Nanopublications LDF server

Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }

• NP135790.RAXgSuWBmHnz8faTUVHPWJEwWingqbm27u3R289USvUgA130_assertion description "[mutation in the ST14 gene is associated with recessive autosomal ichthyosis with hypotrichosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135790.RAXgSuWBmHnz8faTUVHPWJEwWingqbm27u3R289USvUgA130_provenance.
• NP135793.RAXjJwhaIElRGRw5dJ05x9A96V0iYmcKtayfzbNdU5ZRM130_assertion description "[presented a novel form of ichthyosis in a patient, termed hepoxilin A (3) synthase-linked ichthyosis (HXALI), whose scales expressed high levels of 12R-LOX, but were deficient of HXA (3) synthase [hepoxilin A3 synthase]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135793.RAXjJwhaIElRGRw5dJ05x9A96V0iYmcKtayfzbNdU5ZRM130_provenance.
• NP135798.RAUS9emZW9ekVRxAEPaPOfQdVgOP1_UU2CdzAszp07T6k130_assertion description "[the TNNI3 Pro82Ser alteration is likely a disease-modifying mutation in a severely affected individual, and, furthermore, carriers of this alteration (3% of African Americans) might be at increased risk of late-onset cardiac hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135798.RAUS9emZW9ekVRxAEPaPOfQdVgOP1_UU2CdzAszp07T6k130_provenance.
• NP135802.RAVSPUvDdZAs98XkPoRg-P-0ivlHFe5_tUwvfUwEKxpqo130_assertion description "[REVIEW: Cardiac adrenomedullin: its role in cardiac hypertrophy and heart failure ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135802.RAVSPUvDdZAs98XkPoRg-P-0ivlHFe5_tUwvfUwEKxpqo130_provenance.
• NP135809.RAbJb8leoEozABo-qpJ8Cbzw4XBZrlR89pIg5-fSEiC2s130_assertion description "[possible cellular & molecular mechanisms of IL-18-induced myocardial injury include induction of inflammation, increased apoptosis, cardiac hypertrophy, modulation of mitogen activated protein kinase activation, & changes in intracellular Ca [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135809.RAbJb8leoEozABo-qpJ8Cbzw4XBZrlR89pIg5-fSEiC2s130_provenance.
• NP135810.RAdyCArh-kHPwPmKVFvEydAU2eCMJr4pdMcYrHxYNJqJs130_assertion description "[Review concludes that this endogenous calcineurin inhibitor, calcipressin 1, may also play a role in a variety of human diseases, including Alzheimer's disease, Down syndrome and cardiac hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135810.RAdyCArh-kHPwPmKVFvEydAU2eCMJr4pdMcYrHxYNJqJs130_provenance.
• NP135812.RAd0-jFklTgP1wFc_FmeRZAf8Tp3HbSJDrWw2DHxUyvMM130_assertion description "[Gab1-SHP2 interaction plays a crucial role in gp130-dependent longitudinal elongation of cardiomyoctes and cardiac hypertrophy through activation of ERK5 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135812.RAd0-jFklTgP1wFc_FmeRZAf8Tp3HbSJDrWw2DHxUyvMM130_provenance.
• NP135817.RAScMpCJZhNwq9piIDCatG9PXegkW9bA-6UXRYOdmBE3o130_assertion description "[Activation of NHE1 is sufficient to generate Ca2+ signals that induce cardiac hypertrophy and heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135817.RAScMpCJZhNwq9piIDCatG9PXegkW9bA-6UXRYOdmBE3o130_provenance.
• NP135818.RAX8LuqWDUGoOXrlB4gAO-21iMm_1RnAqPoTV9VGgKiGA130_assertion description "[Enhanced activity of the cardiac Na+/H+ exchanger (NHE-1) after myocardial stretch is considered a key step of the signaling pathway leading to cardiac hypertrophy [REVIEW].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135818.RAX8LuqWDUGoOXrlB4gAO-21iMm_1RnAqPoTV9VGgKiGA130_provenance.
• NP135824.RAVnrXf30AJvzikPn9mC8toTljU-vbBJa5sTdL4H6xcbE130_assertion description "[Polymorphism A1166C contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy/mutated receptor has changed sensitivity to Angiotensine II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135824.RAVnrXf30AJvzikPn9mC8toTljU-vbBJa5sTdL4H6xcbE130_provenance.
• NP135829.RARmEpSSmCb1oGSYVyK3g_BD8kkQe-zca9wPvGIPjeY_I130_assertion description "[Specific phosphorylation events on ERK1/2 integrate differing upstream signals to induce cardiac hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135829.RARmEpSSmCb1oGSYVyK3g_BD8kkQe-zca9wPvGIPjeY_I130_provenance.
• NP135830.RAZ_o7U6Z-ffi2EJw1oOO3U8fL7lDYP-S0P2zkqODZ7Uk130_assertion description "[Lats2 affects both growth and death of cardiac myocytes, but it primarily regulates the size of the heart and acts as an endogenous negative regulator of cardiac hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135830.RAZ_o7U6Z-ffi2EJw1oOO3U8fL7lDYP-S0P2zkqODZ7Uk130_provenance.
• NP135831.RAb8rfgqxzGItLLq7Lopc4lW-vq-wNz79Ui5aUORGSP00130_assertion description "[Polymorphism of the NFATC4 gene plays a role in the development of human cardiac hypertrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135831.RAb8rfgqxzGItLLq7Lopc4lW-vq-wNz79Ui5aUORGSP00130_provenance.
• NP135833.RATFL1BP_rmDPjFMZTMi8jCdiL-XHYgH497bc-bFEZNp4130_assertion description "[corin gene single nucleotide polymorphism associated with hypertension and cardiac hypertrophy impair corin zymogen activation and natriuretic peptide processing activity ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135833.RATFL1BP_rmDPjFMZTMi8jCdiL-XHYgH497bc-bFEZNp4130_provenance.
• NP135839.RAUO1UIfo5Ob-X5rpkAUPjSyCdsGItuGeUHyzu2RDF53Y130_assertion description "[Diminished GP130 Abundance in congestive heart failure ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135839.RAUO1UIfo5Ob-X5rpkAUPjSyCdsGItuGeUHyzu2RDF53Y130_provenance.
• NP135847.RATJjx6cnFFKpsa37EBB8UmxkLLpohT3ZGjUqmRFxH6Js130_assertion description "[the heart and the lungs release adrenomedullin peptides in moderate congestive heart failure and this secretion breaks down in severe CHF ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135847.RATJjx6cnFFKpsa37EBB8UmxkLLpohT3ZGjUqmRFxH6Js130_provenance.
• NP135849.RAa1F40HQ4Czrm4VlzyeJLO2XPlBTmQQRfvPF7uLXmghY130_assertion description "[HDAC4 as a specific downstream substrate of CaMKIIdeltaB in cardiac cells and have broad applications for the signaling pathways leading to cardiac hypertrophy and heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135849.RAa1F40HQ4Czrm4VlzyeJLO2XPlBTmQQRfvPF7uLXmghY130_provenance.
• NP135853.RAdPqgHOZL5JeKvd1zPzNM0n1bBB5S3HrJPTMPNFL-AYw130_assertion description "[TGF-beta1/bFGF and ET-1 have different roles in graft fibrosis in heart failure patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135853.RAdPqgHOZL5JeKvd1zPzNM0n1bBB5S3HrJPTMPNFL-AYw130_provenance.
• NP135862.RAS37vL8UKw7V3gz1-GZ6lIvQ7BjM-WP83goIlhVAAUs4130_assertion description "[exaggerated urinary excretion of AQP-2 is dependent on baroreceptor-mediated release of arginine vasopressin in patients with congestive heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135862.RAS37vL8UKw7V3gz1-GZ6lIvQ7BjM-WP83goIlhVAAUs4130_provenance.
• NP135880.RAWBXListY1foEmRNADQbE8yHY5J7lF92yDMoAkaoFNjM130_assertion description "[report that an inherited human dilated cardiomyopathy with refractory congestive heart failure is caused by a dominant Arg -- > Cys missense mutation at residue 9 (R9C) in phospholamban ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135880.RAWBXListY1foEmRNADQbE8yHY5J7lF92yDMoAkaoFNjM130_provenance.
• NP135881.RATp20xPgUsJtMKzRLCu9j22je1ZHcHq6EkhbEpTe04mw130_assertion description "[although activation of PPARgamma appears to have beneficial effects on atherosclerosis and heart failure, it is still largely uncertain whether PPARgamma ligands prevent the development of cardiovascular diseases-REVIEW ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135881.RATp20xPgUsJtMKzRLCu9j22je1ZHcHq6EkhbEpTe04mw130_provenance.
• NP135884.RAfU0YQCGkhbYwfCMYgyON-zuEDazigw5cP6kdRWmd_E0130_assertion description "[Elevated in the aortic root of congestive heart failure/at least in part from the microcirculation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135884.RAfU0YQCGkhbYwfCMYgyON-zuEDazigw5cP6kdRWmd_E0130_provenance.
• NP135885.RAdGZIsRX1Ctq0zttfGQsTyVJY7meL3r4kaZ0WDoK7xeA130_assertion description "[Differential expression of apelin in patients with chronic heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135885.RAdGZIsRX1Ctq0zttfGQsTyVJY7meL3r4kaZ0WDoK7xeA130_provenance.
• NP135901.RARKyFV4pRtaP7REn5YuSjhNBhUsv3xLHhUVACMVwvODs130_assertion description "[The known effect of B cells in periodontitis would be partly mediated by salivary BAFF in patients with primary Sjogren's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135901.RARKyFV4pRtaP7REn5YuSjhNBhUsv3xLHhUVACMVwvODs130_provenance.
• NP135904.RAWE1QpNrgyKCB2dt7J81esJQAPeA_mkx_-l8deksZFiI130_assertion description "[promoter polymorphisms is associated with susceptibility to primary Sjogren's syndrome in Taiwan ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135904.RAWE1QpNrgyKCB2dt7J81esJQAPeA_mkx_-l8deksZFiI130_provenance.
• NP135907.RAc8DsIGmHKdx2zKg8m5E9dWq1oRJAb_OfiBGQxoWYy2Y130_assertion description "[Primary Sjogren's syndrome and systemic lupus erythematosus share IRF gene polymorphisms as a common genetic susceptibility factor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135907.RAc8DsIGmHKdx2zKg8m5E9dWq1oRJAb_OfiBGQxoWYy2Y130_provenance.
• NP135910.RAf2DZlbsyL6arkSXKxCZ7FsQyhPKh-kZcExnoUR-PdDE130_assertion description "[This study indicates that the increased type I IFN activity observed in Sjogren's syndrome patients is not only a local but also a systemic phenomenon and points to plasmacytoid dendritic cells as a possible source of this activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135910.RAf2DZlbsyL6arkSXKxCZ7FsQyhPKh-kZcExnoUR-PdDE130_provenance.
• NP135912.RASZfWozbA0j4PE7v6uk3nbU88qdJnpMztpgqtd3YE67c130_assertion description "[Abnormal STAT3 signalling in T cells from Sjogren's syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135912.RASZfWozbA0j4PE7v6uk3nbU88qdJnpMztpgqtd3YE67c130_provenance.
• NP135914.RAR80xW9FG-lpIp5JsOmXK3yBdYFbrcbwB8b45xAgC4U0130_assertion description "[Increased Ro/SSA 60 and La/SSB mRNA expression in minor salivary glands in primary Sjogren's syndrome (pSS) suggest that these these 2 autoantigens, but not Ro/SSA 52, are involved in the tissue-specific autoimmune response in pSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135914.RAR80xW9FG-lpIp5JsOmXK3yBdYFbrcbwB8b45xAgC4U0130_provenance.
• NP135917.RAcBam_LHEiv758enRHo89N5ynkBL4wVKPgPbVz6uCfv8130_assertion description "[Increased expression of Ro52 in patients may be directly involved in the reduced cellular proliferation and increased apoptotic cell death observed in Sjogren's syndrome and systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135917.RAcBam_LHEiv758enRHo89N5ynkBL4wVKPgPbVz6uCfv8130_provenance.
• NP135918.RAS2cQ-IVQN9rsk1wqghUFxdX94fek3GblfOFmyUxwqu4130_assertion description "[The in vivo role of alpha-fodrin autoantigen in primary Sjogren's syndrome was analyzed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135918.RAS2cQ-IVQN9rsk1wqghUFxdX94fek3GblfOFmyUxwqu4130_provenance.
• NP135937.RAcCEMKw-fZrpEtvu20tLjadPU2AsULMxnlgDqPyANePs130_assertion description "[The mean sFas values were found higher in rheumatoid arthritis (RA), polymyositis/dermatomyositis (PM/DM) and osteoarthritis (OA) than in control although no differences were found in systemic sclerosis (SSc) and Sjogren's syndrome (SS) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135937.RAcCEMKw-fZrpEtvu20tLjadPU2AsULMxnlgDqPyANePs130_provenance.
• NP135952.RAdSKQYmRIvyuToHinNfBeobrbL5dEu0Hug8Azp_sjP90130_assertion description "[Progressive GAA expansions of FXN protein in dorsal root ganglia of Friedreich's ataxia patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135952.RAdSKQYmRIvyuToHinNfBeobrbL5dEu0Hug8Azp_sjP90130_provenance.
• NP135958.RAX7o3BDOX7uNIpz-NMfEmzgRkLM2HlyR5KGRNM9ZbzWc130_assertion description "[Frataxin and cardiac troponin T gene mutations co-exist in a child with Friedreich ataxia and familial hypertrophic cardiomyopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135958.RAX7o3BDOX7uNIpz-NMfEmzgRkLM2HlyR5KGRNM9ZbzWc130_provenance.
• NP135961.RAXCql7w4J0rwxOE40Xi3VBAIaqDMvbRuVc9qia0i8wck130_assertion description "[These data suggest that increased proneness to caspase activation in lymphocytes could reflect an ongoing systemic response in neurodegenerative disease with pathogenetic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135961.RAXCql7w4J0rwxOE40Xi3VBAIaqDMvbRuVc9qia0i8wck130_provenance.
• NP135962.RAQtFxvhApNCOocnfdUmtWDXatp2ee2mabWOJj-9tJ7NY130_assertion description "[Calpain activation in neurodegenerative diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135962.RAQtFxvhApNCOocnfdUmtWDXatp2ee2mabWOJj-9tJ7NY130_provenance.
• NP135971.RAc85XpfwTW9MBUZayyEqHphnfAMYIl5OdXtct9tusWTs130_assertion description "[Trinucleotide repeat expansions of ataxin 7 may be involved in neurodegenerative diseases such as cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135971.RAc85XpfwTW9MBUZayyEqHphnfAMYIl5OdXtct9tusWTs130_provenance.
• NP135977.RARu8vFHRNogPOtCknW6O2CTLdsV-FtAWU2okd7Rl-xGU130_assertion description "[The present observations indicate modifications in the expression of constitutive Dyrk1A in the cytoplasm and nuclei of neurons in various neurodegenerative diseases associated with tau phosphorylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135977.RARu8vFHRNogPOtCknW6O2CTLdsV-FtAWU2okd7Rl-xGU130_provenance.
• NP135987.RAdfHdzLk62-0cuFte84SphIOMODRgkjBCVEhBFX-20MM130_assertion description "[Reviewer states that the role (s) of Bax in neuronal dysfunction and/or death may be dependent on the disease context/studies will determine whether Bax plays a broad role in death and dysfunction of neurons in neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135987.RAdfHdzLk62-0cuFte84SphIOMODRgkjBCVEhBFX-20MM130_provenance.
• NP135995.RAUxHUYSGI2Mp9u6wDRxnTaQXb8eFOYrPES_wRQYFXUc8130_assertion description "[can modulate the function of microglia and influence inflammatory changes such as those seen in neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135995.RAUxHUYSGI2Mp9u6wDRxnTaQXb8eFOYrPES_wRQYFXUc8130_provenance.
• NP135996.RAaUXqLCeSZXFy8yNIJbO5Yn_XTRns2HwhXN2p2-gAa9c130_assertion description "[results suggest that interactions between alpha-synuclein and tau can promote their fibrillization and drive the formation of pathological inclusions in human neurodegenerative diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135996.RAaUXqLCeSZXFy8yNIJbO5Yn_XTRns2HwhXN2p2-gAa9c130_provenance.
• NP135999.RAerJMpJFSUhF8XcSz2iFkJQtpqa_2vveMSk4KUCTQZjs130_assertion description "[Deciphering the precise role of VEGF at the neurovascular interface promises to uncover new insights into the development and pathology of the nervous system, helpful to design novel strategies to treat (motor) neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135999.RAerJMpJFSUhF8XcSz2iFkJQtpqa_2vveMSk4KUCTQZjs130_provenance.
• NP136000.RAdXmzUWt3nwCsuSafVmoBRRaBzmc5fbS92IpNGeaE5_o130_assertion description "[These data suggest that increased proneness to caspase activation in lymphocytes could reflect an ongoing systemic response in neurodegenerative disease with pathogenetic implications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136000.RAdXmzUWt3nwCsuSafVmoBRRaBzmc5fbS92IpNGeaE5_o130_provenance.
• NP136002.RAcKj8Sg33IBPNvKcP3VJ5gYJWXRnpQQ9go0-XlYtvGHM130_assertion description "[Neuroprotective role for SCF in cortical neurons, an effect mediated by Akt and ERK, as well as NFkappaB-mediated gene transcription/represents a novel therapeutic target in the treatment of neurodegenerative disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136002.RAcKj8Sg33IBPNvKcP3VJ5gYJWXRnpQQ9go0-XlYtvGHM130_provenance.
• NP136012.RAWFbnvaz7VfYxc0n0hDol8IIjk-vRFk-o4WV6XNSqaHg130_assertion description "[The intronic GAA repeat expansion in the FXN gene causes the hereditary neurodegenerative disorder Friedreich ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136012.RAWFbnvaz7VfYxc0n0hDol8IIjk-vRFk-o4WV6XNSqaHg130_provenance.
• NP136013.RAXxAdWYGTS2JmIswMAc1ybgvgU0Wwl7iKtFkMYf7jbvU130_assertion description "[Mitochondrial UCPs precondition neurons by dissociating cellular energy production from that of free radicals to withstand the harmful effects of cellular stress occurring in a variety of neurodegenerative disorders, including epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136013.RAXxAdWYGTS2JmIswMAc1ybgvgU0Wwl7iKtFkMYf7jbvU130_provenance.
• NP136014.RAUwB-BAZtWdsOteWTB3-fwnFC4BWW9KWtauARRpzFZOQ130_assertion description "[neuroprotection in the thalamus correlated with a high expression of UCP2, which is neuroprotective in a number of models of neurodegenerative diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136014.RAUwB-BAZtWdsOteWTB3-fwnFC4BWW9KWtauARRpzFZOQ130_provenance.
• NP136016.RAT_l3H7Hdl_mREBKHkffl25npbB6Lm5-36CNMD8NE4Q4130_assertion description "[GDNF-mediated, autoregulatory long-lasting feedback loop could have important implications for GDNF's potential value as a treatment for addiction and neurodegenerative diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136016.RAT_l3H7Hdl_mREBKHkffl25npbB6Lm5-36CNMD8NE4Q4130_provenance.
• NP136017.RAfAFQe0ne3L22tzsrMLVRvDL64P7RuYJjtpeM5BfXo0I130_assertion description "[insulin-like growth factor I signaling has a role in neurodegenerative diseases (review) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136017.RAfAFQe0ne3L22tzsrMLVRvDL64P7RuYJjtpeM5BfXo0I130_provenance.
• NP136019.RAV0fepiyJCQgAqEmqtiRNP1Cjg80JtY7UosHhhjEco2M130_assertion description "[There are many precedents in neurodegenerative disease in which rare single-gene mutations have given great insight into understanding disease processes, which is why the TDP-43 mutations are potentially very important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136019.RAV0fepiyJCQgAqEmqtiRNP1Cjg80JtY7UosHhhjEco2M130_provenance.
• NP136021.RAQs4gZgGrLQvr_pv4WJYwVX3qifLrFPAzbojNon0hOGE130_assertion description "[Therefore, Bcl-X (L), a promising therapeutic candidate for ischemia and neurodegenerative diseases, is only of partial efficacy in preventing the direct neurotoxicity of pneumolysin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136021.RAQs4gZgGrLQvr_pv4WJYwVX3qifLrFPAzbojNon0hOGE130_provenance.
• NP136022.RAS_6DT0_3VvsdBWnqhKXxEl25oy3kAq4VP48vNjgWJpQ130_assertion description "[Mitochondrial HSP60 chaperonopathy causes an autosomal-recessive neurodegenerative disorder linked to brain hypomyelination and leukodystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136022.RAS_6DT0_3VvsdBWnqhKXxEl25oy3kAq4VP48vNjgWJpQ130_provenance.
• NP136024.RAbqPVol8fdctIUmq4Hk91zBJD-WcTEQdGrkcSNnwUWaY130_assertion description "[Wnt/beta-catenin signaling has a role in neurodevelopment as well as in neurodegenerative diseases [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136024.RAbqPVol8fdctIUmq4Hk91zBJD-WcTEQdGrkcSNnwUWaY130_provenance.
• NP136031.RAawSXLEiFS8XgdzI2RlFfpg3vymctb88ANhK6_h4eg3o130_assertion description "[dysfunction of PQBP-1 induces mitochondrial stress, a key molecular pathomechanism that is shared among human neurodegenerative disorders ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136031.RAawSXLEiFS8XgdzI2RlFfpg3vymctb88ANhK6_h4eg3o130_provenance.
• NP136034.RAdtlINfkJqyRh00XQEtt3PkK6YulSCVJtugwpZwv-2yw130_assertion description "[Polymorphism is associated with neurodegenerative diseases, notably Alzheimer disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136034.RAdtlINfkJqyRh00XQEtt3PkK6YulSCVJtugwpZwv-2yw130_provenance.
• NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_assertion description "[Variant-specific causal involvement of AChE in the progression of both neurodegenerative diseases and neuromuscular syndromes raises the possibility that future therapeutic drugs might target specific AChE variant (s) or the corresponding RNA transcripts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136037.RAeTGvdE_er2j4YeQieEnSlqOduKxSlBtZnoeOxSt73jE130_provenance.
• NP136038.RAb4rJrnDaUoq-geRa797LgQPMeihfl2Hznn1kOL2e0FE130_assertion description "[Synphilin-1A may contribute to neuronal degeneration in alpha-synuclein mutations and provides insights into the role of inclusion bodies in neurodegenerative disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136038.RAb4rJrnDaUoq-geRa797LgQPMeihfl2Hznn1kOL2e0FE130_provenance.
• NP136059.RAcTu6VAz99rKL2IWLbuJ9to0o3arWpbYR-kAskfx1O-s130_assertion description "[TROPONIN I mutations in familial hypertrophic cardiomyopathy affect the regulatory processes involving TROPONIN I and increased the Ca (2+) sensitivity of cardiac muscle contraction ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136059.RAcTu6VAz99rKL2IWLbuJ9to0o3arWpbYR-kAskfx1O-s130_provenance.
• NP136070.RAYkU-jsCjtd_guDbXZ6h2kridbJ4dgxms080rgTgvzKs130_assertion description "[children with sickle cell anemia with poor growth had significantly more proteolyzed IGFBP-3 in serum compared to children with normal growth ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136070.RAYkU-jsCjtd_guDbXZ6h2kridbJ4dgxms080rgTgvzKs130_provenance.
• NP136075.RAUvs-rYKLfyudUxL6eAKqROsvMTk9CXrXl0nK8JnRz8Q130_assertion description "[B-CAM/LU is the most critical receptor mediating adhesion to laminin under both static and flow conditions in sickle cell anemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136075.RAUvs-rYKLfyudUxL6eAKqROsvMTk9CXrXl0nK8JnRz8Q130_provenance.
• NP136078.RAZ0CbN1L496SLJkX88TNGb9f6hWnti_IJEUG66njEKjk130_assertion description "[FY- status was strongly associated with chronic organ damage and proteinuria in sickle cell anemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136078.RAZ0CbN1L496SLJkX88TNGb9f6hWnti_IJEUG66njEKjk130_provenance.
• NP136091.RAS8IhjwPkAfLuE16phFlPrGSi9KG0cm8U0MlaJXsBvxI130_assertion description "[Review/effects of alpha-globin genotype on the pathophysiology of sickle cell anemia, HbSC disease, and sickle beta-thalassemia are studied.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136091.RAS8IhjwPkAfLuE16phFlPrGSi9KG0cm8U0MlaJXsBvxI130_provenance.
• NP136093.RAf2eINAKRbjEVWgoK94Np3abETgwGsWyjuR2Gx4rjeDg130_assertion description "[Aberrant Cdx2 expression in pyloric gland adenoma of the gallbladder is closely associated with nuclear beta-catenin expression and squamous morule in contrast with intestinal metaplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136093.RAf2eINAKRbjEVWgoK94Np3abETgwGsWyjuR2Gx4rjeDg130_provenance.
• NP136096.RAbiOhbYhjBYrDawk4ht3ZVT4RPnYoop0Qo4EwQ_b7RCE130_assertion description "[expression of CDX2 precedes expression of CDX1 during the progression of intestinal metaplasia; expression of CDX2 may trigger the initiation and development of intestinal metaplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136096.RAbiOhbYhjBYrDawk4ht3ZVT4RPnYoop0Qo4EwQ_b7RCE130_provenance.
• NP136102.RAXURApHR0Nr68YoTfJINA0VB3-rktQ4MoMSo-UFS11LI130_assertion description "[We found a 60% increase in risk of intestinal metaplasia (IM) and dysplasia combined (OR 1.62, 95% CI: 1.10-2.38) among the carriers of the IL10-1082 low activity allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136102.RAXURApHR0Nr68YoTfJINA0VB3-rktQ4MoMSo-UFS11LI130_provenance.
• NP136103.RAUCXeQDLDa_dC7L-i4Dsh8Ez8hl375DBIIQXNh4t8-Ic130_assertion description "[Among host genetic factors contributing to H.pylori disease outcome, IL-10 -819 TT genotype favors intestinal metaplasia and non-cardia gastric cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136103.RAUCXeQDLDa_dC7L-i4Dsh8Ez8hl375DBIIQXNh4t8-Ic130_provenance.
• NP136104.RAVVVLrINC0uQNPScpYvW_AENpFTS6j1d4ZLyEUTJigV4130_assertion description "[Changing pattern of cytokeratin 7 and 20 expression from normal epithelium to intestinal metaplasia of the gastric mucosa and gastroesophageal junction ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136104.RAVVVLrINC0uQNPScpYvW_AENpFTS6j1d4ZLyEUTJigV4130_provenance.
• NP136107.RAfrq-re3yGytkNSNsquBkSdcX2D3V6XIOu8jgKELvRss130_assertion description "[p53 mutations reflected histological progression in Barrett's patients with p53 mutations found in 30% of metaplasia patients (P = 0.4) and low-grade dysplasia patients (P = 0.33).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136107.RAfrq-re3yGytkNSNsquBkSdcX2D3V6XIOu8jgKELvRss130_provenance.
• NP136113.RAf_VDiVaunvDoSUxm5V0n31TC5rDcdD5rFqBha6gWB3g130_assertion description "[The stronger Shh expression in intestinal metaplasia and gastric adenoma indicates that hedgehog protein is involved at an early phase of gastric carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136113.RAf_VDiVaunvDoSUxm5V0n31TC5rDcdD5rFqBha6gWB3g130_provenance.
• NP136120.RAcuphn0ZW1ICscelJ5-q9wDBXOdH3ylpAevwT3ZXU6KM130_assertion description "[Demethylation of the CDX1 promoter may be the key to the induction and maintenance of its expression and so of the Barrett's metaplasia phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136120.RAcuphn0ZW1ICscelJ5-q9wDBXOdH3ylpAevwT3ZXU6KM130_provenance.
• NP136126.RATVGPQ3aWsmOwtR0Huci7xKlz-G5PAYEPMqkbetiCXwc130_assertion description "[SPRR1B is a valid biomarker for the study of the molecular mechanisms of squamous metaplasia/is a definitive link between inflammation and squamous metaplasia in autoimmune-mediated dry eye disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136126.RATVGPQ3aWsmOwtR0Huci7xKlz-G5PAYEPMqkbetiCXwc130_provenance.
• NP136127.RAf8TLmw0QxX696kSFSz_YvzUXJeil1sCm9uDfHtLxxJU130_assertion description "[Claudin tight junction proteins in endoscopy biopsy samples showed Barrett's metaplasia contains more claudin-2 and claudin-3 than found in normal esophageal mucosa, but markedly lower claudins 1 and 5, indicating very different tight junction barriers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136127.RAf8TLmw0QxX696kSFSz_YvzUXJeil1sCm9uDfHtLxxJU130_provenance.
• NP136128.RAcpqZNOfbhqEV1vhvxxQ7rQOYYJDk5arqjoAd2WLlatY130_assertion description "[The expression of VEGF in intestinal metaplasia and gastric dysplasia, which could signify an early angiogenic switch during tumorigenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136128.RAcpqZNOfbhqEV1vhvxxQ7rQOYYJDk5arqjoAd2WLlatY130_provenance.
• NP136130.RAXh665tJ9_0CQpX2JVNUEPxx0XWVnDnIXVH9YB_C488s130_assertion description "[Increasing COX-2 expression in Barrett's metaplasia is significantly associated with a change in the local inflammatory reaction, but not during further progression through dysplasia to cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136130.RAXh665tJ9_0CQpX2JVNUEPxx0XWVnDnIXVH9YB_C488s130_provenance.
• NP136136.RAcXHHMJW6niBnBikWXDrbl4DAUJbM6n9SNJXAFfdb-es130_assertion description "[CYP2E1 polymorphisms are associated with incomplete intestinal metaplasia in a high-risk area of stomach cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136136.RAcXHHMJW6niBnBikWXDrbl4DAUJbM6n9SNJXAFfdb-es130_provenance.
• NP136139.RAYt1zbwTy3gTdaOI5LPwE4BuXf0JexHAKG-PwCEDQpcs130_assertion description "[FAS and FASL genotypes of the hosts are important determinants in the pathogenesis of gastric atrophy and intestinal metaplasia in H.pylori-infected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136139.RAYt1zbwTy3gTdaOI5LPwE4BuXf0JexHAKG-PwCEDQpcs130_provenance.
• NP136140.RATvOkK8A_9QCX1FHiwQRqrP83t2RrKJr1Bchb7uPdSS0130_assertion description "[CD1a may be a novel biomarker for Barrett metaplasia and that its expression may help to predict the prognosis of this pathology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136140.RATvOkK8A_9QCX1FHiwQRqrP83t2RrKJr1Bchb7uPdSS0130_provenance.
• NP136145.RAQGsSeCE6oTjWUF0wtqtPwPmQuefWZB4fLjws9zbOrcQ130_assertion description "[Cdx2 plays an important role in the regulation of intestinal claudin expression not only in gastric mucosa with intestinal metaplasia but also gastric carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136145.RAQGsSeCE6oTjWUF0wtqtPwPmQuefWZB4fLjws9zbOrcQ130_provenance.
• NP136153.RAWVX9zuVTtZZudiI_R1ngsVTnHAw0xO5BLa9T2sZc6pM130_assertion description "[ER-B1, ER-B2, ER-B3 and ER-B5 are overexpressed in esophageal adenocarcinoma compared to its precursor lesion, Barrett's metaplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136153.RAWVX9zuVTtZZudiI_R1ngsVTnHAw0xO5BLa9T2sZc6pM130_provenance.
• NP136155.RAeuvOcjKD4_QSYE17mHDNYqK7k9Dx_q7OZz81cb1enoc130_assertion description "[Transformation associated with reflux at the gastroesophageal junction reflects activation by bile acid and acid of a transcriptional program involving NF-kappaB and Cdx2, which mediate intestinal metaplasia and ectopic expression of GC-C.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136155.RAeuvOcjKD4_QSYE17mHDNYqK7k9Dx_q7OZz81cb1enoc130_provenance.
• NP136158.RASClTHVfx6hJO11rwoNGgTeGw159F9uyOPOmk545CPA0130_assertion description "[Describe a novel dominant pathogenic GJB2 mutation in a family affected with bilateral mild/moderate high-frequency hereditary non-syndromic sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136158.RASClTHVfx6hJO11rwoNGgTeGw159F9uyOPOmk545CPA0130_provenance.
• NP136159.RAd8t7GVN3KEO13b8wyJI_YV-kbdrfRRTwWC8bP4UbRt8130_assertion description "[Mutations in GJB2, encoding the gap junction beta-2 protein Connexin 26, are associated with autosomal recessive nonsyndromic sensorineural hearing loss (NSHL), autosomal dominant NSHL, and several forms of syndromic sensorineural hearing loss ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136159.RAd8t7GVN3KEO13b8wyJI_YV-kbdrfRRTwWC8bP4UbRt8130_provenance.
• NP136160.RAX59YFoDz6g3egslcCJ-cmKmYQDbVagzNVI0MCpIipck130_assertion description "[findings suggest that loci other than GJB2 and GJB6 contribute to the pathogenesis of autosomal recessive-nonsyndromic sensorineural hearing loss and that the full spectrum of GJB2 sequence changes is not yet fully elucidated ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136160.RAX59YFoDz6g3egslcCJ-cmKmYQDbVagzNVI0MCpIipck130_provenance.
• NP136161.RAamjUiEt-u20KLa1C9qJGq0FctizvNB_fOVVzJfP9XZ8130_assertion description "[Clinical data showed a bilateral sensorineural hearing loss for children with GJB2 35delG/35delG genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136161.RAamjUiEt-u20KLa1C9qJGq0FctizvNB_fOVVzJfP9XZ8130_provenance.
• NP136165.RAfVjfbhtFnBdKJ5CjHXfmvo2Q0pxoxj50WCZnPzzuOCc130_assertion description "[Heterozygous missense mutation in sensorineural hearing loss, striate palmoplantar hyperkeratosis and knuckle pads.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136165.RAfVjfbhtFnBdKJ5CjHXfmvo2Q0pxoxj50WCZnPzzuOCc130_provenance.
• NP136169.RAZyVZ2xV1ciuIJ1y0Zc7HM1RpWF2Zna7ddbmaDvL-FpI130_assertion description "[eNOS gene affects the red blood cell deformability, so possibly contributing to idiopathic sudden sensorineural hearing loss ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136169.RAZyVZ2xV1ciuIJ1y0Zc7HM1RpWF2Zna7ddbmaDvL-FpI130_provenance.
• NP136173.RAfQgFgHCIj0SxuBjyCNQodOx3vrtTmsHEWNevrf5NscU130_assertion description "[one-third (3 out of 9) autosomal dominant low frequency sensorineural hearing loss (LFSNHL) families had mutations in WFS1, indicating that in non-syndromic hearing loss WFS1 is restrictively & commonly found within autosomal dominant LFSNHL families ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136173.RAfQgFgHCIj0SxuBjyCNQodOx3vrtTmsHEWNevrf5NscU130_provenance.
• NP136175.RAXRLGliuGT9CSkHeZ4wpxQ74_euQJZ2PlrshpvfdlpjU130_assertion description "[a novel heterozygous missense mutation in exon 8 of WFS1 (i.e., Y669H) which is likely responsible for the low-frequency sensorineural hearing loss (LFSNHL) phenotype in a Taiwanese family was discovered ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136175.RAXRLGliuGT9CSkHeZ4wpxQ74_euQJZ2PlrshpvfdlpjU130_provenance.
• NP136185.RAcXRJfFQTuAhm4sW1n1Mv3XdjH_eqgALrOSzEKc0XT0s130_assertion description "[Patient with HLA-DRB1 phenotype are genetically susceptible for sudden sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136185.RAcXRJfFQTuAhm4sW1n1Mv3XdjH_eqgALrOSzEKc0XT0s130_provenance.
• NP136188.RASqlmzLaECXzqVuHob2EUVsPM_xj_ihUgrvlDj4Ue_KQ130_assertion description "[Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136188.RASqlmzLaECXzqVuHob2EUVsPM_xj_ihUgrvlDj4Ue_KQ130_provenance.
• NP136189.RAUKZKL27R5o7MPhPETCyu_kyWHJwjp_UJfJbNqXr9FQY130_assertion description "[Multiple mutations of MYO1A, a cochlear-expressed gene, were studied in sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136189.RAUKZKL27R5o7MPhPETCyu_kyWHJwjp_UJfJbNqXr9FQY130_provenance.
• NP136194.RAWUN79i56iK7FxO5qMkhX8a1Zih2BWk8U5yVGTLf1Qug130_assertion description "[findings suggest that loci other than GJB2 and GJB6 contribute to the pathogenesis of autosomal recessive-nonsyndromic sensorineural hearing loss and that the full spectrum of GJB2 sequence changes is not yet fully elucidated ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136194.RAWUN79i56iK7FxO5qMkhX8a1Zih2BWk8U5yVGTLf1Qug130_provenance.
• NP136202.RAYfUgPZDTGntxVgtn5NyAW--n3PyNvR8MRbQbqPzTGWE130_assertion description "[An increase in fasting insulin levels is associated with an 8.6- to 14.8-fold increased risk of presenting with colonic adenomas in acromegaly ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136202.RAYfUgPZDTGntxVgtn5NyAW--n3PyNvR8MRbQbqPzTGWE130_provenance.
• NP136213.RAUtroTBeamB685tJd7okZ9WwcSFtylalov7zwkkbIs2o130_assertion description "[it is proposed that absence of NOD2/TLR4 cross-tolerance as a central mechanism for the increased susceptibility to Crohn's disease in individuals with 3020insC NOD2 mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136213.RAUtroTBeamB685tJd7okZ9WwcSFtylalov7zwkkbIs2o130_provenance.
• NP136216.RAf7qDl22rniyE-sFXImNUyO_5uamKvRleTVDtJEnmG_4130_assertion description "[The effect of NOD2 activation on TLR2-mediated cytokine responses is dependent on activation dose and NOD2 genotype in Crohn's Disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136216.RAf7qDl22rniyE-sFXImNUyO_5uamKvRleTVDtJEnmG_4130_provenance.
• NP136220.RAdKB7vX0gUhS7ykmp4vK3Mq8aM9ZbkdsejgCY_b4MWqY130_assertion description "[Differential up-regulation of CD103 expression on lamina propria lymphocytes in Crohn's disease may indicate differential humoral or cellular regulation in inducing CD103 molecules on lymphocytes in patients with this disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136220.RAdKB7vX0gUhS7ykmp4vK3Mq8aM9ZbkdsejgCY_b4MWqY130_provenance.
• NP136222.RAYSmhSiIN5U62cz-UNTc756srNlJolBrQLiL341zYCo8130_assertion description "[The up-regulation of PDX-1 may be an important mechanism in the induction of the Ulcer-associated cell lineage in Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136222.RAYSmhSiIN5U62cz-UNTc756srNlJolBrQLiL341zYCo8130_provenance.
• NP136231.RAaCqqpNTZ82qmrNurK0Nkf9IcOdN9anCBALivGVYR-mA130_assertion description "[IL-4 and IL-13 mediate the hypercontractility of intestinal muscle via a STAT6 pathway at the level of the smooth muscle cell/STAT6 pathway may contribute to the hypercontractility of intestinal muscle in Crohn's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136231.RAaCqqpNTZ82qmrNurK0Nkf9IcOdN9anCBALivGVYR-mA130_provenance.
• NP136235.RAQ-6bugifv-khyjYYhprKAF7qLK4KkAHnOYK1PLtR0WM130_assertion description "[variations in MASP2 appear to be of limited importance in the pathogenesis of Crohn's disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136235.RAQ-6bugifv-khyjYYhprKAF7qLK4KkAHnOYK1PLtR0WM130_provenance.
• NP136236.RAW6Ury-J1wHEXzqeU6NWDDiyVIepuoFgetumXtIHomZg130_assertion description "[FcgammaRI is hyperexpressed in the intestinal mast cells of Crohn disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP136236.RAW6Ury-J1wHEXzqeU6NWDDiyVIepuoFgetumXtIHomZg130_provenance.

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