Analysis of calpain-3 protein in muscle biopsies of different muscular dystrophies from India

por Renjini, R., Gayathri, N., Nalini, A., Bharath, M.M. Srinivas
Publicado 2012

Schwartz–Jampel syndrome

por Chandra, Sadanandavalli Retnaswami, Issac, Thomas Gregor, Gayathri, N., Shivaram, Sumanth
Publicado 2015

A typical case of myoclonic epilepsy with ragged red fibers (MERRF) and the lessons learned

por Chandra, SR, Issac, TG, Gayathri, N, Gupta, N, Abbas, MM
Publicado 2015

Key players in regulatory RNA realm of bacteria

por Mahendran, Gowthami, Jayasinghe, Oshadhi T., Thavakumaran, Dhanushika, Arachchilage, Gayan Mirihana, Silva, Gayathri N.
Publicado 2022

VALIDATION OF ASHWAGANDHA CHURNAM

por Nagavalli, D., Vetrichelvan, T., Gayathri, N., Poongothai, P., Sivasankari, K. P., Vadamalai, S.V.
Publicado 2001

Carfilzomib: A Promising Proteasome Inhibitor for the Treatment of Relapsed and Refractory Multiple Myeloma

por Jayaweera, Shansa Pranami E., Wanigasinghe Kanakanamge, Sacheela Prasadi, Rajalingam, Dharshika, Silva, Gayathri N.
Publicado 2021

Fabry's disease: An ultrastructural study of nerve biopsy

por Gayathri, N., Yasha, T. C., Kanjalkar, Makarand, Agarwal, Santosh, Sagar, B. K. Chandrashekar, Santosh, Vani, Shankar, S. K.
Publicado 2008

Speech-Language and swallowing manifestations and rehabilitation in an 11-year-old girl with MELAS syndrome

por Vandana, V. P., Bindu, Parayil Sankaran, Sonam, Kothari, Taly, Arun B., Gayathri, N., Madhu, N., Sinha, S.
Publicado 2015

Active dendritic integration and mixed neocortical network representations during an adaptive sensing behavior

por Ranganathan, Gayathri N., Apostolides, Pierre F., Harnett, Mark T., Xu, Ning-Long, Druckmann, Shaul, Magee, Jeffrey C.
Publicado 2018

Tangier's disease: An uncommon cause of facial weakness and non-length dependent demyelinating neuropathy

por Nagappa, Madhu, Taly, Arun B., Mahadevan, Anita, Pooja, M., Bindu, P. S., Chickabasaviah, Y. T., Gayathri, N., Sinha, Sanjib
Publicado 2016

Hereditary inclusion body myopathy: A myopathy with unique topography of weakness, yet frequently misdiagnosed: Case series and review of literature

por Das, Biplab, Goyal, Manoj Kumar, Bhatkar, Sanat Ramchandra, Vinny, Pulikottil Wilson, Modi, Manish, Lal, Vivek, Gayathri, N., Mahadevan, Anitha, Radotra, Bishan Dass
Publicado 2016

Organic cation transporter 1 (OCT1) is involved in pentamidine transport at the human and mouse blood-brain barrier (BBB)

por Sekhar, Gayathri N., Georgian, Ana R., Sanderson, Lisa, Vizcay-Barrena, Gema, Brown, Rachel C., Muresan, Paula, Fleck, Roland A., Thomas, Sarah A.
Publicado 2017

Variations in HLA-B cell surface expression, half-life and extracellular antigen receptivity

por Yarzabek, Brogan, Zaitouna, Anita J, Olson, Eli, Silva, Gayathri N, Geng, Jie, Geretz, Aviva, Thomas, Rasmi, Krishnakumar, Sujatha, Ramon, Daniel S, Raghavan, Malini
Publicado 2018

Detection of Dysferlin Gene Pathogenic Variants in the Indian Population in Patients Predicted to have a Dysferlinopathy Using a Blood-based Monocyte Assay and Clinical Algorithm:...

por Dastur, Rashna Sam, Gaitonde, Pradnya Satish, Kachwala, Munira, Nallamilli, Babi R. R., Ankala, Arunkanth, Khadilkar, Satish V., Atchayaram, Nalini, Gayathri, N., Meena, A. K., Rufibach, Laura, Shira, Sarah, Hegde, Madhuri
Publicado 2017

Drug reformulation for a neglected disease. The NANOHAT project to develop a safer more effective sleeping sickness drug

por Sanderson, Lisa, da Silva, Marcelo, Sekhar, Gayathri N., Brown, Rachel C., Burrell-Saward, Hollie, Fidanboylu, Mehmet, Liu, Bo, Dailey, Lea Ann, Dreiss, Cécile A., Lorenz, Chris, Christie, Mark, Persaud, Shanta J., Yardley, Vanessa, Croft, Simon L., Valero, Margarita, Thomas, Sarah A.
Publicado 2021