Nanopublications

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

Showing items 44,801 to 44,900 of ±4,851,667 with 100 items per page.

first
previous
next

NP45945.RAkxgxM9yDEX_E3kqM2Knj4rJz5rMEcunUmXYg3F_i7OE130_assertion description "[In addition, we identified the same MYOC mutation, implicated for primary open angle glaucoma, in three additional PCG patients who did not harbor any mutation in CYP1B1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45945.RAkxgxM9yDEX_E3kqM2Knj4rJz5rMEcunUmXYg3F_i7OE130_provenance.
NP45950.RAt-R8h87CmDqFY4_XK0CsbXwX0lMpnVCPucZhFXcYJ2o130_assertion description "[Genetic susceptibility to distinct bladder cancer subphenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45950.RAt-R8h87CmDqFY4_XK0CsbXwX0lMpnVCPucZhFXcYJ2o130_provenance.
NP45966.RAokL9cevxO3l5PpQ6ZNC83JfIr4Ve26BUBfchJkSue4U130_assertion description "[Overall, there is no conclusive evidence that genetic variants in genes involved in the estrogen metabolic pathway are associated with mammographic density in postmenopausal women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45966.RAokL9cevxO3l5PpQ6ZNC83JfIr4Ve26BUBfchJkSue4U130_provenance.
NP45969.RAtzDYbLZUmE0wiJUQp6ftLom1vSXORynP7qivZpW-L1Q130_assertion description "[Genetic polymorphisms of estrogen metabolizing enzyme and breast cancer risk in Thai women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45969.RAtzDYbLZUmE0wiJUQp6ftLom1vSXORynP7qivZpW-L1Q130_provenance.
NP45970.RAvpkTEncx2VXILIi7-y9Tkwt55CyzN5D0xcGKMmJQC28130_assertion description "[Coffee intake and CYP1A2*1F genotype predict breast volume in young women: implications for breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45970.RAvpkTEncx2VXILIi7-y9Tkwt55CyzN5D0xcGKMmJQC28130_provenance.
NP45979.RAuatbXeyKbyd_HH3xR-8XZiu82Su7i4_wwSAkqQX1z1U130_assertion description "[When CYP1A1, CYP1A2, and CYP1B1 genotypes were combined and ranked by the number of putative low-risk genotypes carried, women with four or five low-risk genotypes had a reduced risk of endometrial cancer (OR, 0.29; 95% CI, 0.15-0.56) compared with women with one or none.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45979.RAuatbXeyKbyd_HH3xR-8XZiu82Su7i4_wwSAkqQX1z1U130_provenance.
NP45986.RAsYKyau4w7RN4vyrvNUiTJb6cDLv4MqZxcC3U8rvs8T0130_assertion description "[Interaction between CYP1A2-T2467DELT polymorphism and smoking in adenocarcinoma and squamous cell carcinoma of the lung.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45986.RAsYKyau4w7RN4vyrvNUiTJb6cDLv4MqZxcC3U8rvs8T0130_provenance.
NP45987.RAvD5uZXOGiue3nJhMGsHK6UF0qxzWp1ypvEKpYXNMPjA130_assertion description "[Development of lung cancer before the age of 50: the role of xenobiotic metabolizing genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45987.RAvD5uZXOGiue3nJhMGsHK6UF0qxzWp1ypvEKpYXNMPjA130_provenance.
NP45990.RAiXNxsvYRR8haYKTE_aFylBoMikbF_3ikGE0c-spHb0A130_assertion description "[Phase I metabolic genes and risk of lung cancer: multiple polymorphisms and mRNA expression.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45990.RAiXNxsvYRR8haYKTE_aFylBoMikbF_3ikGE0c-spHb0A130_provenance.
NP45996.RAili0EX60AQM_1_YnxejiF8EHim8lzy2nNxDc2oE0ayU130_assertion description "[These frequencies are higher than those previously reported for other human populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP45996.RAili0EX60AQM_1_YnxejiF8EHim8lzy2nNxDc2oE0ayU130_provenance.
NP46002.RApXHlYkaxDeihD9cxOHBrjlqZC7vRTPSIl_atgjKOaPU130_assertion description "[Genetic determinants in the metabolism of bladder carcinogens in relation to risk of bladder cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46002.RApXHlYkaxDeihD9cxOHBrjlqZC7vRTPSIl_atgjKOaPU130_provenance.
NP46022.RAnl1f5OBnIWrDwEoFUuGrNka7Tkzpspp3LQSP0Yv59l4130_assertion description "[The frequencies of CYP1A1*2A; CYP1A1*2C; CYP1B1*3; CYP3A4*1B CYP3A4*2 polymorphisms were determined in 71 patients aged 36-87, with primary breast cancer and 100 healthy individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46022.RAnl1f5OBnIWrDwEoFUuGrNka7Tkzpspp3LQSP0Yv59l4130_provenance.
NP46027.RAh1t2oSeBHz-Xa_Ck81JOoSryNh4aCLrlHHAOMT8fHe4130_assertion description "[Results from this study suggest that rs4680 in the COMT gene and rs4646903 in the CYP1A1 gene may be genetic markers for breast cancer prognosis in Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46027.RAh1t2oSeBHz-Xa_Ck81JOoSryNh4aCLrlHHAOMT8fHe4130_provenance.
NP46028.RAndZWAaFNY5Yo3Nx51OzIb8qSr77C0BZlezceEQcXK0w130_assertion description "[Potential differences in breast cancer risk factors based on CYP1A1 MspI and African-American-specific genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46028.RAndZWAaFNY5Yo3Nx51OzIb8qSr77C0BZlezceEQcXK0w130_provenance.
NP46036.RAs-w1dCYPcW9p8UAweYevmRm87NU4g4fvx2-e3ABg8dE130_assertion description "[Our results suggest that the XRCC1 399Gln allele is a potentially important determinant of susceptibility to smoking-induced pancreatic cancer. Our findings, including stronger associations and interactions among women, require replication in additional study populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46036.RAs-w1dCYPcW9p8UAweYevmRm87NU4g4fvx2-e3ABg8dE130_provenance.
NP46042.RAuZkA9Zn-nnSYI9QDC0fGNelpUqehuFpxl7EvuiShbB0130_assertion description "[We investigated CYP1A1*2A, CYP1A1*2C, CYP1A2*1C, CYP1A2*1F, GSTM1 and NAT2 gene polymorphisms, involving enzymes which metabolize many carcinogens, with reference to colorectal cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46042.RAuZkA9Zn-nnSYI9QDC0fGNelpUqehuFpxl7EvuiShbB0130_provenance.
NP46055.RAiNmPw5VG3zrmkxSToKwlEFMbiaAKHIKc_8ewIrzTnuU130_assertion description "[our data suggested that CYP1B1 germ line-inactivating mutations might increase the incidence of HCA in women with HNF1alpha mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46055.RAiNmPw5VG3zrmkxSToKwlEFMbiaAKHIKc_8ewIrzTnuU130_provenance.
NP46062.RAncJOHGSesHrlZkPqoG5ZLifPXLWgxXCqGyarMRvIVF8130_assertion description "[The estimated head and neck cancer risk for the combination of either CYP1A1 Ile462Val or CYP1A1 Val462Val genotype with either GSTP1 Ile105Val or Val105Val genotype (OR=2.89, 95% CI: 0.71-11.71) and for the combination of either CYP1A1 Ile462Val or CYP1A1 Val462Val genotype with GSTT1 null genotype (OR=2.62, 95% CI: 0.64-10.85) suggested the absence of the modifying effect of combined variant alleles on head and neck cancer susceptibility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46062.RAncJOHGSesHrlZkPqoG5ZLifPXLWgxXCqGyarMRvIVF8130_provenance.
NP46072.RAmgQRB9WtA3IdnIJxdIZ-8jal5coEVMznMq5ODbYNJpU130_assertion description "[Susceptibility to endometriosis in women of Han Nationality in Guangdong Province associated with Msp I polymorphisms of cytochrome P450 1A1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46072.RAmgQRB9WtA3IdnIJxdIZ-8jal5coEVMznMq5ODbYNJpU130_provenance.
NP46075.RAnIhX7XJVgGEN7S3fl0F-R3V3F3pCf7S-GEQKeC6EaT4130_assertion description "[Estrogen bioactivation, genetic polymorphisms, and ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46075.RAnIhX7XJVgGEN7S3fl0F-R3V3F3pCf7S-GEQKeC6EaT4130_provenance.
NP46076.RAqiaSUBhuxxizmPxFVEzluWp5pPO82r5SOGwFmL5A32U130_assertion description "[Ovarian cancer risk and polymorphisms involved in estrogen catabolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46076.RAqiaSUBhuxxizmPxFVEzluWp5pPO82r5SOGwFmL5A32U130_provenance.
NP46077.RApMZWQZfLG_OTkcyo0SpRxjajwoTd1Ha-dmb6AvuNRl8130_assertion description "[Coffee intake, variants in genes involved in caffeine metabolism, and the risk of epithelial ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46077.RApMZWQZfLG_OTkcyo0SpRxjajwoTd1Ha-dmb6AvuNRl8130_provenance.
NP46079.RAty0qQ7dHBSP8V0Bb6SYGJSLXMCyN5UIcvbKj168OcpA130_assertion description "[Validating genetic risk associations for ovarian cancer through the international Ovarian Cancer Association Consortium.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46079.RAty0qQ7dHBSP8V0Bb6SYGJSLXMCyN5UIcvbKj168OcpA130_provenance.
NP46085.RAjZMjQIuIEX6xQq03lcWY8J2O9BCPPcJd7pV7zl3L4oM130_assertion description "[Oxidative stress-related gene interactions with preterm delivery in Korean women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46085.RAjZMjQIuIEX6xQq03lcWY8J2O9BCPPcJd7pV7zl3L4oM130_provenance.
NP46087.RAkL310uG54nlQT2D97wtw_YbavBfe6EJi4ffscUSmn1Y130_assertion description "[We evaluated the association between polymorphisms in the cytochrome P-450 CYP1A1 (CYP1A1) and glutathione S-transferase M1 (GSTM1) genes and genetic susceptibility to prostate cancer in Chinese men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46087.RAkL310uG54nlQT2D97wtw_YbavBfe6EJi4ffscUSmn1Y130_provenance.
NP46093.RAmYnfbkOizWW6qJD5wFeLd4bcnoJDIb5eWViRRX4jv4M130_assertion description "[Our findings suggest that the interaction between genetic polymorphisms in GST (T1; M1) and CYP1A1-M1* would play a significant role as a modifying factor on PCa risk in Chilean people.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46093.RAmYnfbkOizWW6qJD5wFeLd4bcnoJDIb5eWViRRX4jv4M130_provenance.
NP46095.RAiPFRF7A2PUJOe2rR8Dv9fQG4A8DQrFxzT5a1P5h9drk130_assertion description "[These gene polymorphisms may play a role in the development prostate cancer (PCa) in Turkish populations; we therefore assessed the association of CYP1A1 and GSTM1 polymorphisms in patients with PCa in our population through a case-control study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46095.RAiPFRF7A2PUJOe2rR8Dv9fQG4A8DQrFxzT5a1P5h9drk130_provenance.
NP46096.RAh7daxgQ2s4BYK6lsO5yagrUxbreUqBWXKbWkyv50Jb0130_assertion description "[Gene-environment interaction involved in oral carcinogenesis: molecular epidemiological study for metabolic and DNA repair gene polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46096.RAh7daxgQ2s4BYK6lsO5yagrUxbreUqBWXKbWkyv50Jb0130_provenance.
NP46106.RAqF25RvOT79d5z6jtXWN17tGKIsC93EnZanEeVHzQWbo130_assertion description "[DNA was obtained from blood samples and we studied by PCR-RFLP the distribution of CYP1A1 *2B (n=248) and *4 (n=222) polymorphisms in healthy controls and 222 lung cancer patients from a Mexican population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46106.RAqF25RvOT79d5z6jtXWN17tGKIsC93EnZanEeVHzQWbo130_provenance.
NP46108.RArhaX4rAL20Q5yl_46pXKPhY1AvFByYoqoTsPgEPcrkA130_assertion description "[The frequencies of the CYP1A1 valine allele, homozygous deletions of GSTM1 and GSTT1, and two point mutations of the NAT2 gene, (C481-->T) and S2 (G590-->A), were compared in healthy children and children having bronchial asthma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46108.RArhaX4rAL20Q5yl_46pXKPhY1AvFByYoqoTsPgEPcrkA130_provenance.
NP46115.RAkOuLUA628UH3pIhtqdWzTBGUWA4FVVvOzwbsbp1JXVg130_assertion description "[CYP1A1MspI and HincII genotypes modified the association between passive smoking and primary dysmenorrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46115.RAkOuLUA628UH3pIhtqdWzTBGUWA4FVVvOzwbsbp1JXVg130_provenance.
NP46127.RAhPnRs8u89i4KKkze8Av_kRdC_BXFr8RTKWYAv-9a7wE130_assertion description "[No differences in allele frequencies were seen by age, sex, or type of controls (hospital patients versus population controls). No examples of linkage disequilibrium between the different loci were detected based on comparison of observed and expected frequencies for combinations of specific alleles.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46127.RAhPnRs8u89i4KKkze8Av_kRdC_BXFr8RTKWYAv-9a7wE130_provenance.
NP46128.RAitn1WEVyVyLy4DaDVG8Eyw5fLw5-RyBzD0xgpUYZajs130_assertion description "[Women withthe simultaneous occurrence of two or more genetic polymorphisms in the above-mentioned biotransformation enzymes, most probably resulting in a disturbed detoxification capacity, may be at increased risk for pre-eclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46128.RAitn1WEVyVyLy4DaDVG8Eyw5fLw5-RyBzD0xgpUYZajs130_provenance.
NP46131.RAlkR_bjfnrVAXfxHcZ7CbBYVl1-zJxudmNUFQgHXawbo130_assertion description "[Profile of polymorphisms of drug-metabolising enzymes and the risk of therapy-related leukaemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46131.RAlkR_bjfnrVAXfxHcZ7CbBYVl1-zJxudmNUFQgHXawbo130_provenance.
NP46138.RAubKto5P2R7eqMeVT-mbamcqTJAarYVkFTYT1upqAviY130_assertion description "[Combination of TNF-RII, CYP1A1 and GSTM1 polymorphisms and the risk of Japanese SLE: findings from the KYSS study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46138.RAubKto5P2R7eqMeVT-mbamcqTJAarYVkFTYT1upqAviY130_provenance.
NP46143.RAo5Gnon6EgZKj2Ym1WOO6QvGnZeEziqoxallCTXfekB0130_assertion description "[Most of the variants in the candidate breast cancer genes evaluated in this study are not strong predictors of breast density. However, our findings of differences in associations for UGT1A1 and AIB1 genotypes with breast density by menopausal status needs additional corroboration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46143.RAo5Gnon6EgZKj2Ym1WOO6QvGnZeEziqoxallCTXfekB0130_provenance.
NP46147.RApNNCPaGePuQ2M_lk1I65LsU3nred4iH0nhwsFhwJ_Tk130_assertion description "[Our data offer insufficient support for an association between variation in ESR1, ESR2, PGR, CYP19A1, and HSD17B2 and risk for developing colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46147.RApNNCPaGePuQ2M_lk1I65LsU3nred4iH0nhwsFhwJ_Tk130_provenance.
NP46149.RAtzzkD7f7GdjAP9lAzXLeLygwB6wLXGq6j-cx2YLNeiQ130_assertion description "[Association of endometriosis risk and genetic polymorphisms involving sex steroid biosynthesis and their receptors: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46149.RAtzzkD7f7GdjAP9lAzXLeLygwB6wLXGq6j-cx2YLNeiQ130_provenance.
NP46155.RAs7v2XwYU64VP7dC9fMA9lb-OvlXfGjOf_hmTAdJa_7E130_assertion description "[Study on the relationship between polymorphisms of genes (CYP17, CYP19 and SULT1A1) and susceptibility to breast cancer in Chinese women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46155.RAs7v2XwYU64VP7dC9fMA9lb-OvlXfGjOf_hmTAdJa_7E130_provenance.
NP46156.RAks-QtubA40r7ZXrcG2PeQTIpcjgJfYtSdZfTCPREP9U130_assertion description "[In order to determine if polymorphisms of the CYP19 gene are associated with breast cancer risk, we analyzed the frequency of tetranucleotide (TTTA) tandem repeats and a 3-bp insertion (I)/deletion (D) polymorphism in intron 4 of the CYP19 gene in genomic DNA from 70 Korean breast cancer patients and 102 age-matched, healthy women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46156.RAks-QtubA40r7ZXrcG2PeQTIpcjgJfYtSdZfTCPREP9U130_provenance.
NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion description "[Pairwise analysis showed that combinations of the ERalpha G allele with the homozygous Trp genotype of CYP19A1 codon 39 (rs2236722), the methionine (Met) allele of COMT codon 158 (rs4680) or Pro allele of p53 codon 72 (rs1042522) were more frequent in ER-positive than ER-negative breast cancer, especially in patients less than 50-year old.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_provenance.
NP46162.RAnFLd_1vjFwdjpyFTQ7ayHStNdB2_4gtA328vlimVeks130_assertion description "[Functional genetic polymorphisms in the aromatase gene CYP19 vary the response of breast cancer patients to neoadjuvant therapy with aromatase inhibitors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46162.RAnFLd_1vjFwdjpyFTQ7ayHStNdB2_4gtA328vlimVeks130_provenance.
NP46163.RAgTS09tA5M_EmaNPUNbw5fY0z2pBLaco5fvWlFwr9u4U130_assertion description "[Association between CYP19 polymorphisms and breast cancer risk: results from 10,592 cases and 11,720 controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46163.RAgTS09tA5M_EmaNPUNbw5fY0z2pBLaco5fvWlFwr9u4U130_provenance.
NP46174.RAlOZKiUSdOoMMu7VsTbWlpOCOBdrhI5FMKcv-HGSMmtU130_assertion description "[Although CYP19 may not be a major genetic determinant of PCOS, it may act as a genetic modifier of the hyperandrogenic phenotype of PCOS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46174.RAlOZKiUSdOoMMu7VsTbWlpOCOBdrhI5FMKcv-HGSMmtU130_provenance.
NP46178.RAsOlgJ0AlCly4_6Nc03akxLr3CuHcm7PYtZ_VY5mL3g0130_assertion description "[It may be suggested that more aggressive clinically and frequently receptor-negative type II of endometrial cancer is associated with indirect signs of mainly intratumoral hyperproduction of estrogens (excess of CYP19 A6A6 genotype) without their sufficient inactivation into methoxyderivatives that warrants further study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46178.RAsOlgJ0AlCly4_6Nc03akxLr3CuHcm7PYtZ_VY5mL3g0130_provenance.
NP46188.RApkGS3fHG3A1VpJQWnMS0yDJwUldPWg8rsAOa34kfv2A130_assertion description "[Aromatase and interleukin-10 genetic variants interactively modulate Alzheimer's disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46188.RApkGS3fHG3A1VpJQWnMS0yDJwUldPWg8rsAOa34kfv2A130_provenance.
NP46190.RAsmVK1QgrzL9XzOYgJDEs_Dalu2xkYfrIFlhq4S-mc00130_assertion description "[ Polymorphisms in HSD3B1, CYP19, AKR1C3 genes may be associated with an enlarged prostate in older men. These data provide insights into genes that should be examined further for their potential role in the pathogenesis of BPH. (c) 2005 Wiley-Liss, Inc.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46190.RAsmVK1QgrzL9XzOYgJDEs_Dalu2xkYfrIFlhq4S-mc00130_provenance.
NP46193.RAjM8oN7cpe6jEWROF3lTEey17unxqRRDZsgDMOF-Ud2I130_assertion description "[Common variations of CYP19-aromatase are associated with differences in BMD that seem to be important from an individual as well as from a population perspective.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46193.RAjM8oN7cpe6jEWROF3lTEey17unxqRRDZsgDMOF-Ud2I130_provenance.
NP46197.RAi-lQ84olqOxKq7LoIhpnXimQ803duhMN1ygfjTucHRk130_assertion description "[For single polymorphisms, a significant association of the T/T genotype of the PvuII site in the ER alpha gene (odds ratio OR, 3.44; 95% confidence interval CI, 1.97-5.99; P = 0.0028), and the C/T and T/T genotypes of the CYP19 gene (OR, 1.77; 95% CI, 1.02-3.09; P = 0.037) with prostate carcinoma risk, was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46197.RAi-lQ84olqOxKq7LoIhpnXimQ803duhMN1ygfjTucHRk130_provenance.
NP46207.RAhmU_LM15AghMIaz1wLs8oWSYGwjoefs3KgmszyLbvDE130_assertion description "[Concerning the CYP17 MspA1 polymorphism and breast cancer risk: a meta-analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46207.RAhmU_LM15AghMIaz1wLs8oWSYGwjoefs3KgmszyLbvDE130_provenance.
NP46209.RAgMjzJA4ARknuRm7ZF2Jr45b15b4IVJ_Pw3AbrIXiuVM130_assertion description "[Most of the variants in the candidate breast cancer genes evaluated in this study are not strong predictors of breast density. However, our findings of differences in associations for UGT1A1 and AIB1 genotypes with breast density by menopausal status needs additional corroboration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46209.RAgMjzJA4ARknuRm7ZF2Jr45b15b4IVJ_Pw3AbrIXiuVM130_provenance.
NP46221.RAvCNXp-2W4jEfGlSstDyHSOMEDojJQK-OXnh46oi5SPo130_assertion description "[Possession of the A2 variant of CYP17 appears to increase risk for ovarian cancer, whereas possession of the Val/Met variant of COMT decreases the risk for mucinous tumors. Confirmation in other populations and further exploration of potential pathogenetic mechanisms will be necessary.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46221.RAvCNXp-2W4jEfGlSstDyHSOMEDojJQK-OXnh46oi5SPo130_provenance.
NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_assertion description "[These observations have suggested that the CYP17 A2/A2, CYP1B1 Val/Val, and CYP2D6 genotypes may be associated with an altered risk of prostate cancer, while the CYP2D6 and SRD5A2 V89L polymorphism have no association with its risk in the North Indian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46232.RAqIhnrGkimrrnP_DG7C7Rdv6gq5iVdMYva6HmeSHHtd8130_provenance.
NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_assertion description "[These results suggested that common variants of the CYP17 gene are associated with prostate enlargement and therefore may increase the risk of development of BPH in this population, while infrequent variants of the aromatase gene (CYP19) could be of a protective nature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46234.RArwkenIKenhLbRG1oFcYRIZ93cfm_HBlG81j95GN7tWg130_provenance.
NP46239.RAlt2HW2-z64pO2KoMdfOF0xyz8glMmur9SBZ9LviUHbg130_assertion description "[Among these women, the risk of endometrial cancer was higher for women homozygous for the CYP17 T allele (OR, 4.10; 95% CI, 1.64-10.3), but not for women with the C allele (OR, 1.31; 95% CI, 0.53-3.21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46239.RAlt2HW2-z64pO2KoMdfOF0xyz8glMmur9SBZ9LviUHbg130_provenance.
NP46240.RAmfHGOW-_KGfd3tSwPYoyOTVd2pGGgRpBlzcFT0wKxIw130_assertion description "[Thus, specific set of genetic polymorphisms (carrying of CYP17 A1 allele and combination of longest A6 or A7 CYP19 alleles) may predispose to the induction of higher rate of local estrogen biosynthesis in malignant endometrium, that in its turn may support growth of the latter. Further studies are warranted to connect revealed regularities with the type I or II of EC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46240.RAmfHGOW-_KGfd3tSwPYoyOTVd2pGGgRpBlzcFT0wKxIw130_provenance.
NP46242.RAqcGSI7zaK7MLn7PoNxUt4TLIWpC-ZqXMIj5ZbKj8keE130_assertion description "[Distribution of allelic polymorphisms of CYP17 (17alpha-hydroxylase/17,20-lyase), CYP19 (aromatase), catechol-O-methyltransferase (COMT) and CYP1B1 (primarily, estrogen 4-hydroxylase) genes was compared totally in 156 endometrial cancer patients, approximately two-third of who belonged (on the basis of case history and some characteristics of host and tumor) to type I of the disease, and one-third to type II.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46242.RAqcGSI7zaK7MLn7PoNxUt4TLIWpC-ZqXMIj5ZbKj8keE130_provenance.
NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_assertion description "[This study suggests that the A2 allele may significantly decrease the overall risk of developing RA. In women, the protective effect of A2 mainly affects the older age group. In men, the clinical severity of RA may decrease in patients with the A2/A2 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46250.RApiG8RpFa2mP4RNBXsnJ6P1N82JoDDi4OzxN4F_w1uwM130_provenance.
NP46252.RAh7dgBkM-YCpn-efiLrpF56vywsTM15UmqPvTiB_pjgk130_assertion description "[The polymorphic CYP17 allele is not found with increased frequency in systemic lupus erythematosus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46252.RAh7dgBkM-YCpn-efiLrpF56vywsTM15UmqPvTiB_pjgk130_provenance.
NP46259.RApy0vaaFXRbDmDqaPKE2KINAnivEqPM_LHhodzi47VWc130_assertion description "[Association of the -344T/C aldosterone synthase gene variant with essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46259.RApy0vaaFXRbDmDqaPKE2KINAnivEqPM_LHhodzi47VWc130_provenance.
NP46263.RAmkMxpG2WVECViy2g3H5K66ATaIihNqT4_UiiANVi1iA130_assertion description "[Participation of CYP11B2 and REN and possibly AGT genes in development of low renin AH was convincingly shown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46263.RAmkMxpG2WVECViy2g3H5K66ATaIihNqT4_UiiANVi1iA130_provenance.
NP46264.RAno5OcHJ41PNxsXQl0Pr-ofNQ2MaB6cdYQoaJbuB76pQ130_assertion description "[Individual coronary risk might be related to the presence of a critical accumulation detrimental polymorphisms]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46264.RAno5OcHJ41PNxsXQl0Pr-ofNQ2MaB6cdYQoaJbuB76pQ130_provenance.
NP46265.RAr_Tn5MQNdJ545ztOy8CSNEcb9-k2GtC49MjGT6Q7JMM130_assertion description "[ An increasing number of risk alleles are associated with an elevated risk for CAD. An analysis of multiple polymorphisms, some several hundred, each with a small impact, may allow improved assessment of the individual genetic burden for CAD. Larger studies are needed to prove this hypothesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46265.RAr_Tn5MQNdJ545ztOy8CSNEcb9-k2GtC49MjGT6Q7JMM130_provenance.
NP46269.RArOl1poO2LNig8vQ7fSfrm5LTghORgY6hPZWYmU8245c130_assertion description "[We studied retrospectively the role of angiotensinogen (AGT) M235T, angiotensin converting enzyme (ACE) insertion/deletion (I/D), angiotensin II type 1 receptor (AT1R) A1166C, aldosterone syntase (CYP11B2) -344C/T and intron 2 W/C polymorphisms in conjunction with clinical and biochemical covariables on the rate of progression of renal insufficiency in a group of patients with ESRD of various etiologies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46269.RArOl1poO2LNig8vQ7fSfrm5LTghORgY6hPZWYmU8245c130_provenance.
NP46271.RAm-QNrgkhEjUrXUDLbiE9nNbxuHuxxVcRh7yCDdjDo4c130_assertion description "[ AT1 receptor genotypes could influence arterial ageing in hypertensive subjects. These results also show that the association between genotypes and arterial stiffness may manifest itself later in life.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46271.RAm-QNrgkhEjUrXUDLbiE9nNbxuHuxxVcRh7yCDdjDo4c130_provenance.
NP46272.RAl2wESJ0_aoKK6Qvhvn8NyAVt1st8KW4kYMCRQzwREDk130_assertion description "[ In addition to the angiotensin-converting enzyme (ACE) and angiotensinogen (AGT) gene variants, gene-gene interactions may be important causative factors in a complex disease such as young-onset essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46272.RAl2wESJ0_aoKK6Qvhvn8NyAVt1st8KW4kYMCRQzwREDk130_provenance.
NP46274.RAiubTrQbeRVwx_XEM3JwCAwX_2Hj8Cq5cRiOcrl56do8130_assertion description "[ A CYP11B2 gene variant predicts the variable improvement in LV ejection fraction that occurs subsequent to initiating medical therapy in IDC. These data suggest a role for the aldosterone synthase locus in regulating the progression of heart failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46274.RAiubTrQbeRVwx_XEM3JwCAwX_2Hj8Cq5cRiOcrl56do8130_provenance.
NP46280.RAvLhdOSx2Oaq6kPHjRxZbl1uz218RuvmIAWF8T_1HqaU130_assertion description "[Polymorphic differences from normal in the aldosterone synthase gene (CYP11B2) in patients with primary hyperaldosteronism and adrenal tumour (Conn's syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46280.RAvLhdOSx2Oaq6kPHjRxZbl1uz218RuvmIAWF8T_1HqaU130_provenance.
NP46281.RAvKFB2GMgfOtz-jGI6dlULvVm_N47PCRfxbwRviAfh1w130_assertion description "[Association between the TNFRII 196R allele and diagnosis of rheumatoid arthritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46281.RAvKFB2GMgfOtz-jGI6dlULvVm_N47PCRfxbwRviAfh1w130_provenance.
NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_assertion description "[ In agreement with previous studies, we found that the TT genotype of T-344C polymorphism of aldosterone synthase gene was associated with significantly higher levels of PRA in normotensive men. In subjects with high PRA, the TT genotype was associated with higher values of the LVMI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46282.RAuGu9GYRkzXIEtRn40UhbpTKWZKZy43uPi3roStcaM4o130_provenance.
NP46283.RAvIuxNMG-RTUQSjM5PTz3azpEAU8AVjAAMvFz_9rK7Rg130_assertion description "[ Our data suggest that -344C/T polymorphism affects LV mass and thickness in essential hypertension, independent of adrenal aldosterone. A role for intracardiac aldosterone synthesis is hypothesized.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46283.RAvIuxNMG-RTUQSjM5PTz3azpEAU8AVjAAMvFz_9rK7Rg130_provenance.
NP46288.RAvi0EV62SmQqUa2MICuZAEL9iSFDpugmz0pvRWDtSy1o130_assertion description "[CT genotype of CYP11B2 gene may be one of factors responsible for the pathogenesis of HCM in a proportion of patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46288.RAvi0EV62SmQqUa2MICuZAEL9iSFDpugmz0pvRWDtSy1o130_provenance.
NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_assertion description "[Our data did not support the association between Mendelian disease gene variants and essential hypertension in the Japanese. However, the present study did not definitively resolve this issue and further investigation is certainly warranted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46292.RAiq1jjub0xQIG0gvBbriDxzSmG5Gxz080efOK7LoX6OQ130_provenance.
NP46295.RAh9KUIs1gJ33fl41otEldN3ltQBQ8gEKbxIAU8DAx57s130_assertion description "[The aim of this study was to investigate the association of DNA polymorphisms within steroid synthesis genes (CYP11B2, CYP11B1) and the postoperative resolution of hypertension in Chinese patients undergoing adrenalectomy for aldosterone-producing adenomas (APA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46295.RAh9KUIs1gJ33fl41otEldN3ltQBQ8gEKbxIAU8DAx57s130_provenance.
NP46300.RAu9uZYt0NNwQ0p1IzRWVBXjA84z-VIzLcRh1sSm2lKnc130_assertion description "[Role of androgen metabolism genes CYP1B1, PSA/KLK3, and CYP11alpha in prostate cancer risk and aggressiveness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46300.RAu9uZYt0NNwQ0p1IzRWVBXjA84z-VIzLcRh1sSm2lKnc130_provenance.
NP46304.RAkTq6feINTo0S7XCUNCDfIHIsVYy9dW951oqtoJYr2ZE130_assertion description "[Polymorphisms in mitochondrial genes and prostate cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46304.RAkTq6feINTo0S7XCUNCDfIHIsVYy9dW951oqtoJYr2ZE130_provenance.
NP46305.RAhE_KiBdjTzdVV5pl93lJidGATjrh-J_jlplYUtk_9HM130_assertion description "[The presence of the CYP11A1 (TTTTA)6 allele increases the risk of biochemical relapse in organ confined and low-grade prostate cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46305.RAhE_KiBdjTzdVV5pl93lJidGATjrh-J_jlplYUtk_9HM130_provenance.
NP46308.RAkIre98yPgIGaemi-qeO-VaedOOG210AGMObROdfO0cw130_assertion description "[The results from this study indicate that the TAAAA repeat polymorphism near the promoter region of the CYP11A gene may be an important susceptibility factor for breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46308.RAkIre98yPgIGaemi-qeO-VaedOOG210AGMObROdfO0cw130_provenance.
NP46309.RAu-0PEFttRQUaa9JIbDzn_c1tv5tqJDwyxrizHMv_yRw130_assertion description "[A systematic assessment of common genetic variation in CYP11A and risk of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46309.RAu-0PEFttRQUaa9JIbDzn_c1tv5tqJDwyxrizHMv_yRw130_provenance.
NP46310.RAvRlkvW0MCztEzALHiUNXFrMztyZn5neNB-ExEhGHZ1E130_assertion description "[Haplotype analysis of CYP11A1 identifies promoter variants associated with breast cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46310.RAvRlkvW0MCztEzALHiUNXFrMztyZn5neNB-ExEhGHZ1E130_provenance.
NP46316.RAhsEGGHeZFP_Y2Nd0YL8HNd8tlp2qxHYRGDQQ7vFuwww130_assertion description "[ Among subjects of a Mediterranean population with low risk for CHD, the presence of DD ACE genotype could be a risk factor for myocardial infarction, and we confirm the linkage disequilibrium between two nucleotide positions of the ACE gene and the polymorphism for an Alu insertion.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46316.RAhsEGGHeZFP_Y2Nd0YL8HNd8tlp2qxHYRGDQQ7vFuwww130_provenance.
NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_assertion description "[However, studies on the association of the C242T polymorphism in the p22phox gene with CAD have produced conflicting results, and the relation of this polymorphism with CAD is not well known in a population with acquired risk factors enhancing the NADPH-dependent superoxide production.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46319.RAg2xx-JvXGcOu3EprfjDt-uyYr_RY3SAceUl7rRnCDKY130_provenance.
NP46322.RAg5JeyzWH1LU-ejbvZ4ob34tqReV9FRQCnQdEU3REBQI130_assertion description "[Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46322.RAg5JeyzWH1LU-ejbvZ4ob34tqReV9FRQCnQdEU3REBQI130_provenance.
NP46330.RAsbDlW7nZgQxsv33RkokHRF31F0uG8QT8cYcEVXvjN7g130_assertion description "[Non-effect of p22-phox -930A/G polymorphism on end-organ damage in Brazilian hypertensive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46330.RAsbDlW7nZgQxsv33RkokHRF31F0uG8QT8cYcEVXvjN7g130_provenance.
NP46337.RAjsZuVrnZXhLjUbgDwYbK9y4kKfxCWdjrfi7eF4mnmvo130_assertion description "[To investigate the relationship between genetic factors associated with endothelial function and the development of coronary artery disease (CAD), endothelial nitric oxide synthase (ecNOS) gene a/b polymorphism and NADH/NADPH oxidase p22 phox gene C242T polymorphism were examined in 305 Korean male CAD patients and 215 healthy male control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46337.RAjsZuVrnZXhLjUbgDwYbK9y4kKfxCWdjrfi7eF4mnmvo130_provenance.
NP46342.RAk5eiPijfKspHaZpUy5oL8hRIG_X4XSNhDE5DYkMA-AI130_assertion description "[ Nuclear genetic polymorphisms related to oxidative stress or apoptosis may modify the age at onset of LHON.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46342.RAk5eiPijfKspHaZpUy5oL8hRIG_X4XSNhDE5DYkMA-AI130_provenance.
NP46343.RAspDegN9BPrSVZmOkU8q3k-FYXKFj827AqH-PTcVSxrk130_assertion description "[These results show that the C242T mutation in the p22 phox gene is associated with progression of asymptomatic atherosclerosis in the subjects with type 2 diabetes and is also associated with insulin resistance in nondiabetic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46343.RAspDegN9BPrSVZmOkU8q3k-FYXKFj827AqH-PTcVSxrk130_provenance.
NP46344.RAnb0Y1GGs687_u75WmaFvSjSrcSJ6szpefsmZgi2MYkE130_assertion description "[Association of the CYBA, PPARGC1A, PPARG3, and PPARD gene variants with coronary artery disease and metabolic risk factors of coronary atherosclerosis in a Russian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46344.RAnb0Y1GGs687_u75WmaFvSjSrcSJ6szpefsmZgi2MYkE130_provenance.
NP46351.RApVQFK49Ec1CcBmakbmanwPZbi3rvRRb7XRgMiHXLncE130_assertion description "[ These results suggest that assessment of the combination of NADPH p22phox C242T and RAGE G1704T polymorphisms may be useful in identifying the risk for developing diabetic nephropathy in type 2 diabetic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46351.RApVQFK49Ec1CcBmakbmanwPZbi3rvRRb7XRgMiHXLncE130_provenance.
NP46352.RAhoHW0VgnyyCQtzGlV3QlILEP1IthG-VFcWm1hqjf4FM130_assertion description "[ These results show that the C242T mutation in the p22 phox gene is associated with progression of asymptomatic atherosclerosis in the subjects with type 2 diabetes and is also associated with insulin resistance in nondiabetic subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46352.RAhoHW0VgnyyCQtzGlV3QlILEP1IthG-VFcWm1hqjf4FM130_provenance.
NP46353.RAtTUUpYho08k24iPopUnAYdus0UgYjSjYY2goMo2LKlQ130_assertion description "[The nonreplication of association suggests differential genetic susceptibility of the two populations to diabetic chronic renal insufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46353.RAtTUUpYho08k24iPopUnAYdus0UgYjSjYY2goMo2LKlQ130_provenance.
NP46356.RAhBDW8AtLB2hnpQgm38fd83MFjQ_x3chJyx8m8SXIRQo130_assertion description "[Distribution of four HIV type 1-resistance polymorphisms (CCR5-Delta32, CCR5-m303, CCR2-64I, and SDF1-3'A) in the Bahraini population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46356.RAhBDW8AtLB2hnpQgm38fd83MFjQ_x3chJyx8m8SXIRQo130_provenance.
NP46357.RAjkH8I88acxpEfu9cPirW87K0ClxTDnamuxkr-JuXkrg130_assertion description "[Therefore, this study not only reports the frequencies for the CX(3)CR1 and CCR5 promoter haplotypes in a Chinese population living in Taiwan, but also identifies a statistical link between the P1/P1 haplotype and the elevated CCR5 expression levels in the study group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46357.RAjkH8I88acxpEfu9cPirW87K0ClxTDnamuxkr-JuXkrg130_provenance.
NP46362.RAkWVS9EPgTxo1vETTPBS0DCFyQJwIHSuFiTQV8Gms1X8130_assertion description "[On the basis of our findings we can exclude the possibility that either the chemokine receptor polymorphisms or the SDF-1 polymorphism explain the beneficial outcome of GBV-C infected patients with HIV infection]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46362.RAkWVS9EPgTxo1vETTPBS0DCFyQJwIHSuFiTQV8Gms1X8130_provenance.
NP46363.RAn0nRMfrA2aQjjVIA1XtbhgJnRMXuvCveLvkuS46XgQg130_assertion description "[ The CCR5-Delta32 and CCR2-64I alleles had a strong protective effect on progression of HIV-1 infection, but SDF-1 3'A homozygosity carried no such protection.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46363.RAn0nRMfrA2aQjjVIA1XtbhgJnRMXuvCveLvkuS46XgQg130_provenance.
NP46369.RAp-p9YVrdZ1cgpA7FmIi5h304_dHKLep1sqn7u-A_OYw130_assertion description "[Distribution of four HIV type 1-resistance polymorphisms (CCR5-Delta32, CCR5-m303, CCR2-64I, and SDF1-3'A) in the Bahraini population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46369.RAp-p9YVrdZ1cgpA7FmIi5h304_dHKLep1sqn7u-A_OYw130_provenance.
NP46386.RAgkC1ytAXTmo_MwrzSGx9BEFPXRQw95XmirkkzgP2jEY130_assertion description "[In two recent studies from Germany, a strong association was found between the allelic variant T of the amino acid substitution encoding polymorphism 224 C/T (A38V) in exon 2 of the cathepsin D gene (CTSD) and late onset Alzheimer disease (AD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46386.RAgkC1ytAXTmo_MwrzSGx9BEFPXRQw95XmirkkzgP2jEY130_provenance.
NP46401.RApe-o80mk6Uo72fUm99UUfDKh_KpW35j6Qty8kgmYK5E130_assertion description "[Prevalence of mutations in APC, CTNNB1, and BRAF in Tunisian patients with sporadic colorectal cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46401.RApe-o80mk6Uo72fUm99UUfDKh_KpW35j6Qty8kgmYK5E130_provenance.
NP46406.RAu4KlwChNhvrsLohxEI_17I2gzc4gCfUPuDmCPkpvMA8130_assertion description "[Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46406.RAu4KlwChNhvrsLohxEI_17I2gzc4gCfUPuDmCPkpvMA8130_provenance.
NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_assertion description "[The frequency of CTLA-4 +49A>G polymorphism is not different in children and adults with GD compared to the normal control population and does not seem to contribute independently to the severity of the clinical presentation of GD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP46409.RAhbzbSodR2kqOPRxGNqu8bvMKRP9OHQF4gN7gxRCtctY130_provenance.

first
previous
next