Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Alireza, Mowjoodi"'
Publikováno v:
BioTechniques, Vol 57, Iss 6, Pp 313-316 (2014)
Allelic discrimination using TaqMan 5′-nuclease assay chemistry has been in routine use for many years, and the catalog of Life Technologies— predesigned SNP genotyping assays now exceeds 4 million entries. However, predesigned assays are often n
Externí odkaz:
https://doaj.org/article/f32b865ee2584413ba7b366bc2991784
Publikováno v:
BioTechniques. 57:313-316
Allelic discrimination using TaqMan 5′-nuclease assay chemistry has been in routine use for many years, and the catalog of Life Technologies— predesigned SNP genotyping assays now exceeds 4 million entries. However, predesigned assays are often n
Autor:
Michael Ho, Alireza Mowjoodi, Michael W. Steffes, Rinku Sutradhar, Bhupinder Bharaj, A. Peter Maxwell, Amy Jayne McKnight, William C. Speed, Lei Sun, Judith R. Kidd, Patricia A. Cleary, Paul S. Thorner, Jean M. Bucksa, Michelle Liu, Trevor J. Orchard, Xinlei Xie, Wanjie Sun, Hussam Al-Kateb, Rachel G. Miller, David A. Savage, Valerie L. Arends, Shelley B. Bull, Andrew D. Paterson, Andrew P. Boright, Kenneth K. Kidd, Lucia Mirea, John M. Lachin
Publikováno v:
Diabetes. 57:218-228
BACKGROUND— Despite familial clustering of nephropathy and retinopathy severity in type 1 diabetes, few gene variants have been consistently associated with these outcomes. RESEARCH DESIGN AND METHODS— We performed an individual-based genetic ass
Autor:
Lucia Mirea, Shelley B. Bull, Alireza Mowjoodi, Stephen W. Scherer, Bernard Zinman, Andrew D. Paterson, Andrew P. Boright
Publikováno v:
Diabetes. 54:1238-1244
The development and progression of microvascular complications have been extensively documented in a cohort of type 1 diabetic subjects enrolled in the Diabetes Control and Complications Trial (DCCT) and followed in the Epidemiology of Diabetes Inter
Autor:
Hussam, Al-Kateb, Andrew P, Boright, Lucia, Mirea, Xinlei, Xie, Rinku, Sutradhar, Alireza, Mowjoodi, Bhupinder, Bharaj, Michelle, Liu, Jean M, Bucksa, Valerie L, Arends, Michael W, Steffes, Patricia A, Cleary, Wanjie, Sun, John M, Lachin, Paul S, Thorner, Michael, Ho, Amy Jayne, McKnight, A Peter, Maxwell, David A, Savage, Kenneth K, Kidd, Judith R, Kidd, William C, Speed, Trevor J, Orchard, Rachel G, Miller, Lei, Sun, Shelley B, Bull, Andrew D, Paterson
Publikováno v:
Diabetes. 57(1)
Despite familial clustering of nephropathy and retinopathy severity in type 1 diabetes, few gene variants have been consistently associated with these outcomes.We performed an individual-based genetic association study with time to renal and retinal
Autor:
Seyed A, Mesbah-Namin, Mohammad H, Sanati, Alireza, Mowjoodi, Philip J, Mason, Tom J, Vulliamy, Mohammad R, Noori-Daloii
Publikováno v:
British journal of haematology. 117(3)
We report the first investigation of glucose- 6-phosphate dehydrogenase (G6PD) deficiency among the Mazandaranians in the north of Iran. We analysed the G6PD gene in 74 unrelated G6PD-deficient men with a history of favism. Molecular analysis reveale
Autor:
Mohammad Hossein Sanati, Tom Vulliamy, Seyed Alireza Mesbah-Namin, Alireza Mowjoodi, Mohammad Reza Noori-Daloii, Philip J. Mason
Publikováno v:
British Journal of Haematology. 117:763-764
Summary. We report the first investigation of glucose- 6-phosphate dehydrogenase (G6PD) deficiency among the Mazandaranians in the north of Iran. We analysed the G6PD gene in 74 unrelated G6PD-deficient men with a history of favism. Molecular analysi
Autor:
Cunanan, Joanna, Rajyam, Sarada Sriya, Sharif, Bedra, Udwan, Khalil, Rana, Akanchaya, De Gregorio, Vanessa, Ricardo, Samantha, Elia, Andrew, Brooks, Brian, Weins, Astrid, Pollak, Martin, John, Rohan, Barua, Moumita
Publikováno v:
American Journal of Physiology: Renal Physiology; May2024, Vol. 326 Issue 5, pF704-F726, 23p
Publikováno v:
Pediatrics Week; 5/3/2024, p1302-1302, 1p
Autor:
Zarrei, Mehdi, Merico, Daniele, Kellam, Barbara, Engchuan, Worrawat, Scriver, Tara, Jokhan, Rikash, Wilson, Michael D., Parr, Jeremy, Lemire, Edmond G., Stavropoulos, Dimitri J., Scherer, Stephen W.
Publikováno v:
American Journal of Medical Genetics. Part A; May2017, Vol. 173 Issue 5, p1287-1293, 7p