Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sarla Pandita"'
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:
Swarkar Sharma, Hemender Singh, Shipra Kowra, Manish Gupta, Poorvi Bhau, Tania Chalotra, Ruchi Manotra, Nital Gupta, Geetanjali Gupta, Ajay Pandita, Mohammad Butt, Rajesh Sharma, Sarla Pandita, Vinod Singh, Bhavuk Garg, Ekta Rai
Variant rs11190870 is located 7.5 kb downstream of LBX1 gene and several studies have implicated its association with Adolescent Idiopathic Scoliosis (AIS) in different populations. However, any genetic study is altogether lacking in South-Asian Indi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc8df642387ecd5bc4494c25805b303d
https://doi.org/10.21203/rs.3.rs-1866650/v1
https://doi.org/10.21203/rs.3.rs-1866650/v1
Autor:
Hemender Singh, null Shipra, Manish Gupta, Poorvi Bhau, Tania Chalotra, Ruchi Manotra, Nital Gupta, Geetanjali Gupta, Ajay K. Pandita, Mohammad Farooq Butt, Rajesh Sharma, Sarla Pandita, Vinod Singh, Bhavuk Garg, Ekta Rai, Swarkar Sharma
LBX1 is a developmental gene involved in skeletal muscle development and somatosensory functioning and proven to be an important gene involved in Adolescent Idiopathic Scoliosis (AIS) etiology. Variant rs11190870 is located 7.5 kb downstream of LBX1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::917d8eb6ab719fd51b96a76d2ed6af38
https://doi.org/10.1101/2022.06.28.22276987
https://doi.org/10.1101/2022.06.28.22276987
Autor:
Hemender, Singh, Shipra, Varun, Sharma, Indu, Sharma, Akash, Sharma, Sonakshi, Modeel, Nital, Gupta, Geetanjali, Gupta, Ajay K, Pandita, Mohammad Farooq, Butt, Rajesh, Sharma, Sarla, Pandita, Vinod, Singh, Ekta, Rai, Shiro, Ikegawa, Swarkar, Sharma
Publikováno v:
Am J Transl Res
AIS is a heterogeneous 3D spinal deformity with Cobb angle ≥10°. It affects children in the age group of 10-16 years globally with 2-3% prevalence and significant female predominance. The exact etiology of AIS is not known however, it is supposed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ece02d0b368feca60f55bc3712ac71d
https://pubmed.ncbi.nlm.nih.gov/35273713
https://pubmed.ncbi.nlm.nih.gov/35273713
Publikováno v:
Clinical Cases in Mineral and Bone Metabolism. 14:105
Manifestations of primary hypoparathyroidism are produced by neuromuscular irritability or by extraosseous calcifications. We present a patient of primary hypoparathyroidism who had extensive calcification of brain parenchyma, and was suffering from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff9d484e139a04f8845703f2e79d52e1
https://doi.org/10.11138/ccmbm/2017.14.1.105
https://doi.org/10.11138/ccmbm/2017.14.1.105
Publikováno v:
Annals of Thoracic Medicine
Annals of Thoracic Medicine, Vol 5, Iss 1, Pp 56-57 (2010)
Annals of Thoracic Medicine, Vol 5, Iss 1, Pp 56-57 (2010)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85eb6b4debd41ab3022513100ecb3456
http://europepmc.org/articles/PMC2841816
http://europepmc.org/articles/PMC2841816