Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP30164.RAYXo7JqvdZEC1eNtN7nXk2QUyvPE1Ln0Vq-1JMCTv50Q130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30164.RAYXo7JqvdZEC1eNtN7nXk2QUyvPE1Ln0Vq-1JMCTv50Q130_provenance.
- NP30166.RARIP8DM9vXxRXe76ygb2es3xBHmx9IhrqQPi1XGezhYA130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30166.RARIP8DM9vXxRXe76ygb2es3xBHmx9IhrqQPi1XGezhYA130_provenance.
- NP30170.RAYcJemL4hpR5btn43dH_LuI9Fg6vX9rpJ0UkUgG3xLdU130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30170.RAYcJemL4hpR5btn43dH_LuI9Fg6vX9rpJ0UkUgG3xLdU130_provenance.
- NP30184.RAVvEcqaBdB-3Fh9Ar6JuQySqCYO0d6HZ-U31VnwydGKA130_assertion description "[Genetic factors in congenital diaphragmatic hernia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30184.RAVvEcqaBdB-3Fh9Ar6JuQySqCYO0d6HZ-U31VnwydGKA130_provenance.
- NP30185.RAfPfQgJY78GCKCdK6R9aBPyp1B7mC3SzzFxbMAh_DHEY130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30185.RAfPfQgJY78GCKCdK6R9aBPyp1B7mC3SzzFxbMAh_DHEY130_provenance.
- NP30187.RARSThne10dU1tI8ZADTIQxj8h-JI4OkyFIBh1Map1WWA130_assertion description "[Here we demonstrate that loss of a neuron-specific transmembrane protein, SLIT and NTRK-like protein-5 (Slitrk5), leads to OCD-like behaviors in mice, which manifests as excessive self-grooming and increased anxiety-like behaviors, and is alleviated by the selective serotonin reuptake inhibitor fluoxetine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30187.RARSThne10dU1tI8ZADTIQxj8h-JI4OkyFIBh1Map1WWA130_provenance.
- NP30201.RAfTDore2sL8BfThl5aJZoRrKvp-Yb4EzWxvS9QmXxyPE130_assertion description "[Expression and location of Smad2, 4 mRNAs during and after liver fibrogenesis of rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30201.RAfTDore2sL8BfThl5aJZoRrKvp-Yb4EzWxvS9QmXxyPE130_provenance.
- NP30214.RAf_PTfBQARLDVDhCJ6vD7X5_XfZ510RvriBIccpu8Fw8130_assertion description "[Of these genes, five (TP53, CDKN2A, SMAD4, ARID1A and PIK3CA) have previously been implicated in EAC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30214.RAf_PTfBQARLDVDhCJ6vD7X5_XfZ510RvriBIccpu8Fw8130_provenance.
- NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30218.RAQqW_bdH22jz5JqWz_f98_WqLJikMkZ-XLwV-JYQWG0A130_provenance.
- NP30219.RAXXtwk1wQLYV_n6RVseHprKLzbBf6nW22m_gy8JOPNow130_assertion description "[SMAD4 levels and response to 5-fluorouracil in colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30219.RAXXtwk1wQLYV_n6RVseHprKLzbBf6nW22m_gy8JOPNow130_provenance.
- NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_assertion description "[Using exome sequencing of individuals with Myhre syndrome, we identified SMAD4 as a candidate gene that contributes to this syndrome on the basis of its pivotal role in the bone morphogenetic pathway (BMP) and transforming growth factor (TGF)- signaling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30222.RASvMs93JchOYeJ3cInjw0OGL6RbeBYKHj4aoVMtFu_n8130_provenance.
- NP30224.RAWZRiPpZhHaVxP1Y6FUNFblLRXuccCU5Ls3lRRTHfmqo130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30224.RAWZRiPpZhHaVxP1Y6FUNFblLRXuccCU5Ls3lRRTHfmqo130_provenance.
- NP30225.RAX_fvD9RKHY2Ygb9KBszzfUPcHABwizCqYXOUkhs2K70130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30225.RAX_fvD9RKHY2Ygb9KBszzfUPcHABwizCqYXOUkhs2K70130_provenance.
- NP30227.RAQtnE7FDDe3ty16QT_6mWaN60O5TJ35z282Ig5X8GzvI130_assertion description "[Exome sequencing of liver fluke-associated cholangiocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30227.RAQtnE7FDDe3ty16QT_6mWaN60O5TJ35z282Ig5X8GzvI130_provenance.
- NP30228.RAUB7XZ3-Xbc4CxwwBCeNsXKgdHUzCeOSpv-KpyxxD6so130_assertion description "[Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30228.RAUB7XZ3-Xbc4CxwwBCeNsXKgdHUzCeOSpv-KpyxxD6so130_provenance.
- NP30233.RARPz8HjIcZEslLpqIw1WbJX9fAndy6tGr7mMM9GrFagA130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30233.RARPz8HjIcZEslLpqIw1WbJX9fAndy6tGr7mMM9GrFagA130_provenance.
- NP30237.RAUDi4KP_0j8VQeWKSV241RccOyvPdcPoDSSyRpvLF7g8130_assertion description "[We identified 70 genes that were recurrently mutated in Burkitt lymphomas, including ID3, GNA13, RET, PIK3R1 and the SWI/SNF genes ARID1A and SMARCA4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30237.RAUDi4KP_0j8VQeWKSV241RccOyvPdcPoDSSyRpvLF7g8130_provenance.
- NP30238.RAfTwKMnFZ1uPePQi4eWucSOEu_SnYs6cn6LmCP2C9Ym8130_assertion description "[Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30238.RAfTwKMnFZ1uPePQi4eWucSOEu_SnYs6cn6LmCP2C9Ym8130_provenance.
- NP30243.RAfcI2BQaIuqIfI01UOcgp8uC9NR3YyhBppHg24XgkMWI130_assertion description "[Varied pathways of stage IA lung adenocarcinomas discovered by integrated gene expression analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30243.RAfcI2BQaIuqIfI01UOcgp8uC9NR3YyhBppHg24XgkMWI130_provenance.
- NP30244.RAWU-4TSbbUwnS_y91sI60dAwejGAja1sSKCVsHSrYjPk130_assertion description "[Varied pathways of stage IA lung adenocarcinomas discovered by integrated gene expression analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30244.RAWU-4TSbbUwnS_y91sI60dAwejGAja1sSKCVsHSrYjPk130_provenance.
- NP30248.RAUh6MUOTX-PkaTgm0zictvs8y5c6vh1w3kbqu0ktZ15I130_assertion description "[The mutational landscape of adenoid cystic carcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30248.RAUh6MUOTX-PkaTgm0zictvs8y5c6vh1w3kbqu0ktZ15I130_provenance.
- NP30254.RAW6T7amkEACtOXLB9sF7d_Zf1QWpWbq4VPH7nEhcwB3A130_assertion description "[Collectively, these results substantiate a sequence independent role of SMN's C-terminus in protein stability and provide the first in vivo evidence supporting translational readthrough as a therapeutic strategy for the treatment of SMA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30254.RAW6T7amkEACtOXLB9sF7d_Zf1QWpWbq4VPH7nEhcwB3A130_provenance.
- NP30255.RAalj-ps6O7Kw6VxIPG2v3Yt1rOWlL1xng1vfJrSvykt8130_assertion description "[Disruption of the Survival Motor Neuron (SMN) gene in pigs using ssDNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30255.RAalj-ps6O7Kw6VxIPG2v3Yt1rOWlL1xng1vfJrSvykt8130_provenance.
- NP30257.RAVr9sSuoy742zbdhCICBce_6JTlmf8VPlBVGxM5XMjAU130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30257.RAVr9sSuoy742zbdhCICBce_6JTlmf8VPlBVGxM5XMjAU130_provenance.
- NP30265.RAYPhiUk_QLcZe0Z3msxp2i0JwM4deIMA7t1oQH9q6nhE130_assertion description "[Missense mutations in SMOH in sporadic basal cell carcinomas of the skin and primitive neuroectodermal tumors of the central nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30265.RAYPhiUk_QLcZe0Z3msxp2i0JwM4deIMA7t1oQH9q6nhE130_provenance.
- NP30266.RAXYd3IHEEtgDTQ5WgIP4g4RJdYtg5ShRizkMfNaIXL1w130_assertion description "[Polyamine oxidase and acrolein as novel biochemical markers for diagnosis of cerebral stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30266.RAXYd3IHEEtgDTQ5WgIP4g4RJdYtg5ShRizkMfNaIXL1w130_provenance.
- NP30268.RAd_V7qM5S1EEletabQNT_6HK_ZoL7fCeXNNsbEOLrBF0130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30268.RAd_V7qM5S1EEletabQNT_6HK_ZoL7fCeXNNsbEOLrBF0130_provenance.
- NP30275.RAd6q_2odBZplG-xBva3k0XFXJi1YFWDCneGyN-ndfAFo130_assertion description "[Multiple recurrent genetic events converge on control of histone lysine methylation in medulloblastoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30275.RAd6q_2odBZplG-xBva3k0XFXJi1YFWDCneGyN-ndfAFo130_provenance.
- NP30282.RAWRUZnBrkasV8WkwX2p6rLr9NJnD1W36T9Skoezxtld0130_assertion description "[Chemical genomic screening for methylation-silenced genes in gastric cancer cell lines using 5-aza-2'-deoxycytidine treatment and oligonucleotide microarray.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30282.RAWRUZnBrkasV8WkwX2p6rLr9NJnD1W36T9Skoezxtld0130_provenance.
- NP30284.RAVNIKKLEeNFhzcHFzAyZUtYOC57ela634GglanabnX8A130_assertion description "[Discovery of deregulation of zinc homeostasis and its associated genes in esophageal squamous cell carcinoma using cDNA microarray.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30284.RAVNIKKLEeNFhzcHFzAyZUtYOC57ela634GglanabnX8A130_provenance.
- NP30288.RAaC1f4vuQssrNBwc89iRJvkFebXnwOCULU2aqHwbMYzI130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30288.RAaC1f4vuQssrNBwc89iRJvkFebXnwOCULU2aqHwbMYzI130_provenance.
- NP30297.RAVyzOWafKZVnrGsRp7gYRkrynemJlyITPIZXPQ30f-NY130_assertion description "[Pharmacogenetics of methylphenidate response in preschoolers with ADHD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30297.RAVyzOWafKZVnrGsRp7gYRkrynemJlyITPIZXPQ30f-NY130_provenance.
- NP30304.RAWNu2EYB1N2xjtPLEe_hCOTvpBhCWly3HKsdqCMsBz-c130_assertion description "[Alpha-synuclein-glucocerebrosidase interactions in pharmacological Gaucher models: a biological link between Gaucher disease and parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30304.RAWNu2EYB1N2xjtPLEe_hCOTvpBhCWly3HKsdqCMsBz-c130_provenance.
- NP30305.RAapcc6Lk5Tx_JsSbvK13sDejPtKDE8fOWaliyGAu4shc130_assertion description "[Evidence of oxidative stress in the neocortex in incidental Lewy body disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30305.RAapcc6Lk5Tx_JsSbvK13sDejPtKDE8fOWaliyGAu4shc130_provenance.
- NP30308.RAXb4hMNu2W9-8gpfeDyRZ3xcV0X8pRMXaRgxVc9afba8130_assertion description "[The metal transporter SMF-3/DMT-1 mediates aluminum-induced dopamine neuron degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30308.RAXb4hMNu2W9-8gpfeDyRZ3xcV0X8pRMXaRgxVc9afba8130_provenance.
- NP30309.RAbeIBV8gx6DYewxwwCfZCfZBRAc9vCblZbYS5W5FvfO0130_assertion description "[Adult-onset neurodegeneration with brain iron accumulation and cortical alpha-synuclein and tau pathology: a distinct clinicopathological entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30309.RAbeIBV8gx6DYewxwwCfZCfZBRAc9vCblZbYS5W5FvfO0130_provenance.
- NP30311.RAaRRO8-3IoILQ4DSPN9UOSUe2Gt5ejDcJtYFWt7Gu2Jk130_assertion description "[A proteomic analysis of MCLR-induced neurotoxicity: implications for Alzheimer's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30311.RAaRRO8-3IoILQ4DSPN9UOSUe2Gt5ejDcJtYFWt7Gu2Jk130_provenance.
- NP30314.RAZsd0NMJnWRZcPJQ_LjiTrqRQKx89zNDHlbpDRE40Hrg130_assertion description "[Neuronal vulnerability in Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30314.RAZsd0NMJnWRZcPJQ_LjiTrqRQKx89zNDHlbpDRE40Hrg130_provenance.
- NP30317.RAeeimvFdoORQQCdB6l-HP4mmtRdMqJ9MmxkjW7xbY0sk130_assertion description "[-Synuclein gene may interact with environmental factors in increasing risk of Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30317.RAeeimvFdoORQQCdB6l-HP4mmtRdMqJ9MmxkjW7xbY0sk130_provenance.
- NP30320.RAXSpqZiujBSaIArtyyWiF8n5ddZwQVG1bsKBlBK_RPpo130_assertion description "[Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30320.RAXSpqZiujBSaIArtyyWiF8n5ddZwQVG1bsKBlBK_RPpo130_provenance.
- NP30321.RAUiK8XXYrnM2QX8aV3iWfC7iEUnpOomNaB-sz3p4wtnY130_assertion description "[Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30321.RAUiK8XXYrnM2QX8aV3iWfC7iEUnpOomNaB-sz3p4wtnY130_provenance.
- NP30325.RAbnbiTvYSNDXQy7IGDs_CXTjat6_VyKnkGFjYQI8MpVw130_assertion description "[Study of association between alpha-synuclein gene polymorphism and methamphetamine psychosis/dependence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30325.RAbnbiTvYSNDXQy7IGDs_CXTjat6_VyKnkGFjYQI8MpVw130_provenance.
- NP30332.RAX8u6y6buT2dpoqLiwBkHT1n86lYhxjIc8ZksFEdNhi8130_assertion description "[Global gene expression profiling of chemically induced rat mammary gland carcinomas and adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30332.RAX8u6y6buT2dpoqLiwBkHT1n86lYhxjIc8ZksFEdNhi8130_provenance.
- NP30334.RAWOMMr3Nb__Fwc9RDS-WkhLZ0SnOaY7AzE6yXWX3Nnto130_assertion description "[A comparison of transcriptomic and metabonomic technologies for identifying biomarkers predictive of two-year rodent cancer bioassays.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30334.RAWOMMr3Nb__Fwc9RDS-WkhLZ0SnOaY7AzE6yXWX3Nnto130_provenance.
- NP30338.RAeFOkKmGejUcB1p4DU_CjiAdI8GCxTX40Z37BSS191J4130_assertion description "[Global gene expression profiling of chemically induced rat mammary gland carcinomas and adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30338.RAeFOkKmGejUcB1p4DU_CjiAdI8GCxTX40Z37BSS191J4130_provenance.
- NP30339.RAf61kohbOy4Igeg6G_hl9x5ERppJr47slMJtkc9bsTAo130_assertion description "[Host cell gene expression during human immunodeficiency virus type 1 latency and reactivation and effects of targeting genes that are differentially expressed in viral latency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30339.RAf61kohbOy4Igeg6G_hl9x5ERppJr47slMJtkc9bsTAo130_provenance.
- NP30340.RAcyvXyq2Z4_5JjDYR-0k0tjnNeMSKsmCJUR-jJINvwOw130_assertion description "[Global gene expression profiling of chemically induced rat mammary gland carcinomas and adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30340.RAcyvXyq2Z4_5JjDYR-0k0tjnNeMSKsmCJUR-jJINvwOw130_provenance.
- NP30341.RARDYHWxadlCoB7fnGFvbzLuEKDeiYznlStUGtV2nbsEk130_assertion description "[Global gene expression profiling of chemically induced rat mammary gland carcinomas and adenomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30341.RARDYHWxadlCoB7fnGFvbzLuEKDeiYznlStUGtV2nbsEk130_provenance.
- NP30349.RAfbV-1LIfyBZx16lHo2WOAOfNgblvgl8V2G9p9W8_jyY130_assertion description "[A gene expression signature of acquired chemoresistance to cisplatin and fluorouracil combination chemotherapy in gastric cancer patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30349.RAfbV-1LIfyBZx16lHo2WOAOfNgblvgl8V2G9p9W8_jyY130_provenance.
- NP30354.RAVXW0oth9wQfbIpPsWdnUpYNUpQEx6Y3PkWGUsNeAfSA130_assertion description "[We examined SOCS1 gene methylation in >200 patients with chronic liver disease and found that the severity of liver fibrosis is strongly correlated with SOCS1 gene methylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30354.RAVXW0oth9wQfbIpPsWdnUpYNUpQEx6Y3PkWGUsNeAfSA130_provenance.
- NP30355.RAQfoh_zwSu6WtmekalqKEstEBkm6judv8a0hwr1PIHzg130_assertion description "[We examined SOCS1 gene methylation in >200 patients with chronic liver disease and found that the severity of liver fibrosis is strongly correlated with SOCS1 gene methylation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30355.RAQfoh_zwSu6WtmekalqKEstEBkm6judv8a0hwr1PIHzg130_provenance.
- NP30358.RAYVyiG3M75HOlC4giGGMoaFBTIM9ZjuyFVbF7Vi9kpqE130_assertion description "[Pravastatin prevents aortic atherosclerosis via modulation of signal transduction and activation of transcription 3 (STAT3) to attenuate interleukin-6 (IL-6) action in ApoE knockout mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30358.RAYVyiG3M75HOlC4giGGMoaFBTIM9ZjuyFVbF7Vi9kpqE130_provenance.
- NP30360.RAcQA78oufwd1inZWzMZTuYCfTf2hksnlrjlsPYL0ANfQ130_assertion description "[]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30360.RAcQA78oufwd1inZWzMZTuYCfTf2hksnlrjlsPYL0ANfQ130_provenance.
- NP30361.RAdwsbDL0hGmhcTHNcZ-y1Rr2ApXjBUPWn098PNFbCm9A130_assertion description "[Transcriptional profiling endometrial carcinomas microdissected from DES-treated mice identifies changes in gene expression associated with estrogenic tumor promotion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30361.RAdwsbDL0hGmhcTHNcZ-y1Rr2ApXjBUPWn098PNFbCm9A130_provenance.
- NP30363.RAYQgiK287kC7o7G9O5YBR24wTpqihuuVDFGTcAcFjoBk130_assertion description "[Cardioplegia prevents ischemia-induced transcriptional alterations of cytoprotective genes in rat hearts: a DNA microarray study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30363.RAYQgiK287kC7o7G9O5YBR24wTpqihuuVDFGTcAcFjoBk130_provenance.
- NP30367.RAcQzgh1dgi94eAxSa2IN5ZkL1fJC__BdTLKB93u58xfY130_assertion description "[Rapid one-step purification of native dimeric ALS-associated human Cu/Zn superoxide dismutase from transgenic rat tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30367.RAcQzgh1dgi94eAxSa2IN5ZkL1fJC__BdTLKB93u58xfY130_provenance.
- NP30370.RAb3OuFbCPdJYAzQL_z7nYfh4loGsxka4xyG46Pq7n9no130_assertion description "[Superoxide dismutase 1 mutants related to amyotrophic lateral sclerosis induce endoplasmic stress in neuro2a cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30370.RAb3OuFbCPdJYAzQL_z7nYfh4loGsxka4xyG46Pq7n9no130_provenance.
- NP30394.RAa5SarERZ6uUmsVTHZxPeeiUL4OmPEktRfZIx2I9xLVs130_assertion description "[This study strongly supports a role for COX-2 in the pathophysiology of ALS and provides the first experimental evidence that prophylactic treatment with COX-2 inhibitors can significantly delay the onset of motor dysfunction in the SOD1-G93A transgenic mouse model of ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30394.RAa5SarERZ6uUmsVTHZxPeeiUL4OmPEktRfZIx2I9xLVs130_provenance.
- NP30397.RAS8j-eNDmFrAmPUeT0K7o5IPPO839V_wsly7bJusbJDw130_assertion description "[In this study, to prove the efficacy of BRC in ALS, we conducted a set of preclinical studies using a transgenic ALS mouse model carrying the H46R mutation in the human Cu/Zn superoxide dismutase (SOD1) gene ALS(SOD1(H46R)) by the post-onset administration of BRC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30397.RAS8j-eNDmFrAmPUeT0K7o5IPPO839V_wsly7bJusbJDw130_provenance.
- NP30398.RASuV0tiIscMNc-FYxd-QCaB_zeNXMv9rp9aArVyibTV4130_assertion description "[Our cellular systems reproduce many of the biochemical changes observed in patients with DS or ALS, and in transgenic mice overexpressing mutant SOD1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30398.RASuV0tiIscMNc-FYxd-QCaB_zeNXMv9rp9aArVyibTV4130_provenance.
- NP30401.RAWBpH7T3nbm-NXtFakoK-oG8T7JqlakIS5YMa846HjoY130_assertion description "[Changes in pro/antioxidant balance in smoking and non-smoking pregnant women with intrauterine growth restriction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30401.RAWBpH7T3nbm-NXtFakoK-oG8T7JqlakIS5YMa846HjoY130_provenance.
- NP30408.RAXBS-6aHmR7xroedqgO0KZRQ_asuTDyKwa6IEI1bqxhI130_assertion description "[Treatment with liposome-encapsulated SOD reduced blood pressure by 50 mm Hg in angiotensin II-infused rats while having no effect on blood pressure in control rats or rats with norepinephrine-induced hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30408.RAXBS-6aHmR7xroedqgO0KZRQ_asuTDyKwa6IEI1bqxhI130_provenance.
- NP30410.RAbXIoBpdeMFLZHwg6RKUeh4dx6wKURbZOlWN6OI8baXo130_assertion description "[Overexpression of Cu,Zn superoxide dismutase (SOD1) reduces ischemic injury in some stroke models but exacerbates injury in a neonatal stroke model and in other settings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30410.RAbXIoBpdeMFLZHwg6RKUeh4dx6wKURbZOlWN6OI8baXo130_provenance.
- NP30411.RAVLJOFtwKMhFaLssY2S_hCzqIMepMrzDGCYYzga-xWso130_assertion description "[Overexpression of copper/zinc superoxide dismutase in transgenic mice protects against neuronal cell death after transient focal ischemia by blocking activation of the Bad cell death signaling pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30411.RAVLJOFtwKMhFaLssY2S_hCzqIMepMrzDGCYYzga-xWso130_provenance.
- NP30412.RAdsnGXrCqCQQgYoA5U46g7F4OJdag976kF8vXeghCNts130_assertion description "[Oxidative stress transiently decreases the IKK complex (IKKalpha, beta, and gamma), an upstream component of NF-kappaB signaling, after transient focal cerebral ischemia in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30412.RAdsnGXrCqCQQgYoA5U46g7F4OJdag976kF8vXeghCNts130_provenance.
- NP30413.RAVPW99cbbTIvAiO7pbIJat31j1SZsnCvF-TMDtMVgyaM130_assertion description "[Activation of the Akt/GSK3beta signaling pathway mediates survival of vulnerable hippocampal neurons after transient global cerebral ischemia in rats.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30413.RAVPW99cbbTIvAiO7pbIJat31j1SZsnCvF-TMDtMVgyaM130_provenance.
- NP30415.RAcd5N1SbgoTvY-SnyPPGF5gqTXITQHMAhlEDRMK32SYM130_assertion description "[Comprehensive characterization of serum clinical chemistry parameters and the identification of urinary superoxide dismutase in a carbon tetrachloride-induced model of hepatic fibrosis in the female Hanover Wistar rat.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30415.RAcd5N1SbgoTvY-SnyPPGF5gqTXITQHMAhlEDRMK32SYM130_provenance.
- NP30432.RAYwU-nxXqOQ1bZtouQWiZ3tPYAavSgS4cKWPXU_XmK3Q130_assertion description "[Overexpression of human copper/zinc superoxide dismutase (SOD1) suppresses ischemia-reperfusion injury and subsequent development of graft coronary artery disease in murine cardiac grafts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30432.RAYwU-nxXqOQ1bZtouQWiZ3tPYAavSgS4cKWPXU_XmK3Q130_provenance.
- NP30442.RAVXLjds4r423xXyCY0249jthvXI0kfs38SFdiYqHtHTI130_assertion description "[Proteomic changes related to `bewildered` circulating platelets in the acute coronary syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30442.RAVXLjds4r423xXyCY0249jthvXI0kfs38SFdiYqHtHTI130_provenance.
- NP30445.RAUE0POmKCqsQb9--APifcSF1uz3DHBg7GCBBqfby_Eis130_assertion description "[Proteomic analysis of intestinal epithelial cells expressing stabilized beta-catenin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30445.RAUE0POmKCqsQb9--APifcSF1uz3DHBg7GCBBqfby_Eis130_provenance.
- NP30451.RAftlM7km_iOsUYX0T0pF-_b_7_TtM_TAvDuIOF06wunU130_assertion description "[Mice irradiated and reconstituted with hematopoietic cells lacking manganese superoxide dismutase (SOD2) show a persistent hemolytic anemia similar to human sideroblastic anemia (SA), including characteristic intra-mitochondrial iron deposition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30451.RAftlM7km_iOsUYX0T0pF-_b_7_TtM_TAvDuIOF06wunU130_provenance.
- NP5.RAwQyGERKSgVsGJXsfeXsp5KeuSV1Usv2NCpJ6K6IcrKQ130_assertion description "[The mutational spectrum in a cohort of Charcot-Marie-Tooth disease type 2 among the Han Chinese in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP5.RAwQyGERKSgVsGJXsfeXsp5KeuSV1Usv2NCpJ6K6IcrKQ130_provenance.
- NP7.RAwjxsrmSm48aXD8NWx8WLhzVflFyEqEz_reSEJpRIU2k130_assertion description "[Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7.RAwjxsrmSm48aXD8NWx8WLhzVflFyEqEz_reSEJpRIU2k130_provenance.
- NP9.RA0i27X4O9VvqroA2MH2IamMnily5GRuAf6JnboeR054c130_assertion description "[Novel ABCA12 mutations identified in two cases of non-bullous congenital ichthyosiform erythroderma associated with multiple skin malignant neoplasia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP9.RA0i27X4O9VvqroA2MH2IamMnily5GRuAf6JnboeR054c130_provenance.
- NP10.RAyK9TQ-Ui6GHKfYY8i1_0Lrxq2iITns9uHHB6YP_gdHE130_assertion description "[Novel compound heterozygous nonsense and missense ABCA12 mutations lead to nonbullous congenital ichthyosiform erythroderma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10.RAyK9TQ-Ui6GHKfYY8i1_0Lrxq2iITns9uHHB6YP_gdHE130_provenance.
- NP20.RAzZ2k1TUt-kQU3ciWEjeYf-uXYFLZSqPHJGlW_KkvUkU130_assertion description "[Clinical variant of Tangier disease in Japan: mutation of the ABCA1 gene in hypoalphalipoproteinemia with corneal lipidosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20.RAzZ2k1TUt-kQU3ciWEjeYf-uXYFLZSqPHJGlW_KkvUkU130_provenance.
- NP21.RA8C2c9SrO5l5ksCB5trnBHjWv29h9mYyh3YR4W480sXw130_assertion description "[Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21.RA8C2c9SrO5l5ksCB5trnBHjWv29h9mYyh3YR4W480sXw130_provenance.
- NP24.RA-zq_bylinUwJXeHX-UZcvYv7tko5ilPj0h8Kr3BxMDo130_assertion description "[The application of the test to the molecular analysis of a new patient with familial HDL-deficiency (Tangier disease) led to a discovery of two novel ABCA1 mutations: C2665del and C4457T.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP24.RA-zq_bylinUwJXeHX-UZcvYv7tko5ilPj0h8Kr3BxMDo130_provenance.
- NP25.RAzKjBqrM80otNc-Bzq3IZdBTXpx8tHXfXF_Qrr3zV6FY130_assertion description "[Common and rare ABCA1 variants affecting plasma HDL cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25.RAzKjBqrM80otNc-Bzq3IZdBTXpx8tHXfXF_Qrr3zV6FY130_provenance.
- NP28.RA32oemnp-VqO17kpSopxeq_y0S8wCQv5YV3MZWr11LIA130_assertion description "[Novel ABCA1 compound variant associated with HDL cholesterol deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP28.RA32oemnp-VqO17kpSopxeq_y0S8wCQv5YV3MZWr11LIA130_provenance.
- NP30.RA2P8JIv2f7Hzw_n6nDBQLqfz5_ECEBM_NE5kkzZ3OM7M130_assertion description "[Frequency of ABCA4 mutations in 278 Spanish controls: an insight into the prevalence of autosomal recessive Stargardt disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP30.RA2P8JIv2f7Hzw_n6nDBQLqfz5_ECEBM_NE5kkzZ3OM7M130_provenance.
- NP33.RA4m_6IscLgMTX7rwJxEZnFqabzPH-6vCqZsFOhWxMCU8130_assertion description "[In order to further characterize the complex genotype-phenotype relationships involving this gene, we have performed a mutation analysis of ABCA4 in 14 Spanish patients comprising eight STGD (Stargardt), four FFM (fundus flavimaculatus), and two CRD (Cone-rod dystrophy) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33.RA4m_6IscLgMTX7rwJxEZnFqabzPH-6vCqZsFOhWxMCU8130_provenance.
- NP34.RA3_Fr_Ff7MnPDUpRkoAekBepg9kRA7XH4R5zGDurSgqc130_assertion description "[Analysis of the ABCR (ABCA4) gene in 4-aminoquinoline retinopathy: is retinal toxicity by chloroquine and hydroxychloroquine related to Stargardt disease?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP34.RA3_Fr_Ff7MnPDUpRkoAekBepg9kRA7XH4R5zGDurSgqc130_provenance.
- NP35.RA4iiVIkfIe5MsYCEiL2d8vThYvBkVQrIhK9lo8eZjO2g130_assertion description "[Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR (ABCA4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP35.RA4iiVIkfIe5MsYCEiL2d8vThYvBkVQrIhK9lo8eZjO2g130_provenance.
- NP43.RAz6o48AglfV22vXkEEcHJ-gaFjQto4che9u2KIUYZVng130_assertion description "[Mutations in the ABCA4 (ABCR) gene are the major cause of autosomal recessive cone-rod dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP43.RAz6o48AglfV22vXkEEcHJ-gaFjQto4che9u2KIUYZVng130_provenance.
- NP44.RA1MuXHSb1Wj16-hnv67H4C8M_HTSlqSGHtB76Z1i4hfo130_assertion description "[A comprehensive survey of sequence variation in the ABCA4 (ABCR) gene in Stargardt disease and age-related macular degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP44.RA1MuXHSb1Wj16-hnv67H4C8M_HTSlqSGHtB76Z1i4hfo130_provenance.
- NP47.RAy_D1YDk9tCfCvaYlvIvJhH54jYsnEqmysGZmk4aupgQ130_assertion description "[Mutations in ABCR (ABCA4) in patients with Stargardt macular degeneration or cone-rod degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP47.RAy_D1YDk9tCfCvaYlvIvJhH54jYsnEqmysGZmk4aupgQ130_provenance.
- NP49.RA-FZgkW56Au2wONR_3ejbAfvlIsXeCLgL1fUIfAnyySs130_assertion description "[Molecular analysis of the ABCA4 gene for reliable detection of allelic variations in Spanish patients: identification of 21 novel variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP49.RA-FZgkW56Au2wONR_3ejbAfvlIsXeCLgL1fUIfAnyySs130_provenance.
- NP52.RA4clh6gO-Tgj8dvp_Wv6vL4F2X5L3rssMzHeKkUvSVEI130_assertion description "[Impaired expression and function of the bile salt export pump due to three novel ABCB11 mutations in intrahepatic cholestasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP52.RA4clh6gO-Tgj8dvp_Wv6vL4F2X5L3rssMzHeKkUvSVEI130_provenance.
- NP53.RA_wwLO6tXXrIe4uuQx2rvf19ieVRjRJ1BqIZBLFzXRhI130_assertion description "[FIC1 and BSEP defects in Taiwanese patients with chronic intrahepatic cholestasis with low gamma-glutamyltranspeptidase levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP53.RA_wwLO6tXXrIe4uuQx2rvf19ieVRjRJ1BqIZBLFzXRhI130_provenance.
- NP68.RA-x23_izSrOUiTeY8M1s5ZfIcli-_9S9RXR91gW4Toqk130_assertion description "[Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP68.RA-x23_izSrOUiTeY8M1s5ZfIcli-_9S9RXR91gW4Toqk130_provenance.
- NP70.RA7O5SwQbucwKRup4rN1f7UyT7UoEfhfLNZIXfrP5QorI130_assertion description "[Spectrum of genetic variation at the ABCC6 locus in South Africans: Pseudoxanthoma elasticum patients and healthy individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP70.RA7O5SwQbucwKRup4rN1f7UyT7UoEfhfLNZIXfrP5QorI130_provenance.
- NP72.RA2chcf-39HpUnqErOCuKWFCrBa_gOhgMnzYguS_AZD0k130_assertion description "[Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP72.RA2chcf-39HpUnqErOCuKWFCrBa_gOhgMnzYguS_AZD0k130_provenance.
- NP73.RA22uwGJJo-BlHbkxez_5vj5VXvt7ZS1_NZOJzkYwhGcs130_assertion description "[ABCC6 mutations in Italian families affected by pseudoxanthoma elasticum (PXE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP73.RA22uwGJJo-BlHbkxez_5vj5VXvt7ZS1_NZOJzkYwhGcs130_provenance.
- NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_assertion description "[Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP83.RA49uXg7dDECLelWVzhwS9cDY9W6Qq1x77IlAbvA5SU7Q130_provenance.
- NP84.RA6MiOwdvxyy1Od7S1_6teM_Xi90RE9uvucFNm2vttl-I130_assertion description "[Acute insulin response tests for the differential diagnosis of congenital hyperinsulinism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84.RA6MiOwdvxyy1Od7S1_6teM_Xi90RE9uvucFNm2vttl-I130_provenance.
- NP93.RA7M39SmuwLn5yIvHTWS5c1lRPoOZXHNjSy_pzQZuVn4I130_assertion description "[Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP93.RA7M39SmuwLn5yIvHTWS5c1lRPoOZXHNjSy_pzQZuVn4I130_provenance.
- NP95.RA0DkcVbcjyVY_rYEt1_JeqerHuvdnBXJqqkumBYWCgGU130_assertion description "[KATP channel mutation confers risk for vein of Marshall adrenergic atrial fibrillation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95.RA0DkcVbcjyVY_rYEt1_JeqerHuvdnBXJqqkumBYWCgGU130_provenance.
- NP99.RAyw-4GgVp8sxWTccwHhhfSX9ECT3VnBJP3Z4oQuPzk7k130_assertion description "[X-linked adrenoleukodystrophy (X-ALD) is a progressive peroxisomal disorder affecting adrenal glands, testes and myelin stability that is caused by mutations in the ABCD1 (NM_000033) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99.RAyw-4GgVp8sxWTccwHhhfSX9ECT3VnBJP3Z4oQuPzk7k130_provenance.
- NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_assertion description "[Eight novel ABCD1 gene mutations and three polymorphisms in patients with X-linked adrenoleukodystrophy: The first polymorphism causing an amino acid exchange.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP102.RAy0v4Wg-Yj9JVnnMCwxDO_WBregmcrvNc2XkB-B74LUA130_provenance.