Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Deepshi, Thakral"'
Publikováno v:
Journal of the Egyptian National Cancer Institute, Vol 34, Iss 1, Pp 1-14 (2022)
Abstract Background Mature B-cell non-Hodgkin lymphomas are one of the most common hematological malignancies with a divergent clinical presentation, phenotype, and course of disease regulated by underlying genetic mechanism. Main body Genetic and mo
Externí odkaz:
https://doaj.org/article/c11555bb059b46dfbc9124499dd45082
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
The circulating cell-free nucleic acids (ccfNAs) consist of a heterogenous cocktail of both single (ssNA) and double-stranded (dsNA) nucleic acids. These ccfNAs are secreted into the blood circulation by both healthy and malignant cells via various m
Externí odkaz:
https://doaj.org/article/1f8a4ec083cc44a18834ef80cbf69266
Autor:
Chitrita Goswami, Smriti Chawla, Deepshi Thakral, Himanshu Pant, Pramod Verma, Prabhat Singh Malik, Jayadeva ▮, Ritu Gupta, Gaurav Ahuja, Debarka Sengupta
Publikováno v:
BMC Genomics, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Early diagnosis is crucial for effective medical management of cancer patients. Tissue biopsy has been widely used for cancer diagnosis, but its invasive nature limits its application, especially when repeated biopsies are needed.
Externí odkaz:
https://doaj.org/article/299bb670c54a462791afb91469cc7718
Autor:
Sushmita Chakraborty, Devika Gupta, Deepshi Thakral, Sameer Bakhshi, Prabin Kumar, Sushil Kabra, Rakesh Lodha, Dipendra Mitra
Publikováno v:
Central European Journal of Immunology, Vol 45, Iss 1, Pp 117-121 (2020)
Leukocyte adhesion deficiencies (LADs) are a type of primary immunodeficiencies characterized by delayed detachment of the umbilical cord, impaired wound healing, leukocytosis, and recurrent infections. The disease is caused by genetic defects affect
Externí odkaz:
https://doaj.org/article/740c2a6d66e444bfa49046c336dbc7ee
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 2, Pp 279-282 (2019)
Griscelli syndrome is a rare autosomal recessive inherited disorder characterized by hypopigmentation, silver colored hair, and associated immunological deficiency, which proves fatal in the absence of timely intervention. Our patients diagnosed with
Externí odkaz:
https://doaj.org/article/8ced02b54eec4a948496cf5b87f8c55d
Autor:
Nupur Das, Deepshi Thakral, Geetika Singh, Ankit Malhotra, Ravi Hari Phulware, Ajay Gogia, Ritu Gupta
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 62, Iss 4, Pp 614-617 (2019)
Pediatric small round cell tumors (PSRCTs) constitute a large proportion of childhood malignancies with overlapping diagnostic and clinical features but radically different therapies. Here, we report a case of 16-year-old male child presenting with d
Externí odkaz:
https://doaj.org/article/b6293f17f50e472e80c5290371624ac5
Autor:
Deepshi Thakral, Ritu Gupta, Ranjit Kumar Sahoo, Pramod Verma, Indresh Kumar, Sangeeta Vashishtha
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
The clonal evolution of acute myeloid leukemia (AML), an oligoclonal hematological malignancy, is driven by a plethora of cytogenetic abnormalities, gene mutations, abnormal epigenetic patterns, and aberrant gene expressions. These alterations in the
Externí odkaz:
https://doaj.org/article/0fb8ebea475847aaad4ac1c1b208a7c7
Autor:
Smeeta Gajendra, Ritu Gupta, Deepshi Thakral, Sanjeev Kumar Gupta, Garima Jain, Sameer Bakhshi, Atul Sharma, Ranjeet Kumar Sahoo, Lalit Kumar, Sandeep Rai, Saroj Singh, Ashish Datt Upadhyay
Publikováno v:
International Journal of Laboratory Hematology. 45:221-228
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 61, Iss 1, Pp 137-140 (2018)
X-linked hyperimmunoglobulin M (HIGM) syndrome may increase the susceptibility of patients to disseminated cryptococcal infections primarily due to CD40L deficiency that causes defective cross talk between T- and B-cells, thus preventing class switch
Externí odkaz:
https://doaj.org/article/8dd32e1d1dfd422f863983419e499c0e
Autor:
Raja Pramanik, Avinash Upadhyay, Sachin Khurana, Lalit Kumar, Prabhat S. Malik, Sunesh Kumar, M. D. Ray, S. V. S. Deo, Ritu Gupta, Deepshi Thakral, Sanjay Thulkar, V. L. Ramprasad
Publikováno v:
Indian Journal of Medical and Paediatric Oncology. 43:361-368
Introduction Ovarian cancer is the third most common cancer among Indian women. The data on the hereditary predisposition of these cancers and the clinical outcomes of those with pathogenic mutations is meager in India. Objective The aim of the curre