Matches in Nanopublications for { ?s <http://purl.org/dc/terms/description> ?o ?g. }
- NP120485.RATXwGqducKEQstUP49wN82vJJAImAOS4HPN_mq_sEYHA130_assertion description "[PFKFB-4 and PFKFB-3 genes are expressed in gastric and pancreatic cancer cells, they strongly respond to hypoxia via a HIF-1alpha dependent mechanism and possibly have a significant role in the Warburg effect which is found in malignant cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120485.RATXwGqducKEQstUP49wN82vJJAImAOS4HPN_mq_sEYHA130_provenance.
- NP120494.RAYm2dS7EK_bXAReVzGgqFZMmkZxGXn7y1s_NcKudGWGU130_assertion description "[Hypoxic induction of Ero1-L alpha is key adaptive response in a previously unrecognized HIF-1-mediated pathway that operates to improve protein secretion under hypoxia and might be used for inhibiting tumor growth via inhibiting VEGF-driven angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120494.RAYm2dS7EK_bXAReVzGgqFZMmkZxGXn7y1s_NcKudGWGU130_provenance.
- NP120496.RAfbGNyK5wgi_bsxulrH2uIMkALpAyboPpWYucV2z9YTk130_assertion description "[MMP1 mRNA remains associated with polysomes during hypoxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120496.RAfbGNyK5wgi_bsxulrH2uIMkALpAyboPpWYucV2z9YTk130_provenance.
- NP120500.RAeWsaU8jYiA2lJYeGGZwomgC5s6qeePpxaYJ7XEvgmXE130_assertion description "[IGFBP-1 phosphorylation may be a novel mechanism of an adaptive response to hypoxia and nutrient restriction in a tumor cell line.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120500.RAeWsaU8jYiA2lJYeGGZwomgC5s6qeePpxaYJ7XEvgmXE130_provenance.
- NP120502.RAVTZ93y6vSpSYqj7pU30RDP3T7pRq8cgrgxk92k4uH6g130_assertion description "[Hypoxia and epidermal growth factor receptor signal coexisted in the tumor microenvironment and might promote angiogenesis through HIF-1 alpha-mediated upregulation of SCF and other angiogenic factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120502.RAVTZ93y6vSpSYqj7pU30RDP3T7pRq8cgrgxk92k4uH6g130_provenance.
- NP120504.RAV7Bx6zmHf9QZbHQd-NWDmY2_HnIR0chgfcbW2es96is130_assertion description "[Prx I and Trx expression is increased in lung cancer cells following hypoxia and in human lung cancer tissues ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120504.RAV7Bx6zmHf9QZbHQd-NWDmY2_HnIR0chgfcbW2es96is130_provenance.
- NP120506.RAZrQKb-mRiQjjoKvASONVnPxzg04fT8IQUzJl80orHTk130_assertion description "[Effect of acute hypoxia on cloned homo- and heteromeric P2X3 receptors expressed in human embryonic kidney 293 cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120506.RAZrQKb-mRiQjjoKvASONVnPxzg04fT8IQUzJl80orHTk130_provenance.
- NP120508.RAWrJC94QUG2LP_5Ik2PKLXisinkfWvryfWgStztvhGls130_assertion description "[This paper describes a previously unknown link between hypoxia and STAT1 expression down-regulation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120508.RAWrJC94QUG2LP_5Ik2PKLXisinkfWvryfWgStztvhGls130_provenance.
- NP120512.RAQZjgLoz9ugxO3OIR0jQ7u4H2I2Rk4AadeyP-lluRrEc130_assertion description "[Accumulated EGLN1 in hypoxia acts as a negative-feedback mechanism to modulate HIF-1alpha target gene expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120512.RAQZjgLoz9ugxO3OIR0jQ7u4H2I2Rk4AadeyP-lluRrEc130_provenance.
- NP120520.RAZJuW7doUf1qMo-Ga8ZtNwl7BLzQFbdopP34MR7lFYXs130_assertion description "[The present study demonstrates for the first time, differential expression of mRNA and secretion for angiogenin and VCAM-1 from placental explants and trophoblasts in culture subjected to hypoxia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120520.RAZJuW7doUf1qMo-Ga8ZtNwl7BLzQFbdopP34MR7lFYXs130_provenance.
- NP120526.RASW57BIHqZIoPvuQOCBDf_p1BZB5tx7YK6Iva_WwFxH4130_assertion description "[SUMO-1 has a role in modifying cAMP-response element-binding protein (CREB) in prolonged hypoxia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120526.RASW57BIHqZIoPvuQOCBDf_p1BZB5tx7YK6Iva_WwFxH4130_provenance.
- NP120527.RAaTrrOnUF-WXdtLoRCFS7nxD58WFSEBwOZUuIZ9hHNEY130_assertion description "[This review presents a model incorporating hypoxia responsive facilitative GLUT1 and GLUT3 as putative components of the glucose sensing apparatus in chondrocytes ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120527.RAaTrrOnUF-WXdtLoRCFS7nxD58WFSEBwOZUuIZ9hHNEY130_provenance.
- NP120528.RAYayKiTBYvV2Okh9wSdD5ROPMzEPe7BUxxIllVIVFS5o130_assertion description "[During trophoblast hypoxia glucose transporters (GLUT1/3) are upregulated via HIF-1 alpha pathway.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120528.RAYayKiTBYvV2Okh9wSdD5ROPMzEPe7BUxxIllVIVFS5o130_provenance.
- NP120533.RAWu2C9W15G3s5X5gMGDk6d1iQ-BFhWI923qDVu0KXMiQ130_assertion description "[DNA damage and hypoxia are two important physiologic activators of p53.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120533.RAWu2C9W15G3s5X5gMGDk6d1iQ-BFhWI923qDVu0KXMiQ130_provenance.
- NP120546.RAaxtd32f4z1S_qjpddS0KW9tq2ZKuDY4H2H1Q9LpWA-I130_assertion description "[up-regulation of uPAR expression by Bcl-2 in hypoxia is modulated by Sp1 DNA binding activity through the ERK signaling pathway ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120546.RAaxtd32f4z1S_qjpddS0KW9tq2ZKuDY4H2H1Q9LpWA-I130_provenance.
- NP120549.RAbZbSZmpbDTt2BElUG2FsD2h-AcXpUJICx5VuPATo6AU130_assertion description "[functional cooperation between Bax and Bak in cell hypoxia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120549.RAbZbSZmpbDTt2BElUG2FsD2h-AcXpUJICx5VuPATo6AU130_provenance.
- NP120551.RATvTDIUsQtyLZMiAjt2lOyrRir5H263w5djaKeFcTWoI130_assertion description "[a novel Sp1-dependent regulatory pathway for CD39 indicate the likelihood that CD39 is central to protective responses to hypoxia/ischemia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120551.RATvTDIUsQtyLZMiAjt2lOyrRir5H263w5djaKeFcTWoI130_provenance.
- NP120552.RAahEfLSTxBqjl8VqZ1hcBOAKOQN_B3jaiYwvX_001dvc130_assertion description "[The expression of 11 beta-hydroxysteroid dehydrogenase type 2 is induced during trophoblast differentiation: effects of hypoxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120552.RAahEfLSTxBqjl8VqZ1hcBOAKOQN_B3jaiYwvX_001dvc130_provenance.
- NP120555.RATDPWOu1PmGDHL1uZEFSVpFFyA4rKlII16f1G-M85TeM130_assertion description "[Data show that TAK1 forms a stable complex with JIP1 and regulates the activation of JNK, which in turn determines the cellular stress response to hypoxia; this activation of TAK1-JIP1-JNK is suppressed by vaccinia-related kinase 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120555.RATDPWOu1PmGDHL1uZEFSVpFFyA4rKlII16f1G-M85TeM130_provenance.
- NP120556.RAYisewfq3i2813mkNfjL7-U20Wds2z4Nv4IWIChdlfBg130_assertion description "[VHL-mediated hypoxia regulation of cyclin D1 in renal carcinoma cells.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120556.RAYisewfq3i2813mkNfjL7-U20Wds2z4Nv4IWIChdlfBg130_provenance.
- NP120563.RAbXxLJOFS3a5RYtsuZToWXyPDpd850UFNgoxzJ82AhfM130_assertion description "[expression induced by interleukin-1beta and amyloid beta 42 peptide is potentiated by hypoxia in primary human neural cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120563.RAbXxLJOFS3a5RYtsuZToWXyPDpd850UFNgoxzJ82AhfM130_provenance.
- NP120567.RAeumNSMPCkihYFWeu1vfmLd31omdkVq47yPt7YQTlTIA130_assertion description "[s-FKN is shed from endothelial cells following hypoxia/reoxygenation and acts through CX3CR1 on them to increase ICAM-1 expression and promote neutrophil adhesion through activation of the Jak-Stat5 pathway ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120567.RAeumNSMPCkihYFWeu1vfmLd31omdkVq47yPt7YQTlTIA130_provenance.
- NP120572.RATKU31jnvvAL4zWnGH9hSryXcgPGMfn67cUzh25lqahY130_assertion description "[Expression of GLUT-1 in psoriasis and the relationship between GLUT-1 upregulation induced by hypoxia and proliferation of keratinocyte growth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120572.RATKU31jnvvAL4zWnGH9hSryXcgPGMfn67cUzh25lqahY130_provenance.
- NP120574.RASpbPL3uAUTo-UevJ6b9vGYMYXGELXa-8JzeOsslaAkw130_assertion description "[Under hypoxia enhanced levels of VEGFR1 on human umbilical vein endothelial cells were observed, while in human colonic microvascular endothelial cells there was a variable reaction to hypoxia, with cases of enhanced, unchanged and reduced expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120574.RASpbPL3uAUTo-UevJ6b9vGYMYXGELXa-8JzeOsslaAkw130_provenance.
- NP120584.RATD3-lzBuCN6zvCfJziNOt1bGf1dFMQHfZilUWFRhX6s130_assertion description "[HO-1 induction protected human hepatocytes against warm and cold hypoxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120584.RATD3-lzBuCN6zvCfJziNOt1bGf1dFMQHfZilUWFRhX6s130_provenance.
- NP120585.RAQ00XQ2nn0Htty-O7JD-CGmC_I1gG2eno2Su_bDwfS6Y130_assertion description "[androgen receptor is involved in VEGF and hypoxia sensing via hypoxia-inducible factors HIF-1a, HIF-2a, and the prolyl hydroxylases in human prostate cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120585.RAQ00XQ2nn0Htty-O7JD-CGmC_I1gG2eno2Su_bDwfS6Y130_provenance.
- NP120590.RAWpvzwtW6pYk6FZ6a-SISF024Y7YfIjoNBY5elQ0C8Sg130_assertion description "[Stress-related signaling pathways in epithelial cells are modulated by hypoxia and confer protection from reoxygenation, since hypoxia and chemical inhibition of p38mapk and MEK1/2 similarly increase cytolysis resulting from O2-.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120590.RAWpvzwtW6pYk6FZ6a-SISF024Y7YfIjoNBY5elQ0C8Sg130_provenance.
- NP120591.RAf54_6wOo6NJ3VoqesB1UMLYm9lsetx9ojxyM1YMc0o4130_assertion description "[CK2 may be a key mediator for HDAC1 and HDAC2 activation under hypoxia in tumor cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120591.RAf54_6wOo6NJ3VoqesB1UMLYm9lsetx9ojxyM1YMc0o4130_provenance.
- NP120593.RAb-TrP0jWTyEuupbIacdoZB1Yy3O6NzBz9srOPagSuQo130_assertion description "[Findings suggest that PNUTS may play an important role in controlling cell death in response to cellular stresses such as hypoxia through the post-translational modification of p53 and MDM2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120593.RAb-TrP0jWTyEuupbIacdoZB1Yy3O6NzBz9srOPagSuQo130_provenance.
- NP120596.RATeBEZqbAIF8khzy4xv5hj0yKsj3sLIsAp7Kqaz4M11k130_assertion description "[Repression of alpha-fetoprotein gene expression under hypoxic conditions in human hepatoma cells: characterization of a negative hypoxia response element that mediates opposite effects of hypoxia inducible factor-1 and c-Myc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120596.RATeBEZqbAIF8khzy4xv5hj0yKsj3sLIsAp7Kqaz4M11k130_provenance.
- NP120597.RAT3hDqNLBReOBVbH7YKB-0arKSyb44nr5J5RSjAw44OQ130_assertion description "[Myc is an integral part of a novel HIF-1alpha pathway, which regulates a distinct group of Myc target genes in response to hypoxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120597.RAT3hDqNLBReOBVbH7YKB-0arKSyb44nr5J5RSjAw44OQ130_provenance.
- NP120600.RAbXPdHz1GPTwQHRBcAiugPcGetxkQLURvgKxhcmAg3aM130_assertion description "[Both hypoxia and heat shock prevented the lipopolysaccharide-induced increase in adult CD11b although it was unaltered in neonates.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120600.RAbXPdHz1GPTwQHRBcAiugPcGetxkQLURvgKxhcmAg3aM130_provenance.
- NP120604.RAd_T3u_UvpxA1kq7Mfoub7Pq_sIipqzGqo8m8RGPSCwo130_assertion description "[regulation of TGF-beta3 promoter activity by HIF-1 represents a mechanism for trophoblast differentiation during hypoxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120604.RAd_T3u_UvpxA1kq7Mfoub7Pq_sIipqzGqo8m8RGPSCwo130_provenance.
- NP120606.RAdX-7WcXPGR7OZqemx60hbLkRpGllVCW_4HTmZp9mf8w130_assertion description "[renal failure patients mounted an EPO response to hypoxia but at lower EPO levels ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120606.RAdX-7WcXPGR7OZqemx60hbLkRpGllVCW_4HTmZp9mf8w130_provenance.
- NP120607.RATGVQWxR3QfI4QRf615U289iZHp-7Ku36UmzKh_pGLwE130_assertion description "[Serum erythropoietin levels (s- [epo]), haemoglobin concentration ([ Hb]), haematocrit (hct), and ferritin concentration ([ fer]) were measured in seven healthy male volunteers (20-23 years) exposed continuously to hypoxia (PO (2) 14 kPa) for 10 days ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120607.RATGVQWxR3QfI4QRf615U289iZHp-7Ku36UmzKh_pGLwE130_provenance.
- NP120610.RAYplHijYw-eoxSyHcGLE-Hh13Rw42woTo1WDKmUdH4OQ130_assertion description "[The amount of ecNOS in the placenta is not deficient in pre-eclampsia, excluding a possible pathogenic role for eNOS in this disease; furthermore, placental hypoxia, which is associated with pre-eclampsia, does not induce an upregulation of ecNOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120610.RAYplHijYw-eoxSyHcGLE-Hh13Rw42woTo1WDKmUdH4OQ130_provenance.
- NP120616.RAWKaUVZLBHe7P64mNZxYQsFS6xO7CdxkpO9zx-67KLcE130_assertion description "[The subtype SK2 channels were up-regulated under hypoxia, shown with pharmacological tools and with mRNA analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120616.RAWKaUVZLBHe7P64mNZxYQsFS6xO7CdxkpO9zx-67KLcE130_provenance.
- NP120634.RAYqEvGSR7z2_90Bn43W6IoU81yk0FZpwq2aw1iWOcnVk130_assertion description "[Studies of binding of KLF6 to the human iNOS promoter reveal CACCC binding sites and transactivation of iNOS promoter in diverse pathophysiological conditions: NaCN-induced hypoxia, heat shock, serum starvation, and PMA/ionophore stimulation ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120634.RAYqEvGSR7z2_90Bn43W6IoU81yk0FZpwq2aw1iWOcnVk130_provenance.
- NP120635.RASkOGafnRMu85ys5oT5tLURNYEg5WPayGDngQD3PMCAo130_assertion description "[HIF-1 and HIF-2 have roles in SK1 upregulation during hypoxia in glioma cells ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120635.RASkOGafnRMu85ys5oT5tLURNYEg5WPayGDngQD3PMCAo130_provenance.
- NP120636.RAX2fIWWx6VYfWImyBCPVDItiZAh_oMZElDnohuanNqnY130_assertion description "[Induction of hepatocyte growth factor activator gene expression under hypoxia activates the hepatocyte growth factor/c-Met system via hypoxia inducible factor-1 in pancreatic cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120636.RAX2fIWWx6VYfWImyBCPVDItiZAh_oMZElDnohuanNqnY130_provenance.
- NP120638.RAUs37Ioh-RpK0KJKPvA8PcoMutKZCEKqfy5qAFbBWm8o130_assertion description "[Acute and chronic cell hypoxia regulate sodium currents by recombinant hNa (v) 1.5 alpha.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120638.RAUs37Ioh-RpK0KJKPvA8PcoMutKZCEKqfy5qAFbBWm8o130_provenance.
- NP120644.RAVxN4BEICsba-1F8INujaCIfEn33QwtkihDHehW9YwQ4130_assertion description "[basal endoglin transcription (highly dependent on Sp1) may switch from a constitutive to an inducible state through Sp1 interaction with HIF-1 and Smad transcription factors, induced by hypoxia and TGF-beta, respectively ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120644.RAVxN4BEICsba-1F8INujaCIfEn33QwtkihDHehW9YwQ4130_provenance.
- NP120652.RAUaA_82OZg3sDVUDgjGAB5jPA7JkmrKaPPUZq4Kbfz_M130_assertion description "[Receptor estrogen-related receptors alpha, beta and gamma physically interact with HIF and stimulate HIF-induced transcription in tumor cells cultured under hypoxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120652.RAUaA_82OZg3sDVUDgjGAB5jPA7JkmrKaPPUZq4Kbfz_M130_provenance.
- NP120658.RAf4m3Nse0aKQN6CY8_LJThlfgKsdcQrnVqu1FYNM6wNE130_assertion description "[These results suggest that hypoxia is an important negative regulator of monocyte chemotaxis to the renal inflamed interstitium, by reducing MCP-1 expression ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120658.RAf4m3Nse0aKQN6CY8_LJThlfgKsdcQrnVqu1FYNM6wNE130_provenance.
- NP120659.RAZ7O2BVQOyyOk7XfuXAxSNckJysd5hUZ6jHYWwjwimQY130_assertion description "[induction by hypoxia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120659.RAZ7O2BVQOyyOk7XfuXAxSNckJysd5hUZ6jHYWwjwimQY130_provenance.
- NP120666.RAXaWluZTqz2g3WgroRtq0NCefC71hK0F80OjG_tq1w78130_assertion description "[Repression of alpha-fetoprotein gene expression under hypoxic conditions in human hepatoma cells: characterization of a negative hypoxia response element that mediates opposite effects of hypoxia inducible factor-1 and c-Myc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120666.RAXaWluZTqz2g3WgroRtq0NCefC71hK0F80OjG_tq1w78130_provenance.
- NP120669.RAfFdUsp2a5pEDoJvldb6b_TxNV8eUgxxy_C07cKVt4Rc130_assertion description "[Increase in serum M-CSF levels precedes development of preeclampsia/of serum M-CSF supports M-CSF elevation in placenta/elevation at 18 weeks of gestation may be related to placental hypoxia, considered cause of preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120669.RAfFdUsp2a5pEDoJvldb6b_TxNV8eUgxxy_C07cKVt4Rc130_provenance.
- NP120674.RAdoVB-sUKPklIe_f0pXSBKatC0aJNKdS0g3TRak8466I130_assertion description "[tumor hypoxia may trigger overexpression of STK15 observed in various tumors ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120674.RAdoVB-sUKPklIe_f0pXSBKatC0aJNKdS0g3TRak8466I130_provenance.
- NP120679.RAQpF5knymKn3k7vrK6exs1Q1-22CC5D219bstqvJqIMU130_assertion description "[Protein kinase C-delta is activated by hypoxia, increases the stability and transcriptional activity of hypoxia-inducible factor-1 alpha and demonstrates a new role as regulator of hypoxia-induced angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120679.RAQpF5knymKn3k7vrK6exs1Q1-22CC5D219bstqvJqIMU130_provenance.
- NP120682.RAVEH0tBervqcXZ-WrKiuswHwOkffldwNxD_sjB708soU130_assertion description "[Stress-related signaling pathways in epithelial cells are modulated by hypoxia and confer protection from reoxygenation, since hypoxia and chemical inhibition of p38mapk and MEK1/2 similarly increase cytolysis resulting from O2-.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120682.RAVEH0tBervqcXZ-WrKiuswHwOkffldwNxD_sjB708soU130_provenance.
- NP120689.RAQe4SsT3aL8ZMvJSSFiqiXLhs_PMD3KnuRwqFSkDY85M130_assertion description "[CCL27 expression is under the control of NF-kappaB, and that NF-kappaB, as indicated by others, may be an attractive target for therapy in inflammatory skin diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120689.RAQe4SsT3aL8ZMvJSSFiqiXLhs_PMD3KnuRwqFSkDY85M130_provenance.
- NP120694.RASZQPrZoZlYnLlL19CXdDLlVDj0QEmLHZXpbjfg61Has130_assertion description "[Focal palmoplantar keratoderma in gap junction skin disease may be specifically associated with connexin trafficking defects as well as with mutations affecting its extracellular domains, thus broadening the spectrum of GJB2-associated diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120694.RASZQPrZoZlYnLlL19CXdDLlVDj0QEmLHZXpbjfg61Has130_provenance.
- NP120705.RAQppt4bUb2wzepVNzj13krse9LRmMqANcozgUyclMkd4130_assertion description "[mutation causes multiple epiphyseal dysplasia; genetic heterogeneity ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120705.RAQppt4bUb2wzepVNzj13krse9LRmMqANcozgUyclMkd4130_provenance.
- NP120711.RASrVbnwm0K4QXMUacmUJsxhfcTnZJxPsPcZdXMxyl1yE130_assertion description "[MATN3 mutations is associated with multiple epiphyseal dysplasia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120711.RASrVbnwm0K4QXMUacmUJsxhfcTnZJxPsPcZdXMxyl1yE130_provenance.
- NP120714.RAQ4jmO0-XfpIluUXDit_pWpP12G6unl_2Zcmbmv8Qvgg130_assertion description "[Familial mutation of G504S of collagen type II alpha (COL2A1) gene results in distinctive spondyloepiphyseal dysplasia congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120714.RAQ4jmO0-XfpIluUXDit_pWpP12G6unl_2Zcmbmv8Qvgg130_provenance.
- NP120719.RAW-kziBeJ5ITCZfnRae5vuNpOGUjM5GID8i-TVq1fvuY130_assertion description "[A previously unreported deletion of T in exon 5 of SEDL gene (293delT) was observed in 2 spondyloepiphyseal dysplasia probands in a Chinese family; seven individuals in the family carry the mutation resulting in frameshift and a putative truncated protein ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120719.RAW-kziBeJ5ITCZfnRae5vuNpOGUjM5GID8i-TVq1fvuY130_provenance.
- NP120736.RAfj2eFsvO6Faofs3XJvJdBxQotTqDXwGZ_4_TwFfs1f8130_assertion description "[The frequency for the 35delG/GJB2 was 27.5% in Venezuelan patients with autosomal recessive nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120736.RAfj2eFsvO6Faofs3XJvJdBxQotTqDXwGZ_4_TwFfs1f8130_provenance.
- NP120745.RAcUQxTdEligKE1uAGLygTXdriIyc3lC9_vpxTF3rp8W8130_assertion description "[Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120745.RAcUQxTdEligKE1uAGLygTXdriIyc3lC9_vpxTF3rp8W8130_provenance.
- NP120746.RAR0uVHgQ-x2baHAlDW-2_F-XOMNHpl9dQC8vQmKOsRsU130_assertion description "[Then HaeIII polymorphic restriction site in the gene of 12S rRNA site was found in 4 out of 100 patients with non-syndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120746.RAR0uVHgQ-x2baHAlDW-2_F-XOMNHpl9dQC8vQmKOsRsU130_provenance.
- NP120748.RAUVdeCOksx4geDPz16IpB8YgccO4VQadSrld_vQdrz8Q130_assertion description "[A new heterozygous missense mutation (c.2557C > T; p.R853C) was found in autosomal dominant non-syndromic hearing loss that changes an invariant residue of the fifth IQ motif, a putative calmodulin (CaM) binding domain.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120748.RAUVdeCOksx4geDPz16IpB8YgccO4VQadSrld_vQdrz8Q130_provenance.
- NP120751.RAe_YYcpoXxySOg-weXMMRjzPCbPJgF0lX46_V97LN-0s130_assertion description "[the sensorineural hearing impairment in TECTA mutations may be characterized as a cochlear conductive hearing impairment ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120751.RAe_YYcpoXxySOg-weXMMRjzPCbPJgF0lX46_V97LN-0s130_provenance.
- NP120754.RAVOPQSWBuzK6xHaR_zjsPO_ktCiIF16GKhKP6kVk2qc0130_assertion description "[GRM7 contributes to risk of developing age-related hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120754.RAVOPQSWBuzK6xHaR_zjsPO_ktCiIF16GKhKP6kVk2qc0130_provenance.
- NP120755.RAbb5hG9kU0Rzzj7PkkVVSiZr_w-BXNTeFC65H6YY1DKc130_assertion description "[the G11696A mutation may act in synergy with the primary deafness-associated 12S rRNA A1555G mutation in a Chinese family, thereby increasing the penetrance and expressivity of hearing loss in this Chinese pedigree [case report]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120755.RAbb5hG9kU0Rzzj7PkkVVSiZr_w-BXNTeFC65H6YY1DKc130_provenance.
- NP120763.RAd2xEgIfP7MbHhWX1NbviXpqIuTHvGaTQK_gzV-DIjHs130_assertion description "[Our results suggest that GJB2 and SLC26A4 mutations together make up a major cause of congenital hearing loss in the Korean population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120763.RAd2xEgIfP7MbHhWX1NbviXpqIuTHvGaTQK_gzV-DIjHs130_provenance.
- NP120768.RAVaXc7dNUNCa0Z9sB-Xf5uUsB798rxc8mterVLmG_DI8130_assertion description "[Results shows KCNQ4 SNPs were significantly associated with Age-related hearing impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120768.RAVaXc7dNUNCa0Z9sB-Xf5uUsB798rxc8mterVLmG_DI8130_provenance.
- NP120776.RAbRfGafqZrXqxeS7aaMMGP5lw2CKU7kTo1JOUWNnrHco130_assertion description "[This study establishes a firm causal relationship between the Arg455His mutation, optic atrophy, and associated hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120776.RAbRfGafqZrXqxeS7aaMMGP5lw2CKU7kTo1JOUWNnrHco130_provenance.
- NP120780.RAUCwHOTKyrMvUj8dXvqWekLjbQHhuKNXW6ojrfimTwJQ130_assertion description "[Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120780.RAUCwHOTKyrMvUj8dXvqWekLjbQHhuKNXW6ojrfimTwJQ130_provenance.
- NP120784.RAQf0C-ePOrJdYFcWVJvd12XYe0jYTFAFP6QaPHocRChk130_assertion description "[A region suggestive of linkage was found on chromosome 3q, with a logarithm of the odds score of 2.5 in the same region of this chromosome where the DFNA18 locus resides, which has been reported to cause a form of progressive hereditary hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120784.RAQf0C-ePOrJdYFcWVJvd12XYe0jYTFAFP6QaPHocRChk130_provenance.
- NP120785.RAUZBgpZqsuQ7L-ikHsIu_-42C9COAlxKiawD_n-fJHh0130_assertion description "[Families carrying both G7444A and A1555G mutations in the Mitochondrial tRNASer (UCN) gene displayed high penetrance of hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120785.RAUZBgpZqsuQ7L-ikHsIu_-42C9COAlxKiawD_n-fJHh0130_provenance.
- NP120791.RAVQltsOPv7zzES9G6yd1YDM0nvP_DVeXkpTVFXIrfhyY130_assertion description "[frequency of 35delG was about 18.5%, however, del (GJB6-D13S1830) was not found in the studied patients with autosomal recessive non-syndromic hearing loss; results support founder effect regarding these mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120791.RAVQltsOPv7zzES9G6yd1YDM0nvP_DVeXkpTVFXIrfhyY130_provenance.
- NP120799.RARyDs04zgs8pCpOQK2PzFwAnPlnbaieQ7QJrpr-fowk4130_assertion description "[oxLDL-induced upregulation of aldose reductase in human macrophages is proinflammatory in foam cells and may represent a potential link among hyperlipidemia, atherosclerosis, and diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120799.RARyDs04zgs8pCpOQK2PzFwAnPlnbaieQ7QJrpr-fowk4130_provenance.
- NP120801.RAf0JI023UDtF0bl744buHyGLGMcCO0q_SOYof_hVKkhI130_assertion description "[GPX1 was measured in the blood from patients with diabetes mellitus, insulin-dependent.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120801.RAf0JI023UDtF0bl744buHyGLGMcCO0q_SOYof_hVKkhI130_provenance.
- NP120809.RAUTlup1NrSv5E_eeQg9ypHnIool7cY7DasVgEm0leYP0130_assertion description "[Slovak patients with type 1A diabetes mellitus were typed for class II HLA genes/of 14 DQA1 alleles the highest occurrence rate showed DQA1*0301 and DQA1*0501, while DQA1*0102 and DQA1*0201, respectively, were found to be the least frequent ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120809.RAUTlup1NrSv5E_eeQg9ypHnIool7cY7DasVgEm0leYP0130_provenance.
- NP120814.RAU1UP5uj3VmMaaL0zFW78NVB2-Ai6I-TpUbdvA6D33Lo130_assertion description "[Several polymorphisms of leptin gene and its receptor have been described as potential developmental factors of pregnancy complications such as diabetes mellitus or pregnancy induced hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120814.RAU1UP5uj3VmMaaL0zFW78NVB2-Ai6I-TpUbdvA6D33Lo130_provenance.
- NP120816.RAenkNwJ0HyiQegjJDHKJKWQ3pMRcqx0Lzr1KeZMmK5vA130_assertion description "[Several polymorphisms of leptin gene and its receptor have been described as potential developmental factors of pregnancy complications such as diabetes mellitus or pregnancy induced hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120816.RAenkNwJ0HyiQegjJDHKJKWQ3pMRcqx0Lzr1KeZMmK5vA130_provenance.
- NP120817.RAWudPV6Vp1YD4c-Hz3L1DG9BXMDZ_zu8O-I5lKGPLq6Y130_assertion description "[RAGE was found throughout the testis, caput epididymis, particularly the principle cells apical region, and on sperm acrosomes in men with diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120817.RAWudPV6Vp1YD4c-Hz3L1DG9BXMDZ_zu8O-I5lKGPLq6Y130_provenance.
- NP120823.RAfmFywcmQEgXIg4GRGvytlMX2691dUGLbMB1ikLgyDdc130_assertion description "[Both the 6q24 abnormality and KCNJ11 mutation are major causes of neonatal diabetes mellitus in Japanese patients ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120823.RAfmFywcmQEgXIg4GRGvytlMX2691dUGLbMB1ikLgyDdc130_provenance.
- NP120825.RAT3V4QwNuzuvZsxbTwFUwpILyRNjHnDb6njDgQcxTEVo130_assertion description "[study has shown that mutations in the KCNJ11 and ABCC8 are a major cause of transient neonatal diabetes mellitus, accounting for 29% of all cases and 89% of non-6q24 transient neonatal diabetes mellitus ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120825.RAT3V4QwNuzuvZsxbTwFUwpILyRNjHnDb6njDgQcxTEVo130_provenance.
- NP120827.RAf5K-LUXpEY3IDHpOkFelRR-7m30Y9BwWypYANurYEW4130_assertion description "[The GSTM1, GSTT1 and GSTP1 gene polymorphisms in diabetic patients and healthy individuals were investigated to test whether polymorphisms in GST genes are associated with diabetes mellitus (DM) in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120827.RAf5K-LUXpEY3IDHpOkFelRR-7m30Y9BwWypYANurYEW4130_provenance.
- NP120832.RATTgYY7m00CB0J7M5RDiKgVp7s1uSs0jK6jdYDYV2k2o130_assertion description "[The novel G-- > A mutation in exon 9 changes the essential amino acid Arg 354 to Cys 354 and may be responsible for the decreased catalase activity causing diabetes mellitus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120832.RATTgYY7m00CB0J7M5RDiKgVp7s1uSs0jK6jdYDYV2k2o130_provenance.
- NP120845.RAQ4znYx0h5MHfBBbSlg6v0OqNcR2t8b6hPVAn0ks41Kw130_assertion description "[maternally inherited combination of diabetes mellitus and hearing impairment in three members of a family was found to be associated with autosomal dominant transmission of the E864K mutation of the WFS1 gene ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120845.RAQ4znYx0h5MHfBBbSlg6v0OqNcR2t8b6hPVAn0ks41Kw130_provenance.
- NP120847.RAceaLFdvnehU0EM2_VK71gdZstf8xhl4yMdqgx1vqa70130_assertion description "[genotype distribution of the SOD1 in patients with diabetes mellitus can differ from nondiabetic individuals ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120847.RAceaLFdvnehU0EM2_VK71gdZstf8xhl4yMdqgx1vqa70130_provenance.
- NP120850.RAWSLvJLLZCTbVTKnGafKhhV93FTWaHq4pfzh8WZwP-vI130_assertion description "[analysis of the structure and function of visfatin and its relation to diabetes mellitus and other dysfunctions [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120850.RAWSLvJLLZCTbVTKnGafKhhV93FTWaHq4pfzh8WZwP-vI130_provenance.
- NP120853.RAZ6jslbXfRANEzDJmhwMjvXmvvaFANPs5jDvOFHxFBlM130_assertion description "[high serum levels of IL-18 and TNF-alpha suggested that they might play a role in the pathogenesis of diabetes mellitus and in the development of nephropathy in diabetic patients whether of type 1 or 2 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120853.RAZ6jslbXfRANEzDJmhwMjvXmvvaFANPs5jDvOFHxFBlM130_provenance.
- NP120864.RAVsqOi_E8jqv53GypVvSEcpPM21GL1aA3YeC69uPEPPI130_assertion description "[Diabetes mellitus type 2 is associated with mildly increased levels of myeloperoxidase, independent of other clinical variables.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120864.RAVsqOi_E8jqv53GypVvSEcpPM21GL1aA3YeC69uPEPPI130_provenance.
- NP120876.RASoKFXyYYXT-jguK6ZtJDqJx2S4L3aDRSYuKA2V42X4c130_assertion description "[Patients with diabetes mellitus who are carriers of a CYP2C9*3 allele require lower doses of tolbutamide to regulate their serum glucose levels compared to patients with the wild-type genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120876.RASoKFXyYYXT-jguK6ZtJDqJx2S4L3aDRSYuKA2V42X4c130_provenance.
- NP120889.RAZe-OaiTesT6DDqLjW2QBDSUgpVQM1exxRzY7TGdzSY4130_assertion description "[association of polymorphic trinucleotide repeat (GAA) n with diabetes mellitus type 2 in the Moscow population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120889.RAZe-OaiTesT6DDqLjW2QBDSUgpVQM1exxRzY7TGdzSY4130_provenance.
- NP120891.RAecuuDcLI2-axUKEDe9Fo022QgPzPRZVji4aiuLKHFU8130_assertion description "[Reduced frequency in children with diabetes mellitus type 1, associated with enterovirus RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120891.RAecuuDcLI2-axUKEDe9Fo022QgPzPRZVji4aiuLKHFU8130_provenance.
- NP120899.RAegVTaFz_CYtjjn5gkl3oCzOC-dwOtw2BD1FD1VXqLr4130_assertion description "[DNA sequence differences in the promoter of PRKCB1 contribute to diabetic nephropathy susceptibility in type I diabetes mellitus ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120899.RAegVTaFz_CYtjjn5gkl3oCzOC-dwOtw2BD1FD1VXqLr4130_provenance.
- NP120901.RAYQz6YN4cglWObHxkAr5rT429-pwZgTZCE14Z2_FDGtI130_assertion description "[TLR2 polymorphisms are associated with diabetes mellitus, type 1 (T1DM), and distribution differences between T1DM vs controls were not influenced by the HLA genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120901.RAYQz6YN4cglWObHxkAr5rT429-pwZgTZCE14Z2_FDGtI130_provenance.
- NP120903.RAdaJEwMSGHDn2TWVLqwEIvswIQozupHTA2X4vbPyeB7c130_assertion description "[An amino acid substitution in ABCA1 is associated with low levels of HDL and diabetes mellitus, type 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120903.RAdaJEwMSGHDn2TWVLqwEIvswIQozupHTA2X4vbPyeB7c130_provenance.
- NP120904.RAQcqjZkfPD5hgF86EGkq4ePH73ciT_AOjQt1ic6-7B8U130_assertion description "[The GSTM1, GSTT1 and GSTP1 gene polymorphisms in diabetic patients and healthy individuals were investigated to test whether polymorphisms in GST genes are associated with diabetes mellitus (DM) in the Turkish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120904.RAQcqjZkfPD5hgF86EGkq4ePH73ciT_AOjQt1ic6-7B8U130_provenance.
- NP120909.RAfJUUx57jOy8um-I-GW331Oliu9XesUXf3i9FIdPZgiQ130_assertion description "[data suggest that paraoxonase-1 activity loss is an event occurring later in the course of diabetes mellitus and it does not affect oxidation of circulating LDL ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120909.RAfJUUx57jOy8um-I-GW331Oliu9XesUXf3i9FIdPZgiQ130_provenance.
- NP120919.RAaAdcbIvyxrq1SkVZ8740-wOrMB9XhJEWWynKasYMuO8130_assertion description "[findings suggest that Pro12Ala proliferator-activated receptor-gamma (PPAR-gamma) gene polymorphism may be protective against insulin resistance and development of diabetes mellitus in the first-degree relatives of subjects with polycystic ovary syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120919.RAaAdcbIvyxrq1SkVZ8740-wOrMB9XhJEWWynKasYMuO8130_provenance.
- NP120928.RAS7AxB2yh7e_Ta9Q5v3y7FK_-Q0S2n_3pjCN6W8amQ1I130_assertion description "[a L162V polymorphism at the peroxisome proliferator activated receptor alpha locus modulates the risk of cardiovascular events associated with insulin resistance and diabetes mellitus ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120928.RAS7AxB2yh7e_Ta9Q5v3y7FK_-Q0S2n_3pjCN6W8amQ1I130_provenance.
- NP120933.RAYAi3bHATBMMIa6NrxlOoZE0gLL794GMk_w6fJWzdMn4130_assertion description "[Mutations in MKS1 is associated with Bardet-Biedl syndrome ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120933.RAYAi3bHATBMMIa6NrxlOoZE0gLL794GMk_w6fJWzdMn4130_provenance.
- NP120936.RAZ6TIhVdQbZtvkp1bHSEfgyPlmy6C_K7XGdxlWKNqDCk130_assertion description "[A novel Bardet-Biedl syndrome protein is identified anad characterized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120936.RAZ6TIhVdQbZtvkp1bHSEfgyPlmy6C_K7XGdxlWKNqDCk130_provenance.
- NP120945.RAbXCY1vrkFzfT-lFSZnQMWeQwvMY78VtMpZ15pzEXHec130_assertion description "[Comparative genomics and gene expression analysis identifies PHTB1 protein as BBS9, a new Bardet-Biedl syndrome gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120945.RAbXCY1vrkFzfT-lFSZnQMWeQwvMY78VtMpZ15pzEXHec130_provenance.
- NP120949.RAYCrnuiDgVR30Xj5fPyVPFHOaoltfX8idB0lmQGSweXY130_assertion description "[A novel missense mutation found in BBS2 exon 4 and a novel intronic point mutation found in Bardet-Biedl syndrome patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120949.RAYCrnuiDgVR30Xj5fPyVPFHOaoltfX8idB0lmQGSweXY130_provenance.
- NP120953.RAdvbuWIzL2T3ZyRhw5xRVUnkYlZBuDP2Q-MK5_ryvHz4130_assertion description "[PK can function as an autoimmune target and that this immunoreactivity may be associated with Tourette syndrome, obsessive compulsive disorder, and associated disorders ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP120953.RAdvbuWIzL2T3ZyRhw5xRVUnkYlZBuDP2Q-MK5_ryvHz4130_provenance.