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Clinical Biochemistry
|
September 12, 2018
Utility of amniotic fluid chitotriosidase in the prenatal diagnosis of lysosomal storage disorders
Srilatha Kadali, Tumuluri Madalasa, Gummadi Maheshwar Reddy, et al.
Indian Journal of Biochemistry & Biophysics
|
April 30, 2014
Association of genetic variants of xenobiotic metabolic pathway with systemic lupus erythematosus
Yedluri Rupasree, Shaik Mohammad Naushad, Liza Rajasekhar, et al.
Neuroscience Letters
|
March 11, 2021
Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling
Shaik Mohammad Naushad, Tajamul Hussain, Salman Alrokayan, et al.
Gene
|
June 22, 2017
FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
Akella Radha Rama Devi, Nagesh Narayan Panday, Shaik Mohammad Naushad
Pharmacological Reports : PR
|
August 6, 2022
Development of pharmacogenomic algorithm to optimize nateglinide dose for the treatment of type 2 diabetes mellitus
Shaik Mohammad Naushad, Tajamul Hussain, Salman A Alrokayan, et al.
Pharmacological Reports : PR
|
June 9, 2021
Pharmacogenetic determinants of warfarin in the Indian population
Shaik Mohammad Naushad, Vijay Kumar Kutala, Tajamul Hussain, et al.
The Annals of Pharmacotherapy
|
March 22, 2021
Influence of RFC1 c.80A>G Polymorphism on Methotrexate-Mediated Toxicity and Therapeutic Efficacy in Rheumatoid Arthritis: A Meta-analysis
Shaik Mohammad Naushad, Salman A Alrokayan, Fahad N Almajhdi, et al.
Molecular Biology Reports
|
August 18, 2020
Probing the epigenetic signatures in subjects with coronary artery disease
Bobbala Indumathi, Sai Satish Oruganti, Shaik Mohammad Naushad, et al.
The Journal of Gene Medicine
|
October 26, 2020
Pharmacogenetic profiling of dihydropyrimidine dehydrogenase (DPYD) variants in the Indian population
Shaik Mohammad Naushad, Tajamul Hussain, Salman A Alrokayan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 5, 2023
Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease
Ananthaneni Radhika, Sandeepta Burgula, Chandan Badapanda, et al.
Page
of 9
Search research articles
Search
Showing results (11-20 of 84) with videos related to
Sort By:
Page
of 9
Clinical Biochemistry
|
September 12, 2018
Utility of amniotic fluid chitotriosidase in the prenatal diagnosis of lysosomal storage disorders
Srilatha Kadali, Tumuluri Madalasa, Gummadi Maheshwar Reddy, et al.
Indian Journal of Biochemistry & Biophysics
|
April 30, 2014
Association of genetic variants of xenobiotic metabolic pathway with systemic lupus erythematosus
Yedluri Rupasree, Shaik Mohammad Naushad, Liza Rajasekhar, et al.
Neuroscience Letters
|
March 11, 2021
Alpha synuclein (SNCA) rs7684318 variant contributes to Parkinson's disease risk by altering transcription factor binding related with Notch and Wnt signaling
Shaik Mohammad Naushad, Tajamul Hussain, Salman Alrokayan, et al.
Gene
|
June 22, 2017
FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
Akella Radha Rama Devi, Nagesh Narayan Panday, Shaik Mohammad Naushad
Pharmacological Reports : PR
|
August 6, 2022
Development of pharmacogenomic algorithm to optimize nateglinide dose for the treatment of type 2 diabetes mellitus
Shaik Mohammad Naushad, Tajamul Hussain, Salman A Alrokayan, et al.
Pharmacological Reports : PR
|
June 9, 2021
Pharmacogenetic determinants of warfarin in the Indian population
Shaik Mohammad Naushad, Vijay Kumar Kutala, Tajamul Hussain, et al.
The Annals of Pharmacotherapy
|
March 22, 2021
Influence of RFC1 c.80A>G Polymorphism on Methotrexate-Mediated Toxicity and Therapeutic Efficacy in Rheumatoid Arthritis: A Meta-analysis
Shaik Mohammad Naushad, Salman A Alrokayan, Fahad N Almajhdi, et al.
Molecular Biology Reports
|
August 18, 2020
Probing the epigenetic signatures in subjects with coronary artery disease
Bobbala Indumathi, Sai Satish Oruganti, Shaik Mohammad Naushad, et al.
The Journal of Gene Medicine
|
October 26, 2020
Pharmacogenetic profiling of dihydropyrimidine dehydrogenase (DPYD) variants in the Indian population
Shaik Mohammad Naushad, Tajamul Hussain, Salman A Alrokayan, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
September 5, 2023
Elucidation of genetic determinants of dyslipidaemia using a global screening array for the early detection of coronary artery disease
Ananthaneni Radhika, Sandeepta Burgula, Chandan Badapanda, et al.
Page
of 9