Nanopublications

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

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NP131583.RASg9vKJp_K-T9sVxJbjtDKxnrjMIcuu5L_cgjFxQu8n4130_assertion description "[Individuals homozygous with respect to the at-risk allele have a 2.3-times higher risk of celiac disease (P = 1.55 x 10 (-5)).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131583.RASg9vKJp_K-T9sVxJbjtDKxnrjMIcuu5L_cgjFxQu8n4130_provenance.
NP131587.RAaGkLscFRt5G6ogHxoWhkT7IsP6k-r3S2vytACPi4Ck0130_assertion description "[Autoantigen in celiac disease/. ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131587.RAaGkLscFRt5G6ogHxoWhkT7IsP6k-r3S2vytACPi4Ck0130_provenance.
NP131597.RAR3PaPMwFlBFxJ1wtnCWQFMZdCkiQK4hYn21Utr2PW8U130_assertion description "[novel allele in the transmembrane region of the MICA gene consisting of seven GCT repeats found in a family based study of MICA polymorphism in celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131597.RAR3PaPMwFlBFxJ1wtnCWQFMZdCkiQK4hYn21Utr2PW8U130_provenance.
NP131606.RAWMn_yZRgLKPb9c0a8yLOSlQHejXHB0cCt6CHUB-QPys130_assertion description "[Results suggest that the simultaneous presence of IL-1B and TNF-alpha two-positions risk haplotypes enhances the susceptibility for celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131606.RAWMn_yZRgLKPb9c0a8yLOSlQHejXHB0cCt6CHUB-QPys130_provenance.
NP131609.RAS2hmCASiZATdSUKP2dVpt8Krutc6T7DnQwa2VEjP3zo130_assertion description "[Female more often than males carry DQ2/DQ8 molecules while the majority of negative cases of celiac disease are male ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131609.RAS2hmCASiZATdSUKP2dVpt8Krutc6T7DnQwa2VEjP3zo130_provenance.
NP131612.RAYMgWNTnAvAQcFYFisNKh35m8X7uzMT-BWOMJe7AR2IA130_assertion description "[Plasma levels of motilin were studied in 16 untreated Celiac disease patients and in an age-matched control group of 18 healthy subjects by radioimmunoassay and by high-performance liquid chromatography (HPLC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131612.RAYMgWNTnAvAQcFYFisNKh35m8X7uzMT-BWOMJe7AR2IA130_provenance.
NP131615.RAZa2UYzhecn-j18OxxShlcxIlMRZVUAJDVLyDcYWxE9U130_assertion description "[Polymorphisms within the vitamin D receptor gene are markers of susceptibility to or protection from autoimmune diseases, although association of variants with celiac disease and type 1 diabetes seems to be heterogeneous.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131615.RAZa2UYzhecn-j18OxxShlcxIlMRZVUAJDVLyDcYWxE9U130_provenance.
NP131621.RAfpOCRUn9OMwPSKi24stMc2oj25OdMh9UjOm0nSotAu4130_assertion description "[Female more often than males carry DQ2/DQ8 molecules while the majority of negative cases of celiac disease are male.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131621.RAfpOCRUn9OMwPSKi24stMc2oj25OdMh9UjOm0nSotAu4130_provenance.
NP131624.RAW6SgE93t1QaKVCKJIDJNQYMGnDJjk1I2d_FDiK9mJKw130_assertion description "[HLA DQA1-DQB1 genotypes in Bedouin families with celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131624.RAW6SgE93t1QaKVCKJIDJNQYMGnDJjk1I2d_FDiK9mJKw130_provenance.
NP131633.RATT_9yb4CclZS5YQZVd3PJV2yUq8AoDN3l8QfpiDNwqg130_assertion description "[possible associations between common serological markers of celiac disease with the -1087 IL10 and -308 TNFA polymorphisms ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131633.RATT_9yb4CclZS5YQZVd3PJV2yUq8AoDN3l8QfpiDNwqg130_provenance.
NP131635.RAQx_DUNagS09AV-cvCowJI7Wjcu-5MYJjXIkrvo5WXyA130_assertion description "[Results suggest that the simultaneous presence of IL-1B and TNF-alpha two-positions risk haplotypes enhances the susceptibility for celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131635.RAQx_DUNagS09AV-cvCowJI7Wjcu-5MYJjXIkrvo5WXyA130_provenance.
NP131636.RARfsn1BVFrWGaLYT2UvUz8H5_B4GUTgbZSysYWVrSsBQ130_assertion description "[In our study cohort we cannot confirm an association of the tagging SNPs of the IBD5 locus (included OCTN1 and 2 variants) with celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131636.RARfsn1BVFrWGaLYT2UvUz8H5_B4GUTgbZSysYWVrSsBQ130_provenance.
NP131637.RAcMieVJDK2Y3xg3CvC__1TqD7uzO4wBUuAINR7dBwDxM130_assertion description "[Association of KIR2DL5B gene with celiac disease supports the susceptibility locus on 19q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131637.RAcMieVJDK2Y3xg3CvC__1TqD7uzO4wBUuAINR7dBwDxM130_provenance.
NP131640.RAea9pd0o63ddFhL8gmF30VvYJWJnwadSe2JWfebuPuto130_assertion description "[no difference was found in the genotype and allele frequencies of TLR4 between patients with type 1 diabetes mellitus (T1DM), celiac disease (CD), both T1DM and CD and controls ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131640.RAea9pd0o63ddFhL8gmF30VvYJWJnwadSe2JWfebuPuto130_provenance.
NP131643.RAX3BWcYAMAfZlzQqvsvNKVRnvnRApjErVd6H59gT8BJY130_assertion description "[children with active celiac disease have an altered expression of TGF-beta1 and TGF-beta3 in the small intestine ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131643.RAX3BWcYAMAfZlzQqvsvNKVRnvnRApjErVd6H59gT8BJY130_provenance.
NP131650.RAW_z67Goc9WJhXbwBtzeX-xCOyWybU9QmQWWy5nmFNWo130_assertion description "[Results suggest that tissue ghrelin levels do not correlate with gastric emptying rate in adult celiac disease patients and in controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131650.RAW_z67Goc9WJhXbwBtzeX-xCOyWybU9QmQWWy5nmFNWo130_provenance.
NP131652.RAZGZLCxkBl25_19VOftnUxB-3njswGHHS7aoB8hfEG3Y130_assertion description "[It appears that IL23R is a susceptibility locus for celiac disease and multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131652.RAZGZLCxkBl25_19VOftnUxB-3njswGHHS7aoB8hfEG3Y130_provenance.
NP131655.RARBdO0iNMGgwJvYOfS0acMN1kSNA7G5JrOksE1xbThgU130_assertion description "[This is the first report that the FcgRIIa*519GG genotype predisposes to type 1 diabetes and celiac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131655.RARBdO0iNMGgwJvYOfS0acMN1kSNA7G5JrOksE1xbThgU130_provenance.
NP131656.RAQOlbK3fRi6OLy92zDStSIi9z73pZWt5waaTGIrRVXS0130_assertion description "[the mRNA expression of PREGNANCY-SPECIFIC BETA-1-GLYCOPROTEIN is up-regulated in cells circulating within blood from women with preeclampsia, and is positively correlated with cliical severity ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131656.RAQOlbK3fRi6OLy92zDStSIi9z73pZWt5waaTGIrRVXS0130_provenance.
NP131663.RAdzT3ly5s1T3yLVgAw_RfJ29TLrAsNMAT1hZH6ulNHFo130_assertion description "[sFlt-1 and PlGF and their ratio relative to one another may play a role in the development of preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131663.RAdzT3ly5s1T3yLVgAw_RfJ29TLrAsNMAT1hZH6ulNHFo130_provenance.
NP131665.RAaXkHc5llyxY_9-kH0NSBYLTK0V93NyZ1FuVhB3twczg130_assertion description "[calreticulin is increased in peripheral maternal blood early in pregnancy and remains elevated throughout normal gestation; there is a further increase in calreticulin in pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131665.RAaXkHc5llyxY_9-kH0NSBYLTK0V93NyZ1FuVhB3twczg130_provenance.
NP131666.RARH23ZMF-eIyiDbHNe1giBGQkJm9_nX1nOHaGuCDbpQU130_assertion description "[2849 AA genotype is protective against pre-eclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131666.RARH23ZMF-eIyiDbHNe1giBGQkJm9_nX1nOHaGuCDbpQU130_provenance.
NP131670.RAdc9VXWpHTIQaDQ2e83NXS59rlgyA_3vF5sBrjLnuyeI130_assertion description "[Review/endothelin-1 levels are involved in the hypertensive and oxidative stress states in pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131670.RAdc9VXWpHTIQaDQ2e83NXS59rlgyA_3vF5sBrjLnuyeI130_provenance.
NP131672.RAZmhvicI9lOu5LRdHyfwykkLFrGEiDSeRpRuthJwJHJU130_assertion description "[Plasma placenta-specific 1 and GCM1 mRNAs appear promising as noninvasively measurable molecular markers for pre-eclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131672.RAZmhvicI9lOu5LRdHyfwykkLFrGEiDSeRpRuthJwJHJU130_provenance.
NP131676.RAQ4pnIIb-A_WawYtj6mKc4wSJZDyCaG3Ypgnk7mNd74A130_assertion description "[While the TLR-2 +2258 (G > A) and MMP-9 -1562 (C > T) SNPs failed to present any significant association with pre-eclampsia, there was a marked trend for an association between the IL-4 -590 (C > T) SNP and pre-eclampsia (chi (2) = 5.87, P = 0.055) ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131676.RAQ4pnIIb-A_WawYtj6mKc4wSJZDyCaG3Ypgnk7mNd74A130_provenance.
NP131678.RAWiaPcsw5Ex9PGgGqvczFMWp6WPoJUjSKKyf8rCzrnBE130_assertion description "[the G20210A prothrombin gene mutation and the PAI-1 5G/5G genotype have roles in early onset of severe preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131678.RAWiaPcsw5Ex9PGgGqvczFMWp6WPoJUjSKKyf8rCzrnBE130_provenance.
NP131679.RAWcMV_7i4Xks6Rke4r47grSYcSjmi4KHyUnlQ7QdE-x0130_assertion description "[We conclude that down-regulation of nephrin and synaptopodin is associated with proteinuria in women with preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131679.RAWcMV_7i4Xks6Rke4r47grSYcSjmi4KHyUnlQ7QdE-x0130_provenance.
NP131681.RAYA7Suj76QbxlLp8IGQnXDF7BdgFdQ0gctAfgOizQPOo130_assertion description "[The mutant MTHFR 677T allele shows relatively high prevalence in different ethnic groups and potentially associated with preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131681.RAYA7Suj76QbxlLp8IGQnXDF7BdgFdQ0gctAfgOizQPOo130_provenance.
NP131690.RAUOHaRulqar8Lcv9C07IMqN3rv1Z3T1A0wWnvDUIl3DM130_assertion description "[Data provides evidence for association between preeclampsia and a polymorphism of the NOS3 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131690.RAUOHaRulqar8Lcv9C07IMqN3rv1Z3T1A0wWnvDUIl3DM130_provenance.
NP131693.RASuLRw9gwyZ0yQX6_yiq_nsC46rFZjCjR0AURf1MWUGg130_assertion description "[The eNOS Glu298Asp polymorphism and the Asp298-786C-4b haplotype are risk factors for preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131693.RASuLRw9gwyZ0yQX6_yiq_nsC46rFZjCjR0AURf1MWUGg130_provenance.
NP131699.RAV083BdHKtadKFB7zfO_p7xANDfCRUAQ6za0USMmftNc130_assertion description "[Genetic variability in exon 3 and 4 of EPHX may be a risk factor for pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131699.RAV083BdHKtadKFB7zfO_p7xANDfCRUAQ6za0USMmftNc130_provenance.
NP131700.RAavuItoMgse-yyRzjyV9FqPn5bXXKMbdtdzbyAv4FdHw130_assertion description "[Two exonic single nucleotide polymorphisms in the gene are jointly associated with preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131700.RAavuItoMgse-yyRzjyV9FqPn5bXXKMbdtdzbyAv4FdHw130_provenance.
NP131701.RARHBA-H-flsmQSP7U9mbJfJLoo3ZPuvPzeO4xRAiGv3A130_assertion description "[Amniotic fluid S100B protein concentration of the pre-eclampsia & normotensive IUGR cases was significantly higher than that of the control/could be a source responsible for the increased concentration of S100B in amniotic fluid.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131701.RARHBA-H-flsmQSP7U9mbJfJLoo3ZPuvPzeO4xRAiGv3A130_provenance.
NP131704.RATEMG0EtwBKiowx2dHQetCzsrckUtuBRa0F8CNG7j2D4130_assertion description "[LEPR A223G polymorphism may individually modify the risk of severe pre-eclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131704.RATEMG0EtwBKiowx2dHQetCzsrckUtuBRa0F8CNG7j2D4130_provenance.
NP131706.RAWWBGZidsMw8APZG5l_VJ0fZnvglIiO7BqWVQthHN_oQ130_assertion description "[Factor V Leiden mutation in pregnancy may contribute to increase thrombus formation in the placenta and can be a risk factor for hereditary preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131706.RAWWBGZidsMw8APZG5l_VJ0fZnvglIiO7BqWVQthHN_oQ130_provenance.
NP131711.RAWzX57TafayH74BYDFGrLbOkl7MeNvJI1Iamf5eVAVYw130_assertion description "[there is an increase in ceruloplasmin levels in placental tissue in preeclampsia compared to preterm and normal controls ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131711.RAWzX57TafayH74BYDFGrLbOkl7MeNvJI1Iamf5eVAVYw130_provenance.
NP131726.RAeQn9iVXSMr_bQqct4UZj4d2jZ7HVaCZ-Lm_w2iH6Uzc130_assertion description "[A high rate of protein Z deficiency is observed in patients with preeclampsia and fetal demise.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131726.RAeQn9iVXSMr_bQqct4UZj4d2jZ7HVaCZ-Lm_w2iH6Uzc130_provenance.
NP131753.RAT9D2XUpdOr7tarMBU5_kcxsOOE-gPNBTnpoDdLxrLO8130_assertion description "[association between the genotype II and low angiotensin-converting enzyme activity in preeclamptic women and an association between D allele frequency and preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131753.RAT9D2XUpdOr7tarMBU5_kcxsOOE-gPNBTnpoDdLxrLO8130_provenance.
NP131754.RAeWOcZqwB9gh5fp_vgPTy1GGSDOyDwdRJAlEV8XXm_5E130_assertion description "[insertion-deletion polymorphism of angiotensin-converting enzyme is a risk factor for the development of preeclampsia.The deletion genotype could be an important contributing factor for an early onset and recurrent preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131754.RAeWOcZqwB9gh5fp_vgPTy1GGSDOyDwdRJAlEV8XXm_5E130_provenance.
NP131755.RAfPGl-_dGuxGx9IKNjaAkUZ-lLv7IgCUbwwzvFrj_sAI130_assertion description "[Significantly higher levels of pentraxin 3 were found in preeclampsia/growth restriction pregnancies showed intermediate levels between normal and preeclamptic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131755.RAfPGl-_dGuxGx9IKNjaAkUZ-lLv7IgCUbwwzvFrj_sAI130_provenance.
NP131756.RAe32H_NBEqCrVlbpgURVUlJMoX7zSJuRZmJ22FkocnKw130_assertion description "[carriage of the +936T allele of the VEGF gene may be associated with increased susceptibility to the development of preeclampsia and may be an independent risk factor for preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131756.RAe32H_NBEqCrVlbpgURVUlJMoX7zSJuRZmJ22FkocnKw130_provenance.
NP131757.RAT6PmUumWSZxAVqttEGnaci_75LA62sMfqpbr7F6TDH8130_assertion description "[Results suggest that carriers of VEGF (+405) G allele have a decreased susceptibility to pre-eclampsia (PE) and that the progression of PE may be modified by the presence of VEGF (-2578) A allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131757.RAT6PmUumWSZxAVqttEGnaci_75LA62sMfqpbr7F6TDH8130_provenance.
NP131764.RASDi8z3PMWJG0UnCmdgXP_8Wdp8fFuBUC2oD1w17XsAs130_assertion description "[an elevation in serum IL15 is observed in women who have already developed preeclampsia, implying that the increase results from the pathology of preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131764.RASDi8z3PMWJG0UnCmdgXP_8Wdp8fFuBUC2oD1w17XsAs130_provenance.
NP131766.RAc4Np1VZVnOy_x_vZzi8S7BQOSX_7rcy720q9mcl7dWU130_assertion description "[study confirms previous reports of elevated neurokinin B levels in the plasma of preeclampsia women in the third trimester ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131766.RAc4Np1VZVnOy_x_vZzi8S7BQOSX_7rcy720q9mcl7dWU130_provenance.
NP131767.RAX26yxHiUaZFZSJtoCEl3UyZhG5ooPJ0D4sEt02Hb3JA130_assertion description "[In early-onset pre-eclamptic placentae, CYR61 was expressed at a significantly lower level compared with normal matched controls, indicating a potential role of this molecule in the pathogenesis of early-onset pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131767.RAX26yxHiUaZFZSJtoCEl3UyZhG5ooPJ0D4sEt02Hb3JA130_provenance.
NP131774.RASAAaOWakKiSlXUz8c4rgkcZznfOF65rgODqCWQWowXc130_assertion description "[Increased soluble fms-like tyrosine kinase 1 is more likely to be present in women with severe preeclampsia, but it is not present in all women with preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131774.RASAAaOWakKiSlXUz8c4rgkcZznfOF65rgODqCWQWowXc130_provenance.
NP131775.RASZXszsaSsfyRgrfU0vRn-bSXmfIqzRMAgzpxiNLyECQ130_assertion description "[Aldo deficiency due to a compromised methyl oxidase step of Aldo synthesis favors extracellular volume depletion, and may account for an increased risk of placental hypoperfusion and consecutive development of preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131775.RASZXszsaSsfyRgrfU0vRn-bSXmfIqzRMAgzpxiNLyECQ130_provenance.
NP131783.RAYzWr0eETWJIj0LdKlpLAqADLqElG1LMIIhpXIyMuzU8130_assertion description "[hypofibrinolytic genotypes of the PAI-1 gene are associated with the occurrence of mild preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131783.RAYzWr0eETWJIj0LdKlpLAqADLqElG1LMIIhpXIyMuzU8130_provenance.
NP131786.RAcaD_PFLTL6rGhbWRfKPOfuswOVwRbWfEuv7tAB_X6IA130_assertion description "[insertion-deletion polymorphism of angiotensin-converting enzyme is a risk factor for the development of preeclampsia.The deletion genotype could be an important contributing factor for an early onset and recurrent preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131786.RAcaD_PFLTL6rGhbWRfKPOfuswOVwRbWfEuv7tAB_X6IA130_provenance.
NP131788.RAeglvOVJh7Jg5hT4AeRm26XvsUSqqoAK1UTWpmdKFsO8130_assertion description "[Hypoxia alters expression and function of syncytin and its receptor (amino acid transport system B (0)) during trophoblast cell fusion of human placental BeWo cells: implications for impaired trophoblast syncytialisation in pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131788.RAeglvOVJh7Jg5hT4AeRm26XvsUSqqoAK1UTWpmdKFsO8130_provenance.
NP131789.RATLi4UTI4ME4Y9RuTg4Ms9Mj0nrQGc17r_tdWmDnfZds130_assertion description "[Mothers with small for gestational age fetuses had high plasma vascular endothelial growth factor receptor (sVEGFR-1), but lower than preeclampsia patients; those with abnormal uterine and umbilical artery velocimetry had the highest sVEGFR-1 ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131789.RATLi4UTI4ME4Y9RuTg4Ms9Mj0nrQGc17r_tdWmDnfZds130_provenance.
NP131790.RAfDrtuIDTR7bE7zuv5y-E54OWMUO4yh2EvfzndV7rX5E130_assertion description "[sFlt-1 and PlGF and their ratio relative to one another may play a role in the development of preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131790.RAfDrtuIDTR7bE7zuv5y-E54OWMUO4yh2EvfzndV7rX5E130_provenance.
NP131803.RASQfL9-x_9_e1vKLHt0-voHv3ySI8-8tLItEEFwudSAY130_assertion description "[Preeclamptic placental villous explants showed a four-fold increase in sVEGFR-1 over normal pregnancies/levels of sVEGFR-1 in preeclampsia are responsible for inhibiting angiogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131803.RASQfL9-x_9_e1vKLHt0-voHv3ySI8-8tLItEEFwudSAY130_provenance.
NP131804.RAaL017_oRI5fg7s1vqHlUH_dUomUY9en4qHeEMbgV-kA130_assertion description "[A soluble human-specific splicing variant of Flt1 in vascular smooth muscle cells, especially in placental cells in pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131804.RAaL017_oRI5fg7s1vqHlUH_dUomUY9en4qHeEMbgV-kA130_provenance.
NP131806.RARaoGR491tbfhYrv5DEMpU_F2TJZ1Ry-0dkGqSbyhQZw130_assertion description "[In early-onset pre-eclamptic placentae, NOV was expressed at a significantly lower level compared with normal matched controls, indicating a potential role of this molecule in the pathogenesis of early-onset pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131806.RARaoGR491tbfhYrv5DEMpU_F2TJZ1Ry-0dkGqSbyhQZw130_provenance.
NP131809.RARIskvI20oaWLc9OF0_9pZETcCcHsH9Bi7DzRqn16SNo130_assertion description "[Defective levels found in normal placenta compared with pre-eclampsia labor.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131809.RARIskvI20oaWLc9OF0_9pZETcCcHsH9Bi7DzRqn16SNo130_provenance.
NP131813.RAUBkOe2Q_HJuJWuLyGK8e6OVGY0oIhWBpkRBZiNlx_Ho130_assertion description "[Low soluble leptin receptor concentration is associated with a 6.3-fold increased risk of preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131813.RAUBkOe2Q_HJuJWuLyGK8e6OVGY0oIhWBpkRBZiNlx_Ho130_provenance.
NP131814.RAU6K2pNEXz_V2um5VZMakayCDB1Ic2Iu7UlfN-HosIvk130_assertion description "[The insertion-deletion polymorphism in intron 1 of the gamma 2 actin gene is unlikely to play any significant role in obstetric cholestasis or preeclampsia in patients from eastern Finland.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131814.RAU6K2pNEXz_V2um5VZMakayCDB1Ic2Iu7UlfN-HosIvk130_provenance.
NP131817.RAU5hlQkFKRnUoXNw0g1ewYyHDwdfHr0L8YyVfou3Ss4U130_assertion description "[study shows that the M235T variant in the gene encoding angiotensinogen could be a risk factor in mild and severe pre-eclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131817.RAU5hlQkFKRnUoXNw0g1ewYyHDwdfHr0L8YyVfou3Ss4U130_provenance.
NP131818.RAa-ESow5Q-q6YNyLo4DxjlqKLTfHiHkIR6IwpucCsnJI130_assertion description "[CRH, PLAC1, and selectin-P are distributed differently in preeclampsia cases compared to controls and correlate with signs of preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131818.RAa-ESow5Q-q6YNyLo4DxjlqKLTfHiHkIR6IwpucCsnJI130_provenance.
NP131819.RAW3SjKfPayL95wpUi5qaZVAKBdLf0rWcQLJ7b_ZRMeWs130_assertion description "[Our findings suggest that women who experience eclampsia/pre-eclampsia with severe maternal and/or fetal complications are more likely to have a genetic predisposition to produce high levels of TGF-beta 1 as defined by polymorphisms at codon 10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131819.RAW3SjKfPayL95wpUi5qaZVAKBdLf0rWcQLJ7b_ZRMeWs130_provenance.
NP131825.RAeFpuTWEqPUP34kRFyXIBa8GQjjBaA8vz7TjOsT7_CqA130_assertion description "[In women with subsequent preeclampsia, sL-selectin and sVCAM-1 concentrations were significantly lower, whereas sE-selectin, sP-selectin and sICAM-1 levels were significantly higher, compared with controls at mid-pregnancy (p < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131825.RAeFpuTWEqPUP34kRFyXIBa8GQjjBaA8vz7TjOsT7_CqA130_provenance.
NP131836.RAbv0tNwUt8qQnvrXuBpWYw26syqMcn9cvj7Xw0wj-3RY130_assertion description "[Aberrations in the beta-adrenoceptor signalling systems, rather than in the regulation of expression of these receptors may occur in preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131836.RAbv0tNwUt8qQnvrXuBpWYw26syqMcn9cvj7Xw0wj-3RY130_provenance.
NP131845.RAQWMaxwpvTL0aVSpXIaaDLCiZXIGjol-Y8th5TFsz8js130_assertion description "[In women with subsequent preeclampsia, sL-selectin and sVCAM-1 concentrations were significantly lower, whereas sE-selectin, sP-selectin and sICAM-1 levels were significantly higher, compared with controls at mid-pregnancy (p < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131845.RAQWMaxwpvTL0aVSpXIaaDLCiZXIGjol-Y8th5TFsz8js130_provenance.
NP131848.RAalTOHbQEJ1lCfKij4koCw5D5R986F5fHwehSFsdKoUE130_assertion description "[In preeclampsia, regional increases in adrenomedullin mRNA may be induced by hypoxia and mediate local fetal/placental adaptive responses to reduced placental perfusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131848.RAalTOHbQEJ1lCfKij4koCw5D5R986F5fHwehSFsdKoUE130_provenance.
NP131850.RAXGQuqz0DJpsBFkxPoKQPlKwTD6MIvCx8Uo5vQ5Pt7SQ130_assertion description "[in a low-risk population, C-reactive protein levels are already elevated between weeks 10 and 14 in pregnant women who develop preeclampsia or deliver a growth-restricted baby ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131850.RAXGQuqz0DJpsBFkxPoKQPlKwTD6MIvCx8Uo5vQ5Pt7SQ130_provenance.
NP131852.RAQL2KWBgHGRwPAk1Ms4kKSE-kernVQG3VUj3DXpkxfv0130_assertion description "[At the immunohistochemical level Nox1 expression was significantly increased in syncytiotrophoblast and endothelial cells in placentas from patients with preeclampsia as compared to gestational age-matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131852.RAQL2KWBgHGRwPAk1Ms4kKSE-kernVQG3VUj3DXpkxfv0130_provenance.
NP131855.RAQRsbMeuc7kWdQY-bmoGtAt03gJvgiXp_E45kwC6K8C8130_assertion description "[TAFI may contribute to the impairment of fibrinolysis in patients with preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131855.RAQRsbMeuc7kWdQY-bmoGtAt03gJvgiXp_E45kwC6K8C8130_provenance.
NP131856.RAUdWGc6URTa4XTZ74Z87DdSetQW9sQ_OfiV3lwLX3Lyc130_assertion description "[increased levels of serum macrophage colony stimulating factor markedly precede the development of clinical manifestations of preeclampsia ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131856.RAUdWGc6URTa4XTZ74Z87DdSetQW9sQ_OfiV3lwLX3Lyc130_provenance.
NP131858.RAXesVW8YkfYXHmBmgaWJ83MWYXPG0Z8wxZCdrUt1q5Cg130_assertion description "[The approximately 30 kDa HtrA1 form can be correlated to maternal preeclampsia while the significant down-regulation of total HtrA1 can be correlated to placental preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131858.RAXesVW8YkfYXHmBmgaWJ83MWYXPG0Z8wxZCdrUt1q5Cg130_provenance.
NP131860.RAffPAH0DGuidYntYJTD9yFOElHwtD4H0y6teErVACgg8130_assertion description "[CRH, PLAC1, and selectin-P are distributed differently in preeclampsia cases compared to controls and correlate with signs of preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131860.RAffPAH0DGuidYntYJTD9yFOElHwtD4H0y6teErVACgg8130_provenance.
NP131862.RAbUxMqaaw_nEMBmBtyRlusnU7CNi78vcqOuUmcqwVfw0130_assertion description "[data suggest that the ACE polymorphism could be a risk factor for patients with allergic contact dermatitis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131862.RAbUxMqaaw_nEMBmBtyRlusnU7CNi78vcqOuUmcqwVfw0130_provenance.
NP131864.RAfJp_JwOWC2JhN1Ziq1IWdonwL7rMp6U9lG3B_rc39lM130_assertion description "[( NAT2), N-acetyltransferase 2, (rapid acetylation) polymorphism may be involved in the pathogenesis of allergic contact dermatitis to para-pheylenediamine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131864.RAfJp_JwOWC2JhN1Ziq1IWdonwL7rMp6U9lG3B_rc39lM130_provenance.
NP131865.RAcKqwWZE00923SmoYSU-DFhvgxf_iwiz15473vfJA_Wk130_assertion description "[These findings suggest hitherto unknown roles of SMAD transcription factors and of CCL19 in the elicitation phase of allergic contact dermatitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131865.RAcKqwWZE00923SmoYSU-DFhvgxf_iwiz15473vfJA_Wk130_provenance.
NP131866.RAXHpDA5s7FgffPYUQLeFykZ4UFbGkyIxu-RyUPB_s1fQ130_assertion description "[saliva AST and ALP may have roles in development of periodontal diseases ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131866.RAXHpDA5s7FgffPYUQLeFykZ4UFbGkyIxu-RyUPB_s1fQ130_provenance.
NP131869.RAdWmjkTR_vY58kx2NQRasxyaDVgVHlD8x3aR4HCown0A130_assertion description "[results suggest that IL-1RN2 allele positivity is associated with periodontal disease in a Turkish population ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131869.RAdWmjkTR_vY58kx2NQRasxyaDVgVHlD8x3aR4HCown0A130_provenance.
NP131873.RAWhCko6gT4AxHbUx00CNLwaiCuPzYZlY2uupE11rnxgo130_assertion description "[The inflammatory markers, hsCRP, ESR, WBC, fibrinogen, and TNF-alpha, were raised in all patients but were significantly higher in rheumatoid arthritis patients with coronary artery disease who also had periodontal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131873.RAWhCko6gT4AxHbUx00CNLwaiCuPzYZlY2uupE11rnxgo130_provenance.
NP131875.RAVJ0g_UdT56jex8sWbMuV955ccSnucMqWYDV98IM5gr8130_assertion description "[an evident association exists between the carriage of the T-containing genotype and and the extent periodontal disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131875.RAVJ0g_UdT56jex8sWbMuV955ccSnucMqWYDV98IM5gr8130_provenance.
NP131876.RAdDWqqRN-C8tKgZuheyqyVVRNPeFh9J_SNIsGtLUpiVM130_assertion description "[ability to induce either Th1 or Th2 differentiation...important role in periodontal disease [review]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131876.RAdDWqqRN-C8tKgZuheyqyVVRNPeFh9J_SNIsGtLUpiVM130_provenance.
NP131877.RAVlzJ5H2wqnm61lGHzQiKeutp0KkS3aKUJOC-WBOVbqM130_assertion description "[IL-12 and IL-16 may be related to the pathogenesis of periodontal disease, but within the periodontitis sites, IL-16 may be related to disease severity in alcohol drinkers/smokers ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131877.RAVlzJ5H2wqnm61lGHzQiKeutp0KkS3aKUJOC-WBOVbqM130_provenance.
NP131883.RAdjRQkSNnixyxTAYlbRAtVQRAANgDiuEEtn-7YOf6nHY130_assertion description "[increased in gingival tissues of diabetic patients, especially those with periodontal disease ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131883.RAdjRQkSNnixyxTAYlbRAtVQRAANgDiuEEtn-7YOf6nHY130_provenance.
NP131893.RAd77i33WITUU77LGK2VnhVFj9m-DePFYmROjadsTYf60130_assertion description "[Results suggest that the elevated salivary CD14 concentration may be one of the host-response components associated with the clinical manifestations of periodontal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131893.RAd77i33WITUU77LGK2VnhVFj9m-DePFYmROjadsTYf60130_provenance.
NP131902.RARiOByq-MYSjUqysyomZqYDnHqMpXyywUBsOkwiWSmZ4130_assertion description "[MCP-1, MIP-1beta, and IL-8 play important roles in the pathophysiology of Hemophagocytic lymphohistiocytosis (HLH)/addition, the serum concentrations of these chemokines may be sensitive markers for assessing disease activity in patients with HLH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131902.RARiOByq-MYSjUqysyomZqYDnHqMpXyywUBsOkwiWSmZ4130_provenance.
NP131903.RATAnt7g7FvjoleYjnIY8LoSqW84epcw2LXyEh-sd3bnQ130_assertion description "[Mutations in AP3B1 is not associated with familial hemophagocytic lymphohistiocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131903.RATAnt7g7FvjoleYjnIY8LoSqW84epcw2LXyEh-sd3bnQ130_provenance.
NP131914.RAX_FhyYdlL81KJsUAV9TS5hTfbpWLV8nb6uuUZ-hIW5o130_assertion description "[Hemophagocytic lymphohistiocytosis patients with PRF1 mutations demonstrated absent or markedly decreased natural killer cell function.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131914.RAX_FhyYdlL81KJsUAV9TS5hTfbpWLV8nb6uuUZ-hIW5o130_provenance.
NP131917.RAW5tvimVpX5bkie1NJXES06Kmcv8XFMTWm1tJ6gm0LYA130_assertion description "[The genes PRF1, GZMB, UNC13D, and Rab27a involved in hemophagocytic lymphohistiocytosis do not confer a significant risk of association with systemic-onset juvenile idiopathic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131917.RAW5tvimVpX5bkie1NJXES06Kmcv8XFMTWm1tJ6gm0LYA130_provenance.
NP131919.RAdHl5ADKoMeEHmd57t6jcktWpyQZCjO5KUZoYqn4BqfA130_assertion description "[The genes PRF1, GZMB, UNC13D, and Rab27a involved in hemophagocytic lymphohistiocytosis do not confer a significant risk of association with systemic-onset juvenile idiopathic arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131919.RAdHl5ADKoMeEHmd57t6jcktWpyQZCjO5KUZoYqn4BqfA130_provenance.
NP131923.RAXJNAv5aJ8L83WNEmx4dJWPdL28lydleADfbNGEQXAGA130_assertion description "[Extensive genetic and allelic heterogeneity in Familial hemophagocytic lymphohistiocytosis (FHL) and delineate an approach for functionally characterizing missense mutations in RAB27A and UNC13D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131923.RAXJNAv5aJ8L83WNEmx4dJWPdL28lydleADfbNGEQXAGA130_provenance.
NP131926.RAUfDwK0TukAlyAtNwu6s6b-4AlA-E4nvTjRQP3-oF7fM130_assertion description "[HMunc13-4 mutations were shown to cause familial hemophagocytic lymphohistiocytosis; HMunc13-4 is essential for the priming step of cytolytic granules secretion preceding vesicle membrane fusion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131926.RAUfDwK0TukAlyAtNwu6s6b-4AlA-E4nvTjRQP3-oF7fM130_provenance.
NP131927.RAaBn-cjm6CE2RkGhatEJv-xD8lr2J-y7c07AGso5z0hU130_assertion description "[A large group of 63 unrelated patients with Familial hemophagocytic lymphohistiocytosis (FHL) was analysed for mutations in STX11, PRF1, and UNC13D.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131927.RAaBn-cjm6CE2RkGhatEJv-xD8lr2J-y7c07AGso5z0hU130_provenance.
NP131932.RAY2q58CODewb8Jcc9Gd2j_RNLhvjeaUv2THfOAaY4Ygw130_assertion description "[The down-regulation of the SAP gene by ATF5 may represent a common mechanism for the pathogenesis of Hemophagocytic syndrome that is associated with either Epstein-Barr virus infection or immune disorders with dysregulated T-cell activation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131932.RAY2q58CODewb8Jcc9Gd2j_RNLhvjeaUv2THfOAaY4Ygw130_provenance.
NP131933.RAQDnwC4MWgSEht7XbSaIGisqOLLWGLW6rl2hNdrsuy0U130_assertion description "[CD107a surface expression has a role in Munc13-4 defect in familial hemophagocytic lymphohistiocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131933.RAQDnwC4MWgSEht7XbSaIGisqOLLWGLW6rl2hNdrsuy0U130_provenance.
NP131938.RAV_Esd5c-Wxt8AgJuObjMlSmZO_Rq6OVjVTANUXgpxEE130_assertion description "[Mutations in SRGN is not associated with familial hemophagocytic lymphohistiocytosis ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131938.RAV_Esd5c-Wxt8AgJuObjMlSmZO_Rq6OVjVTANUXgpxEE130_provenance.
NP131957.RAUa4OigaXuGixmaWfWDYHf2wyoyL_siTtlT-Qbtz5_r8130_assertion description "[checked for prevalence of the PTPN22 R620W polymorphism in multiplex families affected with systemic lupus erythematosus & other autoimmune diseases; its association with other polymorphisms in mannose binding lectin & FcgammaRIIa genes was also studied ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131957.RAUa4OigaXuGixmaWfWDYHf2wyoyL_siTtlT-Qbtz5_r8130_provenance.
NP131968.RAQI91t3Cc5azpWn2vuJcSFhIeyGNMLhx0K9ndYAHpBKg130_assertion description "[total amount in gingival crevicular fluid significantly decreased in juvenile systemic lupus erythematosus ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131968.RAQI91t3Cc5azpWn2vuJcSFhIeyGNMLhx0K9ndYAHpBKg130_provenance.
NP131978.RAXQj7iLNjS58kudjUjIGKpbp6fokGFWtIv_QxvquvHNg130_assertion description "[Abnormal posttranslational mechanisms of the Elf-1 protein result in defective expression of the functional 98-kDa form of Elf-1, and consequently, the transcriptional defect of TCR zeta-chain in patients with systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131978.RAXQj7iLNjS58kudjUjIGKpbp6fokGFWtIv_QxvquvHNg130_provenance.
NP131983.RAbwDI_1j327Cfsgeidc3XNIV84pPrgUHNlYoYnVdwWWk130_assertion description "[Analysis of the functional relevance of a putative regulatory SNP of PDCD1 associated with systemic lupus erythematosus is reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131983.RAbwDI_1j327Cfsgeidc3XNIV84pPrgUHNlYoYnVdwWWk130_provenance.
NP131985.RAbvQZLlEtc1BT-kz-6PMywnXScD-svl8_0gQeVYYpUmI130_assertion description "[A regulatory polymorphism in this gene is associated with susceptibility to systemic lupus erythematosus in humans (p.666).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131985.RAbvQZLlEtc1BT-kz-6PMywnXScD-svl8_0gQeVYYpUmI130_provenance.
NP131993.RAXFppH5Wx4un1OVMIG4GToTCLzkXlx13ubVv0ujRj-wg130_assertion description "[Data suggest that defects in Notch1 upregulation upon activation of T cells from patients with systemic lupus erythematosus are related to lupus disease activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131993.RAXFppH5Wx4un1OVMIG4GToTCLzkXlx13ubVv0ujRj-wg130_provenance.
NP131994.RAc2azH3b_-RBJNbdl1ONJWoF-3gZx4M_5-W7ou1YkGUk130_assertion description "[These findings suggest allelic variation in this region of CTLA4 is not major independent risk factor for systemic lupus erythematosus, but may contribute to risk of disease in younger African-Americans or in presence of certain immunogenetic markers.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131994.RAc2azH3b_-RBJNbdl1ONJWoF-3gZx4M_5-W7ou1YkGUk130_provenance.

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