Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP146828.RAXGgEJleHAsFwrMgdJG5JMdA6_J1Knz5hLvQtXDmhBHY130_assertion description "[REVIEW: central role in the pathogenesis of idiopathic thrombocytopenic purpura (ITP), andother immune-mediated thrombocytopenias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146828.RAXGgEJleHAsFwrMgdJG5JMdA6_J1Knz5hLvQtXDmhBHY130_provenance.
- NP146829.RAbdrhz9CWHha5BfL4YCxEPWAOWSJvE1dzY6XfN8AVuBw130_assertion description "[mutated FH enables complement activation on the surface of platelets and their activation, which may contribute to the development of thrombocytopenia in Atypical hemolytic uremic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146829.RAbdrhz9CWHha5BfL4YCxEPWAOWSJvE1dzY6XfN8AVuBw130_provenance.
- NP146833.RAVT3vIUZjuAhERUaizbm5YVrJJBQMqN0dmefHfG8TPC0130_assertion description "[Measurement of Cp separated by the present method could be useful for the diagnosis of ITP in the presence of thrombocytopenia and a non- or low-inflammatory state ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146833.RAVT3vIUZjuAhERUaizbm5YVrJJBQMqN0dmefHfG8TPC0130_provenance.
- NP146834.RASIyyfAoMrps99JqyYWskICffkHmiqng1g7Ijvp7EI6o130_assertion description "[subjects with mutations in the motor domain present with severe thrombocytopenia and develop nephritis and deafness before the age of 40, while those with mutations in the tail domain have a much lower risk of complications and higher platelet counts ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146834.RASIyyfAoMrps99JqyYWskICffkHmiqng1g7Ijvp7EI6o130_provenance.
- NP146839.RATuxRpIBWFo7mwn303Ib7FSDXwpwdZRXtemDJITQOKNM130_assertion description "[JAK2 exon 12 mutations were detected in 4 out of 20 polycythemia vera and idiopathic erythrocytosis V617F-negative patients and were only present in the myeloid lineage ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146839.RATuxRpIBWFo7mwn303Ib7FSDXwpwdZRXtemDJITQOKNM130_provenance.
- NP146842.RAQhbYLGjpuar7InQo0HnqMFb6Wid3U0IBQMw6RSWBzv0130_assertion description "[overexpression of PRV-1 to discrimitate essential thrombocythemia and polycythemia vera from secondary thrombocytosis and secondary erythrocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146842.RAQhbYLGjpuar7InQo0HnqMFb6Wid3U0IBQMw6RSWBzv0130_provenance.
- NP146846.RAcA_HtXgGGZEjj9zkcD-MCUfk9LGVzDiTrAFXYaL_3Jc130_assertion description "[Mutation IN Von Hippel Lindau tumor suppressor is associated with polycythemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146846.RAcA_HtXgGGZEjj9zkcD-MCUfk9LGVzDiTrAFXYaL_3Jc130_provenance.
- NP146857.RAblLQr6sYFIv-bAFrrvM7Yjv8TDE42G0CisuzXqF7C7U130_assertion description "[A novel mutation in exon 5 of the ALAS2 gene results in X-linked sideroblastic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146857.RAblLQr6sYFIv-bAFrrvM7Yjv8TDE42G0CisuzXqF7C7U130_provenance.
- NP146864.RAWL75Mk025W7FLaJ7TJUd8jbzV5fBhxzYTWb4kxZF6I4130_assertion description "[Oral contraceptives with desogestrel, drospirenone or cyproterone acetate caused lower free TFPI levels than levonorgestrel, which may explain the mechanism of OC-related APC resistance & thrombotic risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146864.RAWL75Mk025W7FLaJ7TJUd8jbzV5fBhxzYTWb4kxZF6I4130_provenance.
- NP146871.RAaI8QVmVwhAZUyiw3eojd-5pR93SG5WHHuhMlBxZqPDY130_assertion description "[The 2 FV variants FV Hong Kong and FV Cambridge yielded identical APC resistance patterns, with APC responses being intermediate to those of wild-type FV and FV Leiden (Arg506Gln) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146871.RAaI8QVmVwhAZUyiw3eojd-5pR93SG5WHHuhMlBxZqPDY130_provenance.
- NP146879.RAZLiP-MLMeUgdFx9PW_KMcVM21TAo5hdOJrtwDtcVU_g130_assertion description "[the presence of aPT antibodies in patients was significantly associated with the prevalence of prior thromboembolism ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146879.RAZLiP-MLMeUgdFx9PW_KMcVM21TAo5hdOJrtwDtcVU_g130_provenance.
- NP146881.RAf1zmvUR5ORemW8ngLtUEYplN8J-wOw5d1oo03H8V7oA130_assertion description "[A genetic translocation in atypical chronic myeloid leukemia yields a new PCM1-JAK2 fusion gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146881.RAf1zmvUR5ORemW8ngLtUEYplN8J-wOw5d1oo03H8V7oA130_provenance.
- NP146882.RAUcloRrHjG3rFibIfNQN5-fs3sHFeAIJrW1kCymLH8RU130_assertion description "[Atypical chronic myeloid leukemia should be considered as a JAK2 negative chronic myeloid neoplasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146882.RAUcloRrHjG3rFibIfNQN5-fs3sHFeAIJrW1kCymLH8RU130_provenance.
- NP146884.RAUjKyb374E4cOEW1HLiZSzhoBYN5kkimRDPf1TfZK2Ys130_assertion description "[Together, our data indicate the possible correlation between Dkk-1 and human placental choriocarcinoma and suggest potential applications of Dkk-1 in treatment of human placental choriocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146884.RAUjKyb374E4cOEW1HLiZSzhoBYN5kkimRDPf1TfZK2Ys130_provenance.
- NP146886.RAfLN3iP03Z-F_xiFDIWlIGCBjAK1hyHS4UDt_3luyzeo130_assertion description "[These results demonstrate that the InsR regulates choriocarcinoma cell invasion through activation by IGF-II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146886.RAfLN3iP03Z-F_xiFDIWlIGCBjAK1hyHS4UDt_3luyzeo130_provenance.
- NP146891.RATFPOg5d1QccyE1IULoLj6K2xe-3_BJu-Shl_jX90pL4130_assertion description "[Placental leptin expression was examined in representative species of the two most abundant mammalian orders, Rodentia and Chiroptera, and in cultured human choriocarcinoma (BeWo) cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146891.RATFPOg5d1QccyE1IULoLj6K2xe-3_BJu-Shl_jX90pL4130_provenance.
- NP146893.RAUBu4cCyIyqqbpP3uUx93F1BCssuOZwUj0kL_QnhiLlI130_assertion description "[These results demonstrate that the InsR regulates choriocarcinoma cell invasion through activation by IGF-II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146893.RAUBu4cCyIyqqbpP3uUx93F1BCssuOZwUj0kL_QnhiLlI130_provenance.
- NP146895.RAalNB5OZH2wTUvSDsfthEyG70krVhc9ltd4Zlubm9SWU130_assertion description "[Syncytin transcripts were found in first-trimester trophoblast cells with both villous and extravillous phenotypes and also in the JAR and JEG-3 choriocarcinoma cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146895.RAalNB5OZH2wTUvSDsfthEyG70krVhc9ltd4Zlubm9SWU130_provenance.
- NP146896.RAT2RDM1dWBL4zGzjG-MbUHOfq8otvS12xMM-mui9a7o0130_assertion description "[Progesterone receptor isoforms differentially regulate expression of ABCG2 in placental choriocarcinoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146896.RAT2RDM1dWBL4zGzjG-MbUHOfq8otvS12xMM-mui9a7o0130_provenance.
- NP146902.RAQtaoyzYI5eFL-hwe5zdyDzUnsbAiRNTmHJUo9ldEljQ130_assertion description "[RTR mRNA was expressed in the human placental choriocarcinoma cell lines BeWo, JAR, and JEG-3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146902.RAQtaoyzYI5eFL-hwe5zdyDzUnsbAiRNTmHJUo9ldEljQ130_provenance.
- NP146904.RAYIqVCHU_rFQzswzOL-vIPIh_5O7xVc1UiTOS7ojFr5s130_assertion description "[the 5-HT (2A) receptor subtype is fully expressed in the human choriocarcinoma cell lines JEG-3 and BeWo as well as in normal human placental tissue ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146904.RAYIqVCHU_rFQzswzOL-vIPIh_5O7xVc1UiTOS7ojFr5s130_provenance.
- NP146906.RAQNBpOsvt14jU_p4lk2pN5KqArVMTJuhOOAl-uY6NZHE130_assertion description "[17alpha-methyl testosterone is a competitive inhibitor of aromatase activity in Jar choriocarcinoma cells and macrophage-like THP-1 cells in culture.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146906.RAQNBpOsvt14jU_p4lk2pN5KqArVMTJuhOOAl-uY6NZHE130_provenance.
- NP146907.RATAs0VlUz3tecJifucHfO84vn8MjyVh0gyVLKGntzx-k130_assertion description "[using choriocarcinoma cells, it is shown that tyrosine phosphatase mediated suppression of IFN-gamma-inducible JAK and STAT-1 and select IFN-gamma-inducible gene expression in trophoblast cells may contribute to fetal maintenance ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146907.RATAs0VlUz3tecJifucHfO84vn8MjyVh0gyVLKGntzx-k130_provenance.
- NP146910.RARMlA1FEotBUmCEqEBoPpGqZiWG-qDiKcBLoCK4RnX-8130_assertion description "[findings suggest an involvement of PPARgamma in trophoblast differentiation during normal placental development; down-regulation of PPARgamma may contribute to trophoblastic diseases such as hydatidufirm mole and choriocarcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146910.RARMlA1FEotBUmCEqEBoPpGqZiWG-qDiKcBLoCK4RnX-8130_provenance.
- NP146912.RAd-i2wdj1wFJNT5W7K3o3sG-a4KpovfSS9mWmm-frO_M130_assertion description "[Systemic mastocytosis involving the gastrointestinal tract is associated with the usual D816V KIT mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146912.RAd-i2wdj1wFJNT5W7K3o3sG-a4KpovfSS9mWmm-frO_M130_provenance.
- NP146914.RAcj1E-DHaHS0ES7GLwG-L3wp0ZFA7ycDspUFvXUbsEFI130_assertion description "[study found the KIT D816V variant induces cluster formation & expression of several mast cell differentiation & adhesion antigens; it is hypothesized that KIT D816V as a single hit may be sufficient to cause indolent systemic mastocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146914.RAcj1E-DHaHS0ES7GLwG-L3wp0ZFA7ycDspUFvXUbsEFI130_provenance.
- NP146916.RAfqwss71iD0lmIRSoa02ePXFlv8xoFG2k7EqtoGBcozc130_assertion description "[Immunoreactivity for CD25 in gastrointestinal mucosal mast cells is specific for systemic mastocytosis and can be used to confirm the diagnosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146916.RAfqwss71iD0lmIRSoa02ePXFlv8xoFG2k7EqtoGBcozc130_provenance.
- NP146919.RAWdkKu5bhKBRRJ0HwimoRH3LaVN43kjABDofgo3Bfjus130_assertion description "[used fluorescence in situ hybridization to detect deletion of the CHIC2 locus at 4q12 as a surrogate for the FIP1L1-PDGFRA fusion and was observed in bone marrow cells for 3 of 5 patients with systemic mast cell disease associated with eosinophilia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146919.RAWdkKu5bhKBRRJ0HwimoRH3LaVN43kjABDofgo3Bfjus130_provenance.
- NP146925.RAcXOX7fk23ekbFRszUc-ERsKgv2-rRTHsQ96Sn-BR7DY130_assertion description "[The G (beta) 3 C825T polymorphism was associated with SAD in our study sample/finding strengthens the evidence for the involvement of G protein-coupled signal transduction in the pathogenesis of affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146925.RAcXOX7fk23ekbFRszUc-ERsKgv2-rRTHsQ96Sn-BR7DY130_provenance.
- NP146930.RAcFbVUs8pRamaF_CCX7feTkLGJSN23zy9ehS7m2mY36I130_assertion description "[This study does not support the involvement of tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146930.RAcFbVUs8pRamaF_CCX7feTkLGJSN23zy9ehS7m2mY36I130_provenance.
- NP146934.RAcUHkkbdng9zqMDq3prJC_5vnXvYKJZHlpkzERB0tQ6c130_assertion description "[Polymorphisms in GPR50 were compared in bipolar affective disorder (BD), major depressive disorder (MDD), schizophrenia (SCZ) and controls/( Delta502-505) or a variant is a sex-specific risk factor for susceptibility to BD and SCZ.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146934.RAcUHkkbdng9zqMDq3prJC_5vnXvYKJZHlpkzERB0tQ6c130_provenance.
- NP146935.RAaLVVRCIKCrYZ4YlX2dVawUHEuyI_xPHoHXNJogd5CXw130_assertion description "[the SSTR5 gene is involved in the etiology of bipolar affective disorder or may exist in linkage disequilibrium with a susceptibility gene close to SSTR5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146935.RAaLVVRCIKCrYZ4YlX2dVawUHEuyI_xPHoHXNJogd5CXw130_provenance.
- NP146936.RAepSuNnqBcQGYL_NefQojOxs36cuDzI5zUWLxFZ8PPec130_assertion description "[Results from the association studies indicate that GAD1 promoter variants are of importance for the Danish bipolar affective disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146936.RAepSuNnqBcQGYL_NefQojOxs36cuDzI5zUWLxFZ8PPec130_provenance.
- NP146939.RAdd8nob7kLrBFKC35TrGlLYSBE3l_mC5m05ByFn4PWLM130_assertion description "[The hypothesis that gene variants could influence temperamental traits in mood disorders patients was tested/long MAO-A allele was associated with decreased persistence scores among females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146939.RAdd8nob7kLrBFKC35TrGlLYSBE3l_mC5m05ByFn4PWLM130_provenance.
- NP146940.RAb7-Ofq0WqYjBUfKY9dEROWMFv354qHFjtEIxLtOn7gw130_assertion description "[This study does not support the involvement of tyrosine hydroxylase, catechol-O-methyl transferase and Wolfram syndrome 1 polymorphisms in mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146940.RAb7-Ofq0WqYjBUfKY9dEROWMFv354qHFjtEIxLtOn7gw130_provenance.
- NP146942.RASHgx6KRDqP2ZQFObFQunfzJM6Qrke21kSOT90XjiWQw130_assertion description "[Prodynorphin mRNA reduction could modulate endocrine and autonomic mechanisms in subjects with affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146942.RASHgx6KRDqP2ZQFObFQunfzJM6Qrke21kSOT90XjiWQw130_provenance.
- NP146943.RAQnK6R0BUkRSBOqy61GcA7tjP7li4sw7xmbrlHxrFVzY130_assertion description "[The Val66Met polymorphism has been associated with a predisposition to mood disorders and schizophrenia and with therapeutic response to mood stabilizers, antidepressants and antipsychotics (review).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146943.RAQnK6R0BUkRSBOqy61GcA7tjP7li4sw7xmbrlHxrFVzY130_provenance.
- NP146944.RAeG1PLLJb12xhYTAd65DPsayeUoq9ixlBIbGn8n09FUM130_assertion description "[This study investigates the relationship between Val66Met polymorphisms of the BDNF gene and prefrontal cognitive function in 129 patients with schizophrenia and 111 patients with bipolar mood disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146944.RAeG1PLLJb12xhYTAd65DPsayeUoq9ixlBIbGn8n09FUM130_provenance.
- NP146950.RAWxQYeaosNUSENNkC0zW4GlTHS_J2qP4vdFzXhODUE10130_assertion description "[Alterations in 5-HT (1A,) 5-HT (1B), and 5-HT (2A) mRNA levels in the brains of subjects with both mood disorders and schizophrenia add further support for hypothesis of dysregulation of the serotonergic system in these psychiatric disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146950.RAWxQYeaosNUSENNkC0zW4GlTHS_J2qP4vdFzXhODUE10130_provenance.
- NP146959.RAYHCatyJbDn8klx0vJliBUASpQ0wHqRlHK5yLDc3rVSM130_assertion description "[Haplotype-based analysis of TPH2 in patients with UP and BP disorder provides preliminary evidence for protective association in both disorders and thus supports a central role for TPH2 in the pathogenesis of affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146959.RAYHCatyJbDn8klx0vJliBUASpQ0wHqRlHK5yLDc3rVSM130_provenance.
- NP146960.RAafNcocBuIq7IHv9LOW7WJaOArM5wCG1K8C18uo8gEX0130_assertion description "[Disrupted-in-Schizophrenia-1 (DISC1) is now an important candidate risk gene for schizophrenia and affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146960.RAafNcocBuIq7IHv9LOW7WJaOArM5wCG1K8C18uo8gEX0130_provenance.
- NP146974.RATL0l4nfrsz3z1vYpnQ4okep-6PLG7q5VQBisDCGMhAI130_assertion description "[IFN-gamma may play a key role in the regulation of ocular surface inflammation and immunologic reaction in cystic fibrosis (CF) patients/tear level of IFN-gamma may be a candidate marker for evaluation of the clinical status of CF and eye disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146974.RATL0l4nfrsz3z1vYpnQ4okep-6PLG7q5VQBisDCGMhAI130_provenance.
- NP146975.RAczX4Jp7oiAk7CjjcXuzA-ulirHObRuiNn5pMqbdnG5c130_assertion description "[Establishing correlations between the genotype of the von Hippel-Lindau mutation and the phenotype of eye disease may inform us as to how ocular von Hippel-Lindau disease arises, and help guide molecular interventions in ocular von Hippel-Lindau disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146975.RAczX4Jp7oiAk7CjjcXuzA-ulirHObRuiNn5pMqbdnG5c130_provenance.
- NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_assertion description "[study identified a novel MITF mutation of IVS4 -1G -- > C in a Japanese family with Waardenburg syndrome type II ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146978.RAQdxXXvwqDsiA8cLSIjE6mzftvBxVDr9PumKICVzndDs130_provenance.
- NP146982.RASVYK0zEttnKyWydOhz5Gtbay_YGeTsj6CDnWY3m1xpg130_assertion description "[A de novo missense mutation in the gene encoding the SOX10 transcription factor in a Spanish sporadic case of Waardenburg syndrome type IV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146982.RASVYK0zEttnKyWydOhz5Gtbay_YGeTsj6CDnWY3m1xpg130_provenance.
- NP146987.RAc3miwhbVuZvN-CyYZvuSKGvUL6gtrfeBxNxr-IJ6OMk130_assertion description "[PAX3 gene is associated with Waardenburg syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146987.RAc3miwhbVuZvN-CyYZvuSKGvUL6gtrfeBxNxr-IJ6OMk130_provenance.
- NP146990.RAbh8JXPHS44mP8SokPKPGBSLrskuaHX15YyPq4UK37KU130_assertion description "[Increase in serum levels eight days after IVIG treatment in neuromuscular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146990.RAbh8JXPHS44mP8SokPKPGBSLrskuaHX15YyPq4UK37KU130_provenance.
- NP146992.RAWr65aN_4T6c2fMDqB35hiu0TEjRIYZYMmKKIHN5d_P0130_assertion description "[Increase in serum levels eight days after IVIG treatment in neuromuscular disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146992.RAWr65aN_4T6c2fMDqB35hiu0TEjRIYZYMmKKIHN5d_P0130_provenance.
- NP146993.RAaWhiweZS0Ie_xNylVnsCIEXI9q1Fm2Pnf4cvnZzjpAk130_assertion description "[Disruption of DMD and the absence of ACSL4 in a patient are responsible for neuromuscular disease and cognitive impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146993.RAaWhiweZS0Ie_xNylVnsCIEXI9q1Fm2Pnf4cvnZzjpAk130_provenance.
- NP146997.RAf8sf180Ft-P-pqyiMHVxKhGPEueUCZMwx19nQIjaKFI130_assertion description "[IL-6 and IL-8, and probably midkine and VEGF-A, appear to participate in the development of cancer-related cachexia in gastroesophageal malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146997.RAf8sf180Ft-P-pqyiMHVxKhGPEueUCZMwx19nQIjaKFI130_provenance.
- NP147001.RAWluZslDa-hgUr-d0CVlbTmWUTsogtOuTnRZnjOH3cts130_assertion description "[The IL-1B+3954 T allele is a major risk for cachexia from locally advanced gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147001.RAWluZslDa-hgUr-d0CVlbTmWUTsogtOuTnRZnjOH3cts130_provenance.
- NP147002.RAfnSGprW5bJcpEwai4kG38VdyEX9Yrs9x7mYZrRaUWaQ130_assertion description "[potential use of ghrelin and GHS-R agonists in the management of disease-associated cachexia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147002.RAfnSGprW5bJcpEwai4kG38VdyEX9Yrs9x7mYZrRaUWaQ130_provenance.
- NP147005.RAVLOU_3hM4xKoKQwaE9osBZamNYbXPPpoThT6y2NoQ1I130_assertion description "[Overexpression of neuromedin U is associated with bladder tumor formation, lung metastasis and cancer cachexia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147005.RAVLOU_3hM4xKoKQwaE9osBZamNYbXPPpoThT6y2NoQ1I130_provenance.
- NP147011.RAZD0ewvPCiFeZT1MmeAn-IhPKZ--vsWKQMXheAVAoNQk130_assertion description "[the dominant-negative effect, which occurs for human GnRHR mutants isolated from patients with hypogonadotropic hypogonadism, results from receptor retention in the endoplasmic reticulum by mislocalized mutants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147011.RAZD0ewvPCiFeZT1MmeAn-IhPKZ--vsWKQMXheAVAoNQk130_provenance.
- NP147014.RAUO-xk9aQeGiU5i1EB0ag1iIWD0am_RNP_zRDi97KRcg130_assertion description "[GNRHR mutations account for approximately 3.5% of all normosmic and 7%-11% of presumed autosomal recessive idiopathic hypogonadotropic hypogonadism, suggesting that additional genes play an important role in normal puberty.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147014.RAUO-xk9aQeGiU5i1EB0ag1iIWD0am_RNP_zRDi97KRcg130_provenance.
- NP147017.RAUiPPCdy4zUlhYy_yHj3KLRDuvJ8T7QgHqSPbHwCS7WY130_assertion description "[Loss-of-function mutations in PROK2 and PROKR2 underlie both Kallmann syndrome (KS) and normosmic idiopathic hypogonadotropic hypogonadism (IHH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147017.RAUiPPCdy4zUlhYy_yHj3KLRDuvJ8T7QgHqSPbHwCS7WY130_provenance.
- NP147019.RAaTqyYrNaJ0Xbi6FCvqxFmefjoMxmFcyT31KLdA0WWDg130_assertion description "[12% of Kallman syndrome males have KAL1 deletions, but intragenic deletions of the FGFR1, GNRH1, GNRHR, GPR54 and NELF genes are uncommon in Idiopathic hypogonadotropic hypogonadism/Kallman syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147019.RAaTqyYrNaJ0Xbi6FCvqxFmefjoMxmFcyT31KLdA0WWDg130_provenance.
- NP147020.RASpyAYYOeMyLsrEIcatlQGuWCbLy3KaO2e_2x4LDaFN4130_assertion description "[12% of Kallman syndrome males have KAL1 deletions, but intragenic deletions of the FGFR1, GNRH1, GNRHR, GPR54 and NELF genes are uncommon in Idiopathic hypogonadotropic hypogonadism/Kallman syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147020.RASpyAYYOeMyLsrEIcatlQGuWCbLy3KaO2e_2x4LDaFN4130_provenance.
- NP147021.RAYSBLt82etDS0m2qsTwqDIbiwhkMezKPjd6P5bJhoEso130_assertion description "[the reversal of hypogonadotropic hypogonadism in a proband carrying an FGFR1 mutation suggests a role of FGFR1 beyond embryonic GnRH neuron migration, and a loss of function mutation in the FGFR1 gene causing delayed puberty.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147021.RAYSBLt82etDS0m2qsTwqDIbiwhkMezKPjd6P5bJhoEso130_provenance.
- NP147026.RATiWcGHSpzFYDEB5nVg1FZ9hWMLLGXw7OqU0yu2qJsJQ130_assertion description "[A daughter who carried the der Y had the clinical features of Prader-Willi syndrome while a son who carries the der 15 has mild developmental delay and hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147026.RATiWcGHSpzFYDEB5nVg1FZ9hWMLLGXw7OqU0yu2qJsJQ130_provenance.
- NP147028.RAcCMbZtZe118pkB9fArS8i5CnBnBiEJMFzAB2UoCMbEw130_assertion description "[Increased factor V and factor X activity and decreased antithrombin III levels in patients with hypogonadotropic hypogonadism represent a potential hypercoagulable state, which might augment the risk for atherosclerotic and atherothrombotic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147028.RAcCMbZtZe118pkB9fArS8i5CnBnBiEJMFzAB2UoCMbEw130_provenance.
- NP147030.RAUMbZUgevKW5pYFvftmx46ckVx71DayxYajUfBWdOVOY130_assertion description "[study reported patients with adrenal hypoplasia congenita and hypogonadotropic hypogonadism caused by the loss of function mutations of the DAX-1 gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147030.RAUMbZUgevKW5pYFvftmx46ckVx71DayxYajUfBWdOVOY130_provenance.
- NP147037.RAW0JRLnZ9i44tUrs5DS6XlX2jXSIr5PAZLoCQYchUqOA130_assertion description "[Pathologic fractures attributable to hypophosphatasia diagnosed in adulthood, and to missense mutation in TNSALP (C455G > A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147037.RAW0JRLnZ9i44tUrs5DS6XlX2jXSIr5PAZLoCQYchUqOA130_provenance.
- NP147038.RAeZYvg7IUuGeNg6yR70YXaYI8zz6Q7NHDYqRPcZFJ71s130_assertion description "[results suggest that IL-6 is a mediator of the effects of Crohn's serum on in vitro mineralization and may be a contributing factor to the osteopenia associated with Crohn's disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147038.RAeZYvg7IUuGeNg6yR70YXaYI8zz6Q7NHDYqRPcZFJ71s130_provenance.
- NP147040.RAX0rpeLWDGhm6DpBWes6O-El5AO6VLE4k-dByJ5ZPzto130_assertion description "[The purpose of this study was to investigate basal serum levels of OPG, RANKL and leptin, as well as bone mineral density (BMD) at lumbar vertebrae L1-L4, and their evolution during one year in two groups of patients with anorexia nervosa and osteopenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147040.RAX0rpeLWDGhm6DpBWes6O-El5AO6VLE4k-dByJ5ZPzto130_provenance.
- NP147047.RAaCD5mPpmp81cGJMNhMl3AXE2MFw7n673q6hJ-EcGOb0130_assertion description "[downregulation of TLR2 and decreased production of interleukin-12 p40 and tumour necrosis factor-alpha following Mycobacterium avium or lipoteichoic acid stimulation may contribute to host susceptibility to nontuberculous mycobacterial lung disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147047.RAaCD5mPpmp81cGJMNhMl3AXE2MFw7n673q6hJ-EcGOb0130_provenance.
- NP147048.RAZMsPwhYmPBTL9IssyMLrHQnmuTS93sPJZFLKmEnpxT0130_assertion description "[findings indicate differences in early matrix metalloproteinase 9 (MMP-9) bronchoalveolar lavage fluid levels between resolving respiratory distress syndrome and developing chronic lung disease of prematurity ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147048.RAZMsPwhYmPBTL9IssyMLrHQnmuTS93sPJZFLKmEnpxT0130_provenance.
- NP147055.RAQZAOX7-XHjIXlGEbzFtcR5s48ShmcIEHF1UpT5uIHOI130_assertion description "[Elevated CRP levvels may be useful in risk stratification for pulmonary disease in people with metabolic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147055.RAQZAOX7-XHjIXlGEbzFtcR5s48ShmcIEHF1UpT5uIHOI130_provenance.
- NP147056.RAcfkuAZ2V2H33b917bPt6ttJZ0FAIaOcX6-Zox8ENxRk130_assertion description "[PiM2 allele can be considered as genetic risk factor for asthma/and PiZ alleles are very rare in Tunisia in comparison with the European population, leading to a very small contribution in pulmonary diseases pathogenesis in Tunisia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147056.RAcfkuAZ2V2H33b917bPt6ttJZ0FAIaOcX6-Zox8ENxRk130_provenance.
- NP147058.RAZZyFh5KEmULcLITzzEGSRFoVBQAyT9FlS6C3zkQjE-4130_assertion description "[Patients with two identified CFTR mutations which include the R117H/7T anomaly should be followed up routinely as they remain susceptible to severe lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147058.RAZZyFh5KEmULcLITzzEGSRFoVBQAyT9FlS6C3zkQjE-4130_provenance.
- NP147059.RAWrGR9BGMZKPwrNmnonM7rr7M6UnVSPlxnOWFsUFl_pE130_assertion description "[Pre-eminent role for neutrophil elastase as the critical protease responsible for PSP-D depletion in inflammatory lung disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147059.RAWrGR9BGMZKPwrNmnonM7rr7M6UnVSPlxnOWFsUFl_pE130_provenance.
- NP147060.RAZ7DrThFFUwvXVCjLzK425KHKQ1ot2-Fpd3J4fUJUOVU130_assertion description "[CXCR1 cleavage on neutrophils disables bacterial killing in cystic fibrosis lung disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147060.RAZ7DrThFFUwvXVCjLzK425KHKQ1ot2-Fpd3J4fUJUOVU130_provenance.
- NP147062.RAVm5NqFj6O65ETaSmLe790HyNV_bTY6xzfFZxaDd6QGw130_assertion description "[DDR1 contributes to fibroblast survival in the tissue microenvironment of idiopathic pulmonary fibrosis and its up-regulation may occur in other fibroproliferative lung diseases as well.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147062.RAVm5NqFj6O65ETaSmLe790HyNV_bTY6xzfFZxaDd6QGw130_provenance.
- NP147063.RAT4pgrmaER3efRYOJsUgLbrzZ36jKHyt6b2bUwrUeOio130_assertion description "[Membrane-bound MMP-9 on PMN may play pathogenetic roles in inflammatory lung diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147063.RAT4pgrmaER3efRYOJsUgLbrzZ36jKHyt6b2bUwrUeOio130_provenance.
- NP147072.RARzvtb0WkR0DewPXft0RvvdANKPhuv7YrVMkjVysbL8E130_assertion description "[MMP7 and MMP1, are overexpressed in the lung microenvironment and distinguish idiopathic pulmonary fibrosis from other chronic lung diseases/, increased MMP7 concentration may be indicative of asymptomatic ILD and reflect disease progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147072.RARzvtb0WkR0DewPXft0RvvdANKPhuv7YrVMkjVysbL8E130_provenance.
- NP147074.RATuWFoiir2fMFBsvr6jJ_DHv7NdZs26CjXwlVhLBhIWo130_assertion description "[The four haplotype combination groups may have a potential diagnostic use as opposite risk factors for lung disease of prematurity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147074.RATuWFoiir2fMFBsvr6jJ_DHv7NdZs26CjXwlVhLBhIWo130_provenance.
- NP147081.RAYko4M2DVFzbenFmrprKZLc5c3Poo3Ze7VTSGfeFMUVQ130_assertion description "[Decreased levels of SP-A and SP-D have been measured in bronchoalveolar lavage fluid of these patients, as well as patients with acute pneumonia but no chronic lung disease.(review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147081.RAYko4M2DVFzbenFmrprKZLc5c3Poo3Ze7VTSGfeFMUVQ130_provenance.
- NP147092.RAbXREBJET2MKfaRf7UHjJcKsPUL-B3cqxq2DAS2i6QxU130_assertion description "[Decreased levels of SP-A and SP-D have been measured in bronchoalveolar lavage fluid of these patients, as well as patients with acute pneumonia but no chronic lung disease.(review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147092.RAbXREBJET2MKfaRf7UHjJcKsPUL-B3cqxq2DAS2i6QxU130_provenance.
- NP147093.RAXJjZFP95bzm4MNHNnf81snP5-miY04htJReTz366CCI130_assertion description "[Thrombin contributes to the tissue remodeling in inflammatory airways and lung diseases at least partially through PKCdelta activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147093.RAXJjZFP95bzm4MNHNnf81snP5-miY04htJReTz366CCI130_provenance.
- NP147096.RAdSzgdUM7mf6mFbSAM8G7VOy4NJeJANk6ppQkQY1Ny5U130_assertion description "[Overexpression of caveolin-1 in mesangial cells suppresses MAP kinase activation and cell proliferation induced by bFGF and PDGF, two major cytokines in mesangioproliferative nephritis (MN)/expression vector is potential therapy for MN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147096.RAdSzgdUM7mf6mFbSAM8G7VOy4NJeJANk6ppQkQY1Ny5U130_provenance.
- NP147097.RAc67rHgsXL4Ja7_ALtd77hmEnse8wOKvv_vj5VWorGqA130_assertion description "[glomerular Gal-3 expression in renal tissue and serum Gal-3 levels were elevated in patients with SLE nephritis versus healthy controls; moreover, they reflected disease activity; Gal-3 might contribute to the inflammatory process in SLE ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147097.RAc67rHgsXL4Ja7_ALtd77hmEnse8wOKvv_vj5VWorGqA130_provenance.
- NP147099.RAXEiDCQtOQHSywbjgMl5xurCUryzZ6GrNpTQpo3YLzqM130_assertion description "[Significant differences in the NOS2A promoter polymorphism allele and genotype frequency between Henoch-Schonlein Purppura (HSP) patients and controls suggest a potential role for this gene in the susceptibility to HSP and in the development of nephritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147099.RAXEiDCQtOQHSywbjgMl5xurCUryzZ6GrNpTQpo3YLzqM130_provenance.
- NP147102.RAaWFi7y-HaO5RbIndb_5QQT-9OdzlUZpOS7bN3aqIp0k130_assertion description "[cells from patients with diabetic nephritis exhibit significantly lower protein and mRNA expression of p16.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147102.RAaWFi7y-HaO5RbIndb_5QQT-9OdzlUZpOS7bN3aqIp0k130_provenance.
- NP147105.RAaVjZV82YcfE5yp3_2IPmh7FMaGmzZ2-MBn0EZWPqQMU130_assertion description "[TNF-alpha can play a crucial role in the immunopathogenesis of nephritis by the induction of CCL2, ICAM-1 and VCAM-1 expression via the activation of the intracellular MAPK signaling pathway, which may contribute to macrophage and lymphocyte infiltration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147105.RAaVjZV82YcfE5yp3_2IPmh7FMaGmzZ2-MBn0EZWPqQMU130_provenance.
- NP147106.RAdtS_iEljZhvYHujc7EC-Z7LMqvTYLXpx_BiClsXzYw8130_assertion description "[May play role infibrous process in crescentic nephritis, both in glomerular crescentic and tubular epithelial cells/be important in mediating some of the pathological effects of TGF-beta.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147106.RAdtS_iEljZhvYHujc7EC-Z7LMqvTYLXpx_BiClsXzYw8130_provenance.
- NP147110.RAarV88dq1ptyB3vJfMb-INIPBLtPE3RYBPhnj7B_kubY130_assertion description "[TNF-alpha can play a crucial role in the immunopathogenesis of nephritis by the induction of CCL2, ICAM-1 and VCAM-1 expression via the activation of the intracellular MAPK signaling pathway, which may contribute to macrophage and lymphocyte infiltration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147110.RAarV88dq1ptyB3vJfMb-INIPBLtPE3RYBPhnj7B_kubY130_provenance.
- NP147113.RARpJEerUlcSL8zqj_ryy-1_Or-bzOj8SRQbdGwK_u47Q130_assertion description "[In a large cohort of patients a significant association between the occurance of IGA nephritis and the TNF alpha low producer phenotype was found.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147113.RARpJEerUlcSL8zqj_ryy-1_Or-bzOj8SRQbdGwK_u47Q130_provenance.
- NP147117.RAfOna_RHuY2YyxEYVWWJaRpXNzDdcAmxeKMZ70PupG44130_assertion description "[complexes with prolyl 3-hydroxylase 1 (P3H1) to decrease prolyl 3 hydroxylation; dysregulation of prolyl 3 hydroxylation is a mechanism for connective tissue disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147117.RAfOna_RHuY2YyxEYVWWJaRpXNzDdcAmxeKMZ70PupG44130_provenance.
- NP147130.RAWvFm9shDuVFFLKTWN9D7dR7bKfF7LIohuBREasAoWuU130_assertion description "[Genetic variants of TLR-2 were associated with acute reactive arthritis following infection with S.enteritidis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147130.RAWvFm9shDuVFFLKTWN9D7dR7bKfF7LIohuBREasAoWuU130_provenance.
- NP147137.RASbhdj1TvA35OtmcqGrVx2x0lUMxzYqOD6Qr71Uv24pA130_assertion description "[The expression level of IL-17A was significant difference in expression between gingivitis and periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147137.RASbhdj1TvA35OtmcqGrVx2x0lUMxzYqOD6Qr71Uv24pA130_provenance.
- NP147144.RAVXuWKKcGwotC6zZ8RTcG3F4dhXHiDps4Eg5kELtg57k130_assertion description "[There were greater levels of chondroitin sulphate WF6 epitope in gingival crevicular fluid from destructive sites of patients with chronic periodontitis compared with non-destructive sites of patients with gingivitis or chronic periodontitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147144.RAVXuWKKcGwotC6zZ8RTcG3F4dhXHiDps4Eg5kELtg57k130_provenance.
- NP147148.RAVD5yB4Vs4facgiIF5zwri2X6jT0Vb728MsGEzYO4Z7A130_assertion description "[High-producing MBL2 genotypes increase the risk of acute and chronic carditis in patients with history of rheumatic fever.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147148.RAVD5yB4Vs4facgiIF5zwri2X6jT0Vb728MsGEzYO4Z7A130_provenance.
- NP147149.RAaHFUBI8ce_LpJ1VA31zRXZnPFjaFaNUIFMtgtz4Mk8o130_assertion description "[HLA DQA1*03 allele may be a protecting factor in Turkish children with rheumatic fever/combination of the DRB1*04 and DQA1*03 alleles may be a stronger protective factor than the DQA1*03 allele alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147149.RAaHFUBI8ce_LpJ1VA31zRXZnPFjaFaNUIFMtgtz4Mk8o130_provenance.
- NP147152.RAS76YNoYqNOiZzGA9BuOg9kT0Jlozj5Qv_14ppQOZs8o130_assertion description "[the common TLR-2 Arg to Gln polymorphism at position 753 significantly contributes to the pathogenesis of acute rheumatic fever ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147152.RAS76YNoYqNOiZzGA9BuOg9kT0Jlozj5Qv_14ppQOZs8o130_provenance.
- NP147164.RAQe8SZSwIMgepUlExM_8xOpAT61R1C2ICftpnJ_GUBro130_assertion description "[the TLR2 Arg677Trp polymorphism associated with lepromatous leprosy is not a true polymorphism of the TLR2 gene and has resulted from the variation present in the 93% homologous duplicated region of TLR2 exon 3 present approximately 23 kb upstream.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147164.RAQe8SZSwIMgepUlExM_8xOpAT61R1C2ICftpnJ_GUBro130_provenance.
- NP147180.RAVISB6NoIQkx0zrsRe9isXcGsUFea5I_tXdB3MNNiTfM130_assertion description "[Werner syndrome protein co-localizes and associates with gamma H2AX ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147180.RAVISB6NoIQkx0zrsRe9isXcGsUFea5I_tXdB3MNNiTfM130_provenance.
- NP147182.RASJYT-yeyAooVE-qDIUbaMaC52E4s96rTHltckDLR1bo130_assertion description "[Two novel mutations within the WRN gene are associated with Werner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147182.RASJYT-yeyAooVE-qDIUbaMaC52E4s96rTHltckDLR1bo130_provenance.
- NP147183.RAWuchFw5EPHwtb7W9dekyFqqxtwLFTCZhk3tqUamUYvs130_assertion description "[report the identification of two additional factors required in the DNA interstrand cross-links repair process, a previously characterized pre-mRNA splicing complex composed of Pso4/Prp19 and Werner syndrome protein (WRN) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147183.RAWuchFw5EPHwtb7W9dekyFqqxtwLFTCZhk3tqUamUYvs130_provenance.
- NP147189.RAUySYb2z78Z1gbtVB3MTIMK5QqWCJigWHKRXAV0T3jXw130_assertion description "[Results suggest that nuclear DNA helicase II plays a role in promoting the DNA processing function of Werner syndrome helicase, which in turn might be necessary for maintaining genomic stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147189.RAUySYb2z78Z1gbtVB3MTIMK5QqWCJigWHKRXAV0T3jXw130_provenance.
- NP147200.RAe5S41B0ZaUgxJZWCR-PmgEoKx7XjdZr5153qUQaFBPU130_assertion description "[M235 T polymorphism may be associated with persistent pulmonary hypertension in newborns with congenital diaphragmatic hernia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147200.RAe5S41B0ZaUgxJZWCR-PmgEoKx7XjdZr5153qUQaFBPU130_provenance.