Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP207691.RAUFDIiD9WB7Y6lkXqZyuDTRBoPyH0wheq0u5xkiGZik0130_assertion description "[In addition to smoking status, the combination of calcium channel blocker usage and ABCB1 C3435T genotype significantly affected the change of 20 μM ADP-induced MPA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207691.RAUFDIiD9WB7Y6lkXqZyuDTRBoPyH0wheq0u5xkiGZik0130_provenance.
- NP207692.RAfXsHn-SgsTUnKfY-zwHsBVQJs0xhLilackuoOzr2Pqo130_assertion description "[We and others have used genetic linkage studies and mutation analysis to establish that single amino acid substitutions in either the keratin 1 or keratin 10 chains can cause epidermolytic hyperkeratosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207692.RAfXsHn-SgsTUnKfY-zwHsBVQJs0xhLilackuoOzr2Pqo130_provenance.
- NP207695.RAXGrjNFISumuBGblJkW2uGPVtgen_p9gCFThmZgBu8wo130_assertion description "[Here we present data demonstrating that expression of the TL antigen, unlike other class I molecules, is completely independent of the function of the transporter associated with antigen processing (TAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207695.RAXGrjNFISumuBGblJkW2uGPVtgen_p9gCFThmZgBu8wo130_provenance.
- NP207697.RAasiU0VhSjkZlI2Ju6CNp5jJbqxKQTr01yDHYghdVfPA130_assertion description "[Stromal cell-derived factor-1alpha and CXCR4 expression in hemangioblastoma and clear cell-renal cell carcinoma: von Hippel-Lindau loss-of-function induces expression of a ligand and its receptor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207697.RAasiU0VhSjkZlI2Ju6CNp5jJbqxKQTr01yDHYghdVfPA130_provenance.
- NP207702.RAeZZLqSZSIusLNg4RB_o2H3w33iHioUe0iWfYqq2b51E130_assertion description "[Novel mutations in the thymidine kinase 2 gene (TK2) associated with fatal mitochondrial myopathy and mitochondrial DNA depletion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207702.RAeZZLqSZSIusLNg4RB_o2H3w33iHioUe0iWfYqq2b51E130_provenance.
- NP207703.RARrJCyVlVJjN6Y61J4xzzG_8EaLYmjKTefHiFjZEn_r8130_assertion description "[Detection of numeric abnormalities of chromosome 17 and p53 deletions by fluorescence in situ hybridization in pleomorphic adenomas and carcinomas in pleomorphic adenoma. Correlation with p53 expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207703.RARrJCyVlVJjN6Y61J4xzzG_8EaLYmjKTefHiFjZEn_r8130_provenance.
- NP207716.RAcNl8dFtu3uSvSKfCv724UTtFdIro7D0ztp6qWUwc3Ec130_assertion description "[The anti-EGFR monoclonal antibodies panitumumab and cetuximab are approved in the United States for treatment of mCRC refractory to chemotherapy but are not recommended for use in patients with mutations in KRAS codons 12 or 13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207716.RAcNl8dFtu3uSvSKfCv724UTtFdIro7D0ztp6qWUwc3Ec130_provenance.
- NP207721.RAZLrS37swNnz_ZNVPwDqW_XGG8uUFC0Xx0vHoyIyCs8w130_assertion description "[The gonococcal isolates were phenotyped by determining the auxotype/serovar (A/S) class and genotyped by pulsed field gel electrophoresis (PFGE).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207721.RAZLrS37swNnz_ZNVPwDqW_XGG8uUFC0Xx0vHoyIyCs8w130_provenance.
- NP207723.RAW2zQN8nwFYgmjO9kySg9jA0Zv3EH1k9PlNuFW6tWsvY130_assertion description "[To assess whether such an interaction contributes to an increased risk of prostate cancer in humans, we performed a series of epistatic PTEN and CDKN1B interaction analyses in a collection of 188 high-risk hereditary prostate cancer families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207723.RAW2zQN8nwFYgmjO9kySg9jA0Zv3EH1k9PlNuFW6tWsvY130_provenance.
- NP207726.RAb9etmd5GWCXPephgwCcaT4oNwhFB6a5UnlUdI2CVItI130_assertion description "[Overall, 14 out of 15 MM patients carried EDNRB mutations reported in HSCR, some of which had previously been shown to lead to loss of function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207726.RAb9etmd5GWCXPephgwCcaT4oNwhFB6a5UnlUdI2CVItI130_provenance.
- NP207727.RAbSijnd672z9vUTZWRBLXyZwplYz9wA6-Xez3GCUYf0Y130_assertion description "[Functional analysis of a variant of the thyrotropin receptor gene in a family with Graves' disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207727.RAbSijnd672z9vUTZWRBLXyZwplYz9wA6-Xez3GCUYf0Y130_provenance.
- NP207728.RAfzdgcntHuPODw3G1O4bjfb8DbdVpps2B3uZSx_E9aU4130_assertion description "[The coding region single nucleotide polymorphisms (cSNPs) were identified by sequencing of amplimers of PAX2 exon 8 exhibiting variant migration patterns in the course of genomic DNA mutation screening from patients with renal-coloboma syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207728.RAfzdgcntHuPODw3G1O4bjfb8DbdVpps2B3uZSx_E9aU4130_provenance.
- NP207729.RAVeL3sRpRQ7s9-PjOFXRRq3k5Hvt9LND4J19aL1P1nD4130_assertion description "[We thus propose that the muscle wasting typical in DM1 is due to impairment of muscle mass maintenance-regeneration, through premature apoptotic-autophagic activation, rather than altered myogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207729.RAVeL3sRpRQ7s9-PjOFXRRq3k5Hvt9LND4J19aL1P1nD4130_provenance.
- NP207731.RAVDjCkVxIhH93mnwV32GYRR9vhRwX7gF95TC4keRVu7g130_assertion description "[The prevalence of congenital hypothyroidism (CH) associated with mutations in the TSH receptor gene (TSHR) has not been established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207731.RAVDjCkVxIhH93mnwV32GYRR9vhRwX7gF95TC4keRVu7g130_provenance.
- NP207732.RAZxQYqwH8xUg0KLsKeyBJjF6sWrDtUXbPaCdNQWkQo68130_assertion description "[Our findings thus suggest a link between the LTA cascade and the pathogenesis of MI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207732.RAZxQYqwH8xUg0KLsKeyBJjF6sWrDtUXbPaCdNQWkQo68130_provenance.
- NP207735.RASMACHk1f0Q-it00rz4mDYMSXwk-OGMCd4GtPwZ5auHE130_assertion description "[Thus, we investigated the influence of transporters associated with antigen processing (TAP), human leukocyte antigen (HLA)-DQB1, and HLA-DRB1 gene polymorphism in mestizo Colombian patients with pSS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207735.RASMACHk1f0Q-it00rz4mDYMSXwk-OGMCd4GtPwZ5auHE130_provenance.
- NP207740.RAVMRVQtMKgVIAYOgJ2NOTvR_Ex1pW-tV9cYAk2Qk1I0I130_assertion description "[The only tumors found to contain p53 mutations were 3 malignant lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207740.RAVMRVQtMKgVIAYOgJ2NOTvR_Ex1pW-tV9cYAk2Qk1I0I130_provenance.
- NP207744.RAcaO5M1qqHO0wY1jeVS0_MZxjKal3VrCW2rr08K9plAg130_assertion description "[CD24 may thus serve as a new target for directed molecular therapy of cholangiocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207744.RAcaO5M1qqHO0wY1jeVS0_MZxjKal3VrCW2rr08K9plAg130_provenance.
- NP207760.RAeG8R1qcZngvbNmXPWFtwCW8Qe60uKuzI6uxHYe8Npuo130_assertion description "[We examined 10 human breast cancer lesions which were characterized by the presence of microcalcifications and high expression of BSP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207760.RAeG8R1qcZngvbNmXPWFtwCW8Qe60uKuzI6uxHYe8Npuo130_provenance.
- NP207762.RAW2Zkt6e5YgR7ztbohxAYAQjvRESCw286I1IUiNpDFYI130_assertion description "[Single nucleotide polymorphisms of protein C, factor V (e.g., factor V Leiden), and plasminogen activator inhibitor-1 are associated with an increased risk of deep venous thrombosis, pulmonary emboli, acute myocardial infarction, and stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207762.RAW2Zkt6e5YgR7ztbohxAYAQjvRESCw286I1IUiNpDFYI130_provenance.
- NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_assertion description "[Deletions were rare among patients lacking typical DiGeorge syndrome (DGS) or velocardiofacial (VCF) dysmorphic features, and more common in tetralogy of Fallot with pulmonary atresia than tetralogy of Fallot alone.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207765.RAYJQlTytnK4kBIJtIfrTU0kYjLyVzkg_KoCbv5pZFVHw130_provenance.
- NP207766.RARtI3_XJBieookaGjH26rzQoArqWYVNLdf6_naScjNZ4130_assertion description "[RIG-I-like receptors and Toll-like receptors (TLRs) play important roles in the recognition of viral infections.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207766.RARtI3_XJBieookaGjH26rzQoArqWYVNLdf6_naScjNZ4130_provenance.
- NP207777.RAWNIt90EM_Cp1bNQWIiGK5NsBsHItAKZjzyX0NAXGXh8130_assertion description "[Relationships among allergic diseases including asthma and variations in the GST mu (GSTM1) and GST theta (GSTT1) genes were investigated in 1,006 Caucasian subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207777.RAWNIt90EM_Cp1bNQWIiGK5NsBsHItAKZjzyX0NAXGXh8130_provenance.
- NP207778.RAZLyuzIpMUd0J8DEkiwRwRlcCwjmQuz4prvK0DzqKKmc130_assertion description "[Transforming growth factor-beta and p-21: multiple molecular targets of decorin-mediated suppression of neoplastic growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207778.RAZLyuzIpMUd0J8DEkiwRwRlcCwjmQuz4prvK0DzqKKmc130_provenance.
- NP207781.RASQO7GzfqSMFGVVzidCLzEucEVFX6gGyv5You3wUcOtU130_assertion description "[We report here the critical role of the FERM-binding and PDZ- interacting domains of TSLC1 in tumor suppressor activity in non-small cell lung cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207781.RASQO7GzfqSMFGVVzidCLzEucEVFX6gGyv5You3wUcOtU130_provenance.
- NP207786.RAf5Iy9W3TwNGPRAG_xUB5z15_lTiEraCDRTngfwyeFxI130_assertion description "[BRAF mutations represent an alternative molecular pathway in the early tumorigenesis of a subset of KIT/PDGFRA wild-type GISTs and are per se not associated with a high risk of malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207786.RAf5Iy9W3TwNGPRAG_xUB5z15_lTiEraCDRTngfwyeFxI130_provenance.
- NP207787.RAWyyZ0ht1w1aOy-1KM7FZGk5Sbc0O0Xc8P8J5QIOjsGg130_assertion description "[Genetic polymorphisms in MMP7 and reduced serum levels associate with the development of bronchiolitis obliterans syndrome after lung transplantation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207787.RAWyyZ0ht1w1aOy-1KM7FZGk5Sbc0O0Xc8P8J5QIOjsGg130_provenance.
- NP207791.RAeRFSUP_2S9pEZHqnhKIoM-VHBUEHIn61vGbQth9v0pI130_assertion description "[A candidate gene for Hereditary Hemochromatosis (HFE) has been recently cloned from a region 4 cM telomeric to HLA-A on the short arm of chromosome 6.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207791.RAeRFSUP_2S9pEZHqnhKIoM-VHBUEHIn61vGbQth9v0pI130_provenance.
- NP207792.RAUt2oG4vEFz1HK7-IToL3pEaJwX4taKvGXTzWheEi2bw130_assertion description "[Subsequently, associations between CLEC16A and rheumatoid arthritis (RA), Addison's disease and Crohn's disease have been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207792.RAUt2oG4vEFz1HK7-IToL3pEaJwX4taKvGXTzWheEi2bw130_provenance.
- NP207797.RAc-qFMatl3ddYTyQGfpz0-lYkIlbSUNbBK4ccOTme9a4130_assertion description "[Class I, II and III MHC antigens were determined in 41 Mexican mestizo patients with SSc, 113 of their first degree relatives, and 85 ethnically matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207797.RAc-qFMatl3ddYTyQGfpz0-lYkIlbSUNbBK4ccOTme9a4130_provenance.
- NP207799.RAfmxtZD6K_pDDJBVSKG3bkOZBe1Zf8HJ3G9i5c70NABU130_assertion description "[These findings may provide a novel explanation for the antitumorigenic and/or proapoptotic action of MCC-555 in human colorectal cancer and the ability of pharmacologic approaches to be used against diseases caused by alterations of RNA stability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207799.RAfmxtZD6K_pDDJBVSKG3bkOZBe1Zf8HJ3G9i5c70NABU130_provenance.
- NP207804.RAeRmrnI4eq2z9gmLpLE_dvw4R51dpIE9TDPMZ4rFSCFE130_assertion description "[NAT2 polymorphism in Omani gastric cancer patients-risk predisposition and clinicopathological associations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207804.RAeRmrnI4eq2z9gmLpLE_dvw4R51dpIE9TDPMZ4rFSCFE130_provenance.
- NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_assertion description "[All of them have a balanced reciprocal translocation (46,XY or XX, t(7;9) (q11.21;p12) or (46,XY or XX, t(7;9) (p11.2;q12)), but no other members of the family have either the EEC syndrome or chromosome abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207806.RAUSLi_Ho-p4XRI3riWSf5R8DM67WCosZniByb26FGOvU130_provenance.
- NP207810.RAbsWXXxAgT8Y4KjmLzHX2kLHRAUXD6NDJy6Tf0y3zxgY130_assertion description "[Depletion of MAP2 expression and laminar cytoarchitectonic changes in dorsolateral prefrontal cortex in adult autistic individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207810.RAbsWXXxAgT8Y4KjmLzHX2kLHRAUXD6NDJy6Tf0y3zxgY130_provenance.
- NP207816.RATR-hFhhdbagqSxEMdJGYNP8f7dc0sDp8kRp3ayv4OVo130_assertion description "[DNA sequencing of the GH1 genes of the first family (IGHD II) demonstrated heterozygosity for a T-->C transition in the sixth base of the donor splice site of intron III.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207816.RATR-hFhhdbagqSxEMdJGYNP8f7dc0sDp8kRp3ayv4OVo130_provenance.
- NP207824.RAWX2TZcjktB1xBwdvsoYF_PkLL076NYp4fStQX1LXpwU130_assertion description "[Regulation of matrix metalloproteinase-9 by epigenetic modifications and the development of diabetic retinopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207824.RAWX2TZcjktB1xBwdvsoYF_PkLL076NYp4fStQX1LXpwU130_provenance.
- NP207834.RAScCkQW5Cf_JGAXZPRuQ-ZaI_XkWQHCT14svoy3nKC90130_assertion description "[We propose that the link between p38 and c-Met is implicated in the progression of human cholangiocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207834.RAScCkQW5Cf_JGAXZPRuQ-ZaI_XkWQHCT14svoy3nKC90130_provenance.
- NP207836.RAWIcJuVdgfG0a3B0AHHmon0lDU-sugpoEcy635dO9nqA130_assertion description "[Two other sequence changes (L159M and G160D) were associated with keratoconus and PPD, respectively, and involved a region adjacent to the homeodomain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207836.RAWIcJuVdgfG0a3B0AHHmon0lDU-sugpoEcy635dO9nqA130_provenance.
- NP207837.RAV2-TEztfC3S-sP7KW-f7vehMQ8c6y3ZLsBwo65bKRew130_assertion description "[To verify the association of transforming growth factor-beta1(TGF-beta1) (C-509T and T869C), CD14 (C-159T), IL-4 (C-590T), IL-4R (ILe50Val) and ADAM33 (S_2) gene polymorphisms with asthma severity in a sample of patients with mild, moderate and severe persistent atopic asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207837.RAV2-TEztfC3S-sP7KW-f7vehMQ8c6y3ZLsBwo65bKRew130_provenance.
- NP207839.RAdZgenrOWcK75kRjxyNSF_1VoPqx4onVN6D3NzwC3j7g130_assertion description "[Myotonic Dystrophy type 2 (DM2) is caused by a DNA microsatellite expansion within the Zinc Finger Protein 9 gene leading to an abnormal splicing pattern largely responsible for the pathological condition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207839.RAdZgenrOWcK75kRjxyNSF_1VoPqx4onVN6D3NzwC3j7g130_provenance.
- NP207840.RAXVrFMP_ETKCeWArFmDWjPMHFobMmsHIpZ_-5kaBFMzA130_assertion description "[We determined the molecular basis of cystathionine beta-synthase (CBS) deficiency in three siblings with pyridoxine responsive homocystinuria using a significantly improved mutation screening method in bacteria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207840.RAXVrFMP_ETKCeWArFmDWjPMHFobMmsHIpZ_-5kaBFMzA130_provenance.
- NP207841.RAcLqCaAMtuwkxHJ0q9AaoWj-fCpix9KpfopluVaUU_V4130_assertion description "[We identified a significant epistasis effect BCL1 by CHRNA4 showing that carriers of the CC genotype at the BCL1 locus who were also homozygous for the T allele at the CHRNA4 locus had the highest depression scores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207841.RAcLqCaAMtuwkxHJ0q9AaoWj-fCpix9KpfopluVaUU_V4130_provenance.
- NP207845.RAbrvzr3gugCnf9_aFZuuN5_3TBeZMKIEaATzq9Zl21tc130_assertion description "[We did not observe any meaningful gene-environment (calcium and vitamin D) or gene-gene (CYP24A1, CYP27B1, and VDR) interactions with CASR genotypes and colon cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207845.RAbrvzr3gugCnf9_aFZuuN5_3TBeZMKIEaATzq9Zl21tc130_provenance.
- NP207847.RAa603dJj3IMueIacq8xdGorGk6Wz1ETTR2DHjGI36T_8130_assertion description "[Mutations in p53 were infrequent and were present in only three of 47 ALL cases (6%) analyzed; two of these were mixed-lineage leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207847.RAa603dJj3IMueIacq8xdGorGk6Wz1ETTR2DHjGI36T_8130_provenance.
- NP207851.RAe2k-3roFy2_x8-O28mR0feXH4vNdmDRGbirNAkff--M130_assertion description "[Gastroenteropancreatic neuroendocrine tumors (GEP NETs) are relatively rare neoplasias arising from the embryonic neural crest, neuroectoderm and endoderm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207851.RAe2k-3roFy2_x8-O28mR0feXH4vNdmDRGbirNAkff--M130_provenance.
- NP207853.RARnW8IGjiGNbQS1dvJmz47p19Iib3l8A6DhVIgvm_K0A130_assertion description "[TLR9 in fibroblasts appeared to be increased by profibrotic Th2 cytokines (IL-4 and IL-13) and this was true in fibroblasts cultured from the most severe form of IIP, idiopathic pulmonary fibrosis (IPF) SLBs, in non-specific interstitial pneumonia fibroblast lines, and in normal fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207853.RARnW8IGjiGNbQS1dvJmz47p19Iib3l8A6DhVIgvm_K0A130_provenance.
- NP207857.RAeIXt31HMRU2AD5PbJ5TnVd9HJ0FiL8LS6agwWBxrmQE130_assertion description "[RET, GDNF, EDNRB, EDN3, and SOX10 lead to long-segment (L-HSCR) as well as syndromic HSCR but fail to explain the transmission of the much more common short-segment form (S-HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207857.RAeIXt31HMRU2AD5PbJ5TnVd9HJ0FiL8LS6agwWBxrmQE130_provenance.
- NP207859.RAT7nfjztiUgl6hkq9sekay89XACia51oiyEfoHy4-3Ws130_assertion description "[The FHIT gene spans approximately 1 Mb of DNA at chromosome band 3p14.2, which includes the familial renal cell carcinoma chromosome translocation breakpoint (between FHIT exons 3 and 4), the most frequently expressed human constitutive chromosomal fragile site (FRA3B, telomeric to the t(3;8) translocation), and numerous homozygous deletions in various human cancers, frequently involving FHIT exon 5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207859.RAT7nfjztiUgl6hkq9sekay89XACia51oiyEfoHy4-3Ws130_provenance.
- NP207860.RAW1BunS72jEj4oERX5t6CU9CE_YfZF0tNYC_OXWQeI2w130_assertion description "[Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207860.RAW1BunS72jEj4oERX5t6CU9CE_YfZF0tNYC_OXWQeI2w130_provenance.
- NP207866.RAQm1KbiKmecCbb19LabO-lZ-VI_4Frkocu3kinQIcxuw130_assertion description "[It is the deficiency of erythrocyte CD55 and CD59 that accounts for the intravascular hemolysis and hemoglobinuria that are the clinical hallmarks of PNH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207866.RAQm1KbiKmecCbb19LabO-lZ-VI_4Frkocu3kinQIcxuw130_provenance.
- NP207867.RAaaIwdu9F_hnafVCVedzGf9sLmTUdPqZb-5QEalO7Ys0130_assertion description "[X-ray repair cross-complementing group 1 (XRCC1) and xeroderma pigmentosum group D (XPD) are mainly involved in base excision repair (BER) and nucleotide excision repair (NER) of DNA repair pathways, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207867.RAaaIwdu9F_hnafVCVedzGf9sLmTUdPqZb-5QEalO7Ys0130_provenance.
- NP207874.RASyThlIOZPgx1XdNxrIT86tIPvbBnCOXu4B70zGTvD9g130_assertion description "[Groups identified by 5p5m and TNM stage were confirmed as the independent prognostic factors in a multivariate COX proportional hazard model.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207874.RASyThlIOZPgx1XdNxrIT86tIPvbBnCOXu4B70zGTvD9g130_provenance.
- NP207890.RAXZbGRwIYq-yNVYRRFLLMLuxDwUer9Xa-Tjw_mLbuDqA130_assertion description "[The model has been applied to two glioblastoma multiforme (GBM) cases, one with wild type (wt) and another one with mutated (mt) p53 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207890.RAXZbGRwIYq-yNVYRRFLLMLuxDwUer9Xa-Tjw_mLbuDqA130_provenance.
- NP207899.RAbB4nXgt5xNKi1z0K0v4UaINRH71Yy5z78Kt7HHrfqrw130_assertion description "[Hence, heterozygous p35 knockout mice model both cognitive endophenotypes and molecular changes reminiscent of schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207899.RAbB4nXgt5xNKi1z0K0v4UaINRH71Yy5z78Kt7HHrfqrw130_provenance.
- NP207904.RAa-FVO28cnZaGaQBLF0eGptZQgWKUjuQK43VGoJ8EWQM130_assertion description "[Homozygous CD18 null mice develop chronic dermatitis with extensive facial and submandibular erosions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207904.RAa-FVO28cnZaGaQBLF0eGptZQgWKUjuQK43VGoJ8EWQM130_provenance.
- NP207905.RAYpsta6qTep1SxPeFsXL_LVoaYIHryxUrGwJBbJE5hZQ130_assertion description "[Cytogenetic analysis in 14 girls with the Rett syndrome revealed a deletion on the short arm of the X chromosome (del(X) (pter;p22] in one, and a fragile site on chromosome Xp22 in six of the girls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207905.RAYpsta6qTep1SxPeFsXL_LVoaYIHryxUrGwJBbJE5hZQ130_provenance.
- NP207906.RAVv9daGNosXP7MENbKhrZbAQZHaNgpKfSVrbVO-75GuU130_assertion description "[We suggest that BCAS3 is mis-expressed in brain tumors and could serve as a human ES cell and tumor marker.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207906.RAVv9daGNosXP7MENbKhrZbAQZHaNgpKfSVrbVO-75GuU130_provenance.
- NP207907.RAQvZpPq7PTlfNRQXJ_yt7g02ujvfdlgZQTPkl8D7ql4M130_assertion description "[We report 3 cases of FL with unusual expression of CD5.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207907.RAQvZpPq7PTlfNRQXJ_yt7g02ujvfdlgZQTPkl8D7ql4M130_provenance.
- NP207908.RAXLDbKHptirdlH5YNv5B-XUX3YvpJlbJTumlKQci1_iI130_assertion description "[Cytogenetic analysis of a cemento-ossifying fibroma from a patient with nonfamilial bilateral multicentric retinoblastoma revealed three reciprocal translocations with the karyotype 46,XY,t(1;18)(q21;q21.3),t(3;10)(p13;q22),t(6;11)(p22;p15).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207908.RAXLDbKHptirdlH5YNv5B-XUX3YvpJlbJTumlKQci1_iI130_provenance.
- NP207910.RAadJzI3uAhK-FV4h_dj5fA-WqvJ7kXlTY9sxSFUjzmys130_assertion description "[We identified 25 cases (48 samples) of bcl-1+ and CD5- lymphoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207910.RAadJzI3uAhK-FV4h_dj5fA-WqvJ7kXlTY9sxSFUjzmys130_provenance.
- NP207913.RAbpmfZbWGyGuyyMV6QyUdmdq8_7uyJARGxKSJ24MkLDk130_assertion description "[Nine point mutations in the skeletal muscle ryanodine receptor (RYR) gene have so far been identified and shown to correlate with the MH-susceptible phenotype, yet direct evidence linking abnormal Ca2+ homeostasis to mutations in the RYR1 cDNA has been obtained for few mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207913.RAbpmfZbWGyGuyyMV6QyUdmdq8_7uyJARGxKSJ24MkLDk130_provenance.
- NP207919.RAdq_6Qm7x6USSWWAYA_BUPu8x_Z3VNqOcGaahuRUwSxM130_assertion description "[DNMT3B expression might contribute to CpG island methylator phenotype in colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207919.RAdq_6Qm7x6USSWWAYA_BUPu8x_Z3VNqOcGaahuRUwSxM130_provenance.
- NP207928.RAX_OEolCV8TKcAx5WoEo592zhdezZf5xphv-wD59XSqQ130_assertion description "[We studied a series of 53 CMML samples including 31 cases of myeloproliferative form (MP-CMML) and 22 cases of myelodysplastic forms (MD-CMML) using array-comparative genomic hybridisation (aCGH) and sequencing of 13 candidate genes including ASXL1, CBL, FLT3, IDH1, IDH2, JAK2, KRAS, NPM1, NRAS, PTPN11, RUNX1, TET2 and WT1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207928.RAX_OEolCV8TKcAx5WoEo592zhdezZf5xphv-wD59XSqQ130_provenance.
- NP207929.RAY_iBEb96NHoz28dnqlNXmn5Fsv3qsIoqYaH-HAsRMA8130_assertion description "[Enterovirus 71 (EV71) has been shown to induce cyclooxygenase-2 (COX-2) expression in human neuroblastoma SK-N-SH cells through the action of MAPKs, NF-κB, and AP-1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207929.RAY_iBEb96NHoz28dnqlNXmn5Fsv3qsIoqYaH-HAsRMA8130_provenance.
- NP207932.RAQER_Qy7phBApf2TwtP-gHV0EiKYKW5d6sqO5MaH1SN4130_assertion description "[A model, similar to that proposed in APL, involving retinoic acid receptors (RAR) and tissue specific Hox gene expression, is suggested to explain the HDAC effects on embryo development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207932.RAQER_Qy7phBApf2TwtP-gHV0EiKYKW5d6sqO5MaH1SN4130_provenance.
- NP207934.RAQdNCsOsVFQSFQai6MMGqaceJXZdg4J8bhU2p6VISbJA130_assertion description "[Mutations of the aprataxin (APTX) gene cause early-onset ataxia with ocular motor apraxia and hypoalbuminemia (EAOH), also called ataxia with oculomotor apraxia type 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207934.RAQdNCsOsVFQSFQai6MMGqaceJXZdg4J8bhU2p6VISbJA130_provenance.
- NP207935.RAZJmArHau5S20eujngfAWHc-j3pTQSHURdfHqDwzV3LI130_assertion description "[The aim of this study was to evaluate the presence and the role of the serum soluble costimulatory molecule CD28 in patients with systemic lupus erythematosus (SLE), primary Sjögren's syndrome (SS), and systemic sclerosis (SSc).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207935.RAZJmArHau5S20eujngfAWHc-j3pTQSHURdfHqDwzV3LI130_provenance.
- NP207937.RASBv_lKPPPr-7LsmCzMSeiO83hKYHD71Ed4YCHfaPeqo130_assertion description "[To elucidate whether systemic administration of CNP would be a novel medical treatment for chondrodysplasias, for which no drug therapy has yet been developed, we investigated the effect of circulating CNP by using the CNP transgenic mice with an increased circulating CNP under the control of human serum amyloid P component promoter (SAP-Nppc-Tg mice).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207937.RASBv_lKPPPr-7LsmCzMSeiO83hKYHD71Ed4YCHfaPeqo130_provenance.
- NP207944.RAT3CcUVAhq_ji53X62jnYv6aZDbb36zUtf8I8rATnILg130_assertion description "[This activity has been called into question based on evidence in infectious disease and autoimmune models in which IL-27 is not absolutely required for the generation of IFN-gamma, and IL-27 plays a regulatory role in controlling inflammation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207944.RAT3CcUVAhq_ji53X62jnYv6aZDbb36zUtf8I8rATnILg130_provenance.
- NP207946.RAcjbSrmeSdb8Ogn4BdxotbaTDD9n97R9iNhCoW6sS5Y8130_assertion description "[NYGM cells concomitantly expressed MET receptor tyrosine kinase (a product of c-met protooncogene) and its ligand HGF/SF (hepatocyte growth factor/scatter factor), as well as HGF activator and HGF activator inhibitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207946.RAcjbSrmeSdb8Ogn4BdxotbaTDD9n97R9iNhCoW6sS5Y8130_provenance.
- NP207951.RAZsugn4KXFV-GkouK8yYcvKdH5yVa9yVAq_NPlqf-ptw130_assertion description "[In particular, S100A2 was upregulated in squamous cell carcinomas, whereas S100P was mainly increased in adenocarcinomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207951.RAZsugn4KXFV-GkouK8yYcvKdH5yVa9yVAq_NPlqf-ptw130_provenance.
- NP207956.RAQgDhZJORFOdobwffbG_uvealzpOuKAWP2tt2zG_1-HE130_assertion description "[To facilitate the molecular diagnosis of uncharacterized patients with HPFH and delta beta thalassemia, oligonucleotide primers have been designed to enzymatically amplify deletion-specific products for nine known deletions, which include those responsible for HPFH-1, HPFH-2, HPFH-3, Spanish (delta beta)zero thalassemia, hemoglobin (Hb) Lepore, Sicilian (delta beta)zero thalassemia, Chinese G gamma(A gamma delta beta)zero thalassemia, Asian-Indian inversion-deletion G gamma(A gamma delta beta)zero thalassemia, and Turkish inversion-deletion (delta beta)zero thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207956.RAQgDhZJORFOdobwffbG_uvealzpOuKAWP2tt2zG_1-HE130_provenance.
- NP207959.RAdVGUeaiU60qayOQajca6FvdXLu5LDdYWowokcy-OI4E130_assertion description "[Expression of ETV6-NTRK in classical, cellular and mixed subtypes of congenital mesoblastic nephroma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207959.RAdVGUeaiU60qayOQajca6FvdXLu5LDdYWowokcy-OI4E130_provenance.
- NP207964.RAc8p0ZCnNDmhdiNgpLDxsEZkivh-K6mc2dsbtonsliiI130_assertion description "[Human sweet taste perception is mediated by the heterodimeric G protein-coupled receptor encoded by the TAS1R2 and TAS1R3 genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207964.RAc8p0ZCnNDmhdiNgpLDxsEZkivh-K6mc2dsbtonsliiI130_provenance.
- NP207970.RAQNgbs7QfqL83gkgg8WnBRe0qQm9sS2WV6vWKCIsjmDk130_assertion description "[Focusing on a specific subset of genes, we found that the ability of stromal ATF3 to promote cancer progression is mediated by transcriptional repression of CLDN1 and induction of CXCL12 and RGS4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207970.RAQNgbs7QfqL83gkgg8WnBRe0qQm9sS2WV6vWKCIsjmDk130_provenance.
- NP207975.RAXct3F0rM3vglA8RtKaPHDCHVWdTLYFoKAblVK4lyMEY130_assertion description "[A compilation of our data with data from 3 previous SMZL CGH studies revealed a significant heterogeneity between the studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207975.RAXct3F0rM3vglA8RtKaPHDCHVWdTLYFoKAblVK4lyMEY130_provenance.
- NP207978.RAfeA8yRyAM7j84vPiqDXUhSWzGmkG9Zo_0VweZGZRsnw130_assertion description "[We evaluated whether a single-nucleotide polymorphism (SNP) of the TRAF6 gene previously associated with systemic lupus erythematosus and rheumatoid arthritis may be a common risk factor for systemic sclerosis (SSc) and giant cell arteritis (GCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207978.RAfeA8yRyAM7j84vPiqDXUhSWzGmkG9Zo_0VweZGZRsnw130_provenance.
- NP207979.RAS_KUhrmyLBhCCEjPT4tuFxEYAA9TXB7vmPxr6jyjNfE130_assertion description "[The vast majority of cases of APL are associated with t(15; 17) leading to the formation of PML-RAR alpha, RAR alpha-PML and aberrant PML fusion products.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207979.RAS_KUhrmyLBhCCEjPT4tuFxEYAA9TXB7vmPxr6jyjNfE130_provenance.
- NP207980.RAVOAjguZlYEtrMpR8TL1fQw44XbyFu_HzzRRTyr8hVCQ130_assertion description "[To test the hypothesis that FYN, a member of the SRC family of kinases (SFKs), is up-regulated in prostate cancer, as FYN is functionally distinct from other SFKs, and interacts with FAK and paxillin (PXN), regulators of cell morphology and motility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207980.RAVOAjguZlYEtrMpR8TL1fQw44XbyFu_HzzRRTyr8hVCQ130_provenance.
- NP207987.RAWEdZdNybxDqMDhvycYUCgUUvp6eskQtN6FHJjAwI7EA130_assertion description "[Abnormalities in the CDKN2 (p16INK4/MTS-1) gene in human melanoma cells: relevance to tumor growth and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207987.RAWEdZdNybxDqMDhvycYUCgUUvp6eskQtN6FHJjAwI7EA130_provenance.
- NP207990.RAYiRrQ3D9gaR_iTQJFMOnXutum4cnRlspfEaJqZby6Og130_assertion description "[Here we present a second family of this latter type and demonstrate that an AZFc-deleted Y chromosome lacking not only DAZ, but also BPY2 and CDY1, has been transmitted from a father to his three infertile sons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207990.RAYiRrQ3D9gaR_iTQJFMOnXutum4cnRlspfEaJqZby6Og130_provenance.
- NP207991.RAYcH_C3r5FLfJrpl-Enj1FGfIF0NF0z4m_O_gdtSKsp4130_assertion description "[In three families with hypokalemic periodic paralysis (HOPP) we have confirmed the presence of a missense mutation (arginine 528 to histidine) within the gene CACNL1A3 encoding the alpha 1 subunit of the L-type, voltage-sensitive calcium channel.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207991.RAYcH_C3r5FLfJrpl-Enj1FGfIF0NF0z4m_O_gdtSKsp4130_provenance.
- NP207993.RAeTRspUtreqWEhRqQTkLR7J-N6UmhinDoJ2kjL39jZuI130_assertion description "[We found no evidence that could support a major pathogenic role of STH and TAU haplotype in AD, FTD or PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207993.RAeTRspUtreqWEhRqQTkLR7J-N6UmhinDoJ2kjL39jZuI130_provenance.
- NP207995.RAY9w63YndujsHVDqlJWseG26BQAZcOXQfvAauXXiRfO4130_assertion description "[These studies have helped us identify genes that are essential to the development of AAAs (such as MMP9, IL6, and AT1R) and to reveal other genes that may be dispensable in aneurysm formation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP207995.RAY9w63YndujsHVDqlJWseG26BQAZcOXQfvAauXXiRfO4130_provenance.
- NP208001.RAde_uKDlk2sReDyFdeuUp2FkgR5UQQRl2hXf9yQTDT78130_assertion description "[Mutations in SCN5A cause a functional reduction in the availability of cardiac sodium current in Brugada syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208001.RAde_uKDlk2sReDyFdeuUp2FkgR5UQQRl2hXf9yQTDT78130_provenance.
- NP208003.RAZTPB7dmrQSC5g-HWiu_EV9u0YxaK7509rYfJK5zwkT8130_assertion description "[Our previous finding of an association of TLR4 gene sequence variants and prostate cancer risk provides evidence for a role of TLRs in prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208003.RAZTPB7dmrQSC5g-HWiu_EV9u0YxaK7509rYfJK5zwkT8130_provenance.
- NP208004.RAZWbOVIgEQK597QgUkVj6yYLtURCeduKL9UN-AfwJN4k130_assertion description "[We aimed to replicate the previously observed association between acetylcholine receptor subtype M2 (CHRM2) gene polymorphisms and heart rate recovery (HRR) after exercise in patients with a recent acute myocardial infarction (AMI) and assess the prognostic significance of CHRM2 gene variants after AMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208004.RAZWbOVIgEQK597QgUkVj6yYLtURCeduKL9UN-AfwJN4k130_provenance.
- NP208016.RAbmHVjTZ1L4bw0hcKegT-rld05Kq8RjrpowsHj49bAt8130_assertion description "[Decreased levels of brain-derived neurotrophic factor (BDNF) have been implicated in the pathogenesis of Alzheimer's disease and depression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208016.RAbmHVjTZ1L4bw0hcKegT-rld05Kq8RjrpowsHj49bAt8130_provenance.
- NP208017.RATVys0kK2FKyMtLdw8cXadccm32SiBE0uKxWsG3ARDEM130_assertion description "[Identification of sialyltransferase 8B as a generalized susceptibility gene for psychotic and mood disorders on chromosome 15q25-26.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208017.RATVys0kK2FKyMtLdw8cXadccm32SiBE0uKxWsG3ARDEM130_provenance.
- NP208020.RAcZT3w3iUrsxULwaMadL5MiMRxi-8riWSZpaT_u_hb1E130_assertion description "[Most of what is known about the genetic basis of kidney cancer has been learned from study of the inherited forms of kidney cancer: von Hippel Lindau (VHL gene), hereditary papillary renal carcinoma (c-Met gene), Birt Hogg Dubé (BHD gene), and hereditary leiomyomatosis renal cell cancer (fumarate hydratase gene).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208020.RAcZT3w3iUrsxULwaMadL5MiMRxi-8riWSZpaT_u_hb1E130_provenance.
- NP208021.RAaNdjf_nesi2ndOSwIkZ8exaakybXRKRl0W6SekG749I130_assertion description "[Anterior gradient-2 (AGR2) functions in a range of biological systems, including goblet cell formation, limb regeneration, inhibition of p53, and metastasis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208021.RAaNdjf_nesi2ndOSwIkZ8exaakybXRKRl0W6SekG749I130_provenance.
- NP208029.RARE2Y3ZX318ToLaQXfBZdqZI6Znc_7Q7oeDRme1HuPpU130_assertion description "[ETV6/GOT1 fusion in a case of t(10;12)(q24;p13)-positive myelodysplastic syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208029.RARE2Y3ZX318ToLaQXfBZdqZI6Znc_7Q7oeDRme1HuPpU130_provenance.
- NP208031.RAcMdTUNpmhln2lZk7M6Jk4RW0kjMf02987l45veRCyro130_assertion description "[A triple-transgenic mouse model of AD (3xTgAD mice) and nontransgenic control mice were used to test for an affect of chronic mild social stress on blood glucose, plasma glucocorticoids, plasma insulin, anxiety, and hippocampal amyloid β-particle (Aβ), phosphorylated tau (ptau), and brain-derived neurotrophic factor (BDNF) levels.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208031.RAcMdTUNpmhln2lZk7M6Jk4RW0kjMf02987l45veRCyro130_provenance.
- NP208035.RAZyCOxbz8iTIniaw8ldmiwdvsWCfakGzVtQgzlXS-2UY130_assertion description "[In this study we show that Aurora A kinase activity is altered in different ways in three somatic cancer-associated mutations located within the catalytic domain; Aurora A(V174M) shows constitutively increased kinase activity, Aurora A(S155R) activity is decreased primarily due to misregulation, and Aurora A(S361*) activity is ablated due to loss of structural integrity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208035.RAZyCOxbz8iTIniaw8ldmiwdvsWCfakGzVtQgzlXS-2UY130_provenance.
- NP208041.RAYxt21V3Q4ZnUN3gn0bpP81C2G4h9QiVejmJYquyL-XY130_assertion description "[I discuss evidence showing that transgenic expression of a low-avidity IGRP(206-214)-reactive T cell receptor (TCR) efficiently prevents the development of insulitis and diabetes in NOD (non-obese diabetic) mice and that these cells do so by killing autoantigen-loaded antigen presenting cells in the pancreas-draining lymph nodes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208041.RAYxt21V3Q4ZnUN3gn0bpP81C2G4h9QiVejmJYquyL-XY130_provenance.
- NP208046.RAdp91QvVbLqnR0zP1OYaU2unqnn5AK7UaKGPOI1gmaIQ130_assertion description "[To determine if TRK-T1 expression can cause thyroid cancer in vivo, we developed transgenic mice that express the human TRK-T1 fusion protein in the thyroid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208046.RAdp91QvVbLqnR0zP1OYaU2unqnn5AK7UaKGPOI1gmaIQ130_provenance.
- NP208047.RASug8TzHiyZZCIXLtU2oHGHdAWpmYWvBPieQVSkHL0Os130_assertion description "[Polymorphisms in the circadian genes NPAS2, ARNTL, and RORA were also suggested to contribute to depression vulnerability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208047.RASug8TzHiyZZCIXLtU2oHGHdAWpmYWvBPieQVSkHL0Os130_provenance.
- NP208048.RAceDRX8W6BqeWUT2zKZK9ZETBs7IpTQ7AlKPoCbbHUJo130_assertion description "[Expression of PEX1 rescued the cells from the biogenesis defect in human fibroblasts of complementation group 1 (CG1), the largest PBD complementation group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208048.RAceDRX8W6BqeWUT2zKZK9ZETBs7IpTQ7AlKPoCbbHUJo130_provenance.
- NP208050.RAR-C5dpWPO5btrmVNY93dtfJVUVpIUewtVBD55PpYxWc130_assertion description "[Our study thus provides evidence for a pathogenic mechanism for DS in which increased expression of App, in the context of trisomy, causes abnormal transport of NGF and cholinergic neurodegeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208050.RAR-C5dpWPO5btrmVNY93dtfJVUVpIUewtVBD55PpYxWc130_provenance.
- NP208054.RAZ5HnBwFxJjuzrX5q9NPsfzqHySVurJhpRmQDWICnjCY130_assertion description "[Whereas SPARC and IGFBP7 protein were absent in nonmalignant brain vessels, a distinct immunoreactivity patterns were observed in GBM sections whereby SPARC was strongly expressed in perivascular cells adjacent to GBM vessels while GBM endothelial cells were immunostained for IGFBP7.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208054.RAZ5HnBwFxJjuzrX5q9NPsfzqHySVurJhpRmQDWICnjCY130_provenance.