Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: Syndrome and CAT[original query] |
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8.5 Mb deletion at distal 5p in a male ascertained for azoospermia. American journal of medical genetics. Part A 2005 1 133A (2): 189-92. Rossi Elena, de Gregori Manuela, Grazia Patricelli Maria, Pramparo Tiziano, Argentiero Luisa, Giglio Sabrina, Sosta Katiuscia, Foresti Giovanni, Zuffardi Orset |
Gilbert's syndrome: High frequency of the (TA)7 TAA allele in India and its interaction with a novel CAT insertion in promoter of the gene for bilirubin UDP-glucuronosyltransferase 1 gene. World journal of gastroenterology : WJG 2006 Apr 12 (14): 2269-75. Farheen Shabana, Sengupta Sanghamitra, Santra Amal, Pal Suparna, Dhali Gopal Krishna, Chakravorty Meenakshi, Majumder Partha P, Chowdhury Abhij |
Association between polymorphisms in the Clock gene, obesity and the metabolic syndrome in man. International journal of obesity (2005) 2008 Apr 32 (4): 658-62. Scott E M, Carter A M, Grant P |
22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment. European journal of medical genetics 2010 1 53 (2): 61-5. Lundin Johanna, Söderhäll Cilla, Lundén Lina, Hammarsjö Anna, White Iréne, Schoumans Jacqueline, Läckgren Göran, Kockum Christina Clementson, Nordenskjöld Agne |
Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy. European journal of medical genetics 2010 1 53 (2): 55-60. Draaken Markus, Reutter Heiko, Schramm Charlotte, Bartels Enrika, Boemers Thomas M, Ebert Anne-Karoline, Rösch Wolfgang, Schröder Annette, Stein Raimund, Moebus Susanne, Stienen Dietlinde, Hoffmann Per, Nöthen Markus M, Ludwig Micha |
Genetic polymorphisms of antioxidant enzymes in preterm infants. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2012 Oct 25 Suppl 4 131-4. Poggi Chiara, Giusti Betti, Vestri Anna, Pasquini Elisabetta, Abbate Rosanna, Dani Car |
Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities. European journal of human genetics : EJHG 2012 Aug . Lalani SR, Shaw C, Wang X, Patel A, Patterson LW, Kolodziejska K, Szafranski P, Ou Z, Tian Q, Kang SH, Jinnah A, Ali S, Malik A, Hixson P, Potocki L, Lupski JR, Stankiewicz P, Bacino CA, Dawson B, Beaudet AL, Boricha FM, Whittaker R, Li C, Ware SM, Cheung SW, Penny DJ, Jefferies JL, Belmont JW |
Genetic polymorphisms of antioxidant enzymes as risk factors for oxidative stress-associated complications in preterm infants. Free radical research 2012 Sep 46 (9): 1130-9. Giusti Betti, Vestrini Anna, Poggi Chiara, Magi Alberto, Pasquini Elisabetta, Abbate Rosanna, Dani Car |
Association of three polymorphisms of scavenger receptor class BI gene (exon8, exon1, intron5) with coronary stenosis in a coronary Tunisian population. Gene 2012 Dec 511 (2): 383-8. Rejeb Jihène, Omezzine Asma, Boumaiza Imen, Rebhi Lamia, Kacem Slim, Rejeb Nabila Ben, Nabli Naoufel, Abdelaziz Ahmed Ben, Boughzala Essia, Bouslama A |
CYP1A1, GCLC, AGT, AGTR1 gene-gene interactions in community-acquired pneumonia pulmonary complications. Molecular biology reports 2013 Nov 40 (11): 6163-76. Salnikova Lyubov E, Smelaya Tamara V, Golubev Arkadiy M, Rubanovich Alexander V, Moroz Viktor |
Sick building syndrome (SBS) among office workers in a Malaysian university--Associations with atopy, fractional exhaled nitric oxide (FeNO) and the office environment. The Science of the total environment 2015 Dec 536 353-61. Lim Fang-Lee, Hashim Zailina, Md Said Salmiah, Than Leslie Thian-Lung, Hashim Jamal Hisham, Norbäck D |
Genetic variants involved in oxidative stress, base excision repair, DNA methylation, and folate metabolism pathways influence myeloid neoplasias susceptibility and prognosis. Molecular carcinogenesis 2016 Mar . Gonçalves Ana Cristina, Alves Raquel, Baldeiras Inês, Cortesão Emília, Carda José Pedro, Branco Claudia C, Oliveiros Bárbara, Loureiro Luísa, Pereira Amélia, Nascimento Costa José Manuel, Sarmento-Ribeiro Ana Bela, Mota-Vieira Lui |
Gene variants in AKT1, GCKR and SOCS3 are differentially associated with metabolic traits in Mexican Amerindians and Mestizos. Gene 2018 Aug . Cid-Soto Miguel A, Martínez-Hernández Angélica, García-Ortíz Humberto, Córdova Emilio J, Barajas-Olmos Francisco, Centeno-Cruz Federico, Contreras-Cubas Cecilia, Mendoza-Caamal Elvia C, Ciceron-Arellano Isabel, Morales-Rivera Monserrat I, Jimenez-Ruiz Juan L, Salas-Martínez Guadalupe, Saldaña-Álvarez Yolanda, Revilla-Monsalve Cristina, Islas-Andrade Sergio, Orozco Lore |
No evidence for a major effect of three common polymorphisms of the GPx1, MnSOD, and CAT genes on PCOS susceptibility. Journal of cellular biochemistry 2018 Sep . Salahshoor Mohammad Reza, Sohrabi Maryam, Jalili Faramarz, Jalili Parnian, Rezavand Negin, Haghnazari Lida, Jalili Cyr |
Association of GPx1 P198L and CAT C-262T Genetic Variations With Polycystic Ovary Syndrome in Chinese Women. Frontiers in endocrinology 2019 11 10 771. Sun Yuan, Li Suiyan, Liu Hongwei, Gong Yan, Bai Huai, Huang Wei, Liu Qingqing, Guan Linbo, Fan Pi |
Oxidant/Antioxidant Profile in the Thoracic Aneurysm of Patients with the Loeys-Dietz Syndrome. Oxidative medicine and cellular longevity 2020 4 2020 5392454. Soto Maria Elena, Manzano-Pech Lináloe G, Guarner-Lans Verónica, Díaz-Galindo Jorge A, Vásquez Xicoténcatl, Castrejón-Tellez Vicente, Gamboa Ricardo, Huesca Claudia, Fuentevilla-Alvárez Giovanny, Pérez-Torres Isra |
Genetic Variability in Antioxidative and Inflammatory Pathways Modifies the Risk for PCOS and Influences Metabolic Profile of the Syndrome. Metabolites 2020 11 10 (11): . Herman Rok, Jensterle Mojca, Janež Andrej, Gori?ar Katja, Dolžan Vi |
A Novel LC-MS/MS-Based Method for the Diagnosis of ADA2 Deficiency from Dried Plasma Spot. Molecules (Basel, Switzerland) 2021 9 26 (18): . Cafaro Alessia, Pigliasco Federica, Barco Sebastiano, Penco Federica, Schena Francesca, Caorsi Roberta, Volpi Stefano, Tripodi Gino, Gattorno Marco, Cangemi Giulia |
Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population. Laboratory medicine 2022 Aug . Shi Jianrong, Li Wei, Tao Ran, Zhou Dongming, Guo Yajun, Fu Haidong, Sun Anna, Zhang Junfeng, Mao Jianh |
The Predisposition for Type 2 Diabetes Mellitus and Metabolic Syndrome. Balkan journal of medical genetics : BJMG 2023 8 26 (1): 21-26. C Zenoaga-Barb?ro?ie, L Berca, T Vassu-Dimov, M Toma, M I Nica, O A Alexiu-Toma, C Ciornei, A Albu, S Nica, C Nistor, R Ni |
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