Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP316307.RAas4l2RBT9xFS0yofTn1PtuXnPNGKMhqFqI9zNQ_kPUg130_assertion description "[In core binding factor (CBF) acute myeloid leukaemia (AML), realtime quantitative PCR is useful to quantify the fusion transcript ratio (CBFβ-MYH11 and AML1-ETO, in case of inv(16) and t(8;21) respectively) in peripheral blood and bone marrow during the courses of chemotherapy, in order to monitor minimal residual disease (MRD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316307.RAas4l2RBT9xFS0yofTn1PtuXnPNGKMhqFqI9zNQ_kPUg130_provenance.
- NP316310.RAZmXujEXkJAn1hdlxpy28xTRXime4OSJ7J1aN2xuCGa0130_assertion description "[This implicates FAM134B as critical in long-term survival of nociceptive and autonomic ganglion neurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316310.RAZmXujEXkJAn1hdlxpy28xTRXime4OSJ7J1aN2xuCGa0130_provenance.
- NP316315.RAQNKkZqM0kZ6bVs5pquzuLbM2F7SevUbJSMiIOZw6U0o130_assertion description "[This study demonstrates the power and potential weaknesses of in-depth sequencing as a tool to thoroughly investigate the phylogeny of malignant PCs in MM and the IGHV repertoire of normal BMPCs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316315.RAQNKkZqM0kZ6bVs5pquzuLbM2F7SevUbJSMiIOZw6U0o130_provenance.
- NP316318.RAeRAfkuI6Hmo8wZZs6cmlPEBFxFKfVetfaGwK8faikko130_assertion description "[Mutations in the epsilon-sarcoglycan gene (SGCE) can cause autosomal dominant inherited myoclonus-dystonia (M-D).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316318.RAeRAfkuI6Hmo8wZZs6cmlPEBFxFKfVetfaGwK8faikko130_provenance.
- NP316320.RAT2vIYUSew8jDB8x097m-weloebZFNSvGgybPiV-M9n8130_assertion description "[Clinical studies reported a link between increased sPLA2 expression and the presence of cholesterol gallstones.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316320.RAT2vIYUSew8jDB8x097m-weloebZFNSvGgybPiV-M9n8130_provenance.
- NP316324.RAfoNnBwCYtUK7LFao55Dy2ivsifBU6Qd8nQ7pybM6gBI130_assertion description "[Pompe disease is an autosomal recessive lysosomal storage disorder (LSD) caused by deficiency of lysosomal acid alpha-glucosidase (GAA) activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316324.RAfoNnBwCYtUK7LFao55Dy2ivsifBU6Qd8nQ7pybM6gBI130_provenance.
- NP316332.RAU8ezweRNgtob0iFtJ4Jc9Rw5jHmkiqfsWgxNANiBGiQ130_assertion description "[IGFBP7 expression is significantly downregulated in human HCC samples and cell lines compared with normal liver and hepatocytes, respectively, and inversely correlates with the stages and grades of HCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316332.RAU8ezweRNgtob0iFtJ4Jc9Rw5jHmkiqfsWgxNANiBGiQ130_provenance.
- NP316334.RAVpvqIv5clElfy7Fqr5Rioy-AC3FAZIRtlmJCoEwbwss130_assertion description "[Chromosome maintenance protein 1 (CRM1) is a nuclear export receptor involved in the active transport of tumor suppressors (e.g., p53 and nucleophosmin) whose function is altered in cancer because of increased expression and overactive transport.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316334.RAVpvqIv5clElfy7Fqr5Rioy-AC3FAZIRtlmJCoEwbwss130_provenance.
- NP316346.RAbum_ox83mqXT1sQoJ9mUMtMpIDmGHnR7XWkP4leaaGg130_assertion description "[Runt-related transcription factor 3 (RUNX3) is known as a tumor suppressor gene for gastric cancer and other cancers, this gene may be involved in the development of hepatocellular carcinoma (HCC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316346.RAbum_ox83mqXT1sQoJ9mUMtMpIDmGHnR7XWkP4leaaGg130_provenance.
- NP316362.RASeFlIkiA1qoJmktKkOA5y458D2NG4k-I2I2953IpPnQ130_assertion description "[The majority of these diseases result from expanded polyglutamine tracts in the encoded protein as seen in SCA1, SCA2, SCA3, SCA6, SCA7 and Dentatorubral-Pallidoluysian Atrophy (DRPLA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316362.RASeFlIkiA1qoJmktKkOA5y458D2NG4k-I2I2953IpPnQ130_provenance.
- NP316367.RARwAH_QF8vlZFusC7DnTbqItFYDODaeriSDb2OAPonEA130_assertion description "[Polymorphisms in the genes encoding for ERalpha, ERbeta and PR did not correlate with the occurrence of uterine leiomyomas in our Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316367.RARwAH_QF8vlZFusC7DnTbqItFYDODaeriSDb2OAPonEA130_provenance.
- NP316370.RAT9x9p6og2Am03VTgSDZdUq43j9u46zxpL6if8W5xkAE130_assertion description "[Our findings imply that a COX-2 inhibitor might improve the prognosis of patients with lung cancer through the reduction of G-CSF or GM-CSF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316370.RAT9x9p6og2Am03VTgSDZdUq43j9u46zxpL6if8W5xkAE130_provenance.
- NP316373.RAffzX2AVNa1v08KSYywrPSXSnZlPvfdCMCdXzAZ4KZyo130_assertion description "[In contrast, the mitochondrial beta-oxidation of fatty acids can be either increased (as in insulin resistance-associated NASH) or decreased (as in drug-induced NASH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316373.RAffzX2AVNa1v08KSYywrPSXSnZlPvfdCMCdXzAZ4KZyo130_provenance.
- NP316374.RAYp7qNhqfOvyLLa9sCiaIebeLbbZBmCc1PLMPqj35Ge0130_assertion description "[Tgase-2 expressing A549(WT) cells-injected mice group showed increased expressions of N-cadherin and JNK activation, but decreased expression of PP2A in lung cancer tissue comparing with the A549(shTG2) cells-injected group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316374.RAYp7qNhqfOvyLLa9sCiaIebeLbbZBmCc1PLMPqj35Ge0130_provenance.
- NP316375.RAYJNnsCXrgng4fs_A3vn3ZVqPRAUgyu-le1CrObdmjss130_assertion description "[To confirm the association between the MHC2TA -168A-->G polymorphism and MI and to study its putative role for microalbuminuria, the metabolic syndrome (MetS) and cardiovascular mortality.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316375.RAYJNnsCXrgng4fs_A3vn3ZVqPRAUgyu-le1CrObdmjss130_provenance.
- NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_assertion description "[Familial amyloidosis of the Finnish type (FAF) is an autosomal dominant type of systemic amyloidosis caused by a G654A (Asn-187) or G654T (Tyr-187) mutation in the gelsolin gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316379.RAQ4PIhamUZevGfhrjwQRSyptxJZd5ZYQdh4-OWynnBD0130_provenance.
- NP316381.RAbOJy06huZYGEepjBpImc-aA5qAoJqmtsID05BhlCZ8Q130_assertion description "[We previously created a knock-in mutant mouse harboring a dominantly negative mutant thyroid hormone receptor beta (TRbeta(PV/PV) mouse) that spontaneously develops a follicular thyroid carcinoma similar to human thyroid cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316381.RAbOJy06huZYGEepjBpImc-aA5qAoJqmtsID05BhlCZ8Q130_provenance.
- NP316382.RASCXOF3SZBKTfhZa9hmaSgCfrbLiiD8Sm5TANrslRqDM130_assertion description "[We have studied the tumor-specific modulation of CPT1 and FAS in human colorectal cancer (n = 11) and breast carcinomas (n = 24).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316382.RASCXOF3SZBKTfhZa9hmaSgCfrbLiiD8Sm5TANrslRqDM130_provenance.
- NP316414.RAUUn9nbiWQCspYkjLKS8e14yV1aX-8Z_YBEdJKYu2oQc130_assertion description "[Cytochrome p450 profile of colorectal cancer: identification of markers of prognosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316414.RAUUn9nbiWQCspYkjLKS8e14yV1aX-8Z_YBEdJKYu2oQc130_provenance.
- NP316419.RAWvgFv0O9GHJfJDZ3B76Ruujur7sfRXzMmT9z9WupWN0130_assertion description "[These findings suggest that a balance between the expression of Axl and Tyro3 is associated with a molecular switch between a dormant and a proliferative phenotype in PCa metastases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316419.RAWvgFv0O9GHJfJDZ3B76Ruujur7sfRXzMmT9z9WupWN0130_provenance.
- NP316423.RAbGt0QpSzIMK9MLs__Q-RMiKt8iLW6M2a7W2QqcCc-TY130_assertion description "[The transcription factor cyclic AMP response element binding protein (CREB) and the neurotrophin brain-derived neurotrophic factor (BDNF) are targets of diverse classes of antidepressants and are known to be regulated in animal models and in patients suffering from depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316423.RAbGt0QpSzIMK9MLs__Q-RMiKt8iLW6M2a7W2QqcCc-TY130_provenance.
- NP316427.RAampJqArF-UCwuv4wGIDz1E0n8IpLj1E2kLm-7qBDv9o130_assertion description "[In myelodysplasia, c-mpl expression was elevated in 44% of chronic myelomonocytic leukemia (CMML), 42% of refractory anemia with excess myeloblasts (RAEB), and RAEB in transformation to acute leukemia (RAEBt), but not in refractory anemia (RA) and RA with ringed sideroblasts (RARS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316427.RAampJqArF-UCwuv4wGIDz1E0n8IpLj1E2kLm-7qBDv9o130_provenance.
- NP316429.RAeFL5V6SQ2i8bX6A43jAjpxnrTnzNgk96ovWQOGvoTck130_assertion description "[Membrane bound MUC1 was present in higher concentration in SS versus NDE only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316429.RAeFL5V6SQ2i8bX6A43jAjpxnrTnzNgk96ovWQOGvoTck130_provenance.
- NP316431.RAV17TFeiRBvmfbHylRrYb_9R7PZv1N0c30Cp3o7B_6Lo130_assertion description "[Results suggest that the I allele of the angiotensin converting enzyme insertion/deletion polymorphism may interact with the AGT-6G allele to increase mean carotid IMT in the population as a whole.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316431.RAV17TFeiRBvmfbHylRrYb_9R7PZv1N0c30Cp3o7B_6Lo130_provenance.
- NP316435.RAa3wS_JA6kl2uhg2rKhvm8kZcwQu4u4xFgd2zgzvoKEM130_assertion description "[A pilot study on relationships of selected molecular factors (c-myc oncogene average gene copy numbers (AGCN); serum CEA and CA 15.3 antigen levels; tumor cells' DNA values), to the ex vivo chemosensitivity of primary female human breast cancer in a modified adenosine triphosphate cell viability chemosensitivity assay (ATP-CVA), was performed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316435.RAa3wS_JA6kl2uhg2rKhvm8kZcwQu4u4xFgd2zgzvoKEM130_provenance.
- NP316441.RAaAdd7JHwyvHWAfvm3-DvDBd2Rxmijgc54vExivP_XCY130_assertion description "[The role of Chk2 expression in mammary tumorigenesis, however, is still poorly understood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316441.RAaAdd7JHwyvHWAfvm3-DvDBd2Rxmijgc54vExivP_XCY130_provenance.
- NP316442.RAQfodfO0Nm6z94mAooA0KHPZkJSBFCvw8kZesMcNJg4g130_assertion description "[Although the expression of PSA has been shown to correlate with the progression of certain tumors such as small cell lung carcinoma, there have been no studies to determine the roles of PSA in gliomas, the most common type of primary brain tumor in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316442.RAQfodfO0Nm6z94mAooA0KHPZkJSBFCvw8kZesMcNJg4g130_provenance.
- NP316443.RAVvuut98wZJYqOUw2MsIRCZrz5F-cbG7nIxKo-6vpeNc130_assertion description "[In order to determine the relative importance of genetics and the environment on the occurrence of atopic diseases, we investigated the familial aggregation of atopic eczema, allergic rhinitis, and allergic asthma in the relatives of 426 patients with atopic eczema and 628 subjects with no history of eczema (5,136 family members in total).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316443.RAVvuut98wZJYqOUw2MsIRCZrz5F-cbG7nIxKo-6vpeNc130_provenance.
- NP316447.RAVi0_sF1WCF8aTul5ptxxu9iMM6lx1GeWfnqLAN3f3ag130_assertion description "[Hence, S1P and S1P(2) on mast cells are determinants of systemic anaphylaxis and associated pulmonary edema and might be beneficial targets for anaphylaxis attenuation and prophylaxis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316447.RAVi0_sF1WCF8aTul5ptxxu9iMM6lx1GeWfnqLAN3f3ag130_provenance.
- NP316448.RASqNhkxyX5uzkqz1oD-__PRxMq07731_dMy2HdEnAdhg130_assertion description "[Shigella flexneri serotype 2a carries a chromosomal pathogenicity island (PAI), termed the she PAI, that has been implicated in the pathogenesis of diarrhoeal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316448.RASqNhkxyX5uzkqz1oD-__PRxMq07731_dMy2HdEnAdhg130_provenance.
- NP316450.RAaoH5-FmvXMPzLrkyHU7dExLvOPaOxQ24Cd88uDGmf98130_assertion description "[We present our experience of 46 children with CMS, referred to us between 1992-2007 with provisional diagnoses of congenital myopathy (22/46), CMS or limb-girdle myasthenia (9/46), central hypotonia or neurometabolic disease (5/46), myasthenia gravis (4/46), limb-girdle or congenital muscular dystrophy (4/46) and SMA (2/46).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316450.RAaoH5-FmvXMPzLrkyHU7dExLvOPaOxQ24Cd88uDGmf98130_provenance.
- NP316453.RAYoznhgRkxKA3ZwYMRK3Xdg10wYcXF0RRCZ-65tJS01s130_assertion description "[The frequencies of HSPA1L BB genotype and B allele in HCC were more than in CH [odds ratio (OR): 9.83; P = 0.000], but also in HBV-related HCC than Chronic Hepatitis B (CHB) [OR: 3.44; P = 0.004] and HCV-related HCC compared to CHC [OR: 6.32; P = 0.010].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316453.RAYoznhgRkxKA3ZwYMRK3Xdg10wYcXF0RRCZ-65tJS01s130_provenance.
- NP316459.RAZ1mad_vQbs7MKR9pT7luJiyPzr27xm7fON0KnxSx18s130_assertion description "[Expression of the c-erbB-2 gene product and the epidermal growth factor receptor (EGF-R) was investigated in 54 cases of human bladder cancer immunohistologically and by Western blot analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316459.RAZ1mad_vQbs7MKR9pT7luJiyPzr27xm7fON0KnxSx18s130_provenance.
- NP316463.RAaiZKgrtCdowdg9L5zuiqtR2A96ikMa-AwlZeLDv7faM130_assertion description "[These data suggest that the human 5q11.2 breast cancer risk allele marked by rs889312 is mammary gland autonomous, and MIER3 is a candidate breast cancer susceptibility gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316463.RAaiZKgrtCdowdg9L5zuiqtR2A96ikMa-AwlZeLDv7faM130_provenance.
- NP316465.RAbb5IOvpOXKDnDY7jW0fEfXHOKeEDU_4UuRAs_zJXMuw130_assertion description "[A set of initial clinical criteria have been drawn up which it is recommended should be fulfilled before a patient is tested: at least three recurrent bouts, age at disease onset < 20 years and elevated levels of C-reactive protein, especially in individuals with urticaria and moderate fever.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316465.RAbb5IOvpOXKDnDY7jW0fEfXHOKeEDU_4UuRAs_zJXMuw130_provenance.
- NP316466.RAWESHYx0UAmbg6gS6h-sVD82YKkiqVg--HBswhUdhLfo130_assertion description "[A homozygous gene deletion at the glutathione S-transferase M1 (GSTM1) locus of genomic DNA from blood spots was studied by PCR in the group of Slavic populations from the north-western and central-eastern regions of European Russia and in patients with lung cancer (LC), other tumors (OT), endometriosis (E), alcoholic cirrhosis (AC), cystic fibrosis (CF) and chronic bronchitis (CB).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316466.RAWESHYx0UAmbg6gS6h-sVD82YKkiqVg--HBswhUdhLfo130_provenance.
- NP316477.RAbLQ4Uy6kCEM5J0UZl5WzmgVjfaK2QHKN3d_lpQXbUek130_assertion description "[Hereditary thrombotic thrombocytopenic purpura, Upshaw-Schulman syndrome, ADAMTS13 Hereditary thrombotic thrombocytopenic purpura (TTP), also known as Upshaw-Schulman syndrome, is a rare recessively inherited disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316477.RAbLQ4Uy6kCEM5J0UZl5WzmgVjfaK2QHKN3d_lpQXbUek130_provenance.
- NP316483.RAXbvnBtBE6uj7puAKFpulorwGCNCxm7RUpCSm8j0dQg4130_assertion description "[Iron stores and HFE genotypes are not related to increased risk of ischemic stroke. A prospective nested case-referent study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316483.RAXbvnBtBE6uj7puAKFpulorwGCNCxm7RUpCSm8j0dQg4130_provenance.
- NP316490.RATMXhEJ_3vpsGWvMuceuTWnmV8Z5BTd2oLK6jLDAJvIU130_assertion description "[Gigantism is a particular feature of AIP mutations and occurs in more than one third of affected somatotropinoma patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316490.RATMXhEJ_3vpsGWvMuceuTWnmV8Z5BTd2oLK6jLDAJvIU130_provenance.
- NP316495.RAeXj3I8hdlJBQdmfZ_bhJai8XXZAQ8x95PJfqL3B1RSI130_assertion description "[Mutations in CDKL5 and ARX are known causes of early-onset epilepsy and severe developmental delay in males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316495.RAeXj3I8hdlJBQdmfZ_bhJai8XXZAQ8x95PJfqL3B1RSI130_provenance.
- NP316503.RAf8Sd-RvCJxvEKVoOzN6fGBlTW-OaaHJf9UpsU5toxqo130_assertion description "[Naturally occurring BMP15 mutation leads to early ovarian failure in humans, and BMP15 has been shown to activate the Smad1/5/8 pathway in that context.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316503.RAf8Sd-RvCJxvEKVoOzN6fGBlTW-OaaHJf9UpsU5toxqo130_provenance.
- NP316504.RAWZB4Rb44swNhQB058A_kuGV1CFcXumO7DjYNGaCeOw8130_assertion description "[The discovery in the human ocular ciliary body of glaucoma-associated genes (i.e., MYOC, CYP1B1), neuroendocrine processing enzymes, neuroendocrine peptides, steroid-converting enzymes, glutamate transporters, glutamate-metabolizing enzymes, and anti-angiogenic factors requires a reevaluation of its function on aqueous humor secretion, intraocular pressure and its role in glaucoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316504.RAWZB4Rb44swNhQB058A_kuGV1CFcXumO7DjYNGaCeOw8130_provenance.
- NP316508.RAQ35VnqETiYYf1pGmzuam8rqCfWWQGeadu1COVUwIITk130_assertion description "[A meta-analysis was performed to evaluate the association between eNOS Glu298Asp gene polymorphism and ESRD susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316508.RAQ35VnqETiYYf1pGmzuam8rqCfWWQGeadu1COVUwIITk130_provenance.
- NP316512.RAU3mGREQp64An2fHdamtc6gLYCiWvBcr4FwSfZZ1voew130_assertion description "[More than 40% of Japanese people have the inactive form of ALDH2, and inactive ALDH2 is a risk factor for multiple cancer of the esophagus, as well as head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316512.RAU3mGREQp64An2fHdamtc6gLYCiWvBcr4FwSfZZ1voew130_provenance.
- NP316515.RATTVJBR-sq3uSEhXVd-Dz5MHpuLKCR1hUqALFn7n6ByQ130_assertion description "[Genome-wide association studies indicate that IL23R and five additional genes involved in Th17 differentiation (IL12B, JAK2, STAT3, CCR6 and TNFSF15) are associated with susceptibility to Crohn's disease and partly also to ulcerative colitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316515.RATTVJBR-sq3uSEhXVd-Dz5MHpuLKCR1hUqALFn7n6ByQ130_provenance.
- NP316516.RAVK0W6-j1QCjCmwo4x_BZFrUqhcBZ79mISLG2YBsSerE130_assertion description "[The platelet count was higher and the rate of myeloperoxidase (MPO)-positive blasts was lower in AML with MLD than in the other WHO categories.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316516.RAVK0W6-j1QCjCmwo4x_BZFrUqhcBZ79mISLG2YBsSerE130_provenance.
- NP316532.RAewvRsXT7-Bk_Ft1icstQX1g9xCfWQDbmkg9wL_rgsLQ130_assertion description "[In addition, the single-base mutation (C --> T) at position -52 that was identified in a patient with chronic granulomatous disease inhibited the binding of PU.1 to the promoter.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316532.RAewvRsXT7-Bk_Ft1icstQX1g9xCfWQDbmkg9wL_rgsLQ130_provenance.
- NP316534.RAQ9vEbIWXPf0M5PR7fUj4APbxMD4iv7cBZbU-5U0BIxs130_assertion description "[Evidence of oxytocin/oxytocin receptor interplay in human prostate gland and carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316534.RAQ9vEbIWXPf0M5PR7fUj4APbxMD4iv7cBZbU-5U0BIxs130_provenance.
- NP316535.RATOuTN3B51N5fU6e31Ewq8UV1eIeirAHLSR0z8a7BRYI130_assertion description "[Multiple logistic regression analysis with forward stepwise selection using the potential confounders (sex, age, diabetes, hypertension, smoking and alcoholism) and eNOS gene variant revealed that the VNTR polymorphism in intron 4 of the eNOS gene is significantly [adjusted odds ratio=6.23, 95%CI (4.30-9.29), p=0.000] associated with ischemic stroke in the South Indian population from Andhra Pradesh.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316535.RATOuTN3B51N5fU6e31Ewq8UV1eIeirAHLSR0z8a7BRYI130_provenance.
- NP316536.RAdTKCQP2MEQJIp7q7Af877LdYJW2d3nw8EQyH2H1oDpY130_assertion description "[Cholesteryl ester transfer protein concentration is associated with progression of atherosclerosis and response to pravastatin in men with coronary artery disease (REGRESS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316536.RAdTKCQP2MEQJIp7q7Af877LdYJW2d3nw8EQyH2H1oDpY130_provenance.
- NP316537.RAZEYw-gr5skw1c0Z39ZH5ivCLeaA8bqoOfy1LJjgAPbA130_assertion description "[Our data suggest that genetic variants in CRHR1 that associate with differential cortisol activation may also modulate levels of anxiety related to the stress of raising a child with FXS among women who carry an FMR1 premutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316537.RAZEYw-gr5skw1c0Z39ZH5ivCLeaA8bqoOfy1LJjgAPbA130_provenance.
- NP316541.RAR9YUSb4C05omo3U6XE2ivxK1LrxcXxozdjovcGw6Wuc130_assertion description "[This work has addressed these discrepancies by infecting the corneas of mice lacking CD4(+) and CD8(+) T cells with herpes simplex virus type 1 (HSV-1) and monitoring both corneal disease and latent infection of trigeminal ganglia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316541.RAR9YUSb4C05omo3U6XE2ivxK1LrxcXxozdjovcGw6Wuc130_provenance.
- NP316548.RAZtNe97oyazvSfjiyq7FtYi7_DN0Nyl90tM090CD8h-w130_assertion description "[Autosomal dominant inheritance has been found in clinical studies of relatives of PPR-positive epilepsy and nonepilepsy subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316548.RAZtNe97oyazvSfjiyq7FtYi7_DN0Nyl90tM090CD8h-w130_provenance.
- NP316550.RAbTAnCEehinILA4TJssqHe6qwe7HcNxTqaqby-AgQpc8130_assertion description "[In contrast, a large number of studies have reported no association between HFE mutations and coronary heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316550.RAbTAnCEehinILA4TJssqHe6qwe7HcNxTqaqby-AgQpc8130_provenance.
- NP316551.RAYcIMbVTVemTpHtz3RWAhUIuuPREk8PBa6fHfd2OkWwA130_assertion description "[Logistic regression analysis showed that the presence of the S allele of 5-HTTLPR was related to a life-time risk of suicide attempts, but only in male subjects (p=0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316551.RAYcIMbVTVemTpHtz3RWAhUIuuPREk8PBa6fHfd2OkWwA130_provenance.
- NP316552.RAeHFuZWabAp_2TSmDIJzH5l_dbRKqK3W7XwzrCk5sBIQ130_assertion description "[Taken together, we concluded that UCA1 regulated cell cycle through CREB via PI3K-AKT dependent pathway in bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316552.RAeHFuZWabAp_2TSmDIJzH5l_dbRKqK3W7XwzrCk5sBIQ130_provenance.
- NP316554.RARERyILOXMgz_E9YL3W57i5kX5DoZKXPaU1Dyv4aywfc130_assertion description "[Expression and prognostic significance of centromere protein A in human lung adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316554.RARERyILOXMgz_E9YL3W57i5kX5DoZKXPaU1Dyv4aywfc130_provenance.
- NP316555.RAYFx180Szmif3vE1b2RCa-bLUzQ3JRlAO4aHzILvHE9U130_assertion description "[A novel beta1,3-N-acetylglucosaminyltransferase (beta3Gn-T8), which synthesizes poly-N-acetyllactosamine, is dramatically upregulated in colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316555.RAYFx180Szmif3vE1b2RCa-bLUzQ3JRlAO4aHzILvHE9U130_provenance.
- NP316559.RAS22DK0d3F0FEJICKbuCZ96hqfhxxyBJYZN8TaSaKh4I130_assertion description "[Mutations in the genes that encode the presenilin 1 and 2 (PS1 and PS2) proteins cause the majority of familial Alzheimer's disease (FAD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316559.RAS22DK0d3F0FEJICKbuCZ96hqfhxxyBJYZN8TaSaKh4I130_provenance.
- NP316562.RAX_NaKHoSriXtL2UDklUr1CXU9AlPpKKzhgvoLZ2t470130_assertion description "[Overall, our data indicates that YBX1 is down-regulated during myeloid differentiation and the aberrant YBX1 expression in leukemic cells could be a contributing factor in the development of leukemia by blocking their differentiation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316562.RAX_NaKHoSriXtL2UDklUr1CXU9AlPpKKzhgvoLZ2t470130_provenance.
- NP316564.RAUpbUKUO1_VkfE-vPxOlX9wMeD6WP0KDveNTgWlDV72U130_assertion description "[NAT2 rapid acetylators with smoking habit may increase the risk of ALC in Chinese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316564.RAUpbUKUO1_VkfE-vPxOlX9wMeD6WP0KDveNTgWlDV72U130_provenance.
- NP316566.RActfp_rvrJIzVLEsZXdboYhPEaGSRg22ifx4WUgvk2dk130_assertion description "[Deregulation of one or more imprinted genes located at chromosome 11p15.5, of which insulin-like growth factor 2 (IGF2) is the most likely candidate, is believed to cause BWS, whereas the etiology of KTWS is completely obscure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316566.RActfp_rvrJIzVLEsZXdboYhPEaGSRg22ifx4WUgvk2dk130_provenance.
- NP316567.RAVCMj2hwTYXGOT8ZREm3SdxoiXbSed18CkuR-hNi4XpA130_assertion description "[Astrocyte elevated gene-1 (AEG-1), upregulated in various types of human cancers, has been reported to be associated with the carcinogenesis of human cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316567.RAVCMj2hwTYXGOT8ZREm3SdxoiXbSed18CkuR-hNi4XpA130_provenance.
- NP316571.RAfSwrMPmhbnjbqyDghiOaHWxxsjXDfX4PyAuCfDAcepA130_assertion description "[ZNF652, a novel zinc finger protein, interacts with the putative breast tumor suppressor CBFA2T3 to repress transcription.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316571.RAfSwrMPmhbnjbqyDghiOaHWxxsjXDfX4PyAuCfDAcepA130_provenance.
- NP316581.RAaKY6Djg3F18dVwM1nUCc99QSsDT7_0M4iZNSzCY-Evo130_assertion description "[In the actual scenario of the search for further genetic susceptibility factors, a recent paper noted an SNP in the UCP2 gene as a multiple sclerosis (MS) risk factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316581.RAaKY6Djg3F18dVwM1nUCc99QSsDT7_0M4iZNSzCY-Evo130_provenance.
- NP316583.RAb-psKl7m2KwOIEuG7XhTBpRgp4rfiNjgwDsdyL0pXVM130_assertion description "[Deficiencies in the PD-1/programmed death-ligand 1 (PD-L1) pathway are associated with autoimmune diseases, including those of the central nervous system (CNS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316583.RAb-psKl7m2KwOIEuG7XhTBpRgp4rfiNjgwDsdyL0pXVM130_provenance.
- NP316585.RAYnoptVejMyIHx0ff3xi_4-lTgwaTXLOk6Dx779a9rXc130_assertion description "[PD-1 blockade by CT-011, anti-PD-1 antibody, enhances ex vivo T-cell responses to autologous dendritic cell/myeloma fusion vaccine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316585.RAYnoptVejMyIHx0ff3xi_4-lTgwaTXLOk6Dx779a9rXc130_provenance.
- NP316587.RAeHMxMAASXoEAlwrODWjYy6Digd7Swbs0zLfEEZ5t-aQ130_assertion description "[Expression and imprinting of insulin-like growth factor II (IGF2) and H19 genes in uterine leiomyomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316587.RAeHMxMAASXoEAlwrODWjYy6Digd7Swbs0zLfEEZ5t-aQ130_provenance.
- NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316591.RAUcQGvA951znDj6XOvHl39Z0W9lTNdwWctVpae7Zl4vc130_provenance.
- NP316592.RAUKGdxGZVshxZVaf1_Jk-bzROwl3x97aO6OA656QV0Rs130_assertion description "[TRS subtypes were: synovial sarcoma (SS, n=45), myxoid-round cell liposarcoma (MRC-L-sarcoma, n=27), alveolar soft part sarcoma (ASPS, n=4), endometrial stromal sarcoma (ESS, n=3) and clear cell sarcoma (CCS, n=2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316592.RAUKGdxGZVshxZVaf1_Jk-bzROwl3x97aO6OA656QV0Rs130_provenance.
- NP316597.RAUnmIHlnWS1PG84YfU7okjepzO6a7dwT1Q5dKa1jKqYM130_assertion description "[Studies of a number of other benign solid tumors - most of them in tissues of mesenchymal origin - indicated that involvement of HMGIC is not restricted to uterine leiomyomas, suggesting that benign solid tumor formation might have a common genetic denominator.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316597.RAUnmIHlnWS1PG84YfU7okjepzO6a7dwT1Q5dKa1jKqYM130_provenance.
- NP316604.RAUJ0xkvn8iQ--pYwekv_DBd24N2DqYrVkaIFUfgLhTes130_assertion description "[Obstetric cholestasis (OC) is a cholestatic disorder with a prominent genetic background including variation in diverse hepatobiliary lipid transporters, such as ABCB4 (phospholipids) and ABCB11 (bile salts).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316604.RAUJ0xkvn8iQ--pYwekv_DBd24N2DqYrVkaIFUfgLhTes130_provenance.
- NP316607.RAfsOX5V7NekVC1N4do-GAs_ZQ5KmBxjcymFz6jWyqW5Q130_assertion description "[Independent series of bladder tumors showed that transcript and protein levels of galectin-3 were differentially expressed along bladder cancer progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316607.RAfsOX5V7NekVC1N4do-GAs_ZQ5KmBxjcymFz6jWyqW5Q130_provenance.
- NP316608.RAcGEGLI9PMbUW-HRRmbTFY3AB0R7QM-Xn_WcZonT0InU130_assertion description "[Background: Fragile X-associated tremor/ataxia syndrome (FXTAS) is a newly identified neurodegenerative disorder due to intermediate expansion of trinucleotide CGG repeats (55 - 200 repeats) in the 5' untranslated region (UTR) of the Fragile X mental retardation 1 (FMR1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316608.RAcGEGLI9PMbUW-HRRmbTFY3AB0R7QM-Xn_WcZonT0InU130_provenance.
- NP316611.RAX9nE7hAoQrV-reB0DFdv7yXZ2idbLY8CIkscCRcLz6w130_assertion description "[HC2 and GP5+/6+, have shown in large clinical trials that they perform better in the detection of CIN 2+/CIN 3+ lesions than cytology and thus have been clinically validated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316611.RAX9nE7hAoQrV-reB0DFdv7yXZ2idbLY8CIkscCRcLz6w130_provenance.
- NP316613.RAR1FKEbkVO-5tdHBcLmZF4d42blsoc4sdyj0uX7Tz28Q130_assertion description "[The epigenetic changes in pituitary adenomas were identified by evaluating the methylation status of nine genes (RB1, p14(ARF), p16(INK4a), p73, TIMP-3, MGMT, DAPK, THBS1 and caspase-8) in a series of 35 tumours using methylation-specific PCR analysis plus sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316613.RAR1FKEbkVO-5tdHBcLmZF4d42blsoc4sdyj0uX7Tz28Q130_provenance.
- NP316617.RAVZrG2cosDZtbHLgizbuLhg9F3N0pdob7pUJaM2sSgzg130_assertion description "[Our study supports that mutations in the BRAF, KRAS, and PIK3CA genes make at least a minor contribution to OSCC tumorigenesis, and pathway-specific therapies targeting these 2 pathways should be considered for OSCC in a subset of patients with these mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316617.RAVZrG2cosDZtbHLgizbuLhg9F3N0pdob7pUJaM2sSgzg130_provenance.
- NP316619.RAdph8yG_t3AEH8d-6n63NaHJ6a-ddyT9cAx3ke7Kn7tA130_assertion description "[One possible explanation for this disparity is that the gene determines severity of rather than susceptibility to inflammatory polyarthritis (IP) and that the UK and Japanese cohorts differed in terms of outcome.Aim: To examine the association between individual PADI4 single nucleotide polymorphisms (SNPs) and haplotypes, with the development and severity of erosions by five years in patients with IP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316619.RAdph8yG_t3AEH8d-6n63NaHJ6a-ddyT9cAx3ke7Kn7tA130_provenance.
- NP316625.RAfDB_GQS7sfc6R4KcFvWZyly0XXkn2y5Os1U8uA5fpRU130_assertion description "[Genetic tests suitable for the routine laboratory are now available for some important metabolizing enzymes (e.g., CYP2D6, CYP2C19) identifying those individuals who are slow or fast metabolizers of certain drugs, many of which are widely used in the treatment of depression (e.g., tricyclic antidepressants).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316625.RAfDB_GQS7sfc6R4KcFvWZyly0XXkn2y5Os1U8uA5fpRU130_provenance.
- NP316627.RAQAaA4pGgB3py00eKzLIgof4Rr-XpAJjV_95NP3ONDD0130_assertion description "[Germline missense mutations in the tyrosine kinase domain of the hepatocyte growth factor/scatter factor (HGF/SF) receptor, c-Met, are thought to be responsible for hereditary papillary renal carcinoma (HPRC) type 1, a form of human kidney cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316627.RAQAaA4pGgB3py00eKzLIgof4Rr-XpAJjV_95NP3ONDD0130_provenance.
- NP316630.RAe8R71zbHSfJZ46Inf6VprpUuJvekxfpBKFUVTPGvRXI130_assertion description "[Previous studies have shown that insertion/deletion polymorphisms in the angiotensin-converting enzyme (ACE) gene and the endothelial nitric oxide synthase (eNOS) gene are associated with Henoch-Schönlein purpura nephritis (HSPN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316630.RAe8R71zbHSfJZ46Inf6VprpUuJvekxfpBKFUVTPGvRXI130_provenance.
- NP316634.RAVtfOjA_4aBZRhA-2y3yL7lokeRzBCeV3Cod00-yob74130_assertion description "[In mice, immunoblotting with antibodies against cytosolic muscle-type creatine kinase and sarcomeric mitochondrial creatine kinase showed that both of these isoforms decreased as malignancy progressed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316634.RAVtfOjA_4aBZRhA-2y3yL7lokeRzBCeV3Cod00-yob74130_provenance.
- NP316644.RAdXUDaURPyt8xgiWHARWp5qcGEyUfKxvZpA9Tr2a5u4E130_assertion description "[We investigated the role of the divergent transforming growth factor-beta superfamily member, prostate-derived factor (PDF), in regulating response to chemotherapies used in the treatment of colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316644.RAdXUDaURPyt8xgiWHARWp5qcGEyUfKxvZpA9Tr2a5u4E130_provenance.
- NP316645.RASk0oHMUXfDGAXio2tQ23dJT2P2hI9XvFfYHrSwJECDs130_assertion description "[Human leukocyte antigen (HLA)-DRB1 genotyping data of the patients from our previous study was used for the assessment of independent role of TAP genes to SSc susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316645.RASk0oHMUXfDGAXio2tQ23dJT2P2hI9XvFfYHrSwJECDs130_provenance.
- NP316649.RAchkU-mijuVcXcMWJdzTMUxOl8s7xNOS6CPzf6rPopp4130_assertion description "[Furthermore, in vivo administration of GM-CSF at 60 microg/kg body weight daily for 5 consecutive days beginning immediately after injury decreased infarction volume, altered the expression of several apoptosis-related genes (Bcl-2, Bax, caspase 3, and p53), and improved locomotor behavior in the focal cerebral ischemia model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316649.RAchkU-mijuVcXcMWJdzTMUxOl8s7xNOS6CPzf6rPopp4130_provenance.
- NP316652.RAXwXWuJXVq_hl-rw9-j-kMfgpl9WZ1zL4xsxvMpVhKIk130_assertion description "[The culture of NHL B cells in this sytem induced strong upregulation of the expression of CD80 and CD86 as well as other molecules involved in accessory cell functions (HLA class I, CD54, and CD58).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316652.RAXwXWuJXVq_hl-rw9-j-kMfgpl9WZ1zL4xsxvMpVhKIk130_provenance.
- NP316657.RAdAr1kHYzDZbh5wg_0tWXyJDphpe3595-BfOI_A1NtLA130_assertion description "[There is strong evidence that the Chr.5q31-33 region, which contains the immune response cytokine genes [interleukin (IL)-3, IL-4, IL-5, IL-9, and IL-13], is linked to autoimmune thyroid disorders in Chinese and Japanese populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316657.RAdAr1kHYzDZbh5wg_0tWXyJDphpe3595-BfOI_A1NtLA130_provenance.
- NP316658.RAfgK1BGYaPYw1CvCtQ1sI9gLUKXsaFhCl8RKhyjRHQPw130_assertion description "[The insulin-like growth factor (IGF) system is related to EC risk, and IGF-I can inhibit PR transcription in breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316658.RAfgK1BGYaPYw1CvCtQ1sI9gLUKXsaFhCl8RKhyjRHQPw130_provenance.
- NP316659.RAS6IdGR3eZ7vQ14UrJfyJP2sBA_6rbllFuj4GZaTLIdk130_assertion description "[The clear relationship between HER-2/neu status and COX-2 expression in human breast tumors suggests that this mechanism is likely to be operative in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316659.RAS6IdGR3eZ7vQ14UrJfyJP2sBA_6rbllFuj4GZaTLIdk130_provenance.
- NP316661.RAW0dinHTSRdp8a-mNCnzLPZA_tvmx93oQjkivK_O8Brw130_assertion description "[Mutations in at least two genes are linked to autosomal dominant polycystic liver disease (PCLD), PRKCSH and SEC63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316661.RAW0dinHTSRdp8a-mNCnzLPZA_tvmx93oQjkivK_O8Brw130_provenance.
- NP316665.RAUyWgftSL6PKZgFnf3mTRVXrpCoiUs00VzlU-Mr_SRiU130_assertion description "[These observations offer an explanation for the differential genetic susceptibility of DR4+ and DR11+ individuals to the development of chronic Lyme arthritis and, eventually, the progression to antibiotic-refractory Lyme arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316665.RAUyWgftSL6PKZgFnf3mTRVXrpCoiUs00VzlU-Mr_SRiU130_provenance.
- NP316668.RAYA9B5ZHL9u-dZq5Iu2bkLRRJPp645WttRkx8Tz8ZbBc130_assertion description "[The results show statistically significant (p <or= 0.05) differences between genotype frequencies in aggressive and controls (IL-1B +3954 & IL-6 -174); chronic and controls (IL-6 -174 & VDR -1056); chronic and aggressive periodontitis (IL-1A -889); and periodontitis as a whole and controls (VDR -1056, TLR-4 399 & IL-6 -174).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316668.RAYA9B5ZHL9u-dZq5Iu2bkLRRJPp645WttRkx8Tz8ZbBc130_provenance.
- NP316669.RAXPTTnV_bizBR_UhbZJVrptQpOvwQNdRYIMCtPsfJFOg130_assertion description "[Increased NBS1 expression correlated with advanced T stage and recurrence/metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316669.RAXPTTnV_bizBR_UhbZJVrptQpOvwQNdRYIMCtPsfJFOg130_provenance.
- NP316674.RAaQpDadlm7ayQHfX7tAwv3PBtAc_Zpab0iglCz0tVvFw130_assertion description "[We describe the detection and the growth of fibroblasts with human smooth muscle cell differentiation features from bronchoalveolar lavage (BAL) fluid of 53% of patients with scleroderma, but not from healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316674.RAaQpDadlm7ayQHfX7tAwv3PBtAc_Zpab0iglCz0tVvFw130_provenance.
- NP316683.RAZYQfxzNzfXbvKSDP-J3Fu_lmc916kcZYZNgAGKjyK5k130_assertion description "[Three patients with liver cirrhosis in childhood analyzed previously all had PHKG2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316683.RAZYQfxzNzfXbvKSDP-J3Fu_lmc916kcZYZNgAGKjyK5k130_provenance.
- NP316685.RAcwEgz9gBKduUVPy_h6-A8VFfW2uurlI9k3UCZMAUy4c130_assertion description "[Here we evaluated the TMPRSS2-ERG gene fusion in small cell carcinoma of the prostate (n = 12) in comparison with small cell carcinoma of the urinary bladder (n = 12) and lung (n = 11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316685.RAcwEgz9gBKduUVPy_h6-A8VFfW2uurlI9k3UCZMAUy4c130_provenance.
- NP316687.RAYmlw_o1jGVvJh9FYTFWEbGfHsEvVd72PAIxq15C6KV8130_assertion description "[First, we analyzed HSP70-2 polymorphism in risk-associated haplotypes from HLA homozygous cells and normal individuals and confirmed that the HSP70-2 9-kb variant was associated invariably with DR4 (HLA-DRB1*0402, DQB1*0302) and DR2 (HLA-DRB1*01601, DQB1*0502, DQA1*0102 and HLA-DRB1*1501, DQB1*0602) haplotypes, which were the haplotypes found increased in Jewish and non-Jewish patients with CA, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316687.RAYmlw_o1jGVvJh9FYTFWEbGfHsEvVd72PAIxq15C6KV8130_provenance.
- NP316690.RAZCMQuTrJmE0j9eo-JNtM_M_dHgO75s5rsoDxR7zwCoU130_assertion description "[The expression of cyclic nucleotide phosphodiesterase, glial fibrillary acidic protein, myelin-associated glycoprotein, myelin basic protein, and myelin proteolipid protein were assessed in the superior frontal gyrus and the primary motor cortex of control, uncomplicated alcoholic, and cirrhotic alcoholic cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316690.RAZCMQuTrJmE0j9eo-JNtM_M_dHgO75s5rsoDxR7zwCoU130_provenance.
- NP316691.RAQgt0wf3NcjgDJcXwMgIWAJnDsYQ28IAT9s1LMB-7qxw130_assertion description "[Demographic, clinical, and outcome features of children with acute lymphoblastic leukemia and CRLF2 deregulation: results from the MRC ALL97 clinical trial.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316691.RAQgt0wf3NcjgDJcXwMgIWAJnDsYQ28IAT9s1LMB-7qxw130_provenance.
- NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_assertion description "[Human erythrocyte R-type pyruvate kinase deficiency (PKD) is a disorder caused by mutations in the PKLR gene that produces chronic nonspherocytic hemolytic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316697.RATU2fr_L3ngdxODWtEDD3I_I-SUfIT4eeaNtVXePgZSk130_provenance.