Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Madhusoodanan Urulangodi"'
Autor:
Asha Kishore, Marc Sturm, Kanchana Soman Pillai, Christopher Hakkaart, Divya Kalikavil Puthanveedu, Madhusoodanan Urulangodi, Syam Krishnan, Ashwin Ashok Kumar Sreelatha, Roopa Rajan, Pramod Kumar Pal, Ravi Yadav, Gangadhara Sarma, Nicolas Casadei, Thomas Gasser, Peter Bauer, Olaf Riess, Manu Sharma
Publikováno v:
npj Parkinson's Disease, Vol 10, Iss 1, Pp 1-5 (2024)
Abstract The genetic loci implicated in familial Parkinson’s disease (PD) have limited generalizability to the Indian PD population. We tested mutations and the frequency of known mutations in the SNCA gene in a PD cohort from India. We selected 29
Externí odkaz:
https://doaj.org/article/168e33231a6740adb86274bd20fc49b5
Autor:
Anja Waizenegger, Madhusoodanan Urulangodi, Carl P. Lehmann, Teresa Anne Clarisse Reyes, Irene Saugar, José Antonio Tercero, Barnabas Szakal, Dana Branzei
Publikováno v:
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Mus81-Mms4 endonuclease is critical for processing various DNA recombination structures. Here the authors uncover a regulatory mechanism of the endonuclease via posttranslational modifications involving SUMOylation and ubiquitylation that impact on g
Externí odkaz:
https://doaj.org/article/bd031adcb9114b46a9b98466291010e6
Autor:
Valaparambil Karthika Ajit, Sruthi Sivaraman Nair, Sethu Madhavan Anjali, Pravi Vidyadharan, Madhusoodanan Urulangodi, Ramshekhar N. Menon, Soumya Sundaram
Publikováno v:
Neurology and Clinical Neuroscience. 11:93-96
Autor:
Asish Vijayaraghavan, Madhusoodanan Urulangodi, Karthika Ajit Valaparambil, Soumya Sundaram, Syam Krishnan
Publikováno v:
Movement Disorders Clinical Practice.
Autor:
Bharathan Bhavya, Chellapan Anand, Madhusoodanan Urulangodi, Kalapurakkal Sreelakshmi, Akkihebbal Deepti, Girish Menon, Krishnakumar Kesavapisharady, Hariharan Easwer, Srinivas Gopala
Publikováno v:
World Academy of Sciences Journal. 4
C12orf57 pathogenic variants: a unique cause of developmental encephalopathy in a south Indian child
Autor:
F. Alfiya, Manna Jose, Soumya V. Chandrasekharan, Soumya Sundaram, Madhusoodanan Urulangodi, Bejoy Thomas, Ashalatha Radhakrishnan, Moinak Banerjee, Ramshekhar N. Menon
Publikováno v:
Journal of Genetics. 101
Autor:
Madhusoodanan Urulangodi, Anja Waizenegger, José Antonio Tercero, Carl P. Lehmann, Irene Saugar, Barnabas Szakal, Dana Branzei, Teresa Anne Clarisse Reyes
Publikováno v:
Nature Communications
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications, Vol 11, Iss 1, Pp 1-14 (2020)
Digital.CSIC. Repositorio Institucional del CSIC
instname
The Mus81-Mms4 nuclease is activated in G2/M via Mms4 phosphorylation to allow resolution of persistent recombination structures. However, the fate of the activated phosphorylated Mms4 remains unknown. Here we find that Mms4 is engaged by (poly)SUMOy
Publikováno v:
J Cell Commun Signal
Protein post-translational modifications (PTMs) have emerged to be combinatorial, essential mechanisms used by eukaryotic cells to regulate local chromatin structure, diversify and extend their protein functions and dynamically coordinate complex int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e39a7b4c90803f26b4b508b5aa70a95a
https://europepmc.org/articles/PMC7176765/
https://europepmc.org/articles/PMC7176765/
Autor:
Madhuma Madhavan, Sanjay Ganapathi, Madhusoodanan Urulangodi, Linda Koshy, Meenakshi Sharma, Sivadasanpillai Harikrishnan, Panniyammakal Jeemon
Publikováno v:
Meta Gene. 28:100883
Background Inherited cardiomyopathies are a frequent cause of heart failure. A 25-basepair deletion polymorphism MYBPC3Δ25bp (rs36212066) in the MYBPC3 gene found exclusively among individuals of South Asian ancestry, has been shown to be associated
Autor:
George C Vilanilam, C.J. Padmakrishnan, A.N. Deepti, H. V. Easwer, P Rajalakshmi, C.R. Anand, Madhusoodanan Urulangodi, Srinivas Gopala, Bharathan Bhavya, K. Sreelakshmi, Girish Menon, Issac Neena, K Krishnakumar
Publikováno v:
Life Sciences. 264:118673
Aims The study focused on the expression and role of a recent potential cancer therapeutic target protein, MutT Homolog1 (MTH1). MTH1 gets activated in an increased reactive oxygen species (ROS) environment and removes the oxidized nucleotides from t