Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP146594.RAriMOJOoK8ve269eAvrVfYiXTT1u8OvQdIT71H8hPzcU130_assertion description "[Novel R645C mutation was detected in NTRK3 in 2 affected siblings with Hirschsprung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146594.RAriMOJOoK8ve269eAvrVfYiXTT1u8OvQdIT71H8hPzcU130_provenance.
- NP146604.RAp275s1nGg7y-QNWFE1Qi1kQKf7QGRkcIJq0AjgMOgg0130_assertion description "[Missense mutation in the SLC19A2 gene is associated with thiamine-responsive megaloblastic anemia syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146604.RAp275s1nGg7y-QNWFE1Qi1kQKf7QGRkcIJq0AjgMOgg0130_provenance.
- NP146606.RAk7rRSKhB64G-fobKG_u0uPgOBor_erBfC_VuaBgwYao130_assertion description "[molecular basis for TCN2 deficiency in two patients with megaloblastic anemia was identified as variance in RNA editing ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146606.RAk7rRSKhB64G-fobKG_u0uPgOBor_erBfC_VuaBgwYao130_provenance.
- NP146612.RAo2_2I_ELZEKu7dl1OCYPIbuPvPqDunsvrXYxaxfC75A130_assertion description "[Single nucleotide polymorphism (SNP) at location 3435C-- > T plays a significant role in ABCB1 gene function and may be a basis for studies of relationships between ABCB1 genotypes and drug efficacy, drug toxicity, and disease susceptibility phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146612.RAo2_2I_ELZEKu7dl1OCYPIbuPvPqDunsvrXYxaxfC75A130_provenance.
- NP146613.RAl9QlISZrFb82rNB1yTCa57W_fVqmGjWSclfaZyA7YXY130_assertion description "[Anti-cytochrome P450 autoantibodies, identified on the basis of their specific binding in immunoblots, are significantly increased among children on immunosuppressive drugs and in some cases are associated with drug toxicity and organ rejection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146613.RAl9QlISZrFb82rNB1yTCa57W_fVqmGjWSclfaZyA7YXY130_provenance.
- NP146614.RAuOUGgCHcrVR9vWW-D1LYAeKHkk5Hee2iKIT3xAJoM_8130_assertion description "[Anti-cytochrome P450 autoantibodies, identified on the basis of their specific binding in immunoblots, are significantly increased among children on immunosuppressive drugs and in some cases are associated with drug toxicity and organ rejection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146614.RAuOUGgCHcrVR9vWW-D1LYAeKHkk5Hee2iKIT3xAJoM_8130_provenance.
- NP146617.RAoLuwuGILlmdkhtnK1urasfpr1NwaV0QKrYA0fR0_UIE130_assertion description "[variations in NFKB1 appear to affect the risk for alcoholism, particularly contributing to an earlier onset of the disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146617.RAoLuwuGILlmdkhtnK1urasfpr1NwaV0QKrYA0fR0_UIE130_provenance.
- NP146619.RAnqglqWUbu0Aaw0v6qYopfL99EoWbi9HCyMVulW8mhEE130_assertion description "[The promoter region of a gene can influence gene expression, the ALDH1A1 promoter regions were studied to identify polymorphism, to assess their functional significance, and to determine whether they were associated with a risk for developing alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146619.RAnqglqWUbu0Aaw0v6qYopfL99EoWbi9HCyMVulW8mhEE130_provenance.
- NP146622.RAmxCLMX-C5Jq6iF1HOJe0SGi_jbnuFuGv0cfI6rgB6t4130_assertion description "[Among type 1 alcoholics dopamine transporters are lower in nucleus accumbens and dopamine D (2), but not D (1) or D (3) receptors in nucleus accumbens and amygdala/dopamine receptor density is specific for D (2) receptor and for type 1 alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146622.RAmxCLMX-C5Jq6iF1HOJe0SGi_jbnuFuGv0cfI6rgB6t4130_provenance.
- NP146627.RAnDVZXe9lzNv9M-nxbsby76AJiQqTtJzQ1v9OQ6TLjqk130_assertion description "[Monoamine oxidase A polymorphism could play a role in susceptibility to alcoholism, which may differ across sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146627.RAnDVZXe9lzNv9M-nxbsby76AJiQqTtJzQ1v9OQ6TLjqk130_provenance.
- NP146631.RAmNrv6gFlTz5yFC7K5QkpBXmA9k2SsPiipEQDwcazuoQ130_assertion description "[COMT (Val158Met) leads to neurobiology differences in executive cognitive function, stress/anxiety response, and opioid function that increase susceptibility to alcoholism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146631.RAmNrv6gFlTz5yFC7K5QkpBXmA9k2SsPiipEQDwcazuoQ130_provenance.
- NP146637.RAnFf6iKtm68JAkWYQsV7nJmaAy-Cxbbgd9OFkVJFSREo130_assertion description "[Three genetic variants of SLC19A2 gene were identified in Wernicke Korsakoff syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146637.RAnFf6iKtm68JAkWYQsV7nJmaAy-Cxbbgd9OFkVJFSREo130_provenance.
- NP146638.RAqi6hEvogiSljM2OPqFdE5UiMwFggrVp-K0sR3yCA_AI130_assertion description "[presence of high levels of IL-18 in the cord blood of the pre-term infants is correlated with the incidence of periventricular leukomalacia and cerebral palsy and may provide a prognostic marker applicable at birth ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146638.RAqi6hEvogiSljM2OPqFdE5UiMwFggrVp-K0sR3yCA_AI130_provenance.
- NP146640.RAq3dzlUQHHB_YPDfYBug9HY99rzLNq0cRwTdNLdjfi5o130_assertion description "[Increased concentrations of TNF-alpha in cord blood and of IL-6 in cord blood were associated with psychomotor developmental index < 85; Increased concentrations of TNF-alpha in cord blood and IL-8 in cord blood were associated with cerebral palsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146640.RAq3dzlUQHHB_YPDfYBug9HY99rzLNq0cRwTdNLdjfi5o130_provenance.
- NP146650.RAg5wPzwFuk_FxoXSz9Tz9z90wDEaw1_YWhwP80bx6J7I130_assertion description "[We suggest that mtDNA G13513A mutation is an important factor in patients with Leigh syndrome associated with WPW syndrome and/or optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146650.RAg5wPzwFuk_FxoXSz9Tz9z90wDEaw1_YWhwP80bx6J7I130_provenance.
- NP146655.RAlU49OFy66RMQ3RHqk4pxtoPsCzWdcqLbgDGIPLyarpo130_assertion description "[Novel mutation of the OPA1 gene with a clinical phenotype of isolated optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146655.RAlU49OFy66RMQ3RHqk4pxtoPsCzWdcqLbgDGIPLyarpo130_provenance.
- NP146657.RAtMYmRl67qAM_8z3fVHVpwjp_8pkD8mpADiqJsmO7PHw130_assertion description "[The heterozygous R445H mutation in OPA1 was found in five patients with optic atrophy and deafness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146657.RAtMYmRl67qAM_8z3fVHVpwjp_8pkD8mpADiqJsmO7PHw130_provenance.
- NP146659.RArszHkNXW6dUdJoJ0LyW6fRD9hp5gN4xdgve3roihid4130_assertion description "[type III 3-methylglutaconic aciduria (optic atrophy plus syndrome, or Costeff optic atrophy syndrome): identification of the OPA3 gene and its founder mutation in Iraqi Jews ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146659.RArszHkNXW6dUdJoJ0LyW6fRD9hp5gN4xdgve3roihid4130_provenance.
- NP146662.RAmPdw0d8ZFPPstY1PSnW0O-G9iSukabMF4GZ1YsPwz5U130_assertion description "[Our findings show that gross genomic aberrations at the OPA1 gene locus are frequent in Autosomal dominant optic atrophy and substantially contribute to the spectrum and prevalence of OPA1 mutations in ADOA patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146662.RAmPdw0d8ZFPPstY1PSnW0O-G9iSukabMF4GZ1YsPwz5U130_provenance.
- NP146670.RAuW78YJ7hpqRyBkp2JSHZtzn7ww0fIYvVvJyiyUGISoE130_assertion description "[The RNFL (retinal nerve fiber layer) and the layer including the ganglion cell layer are significantly thinner in patients with ADOA (autosomal dominant optic atrophy) associated with an OPA1 gene mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146670.RAuW78YJ7hpqRyBkp2JSHZtzn7ww0fIYvVvJyiyUGISoE130_provenance.
- NP146674.RAtpXkWOilZVRHrKR5LoFQBbA5twPmTv2S3wIhG0UAmtw130_assertion description "[antibodies against human alpha-enolase target antigens in retinal ganglion cells and inner nuclear layer cells and induce the apoptotic death of sensitive cells in rat retinal explants ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146674.RAtpXkWOilZVRHrKR5LoFQBbA5twPmTv2S3wIhG0UAmtw130_provenance.
- NP146676.RAvII6GSRTieGDxpFMjVvSWbysiZAHxO2og7GzyyFsF28130_assertion description "[Dominant optic atrophy (DOA) is characterized by retinal ganglion cell degeneration leading to optic neuropathy/subset of DOA is caused by mutations in the OPA1 gene, encoding for a dynamin-related GTPase required for mitochondrial fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146676.RAvII6GSRTieGDxpFMjVvSWbysiZAHxO2og7GzyyFsF28130_provenance.
- NP146681.RApUq26kxh7A8GodHaMjxuffIn4FMeWAmxT1cz738KBic130_assertion description "[T14484C and T14502C in ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146681.RApUq26kxh7A8GodHaMjxuffIn4FMeWAmxT1cz738KBic130_provenance.
- NP146695.RAuWWswa16Il7_KacfzHta3kQDIuAOOE9Po75l8Un_24c130_assertion description "[mutation in a gene segregating with a peculiar mitochondrial encephalomyopathy associated with COX deficiency in skeletal muscle/is localized in the mitochondrial inner compartment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146695.RAuWWswa16Il7_KacfzHta3kQDIuAOOE9Po75l8Un_24c130_provenance.
- NP146698.RAn07_yD_iHFfRYzjKsKZNyn6W0Af3nqyNXOova_lYeco130_assertion description "[frequency of occurrence of mtDNA with the COII/tRNA (Lys) intergenic 9-bp deletion polymorphism in patients with myoclonic epilepsy with ragged-red fibers or mitochondrial encephalomyopathy syndrome is higher than that of healthy subjects ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146698.RAn07_yD_iHFfRYzjKsKZNyn6W0Af3nqyNXOova_lYeco130_provenance.
- NP146699.RAjrAxjYmv3RlRPL-DYLCSl0wG9HPWaZ6UttnY2Iv76Dw130_assertion description "[the TP53 codon 72 polymorphism could be associated with susceptibility for adrenocortical cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146699.RAjrAxjYmv3RlRPL-DYLCSl0wG9HPWaZ6UttnY2Iv76Dw130_provenance.
- NP146704.RAv4aRNKbju0FqKmc2zqBpKtFxH7jwk8aI5-X1WxpZCYU130_assertion description "[a genetic instability of the 17p13 region, occurring early in adrenocortical cancer development, involves various genes located in this region, including TP53 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146704.RAv4aRNKbju0FqKmc2zqBpKtFxH7jwk8aI5-X1WxpZCYU130_provenance.
- NP146710.RAiqP2h6tmNC6qQi_6uEroEron4CpobfuOOH0gc95zAZE130_assertion description "[Long-term bone marrow cultures (LTBMC) from JAK2617V > F positive essential thrombocythemia patients display a growth pattern more similar to that observed in LTBMC produced by polycythemia vera marrow cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146710.RAiqP2h6tmNC6qQi_6uEroEron4CpobfuOOH0gc95zAZE130_provenance.
- NP146716.RAmV-A0bh9NpSWJjg9jRD2rgXo1KVDJB5c-d4Sf44hs-s130_assertion description "[JAK2V617F-positive essential thrombocythemia and multiple myeloma with IGH/CCND1 gene translocation coexist, but originate from separate clones ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146716.RAmV-A0bh9NpSWJjg9jRD2rgXo1KVDJB5c-d4Sf44hs-s130_provenance.
- NP146723.RAtuXp9FR0g9dbShLPMYpMAxj6p-thrEi8M_9iuTN-xoY130_assertion description "[JAK2 V617F mutation was detected in 124/158 chronic myeloproliferative disease patients; 90.2, 72.1, 63.2 & 50% of polycythemia vera, essential thrombocythemia, idiopathic myelofibrosis & unclassified (U) -MPD cases, respectively, showed the mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146723.RAtuXp9FR0g9dbShLPMYpMAxj6p-thrEi8M_9iuTN-xoY130_provenance.
- NP146731.RAnlxhCSFotx_QLPvHseAc_4hubqMtXsT9zOTqtcbAtEY130_assertion description "[JAK2V617F-positive essential thrombocythemia and multiple myeloma with IGH/CCND1 gene translocation coexist, but originate from separate clones ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146731.RAnlxhCSFotx_QLPvHseAc_4hubqMtXsT9zOTqtcbAtEY130_provenance.
- NP146744.RAmAHhn023_82lGAJqVtulNGx8Xq-h_E7HCgcuYzUkjIA130_assertion description "[Internal tandem duplication of the juxtamembrane domain or by activating point mutations in the second tyrosine kinase domain in FLT3 are associated with leukocytosis and the monocytic FAB subtypes M4 and M5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146744.RAmAHhn023_82lGAJqVtulNGx8Xq-h_E7HCgcuYzUkjIA130_provenance.
- NP146748.RAt6-r4hScNVpFBDxB4A-ZdsT0vL3NETyn-LuD_wxOkpU130_assertion description "[Increased incidence of JAK2 V617F mutation is associated with refractory anemia with ringed sideroblasts and marked thrombocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146748.RAt6-r4hScNVpFBDxB4A-ZdsT0vL3NETyn-LuD_wxOkpU130_provenance.
- NP146750.RAjBc_ajWKReNnC5XOb9FRaRTW-1ziRGkqEDQqK_6N0Jg130_assertion description "[JAK2-V617F mutation may have a role in preventing progression of RARS-T (refractory anemia with ringed sideroblasts and marked thrombocytosis) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146750.RAjBc_ajWKReNnC5XOb9FRaRTW-1ziRGkqEDQqK_6N0Jg130_provenance.
- NP146754.RAvrHYGkDJRFr3F-Mx9TTlKYsF4jVWcBTfPXqEoUJJGcA130_assertion description "[no MPL (myeloproliferative leukemia virus oncogene thrombopoietin recept) W515L/K mutations were found in any patients with refractory anemia with ringed sideroblasts associated with marked thrombocytosis (RARS-T) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146754.RAvrHYGkDJRFr3F-Mx9TTlKYsF4jVWcBTfPXqEoUJJGcA130_provenance.
- NP146766.RAhZjsnecQ9aKBUqXHNBTf6XEDgKV9fuaDrwcx3DUbVvA130_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." NP146766.RAhZjsnecQ9aKBUqXHNBTf6XEDgKV9fuaDrwcx3DUbVvA130_provenance.
- NP146769.RAhHuCqt8i7a4oIAsPLxdWhYdw08sQ1c8YA06K1KbZMHI130_assertion description "[Short AR allelotype (< or = 20 CAG repeats) was associated with a higher incidence of thrombocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146769.RAhHuCqt8i7a4oIAsPLxdWhYdw08sQ1c8YA06K1KbZMHI130_provenance.
- NP146770.RAjCedJsfRyWtLOOMKOESQsnkAWGG626Hu57GUAuQmeW0130_assertion description "[analysis of a family with a splice donor mutation in the thrombopoietin gene that causes hereditary thrombocythemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146770.RAjCedJsfRyWtLOOMKOESQsnkAWGG626Hu57GUAuQmeW0130_provenance.
- NP146775.RAk8OQlP3AJ9cJE8TAXgKgJEJ9Z_B7uaKlJxDXtAVL410130_assertion description "[results of this study showed for the first time that TAFI activity is increased in patients with clonal thrombocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146775.RAk8OQlP3AJ9cJE8TAXgKgJEJ9Z_B7uaKlJxDXtAVL410130_provenance.
- NP146778.RAvCe2snWTYJ9VWtTwwJk4YTRKH2ULHZSBQKMVFGyYqMs130_assertion description "[PCR and fluoresecne in situ hybridization shows that HCMOGT-1 is a novel fusion partner to PDGFRB in juvenile myelomonocytic leukemia with t (5; 17) (q33; p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146778.RAvCe2snWTYJ9VWtTwwJk4YTRKH2ULHZSBQKMVFGyYqMs130_provenance.
- NP146785.RAm769-JRRnVtGBUctQPMBbY9qsTfsCQBNo3lN2G1kW3Y130_assertion description "[patients having juvenile myelomonocytic leukemia with NRAS or KRAS2 glycine to serine substitution received no chemotherapy, but hematologic improvement was observed during a 2- to 4-year follow up.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146785.RAm769-JRRnVtGBUctQPMBbY9qsTfsCQBNo3lN2G1kW3Y130_provenance.
- NP146789.RAqJVs_Z777z_MqZ_axyZOqjmk3bxzbZtxbUrISyyI0Xs130_assertion description "[NO and PAI-1 play pivotal and antagonistic roles in hepatic vein thrombosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146789.RAqJVs_Z777z_MqZ_axyZOqjmk3bxzbZtxbUrISyyI0Xs130_provenance.
- NP146790.RAk8rB77D2VydaK2Bg34NUvIk_qRhmswb43GT6gXKmgA0130_assertion description "[Hyperhomocysteinemia and the homozygous C677T mutation in the MTHFR gene are important risk factors of Budd Chiari syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146790.RAk8rB77D2VydaK2Bg34NUvIk_qRhmswb43GT6gXKmgA0130_provenance.
- NP146794.RAvZ0eYsZWC7Q4YWsNLyjvSEEQtWBgukiljvVYWUoY0jw130_assertion description "[beta3 knockout mice transfused with wild-type platelets generated specific anti-beta3 antibodies which were able to induce thrombocytopenia in wild-type mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146794.RAvZ0eYsZWC7Q4YWsNLyjvSEEQtWBgukiljvVYWUoY0jw130_provenance.
- NP146803.RAmyFOgqnbLB-XDv9CQrTtmJyW4xoPpcYrYJTUrldm0l4130_assertion description "[Mutation analysis in congenital amegakaryocytic thrombocytopenia helps to predict the clinical course and to provide optimal therapy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146803.RAmyFOgqnbLB-XDv9CQrTtmJyW4xoPpcYrYJTUrldm0l4130_provenance.
- NP146808.RAoffzOdu51DPwC4D52lq49-IIlKLda3t-I6a_IGhX5to130_assertion description "[A novel missense mutation in the human gene FLJ14813 is associated with autosomal dominant thrombocytopenia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146808.RAoffzOdu51DPwC4D52lq49-IIlKLda3t-I6a_IGhX5to130_provenance.
- NP146813.RAhJw3qajvQ-MyO7dv75auk3hB_1vtIXmRHSnjLbYQvXo130_assertion description "[Chinese Wiskott-Aldrich Syndrome (WAS) patients had mutations involving exon 1 of the Wiskott-Aldrich syndrome protein (WASP) gene and none had the X-linked thrombocytopenia phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146813.RAhJw3qajvQ-MyO7dv75auk3hB_1vtIXmRHSnjLbYQvXo130_provenance.
- NP146815.RAph96LKIAcMew6raba4kY9CXj5vjnb9-XXLW2xdpzh8M130_assertion description "[Role of interleukin-11 to prevent chemotherapy-induced thrombocytopenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146815.RAph96LKIAcMew6raba4kY9CXj5vjnb9-XXLW2xdpzh8M130_provenance.
- NP146817.RAkTl1Yh2kfp_8GEoauppf6ONm4oUESMBNTrG9DyZFlic130_assertion description "[X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affects DNA binding rather than FOG-1 interaction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146817.RAkTl1Yh2kfp_8GEoauppf6ONm4oUESMBNTrG9DyZFlic130_provenance.
- NP146821.RAnwx1NhrlR_NfF4gbzC9zBTv0Wz5gvyzZ6EdbvXgVfXw130_assertion description "[ADAMTS13 deficiency is associated with severe thrombocytopenia and microangiopathic hemolytic anemia in conjunction with severe bilateral otitis media ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146821.RAnwx1NhrlR_NfF4gbzC9zBTv0Wz5gvyzZ6EdbvXgVfXw130_provenance.
- NP146835.RAlpahxG6eNaspcdRsbHehhuQfL7eZ4aRaDnDSpx3IT9g130_assertion description "[In 77 Italian patients with inherited thrombocytopenia and clinical and laboratory features similar to those of patients with the CYCS missense (Gly41Ser) mutation, no alterations of the open reading frame were identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146835.RAlpahxG6eNaspcdRsbHehhuQfL7eZ4aRaDnDSpx3IT9g130_provenance.
- NP146843.RAnGXT6mehQ8QzpWwiFY9yVe7-gfVI7wXQXMaDIo7SjME130_assertion description "[RT-PCR is the most rapid, reliable, and feasible method for the detection of PRV-1 overexpression in highly purified peripheral blood granulocytes in polycythemia rubra vera and essential thrombocythemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146843.RAnGXT6mehQ8QzpWwiFY9yVe7-gfVI7wXQXMaDIo7SjME130_provenance.
- NP146844.RAskOCzwJ3vgfroGjzUiuaEDoLsJGZkAMIYkRf2AvDYAg130_assertion description "[Biochemical characterization of PHD2 variants associated with polycythemia is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146844.RAskOCzwJ3vgfroGjzUiuaEDoLsJGZkAMIYkRf2AvDYAg130_provenance.
- NP146845.RAijoC-dATTuAZNtfqMmFrZWv5msTRF5i_R6eVQtzNya8130_assertion description "[propose that mutations of the VHL gene represent an important cause of pediatric sporadic polycythemias with an inappropriately high serum erythropoietin concentration ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146845.RAijoC-dATTuAZNtfqMmFrZWv5msTRF5i_R6eVQtzNya8130_provenance.
- NP146849.RAhylyBeNX7GuyD6tgK0YNuqnwy0AVZKGzSZIQHg7rg6M130_assertion description "[Estimated systolic pulmonary artery pressure and plasma concentrations of endothelin-1 and VEGF are increased in patients with Chuvash polycythemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146849.RAhylyBeNX7GuyD6tgK0YNuqnwy0AVZKGzSZIQHg7rg6M130_provenance.
- NP146858.RAsOBv5Tw6AhSrnNVYiujnXZ359mrl3wLyrWCuE3Utw-o130_assertion description "[Missense mutation in pseudouridine synthase 1 causes mitochondrial myopathy and sideroblastic anemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146858.RAsOBv5Tw6AhSrnNVYiujnXZ359mrl3wLyrWCuE3Utw-o130_provenance.
- NP146861.RAjbWNGQPJkvImfD-6OLqZgRaxrY5ZGr-KPhBVR1xZNT4130_assertion description "[REVIEW: mechanisms involving ALAS deficiency, point mutations, post translational processing, and complex formation with succinyl CoA synthetase subunit B in the pathogenesis of hereditary sideroblastic anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146861.RAjbWNGQPJkvImfD-6OLqZgRaxrY5ZGr-KPhBVR1xZNT4130_provenance.
- NP146862.RAr0ICDIIT6ylKSFx8zUl4Qq45atIR4ujTT76Jw1Zf_yI130_assertion description "[Some of SNPs found in the factor V gene may predispose women to acquired activated protein C resistance and recurrent miscarriage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146862.RAr0ICDIIT6ylKSFx8zUl4Qq45atIR4ujTT76Jw1Zf_yI130_provenance.
- NP146863.RAqYJnnvqp8mtVibYvpTlJedY0pN0WvNLvy42dLQbCCNk130_assertion description "[the occurrence of acquired APC resistance in ET and PV patients, probably because of a reduction in free PS levels/APC-resistant phenotype is influenced by the JAK2 (V617F) mutational load.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146863.RAqYJnnvqp8mtVibYvpTlJedY0pN0WvNLvy42dLQbCCNk130_provenance.
- NP146866.RAuz2H3sJf7B6KENN7K17NPA-xfIv6FCp4Vpdsa7DT-Lw130_assertion description "[direct correlation between a major clinical symptom of antiphospholipid syndrome (thrombosis), a diagnostic assay (beta2-GPI-dependent LAC) and a potential mechanism responsible for thrombosis in the antiphospholipid syndrome (increased APC resistance).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146866.RAuz2H3sJf7B6KENN7K17NPA-xfIv6FCp4Vpdsa7DT-Lw130_provenance.
- NP146869.RAtA0fA8oQ6W3Q4T-p0fKkuZW9ZQ0yvo9qQyf48YA-41g130_assertion description "[The prevalence of activated protein C resistance and FVL mutations is increased in patients with retinal vein occlusion compared to controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146869.RAtA0fA8oQ6W3Q4T-p0fKkuZW9ZQ0yvo9qQyf48YA-41g130_provenance.
- NP146885.RAujrmG3rLbp2xEbzEaBeKCPwiLrQxfnAaGAAYxAIW1_I130_assertion description "[Results from RT-PCR, western blotting and confocal microscopy demonstrated that the MT1, MT2 and RORalpha1 melatonin receptors are expressed in the human term placental tissues and in choriocarcinoma cell lines JEG-3 and BeWo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146885.RAujrmG3rLbp2xEbzEaBeKCPwiLrQxfnAaGAAYxAIW1_I130_provenance.
- NP146888.RAiPPOTpGk8Oviz-oP0In_EHt1Mo8gpVkhsulJYFx7a94130_assertion description "[Promoter methylation of the TIMP3 is involved in suppression of TIMP3 expression in choriocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146888.RAiPPOTpGk8Oviz-oP0In_EHt1Mo8gpVkhsulJYFx7a94130_provenance.
- NP146889.RAt4p6uh5LnUnEQcgIRxRMg3hZuBiBNZH5qtt8WXynegQ130_assertion description "[High serum angiogenin levels were associated with choriocarcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146889.RAt4p6uh5LnUnEQcgIRxRMg3hZuBiBNZH5qtt8WXynegQ130_provenance.
- NP146894.RArL2wjGoFOJcWcYhPsxtvTLZDEbCWMeGzYVxAQYczDmk130_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." NP146894.RArL2wjGoFOJcWcYhPsxtvTLZDEbCWMeGzYVxAQYczDmk130_provenance.
- NP146897.RAk2mc9uCs8w7bBqJo6SGiL50XHmF7nyMy2xaBXFkOvsE130_assertion description "[Specific DNA binding activity of two STAT3 variants (STAT3alpha and beta) was observed in immature trophoblasts and appeared to be lost in term placentae/malignant phenotype of choriocarcinoma cells coincides with a high degree of STAT3 activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146897.RAk2mc9uCs8w7bBqJo6SGiL50XHmF7nyMy2xaBXFkOvsE130_provenance.
- NP146901.RApXrWW3WSrJUMsN6VN2ghHj_q_TaAY9aWZ5IcPKFa53g130_assertion description "[Interleukin-1beta stimulates expression in BeWo choriocarcinoma cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146901.RApXrWW3WSrJUMsN6VN2ghHj_q_TaAY9aWZ5IcPKFa53g130_provenance.
- NP146909.RAinWSAsZhxl25Lvi6vIHV6bIsPndXEVZ8DEd8Y9K9J6E130_assertion description "[Two closely spaced Ets-2 binding sites in the proximal promoter of the human chorionic gonadotropin beta5 (hCGbeta5) gene constitute a major enhancer for hCGbeta gene expression in JAr and JEG-3 human choriocarcinoma cells and in mouse NIH3T3 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146909.RAinWSAsZhxl25Lvi6vIHV6bIsPndXEVZ8DEd8Y9K9J6E130_provenance.
- NP146915.RAkjpwC-STMoFS_DFSCh9k6KaJlA3OfX_gE-wg1s_nsUg130_assertion description "[These data suggest that KIT (D816V+) systemic mastocytosis (SM) can co-exist with JAK2 (V617F+) chronic idiopathic myelofibrosis (CIMF) and in some of these SM-CIMF cases, the two mutations are present in the neoplastic cells of both disease components.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146915.RAkjpwC-STMoFS_DFSCh9k6KaJlA3OfX_gE-wg1s_nsUg130_provenance.
- NP146923.RAjDupRKTF7sSNS133K8YfVi7B7AvXHzMuiRZXnW3iaFQ130_assertion description "[mapped a locus for infantile neuroaxonal dystrophy (INAD) and neurodegeneration with brain iron accumulation (NBIA) to chromosome 22q12-q13 and identified mutations in PLA2G6, encoding a group VI phospholipase A2, in NBIA, INAD and Karak syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146923.RAjDupRKTF7sSNS133K8YfVi7B7AvXHzMuiRZXnW3iaFQ130_provenance.
- NP146928.RAgkF23nQaAU1kD-Ufe0RwuK9UgsrHlVmlk362rCndIIM130_assertion description "[Genetic variants within S100B are associated with bipolar affective disorder with psychosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146928.RAgkF23nQaAU1kD-Ufe0RwuK9UgsrHlVmlk362rCndIIM130_provenance.
- NP146929.RAtzIXY-ieLcUXbp3fYOIMJoOaIzqKqc9csI4AVOLhEDk130_assertion description "[reduced GRalpha mRNA expression might be trait-dependent and associated with the pathophysiology of mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146929.RAtzIXY-ieLcUXbp3fYOIMJoOaIzqKqc9csI4AVOLhEDk130_provenance.
- NP146931.RAlmMqnOFn7PqJdLghSucyUxxvkYM1MtpHUaoNkveugUk130_assertion description "[Study suggest that GPR24 variants may confer susceptibility to both bipolar affective disorder and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146931.RAlmMqnOFn7PqJdLghSucyUxxvkYM1MtpHUaoNkveugUk130_provenance.
- NP146933.RAl0tecFxhipMa7RmlT7SXpVjw7y8xH95dyd23CeX1Xfk130_assertion description "[The hypothesis that gene variants could influence temperamental traits in mood disorders patients was tested/containing the DRD4 long allele were marginally associated with low harm avoidance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146933.RAl0tecFxhipMa7RmlT7SXpVjw7y8xH95dyd23CeX1Xfk130_provenance.
- NP146946.RAhHTM3XtVEE_7aUXWTbAHSQcveWZvXAOpanz8Tn3sOnQ130_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 support the 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." NP146946.RAhHTM3XtVEE_7aUXWTbAHSQcveWZvXAOpanz8Tn3sOnQ130_provenance.
- NP146951.RAoxSRLdWfxgJOyCrJgE0Cv3eZSjoJDA71rdmy1wV8_Lo130_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." NP146951.RAoxSRLdWfxgJOyCrJgE0Cv3eZSjoJDA71rdmy1wV8_Lo130_provenance.
- NP146954.RAvepYKb0LOxzmgWmokTj69V2gS93AoUBx_ayx68vcqCQ130_assertion description "[2 new heterozygous missense transitions (C2794T, G3151C) were found in the POLG gene in a family with an autosomal recessive syndrome: progressive external ophthalmoplegia, polyneuropathy, ataxia, sensorineural hearing loss, and affective disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146954.RAvepYKb0LOxzmgWmokTj69V2gS93AoUBx_ayx68vcqCQ130_provenance.
- NP146955.RAtowUvmPgPDXr902m2yabyf6sVO139G6EUmtVlQGcZeU130_assertion description "[Association between GSJ-3beta-50T/C polymorphism and personality and psychotic symptoms in mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146955.RAtowUvmPgPDXr902m2yabyf6sVO139G6EUmtVlQGcZeU130_provenance.
- NP146956.RAlXYg-5sT9eEOydj8bA1PmgIFQDD7Qx-H0UL6WfQUnPQ130_assertion description "[genetic variations in neural cell adhesion molecule 1 or nearby genes could confer risks associated with bipolar affective disorder in Japanese individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146956.RAlXYg-5sT9eEOydj8bA1PmgIFQDD7Qx-H0UL6WfQUnPQ130_provenance.
- NP146964.RAvG3mKIpNuoXJbnnRhTUqnE3jtaT4qsge6s_qASEs3ac130_assertion description "[significantly up-regulated on CD4 and CD8 T cells during acute infectious mononucleosis; regulates lymphocyte activation via signals from cell-surface CD244 (2B4) and SLAM (CD150) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146964.RAvG3mKIpNuoXJbnnRhTUqnE3jtaT4qsge6s_qASEs3ac130_provenance.
- NP146976.RAp9R2ybaYaTb-iPz3ZfNTqtQUQow1U1Y_jCSadFuqc7g130_assertion description "[The findings of this study indicate that an individual's response to age-related eye disease supplements may be related to complement factor H genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146976.RAp9R2ybaYaTb-iPz3ZfNTqtQUQow1U1Y_jCSadFuqc7g130_provenance.
- NP146980.RApm-OgErnm7r6IMtC2qXrtm-aSkulzUiyY798ohldihw130_assertion description "[Detection of both partial and whole gene deletions of MITF increase mutation detection in Waardenburg syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146980.RApm-OgErnm7r6IMtC2qXrtm-aSkulzUiyY798ohldihw130_provenance.
- NP146981.RAvFaMrsTLF5KIjGDbYbOKNFGrvosjpt07sqa-mQ8-Gcw130_assertion description "[Detection of both partial and whole gene deletions of PAX3 increase mutation detection in Waardenburg syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146981.RAvFaMrsTLF5KIjGDbYbOKNFGrvosjpt07sqa-mQ8-Gcw130_provenance.
- NP146988.RAiIswQ2CFg1qIQARb9iWyYvyid3lXFiDNmYvGppy1-k4130_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." NP146988.RAiIswQ2CFg1qIQARb9iWyYvyid3lXFiDNmYvGppy1-k4130_provenance.
- NP146989.RAjWOa_rOEJ_TgcHEOL8yrUjlwdYDKDVwMcNI40jccTRk130_assertion description "[Decrease 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." NP146989.RAjWOa_rOEJ_TgcHEOL8yrUjlwdYDKDVwMcNI40jccTRk130_provenance.
- NP147007.RAhNnfj05ekfIQtk7Hw1C1NpzWclbmC7BNk6iiaihnFhA130_assertion description "[plasma levels are increased in lung cancer cachexia; increased ghrelin may represent a compensatory mechanism under catabolic-anabolic imbalance in cachectic patients with lung cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147007.RAhNnfj05ekfIQtk7Hw1C1NpzWclbmC7BNk6iiaihnFhA130_provenance.
- NP147008.RAkhnK1BtNm4tdwatnTI7eIiTmaQsKl84PrFtW0HKGJAY130_assertion description "[Constitutive expression of cytokines in brain induces changes in gene expression characteristic of chronic inflammation leading to either temporal weight reduction (CNTF) or severe cachexia (leukemia inhibitory factor).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147008.RAkhnK1BtNm4tdwatnTI7eIiTmaQsKl84PrFtW0HKGJAY130_provenance.
- NP147012.RAu5eHpYi5lDjDDZ7tIcmTNeDmE7-2xrJeEDezfSLl1jk130_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." NP147012.RAu5eHpYi5lDjDDZ7tIcmTNeDmE7-2xrJeEDezfSLl1jk130_provenance.
- NP147023.RAgMEMawrytk7T4FM1bw-_0EeDj5jj6a6rjkg8nbYt1QA130_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." NP147023.RAgMEMawrytk7T4FM1bw-_0EeDj5jj6a6rjkg8nbYt1QA130_provenance.
- NP147031.RAlA_WXtJXT3D67gE8KNGUK3ohIgct2sE15Y5lKboGBvA130_assertion description "[LHR mutations may represent an underestimated cause of infertility in women, in addition to being responsible for male hypogonadism with reduced spermatogenesis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147031.RAlA_WXtJXT3D67gE8KNGUK3ohIgct2sE15Y5lKboGBvA130_provenance.
- NP147032.RAs59gUa4hRyqd9RtNTPrqLRDs9PplgYnblXBZ8Y_T11A130_assertion description "[PROP1 mutations should be considered among the growing number of genetic causes of initially isolated hypogonadotropic hypogonadism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147032.RAs59gUa4hRyqd9RtNTPrqLRDs9PplgYnblXBZ8Y_T11A130_provenance.
- NP147033.RAosxr6r3nGnQ_zJ__f7eWz1pw_TQS24wvbejaLKCUgwE130_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." NP147033.RAosxr6r3nGnQ_zJ__f7eWz1pw_TQS24wvbejaLKCUgwE130_provenance.
- NP147035.RAk_Qf_3DgmLZg9MD3OY2GYYMHReQCJRq37sOxS4UAk-s130_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." NP147035.RAk_Qf_3DgmLZg9MD3OY2GYYMHReQCJRq37sOxS4UAk-s130_provenance.
- NP147036.RAlRB_xpop-i9GmFFr-EM7KnjtnPneyanrAPPOsRA88nI130_assertion description "[transgenic mice overexpressing gremlin in the bone microenvironment have decreased osteoblast number and function leading to osteopenia and spontaneous fractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147036.RAlRB_xpop-i9GmFFr-EM7KnjtnPneyanrAPPOsRA88nI130_provenance.
- NP147053.RAieD9iwVEUG1f-uwSq0OOwAdovHmlKGJGlskY0y1JeyY130_assertion description "[results suggest that the guanine-thymine repeat microsatellite polymorphisms in intron II of the human TLR2 gene contribute to the development of nontuberculous mycobacteria lung disease, in a Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147053.RAieD9iwVEUG1f-uwSq0OOwAdovHmlKGJGlskY0y1JeyY130_provenance.
- NP147054.RAsGOBSJ2glfdcww3IckJneVwmkdVRN2hc_7I8jdXu9fs130_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." NP147054.RAsGOBSJ2glfdcww3IckJneVwmkdVRN2hc_7I8jdXu9fs130_provenance.
- NP147057.RAuDdt3-p7qn8LGzGmjkdn2KnSmVA8XI4bnH42Dk4fFmg130_assertion description "[The significantly higher frequency of CFTR mutations among patients with chronic pulmonary disease compared with unaffected controls suggests that these mutations may increase risk for disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147057.RAuDdt3-p7qn8LGzGmjkdn2KnSmVA8XI4bnH42Dk4fFmg130_provenance.
- NP147061.RAtgJrYxmff0iD9i8gNLYpvLlJbt9C2I_oC8Nl5-rt_yU130_assertion description "[IL-8 production is controlled by de novo transcriptional induction as well as posttranscriptional up-regulation of IL-8 by neonatal leukocytes, relating to the development of premature chronic lung disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147061.RAtgJrYxmff0iD9i8gNLYpvLlJbt9C2I_oC8Nl5-rt_yU130_provenance.
- NP147070.RAqb-Qcjiv9yb2oyvj0OtuiZDg1PkJR5xPXMgRXCEHWhA130_assertion description "[TaqI and FokI polymorphisms of the VDR gene do not appear to be responsible for host susceptibility to non-tuberculous mycobacteria lung disease, at least in this Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147070.RAqb-Qcjiv9yb2oyvj0OtuiZDg1PkJR5xPXMgRXCEHWhA130_provenance.
- NP147071.RAgzNywJO4EPAakJ7oNBbX6Q4g35NMfLjNh7x4_Nyabuc130_assertion description "[AHR pathway plays important role in cigarette smoke-mediated COX-2 and prostaglandin production in human lung fibroblasts and may contribute to tobacco-associated inflammation and lung disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP147071.RAgzNywJO4EPAakJ7oNBbX6Q4g35NMfLjNh7x4_Nyabuc130_provenance.