Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP149138.RAoe0eLY_hT5hZDweVwaTFihBS68__9WIF66V3j7iuX3Q130_assertion description "[Imbalanced serum concentration between cathepsin B and cystatin C in patients with pelvic inflammatory disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149138.RAoe0eLY_hT5hZDweVwaTFihBS68__9WIF66V3j7iuX3Q130_provenance.
- NP149147.RAi119DPJWjWf6huuKIVR1Z6XyKQevsUOZaxeuGcMVM5Y130_assertion description "[Upregulation of CD47 in sporadic inclusion body myositis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149147.RAi119DPJWjWf6huuKIVR1Z6XyKQevsUOZaxeuGcMVM5Y130_provenance.
- NP149149.RAggnFtas7lyrY-1eE8rPBcp6EI81PhmnxSzmiy0ktUaM130_assertion description "[CD85j (leukocyte Ig-like receptor 1) is expressed in Polymyositis and sporadic Inclusion body myositis at the sites of partial invasion and in Dermatomyositis in perivascular inflammation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149149.RAggnFtas7lyrY-1eE8rPBcp6EI81PhmnxSzmiy0ktUaM130_provenance.
- NP149150.RAhCsZdCUYkv87RXJgGXj_JO-ecqh7_Dj44FeCR-mF0sU130_assertion description "[role in modulation of integrin-mediated cell adhesion, transendothelial migration, angiogenesis, apoptosis, cell migration, negative regulation of immune cell signalling, autoimmunity, macrophage phagocytosis, IgE-mediated anaphylaxis and thrombosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149150.RAhCsZdCUYkv87RXJgGXj_JO-ecqh7_Dj44FeCR-mF0sU130_provenance.
- NP149152.RAkcB30oi0iiYG72GuzQkaScnuz8yGy4nTvppdNuccUB0130_assertion description "[There are associations between sudden infant death syndrome and particular polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149152.RAkcB30oi0iiYG72GuzQkaScnuz8yGy4nTvppdNuccUB0130_provenance.
- NP149153.RAnf92nx8QPYmO7b3BeMGA-_c8ZAzbnxpzHgHU4VUPYZY130_assertion description "[Four single nucleotide polymorphisms were identified in sudden infant death syndrome: K897T, P967L, R1047L, and Q1068R.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149153.RAnf92nx8QPYmO7b3BeMGA-_c8ZAzbnxpzHgHU4VUPYZY130_provenance.
- NP149156.RAivXk_v1jck05uDJc-rb17P5q1A26wUMBKA8V_f0jfBk130_assertion description "[Cases of infectious death have a higher percentage of both the C allele (p = 0.037 compared to the SIDS cases, p = 0.022 compared to the controls) and the CC genotype (p = 0.05 compared to the SIDS cases, p = 0.016 compared to the controls).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149156.RAivXk_v1jck05uDJc-rb17P5q1A26wUMBKA8V_f0jfBk130_provenance.
- NP149157.RAtDVH16uqgSZRKRB9MyYCO1kNavpCfMrimoaM62Gph3g130_assertion description "[the first molecular and functional evidence implicating CAV3 as a pathogenic basis of Sudden infant death syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149157.RAtDVH16uqgSZRKRB9MyYCO1kNavpCfMrimoaM62Gph3g130_provenance.
- NP149158.RAmQ5Uu3KEGLb4fr4zLecn_eh88VTT_nEDI6N_9_7p3aQ130_assertion description "[significant association between the IL-10 -592*A allele and Sudden Infant Death syndrome, consistent with the earlier findings/study lends support to the hypothesis that IL-10 genotype is related to the susceptibility of babies to SIDS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149158.RAmQ5Uu3KEGLb4fr4zLecn_eh88VTT_nEDI6N_9_7p3aQ130_provenance.
- NP149160.RAsgVfyDP_VcS4qxn-tMGMNHNzoKq82-tuepVdgy2GFvY130_assertion description "[The repetitive scavenger receptor cysteine-rich (SRCR) domains and SRCR-interspersed domains (SID) of DMBT1 define a complex multi-allele system that represents the major basis for the variability of DMBT1 in cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149160.RAsgVfyDP_VcS4qxn-tMGMNHNzoKq82-tuepVdgy2GFvY130_provenance.
- NP149163.RAnDWoUOWCkX00zMykGBigYG3lRyiTQwXEgYqMqDt0Q9k130_assertion description "[3'UTR polymorphism of the serotonin transporter gene is associated with sudden infant death syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149163.RAnDWoUOWCkX00zMykGBigYG3lRyiTQwXEgYqMqDt0Q9k130_provenance.
- NP149166.RAmDmH80uyRXkp0ZII_75gbMFax39WiEr5XANhH3dLDY0130_assertion description "[G6PC1 hepatic activity was abnormally low in 98 SIDS (preterm, n = 13; term, n = 85), and non-SIDS preterm infants (n = 35) compared to term non-SIDS infants (n = 29) and adults (n = 9) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149166.RAmDmH80uyRXkp0ZII_75gbMFax39WiEr5XANhH3dLDY0130_provenance.
- NP149170.RAt4pJCN0OBySRqR7-pGq6q_Ay9qjMYfsoRdA8AKxBdPQ130_assertion description "[Role of genes TPH2, 5-HTT, and MAOA regulating the serotonin metabolic pathway in the brain stain in the etiopathogenesis of the sudden infant death syndrome was studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149170.RAt4pJCN0OBySRqR7-pGq6q_Ay9qjMYfsoRdA8AKxBdPQ130_provenance.
- NP149175.RAl2Ow55AUTj58cTc6VyRCkasFxucN89pN8SST_bgJzvU130_assertion description "[a polymorphism in paired like homeobox (PHOX) 2B gene may have a role in sudden infant death syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149175.RAl2Ow55AUTj58cTc6VyRCkasFxucN89pN8SST_bgJzvU130_provenance.
- NP149176.RAiDSNbnSIgckHFn_LdvO7-PNUp2xZI5nSXcxxkXYSCz4130_assertion description "[Children dying from identified causes have different APOE allele distributions from sudden infant death syndrome (SIDS) cases, but are similar to adults/dying from SIDS have an allele distribution comparable to healthy newborns.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149176.RAiDSNbnSIgckHFn_LdvO7-PNUp2xZI5nSXcxxkXYSCz4130_provenance.
- NP149178.RAoACQhNS0Jslqd_JBnEEFHmOdqHjTrq-C1i_Ou94LrvU130_assertion description "[unfavorable genetic profile in the TNF-alpha gene may be involved in sudden infant death by exposing the infant to both a high level of and prolonged exposure to TNF-alpha ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149178.RAoACQhNS0Jslqd_JBnEEFHmOdqHjTrq-C1i_Ou94LrvU130_provenance.
- NP149182.RApZoQVzCiu_VQAx6hrq67iZEW7PeBX-EfZDcWb3whHZ0130_assertion description "[A functional polymorphism in the tyrosine hydroxylase gene indicates a role of noradrenalinergic signaling in sudden infant death syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149182.RApZoQVzCiu_VQAx6hrq67iZEW7PeBX-EfZDcWb3whHZ0130_provenance.
- NP149183.RAn25jgIX7IVPTlyyspHk4T_Ld0c-Ok0yGEtIyKW9Vv_U130_assertion description "[Role for CFTR gene polymorphism in the progression of alcohol-related pancreatic disease/with homozygous (TG) 11 alleles in intron 8 of the CFTR gene appear to be protected against decreased bicarbonate concentration in pancreatic juice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149183.RAn25jgIX7IVPTlyyspHk4T_Ld0c-Ok0yGEtIyKW9Vv_U130_provenance.
- NP149184.RAqKwbnznU5NuGlaStok8PMOMFoVJqyrmzq3Fd_-NJ0KY130_assertion description "[A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases was perfomed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149184.RAqKwbnznU5NuGlaStok8PMOMFoVJqyrmzq3Fd_-NJ0KY130_provenance.
- NP149195.RAhBv30UGhKE84kUXdGpBs_Pgfm1ttxjsCwfcvB1NayBg130_assertion description "[Findings indicate correlation between the increased expression of p16 during the progression of skin from actinic keratosis to in situ squamous cell carcinoma to invasive squamous cell carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149195.RAhBv30UGhKE84kUXdGpBs_Pgfm1ttxjsCwfcvB1NayBg130_provenance.
- NP149200.RAplcUGYK63wCkaVpn3Jky1r1GGh4BxY8agT-0rBbawB4130_assertion description "[investigation of the involvement of the CDKN2A, CDKN2B and p53 genes in actinic keratosis (AK) and in the progression of AK to squamous cell carcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149200.RAplcUGYK63wCkaVpn3Jky1r1GGh4BxY8agT-0rBbawB4130_provenance.
- NP149208.RAm7Bl93ZRsA20i29dP8k8SAg5LuB4VFbLlF4UPq_O5YA130_assertion description "[A hitherto unknown heteroplasmic mutation at position C2839A base pair in the 16s rRNA region of the mitochondrial genome was evident only in Dupuytren's contracture patients (90%) & may be important in its pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149208.RAm7Bl93ZRsA20i29dP8k8SAg5LuB4VFbLlF4UPq_O5YA130_provenance.
- NP149217.RAjaejswvynXuh9yESMwRR8wwdM5JgR23vATlJk0r5414130_assertion description "[Homozygous SCA2 patients develop levodopa responsive Parkinsonism and dyskinesia and motor fluctuations suggesting a pre-synaptic lesion and eventually progress to dementia with psychosis and ataxia/eye movements are absent at onset but appear later ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149217.RAjaejswvynXuh9yESMwRR8wwdM5JgR23vATlJk0r5414130_provenance.
- NP149221.RAi9lgEFh7usdpTfIqvkH5vn-JC4ThsLP_IK2xWmlewSM130_assertion description "[In our study DRD2 C939T was in strong linkage disequilibrium with TaqIA in tardive dyskinesia in schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149221.RAi9lgEFh7usdpTfIqvkH5vn-JC4ThsLP_IK2xWmlewSM130_provenance.
- NP149224.RAo0bM8D3GHbueHBnawXXPeK6SlnqV151Jm22VOhdscaQ130_assertion description "[The Serbian family further demonstrates that recurrent MR-1 mutations are associated with paroxysmal nonkinesigenic dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149224.RAo0bM8D3GHbueHBnawXXPeK6SlnqV151Jm22VOhdscaQ130_provenance.
- NP149233.RAo2S_vSMozJQ3_t5tYrDpmwfHzMeFkZS7rWrrpd8WJR4130_assertion description "[GLUT1 mutations are a cause of paroxysmal exertion-induced dyskinesias and induce hemolytic anemia by a cation leak ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149233.RAo2S_vSMozJQ3_t5tYrDpmwfHzMeFkZS7rWrrpd8WJR4130_provenance.
- NP149240.RAqjPswlGKs7xA5oVb1zvejQ3lztq59NR3_QAFPujP2V0130_assertion description "[reduced adipose tissue lipoprotein lipase expression, being significantly correlated with the decrease in insulin and prolactin, suggests a role of hyperinsulinemia and hyperprolactinemia in inducing and sustaining obesity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149240.RAqjPswlGKs7xA5oVb1zvejQ3lztq59NR3_QAFPujP2V0130_provenance.
- NP149247.RAn6VRFR83arovZX82JOMMIpD0oENfYBLux6213kXKSSY130_assertion description "[MicroRNA-510 target site of the 3'UTR of HTR3A and HTR3E are associated with the irritable bowel syndrome with diarrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149247.RAn6VRFR83arovZX82JOMMIpD0oENfYBLux6213kXKSSY130_provenance.
- NP149248.RAgB9lLiZ3OMzdT8W2SG-G109_3CfEfvkvmw6EyWw-Nb4130_assertion description "[5-HT3 receptors are known to be involved in mediation of nausea/emesis caused by chemo/radio-therapy and anaesthesia, and more recently have also been found to be involved in irritable bowel syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149248.RAgB9lLiZ3OMzdT8W2SG-G109_3CfEfvkvmw6EyWw-Nb4130_provenance.
- NP149250.RAnzMTZTa8paWA3ceOP4Qxn4uGGbXR_rZzUoO0-tFqlQk130_assertion description "[The serum levels of mannan-binding lectin and the occurrence of spontaneous abortion in women with celiac disease and irritable bowel syndrome are not causally related.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149250.RAnzMTZTa8paWA3ceOP4Qxn4uGGbXR_rZzUoO0-tFqlQk130_provenance.
- NP149252.RAlxH_4Pzxxc3s6fegIYBTtqS9FKM9BqF5SB4FZ58hAog130_assertion description "[Ulcerative colitis and irritable bowel syndrome are associated with similar molecular changes in serotonergic signaling mechanisms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149252.RAlxH_4Pzxxc3s6fegIYBTtqS9FKM9BqF5SB4FZ58hAog130_provenance.
- NP149259.RAgI5CyMmfX16UHYtaeP-Wk3GyAKjdDuJcemb5wfMD4C0130_assertion description "[We present a patient with a homozygous truncating CLDN16 gene mutation (W237X) who had early onset of renal insufficiency despite early diagnosis at 2 months.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149259.RAgI5CyMmfX16UHYtaeP-Wk3GyAKjdDuJcemb5wfMD4C0130_provenance.
- NP149268.RAmR-8nXvM4wsyhhUmKZodwE6alVIk7-6oY6ZdqwEU-gM130_assertion description "[Rheumatoid arthritis patients were less likely to have elevated erythrocyte sedimentation rate (ESR)/depressed C-reactive protein/as a measure of inflammation in rheumatic disease may be limited in infection, renal insufficiency, and low albumin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149268.RAmR-8nXvM4wsyhhUmKZodwE6alVIk7-6oY6ZdqwEU-gM130_provenance.
- NP149269.RAr2oGB-q2uqLc8wgrxe78UHceZD8U_qyRbaWh5yCZKCg130_assertion description "[FGF-23 may be an important determinant in the regulation of mineral metabolism with renal insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149269.RAr2oGB-q2uqLc8wgrxe78UHceZD8U_qyRbaWh5yCZKCg130_provenance.
- NP149274.RAu-HZXd4q4hX1MMZf2YL1VFUp6Sl6tC7oIhtpo9TYsCc130_assertion description "[increased CXCL10 especially in hypothyroid patients with a more aggressive disorder, and normal CCL2 serum levels in autoimmune thyroiditis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149274.RAu-HZXd4q4hX1MMZf2YL1VFUp6Sl6tC7oIhtpo9TYsCc130_provenance.
- NP149275.RAvq4PMFRlisZBWoI5Wpb1xyFXBRtScG-5bTkSEwrRpsA130_assertion description "[High CXCL10 and CCL2 serum levels in patients with mixed cryoglobulinemia and chronic hepatitis c (MC); CXCL10 in MC + autoimmune thyroiditis is significantly higher than that in MC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149275.RAvq4PMFRlisZBWoI5Wpb1xyFXBRtScG-5bTkSEwrRpsA130_provenance.
- NP149283.RAoPhm42KPu9P6CnUAGKdQnoKmMIy8ufwaUUOltv2AxgM130_assertion description "[Additional non-HLA loci contribute to the joint susceptibility to type I diabetes and autoimmune thyroiditis, and two potential candidates include the CTLA-4 and insulin VNTR loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149283.RAoPhm42KPu9P6CnUAGKdQnoKmMIy8ufwaUUOltv2AxgM130_provenance.
- NP149284.RAlo1ufURsgfBw2svHQLcjrSADYnVWCNRfKmH66IF06J8130_assertion description "[High CXCL10 and CCL2 serum levels in patients with mixed cryoglobulinemia and chronic hepatitis c (MC); CXCL10 in MC + autoimmune thyroiditis is significantly higher than that in MC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149284.RAlo1ufURsgfBw2svHQLcjrSADYnVWCNRfKmH66IF06J8130_provenance.
- NP149290.RAjf1eSJBgXsm3Z4d22tQuHqtXZGoyDHwG1eqt1QtrolU130_assertion description "[Long-term follow-up of three patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149290.RAjf1eSJBgXsm3Z4d22tQuHqtXZGoyDHwG1eqt1QtrolU130_provenance.
- NP149291.RAsxGmyWDcL1C19qROwJvn6Dw1dwteEM3xRDDXUHq9B4Y130_assertion description "[The effects of genetic polymorphisms in the ACE on impaired hypoglycemia awareness in 231 Caucasian type 1 diabetes patients, was studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149291.RAsxGmyWDcL1C19qROwJvn6Dw1dwteEM3xRDDXUHq9B4Y130_provenance.
- NP149294.RAnqMt_IjYQE37knzCkcELCaWi4IhyXflknZF2EGa9rh4130_assertion description "[results support the functional importance of insulin in Nrf2-dependent transcriptional upregulation of GCLc in GSH recovery during oxidative challenge and suggest a possible role for hypoglycemia in promoting insulin-mediated GCLc upregulation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149294.RAnqMt_IjYQE37knzCkcELCaWi4IhyXflknZF2EGa9rh4130_provenance.
- NP149298.RAtaA0sN1Z9UIGWAahCMhA6_tgAGSuSMUvqC-nVJInWFY130_assertion description "[Macrosomic infants with transient or persistent hyperinsulinemic hypoglycemia should be screened for HNF4A mutations if there is a family history of youth-onset diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149298.RAtaA0sN1Z9UIGWAahCMhA6_tgAGSuSMUvqC-nVJInWFY130_provenance.
- NP149300.RAnNLGhtat3RHN3Vais9CblK68hPGjoZdRsZc5JdKXsrg130_assertion description "[both mineralocorticoid and glucocorticoid receptors may be involved in the multiple mechanisms controlling counterregulatory responses to hypoglycemia in healthy man ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149300.RAnNLGhtat3RHN3Vais9CblK68hPGjoZdRsZc5JdKXsrg130_provenance.
- NP149301.RAjj26wsDjyNEAvntKJNPhaxP57gVCJH5lNsgaW9_cUmA130_assertion description "[Elevated rate of severe hypoglycemia among patients with higher S-ACE suggests that a genetic determinant for severe hypoglycemia exists.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149301.RAjj26wsDjyNEAvntKJNPhaxP57gVCJH5lNsgaW9_cUmA130_provenance.
- NP149308.RAlw4ptOEFmpYYfoxnk2RIgsOF_P1ifxPvj8GeIxHsd-c130_assertion description "[patients with type 1 diabetes who carry two alleles of the Gly16 variant of ADRB2 are associated with developing hypoglycemia unawareness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149308.RAlw4ptOEFmpYYfoxnk2RIgsOF_P1ifxPvj8GeIxHsd-c130_provenance.
- NP149309.RAn8iSJND0EYkm7OJnbNYcr8gMaDZEm7Z8lCTs9vFutLo130_assertion description "[Variant R620W of PTPN22 play a role in susceptibility to psoriatic arthritis in men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149309.RAn8iSJND0EYkm7OJnbNYcr8gMaDZEm7Z8lCTs9vFutLo130_provenance.
- NP149310.RApTeFY6rocy92Mniv_neoqBuHRfyjcQCWz2izKrvXEfM130_assertion description "[Moderate association of the R620W variant of PTPN22 with psoriatic arthritis in the Toronto population only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149310.RApTeFY6rocy92Mniv_neoqBuHRfyjcQCWz2izKrvXEfM130_provenance.
- NP149313.RAiTeDbFztA2McOTzCb4F7uEWdG1B_ogc__PiisaYSOTM130_assertion description "[An increase in the frequency of the activating KIR2DS1 gene was detected in the psoriatic arthritis (PsA) patients, compared with psoriasis patients negative for PsA and an unaffected American Caucasian control group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149313.RAiTeDbFztA2McOTzCb4F7uEWdG1B_ogc__PiisaYSOTM130_provenance.
- NP149317.RAhJUL0Zy-3YryL8ZmYuFhJEGNmy4ZA7gQWQsbKD-64i4130_assertion description "[Variation within IL23R and IL12B is associated with susceptibility to both psoriasis and psoriatic arthritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149317.RAhJUL0Zy-3YryL8ZmYuFhJEGNmy4ZA7gQWQsbKD-64i4130_provenance.
- NP149327.RAg0BIGBHKEGGBS5Ex10HhQe3YTM7cc5S67-a6GDw8_QA130_assertion description "[Significant associations between Arg381Gln SNP and haplotypes encoding this variant were noted in psoriatic arthritis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149327.RAg0BIGBHKEGGBS5Ex10HhQe3YTM7cc5S67-a6GDw8_QA130_provenance.
- NP149328.RAumetNd5T3sG_c5p8DvPF17N_B2YraYB-4-vCftXGSps130_assertion description "[There was an increased frequency of the (*) 2 allele of HS1, 2-A in dermatitis herpetiformis, plaque psoriatic, and psoriatic arthritis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149328.RAumetNd5T3sG_c5p8DvPF17N_B2YraYB-4-vCftXGSps130_provenance.
- NP149329.RAuDFPpeiN73VILQJx8iejva9u6maMnU03FoR7qF_jzrU130_assertion description "[Certain HLA alleles are found in Chinese patients with psoriasis (HLA-A*30, -Cw*06, -DR*07) and psoriatic arthritis (PsA) (HLA-B*27)/patients with the HLA-B*27 and/or -Cw*12 may have higher risk of developing PsA [HLA-DR].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149329.RAuDFPpeiN73VILQJx8iejva9u6maMnU03FoR7qF_jzrU130_provenance.
- NP149333.RAhiJsAVQt-QT71rchmLRFrpnRxKS5V2VL437d5J0tGgY130_assertion description "[promoter polymorphisms associated with psoriasis vulgaris and psoriatic arthritis but not with pustulosis palmoplantaris ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149333.RAhiJsAVQt-QT71rchmLRFrpnRxKS5V2VL437d5J0tGgY130_provenance.
- NP149337.RAp2oJ-tJcGmsPQidV2GH78Zu9y-xX7WKpRvqR-RyWvjA130_assertion description "[Data suggest that S100 proteins calprotectin and S100A12 are related to radiographic changes rather than disease activity in psoriatic arthritis with low disease activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149337.RAp2oJ-tJcGmsPQidV2GH78Zu9y-xX7WKpRvqR-RyWvjA130_provenance.
- NP149340.RAsas9jcfdYV8juB0MkYE0uIvdK69XxoTZQCwLoLOr-1U130_assertion description "[data indicate that H.pylori infection and IL-1RN*2 synergistically determine susceptibility to duodenal ulcer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149340.RAsas9jcfdYV8juB0MkYE0uIvdK69XxoTZQCwLoLOr-1U130_provenance.
- NP149344.RAl1LWVEH-At2vHGQmwd_B7pAoSa4Q40lvaNCzVdgdrKI130_assertion description "[TNF/LTA genotypes might play an opposite role in the pathogenesis of gastric cancer and duodenal ulcer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149344.RAl1LWVEH-At2vHGQmwd_B7pAoSa4Q40lvaNCzVdgdrKI130_provenance.
- NP149347.RArFl8pdfUIlqV3XB62dsM5VAEE4VeB90VLXvmxSCzYt8130_assertion description "[interacts with Helicobacter pylori isolates from patients with chronic gastritis, duodenal ulcer and gastric cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149347.RArFl8pdfUIlqV3XB62dsM5VAEE4VeB90VLXvmxSCzYt8130_provenance.
- NP149348.RAp5rAWhlbf_BBLJMX_Bqns3dMtS4DqXBOQLIWnZwBqpM130_assertion description "[TNF/LTA genotypes might play an opposite role in the pathogenesis of gastric cancer and duodenal ulcer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149348.RAp5rAWhlbf_BBLJMX_Bqns3dMtS4DqXBOQLIWnZwBqpM130_provenance.
- NP149350.RAs6HhLlyoCatgHjBZLcqV_R2UpLn4xocjULW9memhSFE130_assertion description "[Analysis of CYP2C19 enzyme genotype indicated the patient was a homozygous extensive metabolizer, considered a poor responder for omeprazole treatment for duodenal ulcer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149350.RAs6HhLlyoCatgHjBZLcqV_R2UpLn4xocjULW9memhSFE130_provenance.
- NP149354.RAi8b3hRJemz3hG9__FRxb8FKpHP_eiDrER25zIDwk_aQ130_assertion description "[interacts with Helicobacter pylori isolates from patients with chronic gastritis, duodenal ulcer and gastric cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149354.RAi8b3hRJemz3hG9__FRxb8FKpHP_eiDrER25zIDwk_aQ130_provenance.
- NP149357.RAtgNwiTAhu59mrFL_TBZORHZNYiV_iabxhVhHV4CFZlQ130_assertion description "[association between diabetic complications and LTA, TNF and AGER polymorphisms is complex, with partly different alleles conferring susceptibility in type 1 and type 2 diabetic patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149357.RAtgNwiTAhu59mrFL_TBZORHZNYiV_iabxhVhHV4CFZlQ130_provenance.
- NP149361.RAspHI5wX4VEzpkDQMhwibVJwD1o7WdLNA4keAiMsjwIQ130_assertion description "[Succination of GAPDH and other thiol proteins may provide the chemical link between glucotoxicity and the pathogenesis of diabetic complications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149361.RAspHI5wX4VEzpkDQMhwibVJwD1o7WdLNA4keAiMsjwIQ130_provenance.
- NP149362.RAhQlHJqia98XPEGux5BPE7Pyz_2kiEUWR8F-cbHL0DJw130_assertion description "[association between diabetic complications and LTA, TNF and AGER polymorphisms is complex, with partly different alleles conferring susceptibility in type 1 and type 2 diabetic patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149362.RAhQlHJqia98XPEGux5BPE7Pyz_2kiEUWR8F-cbHL0DJw130_provenance.
- NP149365.RAmUTYo3sqEaRXWigx2YwND6jeanUYau5b-Z742PehVb0130_assertion description "[A decrease in free IGF-I and insulin-like growth factor binding protein 3 levels, along with increases in blood pressure, significantly influenced the presence of diabetic complications ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149365.RAmUTYo3sqEaRXWigx2YwND6jeanUYau5b-Z742PehVb0130_provenance.
- NP149368.RAsB08YYyDCRDDJsQ4IxxJLSgZ_740DZ1o9j5qyP0YZQU130_assertion description "[association between diabetic complications and LTA, TNF and AGER polymorphisms is complex, with partly different alleles conferring susceptibility in type 1 and type 2 diabetic patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149368.RAsB08YYyDCRDDJsQ4IxxJLSgZ_740DZ1o9j5qyP0YZQU130_provenance.
- NP149373.RAkQt886wboEDwx2c1jvIN2dvk4OqjyiIEvViHNw5kUeM130_assertion description "[Higher amounts of MIP-1alpha, MIP-1beta, and RANTES were detected in plasma of HIV-1-positive individuals, particularly those with concomitant pulmonary tuberculosis, although the increase was not found to be statistically significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149373.RAkQt886wboEDwx2c1jvIN2dvk4OqjyiIEvViHNw5kUeM130_provenance.
- NP149375.RAlKbC_GQTN-qUQFugOBiHUyChqhta5wOArH1N2lBcL0Q130_assertion description "[Higher amounts of MIP-1alpha, MIP-1beta, and RANTES were detected in plasma of HIV-1-positive individuals, particularly those with concomitant pulmonary tuberculosis, although the increase was not found to be statistically significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149375.RAlKbC_GQTN-qUQFugOBiHUyChqhta5wOArH1N2lBcL0Q130_provenance.
- NP149379.RAkSEgLK3xIftEj3cSC5i4SBZlLm4_BaiwtzzNpNcvBWU130_assertion description "[HH genotype is high in pulmonary tuberculosis patients and the reduced complement receptor 1 in patients may be an acquired phenomenon related to disease pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149379.RAkSEgLK3xIftEj3cSC5i4SBZlLm4_BaiwtzzNpNcvBWU130_provenance.
- NP149387.RAkM0Wd7rpMkseALfRS5L9tCLPUY4cXmlr9NzGs4_o_MA130_assertion description "[Coding regions of BTNL2 were sequenced to detect known and novel polymorphisms and genotyped 18 SNPs in 432 pulmonary tuberculosis cases and 482 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149387.RAkM0Wd7rpMkseALfRS5L9tCLPUY4cXmlr9NzGs4_o_MA130_provenance.
- NP149391.RAn2Ro9e-D_DgGufOikvfJwj27k5Yij3ETevjb5cX3pJA130_assertion description "[Polymorphisms in the VDR and NRAMP1 gene are statistically associated with susceptibility to pulmonary tuberculosis in the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149391.RAn2Ro9e-D_DgGufOikvfJwj27k5Yij3ETevjb5cX3pJA130_provenance.
- NP149394.RAsxgB3bJEJ0FVkKEmPHA58j_L7Qab9HTSWrTaTQNxrOg130_assertion description "[Polymorphisms of D543N and 3'UTR locus in NRAMP1 gene might affect their susceptibility to pulmonary tuberculosis in Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149394.RAsxgB3bJEJ0FVkKEmPHA58j_L7Qab9HTSWrTaTQNxrOg130_provenance.
- NP149398.RAjTXdcHfUUZTwDLIv1MQhonLyAeA1tjyipFwjuEnU7u8130_assertion description "[DQB1*050301 may be associated with susceptibility to HIV infection as well as development of pulmonary tuberculosis in HIV patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149398.RAjTXdcHfUUZTwDLIv1MQhonLyAeA1tjyipFwjuEnU7u8130_provenance.
- NP149403.RAjC8Fo3cO5_tcfEzJcoJcDwGyPMwq7r3a8vlv_4kZNKI130_assertion description "[T lymphocytes from patients with active pulmonary tuberculosis (PTB) had significantly decreased expression of CD3zeta & absence of the p65/p50 heterodimer of NF- kappa B; findings provide a novel mechanism for the T cell dysfunction in patients with PTB ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149403.RAjC8Fo3cO5_tcfEzJcoJcDwGyPMwq7r3a8vlv_4kZNKI130_provenance.
- NP149404.RAvjZkhpsWkxMZwzSZnJ7wJRkrBAW_fypJtGnPpjKhPwA130_assertion description "[Higher amounts of MIP-1alpha, MIP-1beta, and RANTES were detected in plasma of HIV-1-positive individuals, particularly those with concomitant pulmonary tuberculosis, although the increase was not found to be statistically significant.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149404.RAvjZkhpsWkxMZwzSZnJ7wJRkrBAW_fypJtGnPpjKhPwA130_provenance.
- NP149406.RAt-5NWehSBAHxIXA6Z65vbxddEqoIUjNAy4qP7hb_Ia8130_assertion description "[No significant differences in NOD2 transcriptional responses were detected in pulmonary tuberculosis/some patients, however, NOD2 expression was markedly increased and correlated with toll-like-receptor 2 and 4 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149406.RAt-5NWehSBAHxIXA6Z65vbxddEqoIUjNAy4qP7hb_Ia8130_provenance.
- NP149408.RAsVSEV7uVgLQpjhCNQ-_ccJVOflfHAfsd9_E7qB1UDYo130_assertion description "[cTAGE-1 and cTAGE-5 are new cancer germline antigens and that tumor-specific splicing of cTAGE genes may lead to further candidate proteins for specific immunotherapy of cutaneous T cell lymphoma and other malignancies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149408.RAsVSEV7uVgLQpjhCNQ-_ccJVOflfHAfsd9_E7qB1UDYo130_provenance.
- NP149412.RAsG3A9ln6G5cUoJyyLuN_H1mgveWYvk4GmWkhM0sxW1w130_assertion description "[p53 mutation is not an important mechanism for beta-catenin activation in primary cutaneous T-cell lymphoma; p53 codon 72 polymorphism may influence negative feedback control involving beta-catenin and p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149412.RAsG3A9ln6G5cUoJyyLuN_H1mgveWYvk4GmWkhM0sxW1w130_provenance.
- NP149414.RApW2peL-0XFOzhBdqfg-GK7crAal-0mMVzjZysxaqUVo130_assertion description "[evidence of VEGF production in cutaneous T-cell lymphoma, which is promoted by aberrant activation of Jak3 and the JNKs ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149414.RApW2peL-0XFOzhBdqfg-GK7crAal-0mMVzjZysxaqUVo130_provenance.
- NP149417.RAo4fdusDc6UI22ng8FInOl0FW1fO2unsdqui_tzdPDBQ130_assertion description "[preferential usage of Jbeta1 genes in all cases with advanced stages of cutaneous T-cell lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149417.RAo4fdusDc6UI22ng8FInOl0FW1fO2unsdqui_tzdPDBQ130_provenance.
- NP149424.RAhqPcmtpk-DHLGuDdhmi8xziQ7XA5QgZNB4FuK4O34J4130_assertion description "[This enzyme is expressed in cutaneous infiltrates from patients with cutaneous T-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149424.RAhqPcmtpk-DHLGuDdhmi8xziQ7XA5QgZNB4FuK4O34J4130_provenance.
- NP149429.RAg9b2JQz6sfZmUp1QUrl7bGAAZLSJcHyJFyqjyTtkETA130_assertion description "[SHP2 positively regulates IL-2 induced MAPK activation in malignant T cells/may not be involved in the activation of Stat3 or Stat5 in cutaneous T-cell lymphoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149429.RAg9b2JQz6sfZmUp1QUrl7bGAAZLSJcHyJFyqjyTtkETA130_provenance.
- NP149430.RAose_YcqXzvH7nt656id7hmpySvJ-5vx-Esn4knAdTq8130_assertion description "[ILT2 triggering on cutaneous T-cell lymphoma (CTCL) cells leads to the recruitment of SHP-1 and to the specific inhibition of CTCL malignant cell proliferation in Sezary syndrome induced by CD3/T-cell receptor/TCR) stimulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149430.RAose_YcqXzvH7nt656id7hmpySvJ-5vx-Esn4knAdTq8130_provenance.
- NP149431.RAnPfNB-URcomXBHb4Nllb4XBt02_L_Ap77tupOpJlmN8130_assertion description "[SHP-1 loss correlates with, and may contribute to, progression of cutaneous T-cell lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149431.RAnPfNB-URcomXBHb4Nllb4XBt02_L_Ap77tupOpJlmN8130_provenance.
- NP149436.RAgp0Jt9wV4UD0TpV1G6JMwPlzU7FVnHMNuI6DyC493w4130_assertion description "[High expression of HDAC2 is more common in aggressive than indolent cutaneous T-cell lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149436.RAgp0Jt9wV4UD0TpV1G6JMwPlzU7FVnHMNuI6DyC493w4130_provenance.
- NP149437.RAqaYlJcZ_h8kWTsQUHPB9XFZDeF6GtcCVExh8xXO6eXk130_assertion description "[Nitric oxide induces apoptosis in cutaneous T-cell lymphoma by downregulating constitutive NF-kappAB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149437.RAqaYlJcZ_h8kWTsQUHPB9XFZDeF6GtcCVExh8xXO6eXk130_provenance.
- NP149439.RAtXAWBcF5qaaO2d0ymS3nMIAnx5fMXaA_lFsS_Qt_hBg130_assertion description "[Promoter hypermethylation of thrombospondin 4 is associated with cutaneous T-cell lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149439.RAtXAWBcF5qaaO2d0ymS3nMIAnx5fMXaA_lFsS_Qt_hBg130_provenance.
- NP149440.RArIIuCVxrtQq8HMvXukGkTQJDlNm5za1NOTYOSjV9Q1s130_assertion description "[The immunohistochemical expression of HDAC6 in cutaneous T-cell lymphoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149440.RArIIuCVxrtQq8HMvXukGkTQJDlNm5za1NOTYOSjV9Q1s130_provenance.
- NP149445.RAqUu-me2nsqMCuSEIcPb9KuLlNwvrXoEMD9AqPJ8RzgE130_assertion description "[genetic polymorphism of IFN-gamma may be an important risk factor to develop oral lesions of lichen planus, but an increase in the frequency of -308A TNF-alpha allele may best contribute to the development of additional skin involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149445.RAqUu-me2nsqMCuSEIcPb9KuLlNwvrXoEMD9AqPJ8RzgE130_provenance.
- NP149449.RAlDEFysaI2gwnUp06HyjC56m-f1AFAztOoNYA7vOrElc130_assertion description "[Type I IFN-mediated skin disorders, such as lichen planus, strongly express IDO in lesional skin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149449.RAlDEFysaI2gwnUp06HyjC56m-f1AFAztOoNYA7vOrElc130_provenance.
- NP149458.RAlTiiUz2DgNCLNREgqklh_oRKOtQqpBQ57Mg7C1pUbsM130_assertion description "[a TNF-alpha SNsingle-nucleotide polymorphism may be associated with increased risk of new intracranial hemorrhage in the natural course of brain arteriovenous malformations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149458.RAlTiiUz2DgNCLNREgqklh_oRKOtQqpBQ57Mg7C1pUbsM130_provenance.
- NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_assertion description "[An analysis of the genotype-phenotype correlation is consistent with a more common frequency of pulmonary arteriovenous malformations in patients with ENG mutations than in patients with ACVRL1 mutations in our collective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149461.RAvpCdzNrcU4HXkMqez655C6oCMa1aG1pneMdMYStqf8Q130_provenance.
- NP149463.RAhRDAEvlEbWv29iYH3eFiP_ZNhY_nrCKif9VHCRt0jp4130_assertion description "[key role of abnormal angiogenesis in arteriovenous malformation pathophysiology suggesting that a disruption in systemic VEGF expression may contribute to the natural history of these lesions ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149463.RAhRDAEvlEbWv29iYH3eFiP_ZNhY_nrCKif9VHCRt0jp4130_provenance.
- NP149464.RAmMdh_ZriW8wdUr_UZInz14-diCGO5FAH8jSIazbPC7Q130_assertion description "[ApoE epsilon2 carriers have an increased risk of intracerebral hemorrhage in brain arteriovenous malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149464.RAmMdh_ZriW8wdUr_UZInz14-diCGO5FAH8jSIazbPC7Q130_provenance.
- NP149474.RAt0QW4Ug0SbBwHUlj5ZleuKsPuWKMGT-xx3aHGOSW2Zw130_assertion description "[plays in the role in the pathogenesis of the otitis media with effusion (review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149474.RAt0QW4Ug0SbBwHUlj5ZleuKsPuWKMGT-xx3aHGOSW2Zw130_provenance.
- NP149475.RAu0XCpfZ4VU4KTXjgUgf3cQZxc4eEPwxor4PWBCVsR_E130_assertion description "[MMP-9 and MMP-2 are mediators of inflammation in chronic otitis media with effusion ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149475.RAu0XCpfZ4VU4KTXjgUgf3cQZxc4eEPwxor4PWBCVsR_E130_provenance.
- NP149477.RAoQsdDY-56zZCQ49NA8Ihy7gkuFIKzlcAmQMvND_G5Vk130_assertion description "[Results suggest that increased squamous metaplasia and lower BCL-6 expression in adenoids may be associated with increased susceptibility to otitis media with effusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149477.RAoQsdDY-56zZCQ49NA8Ihy7gkuFIKzlcAmQMvND_G5Vk130_provenance.
- NP149487.RAiCNkBCXebaJqGe4xbsdTREBaDaT57XrO_nxkVCoc5Ss130_assertion description "[data suggest that activity is reduced in the microvillous membrane of placentas from IUGR pregnancies; changes might impair function of Na (+) -coupled transporters and contribute to reduced growth of fetuses ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149487.RAiCNkBCXebaJqGe4xbsdTREBaDaT57XrO_nxkVCoc5Ss130_provenance.
- NP149500.RAqYdPO81Umx-m5POh7jORA25_KpFsFft6BR3CI7Ti4MQ130_assertion description "[Our results reveal the higher levels of maternal and umbilical sCD40L serum levels in pregnancy complicated by pre-eclampsia with and without intrauterine growth retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149500.RAqYdPO81Umx-m5POh7jORA25_KpFsFft6BR3CI7Ti4MQ130_provenance.
- NP149504.RAi7YxZS6FwR5P5DHWF2AwfSU8ujcXWeREqp-wvwqXwTs130_assertion description "[results indicate that TAP gene polymorphisms may have had a role in the development of bronchiectasis in our patient group ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149504.RAi7YxZS6FwR5P5DHWF2AwfSU8ujcXWeREqp-wvwqXwTs130_provenance.
- NP149505.RAh--NeK0_FOYsOv15vxTnZhWzCK_QSkFclbBXf6AIbpo130_assertion description "[results indicate that TAP gene polymorphisms may have had a role in the development of bronchiectasis in our patient group ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP149505.RAh--NeK0_FOYsOv15vxTnZhWzCK_QSkFclbBXf6AIbpo130_provenance.