Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Chenna R. Galiveti"'
Autor:
Shravan Leonard-Murali, Chetana Bhaskarla, Ghanshyam S. Yadav, Sudeep K. Maurya, Chenna R. Galiveti, Joshua A. Tobin, Rachel J. Kann, Eishan Ashwat, Patrick S. Murphy, Anish B. Chakka, Vishal Soman, Paul G. Cantalupo, Xinming Zhuo, Gopi Vyas, Dara L. Kozak, Lindsey M. Kelly, Ed Smith, Uma R. Chandran, Yen-Michael S. Hsu, Udai S. Kammula
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-17 (2024)
Abstract Immune checkpoint inhibition has shown success in treating metastatic cutaneous melanoma but has limited efficacy against metastatic uveal melanoma, a rare variant arising from the immune privileged eye. To better understand this resistance,
Externí odkaz:
https://doaj.org/article/c3827bd8a22341ebb07936043ec06ea7
Autor:
Susanne G van der Grein, Kyra A Y Defourny, Huib H Rabouw, Chenna R Galiveti, Martijn A Langereis, Marca H M Wauben, Ger J A Arkesteijn, Frank J M van Kuppeveld, Esther N M Nolte-'t Hoen
Publikováno v:
PLoS Pathogens, Vol 15, Iss 2, p e1007594 (2019)
Several naked virus species, including members of the Picornaviridae family, have recently been described to escape their host cells and spread infection via enclosure in extracellular vesicles (EV). EV are 50-300 nm sized lipid membrane-enclosed par
Externí odkaz:
https://doaj.org/article/cbf2a20fd85b409791b7c8745997f7da
Publikováno v:
Coronaviruses.
Abstract: Corona Virus Disease 2019 (COVID-19) is reported to be transmitted predominantly by respiratory droplets and fomites. The regular use of a mask can mitigate the airborne transmission of the Severe Acute Respiratory Syndrome Corona Virus-2 (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb55b488e8c79ba2f7d0ebdc16779ae5
https://doi.org/10.2174/2666796704666230330083413
https://doi.org/10.2174/2666796704666230330083413
Autor:
Reinhard Voss, Delf-Magnus Kummerfeld, Boris V. Skryabin, Jochen Seggewiss, Chenna R. Galiveti, Andreas Huge, Anna Wolters, Carsten A. Raabe, Juergen Brosius, Timofey S. Rozhdestvensky
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-9 (2019)
Serotonin 5-HT2C receptor is a G-protein coupled excitatory receptor that regulates several biochemical pathways and has been implicated in obesity, mental state, sleep cycles, autism, neuropsychiatric disorders and neurodegenerative diseases. The ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bc90bc012aea307454ecb4162ae5411
http://europepmc.org/articles/PMC6414643
http://europepmc.org/articles/PMC6414643
Autor:
Delf-Magnus Kummerfeld, Raabe, Carsten A, Voss, Reinhard, Juergen Brosius, Chenna R. Galiveti, Wolters, Anna, Seggewiss, Jochen, Huge, Andreas, Skryabin, Boris, Rozhdestvensky, Timofey S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54b919689a23ad4e39c29478316b2178
Autor:
Anna Wolters, Timofey S. Rozhdestvensky, Boris V. Skryabin, Chenna R. Galiveti, Thomas Robeck, Birte Seeger, Carsten A. Raabe, Jürgen Brosius, Leonid Gubar
Publikováno v:
Scientific Reports
Prader-Willi syndrome (PWS) is a neurogenetic disorder caused by loss of paternally expressed genes on chromosome 15q11-q13. The PWS-critical region (PWScr) contains an array of non-protein coding IPW-A exons hosting intronic SNORD116 snoRNA genes. D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3ac4859ccf4fec82fac9955c3c4e5a7
https://doi.org/10.1038/srep20398
https://doi.org/10.1038/srep20398
Autor:
Boris V. Skryabin, Valentina Sukonina, Marsha Bundman, Sergej Handel, Jürgen Brosius, Chenna R. Galiveti, Timofey S. Rozhdestvensky, Tasneem Khanam, Ursula Jordan
Publikováno v:
Nucleic Acids Research
In a rare occasion a single chromosomal locus was targeted twice by independent Alu-related retroposon insertions, and in both cases supported neuronal expression of the respective inserted genes encoding small non-protein coding RNAs (npcRNAs): BC20
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d53d0b2e6e291a7a8a44dbff8806c539
https://doi.org/10.1093/nar/gkl1082
https://doi.org/10.1093/nar/gkl1082
Publikováno v:
Scientific Reports
Prader-Willi Syndrome (PWS) is a neurogenetic disorder caused by the deletion of imprinted genes on the paternally inherited human chromosome 15q11-q13. This locus harbours a long non-protein-coding RNA (U-UBE3A-ATS) that contains six intron-encoded
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c2bc876cb954170504f1782eba06e1a
Publikováno v:
RNA (New York, N.Y.). 16(2)
In recent years the improvements in high-throughput gene expression analysis have led to the discovery of numerous non-protein-coding RNA (npcRNA) molecules. They form an abundant class of untranslated RNAs that have shown to play a crucial role in d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d1b67fb21213ccbba60f21cbfe84447
https://pubmed.ncbi.nlm.nih.gov/20040593
https://pubmed.ncbi.nlm.nih.gov/20040593
Autor:
Hans Lehrach, Michal Janitz, Jürgen Brosius, Steffen Hennig, Chenna R. Galiveti, Ralf Sudbrak, Zoltán Konthur, James Adjaye
Publikováno v:
GBM Annual Fall meeting Berlin/Potsdam 2005. 2005
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::640d3498eb0ef57a84187ad00435eeb8
https://doi.org/10.1240/sav_gbm_2005_h_001224
https://doi.org/10.1240/sav_gbm_2005_h_001224