Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Ikrormi, Rungsung"'
Autor:
Esam I. Azhar, Thirumalaisamy P. Velavan, Ikrormi Rungsung, Tieble Traore, David S. Hui, Brian McCloskey, Sherif A. El-Kafrawy, Alimuddin Zumla
Publikováno v:
International Journal of Infectious Diseases, Vol 131, Iss , Pp 87-94 (2023)
Objectives: The World Health Organization priority zoonotic pathogen Middle East respiratory syndrome (MERS) coronavirus (CoV) has a high case fatality rate in humans and circulates in camels worldwide. Methods: We performed a global analysis of huma
Externí odkaz:
https://doaj.org/article/0fa4bb90193d4112b5879f17465850c5
Autor:
Tran Thanh Tung, Jürgen Schmid, Vu Xuan Nghia, Le Chi Cao, Le Thi Kieu Linh, Ikrormi Rungsung, Bui Tien Sy, Truong Nhat My, Nguyen Trong The, Nghiem Xuan Hoan, Christian G. Meyer, Heiner Wedemeyer, Peter G. Kremsner, Nguyen Linh Toan, Le Huu Song, C.-Thomas Bock, Thirumalaisamy P. Velavan
Publikováno v:
Pathogens, Vol 11, Iss 12, p 1524 (2022)
Occult hepatitis B infection (OBI) is characterized by the presence of low levels of hepatitis B virus (HBV) DNA and undetectable HBsAg in the blood. The prevalence of OBI in blood donors in Asia ranges from 0.013% (China) to 10.9% (Laos), with no da
Externí odkaz:
https://doaj.org/article/deac7b197ecb4803b4e911860a1fafce
Autor:
Jai Prakash Soni, Shagun Aggarwal, Ikrormi Rungsung, Divya Pasumarthi, Jayesh Sheth, Prajnya Ranganath, Kalpana Gowrishankar, Mohandas Nair, Ishwar C. Verma, Neerja Gupta, V.H. Sankar, Sumita Danda, Ratna Dua Puri, Mehul Mistry, Ashwin Dalal, S Jamal Md Nurul Jain, Katta M. Girisha, Shubha R. Phadke, Madhulika Kabra, Chaitanya Datar, Riddhi Bhavsar, Anju Shukla, Divya Agrawal
Publikováno v:
Journal of Human Genetics. 65:971-984
Mucolipidosis (ML) (OMIM 607840 & 607838) is a rare autosomal recessive inherited disorder that occurs due to the deficiency of golgi enzyme uridine diphosphate (UDP)- N-acetylglucosamine-1-phosphotransferase (GlcNAc-phosphotransferase) responsible f
Autor:
Deepti Saxena, Haseena Sait, Prajnya Ranganath, Priyanka Srivastava, Seema Kapoor, Madhulika Kabra, Ashwin Dalal, Ajitesh Roy, Kausik Mandal, Shubha R. Phadke, Neerja Gupta, Ikrormi Rungsung, Jayalakshmi Pabbati
Publikováno v:
European journal of medical genetics. 64(7)
Background Pycnodysostosis is an autosomal recessive skeletal dysplasia with easily recognizable clinical features and marked molecular heterogeneity. In this study, we explored the clinical and molecular spectrum of 25 Indian patients with pycnodyso
Autor:
Divya, Pasumarthi, Neerja, Gupta, Jayesh, Sheth, S Jamal Md Nurul, Jain, Ikrormi, Rungsung, Madhulika, Kabra, Prajnya, Ranganath, Shagun, Aggarwal, Shubha R, Phadke, Katta M, Girisha, Anju, Shukla, Chaitanya, Datar, Ishwar C, Verma, Ratna Dua, Puri, Riddhi, Bhavsar, Mehul, Mistry, V H, Sankar, Kalpana, Gowrishankar, Divya, Agrawal, Mohandas, Nair, Sumita, Danda, Jai Prakash, Soni, Ashwin, Dalal
Publikováno v:
Journal of human genetics. 65(11)
Mucolipidosis (ML) (OMIM 607840607838) is a rare autosomal recessive inherited disorder that occurs due to the deficiency of golgi enzyme uridine diphosphate (UDP)- N-acetylglucosamine-1-phosphotransferase (GlcNAc-phosphotransferase) responsible for
Publikováno v:
Computational Biology and Chemistry. 76:67-78
LKB1 protein is involved in the regulation of cell polarity by phosphorylating the AMPK under energetic stress conditions. LKB1 protein is expressed in both cytoplasm and nucleus. In the nucleus, LKB1 interacts with orphan nuclear receptor protein Nu
Publikováno v:
Gene Reports. 19:100602
Type IV collagen protein is formed by the interaction of α3. α4. α5 chains and is encoded by COL4A3, COL4A4 and COL4A5 genes located on the chromosome 2 and the X-chromosome. Pathogenic variations in these genes are reported to be associated with
Autor:
Ikrormi Rungsung, Amutha Ramaswamy
The liver kinase B1 (LKB1) is encoded by LKB1 gene. Several pathogenic mutations of LKB1 causing Peutz–Jeghers syndrome and also cancers in breast, gastric, pancreas, and colon have been reported. The present study is focused to analyze the effects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1da7f0837aef6c381f6c71ac8efd3464
Autor:
Ikrormi Rungsung, Amutha Ramaswamy
LKB1, the tumour suppressor, is found mutated in Peutz-Jeghers syndrome (PJS). The LKB1 is a serine-threonine kinase protein that is allosterically activated by the binding of STRADα and MO25α without phosphorylating the Thr212 present at activatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1a0727183d785a67df5e480ff057812