Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.
Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.
Journal Of Psychiatry & Neuroscience : Jpn
Toma, Claudio C; Shaw, Alex D AD; Heath, Anna A; Pierce, Kerrie D KD; Mitchell, Philip B PB; Schofield, Peter R PR; Fullerton, Janice M JM
SIRT1 accelerates the progression of activity-based anorexia.
Nature Communications
Robinette, Timothy M TM; Nicholatos, Justin W JW; Francisco, Adam B AB; Brooks, Kayla E KE; Diao, Rachel Y RY; Sorbi, Sandro S; Ricca, Valdo V; Nacmias, Benedetta B; Brieño-Enríquez, Miguel A MA; Libert, Sergiy S
Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S
Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.
Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27
Variant appearance in text: SIRT1: 994T>C; rs2273773
SIRT1 Allele Frequencies in Depressed Patients of European Descent in Russia.
Frontiers In Genetics
Aftanas, Lyubomir I LI; Anisimenko, Maksim S MS; Berdyugina, Darya A DA; Garanin, Aleksandr Yu AY; Maximov, Vladimir N VN; Voevoda, Mikhail I MI; Vyalova, Natalya M NM; Bokhan, Nikolay A NA; Ivanova, Svetlana A SA; Danilenko, Konstantin V KV; Kovalenko, Sergei P SP
A highly significant association between Cathepsin S gene polymorphisms rs12068264 and chronic obstructive pulmonary disease susceptibility in Han Chinese population.
SIRT1 Polymorphisms and Serum-Induced SIRT1 Protein Expression in Aging and Frailty: The CHAMP Study.
The Journals Of Gerontology. Series A, Biological Sciences And Medical Sciences
Razi, Shajjia S; Cogger, Victoria C VC; Kennerson, Marina M; Benson, Vicky L VL; McMahon, Aisling C AC; Blyth, Fiona M FM; Handelsman, David J DJ; Seibel, Markus J MJ; Hirani, Vasant V; Naganathan, Vasikaran V; Waite, Louise L; de Cabo, Rafael R; Cumming, Robert G RG; Le Couteur, David G DG
Whole-genome sequencing of the world's oldest people.
Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014
Variant appearance in text: SIRT1: L332L; rs2273773
Genetic polymorphisms at SIRT1 and FOXO1 are associated with carotid atherosclerosis in the SAPHIR cohort.
Bmc Medical Genetics
Kedenko, Lyudmyla L; Lamina, Claudia C; Kedenko, Igor I; Kollerits, Barbara B; Kiesslich, Tobias T; Iglseder, Bernhard B; Kronenberg, Florian F; Paulweber, Bernhard B
Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.
Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
The combined effects of genetic variation in the SIRT1 gene and dietary intake of n-3 and n-6 polyunsaturated fatty acids on serum LDL-C and HDL-C levels: a population based study.
Lipids In Health And Disease
Inamori, Tomoko T; Goda, Toshinao T; Kasezawa, Nobuhiko N; Yamakawa-Kobayashi, Kimiko K
Genetic polymorphisms of the main transcription factors for adiponectin gene promoter in regulation of adiponectin levels: association analysis in three European cohorts.
Plos One
Kedenko, Lyudmyla L; Lamina, Claudia C; Kiesslich, Tobias T; Kapur, Karen K; Bergmann, Sven S; Waterworth, Dawn D; Heid, Iris M IM; Wichmann, H-Erich HE; Kedenko, Igor I; Kronenberg, Florian F; Paulweber, Bernhard B