Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Swarkar Sharma"'
SOX9 gene shows association with adolescent idiopathic scoliosis predisposition in Northwest Indians
Autor:
Hemender Singh, Shipra, Manish Gupta, Nital Gupta, Geetanjali Gupta, Ajay K. Pandita, Rajesh Sharma, Sarla Pandita, Vinod Singh, Bhavuk Garg, Ekta Rai, Swarkar Sharma
Publikováno v:
European Journal of Medical Research, Vol 29, Iss 1, Pp 1-6 (2024)
Abstract Background Adolescent idiopathic scoliosis (AIS) is a common structural deformity of the spine affecting adolescent individuals globally. The disorder is polygenic and is accompanied by the association of various genetic loci. Genetic studie
Externí odkaz:
https://doaj.org/article/44511ed3b5fc475ebe0eaa2469ce0867
Autor:
Akshi Spolia, Arshia Angural, Varun Sharma, Shipra, Sushil Razdan, Manoj K. Dhar, Ankit Mahajan, Vijeshwar Verma, Kamal K. Pandita, Swarkar Sharma, Ekta Rai
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Neurofibromatosis type 1 (NF1) is a multisystemic hereditary disorder associated with an increased risk of benign and malignant tumor formation predominantly on the skin, bone, and peripheral nervous system. It has been reported that out of
Externí odkaz:
https://doaj.org/article/528a8fdef95841a9bd8d7ce5e86460da
Autor:
Indermohan Singh Sandhu, Hemender Singh, Anupama Mahajan, Gurinder Mohan, Swarkar Sharma, Prakash Singh, Simranpreet Kaur, Amarjit Singh Bhanwer
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 17, Iss 5, Pp GC01-GC04 (2023)
Introduction: Rheumatoid Arthritis (RA) is a systemic, chronic, inflammatory, and autoimmune disease which is characterised by the progressive ruination of joint structures. The Human Leukocyte Antigens (HLA) genes: HLA-DRB1 and HLA-DQB1, belonging t
Externí odkaz:
https://doaj.org/article/e02507a880da4f83b4cd8d1e7bd0707c
Autor:
Jebi Sudan, Ravinder Singh, Susheel Sharma, Romesh K. Salgotra, Varun Sharma, Gurvinder Singh, Indu Sharma, Swarkar Sharma, Surinder K. Gupta, Sajad Majeed Zargar
Publikováno v:
BMC Plant Biology, Vol 19, Iss 1, Pp 1-15 (2019)
Abstract Background Narrow genetic base, complex allo-tetraploid genome and presence of repetitive elements have led the discovery of single nucleotide polymorphisms (SNPs) in Brassica juncea (AABB; 2n = 4x = 36) at a slower pace. Double digest RAD (
Externí odkaz:
https://doaj.org/article/0ef780bbfc1d482c9f69e4d11efa9203
Autor:
Arshia Angural, Akshi Spolia, Ankit Mahajan, Vijeshwar Verma, Ankush Sharma, Parvinder Kumar, Manoj Kumar Dhar, Kamal Kishore Pandita, Ekta Rai, Swarkar Sharma
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Rare diseases (RDs) are the clinical conditions affecting a few percentage of individuals in a general population compared to other diseases. Limited clinical information and a lack of reliable epidemiological data make their timely diagnosis and the
Externí odkaz:
https://doaj.org/article/87bb555b3a464ee0a785138e5058e6f3
Autor:
Arshia Angural, Inderpal Singh, Ankit Mahajan, Pranav Pandoh, Manoj K Dhar, Sanjana Kaul, Vijeshwar Verma, Ekta Rai, Sushil Razdan, Kamal Kishore Pandita, Swarkar Sharma
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-8 (2017)
Abstract Pantothenate kinase-associated neurodegeneration is a rare hereditary neurodegenerative disorder associated with nucleotide variation(s) in mitochondrial human Pantothenate kinase 2 (hPanK2) protein encoding PANK2 gene, and is characterized
Externí odkaz:
https://doaj.org/article/489c4bd2dfb94413be2ad62d69e5e0bb
Autor:
Ekta Rai, Arshia Angural, Akshi Sapolia, Sushil Razdan, Kamal Kishore Pandita, Swarkar Sharma
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 250-250 (2017)
Rare disorders are poorly understood, most often remain uncharacterized or patients are misdiagnosed due to lack of specific clinical resources. Understanding the basics of inheritance is essential in such cases as it helps to figure out the plausibi
Externí odkaz:
https://doaj.org/article/319f7e3862df49748db2a0601cfb7097
Autor:
Varun Sharma, Indu Sharma, Gurvinder Singh, Itty Sethi, A.J.S. Bhanwer, Vinod Singh, Ekta Rai, Swarkar Sharma
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 257-257 (2017)
Type 2 Diabetes (T2D) is a complex disease and genetic is one of factor contributing to its pathogenesis. Both decreased body sensitivity to insulin and defects in insulin production are involved in T2D development. ND3 is one of the subunit of compl
Externí odkaz:
https://doaj.org/article/37ad778fed4d46a986e79cfe3694f57a
Autor:
Varun Sharma, Itty Sethi, Indu Sharma, Gurvinder Singh, Ankit Mahajan, Arshia Angural, A.J.S. Bhanwer, Manoj K. Dhar, K.K. Pandita, Vinod Singh, Ekta Rai, Swarkar Sharma
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue, Pp 79-79 (2017)
Microtubule Actin Cross linking Factor 1 (MACF1) gene variant rs2296172 has been associated with Type 2 Diabetes (T2D). However, this variant has never been evaluated as such in Indian populations. We replicated this variant in pooled population of N
Externí odkaz:
https://doaj.org/article/3929830120584227b7f79650795758d2
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue, Pp 168-168 (2017)
India is a country with 4,635 different population groups [1]. Jammu and Kashmir is located on the crossroads of Eurasia, bound by China and Tibet from North-East, Afghanistan and Pakistan from North-West. Diversity in Indian population is anticipate
Externí odkaz:
https://doaj.org/article/c0617eb3da654ec09eb6c302f03b4aed