Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP557164.RAVSESdCJRk-h2jMNl070O5MX_zzfOJREkszSNGBd0pPY130_assertion description "[M. tuberculosis cell wall component LAM acts similarly to LPS in activating mononuclear phagocyte cytokine TNF alpha and IL-1 beta release through CD14 and synthesis at the transcriptional level; both cytokines are key participants in the host immune response to tuberculosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557164.RAVSESdCJRk-h2jMNl070O5MX_zzfOJREkszSNGBd0pPY130_provenance.
- NP557174.RARmd5eqfNoW54QHsozUnh2KNEpOwPxyD9xrgEDt-gdpk130_assertion description "[A constant ratio between blood perfusion and oxygen consumption, a stable corticomedullary oxygen gradient, and a relatively low tissue Po(2) are the prerequisites for the function of renal Epo-producing and oxygen-sensing (REPOS) cells, which are located in the juxtamedullary cortex.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557174.RARmd5eqfNoW54QHsozUnh2KNEpOwPxyD9xrgEDt-gdpk130_provenance.
- NP557179.RAf0aL9laL5Ma-s2aqOTUckkw7zs2fkdCvWVEw6ozF2qo130_assertion description "[Targeted deletion of the metastasis-associated phosphatase Ptp4a3 (PRL-3) suppresses murine colon cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557179.RAf0aL9laL5Ma-s2aqOTUckkw7zs2fkdCvWVEw6ozF2qo130_provenance.
- NP557180.RAUjBB0ER5I3JbRgYyVraV1Wse4m9waDKOwWZw-RLmMbQ130_assertion description "[Overexpression of BMI1 confers clonal cells resistance to apoptosis and contributes to adverse prognosis in myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557180.RAUjBB0ER5I3JbRgYyVraV1Wse4m9waDKOwWZw-RLmMbQ130_provenance.
- NP557185.RASHNXseRcycw4DbWk7akWbdwFGtXLLNLb_SvP7WGiLYg130_assertion description "[Granulin-epithelin precursor (GEP) has previously been reported to control cancer growth, invasion, chemo-resistance, and served as novel therapeutic target for cancer treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557185.RASHNXseRcycw4DbWk7akWbdwFGtXLLNLb_SvP7WGiLYg130_provenance.
- NP557191.RAY_vquByAbWoap9dkCKj6YFm09a7CMvNzLZoN12y8HvI130_assertion description "[The functional impact on calcium release of RYR1 mutations linked to central core disease or malignant hyperthermia is different: human myotubes carrying the malignant hyperthermia-linked RYR1 mutation V2168M had a shift in their sensitivity to the RYR agonist 4-chloro-m-cresol to lower concentrations, whereas human myotubes harboring C-terminal mutations linked to central core disease exhibited reduced [Ca2+]i increase in response to 4-chloro-m-cresol, caffeine, and KCl.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557191.RAY_vquByAbWoap9dkCKj6YFm09a7CMvNzLZoN12y8HvI130_provenance.
- NP557203.RAQ11yG_hVaVYqamUTUANtlPmUHQ5VD14kKCarARgWDIY130_assertion description "[The EWS/FLI1 fusion gene found in Ewing's sarcoma and primitive neuroectodermal tumor, is able to transform certain cell lines by acting as an aberrant transcription factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557203.RAQ11yG_hVaVYqamUTUANtlPmUHQ5VD14kKCarARgWDIY130_provenance.
- NP557212.RAcxIDWD0HzjWVx_6WMr0Mrk6fYoqHTGGKkxrOiROaeO8130_assertion description "[Our data imply that RANTES is associated with T1D both genetically and functionally, and contributes to diabetes-prone Th1 cytokine profile.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557212.RAcxIDWD0HzjWVx_6WMr0Mrk6fYoqHTGGKkxrOiROaeO8130_provenance.
- NP557213.RAf1mhCaSg2Mzv96UnkNF225hYbY1nAjicn8ivMPRJZoQ130_assertion description "[These results indicate that CCR6 expression contributes to Th17 cell function in autoimmune disease, especially in autoimmune arthritis such as RA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557213.RAf1mhCaSg2Mzv96UnkNF225hYbY1nAjicn8ivMPRJZoQ130_provenance.
- NP557214.RAeMR8XWMMgufLIYN1lrBClMU-eOjxQehT6OlxX-8BD7Y130_assertion description "[These findings illustrate the interplay between epithelial ovarian CSCs and the EMT, and exert a link to explain tumor heterogeneity and its necessity for ovarian cancer maintenance, metastasis and progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557214.RAeMR8XWMMgufLIYN1lrBClMU-eOjxQehT6OlxX-8BD7Y130_provenance.
- NP557220.RAekdwHoh849q-k6_kMz-MTL7sOesgvUbYw49VCpEk600130_assertion description "[Expression of membrane type-1 matrix metalloproteinase, MT1-MMP in human breast cancer and its impact on invasiveness of breast cancer cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557220.RAekdwHoh849q-k6_kMz-MTL7sOesgvUbYw49VCpEk600130_provenance.
- NP557223.RAfv1rb6-10kBq83cbOFQZcQkMTwo3nYac-HnuyrXiepQ130_assertion description "[Our systematic model revealed that the dynamic response patterns of p38 MAPK and JNK to TNF-α stimulation in MDS were different from that observed in normal marrow cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557223.RAfv1rb6-10kBq83cbOFQZcQkMTwo3nYac-HnuyrXiepQ130_provenance.
- NP557225.RAS7nNWWxmcHSeBjQZfm5chi9KI2sgBUOhD61_FQ8cRfI130_assertion description "[These data suggest a tumour suppressor gene centromeric to 9p21 that may contribute to papillary RCC progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557225.RAS7nNWWxmcHSeBjQZfm5chi9KI2sgBUOhD61_FQ8cRfI130_provenance.
- NP557231.RAaXSzXMjhWyHePT0kbXW-dNEG39qW1mgjWdqs9v-oFwQ130_assertion description "[In addition, treatment of adult worms with TNF-alpha caused a significantly altered expression of 1857 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557231.RAaXSzXMjhWyHePT0kbXW-dNEG39qW1mgjWdqs9v-oFwQ130_provenance.
- NP557233.RAZ4G7XaUYjA8UlrgZj_LOaLgw671xt9hC_VCFev8bDyY130_assertion description "[In addition to discovering novel, recurrently mutated genes (for example, WAC, SMC3, DIS3, DDX41 and DAXX) in AML, we also found two major clonal evolution patterns during AML relapse: (1) the founding clone in the primary tumour gained mutations and evolved into the relapse clone, or (2) a subclone of the founding clone survived initial therapy, gained additional mutations and expanded at relapse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557233.RAZ4G7XaUYjA8UlrgZj_LOaLgw671xt9hC_VCFev8bDyY130_provenance.
- NP557237.RAa3aedD538Ny_YQNb35PKrT0O4ZyVj1Q4FBSkYvNWubc130_assertion description "[Retinol Dehydrogenase 12 (RDH12) was the most frequently mutated gene in the juvenile RP group, and Usher Syndrome 2A (USH2A) and Ceramide Kinase-Like (CERKL) were the most frequently mutated genes in the typical RP group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557237.RAa3aedD538Ny_YQNb35PKrT0O4ZyVj1Q4FBSkYvNWubc130_provenance.
- NP557241.RATrvKA6kI-mADnKReftvSL7y-FeYhZ4dP2fVSauUtfjs130_assertion description "[Polymorphism analysis of the upstream region of the human N-methyl-D-aspartate receptor subunit NR1 gene (GRIN1): implications for schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557241.RATrvKA6kI-mADnKReftvSL7y-FeYhZ4dP2fVSauUtfjs130_provenance.
- NP557247.RAScA_-HwVKq5AKnzBI9fksmxVvIZKqjoOl19xNp8bidM130_assertion description "[Analysis of these nine genes has suggested that early-detected tumors have higher levels of retinoic acid production and higher expression levels of caveolin 2, matrix Gla, and cystatin A, which are already known to be lost during tumor progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557247.RAScA_-HwVKq5AKnzBI9fksmxVvIZKqjoOl19xNp8bidM130_provenance.
- NP557249.RAfPm5nJMyhL7n5m88Rwz-6GjA0iZuUzrC-Uff__sMors130_assertion description "[The Ikaros gene, a central regulator of lymphoid differentiation, fuses to the BCL6 gene as a result of t(3;7)(q27;p12) translocation in a patient with diffuse large B-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557249.RAfPm5nJMyhL7n5m88Rwz-6GjA0iZuUzrC-Uff__sMors130_provenance.
- NP557252.RAaTXLxzwJP7fLNPlKMQHPizLDR_Dt9CAavk_xoTWi6xQ130_assertion description "[For the group of ataxics, the activity of the pyruvate dehydrogenase complex (PDHC) was 68% of the control (P less than 0.01) and that of glutamate dehydrogenase (GDH) was 81% of the control (P less than 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557252.RAaTXLxzwJP7fLNPlKMQHPizLDR_Dt9CAavk_xoTWi6xQ130_provenance.
- NP557258.RAY-zqsiZ01ma6ElWWQvb1oMMbJcvDm_I1ptw3fZRJ52A130_assertion description "[Immunoglobulin G1 (IgG1) and immunoglobulin G3 (IgG3) antibodies to antigens diagnostic of recent infection Pf histidine-rich protein-II (HRP-II) and 6NANP, Pf-vaccine candidates SE36 and 42-kDa region of the 3D7 Pf merozoite surface protein-1 (MSP-1), and tetanus toxoid were measured by indirect enzyme-linked immunoassay.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557258.RAY-zqsiZ01ma6ElWWQvb1oMMbJcvDm_I1ptw3fZRJ52A130_provenance.
- NP557259.RASNPjqGn3-zlIbp8P_gykLXgc-r4tbfImIUQYO_L6mA8130_assertion description "[Specifically, we have shown that diabetic individuals with Hp2-2 are more likely to develop nephropathy, retinopathy, and cardiovascular disease as compared with those with Hp2-1 or Hp1-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557259.RASNPjqGn3-zlIbp8P_gykLXgc-r4tbfImIUQYO_L6mA8130_provenance.
- NP557260.RAQJwI1DpiJ9GqwWGe5XegQiwz4GHQIWEm-v2VNN8NyxA130_assertion description "[Human surfactant protein B: structure, function, regulation, and genetic disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557260.RAQJwI1DpiJ9GqwWGe5XegQiwz4GHQIWEm-v2VNN8NyxA130_provenance.
- NP557262.RAaXQksruwGEz8klH1iy4ciHKDu4Mq6IIDpeW8QcjDu7Q130_assertion description "[Loss of AP-2 results in downregulation of c-KIT and enhancement of melanoma tumorigenicity and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557262.RAaXQksruwGEz8klH1iy4ciHKDu4Mq6IIDpeW8QcjDu7Q130_provenance.
- NP557268.RAdsnyujIXaMNioaFOZRujJkbfk43BBDpR3pT7_U2Zry4130_assertion description "[Recent studies indicated that SPAK and OSR1 are phosphorylated and activated by the WNK1 [with no K (lysine) protein kinase-1] and WNK4, genes mutated in humans affected by Gordon's hypertension syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557268.RAdsnyujIXaMNioaFOZRujJkbfk43BBDpR3pT7_U2Zry4130_provenance.
- NP557270.RAbnqY5cY4KW2J_0JWp56QeUMpGJdLMExOoyToIoCdzxw130_assertion description "[To address the role of Cx43 in melanoma tumor progression, we utilized two melanoma cell lines derived from the same patient in pre-metastasis (WM793B) and following isolation from a lung metastasis in nude mice (1205Lu).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557270.RAbnqY5cY4KW2J_0JWp56QeUMpGJdLMExOoyToIoCdzxw130_provenance.
- NP557276.RAfMQ4wYd6Ac8Ox4v6IG8I6ASje-b2xZ_S6d8dsAYgjN0130_assertion description "[The specific impact of SEL1L in esophageal cancer needs further investigation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557276.RAfMQ4wYd6Ac8Ox4v6IG8I6ASje-b2xZ_S6d8dsAYgjN0130_provenance.
- NP557281.RAc5HRRuY006IuPm2vecdetJycOTcYXWwjY8WeNmcymUs130_assertion description "[Gilbert syndrome is a common inherited disease of unconjugated hyperbilirubinemia due to decreased bilirubin uridine diphosphate-glucuronosyltransferase (B-UGT), and its role in neonatal jaundice has recently been considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557281.RAc5HRRuY006IuPm2vecdetJycOTcYXWwjY8WeNmcymUs130_provenance.
- NP557290.RAd_yg843JA2LTatHLXj7blhvBE9pC9i6Hn1YToIQm7q0130_assertion description "[Compared with controls (18.0%), HPV positivity was significantly more common in BD (68.6%, incidence rate ratio (IRR) 2.94, 95% confidence interval (CI) 1.78-4.85, P<0.001) and EAC (66.7%, IRR 2.87, 95% CI 1.69-4.86, P<0.001), but not in BE (22.1%, IRR 1.06, 95% CI 0.60-1.85, P=0.85).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557290.RAd_yg843JA2LTatHLXj7blhvBE9pC9i6Hn1YToIQm7q0130_provenance.
- NP557291.RAcpqq0kBkf_TryqX7Hhcuc7hxR7PibcRYFGR7vo5ATk0130_assertion description "[A PC-1 amino acid variant (K121Q) is associated with faster progression of renal disease in patients with type 1 diabetes and albuminuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557291.RAcpqq0kBkf_TryqX7Hhcuc7hxR7PibcRYFGR7vo5ATk0130_provenance.
- NP557298.RAXRM3HPmD2E1KsoulP9j4RROwWxxBnvofqf4JG_2tANg130_assertion description "[We studied the MLH1 and MSH2 promoter methylation status in 29 presumably sporadic uterine endometrioid carcinomas (UECs), which had previously been characterized for the MSI phenotype and a subset for DNA MMR gene mutational status.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557298.RAXRM3HPmD2E1KsoulP9j4RROwWxxBnvofqf4JG_2tANg130_provenance.
- NP557302.RAZUFxGpRFKMBicNe0cwz6kwyF9j1me2AjsetPLvBlDq4130_assertion description "[Fragile X syndrome (FXS), the leading monogenic cause of intellectual disability and autism, results from loss of function of the RNA-binding protein FMRP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557302.RAZUFxGpRFKMBicNe0cwz6kwyF9j1me2AjsetPLvBlDq4130_provenance.
- NP557309.RAS3f8GJwu7Jyay0flW-COoYwFRHXtPNBitvCkDXlwThM130_assertion description "[In this Review, we summarize the current evidence regarding the normal function of TDP-43 and the TDP-43 pathology observed in FTLD-TDP, ALS, and other neurodegenerative diseases wherein TDP-43 pathology co-occurs with other disease-specific lesions (for example, with amyloid plaques and neurofibrillary tangles in Alzheimer disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557309.RAS3f8GJwu7Jyay0flW-COoYwFRHXtPNBitvCkDXlwThM130_provenance.
- NP557310.RAaNXl1-gCZHl5dXRfNe4epsq1SXtCztO1vP1916mhuLM130_assertion description "[In adjacent histologically normal lung from lung cancer patients (n = 120), low levels of DNA methylation of the CYP1A1 enhancer were related to high levels of smoking-induced hydrophobic DNA adduct (p < 0.03), and to the presence of TP53 or K-ras mutations in the corresponding lung tumors (p < 0.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557310.RAaNXl1-gCZHl5dXRfNe4epsq1SXtCztO1vP1916mhuLM130_provenance.
- NP557312.RAQsSiMLT-e4WY7mdv-Zf_gveTYUPhwIm1dblbExKwJ10130_assertion description "[BRCA2, FANCC, and FANCG gene mutations are present in a subset of pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557312.RAQsSiMLT-e4WY7mdv-Zf_gveTYUPhwIm1dblbExKwJ10130_provenance.
- NP557313.RAcXhtJA2lcyDfUNNcx_j0XEXyQzGBcfclzkB-yeXEsgM130_assertion description "[Heterozygosity for loss-of-function dominant-negative mutations in STAT1 is responsible for autosomal dominant (AD) Mendelian susceptibility to mycobacterial disease (MSMD), whereas heterozygosity for gain-of-function loss-of-dephosphorylation mutations causes AD chronic mucocutaneous candidiasis (CMC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557313.RAcXhtJA2lcyDfUNNcx_j0XEXyQzGBcfclzkB-yeXEsgM130_provenance.
- NP557317.RAf1wHi5w2AOAq2InBhfUIVsUc5Fh32CP6yJsRN4bjGrU130_assertion description "[The SCL/tal-1 gene on chromosome 1 is disrupted in up to 30% of immature T-cell malignancies, thus representing the most commonly recognized chromosomal abnormality in this disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557317.RAf1wHi5w2AOAq2InBhfUIVsUc5Fh32CP6yJsRN4bjGrU130_provenance.
- NP557318.RAX2_pYCtUiujIqR2Zu9_sqqO3DvbAXXz4c3abGQ5jTks130_assertion description "[Epigenetic inactivation of BCL6B, a novel functional tumour suppressor for gastric cancer, is associated with poor survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557318.RAX2_pYCtUiujIqR2Zu9_sqqO3DvbAXXz4c3abGQ5jTks130_provenance.
- NP557319.RAQleu2QOlYJUsQtskt1-355cMi87Yll01ap_hpQcbrjg130_assertion description "[Our results also provide clues for distinct roles for the CBD-4 and DSP domains of laforin in the etiology of two subsyndromes of LD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557319.RAQleu2QOlYJUsQtskt1-355cMi87Yll01ap_hpQcbrjg130_provenance.
- NP557330.RAb8ODbMyiUk1OSYU6H39zYBI2tuespUixquN79YZ46d0130_assertion description "[Using non-obese diabetic (NOD), severe combined immunodeficient (SCID) or recombination activating gene-1 (RAG1)(-/-) and interleukin-2 receptor gamma-chain (IL-2Rγ)(-/-) mice reconstituted with human peripheral blood mononuclear cells (PBMCs), we have studied the mechanisms of human T cell expansion and activation in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557330.RAb8ODbMyiUk1OSYU6H39zYBI2tuespUixquN79YZ46d0130_provenance.
- NP557332.RAZ4RQvvTHl-wenApnsBtxrYxOVqElwavT7AJQwX8aaSU130_assertion description "[Parathyroid hormone-related protein (PTHrP) is expressed by human prostatic tissue and prostate cancer cell lines, and positively influences primary prostate tumor growth in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557332.RAZ4RQvvTHl-wenApnsBtxrYxOVqElwavT7AJQwX8aaSU130_provenance.
- NP557346.RAVnMq8GIpYORQGmfFSGn6x3jn1Zm7S3erC4qvapgIt-Q130_assertion description "[Five (2.4%) of 211 patients with LQT1-susceptibility mutations had documented AF, compared to 0 of 174 patients with LQT2, 1 of 59 patients with LQT3, 1 of 1 patient with Andersen-Tawil syndrome, and 1 of 34 patients with multiple mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557346.RAVnMq8GIpYORQGmfFSGn6x3jn1Zm7S3erC4qvapgIt-Q130_provenance.
- NP557347.RAVG0fo32LASeA30DdWXTDQUNIHJg3lhbj-ygd97N00dA130_assertion description "[Importantly, the administration of rAAV6:GFP vectors did not induce muscle damage or inflammation except at the highest doses we examined, and administration of a transgene-null vector (rAAV6:MCS) did not cause damage or inflammation at any of the doses tested, demonstrating that GFP-expressing, or transgene-null vectors may be more suitable as experimental controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557347.RAVG0fo32LASeA30DdWXTDQUNIHJg3lhbj-ygd97N00dA130_provenance.
- NP557349.RAa4Kf9a24iehEbwy04mG7mLOLpfpJyw_NB_ff1HpbRKc130_assertion description "[In humans, however, studies investigating the link between resistin and metabolic disease are conflicting.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557349.RAa4Kf9a24iehEbwy04mG7mLOLpfpJyw_NB_ff1HpbRKc130_provenance.
- NP557355.RAXhZPkeQikpjkH2We_nx7zPcCTUWdNkM7GDBrLsWhQh0130_assertion description "[High-level amplification of EIF3S3 was found in 11 of 125 (9%) of pT1/pT2 tumors, 12 of 44 (27%) of pT3/pT4 tumors, and 8 of 37 (22%) of lymph node metastases as well as in 26 of 78 (33%) and 15 of 30 (50%) of hormone refractory locally recurrent tumors and metastases, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557355.RAXhZPkeQikpjkH2We_nx7zPcCTUWdNkM7GDBrLsWhQh0130_provenance.
- NP557357.RAXJSqJaD5fXcfypacDPLJQ6Kz3LZpnLsOJjfwpkwyQPM130_assertion description "[We studied a new FISH method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocation in patients with myeloid neoplasms associated with eosinophilia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557357.RAXJSqJaD5fXcfypacDPLJQ6Kz3LZpnLsOJjfwpkwyQPM130_provenance.
- NP557364.RASJYZNJOaXFr42swv8fTeT73QXai3iFu55noibLs5PTk130_assertion description "[We report here that all three ITCs that caused urinary bladder cancer in rats, including allyl ITC, benzyl ITC, and phenethyl ITC, increased the transactivation of activator protein 1 (AP-1) and AP-1 DNA binding in human bladder cancer UM-UC-3 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557364.RASJYZNJOaXFr42swv8fTeT73QXai3iFu55noibLs5PTk130_provenance.
- NP557371.RAXZW4Qe_u5f6fTbpFRDL4pHNc2MCgNSS_o8SQyNPqb-I130_assertion description "[The aim of this study was to analyze the gene expression of androgen receptor (AR) and type 2 17 beta hydroxysteroid dehydrogenase (17 beta-HSD) in keratinocytes of plucked scalp hairs from hirsute patients and normal subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557371.RAXZW4Qe_u5f6fTbpFRDL4pHNc2MCgNSS_o8SQyNPqb-I130_provenance.
- NP557372.RARumjxQOiEkMsyjL4PXakSjb0HFqwMtqfnAQrMLtivkE130_assertion description "[Here, we identified the modified eukaryotic factor as the abundant nuclear factor poly(ADP-ribose) polymerase-1 (PARP-1), which is important in the pathologies of several disease states typically associated with chronic H. pylori infection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557372.RARumjxQOiEkMsyjL4PXakSjb0HFqwMtqfnAQrMLtivkE130_provenance.
- NP557374.RAS_8gGax6yIpPL31Vs282KGm17oexJtaVEvPspa3Y0pQ130_assertion description "[APS-1 patients develop multiorgan autoimmune diseases including type 1 diabetes (prevalence 12%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557374.RAS_8gGax6yIpPL31Vs282KGm17oexJtaVEvPspa3Y0pQ130_provenance.
- NP557383.RATnx5-8Gx4YpjhJyPa2ivB63w003PlW_EISvtAEIOcjI130_assertion description "[A decrease in the estimated frequency of the extended HLA haplotype B18 CF130 DR3 DQw2 is common to non-insulin-dependent diabetes, juvenile rheumatoid arthritis, and Berger's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557383.RATnx5-8Gx4YpjhJyPa2ivB63w003PlW_EISvtAEIOcjI130_provenance.
- NP557386.RATAGCtJs5CnrVF2S_GujZcrY_P5R2KXtRzC7-QonsfSg130_assertion description "[Two potentially functional genetic variants (IL-23R rs1884444 T>G and rs6682925 T>C) have been found to contribute to solid cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557386.RATAGCtJs5CnrVF2S_GujZcrY_P5R2KXtRzC7-QonsfSg130_provenance.
- NP557390.RAXvMWeUsVN9atBGO1ccl-OYw7powkiy-HEB4Sv_QLMsw130_assertion description "[In contrast, transgenic mice overexpressing TRX1 show an extended life span and are relatively resistant to ischemia- mediated brain damage.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557390.RAXvMWeUsVN9atBGO1ccl-OYw7powkiy-HEB4Sv_QLMsw130_provenance.
- NP557395.RASTIbJOuVQJmCdATrt97RAj0uqXHXxz8CVzJWLXyGjYg130_assertion description "[Using recombinant proteins and a murine model, we demonstrated that an ADAMTS13 variant truncated after either the eighth thrombospondin type 1 repeat or the spacer domain inhibits ferric chloride-induced arterial thrombosis in ADAMTS13(-/-) mice with efficacy similar to that of full-length ADAMTS13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557395.RASTIbJOuVQJmCdATrt97RAj0uqXHXxz8CVzJWLXyGjYg130_provenance.
- NP557400.RAYdoUa92vsI2hMKimnY-0rYTVuDT4YHlUa-v40Qa1mZw130_assertion description "[Based on these results, we performed three different antiangiogenic experiments targeted to inhibit VEGF expression in a human malignant glioma (U87) mouse model: anti-VEGF neutralized antibody intraperitoneal injection; interferon-beta intramusclar injection; and transfection of an endogenous nonspecific angiogenesis inhibitor, thrombospondin-1, into glioma cells caused inhibition of VEGF secretion and/or mRNA expression and resulted in glioma growth inhibition of 70%, 84%, and 50%, respectively, compared with control.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557400.RAYdoUa92vsI2hMKimnY-0rYTVuDT4YHlUa-v40Qa1mZw130_provenance.
- NP557402.RAS3iz9xHz9piGRkbxMApUG5hYPGJcEL93mGHxqlSxX0U130_assertion description "[A subgroup of HER2-positive breast cancer patients with poor prognosis expresses a heterogeneous collection of HER2 carboxy-terminal fragments (CTF) collectively known as p95HER2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557402.RAS3iz9xHz9piGRkbxMApUG5hYPGJcEL93mGHxqlSxX0U130_provenance.
- NP557413.RAXhgA0iCAZkLV8ohCE1lzESYRhhyDmaG8dsRuS1N2bJo130_assertion description "[This in vitro analysis was consistent with the statistical inverse correlation detected between Bmi-1 and PTEN expression in a cohort of human nasopharyngeal carcinoma biopsies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557413.RAXhgA0iCAZkLV8ohCE1lzESYRhhyDmaG8dsRuS1N2bJo130_provenance.
- NP557421.RASgQxS4cBPO0vh8MZwFb0viMWmLf26K3RsXuL0gAfifI130_assertion description "[In order to obtain an alternative tool to diagnose and follow this malignancy, we developed a fluorescence in situ hybridization (FISH) assay that could distinguish between the two most common fusion genes, that is, SS18-SSX1 and SS18-SSX2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557421.RASgQxS4cBPO0vh8MZwFb0viMWmLf26K3RsXuL0gAfifI130_provenance.
- NP557430.RAbX4IQabVlZ2EhZR_s4xcNlL4leC-lvUxRO8_C3YlvbI130_assertion description "[Mutations in emerin and nuclear lamins have been associated with muscular dystrophies and lipodystrophy, raising new questions about the functions of inner nuclear membrane proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557430.RAbX4IQabVlZ2EhZR_s4xcNlL4leC-lvUxRO8_C3YlvbI130_provenance.
- NP557431.RAb8IcteuHVNc4alZoanQXnd1Bfa0cTbkKrUDEedjGQYU130_assertion description "[Genetic polymorphisms of D2-like dopamine receptor genes, DRD2 TaqI A, DRD3 Ser-9-Gly, and DRD4 exon III variable number of tandem repeats, were compared between: (a) MAMP users as a whole and 435 normal controls, and (b) those 154 individuals with MAMP-induced psychosis and the 252 MAMP users with no psychosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557431.RAb8IcteuHVNc4alZoanQXnd1Bfa0cTbkKrUDEedjGQYU130_provenance.
- NP557432.RAc94yTayUCerkjIueXbCzO6K8ARvrwhFhZwCye60kf34130_assertion description "[RNA polymerase III transcription in cancer: the BRF2 connection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557432.RAc94yTayUCerkjIueXbCzO6K8ARvrwhFhZwCye60kf34130_provenance.
- NP557433.RAUVlAHcIQlaaiDENVXuJC7ITkaCxTuEmoUX2hLqBa-EU130_assertion description "[However, the distinctive levels of PKCepsilon, PKCalpha, and caveolin-1 in lung and dermal fibroblasts from scleroderma patients and control subjects indicate that the links between these signaling proteins and MEK/ERK must function differently in the four cell types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557433.RAUVlAHcIQlaaiDENVXuJC7ITkaCxTuEmoUX2hLqBa-EU130_provenance.
- NP557434.RAXeDotZSQhQ2_mHQe5C-osyaHumKoNrs1bHCjS--12Fw130_assertion description "[Positive signal for the appropriate mRNA was detected in tumours associated with Cushing's disease, acromegaly and hyperprolactinaemia, where immunoreactivity for adrenocorticotrophin (ACTH) growth hormone and prolactin had also been confirmed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557434.RAXeDotZSQhQ2_mHQe5C-osyaHumKoNrs1bHCjS--12Fw130_provenance.
- NP557437.RAXKuyqx4fksXjVl8kTHF7cXcb2POwJ_nNd7da2rALLYU130_assertion description "[DMT1 and FP1 are centrally involved in iron uptake/transfer in the duodenum and in the adaptive changes of iron homeostasis to iron deficiency and overload.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557437.RAXKuyqx4fksXjVl8kTHF7cXcb2POwJ_nNd7da2rALLYU130_provenance.
- NP557438.RARyKGeD68Pk8Z8BfRKtuMiboiQHKUH7tI0k-efVt-8UU130_assertion description "[Three genetic loci for the Charcot-Marie-Tooth (CMT) syndromes with slow motor nerve conduction velocities (hereditary motor and sensory neuropathy: HMSN type I) have been mapped to chromosomes 1 (CMT1B), 17 (CMT1A), and the X chromosome (CMTX).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557438.RARyKGeD68Pk8Z8BfRKtuMiboiQHKUH7tI0k-efVt-8UU130_provenance.
- NP557442.RASV3wGm6SO3GTcUC3BXK-VBEqy2Ac2t7GjsOV6807URk130_assertion description "[We describe a child who presented with ataxia and pancytopenia and was found to have a heterozygous mutation, c.845G>A (Arg282His) in TINF2, a gene recently reported to be mutated in a subset of patients with autosomal dominant dyskeratosis congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557442.RASV3wGm6SO3GTcUC3BXK-VBEqy2Ac2t7GjsOV6807URk130_provenance.
- NP557444.RAYQm_cly9A3dy6bbHM7lcJn9Zv2CweJyVoWDGvi2Cz7o130_assertion description "[The expression of growth hormone-releasing hormone (GHRH) and splice variants of its receptor in human gastroenteropancreatic carcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557444.RAYQm_cly9A3dy6bbHM7lcJn9Zv2CweJyVoWDGvi2Cz7o130_provenance.
- NP557446.RAeejjuws0dUD6SlyWZ1jXgEGBQ97nN_UeCZMQmCoNcYc130_assertion description "[Cancer specific promoter CpG Islands hypermethylation of HOP homeobox (HOPX) gene and its potential tumor suppressive role in pancreatic carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557446.RAeejjuws0dUD6SlyWZ1jXgEGBQ97nN_UeCZMQmCoNcYc130_provenance.
- NP557451.RARLqgOBaM0gyiZ09EBCBrVPUWx0-SagvVmql5H0_Zxyk130_assertion description "[To assess whether the major histocompatibility complex (MHC) profile of patients presenting with primary antiphospholipid syndrome (PAPS) is different from that of patients with secondary antiphospholipid syndrome (SAPS), we studied 123 patients, 34 of whom presented PAPS and 35 SAPS due to systemic lupus erythematosus (SLE), 54 SLE patients without antiphospholipid syndrome (APS), and 166 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557451.RARLqgOBaM0gyiZ09EBCBrVPUWx0-SagvVmql5H0_Zxyk130_provenance.
- NP557457.RAT_PcHH21BpVrFc6PPifBdHEJfZzZvJksf_YCob_RTUM130_assertion description "[Here, we use miRNA arrays to compare the global miRNA expression profile of human mesenchymal stem cells (MSC) and ESFT cell lines, and show that ESFT display a distinct miRNA signature that includes induction of the oncogenic miRNA 17-92 cluster and repression of the tumor suppressor let-7 family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557457.RAT_PcHH21BpVrFc6PPifBdHEJfZzZvJksf_YCob_RTUM130_provenance.
- NP557459.RAREsL2bu6YJ_GAIVeA1nE7m4icqXglEwfnEu1Xb59CQs130_assertion description "[Steroid effects on ZAP-70 and SYK in relation to apoptosis in poor prognosis chronic lymphocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557459.RAREsL2bu6YJ_GAIVeA1nE7m4icqXglEwfnEu1Xb59CQs130_provenance.
- NP557464.RAfnEPP_AgD4Cm4NyhE7xA1bwDnJamyiNkqerJup9Wyag130_assertion description "[Here, we have tested 6 key genes of this type, TNF, IL1A, IL1B, IL6, IL1RN and IL10, as candidates for involvement in childhood-onset mood disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557464.RAfnEPP_AgD4Cm4NyhE7xA1bwDnJamyiNkqerJup9Wyag130_provenance.
- NP557466.RAeV4IS9n3wLs4kwMlW5ZILVcXUNxWpgDODKLo76Q7o-M130_assertion description "[To identify genes related to angiogenesis/metastasis that predict locoregional failure in patients with laryngopharyngeal cancer (LPC) undergoing chemoradiotherapy (CRT) treatment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557466.RAeV4IS9n3wLs4kwMlW5ZILVcXUNxWpgDODKLo76Q7o-M130_provenance.
- NP557486.RAYlU04tyLQOz924naeLxYUmweJxlEUq7brc_2xKRETfs130_assertion description "[Leucine-rich repeats and immunoglobin-like domains 3 (LRIG3), a member of LRIG gene family, is down-regulated in various human cancers, but its functions are still unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557486.RAYlU04tyLQOz924naeLxYUmweJxlEUq7brc_2xKRETfs130_provenance.
- NP557488.RAY5qeb-7wtIvXvZfZkeTFu5244bzoj3GxbxoOIAtOptM130_assertion description "[Multiple randomized clinical trials have studied the use of ICD for the primary and secondary SCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557488.RAY5qeb-7wtIvXvZfZkeTFu5244bzoj3GxbxoOIAtOptM130_provenance.
- NP557489.RAbqg5x7XUD2Y1chF98MOHrckqCtjBNQl3i0Mqb-YZBz8130_assertion description "[Therefore, the association of single nucleotide polymorphism of interleukin (IL)-18 promoter region in chronic hepatitis B virus (HBV) infection was examined.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557489.RAbqg5x7XUD2Y1chF98MOHrckqCtjBNQl3i0Mqb-YZBz8130_provenance.
- NP557498.RAWZUhQ8MeTGmW1mVPhqQ7LIkSWqj4IGSj3Ijw0VROK4s130_assertion description "[MDR1 gene polymorphisms: possible association with its expression and clinicopathology characteristics in colorectal cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557498.RAWZUhQ8MeTGmW1mVPhqQ7LIkSWqj4IGSj3Ijw0VROK4s130_provenance.
- NP557503.RAdhhdhjPpEI6qJ0CwTL8YGEbYKgDwaiNhZPkPw9AtEX0130_assertion description "[From 181 patients and 162 healthy controls, we found statistically significant correlations between a 4-SNP SUMO1 haplotype and NSCLP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557503.RAdhhdhjPpEI6qJ0CwTL8YGEbYKgDwaiNhZPkPw9AtEX0130_provenance.
- NP557515.RAYxFz4YT89AjHpSeOh7FLx-MPw0_Lvidq7E8i_hiDDfM130_assertion description "[This report confirms for the first time the in-vitro findings in a single clinical case that TSH as well as HCG leads to spontaneous OHSS in patients with FSHR D567N mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557515.RAYxFz4YT89AjHpSeOh7FLx-MPw0_Lvidq7E8i_hiDDfM130_provenance.
- NP557517.RAbhsv66K7KfaQpk59n9t7_iSl6woWXHcyKHiVidG98rc130_assertion description "[Median p24-antigen and plasma viraemia level decreases below baseline were more pronounced in the triple combination arm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557517.RAbhsv66K7KfaQpk59n9t7_iSl6woWXHcyKHiVidG98rc130_provenance.
- NP557519.RAdZMjDcEJSIqrPuaUWmuYzGzlhwnopLtFlrussnKVMmc130_assertion description "[The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557519.RAdZMjDcEJSIqrPuaUWmuYzGzlhwnopLtFlrussnKVMmc130_provenance.
- NP557520.RARMzTN2_XmST__W_CusnIw0NQuRgP-wUt5tWeqaUZFaE130_assertion description "[Although lncRNA-mediated regulation of INK4b-ARF-INK4a gene is not restricted to ANRIL, both polycomb repressive complex-1 (PRC1) and -2 (PRC2) interact with ANRIL to form heterochromatin surrounding the INK4b-ARF-INK4a locus, leading to its repression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557520.RARMzTN2_XmST__W_CusnIw0NQuRgP-wUt5tWeqaUZFaE130_provenance.
- NP557521.RAUINY2ZuNb-LiWuPjR1PYQMvHPDA_Jg18wiDE14WfQH0130_assertion description "[Hence, our data demonstrate for the first time that underexpressed miR-100 leads to Plk1 overexpression, which in turn contributes to NPC progression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557521.RAUINY2ZuNb-LiWuPjR1PYQMvHPDA_Jg18wiDE14WfQH0130_provenance.
- NP557524.RAcoiKbI6mEbg_GkIGP7VqePFW0FbRBQEEBGyIjwXDimQ130_assertion description "[By a genome-wide association study (320 patients and 1,500 controls) and subsequent replication altogether involving a total of 3,300 Asian SLE patients from Hong Kong, Mainland China, and Thailand, as well as 4,200 ethnically and geographically matched controls, genetic variants in ETS1 and WDFY4 were found to be associated with SLE (ETS1: rs1128334, P = 2.33x10(-11), OR = 1.29; WDFY4: rs7097397, P = 8.15x10(-12), OR = 1.30).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557524.RAcoiKbI6mEbg_GkIGP7VqePFW0FbRBQEEBGyIjwXDimQ130_provenance.
- NP557525.RARoU2Gsg3IH7SKr7iczHf_ZDMKBG4PgUtm5FrUrq7M5c130_assertion description "[Further, loss of RASSF1A has also been reported to occur in premalignant adenomas of the bowel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557525.RARoU2Gsg3IH7SKr7iczHf_ZDMKBG4PgUtm5FrUrq7M5c130_provenance.
- NP557526.RAU1_4_JrG2pN0lroeDp0yit1hPSwRZXcNSnFz8hnrgok130_assertion description "[The AML1 gene encodes a DNA-binding protein that contains the runt domain and is the most frequent target of translocations associated with human leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557526.RAU1_4_JrG2pN0lroeDp0yit1hPSwRZXcNSnFz8hnrgok130_provenance.
- NP557533.RAdqw698RFXe2unTBnyNbusiMGkYeLkdfdAvo7bP90jQA130_assertion description "[The expression of MCM2 mRNA and protein in gastric carcinomas was significantly higher compared to that in normal gastric mucosa (P=0.04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557533.RAdqw698RFXe2unTBnyNbusiMGkYeLkdfdAvo7bP90jQA130_provenance.
- NP557539.RAQp0iYUpzCLHb8S89BK_bgFus9_OeaYeisqKDsdVa5bo130_assertion description "[Seven of 20 (35%) chronic glomerulonephritis (CGN), eight of 20 (40%) diabetes mellitus (DM) with proteinuria, and two of 24 (8.3%) rheumatic diseases were WT1 positive.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557539.RAQp0iYUpzCLHb8S89BK_bgFus9_OeaYeisqKDsdVa5bo130_provenance.
- NP557540.RAR_EfXZ9u_PAUDQYPOfSbaxxAbaho7b8D-nfzzbwyaXA130_assertion description "[HGPS is caused by mutations in LMNA, the gene that encodes nuclear lamins A and C. The most common mutation in subjects with HGPS is a de novo single-base pair substitution, G608G (GGC>GGT), within exon 11 of LMNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557540.RAR_EfXZ9u_PAUDQYPOfSbaxxAbaho7b8D-nfzzbwyaXA130_provenance.
- NP557542.RATgb1sTo_j4GKf7vk2zZIajzPZu3IYay38fKAAtosgrQ130_assertion description "[We evaluated the potential of OSP to induce EAE in rhesus monkeys, an out bred animal model for MS that is immunologically close to humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557542.RATgb1sTo_j4GKf7vk2zZIajzPZu3IYay38fKAAtosgrQ130_provenance.
- NP557546.RAcrocmSyJnAN0Tbs2MeY9H_xioIow8IEEj5BI81lfd8c130_assertion description "[Two naturally occurring amino acid substitutions of the 5-HT2A receptor: similar prevalence in patients with seasonal affective disorder and controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557546.RAcrocmSyJnAN0Tbs2MeY9H_xioIow8IEEj5BI81lfd8c130_provenance.
- NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_assertion description "[Although deletions or structural rearrangements of E2F1 were not detected in 14 primary acute leukemia or myelodysplasia samples with structural abnormalities of chromosome 20q11, the gene was amplified and overexpressed in HEL erythroleukemia cells and translocated to other chromosomes in several established human leukemia cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557548.RARTt-v_tHGpyVoX_qbkhg03AN5QuwRukr-TtuFAAWXps130_provenance.
- NP557553.RASj1Q-UDBAEo_huQVrYLcKKEVux6dwc36FU05DQ9YaCU130_assertion description "[Karyotypic analysis of a patient exhibiting a phenotype of isolated lissencephaly, and of her parents, revealed a de novo balanced translocation, t(8;17)(p11.2; p13.3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557553.RASj1Q-UDBAEo_huQVrYLcKKEVux6dwc36FU05DQ9YaCU130_provenance.
- NP557554.RAWOSspXiTK1aAO0TiuX7DX5xid0zumhX7_4aaUhU8z9s130_assertion description "[In dengue hemorrhagic fever (DHF), which is the life-threatening form of dengue virus (DV) infection, endothelial interactions of cross-reactive antibodies against the DV nonstructural glycoprotein-1 (NS1) are associated with endothelial dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557554.RAWOSspXiTK1aAO0TiuX7DX5xid0zumhX7_4aaUhU8z9s130_provenance.
- NP557560.RAYcSQSJdiP4VSUL_uUkHOt-6MSGvDmidZEn0KgRVXY0Q130_assertion description "[These findings show that: (a) DR3, a genetic marker of autoimmunity, might assist the establishment of chronic HBsAg liver disease in the absence of delta superinfection; (b) DR2 is linked with failure to clear the delta agent, and (c) DR4 may protect from virus B persistence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557560.RAYcSQSJdiP4VSUL_uUkHOt-6MSGvDmidZEn0KgRVXY0Q130_provenance.
- NP557563.RAUriQmN962SNFjvAmkDrOgp_1bXf4vO-2SXtdCNPX160130_assertion description "[These findings suggest that FALS due to an SOD1 gene mutation is potentially a multisystem degenerative disorder, affecting not only neurons, but also astrocytes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557563.RAUriQmN962SNFjvAmkDrOgp_1bXf4vO-2SXtdCNPX160130_provenance.
- NP557568.RAbs0Iuc6aVifgPPdvWPVIHW_O2K4wip_4Aa0QKFQmM3I130_assertion description "[Children (n = 22) who had been diagnosed with salt-losing forms of adrenal hypoplasia (19 isolated cases, 3 familial), and who were negative for mutations in DAX1 (NR0B1) and SF1 (NR5A1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557568.RAbs0Iuc6aVifgPPdvWPVIHW_O2K4wip_4Aa0QKFQmM3I130_provenance.
- NP557573.RAVvKUY1vgeMFoAIGa6bEQMgPtOtBuQPPkDpj-0lLupyE130_assertion description "[CS1 mRNA was expressed in >90% of 532 multiple myeloma cases, regardless of cytogenetic abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557573.RAVvKUY1vgeMFoAIGa6bEQMgPtOtBuQPPkDpj-0lLupyE130_provenance.
- NP557580.RAS2B4_zcE0D1gqUxsU1Brci07oTqmndLw3xCRfxP7rk0130_assertion description "[The TLR adaptors MyD88 and TRIF, as well as TLR4 and TLR3, were found to be dispensable, demonstrating that T. cruzi induces IFN-beta expression in a TLR-independent manner.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557580.RAS2B4_zcE0D1gqUxsU1Brci07oTqmndLw3xCRfxP7rk0130_provenance.
- NP557582.RAXWpgUbyi9YjaeZWehUb3r0wH6CfX2xKD4FDN0HB5aC0130_assertion description "[Apart from its much slower progression, these patients' phenotype closely resembled that of pediatric cases including early onset, absence of CNS symptoms, generalized muscle weakness predominating on axial and proximal muscles but affecting facial, ocular, and respiratory muscles, typical mitochondrial myopathy with a mosaic pattern of COX-negative and ragged-red fibers, combined mtDNA-dependent respiratory complexes deficiency and mtDNA depletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP557582.RAXWpgUbyi9YjaeZWehUb3r0wH6CfX2xKD4FDN0HB5aC0130_provenance.