Artykuły udostępnione publicznie: - Vadlamudi raghavendra raoWięcej informacji
Niedostępne w żadnym miejscu: 2
Dopamine Transporter (DAT1) VNTR Polymorphism and Alcoholism in Two Culturally Different Populations of South India
LVKS Bhaskar, K Thangaraj, S Wasnik, L Singh, V Raghavendra Rao
The American journal on addictions 21 (4), 343-347, 2012
Upoważnienia: Department of Biotechnology, India
Identification of c. 286C> T mutation in the SLURP1 gene in a patient with Mal de Meleda from India
G Gupta, GN Deshmukh, VA Kumar, VR Rao
Polymorphism 9, 23-28, 2022
Upoważnienia: Department of Biotechnology, India
Dostępne w jakimś miejscu: 21
Genomics of rare genetic diseases—experiences from India
S Sivasubbu, V Scaria
Human genomics 13 (1), 52, 2019
Upoważnienia: Council of Scientific and Industrial Research, India, Department of Science …
Burden among Parkinson's disease care givers for a community based study from India
J Sanyal, S Das, E Ghosh, TK Banerjee, L Bhaskar, VR Rao
Journal of the Neurological Sciences 358 (1-2), 276-281, 2015
Upoważnienia: Council of Scientific and Industrial Research, India
Metallomic Biomarkers in Cerebrospinal fluid and Serum in patients with Parkinson’s disease in Indian population
J Sanyal, SSSJ Ahmed, HKT Ng, T Naiya, E Ghosh, TK Banerjee, ...
Scientific reports 6 (1), 35097, 2016
Upoważnienia: Council of Scientific and Industrial Research, India
Association of TCF7L2 and ADIPOQ with body mass index, waist–hip ratio, and systolic blood pressure in an endogamous ethnic group of India
V Gupta, R Khadgawat, HKT Ng, GK Walia, L Kalla, VR Rao, ...
Genetic testing and molecular biomarkers 16 (8), 948-951, 2012
Upoważnienia: Department of Science & Technology, India
Association between neuropeptide Y gene polymorphisms and alcohol dependence: a case-control study in two independent populations
L Bhaskar, K Thangaraj, KP Kumar, G Pardhasaradhi, L Singh, VR Rao
European addiction research 19 (6), 307-313, 2013
Upoważnienia: Department of Biotechnology, India
Next generation sequencing in cardiomyopathy: towards personalized genomics and medicine
A Biswas, VR Rao, S Seth, SK Maulik
Molecular biology reports 41, 4881-4888, 2014
Upoważnienia: Department of Biotechnology, India
NRAS Mutations in de novo acute leukemia: Prevalence and clinical significance
NR Dunna, S Vuree, C Anuradha, K Sailaja, D Surekha, RR Digumarti, ...
NISCAIR-CSIR, India, 2014
Upoważnienia: Department of Science & Technology, India
Loss of function mutation in the P2X7, a ligand-gated ion channel gene associated with hypertrophic cardiomyopathy
A Biswas, A Raza, S Das, M Kapoor, R Jayarajan, A Verma, ...
Purinergic signalling 15, 205-210, 2019
Upoważnienia: Council of Scientific and Industrial Research, India, Department of …
Epidemiology of cardiomyopathy-A clinical and genetic study of hypertrophic cardiomyopathy: The EPOCH-H study
A Biswas, S Das, M Kapoor, S Seth, B Bhargava, VR Rao
Journal of the Practice of Cardiovascular Sciences 1 (2), 143-149, 2015
Upoważnienia: Department of Biotechnology, India
Familial Hypertrophic Cardiomyopathy-Identification of cause and risk stratification through exome sequencing
A Biswas, S Das, M Kapoor, KV Shamsudheen, R Jayarajan, A Verma, ...
Gene 660, 151-156, 2018
Upoważnienia: Council of Scientific and Industrial Research, India, Department of …
EPHX1 Gene Polymorphisms in Alcohol Dependence and their Distribution among the Indian Populations
L Bhaskar, K Thangaraj, M Patel, AM Shah, K Gopal, L Saikrishna, ...
The American Journal of Drug and Alcohol Abuse 39 (1), 16-22, 2013
Upoważnienia: Department of Biotechnology, India
Evaluation of PARKIN gene variants in West Bengal Parkinson’s disease patients
J Sanyal, A Jana, E Ghosh, TK Banerjee, DP Chakraborty, VR Rao
Journal of human genetics 60 (9), 485-492, 2015
Upoważnienia: Council of Scientific and Industrial Research, India
PARK2 and PARK7 Gene Polymorphisms as Risk Factors Associated with Serum Element Concentrations and Clinical Symptoms of Parkinson’s Disease
J Sanyal, A Anirudhan, TK Banerjee, G Guha, R Veerabathiran, ...
Cellular and molecular neurobiology 40, 357-367, 2020
Upoważnienia: Council of Scientific and Industrial Research, India
Epidemiology of cardiomyopathy–A Clinical and Genetic Study of Restrictive Cardiomyopathy: The EPOCH-R Study
M Kapoor, S Das, A Biswas, S Seth, B Bhargava, VR Rao
Journal of the Practice of Cardiovascular Sciences 3 (3), 143-149, 2017
Upoważnienia: Department of Biotechnology, India
Mutations in hotspot region of MYH7 gene exon 23 associated with restrictive cardiomyopathy
M Kapoor, S Das, A Biswas, S Seth, B Bhargava, VR Rao
Cardiogenetics 7 (1), 6358, 2017
Upoważnienia: Department of Biotechnology, India
Role of mica repeat polymorphism in the manifestation of type 1 diabetes mellitus in Bengali Indian patients
O Raha, BN Sarkar, P Veerraju, G Sudhakar, P Raychaudhuri, ...
Genetika 45 (2), 611-619, 2013
Upoważnienia: Department of Science & Technology, India
D190Y mutation in C-terminal tail region of TNNI3 gene causing severe form of restrictive cardiomyopathy with mild hypertrophy in an Indian patient
M Kapoor, S Das, A Biswas, PB Malgulwar, NK Devi, S Seth, B Bhargava, ...
Meta Gene 26, 100777, 2020
Upoważnienia: Department of Biotechnology, India
Dyslipidemia in pre-and post-menopausal women: a study of peri-urban Paundra Kshatriya women
DK Adak, N Bharali, S Biswas, NK Bagchi, TK Biswas, VR Rao
Wydawnictwo Uniwersytetu Łódzkiego, 2023
Upoważnienia: Department of Science & Technology, India
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