Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP177878.RAQvl5s-X5vPpYYfE6vtcqyR0vEeHbfckhiyRSfxWtqDI130_assertion description "[Using comparative genomic hybridization and mutational analysis of APC, KRAS, and TP53 to evaluate 78 colorectal adenomas, we have shown that several of the significant relationships between gene mutations and chromosomal abnormalities reported in colorectal adenocarcinomas also exist at the adenomatous stage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177878.RAQvl5s-X5vPpYYfE6vtcqyR0vEeHbfckhiyRSfxWtqDI130_provenance.
- NP177887.RAUKyEoxnNCEASSsyGfbnqSe9Nq6thTeisURPy2ZMfno8130_assertion description "[We here characterize the impact of K(2P)5.1 (KCNK5; TASK2), a member of the 2-pore domain family of potassium channels, on T-cell function and demonstrate its putative relevance in a T-cell-mediated autoimmune disorder, multiple sclerosis (MS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177887.RAUKyEoxnNCEASSsyGfbnqSe9Nq6thTeisURPy2ZMfno8130_provenance.
- NP177891.RAS9YQ7sF28HXgXHIqeCaiuDfEcXpM9u8maot3YT2g0FA130_assertion description "[Thus, silencing of HIN-1 expression and methylation of its promoter occurs in multiple human cancer types, suggesting that elimination of HIN-1 function may contribute to several forms of epithelial tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177891.RAS9YQ7sF28HXgXHIqeCaiuDfEcXpM9u8maot3YT2g0FA130_provenance.
- NP177892.RAcMQvQtkx-tN_K1sOdUndhrkVJrq0NkQQRr3eyAsYGZQ130_assertion description "[This was investigated in two cross-sectional studies of HIV patients who were immunodeficient when they began antiretroviral therapy (ART) and had stable increases in CD4 T-cell counts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177892.RAcMQvQtkx-tN_K1sOdUndhrkVJrq0NkQQRr3eyAsYGZQ130_provenance.
- NP177912.RAbnU02uEDO3jMVSIQMmwjm_qu0pDciqi9yB4KlJ9VmDY130_assertion description "[Enhancement of calcyclin gene RNA expression in squamous cell carcinoma of the oral mucosa, but not in benign lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177912.RAbnU02uEDO3jMVSIQMmwjm_qu0pDciqi9yB4KlJ9VmDY130_provenance.
- NP177914.RAdfQNOBIbW9U1694hpGeKdPfkW5zSA9w1PIHt9XvULm8130_assertion description "[CUL1 also mediates degradation of IκBα and p27, levels of which has been associated with RA etiology and drug response, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177914.RAdfQNOBIbW9U1694hpGeKdPfkW5zSA9w1PIHt9XvULm8130_provenance.
- NP177923.RAeeFhZuBxWbaIhwydudtYvH1k_Q5FYKzuI8PbpZAiSpo130_assertion description "[We found that p53 accumulates selectively in the erythroid lineage in primary human hematopoietic progenitor cells after expression of shRNAs targeting RPS14, the ribosomal protein gene deleted in the 5q-syndrome, or RPS19, the most commonly mutated gene in DBA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177923.RAeeFhZuBxWbaIhwydudtYvH1k_Q5FYKzuI8PbpZAiSpo130_provenance.
- NP177928.RAQ8Dc3ILvuNZB3wyqrsQrjB5_8Ve-HhS45wSak6pWmDM130_assertion description "[RB1CC1 activates the promoter and expression of RB1 in human cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177928.RAQ8Dc3ILvuNZB3wyqrsQrjB5_8Ve-HhS45wSak6pWmDM130_provenance.
- NP177943.RATXaI-KecJn-uCCddOoaHF7cMxPMpB2yigCMa3J0ABao130_assertion description "[Although most of the patients had solitary GEP-NETs, 6 were diagnosed with GEP-NET as a part of multiple endocrine neoplasia type 1 and 1 as a part of neurofibromatosis type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177943.RATXaI-KecJn-uCCddOoaHF7cMxPMpB2yigCMa3J0ABao130_provenance.
- NP177944.RAaG-SFH98QqPtW8nsf1fMYvuKPOXh_0ZZkmFwBspJUw4130_assertion description "[Loss of p53 function appears to be a critical determinant for bypassing this checkpoint and the subsequent progression to invasive adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177944.RAaG-SFH98QqPtW8nsf1fMYvuKPOXh_0ZZkmFwBspJUw4130_provenance.
- NP177945.RAT7r9X25En43SaZJ5X1Tpirlyn8BcOw9wnrjdhjaaF5E130_assertion description "[A region of strong association resides within the ULBP (cytomegalovirus UL16-binding protein) gene cluster on chromosome 6q25.1, encoding activating ligands of the natural killer cell receptor NKG2D that have not previously been implicated in an autoimmune disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177945.RAT7r9X25En43SaZJ5X1Tpirlyn8BcOw9wnrjdhjaaF5E130_provenance.
- NP177946.RAVTlIIKMAeB3tGNh7g-z6ZKTM_XbbHUfJZqHcWBTkDCQ130_assertion description "[It is unusual among the epithelial carcinomas because tumorigenesis can occur by two distinct pathways: low-grade, recurring papillary tumours usually contain oncogenic mutations in FGFR3 or HRAS, whereas high-grade, muscle-invasive tumours with metastatic potential generally have defects in the pathways controlled by the tumour suppressors p53 and retinoblastoma (RB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177946.RAVTlIIKMAeB3tGNh7g-z6ZKTM_XbbHUfJZqHcWBTkDCQ130_provenance.
- NP177953.RAfONwq1xM50Ke6FHxmpEpTd4aihz8hZUjiFhKS8fno8c130_assertion description "[A total of 386 CT or MRI proven stroke patients were included; 193 each had ischemic stroke and ICH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177953.RAfONwq1xM50Ke6FHxmpEpTd4aihz8hZUjiFhKS8fno8c130_provenance.
- NP177958.RAdv-1oxjAnqVERrAJdEywbrwA5u5PoN39rO6N2VuPAjY130_assertion description "[In analogy, we propose that deregulation of the MAPK/ERK pathway in SoS results in altered hypertrophic differentiation of NSD1 expressing chondrocytes and may be a determining factor in statural overgrowth and accelerated skeletal maturation in SoS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177958.RAdv-1oxjAnqVERrAJdEywbrwA5u5PoN39rO6N2VuPAjY130_provenance.
- NP177959.RAaJfjjHPxU7OoDfsxJc-cg1J1Peixf_mf2WruOcwOshM130_assertion description "[A chemokine receptor, CXCR4, and its endogenous ligand, stromal cell-derived factor-1 (SDF-1), have been recognized to be involved in the metastasis of several types of cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177959.RAaJfjjHPxU7OoDfsxJc-cg1J1Peixf_mf2WruOcwOshM130_provenance.
- NP177967.RAaBbo0pKlevCjOKx-YO3g6G30OEpTa4wmbHUyJ0VsHXQ130_assertion description "[Six different mutations in the fibroblast growth factor receptor 2 have been identified in patients with the clinical diagnosis of JWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177967.RAaBbo0pKlevCjOKx-YO3g6G30OEpTa4wmbHUyJ0VsHXQ130_provenance.
- NP177979.RAbJUiXwFbgx2n9ZiK9adrvpGUWfNxYtDquqyR0UyD5CA130_assertion description "[Our findings confirm the importance of genetic factors in body weight change induced by long-term AAP treatment in patients with schizophrenia and indicate a role of DRD2 in body weight regulation during long-term AAP treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177979.RAbJUiXwFbgx2n9ZiK9adrvpGUWfNxYtDquqyR0UyD5CA130_provenance.
- NP177981.RAeDpQkgy4uuUMXfsC2djJ9IeeXaslZdJz-dnVbx6L5Qc130_assertion description "[Anaplastic lymphoma kinase (ALK)-positive diffuse large B-cell lymphoma (DLBCL) is a rare tumor that is frequently associated with t(2;17)(p23;q23), a translocation fusing the ALK gene at 2p23 to the clathrin heavy chain gene (CLTC) at 17q23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177981.RAeDpQkgy4uuUMXfsC2djJ9IeeXaslZdJz-dnVbx6L5Qc130_provenance.
- NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_assertion description "[We report here the identification of 10 novel mutations, of which eight are localized in FGA, thus increasing the total number of causative mutations identified to 72 and confirming the relative importance of FGA in the molecular basis of fibrinogen deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177982.RAVZ-05bVFf7EPKBvj_fUXoCVJvNzninGGO3Vmr7OXVms130_provenance.
- NP177986.RAWTzdtXWCGLvweP76f1YHl1kv0uS9DqV7EZ3zNWBTZYw130_assertion description "[The general expression level of ING1 and the transcription levels of ING1a and ING1b in 31 pairs of hepatocellular carcinoma and matched nontumorous tissues were evaluated by using immunostaining and semi-quantitative reverse transcript polymerase chain reaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177986.RAWTzdtXWCGLvweP76f1YHl1kv0uS9DqV7EZ3zNWBTZYw130_provenance.
- NP177992.RAVjEEJQXZAkbAJRsTYxHfVNVuzWyArDhR-J6HTAuAr7I130_assertion description "[Epithelial-to-mesenchymal transition (EMT) is strongly associated with cancer progression, but its potential role during premalignant development has not been studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177992.RAVjEEJQXZAkbAJRsTYxHfVNVuzWyArDhR-J6HTAuAr7I130_provenance.
- NP177994.RATHmZkGMDzEBWquYe6s3IwUpANu72llHH0Xu59tzKHtg130_assertion description "[In this group of Hispanic children at high risk of type 2 diabetes, 1) pre-diabetes is highly variable from year to year; 2) the prevalence of persistent pre-diabetes over 3 years is 13%; and 3) children with persistent pre-diabetes have lower BCF, due to a lower AIR, and increasing visceral fat over time.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177994.RATHmZkGMDzEBWquYe6s3IwUpANu72llHH0Xu59tzKHtg130_provenance.
- NP177998.RAV4BCz5hI6BSaY-Dbb3wkT6XJUobe60aV8cPvvI26y9k130_assertion description "[Mutations of RET are associated to a subset of colorectal cancer and are commonly found in hereditary and sporadic thyroid cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP177998.RAV4BCz5hI6BSaY-Dbb3wkT6XJUobe60aV8cPvvI26y9k130_provenance.
- NP178000.RAW9jraU5TvjJs95I2auBPjT6Wju5zne9zkjHeGXAY3as130_assertion description "[Association of a disintegrin and metalloprotease 33 (ADAM33) gene with asthma in ethnically diverse populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178000.RAW9jraU5TvjJs95I2auBPjT6Wju5zne9zkjHeGXAY3as130_provenance.
- NP178013.RAWnxHWOLOEm4RZ69h0oC23t0LY2FhG-tZXhswXrlYTBQ130_assertion description "[We discuss the implications of our results for the use of positive immunostaining in clinical diagnosis, and the involvement of p53 in skin carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178013.RAWnxHWOLOEm4RZ69h0oC23t0LY2FhG-tZXhswXrlYTBQ130_provenance.
- NP178017.RAY-gygnWChU04F03uVMOtisFXTG2TuFEcytCOzyerIoY130_assertion description "[In order to determine whether concurrent loss of PEDF is sufficient to promote adipogenesis and tumorigenesis in the pancreas, the authors ablated PEDF in an EL-Kras(G12D) mouse model of non-invasive cystic papillary neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178017.RAY-gygnWChU04F03uVMOtisFXTG2TuFEcytCOzyerIoY130_provenance.
- NP178018.RAdlkUJu_YCWI2vrSXTU7iT4qoYEQOQwYe06GZXb31kLU130_assertion description "[Mechanistically, we show that loss of the SNF5 tumor suppressor leads to elevated expression of the Polycomb gene EZH2 and that Polycomb targets are broadly H3K27-trimethylated and repressed in SNF5-deficient fibroblasts and cancers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178018.RAdlkUJu_YCWI2vrSXTU7iT4qoYEQOQwYe06GZXb31kLU130_provenance.
- NP178020.RAYugkQZxHmZ9PzDtn214AK1nU0LxTNjkoeBI3hfV6FJ8130_assertion description "[There was a significant survival advantage for patients with low tumour PCNA-indices (< 3.5%) compared with those with high indices (> 3.5%, p = 0.019), a difference also found for patients with non-metastatic disease (p = 0.012).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178020.RAYugkQZxHmZ9PzDtn214AK1nU0LxTNjkoeBI3hfV6FJ8130_provenance.
- NP178023.RAcuxWvRtZnfY6NRKMWORWQiFNGKsde3bCmE2JuKUvrK4130_assertion description "[This study addressed the hypothesis that variation in genes associated with dopamine function (SLC6A3, DRD2, DRD4), serotonin function (SLC6A4, and regulation of monoamine levels (MAOA) may be predictive of BMI categories (obese and overweight + obese) in young adulthood and of changes in BMI as adolescents transition into young adulthood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178023.RAcuxWvRtZnfY6NRKMWORWQiFNGKsde3bCmE2JuKUvrK4130_provenance.
- NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_assertion description "[Molecular genetics has identified some inherited mutations (such as at APC and the mismatch repair loci) that predispose to colon cancer and some somatic mutations (such as at APC and p53) that cause sporadic colon tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178025.RAYDMgQf3B2IER1NKueLexus3qvsRzVpfV-_6RT6GnYHk130_provenance.
- NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_assertion description "[Mutations in RET and in two members of the GDNF ligand family are associated with Hirschsprung disease (HSCR), a congenital absence of the enteric ganglia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178029.RARBLftLF_tieekPhZkygifwjrNsVBVNCf0i6LOSf-qBk130_provenance.
- NP178034.RAaLdZ5QIHMBIdAkDcNXN21q34kcyvh375hSRs27kywj4130_assertion description "[Our results indicate that FLT3 alterations are associated in APL with more aggressive clinical features and suggest that these lesions may not play a major role in leukemia progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178034.RAaLdZ5QIHMBIdAkDcNXN21q34kcyvh375hSRs27kywj4130_provenance.
- NP178037.RAeEFPrOwAhGTkh-v4J_K1dajNwnufkXxENv0KROip0bE130_assertion description "[Factor V Leiden (R507Q) and factor II (prothrombin) mutation (G20210A) are the two most common inherited hypercoagulability disorders among populations of European origin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178037.RAeEFPrOwAhGTkh-v4J_K1dajNwnufkXxENv0KROip0bE130_provenance.
- NP178052.RAaFSwEY-qDUPGgBdHUHaZQoNgbxojylqkJmlLlAiDgWM130_assertion description "[Univariate analyses demonstrated that SCCRO overexpression correlated with nodal metastases (P = 0.05) and advanced stage (P = 0.02), whereas PIK3CA overexpression was associated with vascular invasion (P = 0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178052.RAaFSwEY-qDUPGgBdHUHaZQoNgbxojylqkJmlLlAiDgWM130_provenance.
- NP178060.RAfMO2zoDs6RfBG9x7t-PX_OhkR6I1As8BDxCGnawTiNs130_assertion description "[Mutations in the dystrophin gene give rise to Duchenne and Becker muscular dystrophies (DMD and BMD), in which both skeletal and cardiac muscles are affected, but also to X-linked dilated cardiomyopathy (XLDC), a condition characterised by exclusive cardiac involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178060.RAfMO2zoDs6RfBG9x7t-PX_OhkR6I1As8BDxCGnawTiNs130_provenance.
- NP178065.RAToYEQAw27hdZA9_xEP4PQn-JwkjWeUD2QcKxyveqr9M130_assertion description "[Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178065.RAToYEQAw27hdZA9_xEP4PQn-JwkjWeUD2QcKxyveqr9M130_provenance.
- NP178071.RAdx4IIOqyeVdCcGGgYGY_jT5hhl0MCVOHpt7_2YJYGkI130_assertion description "[More extensive hemihypertrophy extending to body sites remote from the vascular malformation itself could have a higher risk of Wilms tumor, although the magnitude of this risk is uncertain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178071.RAdx4IIOqyeVdCcGGgYGY_jT5hhl0MCVOHpt7_2YJYGkI130_provenance.
- NP178074.RAS8FVqtU13t3SbpFFa0GBYpHU4koF-534c15qsRMgSf8130_assertion description "[High levels of S100A4 were found to significantly correlate with histological grade (P=0.030) and loss of oestrogen receptor (P=0.046), but not to the time interval between surgery and development of distant metastasis (P=0.51) or to patient survival (P=0.89).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178074.RAS8FVqtU13t3SbpFFa0GBYpHU4koF-534c15qsRMgSf8130_provenance.
- NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_assertion description "[Missense variants of the ATM gene are a rare event in childhood Hodgkin disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178080.RAeJIgjln92Jt3VHrORWD4F-NR_IlWr9Acn5nQoEXCC04130_provenance.
- NP178086.RATi5NQvPe3qTloBYhy0Mk3qtbLZUrcRLoCi0u17BskAA130_assertion description "[A C825T polymorphism of a gene encoding the beta3 subunit of heterotrimeric G proteins (GNB3) was reported to be associated with several pathological conditions, such as hypertension and depressive disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178086.RATi5NQvPe3qTloBYhy0Mk3qtbLZUrcRLoCi0u17BskAA130_provenance.
- NP178094.RAVMM4HEL8sINyVIpxXae1qzcgMz0Q0oOEue4TAu_Ym3k130_assertion description "[Mutations in the gene encoding the human cardiac sodium channel (SCN5A) have been associated with three distinct cardiac arrhythmia disorders: the long QT syndrome, the Brugada syndrome and cardiac conduction disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178094.RAVMM4HEL8sINyVIpxXae1qzcgMz0Q0oOEue4TAu_Ym3k130_provenance.
- NP178095.RAf7Ja2yVU_C1YTixTkQKN5fJ9UWzSk3f0CyAEbKtZ8DM130_assertion description "[A tissue microarray was constructed from paraffin-embedded blocks of 48 MTCs (13 familial, 35 sporadic) previously evaluated for germ line and somatic RET mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178095.RAf7Ja2yVU_C1YTixTkQKN5fJ9UWzSk3f0CyAEbKtZ8DM130_provenance.
- NP178107.RASJq4ipP4d0I2AMLNZnLrqbde1xjbvK22GibhWH7pvv0130_assertion description "[Molecular characterization of a (1;10)(p22;q21) constitutional translocation from a patient with neuroblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178107.RASJq4ipP4d0I2AMLNZnLrqbde1xjbvK22GibhWH7pvv0130_provenance.
- NP178108.RAb0np-dkYsOU_byy1mY0pEUpzXRmAIY9G_0cCUfPJoWQ130_assertion description "[Chromosomal translocations involving the immunoglobulin heavy chain (IGH) locus at chromosome 14q32 represent a common mechanism of oncogene activation in lymphoid malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178108.RAb0np-dkYsOU_byy1mY0pEUpzXRmAIY9G_0cCUfPJoWQ130_provenance.
- NP178115.RAT91dB3MpMkm_oOjF5D3j2YcgRyfSijOrO0kCebsGJoY130_assertion description "[To investigate the association between a single-nucleotide polymorphism (SNP) of ERCC1, Asn118Asn (C → T), and the response of patients with late-stage non-small cell lung cancer (NSCLC) (n = 142) to cisplatin-based chemotherapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178115.RAT91dB3MpMkm_oOjF5D3j2YcgRyfSijOrO0kCebsGJoY130_provenance.
- NP178119.RAXP_XMME4KD_5budxmM0WSTQzU6hc6cro8IaXgEyQgzM130_assertion description "[We also discuss how this model of H2AX function could account for some aspects of the genomic instability and cancer prone human phenotypes associated with Ataxia Telangiectasia (AT), Nijmegen Breakage Syndrome (NBS), Ataxia Telangiectasia Like Disorder (ATLD), and Bloom's Syndrome (BS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178119.RAXP_XMME4KD_5budxmM0WSTQzU6hc6cro8IaXgEyQgzM130_provenance.
- NP178121.RAXxuVg4fy0l5oGHlxTeScDrxeMNgNXUUJtFdP6tNh2Cg130_assertion description "[While MAL was largely unmethylated at the transcription start site (Region 1; -48 to +73 bp) in primary serous ovarian cancers, methylation of an upstream region (Region 2; -452 to -266 bp) was inversely correlated with MAL transcription in the primary cancers (R = -0.463) and ovarian cancer cell lines (R = -0.444).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178121.RAXxuVg4fy0l5oGHlxTeScDrxeMNgNXUUJtFdP6tNh2Cg130_provenance.
- NP178124.RAZEbBEmCw5GP496jGcMxPz7PIMH2_iTbG_dbd4zmLa8g130_assertion description "[Indeed, many studies in human breast cancers show both positive and negative associations between the infiltration of various immune effectors (e.g., CD4 and CD8 T cells) and the propensity to relapse with metastatic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178124.RAZEbBEmCw5GP496jGcMxPz7PIMH2_iTbG_dbd4zmLa8g130_provenance.
- NP178130.RAcmCJIc4kf5SyecMS61ruAfbhBkNbvtHl_tLuXeFbAv8130_assertion description "[The level of miR-612 in HCC patients was inversely associated with tumor size, stage, EMT, and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178130.RAcmCJIc4kf5SyecMS61ruAfbhBkNbvtHl_tLuXeFbAv8130_provenance.
- NP178135.RAWaOzBkkY3BuvkI9mrL1IKLRnCCl3f_0Dnnp-0aPM88Q130_assertion description "[Attempts to prove the BDNF hyperactivity hypothesis may lead investigators in a new direction for the study of the pathogenesis of autism and the development of an effective intervention of this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178135.RAWaOzBkkY3BuvkI9mrL1IKLRnCCl3f_0Dnnp-0aPM88Q130_provenance.
- NP178141.RAe9X_vui2IRMv3WsGDFEWIxCNtACKLQPHneLnRYfV99Y130_assertion description "[MA and p53 mutations were found to be significantly associated with recurrence of disease (p = 0.033 and 0.026, respectively).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178141.RAe9X_vui2IRMv3WsGDFEWIxCNtACKLQPHneLnRYfV99Y130_provenance.
- NP178143.RAQVL2fGqL6xa74Rm5IDyCkyGBoOSEmISFjVMUjRWf_ZI130_assertion description "[Aberrant methylation of exon-1 sequences within the nontranscribed vimentin gene is a novel molecular biomarker of colon cancer and can be successfully detected in fecal DNA to identify nearly half of individuals with colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178143.RAQVL2fGqL6xa74Rm5IDyCkyGBoOSEmISFjVMUjRWf_ZI130_provenance.
- NP178144.RARW3I4aTLTHf7ywdDARgpNHKQU_w7g-PDm5sdK1U795w130_assertion description "[Our findings support the concept that in vivo PPARγ and NF-κB pathways are implicated in the inhibitory effects of 15dPGJ2 on inflammatory mediators at different times depending on whether the infection is caused by the lethal or non-lethal T. cruzi strain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178144.RARW3I4aTLTHf7ywdDARgpNHKQU_w7g-PDm5sdK1U795w130_provenance.
- NP178148.RARU1SAKz9tHmnm_jjlXXC3CwT4tF0oRqEV5tZjDGLaDY130_assertion description "[We investigated the role of the MDR1 P-gp gene in predicting the induction of mania in bipolar patients (BP) treated with proserotonergic drugs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178148.RARU1SAKz9tHmnm_jjlXXC3CwT4tF0oRqEV5tZjDGLaDY130_provenance.
- NP178155.RASUMarXqE6mga0KhwHtYXEviNNxc050JcBQlxJMG-RHQ130_assertion description "[We identified and characterized a gene encoding a homologue of the B subunits of cholera toxin (CTB) and heat-labile enterotoxin (LTB) of Escherichia coli from a clinical isolate of Citrobacter freundii that was found to produce a factor in the culture supernatant that cross-reacted with antibodies to CTB and LTB when assayed by enzyme-linked immunosorbent assay (ELISA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178155.RASUMarXqE6mga0KhwHtYXEviNNxc050JcBQlxJMG-RHQ130_provenance.
- NP178158.RAawSskxE4J_q-E6LACtjlC18EXeO1-0F6oJM0ilmy9_0130_assertion description "[Today 2010 there are over 19 000 publications in the area of biomarkers and prostate cancer, but only one biomarker, PSA, is used in the clinic today!]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178158.RAawSskxE4J_q-E6LACtjlC18EXeO1-0F6oJM0ilmy9_0130_provenance.
- NP178161.RAVZqPYRtL1sNBKbTWerzP6uzBPbvs8jjP9EYC_O5-Uyg130_assertion description "[Monoclonal antibodies (MoAb) and tyrosine kinase inhibitors (TKI) targeting the EGFR (Epidermal Growth Factor Receptor) pathways are currently used in colorectal cancer treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178161.RAVZqPYRtL1sNBKbTWerzP6uzBPbvs8jjP9EYC_O5-Uyg130_provenance.
- NP178162.RASgnQu8hoc_V3b4RxELRlt5A1aa5FwyrckzUi8YzbUDk130_assertion description "[After a 5-year follow-up, the elderly carriers of T-allele of TNF-α rs1799724 were at an increased risk of dementia (p = 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178162.RASgnQu8hoc_V3b4RxELRlt5A1aa5FwyrckzUi8YzbUDk130_provenance.
- NP178163.RAavcdiWeuejD05ndyIApVij-N5v8dgQX_yNRAxeKBnTQ130_assertion description "[Recent studies by ourselves and others have demonstrated breakpoint clustering in acute leukemias bearing translocations involving 11q23, and a Drosophila trithorax gene homologue (called MLL, HRX, or ALL-1) has been shown to span the 11q23 breakpoints of these translocations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178163.RAavcdiWeuejD05ndyIApVij-N5v8dgQX_yNRAxeKBnTQ130_provenance.
- NP178171.RAYdoZfpcNZYOerRk5GhVXAcG6Njl7K5VdD6RZjECljr4130_assertion description "[Furthermore, ataxin-2 (encoded by the gene ATXN2), a polyglutamine containing protein elongated in spinocerebellar ataxia type 2, has been shown to be a modulator of TDP-43 induced toxicity in ALS animal and cell models.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178171.RAYdoZfpcNZYOerRk5GhVXAcG6Njl7K5VdD6RZjECljr4130_provenance.
- NP178172.RAbceEi8QzSS04jQxu3QKKp1NbB4UOJHReJCs5jObxZRk130_assertion description "[The results of an in vivo drug sensitivity assay confirmed that DARPP-32 may play a specific role in the MDR of gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178172.RAbceEi8QzSS04jQxu3QKKp1NbB4UOJHReJCs5jObxZRk130_provenance.
- NP178181.RAVrX1mIxqDkl3APUimFN4Aq48bkqobpFnAzLEsgooRvY130_assertion description "[Since benefit from statin therapy in elderly patients has been primarily shown among those with prior vascular disease, we performed analyses in PROSPER patients with prior disease and found that pravastatin therapy significantly reduced events in 719Arg carriers [hazards ratio (HR): 0.66, 95% confidence interval (CI): 0.52-0.86] but not in noncarriers (HR: 0.94, 95% CI: 0.69-1.28), P=0.09 for interaction between treatment and carrier status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178181.RAVrX1mIxqDkl3APUimFN4Aq48bkqobpFnAzLEsgooRvY130_provenance.
- NP178186.RAe9PNbo7iwYJ_f8RXUhcJy-ppiP9AuA20aCLZybLJIFE130_assertion description "[Furthermore, we used quantitative real-time RT-PCR to quantify the levels of NDRG2 and MYC mRNA in thyroid gland cancer and breast cancer, using a distinct set of normal and tumor samples.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178186.RAe9PNbo7iwYJ_f8RXUhcJy-ppiP9AuA20aCLZybLJIFE130_provenance.
- NP178188.RATe6Y5yL87v79C9v1as5xrREjmERYDj7AGab2mqhygeI130_assertion description "[We suggest that REIC/Dkk-3 is a novel target for breast cancer treatment and that Ad-REIC might be an attractive agent against drug-resistant cancer in combination with conventional antineoplastic agents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178188.RATe6Y5yL87v79C9v1as5xrREjmERYDj7AGab2mqhygeI130_provenance.
- NP178194.RAar76RiRrqrVcb2ylqRR_twc9KOXIIq4GJSq97SBpbZ8130_assertion description "[Aberrant expression and constitutive activation of STAT3 in cervical carcinogenesis: implications in high-risk human papillomavirus infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178194.RAar76RiRrqrVcb2ylqRR_twc9KOXIIq4GJSq97SBpbZ8130_provenance.
- NP178195.RATjUhI4SiI9HEB43BF0E7doR1nFZPr1LkouZvFQLYFVA130_assertion description "[We speculated that the adipokine leptin might play a role in regulating iron metabolism in the overweight population because it shares a number of common biological features with IL-6, a major factor in the development of the anemia of chronic disease via its stimulatory actions on the production and release of the iron regulatory hormone hepcidin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178195.RATjUhI4SiI9HEB43BF0E7doR1nFZPr1LkouZvFQLYFVA130_provenance.
- NP178197.RAQ9hrQpsur0rROEI2tNO-uFpP_IKPAWrq4aBcxtarmGk130_assertion description "[Our data suggest that the HER-1 R497K and EGFR intron 1 (CA)(n) repeat polymorphisms may be potential indicators of radiosensitivity in patients with rectal cancer treated with chemoradiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178197.RAQ9hrQpsur0rROEI2tNO-uFpP_IKPAWrq4aBcxtarmGk130_provenance.
- NP178209.RAaUp7ho0DsuMoLPawJdh4avEv0Z5otiZVoPvQeE7-wS4130_assertion description "[Ataxia with ocular motor apraxia type 1 (AOA1) is an autosomal recessive cerebellar ataxia (ARCA) associated with oculomotor apraxia, hypoalbuminaemia and hypercholesterolaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178209.RAaUp7ho0DsuMoLPawJdh4avEv0Z5otiZVoPvQeE7-wS4130_provenance.
- NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_assertion description "[Single-nucleotide polymorphisms (SNPs) in the major histocompatibility complex class II transactivator (MHC2TA) gene encoding the class II transactivator have been associated with multiple sclerosis, rheumatoid arthritis, and myocardial infarction in the Swedish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178214.RAdBxsvD52GdJ0YRvulX1Bn33VSvvO121KwkIuwO6c6Mc130_provenance.
- NP178217.RAaIDITznkXHQgk_vJbdI0XLh10QLP5wnlk_8IkV_KTDY130_assertion description "[Germline mutations in the mitochondrial complex II genes, SDHB, SDHC, and SDHD, cause hereditary paraganglioma (PGL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178217.RAaIDITznkXHQgk_vJbdI0XLh10QLP5wnlk_8IkV_KTDY130_provenance.
- NP178219.RAcp3G87y06sQ4Q5guo-BD8acHldfU7-_31cu5h0vr--E130_assertion description "[Other phenotypes associated with expression of mutated WASP are X-linked thrombocytopenia and neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178219.RAcp3G87y06sQ4Q5guo-BD8acHldfU7-_31cu5h0vr--E130_provenance.
- NP178221.RAVQpTyvT5SMETQJ_4kS7LS2j3qsuZ-EWLEp7ZjJvLdoY130_assertion description "[Cases caused by Kir6.2 mutation usually result in permanent NDM (PNDM) rather than transient NDM (TNDM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178221.RAVQpTyvT5SMETQJ_4kS7LS2j3qsuZ-EWLEp7ZjJvLdoY130_provenance.
- NP178222.RAdcOXiZpKhymUMCo6dsQZNnfZI0xktQhp9BlUmGZh6as130_assertion description "[Erythromelalgia due to heterozygous gain-of-function SCN9A mutations usually presents as a pure sensory-autonomic disorder characterized by recurrent episodes of burning pain and redness of the extremities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178222.RAdcOXiZpKhymUMCo6dsQZNnfZI0xktQhp9BlUmGZh6as130_provenance.
- NP178223.RAd8saD9elYlwXjvMlFYxR0PwSkToas3vk5C7cQfQhbXM130_assertion description "[A deficiency of citrin, which is encoded by the SLC25A13 gene, causes both adult-onset type II citrullinemia (CTLN2) and neonatal intrahepatic cholestasis (NICCD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178223.RAd8saD9elYlwXjvMlFYxR0PwSkToas3vk5C7cQfQhbXM130_provenance.
- NP178225.RAQIvftRVDpF6XcmLIiDe8JyW-6orExuq48MRXT0BYkQQ130_assertion description "[Development of engineered antibodies specific for the Müllerian inhibiting substance type II receptor: a promising candidate for targeted therapy of ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178225.RAQIvftRVDpF6XcmLIiDe8JyW-6orExuq48MRXT0BYkQQ130_provenance.
- NP178228.RAcHCBVxWDqwqPC0s-Dd5uDSecaKveE394s0ECbKekFY8130_assertion description "[This study investigated three single-nucleotide polymorphisms (SNPs) of BDNF (rs6265 (Val66Met), rs11030104 and rs7103411) in Japanese patients with PD and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178228.RAcHCBVxWDqwqPC0s-Dd5uDSecaKveE394s0ECbKekFY8130_provenance.
- NP178230.RAZ_ZznxIpxzDSJBc8pelyU5ioRsLyaEOzJcbAQc4sXi0130_assertion description "[Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178230.RAZ_ZznxIpxzDSJBc8pelyU5ioRsLyaEOzJcbAQc4sXi0130_provenance.
- NP178237.RAXo2Hl0DO0TNJQnVo2LdV9M3-KxjvS7t4O7FhFuUcKUI130_assertion description "[Silencing of heparanase by siRNA inhibits tumor metastasis and angiogenesis of human breast cancer in vitro and in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178237.RAXo2Hl0DO0TNJQnVo2LdV9M3-KxjvS7t4O7FhFuUcKUI130_provenance.
- NP178238.RASd87RvHXmCNzpTxixkdDWl2poVX5KqZn0IN94oTQEFo130_assertion description "[Thus, it can be hypothesized that in a proportion of MBCs, particularly in BRCA2-associated MBCs, the level of estrogens and environmental carcinogens exposure might be increased suggesting a link between gene and environmental exposure in the pathogenesis of MBC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178238.RASd87RvHXmCNzpTxixkdDWl2poVX5KqZn0IN94oTQEFo130_provenance.
- NP178246.RAQIYRGJdqZe0SDmzYit-wHl2owyyx6HY8kOkMSIZ8vKE130_assertion description "[Effects of pegylated interferon alpha-2a on hepatitis-C-virus-associated glomerulonephritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178246.RAQIYRGJdqZe0SDmzYit-wHl2owyyx6HY8kOkMSIZ8vKE130_provenance.
- NP178252.RAfngZ9Vh17dEnZOuQPZCbhITQjQTpRwrk8fgoBdA7L94130_assertion description "[EGFR activation results in enhanced cyclooxygenase-2 expression through p38 mitogen-activated protein kinase-dependent activation of the Sp1/Sp3 transcription factors in human gliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178252.RAfngZ9Vh17dEnZOuQPZCbhITQjQTpRwrk8fgoBdA7L94130_provenance.
- NP178253.RAa0Iaf19i3idNLLCN3e1wU-JRWwFbbDtnPe-sNxUhb8M130_assertion description "[In fact PTC is the product of the fusion of the tyrosine kinase domain of the ret proto-oncogene with the 5'-terminal region of another gene that we have named H4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178253.RAa0Iaf19i3idNLLCN3e1wU-JRWwFbbDtnPe-sNxUhb8M130_provenance.
- NP178261.RAS-4CfF8jUPlorx_t6aqsnQt59jROcolcDuKdNZVPn_A130_assertion description "[We have, therefore, excluded HRY as the gene for dominant optic atrophy by sequence analysis, mapped it genetically, and identified a polymorphism in our population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178261.RAS-4CfF8jUPlorx_t6aqsnQt59jROcolcDuKdNZVPn_A130_provenance.
- NP178262.RAb-Y4E88NJyWLaB27ZGBIj3ybZgNIA9jifZJy7TZ90uc130_assertion description "[Of 20 gastric carcinomas examined, 10 (50%) and 12 (60%) expressed TRF1 and TRF2 at higher levels than did non-neoplastic mucosa, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178262.RAb-Y4E88NJyWLaB27ZGBIj3ybZgNIA9jifZJy7TZ90uc130_provenance.
- NP178263.RAfm_A0D1sCaKXnswISuAO-yk2MZ9y3pPNRDc9QezeDiE130_assertion description "[Despite efficient homeostatic proliferation of total CD4 and CD8 T cells, the frequency of CD8 T cells specific for Melan-A and cancer-testis antigens remained relatively low.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178263.RAfm_A0D1sCaKXnswISuAO-yk2MZ9y3pPNRDc9QezeDiE130_provenance.
- NP178275.RAXFD6ypbi-X2jU1I5a9fT4EcK0gi5_Gy8MyG3QVh_lfM130_assertion description "[In prostate, ovarian and breast cancer, downregulation of galectin-3 is associated with malignancy and tumor progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178275.RAXFD6ypbi-X2jU1I5a9fT4EcK0gi5_Gy8MyG3QVh_lfM130_provenance.
- NP178277.RAeK1s_KOPCtVo2YPsFo1oPkcRlSfQ20pw02CPzDrXd_s130_assertion description "[The human lung T cell compartment contains many CD8⁺ T cells specific for respiratory viruses, suggesting that the lung is protected from recurring respiratory infections by a resident T cell pool.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178277.RAeK1s_KOPCtVo2YPsFo1oPkcRlSfQ20pw02CPzDrXd_s130_provenance.
- NP178280.RAWH9RnK0-zY3KuDmDFdhh8v6ONRnt-dAqbnemS3YkJ3w130_assertion description "[LRP1 mRNA and protein were not related to CAA severity and presence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178280.RAWH9RnK0-zY3KuDmDFdhh8v6ONRnt-dAqbnemS3YkJ3w130_provenance.
- NP178283.RAat0DV0IuM4AKsNBIioSoIhkMrneCYZc8d50yOkyw59o130_assertion description "[Sjögren-Larsson syndrome (SLS; MIM#270200) is an autosomal recessive neurocutaneous disease caused by mutations in the ALDH3A2 gene for fatty aldehyde dehydrogenase (FALDH), a microsomal enzyme that catalyzes the oxidation of medium- and long- chain aliphatic aldehydes fatty acids.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178283.RAat0DV0IuM4AKsNBIioSoIhkMrneCYZc8d50yOkyw59o130_provenance.
- NP178285.RAZK1KiCzEulRvb4IGkLkGNJRtVYRVOZ0xtt-iXTeLK4A130_assertion description "[Alterative splicing of Aurora-B produces different sizes of proteins in HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178285.RAZK1KiCzEulRvb4IGkLkGNJRtVYRVOZ0xtt-iXTeLK4A130_provenance.
- NP178292.RAWWxJV30FuMmpP_ozzapKdRUHDLXhDQqVvZTLfvhgORc130_assertion description "[However, 3 cancer/testis antigen genes (PAGE4, SCP-1, and SPANX) and 3 clinicopathologic parameters (lymph node involvement, vessel cancer embolus, and tumor invasion depth) correlated significantly with liver metastasis of colorectal cancer (P < .05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178292.RAWWxJV30FuMmpP_ozzapKdRUHDLXhDQqVvZTLfvhgORc130_provenance.
- NP178295.RAd_D_Ki2fmaWjm-i4pnkXjEWHlqxmCSrWQ0I783PXhNo130_assertion description "[The family-based analysis did not reveal any association between DAT1 alleles and ADHD either when it was considered as a dichotomous trait (Z = 0.16, p =.86) or as a continuous trait (Wender Scale Z = -1.67, p =.09; Brown ADD Scale Z = 0.28, p =.77).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178295.RAd_D_Ki2fmaWjm-i4pnkXjEWHlqxmCSrWQ0I783PXhNo130_provenance.
- NP178302.RAduEHhhhDjzOVX0mR7zkRJ-r8CVV4EIrKlAzm_-ZMVwQ130_assertion description "[Three genes have been identified which, when mutated, cause Familial Alzheimer disease (FAD): the presenilin-1 (PS1), the presenilin-2 (PS2) and the amyloid precursor protein (APP) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178302.RAduEHhhhDjzOVX0mR7zkRJ-r8CVV4EIrKlAzm_-ZMVwQ130_provenance.
- NP178304.RAQdwuw9lSFkap8L8wSEBsAKBdxv51Nn2HItC2F_MDXG0130_assertion description "[In summary, our case-control study of lung cancer revealed that the effect of these polymorphisms is not very marked for different genotypic combinations of GSTP1, GSTM1 and GSTT1 in the context of developing lung cancer in a north Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178304.RAQdwuw9lSFkap8L8wSEBsAKBdxv51Nn2HItC2F_MDXG0130_provenance.
- NP178305.RAZhzGThM0EsPuRj_tVtK-iHKJP2snhxlaziIqQy-5nuM130_assertion description "[Twenty-nine hepatoblastomas were evaluated for possible prognostic correlation between p27 expression in different histotypes of hepatoblastoma, changes during chemotherapy, and outcome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178305.RAZhzGThM0EsPuRj_tVtK-iHKJP2snhxlaziIqQy-5nuM130_provenance.
- NP178306.RAZlWRBI9ocBo7E5EeeOCQ_HekTscJDqYubjLSOi-neg8130_assertion description "[This is the first evidence that the coexistence of somatic and germline alterations in the APC gene is involved in the development of a jejunal adenoma causing small-bowel intussusception.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178306.RAZlWRBI9ocBo7E5EeeOCQ_HekTscJDqYubjLSOi-neg8130_provenance.
- NP178309.RAbYsBXV_F1wjiDFZp4igoiTZeRfVcXvqtVM2wteGCOhk130_assertion description "[This study investigated the susceptibility and prognostic implications of the CYP2E1, CYP2C19, CYP2D6, mEH and NAT2 gene polymorphisms in breast carcinoma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178309.RAbYsBXV_F1wjiDFZp4igoiTZeRfVcXvqtVM2wteGCOhk130_provenance.
- NP178314.RASZ4GHvIUCnY2KwjaJc1mza_PdcE7x2fERhZA67i52ec130_assertion description "[Several PGK variants have been characterized in asymptomatic individuals or in patients with hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178314.RASZ4GHvIUCnY2KwjaJc1mza_PdcE7x2fERhZA67i52ec130_provenance.
- NP178317.RAW28vapFk_IUPReiE_pnXe84EVfTXvrf-6X0yW3QZcWg130_assertion description "[We conclude that RFP2, c13ORF1, and a chromosome 13-specific ST13-like gene, FAM10A4, are the most likely candidates for such a type of B-CLL TSG.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178317.RAW28vapFk_IUPReiE_pnXe84EVfTXvrf-6X0yW3QZcWg130_provenance.
- NP178322.RAaAAUzbau73KA1i4DDwUm7wX85H_3UEi2IkkvFmZFkrQ130_assertion description "[These observations are in line with recent reports showing that at least certain cell lines from other chromosome breakage syndromes, such as ataxia telangiectasia and Bloom syndrome, may be also defective for radiation-induced increase of p53 protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP178322.RAaAAUzbau73KA1i4DDwUm7wX85H_3UEi2IkkvFmZFkrQ130_provenance.