Nanopublications

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

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NP220917.RArkMarPqvNRQtdIyjSvol2Q0J5JRnzJbLvs9uvtvwtAA130_assertion description "[A 9-bp deletion (2320del9) was detected in the arylsulfatase A genes of a patient with late infantile metachromatic leukodystrophy and of a patient with nonprogressive neurological symptoms and very low arylsulfatase A activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220917.RArkMarPqvNRQtdIyjSvol2Q0J5JRnzJbLvs9uvtvwtAA130_provenance.
NP220919.RAuZEZ2DrTVGEGMQIOvSbCmqC7gjt53Lula-Nw9mBs13I130_assertion description "[Furthermore, FLT3 mutated ETP-ALL was characterized by a specific immunophenotype (CD2+/CD5-/CD13+/CD33-), a distinct gene expression pattern (aberrant expression of IGFBP7, WT1, GATA3) and mutational status (absence of NOTCH1 mutations and a low frequency, 21%, of clonal TCR rearrangements).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220919.RAuZEZ2DrTVGEGMQIOvSbCmqC7gjt53Lula-Nw9mBs13I130_provenance.
NP220935.RAjNIu386uMrfCfulaZa8hyuhlYflB66-W24EDLnaCNUE130_assertion description "[BDNF directly induced N-methyl-D-aspartate currents in dentate granule cells of TLE patients with HS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220935.RAjNIu386uMrfCfulaZa8hyuhlYflB66-W24EDLnaCNUE130_provenance.
NP220943.RAu-i_OvU-bKAp3R5MwyMSQk7NXbwKNL8SyWjU2mLL_lA130_assertion description "[In a study of 120 asthmatic children cared for in a single pediatric pulmonary practice, intensity of medical treatment over the year prior was modeled as a function of null mutations of glutathione S transferase (GST) M1 and T1, ile105val variant of GSTP1, and pro187ser variant of NAD(P)H:quinone oxidoreductase 1 (NQO1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220943.RAu-i_OvU-bKAp3R5MwyMSQk7NXbwKNL8SyWjU2mLL_lA130_provenance.
NP220944.RAk-QIm97_jDIzS-CQgL71sIY7vll6Ot1hxTyoUhR2XUk130_assertion description "[Mutations in the genes encoding the tumour necrosis factor (TNF) superfamily receptors transmembrane activator and calcium-modulating ligand interactor (TACI) and B cell activation factor of the TNF family receptor (BAFF-R), CD19 and the co-stimulatory molecule inducible co-stimulator molecule (ICOS) all lead to CVID and illustrate the complex interplay required to co-ordinate an effective humoral immune response.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220944.RAk-QIm97_jDIzS-CQgL71sIY7vll6Ot1hxTyoUhR2XUk130_provenance.
NP220945.RAooHc4LWm3NaBv4LLFi6lSGL39MidpGlEjx5GA7jE4C0130_assertion description "[Then, to examine whether t(2;5)(p23;q35) was present on biopsied lymphomas, reverse transcriptase-polymerase chain reaction (RT-PCR) covering the fusion junction of p80 mRNA was performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220945.RAooHc4LWm3NaBv4LLFi6lSGL39MidpGlEjx5GA7jE4C0130_provenance.
NP220946.RAsKkgj18HimprACbnpKu-_m25ORDAOcghkU66xYRT5JM130_assertion description "[The multivariate logistic regression showed that HPV viral load was associated with an increased odds of LSIL/HSIL, odds ratio of 10.7 (95% CI 2.0 - 57.7) for those that were HC2 positive and had a viral load of <or= 181.1 RLU (the median HPV viral load), and 33.8 (95% CI 6.4 - 178.9) for those that were HC2 positive with a HPV viral load > 181.1 RLU.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220946.RAsKkgj18HimprACbnpKu-_m25ORDAOcghkU66xYRT5JM130_provenance.
NP220948.RAhSelNYY6h8_Wq-m4Dt6T9nUuQLMTvTbzHmouAtcAQMQ130_assertion description "[The mild iron overload associated with heterozygosity for C282Y HFE mutation confers susceptibility to nonalcoholic fatty liver disease, causing relative insulin deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220948.RAhSelNYY6h8_Wq-m4Dt6T9nUuQLMTvTbzHmouAtcAQMQ130_provenance.
NP220950.RAlHBnlu1x9g9V9n3YLy_h8KXBshVZhdvPxCZYWmmXXwA130_assertion description "[In our previous study, we found a higher expression of pY307-PP2A in HER-2/neu positive breast tumour samples and significantly correlated to tumour progression, and in this context, it could function as a proto-oncogene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220950.RAlHBnlu1x9g9V9n3YLy_h8KXBshVZhdvPxCZYWmmXXwA130_provenance.
NP220959.RAklDLcIKqGF7NycVVgWNPahN17B65JQZolQEPEmYds1Y130_assertion description "[The human transcription factors (TFs) GATA4, NKX2.5 and TBX5 form part of the core network necessary to build a human heart and are involved in Congenital Heart Diseases (CHDs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220959.RAklDLcIKqGF7NycVVgWNPahN17B65JQZolQEPEmYds1Y130_provenance.
NP220960.RAh8RGKEZeLBLQ_2gTwhqGtpTiV1o1-UX2gJtWrMNWTc8130_assertion description "[Susceptibility to a variety of malignancies has been linked to human leukocyte antigen (HLA) genes, including the HLA class II allele DQB1*0301.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220960.RAh8RGKEZeLBLQ_2gTwhqGtpTiV1o1-UX2gJtWrMNWTc8130_provenance.
NP220975.RAqa7YRBIqSntcy2h-gqaSr67crrDhNaqqEDiGe797HSw130_assertion description "[The UGT2B15 allele exhibits 2-fold decreased activity for dihydrotestosterone, which was suggested to be associated with the risk of prostate cancer based on in vitro functional analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220975.RAqa7YRBIqSntcy2h-gqaSr67crrDhNaqqEDiGe797HSw130_provenance.
NP220977.RArLRiDkeXrUrkNSbutxDBR2SstP4Iw1dg8HHyzW4Rnv8130_assertion description "[These studies suggest that endogenous PF4 release may have biologic consequences for APC generation and survival in clinical sepsis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220977.RArLRiDkeXrUrkNSbutxDBR2SstP4Iw1dg8HHyzW4Rnv8130_provenance.
NP220978.RAlEkbhTOSc8O9V0lAypqAixkYVHqDzPXqcDkM3fDC5wA130_assertion description "[The LPL G allele frequency was also lower in ischemic stroke patients (5.2%) vs. controls (10.7%, p<0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220978.RAlEkbhTOSc8O9V0lAypqAixkYVHqDzPXqcDkM3fDC5wA130_provenance.
NP220990.RAuZsZpD9ZtzUHF9y0biz7Vr16Agay5jvmUtUrjsNQE1A130_assertion description "[We also analyzed ACSL4 and DLG3, which have previously been known to cause XLMR and IL1RAPL2, a homologous gene for IL1RAPL1 that is mutated in autism and XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220990.RAuZsZpD9ZtzUHF9y0biz7Vr16Agay5jvmUtUrjsNQE1A130_provenance.
NP220991.RAg3TsFBSfcMkstzTUl_ZdI0PwUzW_Ti5wTMO_JzMgv1c130_assertion description "[Our findings further illustrate the role of BDNF genetic variants in drug abuse and dependence and this study will help to identify who are at risk of becoming heroin dependence in the future and decide the more appropriate timing that interventions should be taken in the high-risk groups.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220991.RAg3TsFBSfcMkstzTUl_ZdI0PwUzW_Ti5wTMO_JzMgv1c130_provenance.
NP220993.RAhLG3QwsCnkgpCH-MHA6Wco5kY702tKS-1jhIlSeK-CQ130_assertion description "[We report a rare case of intractable frontal lobe epilepsy with mental deterioration, in which the measles virus gene was detected from the cerebrospinal fluid (CSF) and peripheral mononuclear cells (PBMC) obtained 9 years after the first epileptic episode using reverse transcriptase-polymerase chain reaction (RT-PCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220993.RAhLG3QwsCnkgpCH-MHA6Wco5kY702tKS-1jhIlSeK-CQ130_provenance.
NP220997.RAhv38UfQ_vmQebbdG61ux6z9GueSSAdSPOh___yzOodA130_assertion description "[Prostate-specific membrane antigen (PSMA) is a potential target in prostate cancer patients because it is very highly expressed and because it has been reported to be upregulated by androgen deprivation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220997.RAhv38UfQ_vmQebbdG61ux6z9GueSSAdSPOh___yzOodA130_provenance.
NP220998.RAn-Vxq0Jw-VJWiwB-AUZHL4_k-XKEOrsHc7Nzb3KnKQM130_assertion description "[In order to determine the expression profile of MMR genes in impaired human spermatogenesis, we performed transcript levels analysis of MMR genes (MLH1, MLH3, PMS2, MSH4, and MSH5), and other meiosis-involved genes (ATR, HSPA2, and SYCP3) as controls, by real-time reverse transcription-polymerase chain reaction in testis from 13 patients with spermatogenic failure, 5 patients with primary germ cell tumors, and 10 controls with conserved spermatogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220998.RAn-Vxq0Jw-VJWiwB-AUZHL4_k-XKEOrsHc7Nzb3KnKQM130_provenance.
NP220999.RAm2miG7iRsvbTjE4z8FvmCshMJPI25d4r3Bcmvl73cK8130_assertion description "[Based on the available NF2 mutation data, the most dominant influence on the spectra of mutations in exons 1-15 are C>T transitions that change arginine codons (CGA) to stop codons (TGA) due to spontaneous deamination of methylcytosine to thymine in CpG dinucleotides.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220999.RAm2miG7iRsvbTjE4z8FvmCshMJPI25d4r3Bcmvl73cK8130_provenance.
NP221004.RAvcMoCLRhHUeHPv_dL6AGGbRPQaGe_vcc1tr6hdCJrjM130_assertion description "[Familial dysalbuminemic hyperthyroxinemia (FDH) is a familial autosomal dominant syndrome caused by abnormal albumin with an increased affinity for thyroxine (T4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221004.RAvcMoCLRhHUeHPv_dL6AGGbRPQaGe_vcc1tr6hdCJrjM130_provenance.
NP221006.RAtKMC-E3md8yGEC9PZtBBTXEwcVlsbMm4vMfSu3qgpeo130_assertion description "[A NUP98-positive acute myeloid leukemia with a t(11;12)(p15;q13) without HOXC cluster gene involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221006.RAtKMC-E3md8yGEC9PZtBBTXEwcVlsbMm4vMfSu3qgpeo130_provenance.
NP221007.RAp-8Eihgo3T3CqCSWJiMSzy7sGIUuYGXA6cdX44LZmd0130_assertion description "[Thus, EGFR mutations can be implicated in carcinogenesis of lung adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221007.RAp-8Eihgo3T3CqCSWJiMSzy7sGIUuYGXA6cdX44LZmd0130_provenance.
NP221011.RAjSgipGUKGH0Tq_w8ylMITiqX4_NVFHZ8Ke5ZdSNLn2Q130_assertion description "[We report a novel homozygous missense mutation in exon 15 (c.2039C>G, HK [hexokinase] Utrecht) of HK1, the gene that encodes red blood cell-specific hexokinase-R, in a patient previously diagnosed with hexokinase deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221011.RAjSgipGUKGH0Tq_w8ylMITiqX4_NVFHZ8Ke5ZdSNLn2Q130_provenance.
NP221012.RAmsad5f57zNH3J4yWu3UYXIoPMOh7vvMlzV6DmBut4QA130_assertion description "[The notable features of this case include the consequences of non-concordance with treatment, the use of continuous subcutaneous insulin infusion to treat insulin-resistant diabetes and the need for repeated plasmapheresis during pregnancy to avert pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221012.RAmsad5f57zNH3J4yWu3UYXIoPMOh7vvMlzV6DmBut4QA130_provenance.
NP221013.RAkRiK23_PaC-BC5Mmq7C-u6oBtC-Rcp5DhXW017YgAr4130_assertion description "[Deficit in stimulus filtering, an endophenotype of schizophrenia, can be demonstrated using the auditory P50 paired-click gating paradigm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221013.RAkRiK23_PaC-BC5Mmq7C-u6oBtC-Rcp5DhXW017YgAr4130_provenance.
NP221021.RAgZ4VAtqDIci0c4mh5kgVM2OfQsAxxoUSnFKVEGA0PuQ130_assertion description "[Taken together, these results imply that the basic amino acids at position 13, which is present only on the DR2 and DR4 B1 molecules (Arg on DR2 and His on DR4), are most important for determining the predisposition to autoimmune hepatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221021.RAgZ4VAtqDIci0c4mh5kgVM2OfQsAxxoUSnFKVEGA0PuQ130_provenance.
NP221025.RAjrIi9RLqLB7Oc_JxAFPUQ4DedEvPDUZE4IgQXq-0JLQ130_assertion description "[In light of studies investigating polymorphisms in SHBG and T2DM, our group and others have hypothesized that SHBG may represent a candidate gene for PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221025.RAjrIi9RLqLB7Oc_JxAFPUQ4DedEvPDUZE4IgQXq-0JLQ130_provenance.
NP221030.RAo1hYA5jyOx7U3_TAETk9Ajh1Lf9K8F4vq9dRwnV4-lc130_assertion description "[miR-192 overexpression increased tumor volume in an orthotopic pancreatic cancer mouse model, coupled with suppression of SIP1 and elevation of collagen I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221030.RAo1hYA5jyOx7U3_TAETk9Ajh1Lf9K8F4vq9dRwnV4-lc130_provenance.
NP221036.RAmaqEtNBkZPWNjZ5W6mdts988BE81qjlUVS9nG4ZOBtU130_assertion description "[This study examines NT secretion, NT receptor and NT-growth responses in androgen-independent prostatic carcinoma (PC3) cells derived from prostate adenocarcinoma metastatic to bone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221036.RAmaqEtNBkZPWNjZ5W6mdts988BE81qjlUVS9nG4ZOBtU130_provenance.
NP221042.RAnt6-m1cM8I0mQelVPPKDEPulGG1DFBLJ85m7Zs2vZBc130_assertion description "[Therefore, decitabine-induced expression of cell growth controlling genes such as NKX3.1 or PMEPA1 underlines the clinical applicability of decitabine in prostate tumors harboring wild type androgen receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221042.RAnt6-m1cM8I0mQelVPPKDEPulGG1DFBLJ85m7Zs2vZBc130_provenance.
NP221045.RAi0yEMg8aPbvg0Qe9EUuUQELRk_fT0XwDpf2jgtcr9iY130_assertion description "[Gene-gene interactions between the homozygous RA-risk PADI4 haplotype and SE alleles were significant in both anti-CCP-positive (AP 0.45, 95% CI 0.20 to 0.71) and -negative RA (AP 0.61, 95% CI 0.29 to 0.92).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221045.RAi0yEMg8aPbvg0Qe9EUuUQELRk_fT0XwDpf2jgtcr9iY130_provenance.
NP221049.RAlhEnAhWBnccDJ_PdnUdAclYHL4yCkxN2NfsUpnyZpB8130_assertion description "[Macrophage migration inhibitory factor (MIF) expression in human malignant gliomas contributes to immune escape and tumour progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221049.RAlhEnAhWBnccDJ_PdnUdAclYHL4yCkxN2NfsUpnyZpB8130_provenance.
NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_assertion description "[We conclude that this kindred demonstrates a considerable overlap between cerebellar ataxia and spastic paraplegia, emphasizing the marked clinical heterogeneity of HSP associated with spastin mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221054.RAv_etp6bnhWkdUP7h2UVn9j41Re75hS2roo7Ppx2Vax4130_provenance.
NP221057.RAr2JUID6sDpwwKXLX6yi71ELF1216G-6ZJ0UJRNfy7yc130_assertion description "[Our study shows that (i) RT-PCR is the most effective approach for the detection of t(12;21) in childhood ALL, (ii) the association of ETV6/AML1 and chromosome 12 and/or 21, seen in 56% of our cases, further confirms existing data, (iii) overall survival of patients with t(12;21) was not better than other cytogenetics groups, and (d) MRD analysis using ETV6/AML1 fusion is specific, but not sensitive enough to avoid false negative results.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221057.RAr2JUID6sDpwwKXLX6yi71ELF1216G-6ZJ0UJRNfy7yc130_provenance.
NP221058.RAga2NRz5n601Se7s6nf23IJn0QWL5cPTOviZJf1i-J6E130_assertion description "[Analysis of the DG10S478 microsatellite, which is outside the 4.3-kb LD block, revealed consistent association of risk allele 8 with type 2 diabetes (odds ratio [OR] = 1.33; P = 0.022) as reported in European populations; however, allele 16 (MAF = 0.016 cases and 0.032 controls) was strongly associated with reduced risk (OR = 0.39; P = 5.02 × 10(-5)) in contrast with previous studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221058.RAga2NRz5n601Se7s6nf23IJn0QWL5cPTOviZJf1i-J6E130_provenance.
NP221060.RAnoNkjDd6T-pTsWpT1O0sDxqe3XoaEApelSazpL7VNlk130_assertion description "[Thus, our study concludes a possible protective influence of distinct polymorphisms in genes involved in GH1 release on breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221060.RAnoNkjDd6T-pTsWpT1O0sDxqe3XoaEApelSazpL7VNlk130_provenance.
NP221063.RAtBPRI9p2GZL3bi4C8qOu656QUd3-m3INQ-XQkRkwflk130_assertion description "[Deletions within the dystrophin gene (DMD) account for >70% of mutations leading to Duchenne and Becker muscular dystrophies (DMD and BMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221063.RAtBPRI9p2GZL3bi4C8qOu656QUd3-m3INQ-XQkRkwflk130_provenance.
NP221069.RAmXl9qXJr2dyjegVhMxzVex48YjaJmars21CQuOF1Ems130_assertion description "[In this work, esiRNAs (endoribonuclease-prepared siRNAs) targeting all of the four open reading frames (ORFs) of HBV genome were prepared.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221069.RAmXl9qXJr2dyjegVhMxzVex48YjaJmars21CQuOF1Ems130_provenance.
NP221072.RAnBIEq-UaKicDB7qUpd8FCeR_BgWKFSuwPg8Lbzg9x-8130_assertion description "[Cellular uptake was studied by flow cytometry and cytotoxicity in 96-h 96-well cultures in cell lines overexpressing Pgp, MRP-1 or wild type (BCRP(R482)) or mutant (BCRP(R482T), BCRP(R482G)) BCRP and in pre-treatment AML marrow cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221072.RAnBIEq-UaKicDB7qUpd8FCeR_BgWKFSuwPg8Lbzg9x-8130_provenance.
NP221073.RAiRgLEjvjxiLxsyQJIDpl2TqRE1Og2Am_WNvYI4YRyFs130_assertion description "[Differential hypermethylation of SOCS genes in ovarian and breast carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221073.RAiRgLEjvjxiLxsyQJIDpl2TqRE1Og2Am_WNvYI4YRyFs130_provenance.
NP221076.RAjZlmQLypDAN98QpRzxS99W-L7BsZt_D3YZeJVL1w918130_assertion description "[To identify a gp100 epitope restricted by the MHC class II allele with the highest prevalence in patients with malignant melanoma (HLA-DRB1*0401), we immunized mice transgenic for a chimeric human-mouse class II molecule (DR4-IE) with recombinant human gp100 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221076.RAjZlmQLypDAN98QpRzxS99W-L7BsZt_D3YZeJVL1w918130_provenance.
NP221077.RAnraOsGPeoiVoaZEum-zt9IvMw1QnH00BgijfDVj3hNU130_assertion description "[Cyclooxygenase (COX2) expression in primary breast cancer correlates with a worse prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221077.RAnraOsGPeoiVoaZEum-zt9IvMw1QnH00BgijfDVj3hNU130_provenance.
NP221082.RAhV2A8I_EwwIaSxMDsxVgnYfwhe7y81SOPP-8L8MGMdk130_assertion description "[The eventual development of proximal weakness led to pathological and genetic testing which identified a A8344G mutation in the mitochondrial tRNA lysine gene, associated with MERRF (myoclonic epilepsy with ragged-red fibers).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221082.RAhV2A8I_EwwIaSxMDsxVgnYfwhe7y81SOPP-8L8MGMdk130_provenance.
NP221088.RAnOBhyRW5pHwMQeSbUa8mfh2lNtXhqpQJMK_DCtcq_d0130_assertion description "[In ectopic and orthotopic mouse models of colorectal cancer, bone marrow-derived CD11b(Itgam)(+)Jagged2 (Jag2)(+) cells infiltrated primary tumors and surrounded tumor cells that exhibited diminished expression of E-cadherin and increased expression of vimentin, 2 hallmarks of EMT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221088.RAnOBhyRW5pHwMQeSbUa8mfh2lNtXhqpQJMK_DCtcq_d0130_provenance.
NP221094.RAlP8QKruiibnTltEYQsAuPVZnC6KLwE_-DIsPK6kuDko130_assertion description "[Polymorphisms in tumour necrosis factor alpha (TNFalpha) gene in patients with acute pancreatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221094.RAlP8QKruiibnTltEYQsAuPVZnC6KLwE_-DIsPK6kuDko130_provenance.
NP221099.RAohEJPiFvsdhXBXT8hSatIGqhelnoWpIaxmLAGitBPUI130_assertion description "[The lethal-spotted mouse which has pigment abnormalities, but also colonic aganglionosis, carries a mutation in the gene coding for endothelin 3 (Edn3), the ligand for the receptor protein encoded by EDNRB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221099.RAohEJPiFvsdhXBXT8hSatIGqhelnoWpIaxmLAGitBPUI130_provenance.
NP221103.RAsUrr63amykhMbjfI3l9hFiQP7P0OeY2qt7cak4vMEMw130_assertion description "[We performed a phase I study of patients with advanced carcinoembryonic antigen (CEA)-expressing malignancies followed by a phase II study of patients with resected hepatic metastases of colon cancer to assess safety and feasibility of administering autologous DC loaded with CEA mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221103.RAsUrr63amykhMbjfI3l9hFiQP7P0OeY2qt7cak4vMEMw130_provenance.
NP221105.RAjpTLxqIZav-jkYY1z0vBcT7Y772gXSud6mfPRV03rvY130_assertion description "[However, while p53-/- mice developed a variety of tumor types, nearly all Gadd45a-/-p53-/- mice developed lymphoblastic lymphoma (LBL), often accompanied by mediastinal masses as is common in human patients with this tumor type.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221105.RAjpTLxqIZav-jkYY1z0vBcT7Y772gXSud6mfPRV03rvY130_provenance.
NP221108.RAoJ_46tyoTQlVDTTo-jI40rSzaAN4xj5_7nSZMaCtQOA130_assertion description "[Patients were classified as cured (negative scan, negative stimulated Tg, 8 patients), with metastasis (positive scan in extrathyroid bed regions, positive Tg, 7 patients), with thyroid remnants (positive scan in thyroid bed, positive Tg, 8 patients), and discordant cases (negative scan, positive Tg, 3 patients).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221108.RAoJ_46tyoTQlVDTTo-jI40rSzaAN4xj5_7nSZMaCtQOA130_provenance.
NP221111.RAvUezWslWzSuuu3j7D9ehvSUl1VYx2bec6wNxYoWjw_c130_assertion description "[Therefore a cooperation of vitamin D and TNF-alpha may play an important role in the control of cell growth in prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221111.RAvUezWslWzSuuu3j7D9ehvSUl1VYx2bec6wNxYoWjw_c130_provenance.
NP221114.RAiLwz3QjLh8hxlSYKlBFK_fZKAsSkivuQiHNG4PvB2Z8130_assertion description "[In western blotting, expression of DAF protein in the cancer tissue was increased, and heterogeneity in the apparent molecular weight of DAF was observed among patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221114.RAiLwz3QjLh8hxlSYKlBFK_fZKAsSkivuQiHNG4PvB2Z8130_provenance.
NP221116.RAgjSwVhZJPBA3W6AmCHGdUgPc4IbV8palCq-2x9GjSS8130_assertion description "[Null mutations in the progranulin gene (PGRN) were recently reported to cause tau-negative frontotemporal dementia linked to chromosome 17.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221116.RAgjSwVhZJPBA3W6AmCHGdUgPc4IbV8palCq-2x9GjSS8130_provenance.
NP221128.RAs_vLWixqv-sX8pm8UHnw4Mkqr_L_3T_d4QMdCcpAcOU130_assertion description "[This variant and two previously reported BDNF SNPs (C270T and Val66Met) were genotyped in 295 patients with AD, 108 with AFDs, 96 with posttraumatic stress disorder (PTSD), 84 with schizophrenia, 327 with alcohol and/or drug dependence, and 250 normal control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221128.RAs_vLWixqv-sX8pm8UHnw4Mkqr_L_3T_d4QMdCcpAcOU130_provenance.
NP221131.RAmI2VTupR9tlK3WhrhSGAS1Nr21bBriKFPhbxNGilSJY130_assertion description "[We have established a PCR assay with allele-specific oligonucleotide primers (ASO) complementary to the CDR3-hypervariable region of the immunoglobulin heavy chain gene of each patient's myeloma clone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221131.RAmI2VTupR9tlK3WhrhSGAS1Nr21bBriKFPhbxNGilSJY130_provenance.
NP221138.RAs4s6yNlauMrI8w_QL8UtGlV5RiSJFs2ZWV4twm5uSKw130_assertion description "[The efficacy of the ACE (angiotensin-converting enzyme) inhibitor perindopril in coronary artery disease [EUROPA (European trial on reduction of cardiac events with perindopril in stable coronary artery disease) study] is associated with the rs12050217 A/G single nucleotide polymorphism in the B1 receptor (bradykinin type 1 receptor) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221138.RAs4s6yNlauMrI8w_QL8UtGlV5RiSJFs2ZWV4twm5uSKw130_provenance.
NP221142.RAtT6VDOJodKhMvVSZa0ATBT5rrmxRxeAK2PVeV-NjLqc130_assertion description "[A number of X-linked AS patients follow a milder course reminiscent of that of patients with heterozygous COL4A3/COL4A4 mutations and TBMN, while at the same time a significant subset of patients with TBMN and familial MH progress to chronic kidney disease (CKD) or end-stage kidney disease (ESKD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221142.RAtT6VDOJodKhMvVSZa0ATBT5rrmxRxeAK2PVeV-NjLqc130_provenance.
NP221145.RAtjxIudfAmVlvNnDonzkEq_Ipe4ecMT9rvr1vgWo7gqs130_assertion description "[MTHFR polymorphism, methyl-replete diets and the risk of colorectal carcinoma and adenoma among U.S. men and women: an example of gene-environment interactions in colorectal tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221145.RAtjxIudfAmVlvNnDonzkEq_Ipe4ecMT9rvr1vgWo7gqs130_provenance.
NP221147.RAv25VitQPwC795Nbh8kYSsxQE1nLV-tcZI28xmralinw130_assertion description "[Apolipoprotein M promoter polymorphisms alter promoter activity and confer the susceptibility to the development of type 1 diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221147.RAv25VitQPwC795Nbh8kYSsxQE1nLV-tcZI28xmralinw130_provenance.
NP221150.RAk7SRosKv7X1xt1eZyKyBQvqJMK1X8J15YP-PuQYu8to130_assertion description "[FANCD2 Western blot as a diagnostic tool for Brazilian patients with Fanconi anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221150.RAk7SRosKv7X1xt1eZyKyBQvqJMK1X8J15YP-PuQYu8to130_provenance.
NP221153.RAs3i_CNTm9A2Wty5wCyCD8GbAYYuqYAa4ehCvWQ8oCdY130_assertion description "[SLPI was localized in the endometrial-type epithelium of endometriomas immunohistochemically.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221153.RAs3i_CNTm9A2Wty5wCyCD8GbAYYuqYAa4ehCvWQ8oCdY130_provenance.
NP221161.RAt3x_Aw0AgRbeJ0b22J8jKO-aHsKhYzZaGsettyTsfKg130_assertion description "[Coexpression of erythropoietin and vascular endothelial growth factor in nervous system tumors associated with von Hippel-Lindau tumor suppressor gene loss of function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221161.RAt3x_Aw0AgRbeJ0b22J8jKO-aHsKhYzZaGsettyTsfKg130_provenance.
NP221164.RAjjtuCCoLzOTTzyzy4Dp5YeXP7CxVc3qrOz6Bm_zykgE130_assertion description "[In the present work the distribution of genotypes and frequency of alleles of the RAD51 G135C polymorphism, XRCC2 Arg 188His and XRCC3 Thr241Met polymorphism in 790 cases of breast cancer were investigated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221164.RAjjtuCCoLzOTTzyzy4Dp5YeXP7CxVc3qrOz6Bm_zykgE130_provenance.
NP221165.RAtRjQCD33g0f_WUmAA80LgZW5-wRE-r9ADxwqD2UkHCQ130_assertion description "[No heterogeneity has been seen with the effects of statin therapy in the elderly compared with younger age groups on classical cardiovascular endpoints of coronary heart disease and stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221165.RAtRjQCD33g0f_WUmAA80LgZW5-wRE-r9ADxwqD2UkHCQ130_provenance.
NP221166.RAliGzcEMvfOBUWyGT3u_x1aBECXYbqdbdaiQW9kEsY3s130_assertion description "[We conclude that total body oxidation of galactose to CO(2) in expired air reflects genotype and that this breath test is a sensitive predictor of verbal dyspraxia in patients with galactosemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221166.RAliGzcEMvfOBUWyGT3u_x1aBECXYbqdbdaiQW9kEsY3s130_provenance.
NP221177.RArNBe5YzopwB46zsCeBpehU1Hee_5rcXN3tfkd1fh3o4130_assertion description "[The prostate-specific antigen or kallikrein-related peptidase 3 (PSA/KLK3) is an established tumor marker for the diagnosis and monitoring of prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221177.RArNBe5YzopwB46zsCeBpehU1Hee_5rcXN3tfkd1fh3o4130_provenance.
NP221180.RAvP9UUAZ8pnprblRi24f3sGRqZhhun9eBXJraFF7M2BU130_assertion description "[In conclusion VEGF, Ang2 and EG-VEGF mRNA may play a role in angiogenesis and carcinogenesis of HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221180.RAvP9UUAZ8pnprblRi24f3sGRqZhhun9eBXJraFF7M2BU130_provenance.
NP221182.RAsFUFEeGHTUDy-fGi2G_4RpoVJAVMru4teauqlsLM0RQ130_assertion description "[Structural genetic changes of tumor suppressor genes MTS-1/INK4A and MTS-2/INK4B were demonstrated in a variety of human cancers but not in thyroid cancer until now.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221182.RAsFUFEeGHTUDy-fGi2G_4RpoVJAVMru4teauqlsLM0RQ130_provenance.
NP221185.RAvCFZr5i9mtqfDPSjIziVxEqn-V8_D7Ijg70MCPk1B0s130_assertion description "[Methylseleninic acid (MSA) inhibits 17β-estradiol-induced cell growth in breast cancer T47D cells via enhancement of the antioxidative thioredoxin/ thioredoxin reductase system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221185.RAvCFZr5i9mtqfDPSjIziVxEqn-V8_D7Ijg70MCPk1B0s130_provenance.
NP221189.RApQvfBmqf-1et5Dj1EfsG5tQKRw6FAAuTossjHgdhJNM130_assertion description "[Whereas mutations in the GH-1 and GHRHR genes account for the majority of mutations detectable in patients with Isolated Growth Hormone Deficiency (IGHD) resulting in postnatal growth failure, the overall detection of genetic defects in these patients remains low with app.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221189.RApQvfBmqf-1et5Dj1EfsG5tQKRw6FAAuTossjHgdhJNM130_provenance.
NP221193.RAj2MeNIct42ICsIeFxcthw0a0nJGWlAtrdS_h4ucDq2c130_assertion description "[mRNA expression of MMP-1, -3, and -13, and ADAMTS5 was attenuated in IL-1β-stimulated human OA chondrocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221193.RAj2MeNIct42ICsIeFxcthw0a0nJGWlAtrdS_h4ucDq2c130_provenance.
NP221194.RAvlaDboz0gFuLCn0gR9QVSZOZUYt0LAqDdYIxNdegxsE130_assertion description "[In conclusion, cyclin E is a strong independent prognostic indicator in patients with early-stage NSCLC, whereas cyclin E2, cyclin A1, and cyclin A2 do not have a prognostic role in NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221194.RAvlaDboz0gFuLCn0gR9QVSZOZUYt0LAqDdYIxNdegxsE130_provenance.
NP221197.RAj-jpwsFJgy_8LHyuKSfgUY7nN9vYmyPKtDmDjAsRYxE130_assertion description "[Decreased levels of the anti-inflammatory cytokine IL-10 further disturb the balance between survival and pro-apoptotic mediators in chronic idiopathic neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221197.RAj-jpwsFJgy_8LHyuKSfgUY7nN9vYmyPKtDmDjAsRYxE130_provenance.
NP221200.RAk3o9nmmq-BMyFXEiOzIMOfTaMatNt-OLytuwiaDfyzk130_assertion description "[Seven out of 16 hypomethylation-induced lymphomas were found to contain an intracisternal A particle (IAP) somatic insertion in the middle of the Notch1 genomic locus, leading to generation of an oncogenic form of Notch1 in the tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221200.RAk3o9nmmq-BMyFXEiOzIMOfTaMatNt-OLytuwiaDfyzk130_provenance.
NP221201.RAlKp2vbuC9cLrsyzd81cwmWR88xNO4P-ijFruF_x7jn8130_assertion description "[c-erbB-2 expression, confirmed also as a cytoplasmic membrane-bound reactivity by immunohistochemical stainings for c-erbB-2 oncoprotein, was significantly related to adenocarcinoma (P less than 0.025), whereas increasing tumor size correlated significantly with increasing c-myc expression (P less than 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221201.RAlKp2vbuC9cLrsyzd81cwmWR88xNO4P-ijFruF_x7jn8130_provenance.
NP221203.RAjExTdFAClhkNf3KRkHV40-otvaeWTVBjJy-bSqG_Q7U130_assertion description "[Our study shows that AQP4 downregulation can occur in muscular dystrophies with either normal or disrupted expression of dystrophin-associated proteins, and that this might be associated with upregulation of AQP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221203.RAjExTdFAClhkNf3KRkHV40-otvaeWTVBjJy-bSqG_Q7U130_provenance.
NP221208.RArm623DzDWmBXq6KnWpfl6-s1NRSkqSxeacTd0E73VhY130_assertion description "[Deletion of the 13q14 chromosomal region is frequent in B cell chronic lymphocytic leukemia (B-CLL) and is believed to inactivate a tumor supressor gene (TSG) next to RB1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221208.RArm623DzDWmBXq6KnWpfl6-s1NRSkqSxeacTd0E73VhY130_provenance.
NP221212.RAmgKrKb2Y4Zeonz1Vb-AqPA__CMAEQ5atkGob0sHJiU0130_assertion description "[To investigate the prognostic significance of p21(WAF1/CIP1) expression and its relationship with p53 accumulation and other apoptotic markers such as Bax, Bcl-2, and apoptotic index in relation to disease-specific survival in oral tongue squamous cell carcinoma (SCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221212.RAmgKrKb2Y4Zeonz1Vb-AqPA__CMAEQ5atkGob0sHJiU0130_provenance.
NP221214.RAqS3kemDMkqYEjXcUjl_LBkevxqhlM2gme__9cSWwdoI130_assertion description "[In the subgroup analysis, we detected no significant association between the COMT 158 Val/Met genotype and prostate cancer risk in Caucasian and Asian populations, while the contrary result for additive model (OR = 2.43, 95 % CI = 1.08-5.43, P (heterogeneity) = 0.04, P = 0.03) in Asian populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221214.RAqS3kemDMkqYEjXcUjl_LBkevxqhlM2gme__9cSWwdoI130_provenance.
NP221221.RAuTovUm_xRU2ha-7dlh9P17phDTjPAIgjYzrxGS9QFHg130_assertion description "[A silent mutation (c.605C-->A) and three missense mutations (c.395C-->G; c.419C-->T; c.771A-->G), respectively, cause the X-linked mental retardation, choreoathetosis, and abnormal behavior (MRXS10) and the hydroxyacyl-CoA dehydrogenase II deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221221.RAuTovUm_xRU2ha-7dlh9P17phDTjPAIgjYzrxGS9QFHg130_provenance.
NP221222.RAkxHDGr2e6S7XKuozKXBdCU1zSD6B1VoCxYK-303tgdg130_assertion description "[Bcl-G expression is reduced in breast cancer tissue but decreased Bcl-G expression showed no correlation with survival, indicating that the most important factors controlling Bcl-G activity are post-translational modification (by Fau and MELK) rather than the rate of transcription of Bcl-G itself.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221222.RAkxHDGr2e6S7XKuozKXBdCU1zSD6B1VoCxYK-303tgdg130_provenance.
NP221224.RAnpWgeMBTu0B-kZ_wcXcmFuHT3XW6mxtcKbPgrsB8r8U130_assertion description "[An insertion-deletion polymorphism in ACE has recently been linked to heart disease, cerebrovascular disease, and AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221224.RAnpWgeMBTu0B-kZ_wcXcmFuHT3XW6mxtcKbPgrsB8r8U130_provenance.
NP221233.RAuaaetXwvBpSF0U72KZsbc0bxIJ5nM8DWA9bzqR5uyqo130_assertion description "[We conclude that loss of transgelin gene expression may be an important early event in tumor progression and a diagnostic marker for breast and colon cancer development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221233.RAuaaetXwvBpSF0U72KZsbc0bxIJ5nM8DWA9bzqR5uyqo130_provenance.
NP221238.RArK6fuSPxSCf7_o_4OgUWN_QJj6GsqR9dnBZWVbJW4Aw130_assertion description "[Collectively, these data support in vivo functional interaction between UBQLN1 and the AD-associated genes, presenilin and APP, and provide further clues regarding the potential role of UBQLN1 in AD pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221238.RArK6fuSPxSCf7_o_4OgUWN_QJj6GsqR9dnBZWVbJW4Aw130_provenance.
NP221240.RAkM_pEOpea59iO1qNdtdBOmnI61v9tGzXQtzH9iCsYiQ130_assertion description "[The older child showed normal elevation of T (up to 7.6 nmol/liter, 2.2 ng/ml), AMH (504 pmol/liter, 70.6 ng/ml), inhibin B (245 pg/ml), FSH, and LH during the first weeks, which led to a presumptive diagnosis of partial androgen insensitivity syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221240.RAkM_pEOpea59iO1qNdtdBOmnI61v9tGzXQtzH9iCsYiQ130_provenance.
NP221243.RAl201elR924MyyowfxlogTwo_qj5K5nV1C_1g2o4_ZuQ130_assertion description "[The SCID defect itself had a clear impact, since, in the chronic phase, SCID.bg and RAG-2(-/-)knockout mice developed less consistent pathological/scintigraphic signs of disease than SCID mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221243.RAl201elR924MyyowfxlogTwo_qj5K5nV1C_1g2o4_ZuQ130_provenance.
NP221244.RAh5-RF6eyh4kL8H33YA6dYebVih0U8piqR89gP6DoWzk130_assertion description "[Hypoparathyroidism-retardation-dysmorphism (HRD) or Sanjad-Sakati syndrome (SSS) (OMIM 241410) is a rare autosomal recessive (AR) inherited condition, characterized by congenital hypoparathyroidism (hypoPTH), retardation, seizures, and a typical facial dysmorphism, consisting of prominent forehead, deep-set eyes, and abnormal external ears.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221244.RAh5-RF6eyh4kL8H33YA6dYebVih0U8piqR89gP6DoWzk130_provenance.
NP221246.RAnkQXhkRp1iRn61GdtSZpBog1o5LHveiVz7szrRHHvsk130_assertion description "[Sarcoidosis CD4+ T cells were primarily responsible for the systemic responses.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221246.RAnkQXhkRp1iRn61GdtSZpBog1o5LHveiVz7szrRHHvsk130_provenance.
NP221247.RAs6hITqtL_GFp55Q4KhOxKiL-rHvHzoYVY0uUCDzJkEg130_assertion description "[Sequencing of the reverse transcriptase-polymerase chain reaction (RT-PCR) products of the Syk mRNA in these pro-B leukemia cells revealed profoundly aberrant coding sequences with deletions or insertions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221247.RAs6hITqtL_GFp55Q4KhOxKiL-rHvHzoYVY0uUCDzJkEg130_provenance.
NP221248.RArlRedQlHrd9zch07cmntIwbf3Cs9oQXkbqU5tZb5eC0130_assertion description "[Genetic variants of the bile salt export pump: inducers and modifiers of liver diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221248.RArlRedQlHrd9zch07cmntIwbf3Cs9oQXkbqU5tZb5eC0130_provenance.
NP221250.RAhUt1lKUYLXCvs3o8uz8Tzrd1NF_lz5igVXJ3-NMc4hg130_assertion description "[PCDHB1 and PCDH7 promoter activities were down-regulated by MeCP2, but not by MBD-deleted MeCP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221250.RAhUt1lKUYLXCvs3o8uz8Tzrd1NF_lz5igVXJ3-NMc4hg130_provenance.
NP221260.RAjSabH7LnkgsooghTdXQeaMRqWF1cUINLcYfjB9AaBYY130_assertion description "[Erythrocyte NAD(P)H2 glutathione oxidoreductase (EC 1.6.4.2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221260.RAjSabH7LnkgsooghTdXQeaMRqWF1cUINLcYfjB9AaBYY130_provenance.
NP221261.RAvjzrY_IP6rUsuupc5d7zrzHWGC4ofEMnL3ifdUtKuuY130_assertion description "[The objective of this study was to determine if mutations in the VHL gene can serve as auxiliary diagnostic criteria in refining histology based subtyping of renal epithelial neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221261.RAvjzrY_IP6rUsuupc5d7zrzHWGC4ofEMnL3ifdUtKuuY130_provenance.
NP221263.RAnJyH1rdKZshDqhekgusGRkEJSHXtaaFMhbHO1lGBQt8130_assertion description "[Partial tandem duplication of ALL1 as a recurrent molecular defect in acute myeloid leukemia with trisomy 11.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221263.RAnJyH1rdKZshDqhekgusGRkEJSHXtaaFMhbHO1lGBQt8130_provenance.
NP221264.RAsZBTsliQL451-74uGQNjXs9N4xcgbzazRFQXYzdaq1M130_assertion description "[The serine/threonine kinase liver kinase B 1 (LKB1) is a multifunctional protein and has been associated with various cancer types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221264.RAsZBTsliQL451-74uGQNjXs9N4xcgbzazRFQXYzdaq1M130_provenance.
NP221271.RAupnGNpIJEGc9eQhbHfSCg4ZoKlwWkNXP-E49VyXJC80130_assertion description "[MODY (Maturity Onset Diabetes of the Young) is an autosomal dominant inherited type of diabetes with significant genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221271.RAupnGNpIJEGc9eQhbHfSCg4ZoKlwWkNXP-E49VyXJC80130_provenance.
NP221273.RAlFtEuI0f_aF50fdUtF4lLpwasWjsEosQ5YZ2hov7inM130_assertion description "[In summary we demonstrate that TLR9 expression is associated with poor differentiation in breast and ovarian cancer specimens, and that TLR9 overexpression and stimulation with hypomethylated DNA augments the migratory capacity of cancer cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221273.RAlFtEuI0f_aF50fdUtF4lLpwasWjsEosQ5YZ2hov7inM130_provenance.
NP221274.RAhnztQYgXr-IYrgdgmH8fmYjdwjWqXzstlsHLPDliyac130_assertion description "[In conclusion, PTEN could modulate the function of VEGF/VEGFR signaling pathway down-regulation of Akt phosphorylation and that PTEN would be a candidate target to be addressed for inhibiting angiogenesis along with the treatment of myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221274.RAhnztQYgXr-IYrgdgmH8fmYjdwjWqXzstlsHLPDliyac130_provenance.
NP221276.RAnMhdG0Ff6bH7_QiQ2o1dy_4qCx8XEMuhmgh19vKz7iE130_assertion description "[Blood samples from 94 breast cancer patients with metastatic disease (M1) were examined for circulating tumour cells by studying the mRNA expression of CK19, p1B, PS2 and EGP2 by real-time PCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221276.RAnMhdG0Ff6bH7_QiQ2o1dy_4qCx8XEMuhmgh19vKz7iE130_provenance.
NP221277.RAtrN4nZgdavqWklBrEW2BAzhB5fuB15Lia0IS4gR3eMo130_assertion description "[Since some sarcoma subtypes, such as Ewing's sarcoma, show characteristics of neuroendocrine differentiation, we wondered whether cancers with neuro-endocrine properties and/or neuroectodermal origin, such as neuroblastoma, small cell lung cancer and melanoma, may express endosialin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221277.RAtrN4nZgdavqWklBrEW2BAzhB5fuB15Lia0IS4gR3eMo130_provenance.

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