ARG1 single nucleotide polymorphisms rs2781666 and rs2781665 confer risk of type 2 diabetes mellitus

Autor: Fawad Ali Shah, Syed, Iqbal, Tahir, Naveed, Nasreen, Akram, Sumaira, Arshad Rafiq, Muhammad, Hussain, Sabir

Genetic polymorphisms mapped in the ARG1 locus (chr6:131894344-131905472) and their functional effects on type 2 diabetes mellitus (T2DM) have not been thoroughly elucidated to date. The present study aimed to investigate an association between varia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9908a1271e5900fceb35554066add3f

Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.

Autor: John, Peter, Tariq, Muhammad, Arshad Rafiq, Muhammad, Amin-ud-din, Muhammad, Muhammad, Dost, Waheed, Ishrat, Ansar, Muhammad, Ahmad, Wasim

Publikováno v: Archives of Dermatological Research; Aug2006, Vol. 298 Issue 3, p135-137, 3p, 1 Color Photograph, 2 Diagrams

Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability.

Autor: Heidari A; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8, Cellular and Molecular Research Center., Tongsook C; Institute of Biochemistry, Graz University of Technology, Graz 8010, Austria., Najafipour R; Cellular and Molecular Research Center., Musante L; Max Planck Institute of Molecular Genetics, Berlin D-14195, Germany., Vasli N; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8., Garshasbi M; Max Planck Institute of Molecular Genetics, Berlin D-14195, Germany, Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran 14117-13116, Iran., Hu H; Max Planck Institute of Molecular Genetics, Berlin D-14195, Germany., Mittal K; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8., McNaughton AJ; Ongwanada Genomics Lab., Sritharan K; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8., Hudson M; Ongwanada Genomics Lab., Stehr H; Department of Medicine, Stanford University, Stanford, CA 94305-5101, USA., Talebi S; Department of Medical Genetics, Medical University of Tehran, Tehran 14167-53955, Iran., Moradi M; Cellular and Molecular Research Center., Darvish H; Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran 4739, Iran., Arshad Rafiq M; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8., Mozhdehipanah H; Department of Neurology, Bou Ali Sina Hospital, Qazvin University of Medical Sciences, Qazvin 34197/59811, Iran., Rashidinejad A; Maternal, Fetal and Neonatal Research Center, Tehran University of Medical Sciences, Tehran 1419733141, Iran., Samiei S; Blood Transfusion Research Center, Tehran 1449613111, Iran., Ghadami M; Department of Medical Genetics, Tehran University of Medical Sciences, Tehran 1417613151, Iran., Windpassinger C; Institute of Human Genetics, Medical University of Graz, Graz 8010, Austria., Gillessen-Kaesbach G; Institut für Humangenetik, Universität zu Lübeck, Lübeck 23562, Germany., Tzschach A; Max Planck Institute of Molecular Genetics, Berlin D-14195, Germany., Ahmed I; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8, Atta-ur-Rehman School of Applied Biosciences, National University of Sciences and Technology, H-12, Islamabad, Pakistan., Mikhailov A; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8., Stavropoulos DJ; Department of Paediatric Laboratory Medicine, The Hospital for Sick Children, Toronto, ON, Canada., Carter MT; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada., Keshavarz S; Cellular and Molecular Research Center., Ayub M; Division of Developmental Disabilities, Department of Psychiatry, Queen's University, Kingston, ON, Canada K7L7X3., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran 19857, Iran, Kariminejad-Najmabadi Pathology and Genetics Center, Tehran 14667, Iran., Liu X; Ongwanada Genomics Lab., Ropers HH; Max Planck Institute of Molecular Genetics, Berlin D-14195, Germany., Macheroux P; Institute of Biochemistry, Graz University of Technology, Graz 8010, Austria., Vincent JB; Molecular Neuropsychiatry and Development (MiND) Lab, The Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health (CAMH), Toronto, ON, Canada M5T 1R8, Department of Psychiatry, University of Toronto, Toronto, ON, Canada M5T 1R8 and Institute of Medical Science, University of Toronto, Toronto, ON, Canada M5S 1A8 john.vincent@camh.ca.

Publikováno v: Human molecular genetics [Hum Mol Genet] 2015 Oct 15; Vol. 24 (20), pp. 5697-710. Date of Electronic Publication: 2015 Jul 23.