Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP150710.RAjDFxoKxqLr0YGPxcbwoQXG6QDVOGQ0d9bZOB16ixgww130_assertion description "[Identify novel mutation in COL7A1 responsible for dominant dystrophic epidermolysis bullosa in a Chinese family/severe phenotype observed in female members.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150710.RAjDFxoKxqLr0YGPxcbwoQXG6QDVOGQ0d9bZOB16ixgww130_provenance.
- NP150711.RAlFHXzv4-geiO-9tOAN9-sDuKqeTK-A0cZq8XgfRKr9U130_assertion description "[Individuals with recessive dystrophic epidermolysis bullosa can develop squamous-cell carcinoma regardless of type VII collagen expression and that additional factors have a role in explaining the high incidence of tumors complicating this genodermatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150711.RAlFHXzv4-geiO-9tOAN9-sDuKqeTK-A0cZq8XgfRKr9U130_provenance.
- NP150712.RApGM4qab5ee3Yv7KQETaGBsdt1PYqT9bNClLhETCYboc130_assertion description "[We report 14 Australian families with different forms of dystrophic epidermolysis bullosa (DEB) with 23 different COL7A1 allelic variants, nine of which were novel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150712.RApGM4qab5ee3Yv7KQETaGBsdt1PYqT9bNClLhETCYboc130_provenance.
- NP150717.RAnJhaO28rPewfgfQXbwd8hG-ip1WUnwi_KZI_QTd_4uY130_assertion description "[Reduced expression of IGFBP-3 in recessive dystrophic epidermolysis bullosa squamous cell carcinoma may provide a partial explanation for the aggressive behavior and poor prognosis of these tumors in this genodermatosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150717.RAnJhaO28rPewfgfQXbwd8hG-ip1WUnwi_KZI_QTd_4uY130_provenance.
- NP150721.RAgLjg5LvoI75EIMdYE6rzggJz8wZccjWKA-CW8WGp5mk130_assertion description "[Mutations in the COL5A2 gene have been identified by DNA sequence analysis in 10 patients with spontaneous vertebral artery dissections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150721.RAgLjg5LvoI75EIMdYE6rzggJz8wZccjWKA-CW8WGp5mk130_provenance.
- NP150722.RApjTfRO6IlQkzBoEeYQfkeRxn9X8ube8imkLdsGDCdqs130_assertion description "[Frequency of the s allele of the CollA1 gene was higher in Russian patients and that of the FokI FF genotype in Tartar patients/data obtained suggest a possible role of these genes in the pathogenesis of syringomyelia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150722.RApjTfRO6IlQkzBoEeYQfkeRxn9X8ube8imkLdsGDCdqs130_provenance.
- NP150725.RAiHd7yWuQEsVHlUxrsJv_55Ewzgkr7dgO9AqxkHDPyEk130_assertion description "[Hereditary otosclerosis linkage to the OTSC4 locus was identified and confirmed in an Israeli family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150725.RAiHd7yWuQEsVHlUxrsJv_55Ewzgkr7dgO9AqxkHDPyEk130_provenance.
- NP150728.RAhv-cmscZTGvQDMR9tef7T4omx6654eCzhFpTmVKHHdU130_assertion description "[identification of susceptibility and protective haplotypes in COL1A1 that are significantly associated with otosclerosis in the Caucasian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150728.RAhv-cmscZTGvQDMR9tef7T4omx6654eCzhFpTmVKHHdU130_provenance.
- NP150734.RAuMhdaD6Lelz2tZeI0191spTWhjGDYiO7TvppA0Hl8iE130_assertion description "[Allele frequency of the G-- > T mutation of this gene is analyzed by an ARMS-PCR in osteoporotic subjects with femoral neck fractures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150734.RAuMhdaD6Lelz2tZeI0191spTWhjGDYiO7TvppA0Hl8iE130_provenance.
- NP150737.RAiEoJD00QQrkxcVemF813tRJ95kS4swVphmz-55ZDzr4130_assertion description "[Corneal amyloidosis with an autosomal dominant mode of inheritance is characterized clinically by the presence of refractile polymorphic corneal opacities, which is caused by an A546D mutation in the TGFBI gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150737.RAiEoJD00QQrkxcVemF813tRJ95kS4swVphmz-55ZDzr4130_provenance.
- NP150743.RArI3sgcK41FuuZffaJ5Tanhn2pM7QO-9HJwJ3xGzCl1s130_assertion description "[in patients with chronic myeloid leukemia, The expression of VEGF (vascular endothelial growth factor) was most pronounced in the Acute phase and it was inversely correlated with degree of splenomegaly and overall survival ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150743.RArI3sgcK41FuuZffaJ5Tanhn2pM7QO-9HJwJ3xGzCl1s130_provenance.
- NP150749.RAlfI7E3o1GvWIwoDaPf6VSoxq-pWCfEwL7oYu9N44dF4130_assertion description "[In proliferative diabetic retionopaathy, intravitreal SST-28 levels are significantly decreased in patients with diabetic macular edema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150749.RAlfI7E3o1GvWIwoDaPf6VSoxq-pWCfEwL7oYu9N44dF4130_provenance.
- NP150753.RApd25qTd5B0IhMmvY3Xio8QVdYMeV1PVczGbHyDIg0DU130_assertion description "[MMP9 sequence variation was significantly associated with variation in leukoaraiosis volume in both African-Americans and Whites.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150753.RApd25qTd5B0IhMmvY3Xio8QVdYMeV1PVczGbHyDIg0DU130_provenance.
- NP150755.RAr-B1IF8-T6gEBHHE4n3e0Ax4mLaHGitehzS4ZUqnq0w130_assertion description "[we have now investigated whether the different apolipoprotein E (APO E) genotypes, in pairwise combinations with the MTHFR 677TT or ACE D/D mutation, could lead to an increased risk of leukoaraiosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150755.RAr-B1IF8-T6gEBHHE4n3e0Ax4mLaHGitehzS4ZUqnq0w130_provenance.
- NP150759.RAkdPFKRL5Z_DJSMTTkbBpYjVf7WOXGSel2j03aan7fFU130_assertion description "[the presence of apoE2/3 genotype, high HDL-cholesterol levels and the absence of apoE3/3 genotype can be regarded as risk factors for superficial fungal disease, especially dermatophytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150759.RAkdPFKRL5Z_DJSMTTkbBpYjVf7WOXGSel2j03aan7fFU130_provenance.
- NP150762.RAreYXaC91UEkk2cIX6JdmtCCxkQ9ubh0Rqfrd7GL2taY130_assertion description "[ApoE4 carrier status was associated with increased risk for early postoperative delirium; results suggest genetic predisposition plays a role & may interact with anesthetic/surgical factors contributing to the development of early postoperative delirium ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150762.RAreYXaC91UEkk2cIX6JdmtCCxkQ9ubh0Rqfrd7GL2taY130_provenance.
- NP150771.RAumu02GohFF95GSvzGeakqbUV9pkLhUgatX29SVG6hs0130_assertion description "[suggest a possible interactive effect of cigarette smoke and the b fibrinogen gene G-455-A polymorphism in the risk of developing Legg-Perthes disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150771.RAumu02GohFF95GSvzGeakqbUV9pkLhUgatX29SVG6hs0130_provenance.
- NP150774.RAjg686Rtu0v3N5pn-GHJxs55a_Qz-GT5lWhMDJHJJV8k130_assertion description "[recombination events may have occurred within the rapsyn gene and that this may have implications in the phenotypic expression of postsynaptic congenital myasthenic syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150774.RAjg686Rtu0v3N5pn-GHJxs55a_Qz-GT5lWhMDJHJJV8k130_provenance.
- NP150779.RAmpBOjwwuK3kqfv6TWqKt3Y_Ocxy5Emd_O6KGiDOcHqY130_assertion description "[E-box mutations in the RAPSN promoter region may have a role in congenital myasthenic syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150779.RAmpBOjwwuK3kqfv6TWqKt3Y_Ocxy5Emd_O6KGiDOcHqY130_provenance.
- NP150783.RAtO9iXqBqbr1ExhPyGUu2vGTCEXMJcllhCrVDX11M3xQ130_assertion description "[study of patients with congenital myasthenic syndromes with mutations in DOK7; none with DOK7 mutations had tubular aggregates in muscle biopsy, implying'limb-girdle myasthenia with tubular aggregates'may be distinct from CMS caused by DOK7 mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150783.RAtO9iXqBqbr1ExhPyGUu2vGTCEXMJcllhCrVDX11M3xQ130_provenance.
- NP150794.RAldoER6kzeTu61hxrxGt4UbVzufidMMN_a2e1LdF0yUw130_assertion description "[Seven in-frame deletion, splicing, missense, nonsense, and frameshift mutations were identified segregating with X-linked congenital stationary night blindness in the NYX gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150794.RAldoER6kzeTu61hxrxGt4UbVzufidMMN_a2e1LdF0yUw130_provenance.
- NP150804.RAq2Z-UrCUc6fZjN3ktlBKTQOz4nfhnsqscFUbtxTfyWM130_assertion description "[Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150804.RAq2Z-UrCUc6fZjN3ktlBKTQOz4nfhnsqscFUbtxTfyWM130_provenance.
- NP150807.RAkAnyoZbACT-i4Q41qOdy9PvlwHcrJiR67GsH-SvEutU130_assertion description "[genetic susceptibility in Beckwith-Wiedemann syndrome; NSD1 could be involved in imprinting of the chromosome 11p15 region ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150807.RAkAnyoZbACT-i4Q41qOdy9PvlwHcrJiR67GsH-SvEutU130_provenance.
- NP150809.RAokWkogjJ2iOmORuVGFBVrOFBtpcerfdKuTnEUGhp58U130_assertion description "[We described a simplified and high-performance test (E-Q-PCR) for rapid assessment of the DNA methylation status at LIT1, a major genetic locus of Beckwith-Wiedemann syndrome (BWS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150809.RAokWkogjJ2iOmORuVGFBVrOFBtpcerfdKuTnEUGhp58U130_provenance.
- NP150812.RAnqzuLmOS1QjdC8QRBeUlT9WPNbv4F25CXfoX8X-1EvU130_assertion description "[In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150812.RAnqzuLmOS1QjdC8QRBeUlT9WPNbv4F25CXfoX8X-1EvU130_provenance.
- NP150813.RArWHlAIC55NF41z4174-nu-kgqLfw4FilCKdkNvkTsH8130_assertion description "[KCNQ1OT1 is part of an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150813.RArWHlAIC55NF41z4174-nu-kgqLfw4FilCKdkNvkTsH8130_provenance.
- NP150815.RApXf-lddZLeMJJFFSovo8XL9kEYFsjUENu0L1W2pgF9M130_assertion description "[LTF at concentration normally found in human colostrum blocks development of S.flexneri-induced inflammatory enteritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150815.RApXf-lddZLeMJJFFSovo8XL9kEYFsjUENu0L1W2pgF9M130_provenance.
- NP150816.RAhxaVMoIiPDPIPLYIYrUg8d7pTT0VTJHw8JQXUHCWRfA130_assertion description "[phenotypic variations of 46, XX girls with mutations in the gene for StAR; majority of StAR 46, XX females developed irregular menses and ovarian cysts [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150816.RAhxaVMoIiPDPIPLYIYrUg8d7pTT0VTJHw8JQXUHCWRfA130_provenance.
- NP150817.RAlvNq75eO7l6XLP1Rxh9rW3IFQBw1wvzczlrTxekG9wE130_assertion description "[our data indicate that an excess of local VEGF with respect to its soluble receptor VEGFR-1 may be a key factor in the onset and maintenance of pathological neo-angiogenesis in ovarian cyst formation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150817.RAlvNq75eO7l6XLP1Rxh9rW3IFQBw1wvzczlrTxekG9wE130_provenance.
- NP150818.RAt38pH3_I24GyHRpW2wnRTt4PGqskxhtMkLt-6ZIk1Qo130_assertion description "[Women with minimal endometriosis had lower PF lactoferrin concentrations compared to both patients with high revised American Fertility Society classification scores and women with follicle ovarian cysts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150818.RAt38pH3_I24GyHRpW2wnRTt4PGqskxhtMkLt-6ZIk1Qo130_provenance.
- NP150820.RAmuhVJQF4sBIzVLb7MtoSmjBwxDHs8nDB-cR1JO78D4s130_assertion description "[our data indicate that an excess of local VEGF with respect to its soluble receptor VEGFR-1 may be a key factor in the onset and maintenance of pathological neo-angiogenesis in ovarian cyst formation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150820.RAmuhVJQF4sBIzVLb7MtoSmjBwxDHs8nDB-cR1JO78D4s130_provenance.
- NP150821.RAtmv-PN9afujyCCz9K4ZD3w-sS-7B-MyjF-NX2aTZX-4130_assertion description "[IL-17 plays an important role in the induction and perpetuation of the immunopathologic processes in herpetic stromal keratitis by modulating the secretion of proinflammatory and neutrophil chemotactic factors by corneal resident fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150821.RAtmv-PN9afujyCCz9K4ZD3w-sS-7B-MyjF-NX2aTZX-4130_provenance.
- NP150822.RAoXtB3QlbAk1vzs7zZPQW559Xxh4wbXgRamEO5tkcAwI130_assertion description "[genotypes/Glu561Asp polymorphism is associated with the susceptibility to HSV keratitis with a protective role for lactoferrin variants comprising Asp561 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150822.RAoXtB3QlbAk1vzs7zZPQW559Xxh4wbXgRamEO5tkcAwI130_provenance.
- NP150824.RAojrZqnrj6JGh2WaQ1c47xrpFfJwq16TCO1T24imWEdA130_assertion description "[Induction of alternatively spliced spermidine/spermine N1-acetyltransferase mRNA in the human kidney cells infected by venezuelan equine encephalitis and tick-borne encephalitis viruses ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150824.RAojrZqnrj6JGh2WaQ1c47xrpFfJwq16TCO1T24imWEdA130_provenance.
- NP150834.RAmkYT4GY-yOpBaU_HeDSsXP6sNIiFy2thh7PILsvr16w130_assertion description "[Increased expression of DMT1 may play an important role in the pathogenesis of cirrhosis-associated hepatic iron overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150834.RAmkYT4GY-yOpBaU_HeDSsXP6sNIiFy2thh7PILsvr16w130_provenance.
- NP150840.RAiZYMueFd3qWX1FtrwZECo-PXLZUHeDrHjwUJvnfcupk130_assertion description "[the S338R mutation results in a mutated ferroportin associated with iron overload and is predicted insensitive to regulation by the iron regulatory hormone hepcidin ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150840.RAiZYMueFd3qWX1FtrwZECo-PXLZUHeDrHjwUJvnfcupk130_provenance.
- NP150845.RApuzqLKPn-lr2m65UB9Cb8CAknwQkvDi23k89jUGt11g130_assertion description "[GDF15 overexpression arising from an expanded erythroid compartment contributes to iron overload in thalassemia syndromes by inhibiting hepcidin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150845.RApuzqLKPn-lr2m65UB9Cb8CAknwQkvDi23k89jUGt11g130_provenance.
- NP150851.RAiSbfUSzyogcdtb7qCYulfpU6lVh4xTXBSbv5JTamZr4130_assertion description "[GDF15 overexpression arising from an expanded erythroid compartment contributes to iron overload in thalassemia syndromes by inhibiting hepcidin expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150851.RAiSbfUSzyogcdtb7qCYulfpU6lVh4xTXBSbv5JTamZr4130_provenance.
- NP150854.RAoeygtWl3W2SkipX0mQFZfGImzxRmHIKa4hLQe4cl3Tc130_assertion description "[Acute visual loss due to nonarteritic anterior ischemic optic neuropathy (NAION) has not previously been reported in CADASIL (heterozygotes for the C406T mutation on exon 3 of the Notch3 gene).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150854.RAoeygtWl3W2SkipX0mQFZfGImzxRmHIKa4hLQe4cl3Tc130_provenance.
- NP150857.RAq7LyLIjAlKAD-lJmonnwDh7FRMUhmAiSN-9JSs6A0nc130_assertion description "[We found an increased prevalence of T (-786) C polymorphism of the eNOS gene in patients with non-arteritic anterior ischemic optic neuropathy (NAION).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150857.RAq7LyLIjAlKAD-lJmonnwDh7FRMUhmAiSN-9JSs6A0nc130_provenance.
- NP150859.RAmhYBLIlJC4MaImiCowL8_U1CV-35Zapow5puT9MKsvw130_assertion description "[Possession of HLA-DRB1*01 increases the risk of Human T cell lymphotropic virus type I (HTLV-I) -associated myelopathy/tropical spastic paraparesis in HTLV-I-infected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150859.RAmhYBLIlJC4MaImiCowL8_U1CV-35Zapow5puT9MKsvw130_provenance.
- NP150867.RAkDk_vYpMT_qR4iUod0dh8V1G00v2bKM7W1BaZ5dtlDM130_assertion description "[Acquisition of the wobble modification in another isoacceptor tRNA is critical for suppressing the MELAS mutation, highlighting the primary role of the UUG decoding deficiency in the molecular pathogenesis of MELAS syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150867.RAkDk_vYpMT_qR4iUod0dh8V1G00v2bKM7W1BaZ5dtlDM130_provenance.
- NP150868.RAlYynaetoVphaDlgA-SqBacdwJJpbSMrSpkoFx737UKw130_assertion description "[Detrimental effects of the m.3243A > G mutation (which causes MELAS syndrome) can be compensated by upregulation of genes coding for oxidative phosphorylation complexes, mitochondrial biogenesis, protein turnover, apoptosis, and muscle regeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150868.RAlYynaetoVphaDlgA-SqBacdwJJpbSMrSpkoFx737UKw130_provenance.
- NP150869.RAj_1DOOkEY-DpMIUbt_GOipWGlC_gZhdajT7KPaYCqLc130_assertion description "[a MELAS syndrome Korean family harbor homoplasmic missense mutation in mitochondrial genom, which confers pathogenicity (Phe251Leu) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150869.RAj_1DOOkEY-DpMIUbt_GOipWGlC_gZhdajT7KPaYCqLc130_provenance.
- NP150874.RAo5qvYPq-RlreLqpuephrqTWRHPSF-QA_-YGB55gZiC4130_assertion description "[1G genotypes of MMP-1 promoter polymorphism are associated with asthma with persistent airway obstruction, and the heterozygous 1G genotype (1G/2G) poses the most susceptibility to persistent airway obstruction in asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150874.RAo5qvYPq-RlreLqpuephrqTWRHPSF-QA_-YGB55gZiC4130_provenance.
- NP150878.RAuE-nwnjpAzKKVxWI09j4mKAaxNW04IjDzAl_UT743Ak130_assertion description "[stimulated expression of MMP-1 and MMP-9 may contribute to the invasive activity and the bone and cartilage loss in pigmented villonodular synovitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150878.RAuE-nwnjpAzKKVxWI09j4mKAaxNW04IjDzAl_UT743Ak130_provenance.
- NP150890.RAo680UxQIRt7e_bf4Rb1fZvKXHGL3Ra4L8xG6eWiy0_k130_assertion description "[According to PrP gene polymorphism and PrP type, 18 cases were classified as MM1-type, two as MV1-type, two as MM2-type and one as MM1 + 2-type sporadic Creutzfeldt-Jakob disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150890.RAo680UxQIRt7e_bf4Rb1fZvKXHGL3Ra4L8xG6eWiy0_k130_provenance.
- NP150891.RAht3qcrL2OGn2dFhn5O68zgRTJsIu0XDjWSuOKbtaddg130_assertion description "[Finds polymorphism at codon 129 of PRNP gene implicated in the development of CJD in Greek population// Val allele frequencies and genotype distribution examined in 348 individuals/Met/Met 50%, Met/Val 39% and Val/Val 11% were observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150891.RAht3qcrL2OGn2dFhn5O68zgRTJsIu0XDjWSuOKbtaddg130_provenance.
- NP150892.RAlWb7199F63KTh4gH0m6VeTPzrmxnYsY9RCGFr_WFiWI130_assertion description "[protease-resistant prion protein (PrPres) in spontaneous lymphoreticular tumors of mice infected with the agent of variant Creutzfeldt-Jakob disease (vCJD) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150892.RAlWb7199F63KTh4gH0m6VeTPzrmxnYsY9RCGFr_WFiWI130_provenance.
- NP150902.RAh4BONs3XDUdDzVEYfGD15hJMnZy1NWn-vwAgyGF2W78130_assertion description "[Immunoreactive patterns of chromogranin A and B [CgA, CgB]were investigated in Creutzfeldt-Jakob disease and Alzheimer's disease/, but not CgA was selectively associated with prion protein deposits, whereas CgA was only seen in amyloid beta plaques ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150902.RAh4BONs3XDUdDzVEYfGD15hJMnZy1NWn-vwAgyGF2W78130_provenance.
- NP150904.RAq22s80YdKZQT450kE5Qe68ZZZ_bKcX-tTF0wAZTyHNo130_assertion description "[Association of a null allele of SPRN with variant Creutzfeldt-Jakob disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150904.RAq22s80YdKZQT450kE5Qe68ZZZ_bKcX-tTF0wAZTyHNo130_provenance.
- NP150906.RAmuKnjkb2T6nd6EoiXKb1vOjzOiyb9oJ0nwCEyqwFNMU130_assertion description "[Significant increased expression levels of AQP1 and AQP4 were seen in Creutzfeldt-Jakob disease, but not in advanced Alzheimer's disease and diffuse Lewy body disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150906.RAmuKnjkb2T6nd6EoiXKb1vOjzOiyb9oJ0nwCEyqwFNMU130_provenance.
- NP150908.RAubDHTF1MK0pCprEsmIz-I7z9X9caRa3oeiMPhqemFNQ130_assertion description "[more AIF-1 immunoreactive macrophages/microglial cells and, interestingly, neurones were observed in Creutzfeldt-Jakob disease patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150908.RAubDHTF1MK0pCprEsmIz-I7z9X9caRa3oeiMPhqemFNQ130_provenance.
- NP150909.RAi5D7zjZhCAgaAAES0OiQ9eUbzFevll5LJGf8J9HRosE130_assertion description "[mutations in GNAT2 are implicated in achromatopsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150909.RAi5D7zjZhCAgaAAES0OiQ9eUbzFevll5LJGf8J9HRosE130_provenance.
- NP150910.RAnChQUweBhFyE9rnsAjSRAQz9RzCwBHWgN8SkghYpVlU130_assertion description "[Novel causative CNGB3 missense mutations found in Achromatopsia patients in the United Kingdom.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150910.RAnChQUweBhFyE9rnsAjSRAQz9RzCwBHWgN8SkghYpVlU130_provenance.
- NP150916.RApbC5aLD39PFNvSFCsNnkhMfwiPq_yAHoqV0unL1Rf-M130_assertion description "[Recombinant activated protein C attenuates endothelial injury and inhibits procoagulant microparticles release in baboon heatstroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150916.RApbC5aLD39PFNvSFCsNnkhMfwiPq_yAHoqV0unL1Rf-M130_provenance.
- NP150922.RAkunFI1yYiA2i7H4hh5qkB3Q-Eti7fJUmaHl9EDxtwho130_assertion description "[significant elevation of anti-protein C antibodies and anti-protein S antibodies in the thrombosis group of uremia patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150922.RAkunFI1yYiA2i7H4hh5qkB3Q-Eti7fJUmaHl9EDxtwho130_provenance.
- NP150923.RAq15-3as7GFKJqIF9KqbpqnSXfRATjUW5vMFeyg5o5LE130_assertion description "[The release of IL-6 from peripheral tissues may act as a signal for the inflammatory response and contribute to functional dysregulation in uremia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150923.RAq15-3as7GFKJqIF9KqbpqnSXfRATjUW5vMFeyg5o5LE130_provenance.
- NP150930.RAj-8KyPI5Dh6cd4Xo68aenf1KubZaBFGv4Ql9kGVCFMA130_assertion description "[PRNP genotyping may be a valuable tool to differentiate between prion disease and other neurodegenerative dementias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150930.RAj-8KyPI5Dh6cd4Xo68aenf1KubZaBFGv4Ql9kGVCFMA130_provenance.
- NP150933.RAi_tXaKFFHluJYzbOgGpl-TahBq3rX7Kjkr9rOG_wI_o130_assertion description "[Mutant PrP is associated with neurodegeneration in prion diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150933.RAi_tXaKFFHluJYzbOgGpl-TahBq3rX7Kjkr9rOG_wI_o130_provenance.
- NP150934.RAkr7znDwdxYeNMXxUF2IPL1jzXhyz75TV8pDKQzpnJjM130_assertion description "[A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150934.RAkr7znDwdxYeNMXxUF2IPL1jzXhyz75TV8pDKQzpnJjM130_provenance.
- NP150935.RAhuS81dAf6EbsRyMnY85cFL2XemXzgVAVj6WHsMfoZ8s130_assertion description "[C.ommon prion protein gene (PRNP) codon 129 polymorphism is a strong susceptibility factor for human prion diseases/of methionine and valine may be a susceptibility factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150935.RAhuS81dAf6EbsRyMnY85cFL2XemXzgVAVj6WHsMfoZ8s130_provenance.
- NP150938.RArHKyD1mpOcbaBYcbiPRWYgOX6vNhh7v2K6CzuLLc-I0130_assertion description "[mechanisms leading to microglial COX-2 expression as well as its potential implication in prion disease pathogenesis remain to be established--REVIEW ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150938.RArHKyD1mpOcbaBYcbiPRWYgOX6vNhh7v2K6CzuLLc-I0130_provenance.
- NP150940.RAlFJsfCvSFh3Iax_iCL7Dw9G61Jv-iWQKdO5TmiBbIro130_assertion description "[Two mutants of PrP, PG14 and A116V, that are associated with familial human prion diseases failed to inhibit the beta-secretase cleavage of APP ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150940.RAlFJsfCvSFh3Iax_iCL7Dw9G61Jv-iWQKdO5TmiBbIro130_provenance.
- NP150949.RAlUUpkWWUcGG3jkMmPOORWK9grBY-5ufFFi6ZmuIv3-8130_assertion description "[ATP7B is a copper-transporting P-type ATPase defective in the copper transport disorder, Wilson disease (WND).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150949.RAlUUpkWWUcGG3jkMmPOORWK9grBY-5ufFFi6ZmuIv3-8130_provenance.
- NP150950.RAjYrnZq_lNStvnSIRC4DarvHXd8afjlcV-gOVw-7WU4A130_assertion description "[A quantitative relationship between mutated ATPase and Menkes/Wilson disease, is shown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150950.RAjYrnZq_lNStvnSIRC4DarvHXd8afjlcV-gOVw-7WU4A130_provenance.
- NP150955.RArVimPDI30LiIzr86eYvmQ6hKa-URT6yt0qF3Lg-T7Cs130_assertion description "[Study describes the database developed for reporting of mutations in ATP7B, the gene defective in Wilson disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP150955.RArVimPDI30LiIzr86eYvmQ6hKa-URT6yt0qF3Lg-T7Cs130_provenance.
- NP163894.RAkMKVYEfCuuYKyw32T54BmvI8xXVdHLhmQFHjsZCqBH4130_assertion description "[Requirement of AP-1 for ceramide-induced apoptosis in human leukemia HL-60 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163894.RAkMKVYEfCuuYKyw32T54BmvI8xXVdHLhmQFHjsZCqBH4130_provenance.
- NP163895.RAo-YPUn89sPjHa-Hk1aYCFBm-Hxm6tO0Ed6coh-sJ6sg130_assertion description "[GSTP-1 mRNA was detected in all the specimens, with slightly increased, but non-significant expression in the neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163895.RAo-YPUn89sPjHa-Hk1aYCFBm-Hxm6tO0Ed6coh-sJ6sg130_provenance.
- NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_assertion description "[The relationship between chromosome 1p and 19q deletions and treatment responsive oligodendrogliomas is discussed, as are the newer advances relating to silencing of the MGMT gene in astrocytomas and mutations in the IDH-1 gene in both astrocytomas and oligodendrogliomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163896.RAp4E3AVEkypOMOAeUHgS5Z2r4nOao9aowQes19cZjXaU130_provenance.
- NP163900.RAkFlpT0fk9eBxRncZnr-2aFHLh7ExE1DAf2uUq18XgnQ130_assertion description "[Endometriomas show lower expression of HER1-3 and no HER4 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163900.RAkFlpT0fk9eBxRncZnr-2aFHLh7ExE1DAf2uUq18XgnQ130_provenance.
- NP163901.RAnvi2VQvqlQUNDeqADeUH3GUv3yiDdsEQ8jIH5lP3vHY130_assertion description "[Growth factor independence 1 antagonizes a p53-induced DNA damage response pathway in lymphoblastic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163901.RAnvi2VQvqlQUNDeqADeUH3GUv3yiDdsEQ8jIH5lP3vHY130_provenance.
- NP163914.RAhvBW9dUVLORQ4i3J_rFudys773PPHRp1nhOa2eqGYKI130_assertion description "[Proinflammatory cytokines (IL-1β and IFN-γ) that mediate β-cell dysfunction in T1D down-regulated HIP14 expression in insulin-secreting INS-1 cells and in isolated rat and human islets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163914.RAhvBW9dUVLORQ4i3J_rFudys773PPHRp1nhOa2eqGYKI130_provenance.
- NP163919.RAiYqYKjHtbl7gXj8BpjFjnrWxnyIycX6M3W_RNqS1Vzw130_assertion description "[Activated leukocyte cell adhesion molecule and OPN mRNA expression has a strong discriminative impact on survival within cancer patients with low or negative expression of ER and HER2, so called 'high-risk' breast cancers, and might help in identifying patients who could benefit from new treatment approaches like targeted therapies in the adjuvant setting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163919.RAiYqYKjHtbl7gXj8BpjFjnrWxnyIycX6M3W_RNqS1Vzw130_provenance.
- NP163920.RAoIXyN1pCmOYgVtnFI2Wdc9j1g2AkGq-1LkC-seBVGw0130_assertion description "[Multiple polymorphisms within the PLCE1 are associated with esophageal cancer via promoting the gene expression in a Chinese Kazakh population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163920.RAoIXyN1pCmOYgVtnFI2Wdc9j1g2AkGq-1LkC-seBVGw0130_provenance.
- NP163933.RApoGzsUV2O7aDKsF34G7893syZeCN5hu9Op7dp_vrT4A130_assertion description "[The use of DNAzyme methodology adds a new potential clinical agent for decreasing uPAR mRNA expression and inhibiting cancer invasion and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163933.RApoGzsUV2O7aDKsF34G7893syZeCN5hu9Op7dp_vrT4A130_provenance.
- NP163935.RAo8SWUWyVPcJHAuj1aJbOdSdz4mT_W0OboBVCu_FEESQ130_assertion description "[A case of ambiguous genitalia presenting with a 45,X/46,Xr(Y)(p11.2;q11.23)/47,X,idic(Y)(p11.2),idic(Y)(p11.2) karyotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163935.RAo8SWUWyVPcJHAuj1aJbOdSdz4mT_W0OboBVCu_FEESQ130_provenance.
- NP163936.RArL9gYKECU537BK_-Hb_h3gl7nT1P9aBxdnkGuu2MhMs130_assertion description "[In the same individuals, we also evaluated the frequency of the coexistence of C677T MTHFR with mutant factor V:Q506, a common risk factor for deep-vein thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163936.RArL9gYKECU537BK_-Hb_h3gl7nT1P9aBxdnkGuu2MhMs130_provenance.
- NP163938.RAvVWwmOKfn3WpsBc2Vvbf8j9onR4nGODufyo0e-26Uh8130_assertion description "[These results suggest that PEDF may be of therapeutic use, especially in retinopathies where pathological neovascularization compromises vision and leads to blindness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163938.RAvVWwmOKfn3WpsBc2Vvbf8j9onR4nGODufyo0e-26Uh8130_provenance.
- NP163940.RAjkVu4fEUxvoUW3OTB7W1OSiQVec3vzHvdZWxP3TLcfE130_assertion description "[Estrogen receptor (ER)-beta is thought to exert anti-proliferative effects in the normal prostate but supports prostate cancer (PCa) cell survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163940.RAjkVu4fEUxvoUW3OTB7W1OSiQVec3vzHvdZWxP3TLcfE130_provenance.
- NP163945.RAha0AhJngCvSuCxv6mkwSqtXNQ4DfJZEUCl318XUnQ-k130_assertion description "[According to the FAB classification, 42 patients presented with RA, 18 with RARS, 37 with RAEB, 22 with CMML, and 29 with RAEB-T. Nine patients showed a secondary MDS (S MDS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163945.RAha0AhJngCvSuCxv6mkwSqtXNQ4DfJZEUCl318XUnQ-k130_provenance.
- NP163948.RAhIAg4rHcyIB5TGanNngKSPvv_W_YYmK0ia6O2Kt3Q3U130_assertion description "[Overexpression of PACAP in transgenic mouse pancreatic beta-cells enhances insulin secretion and ameliorates streptozotocin-induced diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163948.RAhIAg4rHcyIB5TGanNngKSPvv_W_YYmK0ia6O2Kt3Q3U130_provenance.
- NP163950.RAqwF8Q0TaKf9ntHwXaIPDNwVx5gpRDefKWdJWUHUCl24130_assertion description "[We examined HIV-1 subtype C populations in blood and CSF of 43 Malawian children with neurodevelopmental delay or acute neurological symptoms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163950.RAqwF8Q0TaKf9ntHwXaIPDNwVx5gpRDefKWdJWUHUCl24130_provenance.
- NP163957.RAtbEMdiTAXFmp4NeE1VtVNRS20Y65jYwfmE77fBt8pO8130_assertion description "[The APP/NOS2(-/-) bigenic mice progress from Abeta production and amyloid deposition to hyperphosphorylated normal mouse tau at AD-associated epitopes, aggregation and redistribution of tau to somatodendritic regions of neurons and significant neuronal loss including loss of interneurons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163957.RAtbEMdiTAXFmp4NeE1VtVNRS20Y65jYwfmE77fBt8pO8130_provenance.
- NP163967.RAuOCz-d9a2oWJsfQsc0DVWNN8AEtMxhTJ0Wfc3ZMkRqA130_assertion description "[These results show that the occurrence of DNA aneuploidies and nuclear p53 protein expression is a common event in the development of colitis-associated colorectal neoplasias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163967.RAuOCz-d9a2oWJsfQsc0DVWNN8AEtMxhTJ0Wfc3ZMkRqA130_provenance.
- NP163969.RAmD8C3or9O0-9GFbZN2u6cMAllFmc3SCkfbFqtopmo1w130_assertion description "[Hence, factors that influence IDE expression or IDE activity toward Abeta are potentially relevant to the etiology of AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163969.RAmD8C3or9O0-9GFbZN2u6cMAllFmc3SCkfbFqtopmo1w130_provenance.
- NP163974.RAkGY8nS4RU88XjiL2TDgU5tXhdcXLSSBCv_gKyA5t-C8130_assertion description "[Their prognostic significance on prostate-specific antigen (PSA) recurrence was assessed using Kaplan-Meier analysis and Cox regression model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163974.RAkGY8nS4RU88XjiL2TDgU5tXhdcXLSSBCv_gKyA5t-C8130_provenance.
- NP163976.RAluzf81w9UtzPfyUz6uxooCgbN1X60q-61iW-msaEEmw130_assertion description "[MicroRNA-497 targets insulin-like growth factor 1 receptor and has a tumour suppressive role in human colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163976.RAluzf81w9UtzPfyUz6uxooCgbN1X60q-61iW-msaEEmw130_provenance.
- NP163978.RAt8X1Qv7qKkga7odQhtXkwMN9ho2s8l_54w93K3cBcCU130_assertion description "[We performed a genetic association study using four functional polymorphisms of the dopamine receptor 4 (DRD4), dopamine transporter (DAT), mono-amino-oxidase A (MAOA) and cathecol-O-methyl-transferase (COMT) genes in 103 patients with chronic daily headache associated with DA (CDHDA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163978.RAt8X1Qv7qKkga7odQhtXkwMN9ho2s8l_54w93K3cBcCU130_provenance.
- NP163983.RAosZEdoJmxnxdmJifyrapqIYQfKMVGleNfddRZ0rA9c8130_assertion description "[TP53 codon 72 polymorphism is associated with coronary artery disease in Chilean subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163983.RAosZEdoJmxnxdmJifyrapqIYQfKMVGleNfddRZ0rA9c8130_provenance.
- NP163984.RAtRyqBp4gjtKZDMDds2pl-zLhW8vc2h81LxXVUzy4pLE130_assertion description "[Our data opens new possibilities for hornerin and its proteolytic fragments in the control of mammary cell function and breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163984.RAtRyqBp4gjtKZDMDds2pl-zLhW8vc2h81LxXVUzy4pLE130_provenance.
- NP163992.RAi-aeAXKo740Dax-15vMCZG-Aui15akX3lttPVCxoNgI130_assertion description "[Although GCKR CT (46%) and TT (14%) versus CC (40%) genotypes had effects on triglycerides (+0.17 mmol/L; trend, P<0.001), remnant cholesterol (+0.07 mmol/L; P<0.001), and apolipoprotein B (+4.6 mg/dL; P<0.001) similar to those of TRIB1, GCKR did not influence low-density lipoprotein cholesterol levels or risk of IHD or MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163992.RAi-aeAXKo740Dax-15vMCZG-Aui15akX3lttPVCxoNgI130_provenance.
- NP163998.RAi8X2t7hij2HC9UTiOmptZIz28amYj1MXAucNKw6h7vc130_assertion description "[S and the basic core promoter-precore regions (BCP/PC) sequencing was used to identify genotypes and variants relevant to HBV natural history, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP163998.RAi8X2t7hij2HC9UTiOmptZIz28amYj1MXAucNKw6h7vc130_provenance.
- NP164004.RAuQpR66QGEUfw_xeZ6K3wz9TUMmNnQstqHneIEVMghLY130_assertion description "[The significant association of p53 expression in NPC suggested that p53 overexpression seemed to occur at an early stage in the development of NPC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164004.RAuQpR66QGEUfw_xeZ6K3wz9TUMmNnQstqHneIEVMghLY130_provenance.
- NP164009.RAqvtwZIpSdkYprJ7dtP1aDMglxGayJiFOu4lcQqKavno130_assertion description "[Interestingly, the majority (87%) of normal smears had HPV-16 prototype, whereas variants were detected mainly in SIL and ICC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164009.RAqvtwZIpSdkYprJ7dtP1aDMglxGayJiFOu4lcQqKavno130_provenance.
- NP164017.RAi1nE6VFnpAulwf6aSZ4zda4mCyPR5eY27AyHiv-MezE130_assertion description "[Two models of insulin resistance were also evaluated: (a) transgenic mice with a severe insulin receptor defect and (b) gold thioglucose (GTG) mice (obesity with minimal insulin receptor dysfunction).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164017.RAi1nE6VFnpAulwf6aSZ4zda4mCyPR5eY27AyHiv-MezE130_provenance.
- NP164021.RAh5WqzZQMXh6k0WyjghrfV-CSZ2UNeHbrv-olKHw98sc130_assertion description "[Monoclonal antibodies (MAbs) against various adhesion molecules (LFA-1, LFA-3, ICAM-1, VNR, VLA beta I chain) were unable to block TNF production in co-culture of monocytes with a human pancreatic carcinoma (HPC) cell line.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164021.RAh5WqzZQMXh6k0WyjghrfV-CSZ2UNeHbrv-olKHw98sc130_provenance.
- NP164040.RAjslgIj9AiQVOsZ8s6zWtccIXRbpOZyPOtay7qwHdLng130_assertion description "[Ataxia with vitamin E deficiency is a recessive autosomal neurodegenerative disorder resembling the Friedreich ataxia phenotype but is due to mutations in the alpha-tocopherol transfer protein (TTPA) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164040.RAjslgIj9AiQVOsZ8s6zWtccIXRbpOZyPOtay7qwHdLng130_provenance.
- NP164046.RAs9P2W1UHeRicZHKGIDIiiV9WImCMTNHTbpLL2SWeq5g130_assertion description "[Moreover, 25-OCH3-PPD inhibited the growth of prostate cancer xenograft tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164046.RAs9P2W1UHeRicZHKGIDIiiV9WImCMTNHTbpLL2SWeq5g130_provenance.
- NP164048.RArh8j2ytSqTmGZkbF_n7JVSMtLrgX8hd9-E7_AS636W4130_assertion description "[Interleukin-4, interleukin-4 receptor, and interleukin-18 polymorphisms and rheumatoid arthritis: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164048.RArh8j2ytSqTmGZkbF_n7JVSMtLrgX8hd9-E7_AS636W4130_provenance.