Zobrazeno 1 - 10
of 152
pro vyhledávání: '"Trichur R. Raju"'
Autor:
Anu Mary Varghese, Mausam Ghosh, Savita Kumari Bhagat, K. Vijayalakshmi, Veeramani Preethish-Kumar, Seena Vengalil, Pradeep-Chandra-Reddy Chevula, Saraswati Nashi, Kiran Polavarapu, Meenakshi Sharma, Rupinder Singh Dhaliwal, Mariamma Philip, Atchayaram Nalini, Phalguni Anand Alladi, Talakad N. Sathyaprabha, Trichur R. Raju
Publikováno v:
Journal of Neuroinflammation, Vol 17, Iss 1, Pp 1-15 (2020)
Abstract Background Cerebrospinal fluid from amyotrophic lateral sclerosis patients (ALS-CSF) induces neurodegenerative changes in motor neurons and gliosis in sporadic ALS models. Search for identification of toxic factor(s) in CSF revealed an enhan
Externí odkaz:
https://doaj.org/article/56747c5928d646cd97f314edd90ee00d
Autor:
Shruthi Shanmukha, Gayathri Narayanappa, Atchayaram Nalini, Phalguni Anand Alladi, Trichur R. Raju
Publikováno v:
Disease Models & Mechanisms, Vol 11, Iss 4 (2018)
Skeletal muscle atrophy is the most prominent feature of amyotrophic lateral sclerosis (ALS), an adult-onset neurodegenerative disease of motor neurons. However, the contribution of skeletal muscle to disease progression remains elusive. Our previous
Externí odkaz:
https://doaj.org/article/0a94cb27e1f041d3b8a27103426d125b
Autor:
Dhargave Pradnya, Atchayaram Nalini, Raghuram Nagarathna, Raghupathy Sendhilkumar, Tittu Thomas James, Trichur R Raju, Talakad N Sathyaprabha
Publikováno v:
International Journal of Yoga, Vol 14, Iss 2, Pp 133-140 (2021)
Context: Abnormal respiratory function is known to be detectable almost as soon as it can be measured reliably. Studies have identified the effect of respiratory muscle training as well as breathing exercises in improving pulmonary functions in child
Externí odkaz:
https://doaj.org/article/63fdca406e4a4473850ef99c478e4eb2
Autor:
Dhargave Pradnya, Atchayaram Nalini, Raghuram Nagarathna, Trichur R Raju, Ragupathy Sendhilkumar, Adoor Meghana, Talakad N Sathyaprabha
Publikováno v:
International Journal of Yoga, Vol 12, Iss 1, Pp 55-61 (2019)
Background: Duchene muscular dystrophy (DMD) is a progressive muscular disorder. Cardiac disorder is the second-most common cause of death in children with DMD, with 10%–20% of them dying of cardiac failure. Heart rate variability (HRV) is shown to
Externí odkaz:
https://doaj.org/article/ea2c48d97a0e4de9bff46fe2b08570ff
Autor:
V. Ramya, Nisha Sarkar, Savita Bhagat, Raj Kumar Pradhan, Anu Mary Varghese, Atchayaram Nalini, Talakad N. Sathyaprabha, Trichur R. Raju, K. Vijayalakshmi
Publikováno v:
Molecular Neurobiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5bf8d0ae323ac3ccf2dccf57c6f9288
https://doi.org/10.1007/s12035-023-03375-y
https://doi.org/10.1007/s12035-023-03375-y
Autor:
Ganagarajan Inbaraj, Krishnamurthy Arjun, Adoor Meghana, Veeramani Preethish-Kumar, Anu P John, Kiran Polavarapu, Saraswati Nashi, Deepha Sekar, Kaviraja Udupa, Parthipulli V. Prathuysha, Krishna Prasad, Mainak Bardhan, Trichur R. Raju, Boris W. Kramer, Atchayaram Nalini, Talakad N. Sathyaprabha
Publikováno v:
Journal of neuromuscular diseases, 10(2), 227-238. I O S Press
Background and Objective: Duchenne muscular dystrophy (DMD) is a degenerative X-linked muscle disease. Death frequently results from complications in cardiopulmonary systems. Preclinical/early diagnosis of cardiac autonomic abnormalities may aid init
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb3933f4ed629c8151c2f847d343096a
https://cris.maastrichtuniversity.nl/en/publications/70100c2c-28e6-4310-92c7-006274397686
https://cris.maastrichtuniversity.nl/en/publications/70100c2c-28e6-4310-92c7-006274397686
Publikováno v:
Neurotoxicity Research. 39:1892-1907
Parkinson disease (PD) prevalence varies by ethnicity. In an earlier study, we replicated the reduced vulnerability to PD in an admixed population, using 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-susceptible C57BL/6 J, MPTP-resistant CD-1 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd237d86092b88f63ea981a4b2317b7c
https://doi.org/10.1007/s12640-021-00439-6
https://doi.org/10.1007/s12640-021-00439-6
Autor:
Haorei Yarreiphang, D J Vidyadhara, Anand Krishnan Nambisan, Trichur R Raju, BK Chandrashekar Sagar, Phalguni Anand Alladi
Identification of genetic mutations in Parkinson’s disease (PD) promulgates the genetic nature of disease susceptibility. Resilience-associated genes being unknown till date, the normal genetic makeup of an individual may be determinative too. Our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49a391cf9d0e29ae860554a054865069
https://doi.org/10.1101/2022.10.05.511004
https://doi.org/10.1101/2022.10.05.511004
Publikováno v:
Experimental Brain Research. 239:315-327
Amyotrophic lateral sclerosis (ALS) is a late-onset, neurodegenerative disease associated with the loss of motor neurons in the spinal cord, brain stem and primary motor cortex. Deficit in the motor function is one of the clinical features of this di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa161f274a48a20d0bd2d916cff16a4f
https://doi.org/10.1007/s00221-020-05969-7
https://doi.org/10.1007/s00221-020-05969-7
Publikováno v:
Psychopharmacology. 237:2967-2981
Anxiety is one of the most comorbid conditions with major depressive disorder (MDD). Depression-associated anxiety often stems from the dysfunctional hypothalamic-pituitary-adrenal (HPA) axis and its altered regulation by the amygdala. Furthermore, M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::191e5db257a9fc8d9f890d1226f67bfd
https://doi.org/10.1007/s00213-020-05585-x
https://doi.org/10.1007/s00213-020-05585-x