Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rajasekhara Reddy Ravuri"'
Autor:
Cholendra Arja, Rajasekhara Reddy Ravuri, Venugopal N Pulamaghatta, Krishna Mohan Surapaneni, Premanand Raya, Chandrasekhar Adimoolam, Kodanda Reddy Kanala
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e89957 (2014)
The development of chronic obstructive pulmonary disease, upon exposure to tobacco smoke, is the cumulative effect of defects in several genes. With the aim of understanding the genetic structure that is characteristic of our patient population, we s
Externí odkaz:
https://doaj.org/article/3f8f46f56af74f908a9cdddc613b1ad4
Autor:
Adimoolam Chandrasekar, Satish Kumar, Jwalapuram Sreenath, Bishwa Nath Sarkar, Bhaskar Pralhad Urade, Sujit Mallick, Syam Sundar Bandopadhyay, Pinuma Barua, Subihra Sankar Barik, Debasish Basu, Uttaravalli Kiran, Prodyot Gangopadhyay, Ramesh Sahani, Bhagavatula Venkata Ravi Prasad, Shampa Gangopadhyay, Gandikota Rama Lakshmi, Rajasekhara Reddy Ravuri, Koneru Padmaja, Pulamaghatta N Venugopal, Madhu Bala Sharma, Vadlamudi Raghavendra Rao
Publikováno v:
PLoS ONE, Vol 4, Iss 10, p e7447 (2009)
To construct maternal phylogeny and prehistoric dispersals of modern human being in the Indian sub continent, a diverse subset of 641 complete mitochondrial DNA (mtDNA) genomes belonging to macrohaplogroup M was chosen from a total collection of 2,78
Externí odkaz:
https://doaj.org/article/021168f59fb54632aa78ffc17643d7d3
Publikováno v:
The Anthropologist. 14:25-28
KEYWORDS Phenotype. PON1. HDL. SNPs. Vokkaliga ABSTRACT The cardio protective functions of HDL are attributed to the HDL-associated proteins like Paraoxonase 1 (PON1). PON1 is associated with HDL through a N-terminal signal peptide. HDL-associated PO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0d41d56036d92d512e409d7b2247d29
https://doi.org/10.1080/09720073.2012.11891216
https://doi.org/10.1080/09720073.2012.11891216
Autor:
Nageswara Rao, Dunna, Senthil, Rajappa, Raghunadharao, Digumarti, Sugunakar, Vure, Sailaja, Kagita, Surekha, Damineni, V R, Rao, Satish Kumar, Yadav, Rajasekhara Reddy, Ravuri, Vishnupriya, Satti
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 11(6)
Mutations in FLT3 and NPM1 are important prognostic factors in AML, influencing outcome in normal karyotype cases. We here analysed incidences of FLT3/ITD, D 835 and NPM1 mutations in patients with de novo normal karyotype AML using PCR and gene sequ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ae95973640a330e36d4819558e10bb4c
https://pubmed.ncbi.nlm.nih.gov/21338238
https://pubmed.ncbi.nlm.nih.gov/21338238
Autor:
Pinuma Barua, Prodyot Gangopadhyay, Subihra Sankar Barik, Satish Kumar, Koneru Padmaja, Vadlamudi Raghavendra Rao, Madhu Bala Sharma, Bhagavatula Venkata Ravi Prasad, Uttaravalli Kiran, Sujit Mallick, Jwalapuram Sreenath, Rajasekhara Reddy Ravuri, Shampa Gangopadhyay, Syam Sundar Bandopadhyay, Bishwa Nath Sarkar, B. P. Urade, Pulamaghatta N. Venugopal, Ramesh Sahani, Gandikota Rama Lakshmi, Adimoolam Chandrasekar, Debashis Basu
Publikováno v:
PLoS ONE, Vol 4, Iss 10, p e7447 (2009)
PLoS ONE
PLoS ONE
To construct maternal phylogeny and prehistoric dispersals of modern human being in the Indian sub continent, a diverse subset of 641 complete mitochondrial DNA (mtDNA) genomes belonging to macrohaplogroup M was chosen from a total collection of 2,78
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ab2bb9e7b11689bf45e27cc51d62d42
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19823670/pdf/?tool=EBI
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19823670/pdf/?tool=EBI
Autor:
Satish Kumar, Padmaja Koneru, Rajasekhara Reddy Ravuri, Adimoolam Chandrasekar, B. P. Urade, Biswanath Sarkar, Vadlamudi Raghavendra Rao
Publikováno v:
BMC Evolutionary Biology
BMC Evolutionary Biology, Vol 9, Iss 1, p 173 (2009)
BMC Evolutionary Biology, Vol 9, Iss 1, p 173 (2009)
Background An early dispersal of biologically and behaviorally modern humans from their African origins to Australia, by at least 45 thousand years via southern Asia has been suggested by studies based on morphology, archaeology and genetics. However
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1b100de18b055a339053def2fc99545
http://europepmc.org/articles/PMC2720955
http://europepmc.org/articles/PMC2720955
Autor:
Rajasekhara Reddy Ravuri, U Kiran, Pushpa Saviour, Satish Kumar, Vadlamudi Raghavendra Rao, Nallur B. Ramachandra
Publikováno v:
Indian Journal of Human Genetics. 14:99
Dyslexia is a hereditary neurological disorder that manifests as an unexpected difficulty in learning to read despite adequate intelligence, education, and normal senses. The prevalence of dyslexia ranges from 3 to 15% of the school aged children. Ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::799fe459c07d4baf504e43f739b4dc34
https://doi.org/10.4103/0971-6866.45002
https://doi.org/10.4103/0971-6866.45002
Autor:
Vadlamudi Raghavendra Rao, S. Y. Saheb, Satish Kumar, D Xaviour, P B S V Padmanabham, Kiran Uttaravalli, Bipinpal Das, M Kotal, P Aditi Mukherjee, Rajasekhara Reddy Ravuri, Padmaja Koneru
Publikováno v:
BMC Evolutionary Biology, Vol 8, Iss 1, p 230 (2008)
BMC Evolutionary Biology
BMC Evolutionary Biology
Background The "out of Africa" model postulating single "southern route" dispersal posits arrival of "Anatomically Modern Human" to Indian subcontinent around 66–70 thousand years before present (kyBP). However the contributions and legacy of these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b359ff7a5002184ac50deda95918d13f