Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP145659.RAXukYEeEB87zyifbV6EVPO9ECWIC_4e6PmBIfCdgHTNQ130_assertion description "[The T393C SNP is a prognostic marker that could help to identify high risk patients suffering from head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145659.RAXukYEeEB87zyifbV6EVPO9ECWIC_4e6PmBIfCdgHTNQ130_provenance.
- NP145661.RAeLSMtm13_OdeF5HL5cwDczmVYliFrNQkDeOp8vYxBvc130_assertion description "[Microsatellite instability and modifications in the hMLH1 and hMSH2 genes are implicated in a significant proportion of the patients with head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145661.RAeLSMtm13_OdeF5HL5cwDczmVYliFrNQkDeOp8vYxBvc130_provenance.
- NP145667.RATjNhUStyXYz2JeQaitYREB6yoiaVhBsJ-MYn0HbdF54130_assertion description "[The XRCC1 ARG399Gln polymorphism had consistent associations with survival outcomes in head and neck neoplasms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145667.RATjNhUStyXYz2JeQaitYREB6yoiaVhBsJ-MYn0HbdF54130_provenance.
- NP145668.RARdgUxkJciD1gEwm_qaXX2d4hZRZivdiAKlK21jBitts130_assertion description "[Bcl-xL inhibits p53- but not apoptin-induced apoptosis in head and neck neoplasms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145668.RARdgUxkJciD1gEwm_qaXX2d4hZRZivdiAKlK21jBitts130_provenance.
- NP145673.RATeIlhamvpZP-Xy5J2_eRU9bgSQmM3siG3O6zUWSD1w0130_assertion description "[Potentially interesting value of the serum levels of sEGFR and EGF, especially when combined, as markers for non-small cell lung cancer and head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145673.RATeIlhamvpZP-Xy5J2_eRU9bgSQmM3siG3O6zUWSD1w0130_provenance.
- NP145674.RAcWbRvtPd-95FjJaIQGxS3QX4uJiDSQWk61S5HuJe0_w130_assertion description "[analysis of TCF21 epigenetic regulation on 6q23-q24 in lung and head and neck cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145674.RAcWbRvtPd-95FjJaIQGxS3QX4uJiDSQWk61S5HuJe0_w130_provenance.
- NP145678.RAb0rcbnq09r-YjSp7uqbrDIXgcSCGdDtwrxdyM7ik2_0130_assertion description "[MDR1 expression, MRP1 expression, and MRP7 expression are refractory factors in head and neck cancer chemotherapy; induction of MRP7 expression is involved in drug resistance to natural products, especially to docetaxel in salivary gland adenocarcinoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145678.RAb0rcbnq09r-YjSp7uqbrDIXgcSCGdDtwrxdyM7ik2_0130_provenance.
- NP145679.RAbCGPraLB9-bmDoRKDgClzqPISIXFGa1GCwEkTvm712M130_assertion description "[CYP2E1 polymorphism is not associated with the risk of head and neck cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145679.RAbCGPraLB9-bmDoRKDgClzqPISIXFGa1GCwEkTvm712M130_provenance.
- NP145686.RARN9-uZpngYUOIAMk1Kill7y5cf3RMriI_fYbDB99I0I130_assertion description "[Polymorphisms in CYP1A1 is not associated with the risk of head and neck cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145686.RARN9-uZpngYUOIAMk1Kill7y5cf3RMriI_fYbDB99I0I130_provenance.
- NP145691.RAYjsL3VkW0z0LzlOfs84Mzr4QEWh5cKYYlC_haxCJ4Hg130_assertion description "[Increased acetylation of RARbeta1 is associated with head and neck cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145691.RAYjsL3VkW0z0LzlOfs84Mzr4QEWh5cKYYlC_haxCJ4Hg130_provenance.
- NP145693.RARtU4MqxZkjiZ_L0b-WKzdHnbgsXodR1KjvyDKiTWR0Q130_assertion description "[Frequent deletion and decreased mRNA expression of ING4 suggested it as a class two tumor suppressor gene and may play an important role in head and neck cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145693.RARtU4MqxZkjiZ_L0b-WKzdHnbgsXodR1KjvyDKiTWR0Q130_provenance.
- NP145697.RAeo8JQBu_IQ07-Wy8RdxPE0YW5eJISSDsPhTi9crzrkg130_assertion description "[erythropoietin and EPOR are co-expressed in tumor cells, suggesting that erythropoietin may potentially function as an autocrine or paracrine factor in head and neck cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145697.RAeo8JQBu_IQ07-Wy8RdxPE0YW5eJISSDsPhTi9crzrkg130_provenance.
- NP145705.RAcvr_2p8F8q5LB9QUDIP6txrMaMgc4fsLPi3aPXbixZg130_assertion description "[The G308A polymorphism of the TNF-alpha gene did not affect levels of inflammatory markers in patients after surgery for head and neck cancer who were treated with early nutrition.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145705.RAcvr_2p8F8q5LB9QUDIP6txrMaMgc4fsLPi3aPXbixZg130_provenance.
- NP145720.RATqISlK6nDEYLfkBfGyDBTAM7S5l_Drky19T65NwqkRo130_assertion description "[The ability of Cdx1 and c-myc to initiate the earliest stages of transdifferentiation of esophageal keratinocytes toward a cell fate characteristic of Barrett's esophagus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145720.RATqISlK6nDEYLfkBfGyDBTAM7S5l_Drky19T65NwqkRo130_provenance.
- NP145728.RAULlsU-diPstNYD6hCjj1nXom-XzjJq4bWLH-bYbvcF0130_assertion description "[Elevated il 6 levels in Barrett esophagus may contribute to the development of apoptosis resistance, thereby placing this epithelium at higher risk of developing malignancy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145728.RAULlsU-diPstNYD6hCjj1nXom-XzjJq4bWLH-bYbvcF0130_provenance.
- NP145732.RAWSo_F2er-31EbjrCDeCfcngA0-7Q7YyPkw41Y4Ihh0I130_assertion description "[Results describe cathepsin D and aldo-keto reductase 1C2 and 1B10 dysregulation in Barrett's esophagus and esophageal adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145732.RAWSo_F2er-31EbjrCDeCfcngA0-7Q7YyPkw41Y4Ihh0I130_provenance.
- NP145739.RAet2QBGR2w3Zm9vna-COdmFuy3UA-O4sTJLO0AiyI-jg130_assertion description "[Results describe cathepsin D and aldo-keto reductase 1C2 and 1B10 dysregulation in Barrett's esophagus and esophageal adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145739.RAet2QBGR2w3Zm9vna-COdmFuy3UA-O4sTJLO0AiyI-jg130_provenance.
- NP145746.RAaJG8tGNU5hm99AX5JnaWHPUFEOxo1XcNp4HFCOvphXo130_assertion description "[The bile acid receptor FXR is significantly overexpressed in Barrett's esophagus compared to normal mucosa, esophagitis and esophageal adenocarcinoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145746.RAaJG8tGNU5hm99AX5JnaWHPUFEOxo1XcNp4HFCOvphXo130_provenance.
- NP145748.RARhy7UGIrOR3VsWQphVc0qjeiCe5T_FzrjuZ2-TMvhso130_assertion description "[Acid-induced activation of both ERK and p38 causes a significant increase in COX-2 promoter activity, and acid-activated ERK stabilizes COX-2 mRNA in Barrett's esophagus ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145748.RARhy7UGIrOR3VsWQphVc0qjeiCe5T_FzrjuZ2-TMvhso130_provenance.
- NP145754.RAWlVrS_BXYMjU3YFQYOX6BNPPMZFhDptKlk7d5D4JWWw130_assertion description "[Promoter methylation of APC was found in all Barrett esophagus samples & 95% of esophageal adenocarcinomas/methylation of APC correlated with lack of expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145754.RAWlVrS_BXYMjU3YFQYOX6BNPPMZFhDptKlk7d5D4JWWw130_provenance.
- NP145759.RAYGkAb56K8oU97nRcQC-ayAru4HNYsFF4NrBQH15PpU0130_assertion description "[Four pathogenic mutations including a novel, in-frame, 15-bp tandem duplication (806-820) in exon 8 and a novel 751+1G > A splice site mutation in SURF1 in three cases of Leigh Syndrome with cytochrome c oxidase deficiency ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145759.RAYGkAb56K8oU97nRcQC-ayAru4HNYsFF4NrBQH15PpU0130_provenance.
- NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_assertion description "[A patient with typical clinical and neuroradiological features of Leigh syndrome and cytochrome oxidase deficiency was found to have a mutation in the COX15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145761.RAS4FSxln0cZwLszOJKb63CfFJ0ycaU6Ki9FvorHw7_o8130_provenance.
- NP145768.RARiGJDGpuj91ivU9q_19Nl3KM5VCe6wsBBGJfGv-WWPs130_assertion description "[study investigated EGFR protein expression & gene mutations in exons 18, 19 and 21 in 40 renal angiomyolipomas (AML); no EGFR gene mutations of TK domain were detected and strong immunostaining was found in 5% of the renal AML cases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145768.RARiGJDGpuj91ivU9q_19Nl3KM5VCe6wsBBGJfGv-WWPs130_provenance.
- NP145772.RAUw3FViUqcqcdpkil6XEzLDIfSBkAFAGHjIbzJiULB78130_assertion description "[aberrant B-Raf activity in angiomyolipomas leads to abnormal cellular differentiation and migration [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145772.RAUw3FViUqcqcdpkil6XEzLDIfSBkAFAGHjIbzJiULB78130_provenance.
- NP145777.RAYxzT9MVqHWPPPdvZySQlEQFVw8OdhvdfhVRrUU4pNYA130_assertion description "[The data suggest that the OGG1 Ser326Cys polymorphism may be associated with tooth loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145777.RAYxzT9MVqHWPPPdvZySQlEQFVw8OdhvdfhVRrUU4pNYA130_provenance.
- NP145778.RAe9zMk40kyXgJ8uRSYhmNKbWFzxRKo9EXawKgdGEJxWc130_assertion description "[Genetic variations at the MGP locus did not affect the rate of tooth loss in the elderly/, the MGP locus may be associated with some determinants for tooth loss in elderly women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145778.RAe9zMk40kyXgJ8uRSYhmNKbWFzxRKo9EXawKgdGEJxWc130_provenance.
- NP145784.RAaovrddJaiMpXzo0CS-xAf8-iCxnm10xDyM3btK_cDCQ130_assertion description "[Loss of estrogen receptor beta expression is associated with gallbladder cancer progression ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145784.RAaovrddJaiMpXzo0CS-xAf8-iCxnm10xDyM3btK_cDCQ130_provenance.
- NP145786.RAUReA_20Wx2bb3lAARtQoBeCQ0ylDAejNcAdgi7DqKso130_assertion description "[Homozygous deletion, a combination of LOH and promoter hypermethylation, and multiple LOH are major mechanisms of p16 inactivation in gallbladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145786.RAUReA_20Wx2bb3lAARtQoBeCQ0ylDAejNcAdgi7DqKso130_provenance.
- NP145789.RAfuht8fmBoj0vd8aEjmKtqoIhofb22E7nEvkyNJw8S_o130_assertion description "[Individuals with 1/C and 2/C haplotypes of IL-1RN VNTR and -511IL-1B C -- > T polymorphisms were more susceptible to develop gallbladder cancer with gallstones compared to healthy controls in north India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145789.RAfuht8fmBoj0vd8aEjmKtqoIhofb22E7nEvkyNJw8S_o130_provenance.
- NP145791.RAf2mqxFbU6fBHT2RnBCK8ZVLDGcKbqLMIsfPZhiKeNBw130_assertion description "[Individuals with 1/C and 2/C haplotypes of IL-1RN VNTR and -511IL-1B C -- > T polymorphisms were more susceptible to develop gallbladder cancer with gallstones compared to healthy controls in north India.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145791.RAf2mqxFbU6fBHT2RnBCK8ZVLDGcKbqLMIsfPZhiKeNBw130_provenance.
- NP145792.RAcJJx0a5Jl7ibk6XV0J0TZU44xhaMgENClEqqB_P0nPI130_assertion description "[These results suggest that hOGG1 Ser326Cys polymorphism is associated with gallbladder cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145792.RAcJJx0a5Jl7ibk6XV0J0TZU44xhaMgENClEqqB_P0nPI130_provenance.
- NP145795.RASDhlVdfa5szAZsSDbWeUvreGJQisKas7WPerSzstrTc130_assertion description "[Cisplatin enhanced sensitivity to ACNU gallbladder cancer cells expressing MGMT both in vitro and in vivo.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145795.RASDhlVdfa5szAZsSDbWeUvreGJQisKas7WPerSzstrTc130_provenance.
- NP145808.RAfTyMj0RDtHxIdN2AOgkE08d_PYMtZBlvxvc_lEFXbuM130_assertion description "[To find out the association of GST variants with risk of gallbladder cancer, the distribution of polymorphisms in the GST family of genes (GSTT1, GSTM1, GSTP1, and GSTM3) were studied in 106 cancer patients and 201 healthy controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145808.RAfTyMj0RDtHxIdN2AOgkE08d_PYMtZBlvxvc_lEFXbuM130_provenance.
- NP145810.RAScj_TdmkrcAy1tm_9eElcVX5Pnz9Y-EnxAMNArDJ6mc130_assertion description "[Aberrant Nrf2 activation provoked by Keap1 alteration is one of the molecular mechanisms for chemotherapeutic resistance in gallbladder cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145810.RAScj_TdmkrcAy1tm_9eElcVX5Pnz9Y-EnxAMNArDJ6mc130_provenance.
- NP145819.RAU5g8IF1i2Ifn-SEA7_bngnkwqtgK8pifi9nbUex1SbU130_assertion description "[CT60 polymorphism of CTLA-4 maps an important genetic determinant for the risk of both Graves'disease and Hashimoto thyroiditis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145819.RAU5g8IF1i2Ifn-SEA7_bngnkwqtgK8pifi9nbUex1SbU130_provenance.
- NP145823.RAQOiDu2HXsJjgD6gjIo6cA2JvoVVBFxeIttEBdOCoVt0130_assertion description "[CCL5 was significantly increased in Graves'disease patients compared with Hashimoto's thyroiditis or nontoxic nodular thyroid disease subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145823.RAQOiDu2HXsJjgD6gjIo6cA2JvoVVBFxeIttEBdOCoVt0130_provenance.
- NP145828.RAWYBWOn88q6fMe1zz4N6ZDWqLM4nSX58eGABd43qAzpg130_assertion description "[Data do not support a role for ET-1 as a valid quantitative indicator for stage or progression in endemic goiter, Graves'disease or Hashimoto's thyroiditis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145828.RAWYBWOn88q6fMe1zz4N6ZDWqLM4nSX58eGABd43qAzpg130_provenance.
- NP145829.RAU0B99WOVDWfnWFtij37ad9UzgygFz9--a1FBJgzAAXY130_assertion description "[The CYP27B1 promoter (-1260) C/A polymorphism appears to be associated with endocrine autoimmune diseases but the CYP27B1 intron 6 (+2838) C/T polymorphism appears to be associated only with Hashimoto's thyroiditis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145829.RAU0B99WOVDWfnWFtij37ad9UzgygFz9--a1FBJgzAAXY130_provenance.
- NP145831.RAcA0FVmnejoctg6CngHwOiDpz2Gp9c16kJb6P-zcN0qY130_assertion description "[Our findings suggest that the changes in the expression of apoptotic proteins (Fas/FasL and caspase 8) in the thyroid gland of patients with autoimmune Graves Disease and Hashimoto's thyroiditis reflect their involvemetn in the pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145831.RAcA0FVmnejoctg6CngHwOiDpz2Gp9c16kJb6P-zcN0qY130_provenance.
- NP145835.RAcISy54nIXNvHmJhp9JRK9uB4VrQSta4dL-ixwQQFT4M130_assertion description "[It could be concluded that patients who carry the C/C homozygote of the VDR-FokI gene polymorphism in exon 2 may have a higher risk of developing Hashimoto's Thyroiditis in Chinese patients in Taiwan.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145835.RAcISy54nIXNvHmJhp9JRK9uB4VrQSta4dL-ixwQQFT4M130_provenance.
- NP145837.RAUz867L4V4lw5tbDOXHmCyaLSVszacbd5AcKzNEKx-ok130_assertion description "[Our findings suggest that the changes in the expression of apoptotic proteins (Fas/FasL and caspase 8) in the thyroid gland of patients with autoimmune Graves Disease and Hashimoto's thyroiditis reflect their involvemetn in the pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145837.RAUz867L4V4lw5tbDOXHmCyaLSVszacbd5AcKzNEKx-ok130_provenance.
- NP145838.RAS9HVrBwhBsYu32aqBYEq1YYlkgi2-4W7uzG1jG_4VXQ130_assertion description "[there is no significant contribution of common genetic Fas variants to the genetic risk of developing Hashimoto's thyroiditis or Graves'disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145838.RAS9HVrBwhBsYu32aqBYEq1YYlkgi2-4W7uzG1jG_4VXQ130_provenance.
- NP145839.RAQH4Hk9WreiLAhFKx8DU2IFuPaRwMy_vv2mxoCU2Xlvs130_assertion description "[Our findings suggest that the changes in the expression of apoptotic proteins (Fas/FasL and caspase 8) in the thyroid gland of patients with autoimmune Graves Disease and Hashimoto's thyroiditis reflect their involvemetn in the pathogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145839.RAQH4Hk9WreiLAhFKx8DU2IFuPaRwMy_vv2mxoCU2Xlvs130_provenance.
- NP145841.RAWbrj5S4eKIVO885H89cyR_4kiNp745chMdBKD3CZAyk130_assertion description "[Interaction between the HLA-DRB4 and CTLA-4 genes determines the thyroid function of TPO-positive goitrous Japanese Hashimoto's thyroiditis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145841.RAWbrj5S4eKIVO885H89cyR_4kiNp745chMdBKD3CZAyk130_provenance.
- NP145843.RAX8hd7O5TGfrK-u9DkJQUlaM2NsX3mw1LpTEf-aYdzNU130_assertion description "[There are genotypic differences regarding the clinical forms of autoimmune chronic lymphocytic thyroiditis with a strong association between DQB1*03 and the atrophic form only.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145843.RAX8hd7O5TGfrK-u9DkJQUlaM2NsX3mw1LpTEf-aYdzNU130_provenance.
- NP145846.RAQBSaA8l7tsk0aUzJjLnxFLLj7vxsXLjWYf2UFaOXYoY130_assertion description "[Interaction between the HLA-DRB4 and CTLA-4 genes determines the thyroid function of TPO-positive goitrous Japanese Hashimoto's thyroiditis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145846.RAQBSaA8l7tsk0aUzJjLnxFLLj7vxsXLjWYf2UFaOXYoY130_provenance.
- NP145855.RATVuBNjTWQ35coNqvH-vGUmuId364sn0_Wjrs-0FgSFo130_assertion description "[Mutations in GJB2 are responsible for over one quarter of non-syndromic sensorineural deafness in the British Bangladeshi population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145855.RATVuBNjTWQ35coNqvH-vGUmuId364sn0_Wjrs-0FgSFo130_provenance.
- NP145860.RAbaweICDOA1EHpR31VKjR5nHkrcuaCe8c2JbiX6AHBvM130_assertion description "[Barttin mutations is associated with antenatal Bartter syndrome with sensorineural deafness ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145860.RAbaweICDOA1EHpR31VKjR5nHkrcuaCe8c2JbiX6AHBvM130_provenance.
- NP145864.RAeF15fqFKtM-5vY2L7WL8babQWKyhlpUOLh4F80-jCtU130_assertion description "[Direct sequencing after PCR amplification of genomic DNA revealed a novel insertional mutation (405insC) in the GATA3 gene of two patients with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145864.RAeF15fqFKtM-5vY2L7WL8babQWKyhlpUOLh4F80-jCtU130_provenance.
- NP145867.RAd7tayiSOD8nYm1GwBwNgf0o67mjvgireQbZMIoDaCVI130_assertion description "[A novel heterozygous deletion frameshift mutation of GATA3 in a Japanese kindred with the hypoparathyroidism, deafness and renal dysplasia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145867.RAd7tayiSOD8nYm1GwBwNgf0o67mjvgireQbZMIoDaCVI130_provenance.
- NP145878.RAQOq0q6SSM2-_4fObdw5Zwe7fW1Qy4BhMaVPgu1WxVew130_assertion description "[Mice lacking SLC12A7 function suffer from deafness and renal metabolic acidosis/phenotype suggests a function in inner ear potassium recycling/function in the proton secreting alpha-intercalating cells of the kidney is shown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145878.RAQOq0q6SSM2-_4fObdw5Zwe7fW1Qy4BhMaVPgu1WxVew130_provenance.
- NP145879.RAXs7zA-thl2Za5Rze39vVDu5OqwU2P48ho4kD5p3HecA130_assertion description "[Familial deafness, congenital heart defects, and posterior embryotoxon caused by cysteine substitution in the first epidermal-growth-factor-like domain of jagged 1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145879.RAXs7zA-thl2Za5Rze39vVDu5OqwU2P48ho4kD5p3HecA130_provenance.
- NP145882.RAby8nsXf5JzFC_jyfoAss9lRvt4yO8RDY7t3lcIz3fDI130_assertion description "[Interactions with ZO-1 and ZO-2, in particular, may mediate recruitment of armadillo repeat gene deletes in velocardiofacial syndrome protein to the plasma membrane and the nucleus ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145882.RAby8nsXf5JzFC_jyfoAss9lRvt4yO8RDY7t3lcIz3fDI130_provenance.
- NP145883.RAVZVIXfbAtnhQfc-jT1_FxAQG1QrjtDTldDWzZr_WyHk130_assertion description "[a novel nuclear localization signal in Tbx1 is deleted in DiGeorge syndrome patients harboring the 1223delC mutation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145883.RAVZVIXfbAtnhQfc-jT1_FxAQG1QrjtDTldDWzZr_WyHk130_provenance.
- NP145887.RAfR7edUAij7LBB2VNatlipjOTRxSP1fcEH1vBfthIHGQ130_assertion description "[PAP (133-152) and PAP (173-192) were immunogenic and processed from whole PAP in HLA-DRB1*1501 tg mice/peptides were capable of stimulating CD4 T lymphocytes from HLA-DRB1*1501-positive patients with granulomatous prostatitis and normal donors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145887.RAfR7edUAij7LBB2VNatlipjOTRxSP1fcEH1vBfthIHGQ130_provenance.
- NP145897.RAfRGCZpVjN7T4jWg6TMoiJY9dKiPidP44CMu3VqqueUA130_assertion description "[NLC1-A, expressed in human hypothalamus, is considered to be a new resistance gene for human narcolepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145897.RAfRGCZpVjN7T4jWg6TMoiJY9dKiPidP44CMu3VqqueUA130_provenance.
- NP145900.RASOcen30UyrDLxrCfCmUEsc2VUcdxOMIhBh-onoHOfnM130_assertion description "[plasma concentrations of orexin-A-like immunoreactivity (orexin-A-LI) in 156 patients with sleep apnea hypopnea syndrome were significantly decreased.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145900.RASOcen30UyrDLxrCfCmUEsc2VUcdxOMIhBh-onoHOfnM130_provenance.
- NP145911.RARkua1FAFapBFXpMrqseNDr9VK9CobISqOzj92VmDhSk130_assertion description "[A novel mutation (L705V) within the Abeta sequence of AbetaPP in a family with autosomal dominant, recurrent intracerebral hemorrhages.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145911.RARkua1FAFapBFXpMrqseNDr9VK9CobISqOzj92VmDhSk130_provenance.
- NP145915.RASY869Q1PZGBYzk-FwWOGly0gmQgwDtN30HY4NwZZX5E130_assertion description "[Carriers of the epsilon 2 or epsilon 4 APOE allele has an increased risk of both incident and recurrent intracerebral hemorrhage (ICH), and both cortical and deep ICH; most risk estimates are higher in Asians than in Europeans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145915.RASY869Q1PZGBYzk-FwWOGly0gmQgwDtN30HY4NwZZX5E130_provenance.
- NP145917.RAX1h2zeoD0vHshMeUlW3LgzFM-7cL7BlSvmgiGW_BoXU130_assertion description "[angiotensin II type 1 receptor is upregulated in cardiac donors with spontaneous intracerebral hemorrhage ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145917.RAX1h2zeoD0vHshMeUlW3LgzFM-7cL7BlSvmgiGW_BoXU130_provenance.
- NP145921.RAb8j7ojRAnEwf7MY8XIRu-mI7r8zZD6DOnOf22TQpE38130_assertion description "[Accumulating data suggest involvement of cystatin C in the pathogenic processes leading to amyloid deposition in cerebral vasculature and most significantly to cerebral hemorrhage in patients with cerebral amyloid angiopathy { REVIEW } ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145921.RAb8j7ojRAnEwf7MY8XIRu-mI7r8zZD6DOnOf22TQpE38130_provenance.
- NP145923.RARf7y6ptywkd-K7pBsNOWFoJcRpZO61t1hmr25ziMRfQ130_assertion description "[Study shows a significant increase in intracerebral hemorrhage in human apoE4 targeted replacement mice compared with apoE3 mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145923.RARf7y6ptywkd-K7pBsNOWFoJcRpZO61t1hmr25ziMRfQ130_provenance.
- NP145927.RAWZA1v5553yTiB1ybWHop6zBpOYdL2PrylKtN5Ke50sA130_assertion description "[orexin-A/hypocretin-1 may therefore play an important role in the various physiological responses including sleep, feeding, and the overall metabolism in intracerebral hemorrhage patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145927.RAWZA1v5553yTiB1ybWHop6zBpOYdL2PrylKtN5Ke50sA130_provenance.
- NP145932.RAdIRjlp7XZUXyCpL_LUta1ACIcMjYS8huFor8E1mUMXA130_assertion description "[Association analysis of five polymorphic microsatellite markers in cluster headache (CH) patients reveals that genetic variations in the NOS1 gene do not contribute greatly to CH susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145932.RAdIRjlp7XZUXyCpL_LUta1ACIcMjYS8huFor8E1mUMXA130_provenance.
- NP145933.RAe1UXcqpI8OR5HuudHKYlGUXIXX69ion_1xx34LaLCq0130_assertion description "[polymorphism of the HCRTR2 gene may modulate the genetic risk for cluster headache ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145933.RAe1UXcqpI8OR5HuudHKYlGUXIXX69ion_1xx34LaLCq0130_provenance.
- NP145945.RAeC_JGOtBxtZDyV1bSAK5xiuP6q7Rr_rBgH25HKazP6M130_assertion description "[In comparison with controls, the frequency of -1, 082*G alleles was lower in IgA nephropathy and the frequencies of -592*C and -819*C were lower in focal segmental glomerulosclerosis, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145945.RAeC_JGOtBxtZDyV1bSAK5xiuP6q7Rr_rBgH25HKazP6M130_provenance.
- NP145952.RAdY3cgC39hlyAQuH8VIaZ9S9_oj7me0GuPAng_TDRgxw130_assertion description "[in patients with nephrotic syndrome due to biopsy proven focal segmental glomerulosclerosis, AGT-M235T polymorphism was associated with the severity of arterial hypertension ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145952.RAdY3cgC39hlyAQuH8VIaZ9S9_oj7me0GuPAng_TDRgxw130_provenance.
- NP145953.RAVQdDdcXbyop1J6N9wQJBUHvCTNr8F-f6FyDElGTU4u4130_assertion description "[Genetic variation at the MYH9 locus substantially explains the increased burden of focal segmental glomerulosclerosis and hypertensive end-stage kidney diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145953.RAVQdDdcXbyop1J6N9wQJBUHvCTNr8F-f6FyDElGTU4u4130_provenance.
- NP145956.RAZhgCn_Hq8xmWArVZ_Xi0_7uuHXLTDRO911sW_830x2Y130_assertion description "[Relationship between urinary mRNA expression of ACE2 and the degree of proteinuria in type 2 diabetic nephropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145956.RAZhgCn_Hq8xmWArVZ_Xi0_7uuHXLTDRO911sW_830x2Y130_provenance.
- NP145958.RAfOOT_pA8U-cZynMIe8etkxDGjPNeNHZMNjAuOXITlW4130_assertion description "[An inadequate tissue factor pathway inhibitor (TFPI) concentration as a result of elevated tissue factor (TF): tissue factor pathway inhibitor (TFPI) ratio characterizes patients with clinical manifestations of nephrotic syndrome and mild proteinuria.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145958.RAfOOT_pA8U-cZynMIe8etkxDGjPNeNHZMNjAuOXITlW4130_provenance.
- NP145968.RAbOWIWv4W7RNG5IKFcghro6IBVTzMVpuW5zgO9rJzEwo130_assertion description "[B7-H4 was expressed more often in pancreatic ductal carcinoma than was p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145968.RAbOWIWv4W7RNG5IKFcghro6IBVTzMVpuW5zgO9rJzEwo130_provenance.
- NP145975.RAfchUSX9UvQ7Xfjpfe-uj7E-tOgQpRoHJzwxlsq988Mc130_assertion description "[Findings from a large case-control sample of patients with alopecia areata (AA) do not support an association between FCRL3 and susceptibility to AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145975.RAfchUSX9UvQ7Xfjpfe-uj7E-tOgQpRoHJzwxlsq988Mc130_provenance.
- NP145981.RAWK9E77RbnwQum0jNQ7831VZtsNFoQ-R8-lckBwN_xRI130_assertion description "[autoantibodies against the DFS70 are related to the etiology in a certain population of Alopecia areata ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145981.RAWK9E77RbnwQum0jNQ7831VZtsNFoQ-R8-lckBwN_xRI130_provenance.
- NP145982.RAXK1-hkxeZD7lVibwaKqilDmRQefSOmp8S8BPa019FWs130_assertion description "[Expression of CD40, CD54 and HLA-DR were seen in the hair structure including the dermal papilla in alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145982.RAXK1-hkxeZD7lVibwaKqilDmRQefSOmp8S8BPa019FWs130_provenance.
- NP145983.RASDJKVoDyM8GO_ZvVCdkQY0Zj3ycL4mEAnGedCxvzWvw130_assertion description "[study investigated whether there was any association between VDR gene polymorphisms (BsmI, ApaI, and TaqI) and alopecia areata/findings suggest that there is no relationship between VDR gene polymorphisms and alopecia areata.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145983.RASDJKVoDyM8GO_ZvVCdkQY0Zj3ycL4mEAnGedCxvzWvw130_provenance.
- NP145985.RAVV6yqdinGY-rCQa7HFX0fr-3PxP62hJ4VBaAgBfw280130_assertion description "[Alopecia areata might be induced by an aberrant expression of IFN-gamma in individuals whose PBMC produce low amounts of IFN-gamma and TGF-beta1 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145985.RAVV6yqdinGY-rCQa7HFX0fr-3PxP62hJ4VBaAgBfw280130_provenance.
- NP145986.RASZadm6iuwE0Z8YBXgjg4XgXX1B8sfhaChR35yYjltSM130_assertion description "[When alopecia areata (AA) occurs in conjunction with filaggrin-associated atopic disorder, the clinical presentation of AA may be more severe.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145986.RASZadm6iuwE0Z8YBXgjg4XgXX1B8sfhaChR35yYjltSM130_provenance.
- NP145989.RAZIGv4mNdIA1UkFrVb5O3zF3jE2hIYBP0BJOQiTD_bo4130_assertion description "[Fcgamma receptor I Ab and Fcgamma receptor I play an important role in the regulation of alopecia areata (AA), are useful for a marker of the disease prognosis and are worth intense research for the reasonable and specific therapy of AA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145989.RAZIGv4mNdIA1UkFrVb5O3zF3jE2hIYBP0BJOQiTD_bo4130_provenance.
- NP145991.RAYEVQ19KB7njVVMvTPNrsMeIH6XA6s8YddWK4u2B-iYo130_assertion description "[In patients with autoimmune thyroiditis the HLA-DR11 frequency was higher than control values, while in patients with autoimmune polyglandular syndrome type II, the HLA-DR3 frequency was found to be higher.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145991.RAYEVQ19KB7njVVMvTPNrsMeIH6XA6s8YddWK4u2B-iYo130_provenance.
- NP145999.RAccjjSpA3jc9Gs1bLmlKKXtHOl5WRaPTCxAoDpLtUYtM130_assertion description "[correlation between SP levels and diarrhea severity in cryptosporidiosis; may imply that SP plays a role in diarrhea mediation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145999.RAccjjSpA3jc9Gs1bLmlKKXtHOl5WRaPTCxAoDpLtUYtM130_provenance.
- NP146002.RAX6_HV0QWoBV2r11JPFZZDMNDdi85P-mTmrY31oNd9_o130_assertion description "[MicroRNA-510 target site of the 3'UTR of HTR3A and HTR3E are associated with the irritable bowel syndrome with diarrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146002.RAX6_HV0QWoBV2r11JPFZZDMNDdi85P-mTmrY31oNd9_o130_provenance.
- NP146011.RATI8okWtFsYvEH9LPHZp8D04_srD3wnrPb6pR97e7-Uc130_assertion description "[findings demonstrate a unique KIT sequence and expression pattern among mediastinal seminomas; KIT sequencing may assist in differentiating primary from metastatic MS ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146011.RATI8okWtFsYvEH9LPHZp8D04_srD3wnrPb6pR97e7-Uc130_provenance.
- NP146015.RAeLBzLiQp-FoYEZflzFwgwfrG0aamtrI-8tOve7AwJK0130_assertion description "[connexin 43 is downregulated in Sertoli cells and germ cells during the transition from preinvasive carcinoma in situ to seminoma ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146015.RAeLBzLiQp-FoYEZflzFwgwfrG0aamtrI-8tOve7AwJK0130_provenance.
- NP146018.RAYqeGdQ3c9Js89gR3nJKA2feySIsMk1fKXws5V4dxZ5s130_assertion description "[The newly identified neuronal stem cell factor, MCFD2 (SDNSF), were expressed in seminoma cells and they were only present in gonocytes up to the second trimester.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146018.RAYqeGdQ3c9Js89gR3nJKA2feySIsMk1fKXws5V4dxZ5s130_provenance.
- NP146019.RAQ_9iyRaVL-flY1gAF5mIKdiWfpTrlW2vYP9bDn9w_iU130_assertion description "[In conclusion, these data suggest that the SpanX protein family is not exclusively expressed post-meiotically and that seminomas and embryonal carcinomas may originate from SpanX-positive carcinoma-in-situ cell.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146019.RAQ_9iyRaVL-flY1gAF5mIKdiWfpTrlW2vYP9bDn9w_iU130_provenance.
- NP146021.RAU1MeMjcVqPyZSrPmHtdBDtpyebM2VOeJ9VmRBJq6Ed8130_assertion description "[DAD-R, SOX5, and EKI1 map within region of chromosome 12p whose duplication is related to reduced apoptosis in human testicular seminomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146021.RAU1MeMjcVqPyZSrPmHtdBDtpyebM2VOeJ9VmRBJq6Ed8130_provenance.
- NP146026.RAeRrr668q5q9sWYn-nw2Ci9zShn010c3K0wLxQ9qLrKM130_assertion description "[Bax, Bcl-2, fas and Fas-L antigen expression in human seminoma: correlation with the apoptotic index.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146026.RAeRrr668q5q9sWYn-nw2Ci9zShn010c3K0wLxQ9qLrKM130_provenance.
- NP146027.RAbQQHhFIIy9Am-ieurla7KFpM6FD8dbdQo4Metv1c2g0130_assertion description "[Bax, Bcl-2, fas and Fas-L antigen expression in human seminoma: correlation with the apoptotic index.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146027.RAbQQHhFIIy9Am-ieurla7KFpM6FD8dbdQo4Metv1c2g0130_provenance.
- NP146029.RAV0mloXkwETZZtAQU_cUVrblS4e_btG43vTAHNb9kk68130_assertion description "[Diffuse membranous immunoreactivity for podoplanin as detected by monoclonal antibody D2-40 is highly sensitive and specific for primary and metastatic seminoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146029.RAV0mloXkwETZZtAQU_cUVrblS4e_btG43vTAHNb9kk68130_provenance.
- NP146039.RAY08lZkkVS17uB7Do51J3qN5Djz6wmBx6qAibFEgTC74130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146039.RAY08lZkkVS17uB7Do51J3qN5Djz6wmBx6qAibFEgTC74130_provenance.
- NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_assertion description "[R620W polymorphism of PTPN22 is not major risk allele for SLE susceptibility in Caucasians from northern America, the UK, or Finland, but it appears to be risk factor for concurrent autoimmune diseases of autoimmune thyroid disease and SLE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146043.RATtABso-pkrleAsyBk1q6BwrAmJt78W5ciau0onrsYsw130_provenance.
- NP146045.RAa3haAMZNYir6Yi3KHPus9Vs7RnCy2PdNF1ntAPgqFcA130_assertion description "[Polymorphism, Single Nucleotide in ZFAT is associated with autoimmune thyroid disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146045.RAa3haAMZNYir6Yi3KHPus9Vs7RnCy2PdNF1ntAPgqFcA130_provenance.
- NP146051.RAesEGAyvKUZNy5yu0nt-kXiUL4Zj7azhlsbxxU0oK_Gw130_assertion description "[Immunohistochemical CD117 positivity was detected in a wide range of neoplastic and inflammatory thyroid diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146051.RAesEGAyvKUZNy5yu0nt-kXiUL4Zj7azhlsbxxU0oK_Gw130_provenance.
- NP146053.RAVWicAbXhChQf6DyBoW8XDZ5JnUc0cvTCyF_8fqn5TTA130_assertion description "[Positivity in TPO-RT-PCR correlates significantly with metastatic disease in cancer patients and with the presence of thyroid disease in general.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146053.RAVWicAbXhChQf6DyBoW8XDZ5JnUc0cvTCyF_8fqn5TTA130_provenance.
- NP146066.RAUEqz9fNUQTkQfqnkJQsul_vsIBxagJD0ASa71I_1z1k130_assertion description "[Autoimmune thyroid disease induced by thyroglobulin and lipopolysaccharide is inhibited by soluble TNF receptor type I.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146066.RAUEqz9fNUQTkQfqnkJQsul_vsIBxagJD0ASa71I_1z1k130_provenance.
- NP146077.RAX45XdNa5Qjg_axuBP2s99mAz1yAbZ0wnIjRjaJ7I6fc130_assertion description "[IL-5 overexpression is associated with eosinophilia in T-cell lymphomas.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146077.RAX45XdNa5Qjg_axuBP2s99mAz1yAbZ0wnIjRjaJ7I6fc130_provenance.
- NP146080.RAdKKzYWXdx9n-xOZk3QrU6OYV-P5FQu4jyyLpKp-W1-g130_assertion description "[The similar pattern of expression of CXCL13 and PD-1 in angioimmunoblastic T-cell lymphoma provides further evidence that AITL is a neoplasm derived from germinal-center T-helper cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146080.RAdKKzYWXdx9n-xOZk3QrU6OYV-P5FQu4jyyLpKp-W1-g130_provenance.
- NP146081.RAdPtkmDxeJLimylTQfrdCHggBUyMRzx0l1vZS2L-BEto130_assertion description "[NPM/ALK-carrying T cell lymphoma (ALK+TCL) cells secrete IL-10 and TGF-beta and express FoxP3, indicating their T regulatory (Treg) cell phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146081.RAdPtkmDxeJLimylTQfrdCHggBUyMRzx0l1vZS2L-BEto130_provenance.
- NP146082.RAelI1Gk4POvPnlxwM62BtEYrqcj588wQK-DfywAY1V-8130_assertion description "[AKT and IL-15 may be important in extranodal NK/T-cell lymphoma tumor survival ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146082.RAelI1Gk4POvPnlxwM62BtEYrqcj588wQK-DfywAY1V-8130_provenance.
- NP146083.RAbYgQZwHDQULC6i21aiTPBQDP5q0TJuTwQJAAMjiynoQ130_assertion description "[Id2 commonly is overexpressed in highly proliferative T-cell lymphomas, and its expression may result from transcriptional activation of myc in these tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP146083.RAbYgQZwHDQULC6i21aiTPBQDP5q0TJuTwQJAAMjiynoQ130_provenance.