description "[As G-6-PD deficiency is associated with increased hemolysis, we hypothesized that in G-6-PD-deficient neonates who also have the (TA)7/(TA)7 UGT promoter genotype, steady-state hemolysis would be even further increased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187381.RAUEmBbrSugPfzyGqmnPegZjmAPOfOzArx6_snPEpZreA130_provenance.
NP187391.RAVJaji2dDVKwtGiNOg43Yi0S6C9TswFVF1sdx52ezXI4130_assertion description "[Leukosialin, a major O-glycan-containing sialoglycoprotein defining leukocyte differentiation and malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187391.RAVJaji2dDVKwtGiNOg43Yi0S6C9TswFVF1sdx52ezXI4130_provenance.
NP187393.RAdqK8tzn5i-ZUzX64T0Hhgkn4PA2ZpB2Y_jFd5F6GOk8130_assertion description "[Enhanced and prolonged expression of connective tissue growth factor (CTGF) is associated with kidney fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187393.RAdqK8tzn5i-ZUzX64T0Hhgkn4PA2ZpB2Y_jFd5F6GOk8130_provenance.
NP187404.RAYnFMRWb9EwKFTINCAt7iV1hB1EaKcHG1E6xaekij1pE130_assertion description "[Our genetic and functional analyses indicate that germline mutations in SUFU also predispose to meningiomas, particularly to multiple meningiomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187404.RAYnFMRWb9EwKFTINCAt7iV1hB1EaKcHG1E6xaekij1pE130_provenance.
NP187406.RAeoWrFP4Eg_wRJWx112tSZtLdWNDDMkSHdR1Al410SJI130_assertion description "[Gray horses carrying a loss-of-function mutation in ASIP (agouti signaling protein) had a higher incidence of melanoma, implying that increased melanocortin-1 receptor signaling promotes melanoma development in Gray horses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187406.RAeoWrFP4Eg_wRJWx112tSZtLdWNDDMkSHdR1Al410SJI130_provenance.
NP187407.RAUuCCxX2wXzVTUl8IzWl8jZQy6ewjQXTY4hngjl_TE34130_assertion description "[Arginine 16 glycine beta2-adrenoceptor polymorphism and cardiovascular structure and function in patients with heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187407.RAUuCCxX2wXzVTUl8IzWl8jZQy6ewjQXTY4hngjl_TE34130_provenance.
NP187408.RAXpUp4utCsX71fHwxeBFQ9-zVE1T2jFua4jTNYCXGybQ130_assertion description "[A cell line, designated ISOS-1, was established from a tumor formed by transplantation of a human angiosarcoma into mice with severe combined immunodeficiency (SCID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187408.RAXpUp4utCsX71fHwxeBFQ9-zVE1T2jFua4jTNYCXGybQ130_provenance.
NP187411.RAXC3DxDTsUbL1qG3FYJDidTr0Fu5WPKPWoQ2Y1kuWjhA130_assertion description "[Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187411.RAXC3DxDTsUbL1qG3FYJDidTr0Fu5WPKPWoQ2Y1kuWjhA130_provenance.
NP187412.RAcB6ACwTpjhbzo609AuvArMz4mcmuLMzNRlm1oP6dJkM130_assertion description "[Archival tumour material was analysed from 16 patients with CDH1 germline mutations and seven patients fulfilling HDGC criteria without CDH1 germline mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187412.RAcB6ACwTpjhbzo609AuvArMz4mcmuLMzNRlm1oP6dJkM130_provenance.
NP187413.RAbMhX_7WWbSIoyQ4Us5ijpEVFG0hQcyT0UX5QgHlzuPE130_assertion description "[No association was found between IL-8 -251 A/T genotypes and IL-8 mRNA expression in tumour and corresponding normal mucous tissue, as well as susceptibility to sporadic colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187413.RAbMhX_7WWbSIoyQ4Us5ijpEVFG0hQcyT0UX5QgHlzuPE130_provenance.
NP187418.RAZKlOogYnngbHhShemis2mgHepaM1A5nJC_LA6EV8GIc130_assertion description "[alpha-Fetoprotein mRNA in the circulation as a predictor of postsurgical recurrence of hepatocellular carcinoma: a prospective study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187418.RAZKlOogYnngbHhShemis2mgHepaM1A5nJC_LA6EV8GIc130_provenance.
NP187419.RAW4je1UuPRNpDvzzVK7Zc2yOcEakCokZtdWT4YPg2eu4130_assertion description "[The beta-87/VIII showed a configuration of rare polymorphisms in the 5' sub-haplotype, which have been reported to exert an increasing effect on Hb F. They were `T`-158 (G)gamma-globin gene, T-A-G in pre-(G)gamma framework, (TG)(11)(CG)(3) in the (G)gamma-IVS2, (AT)(9)N(12)(AT)(10) in LCR-HS2; in contrast, the haplotype V had, respectively, `C`, T-G-A (TG)(19)(CG)(2)CACG in the (G)gamma-IVS2, and (AT)(10)N(12)(AT)(11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187419.RAW4je1UuPRNpDvzzVK7Zc2yOcEakCokZtdWT4YPg2eu4130_provenance.
NP187423.RAR534CTNPmmNXnZA6TfnjdHv380p_AmIY-PMCFvleoJ8130_assertion description "[Dysfunction of FOXP3 gene product could result in lack of Treg cells and subsequently chronically activated CD4+ T cells which express increased levels of several activation markers and cytokines, resulting in some autoimmune diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187423.RAR534CTNPmmNXnZA6TfnjdHv380p_AmIY-PMCFvleoJ8130_provenance.
NP187428.RAYLhLER70mGLyAL8JJbfY81w8SianbRtNgKUAJUyKpR0130_assertion description "[Using a yeast based p53 functional assay we previously demonstrated that the UVC-induced p53 mutation spectrum appears to be indistinguishable from the one observed in Non Melanoma Skin Cancer (NMSC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP187428.RAYLhLER70mGLyAL8JJbfY81w8SianbRtNgKUAJUyKpR0130_provenance.

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