Zobrazeno 1 - 10
of 165
pro vyhledávání: '"Kudwa A"'
Autor:
Huang, Mei, He, Wenqi, Rajagopal, Lakshmi, Kudwa, Andrea, Grigoriadis, Dimitri E., Meltzer, Herbert Y.
Publikováno v:
In Pharmacology, Biochemistry and Behavior March 2020 190
A Previously Uncharacterized Role for Estrogen Receptor β: Defeminization of Male Brain and Behavior
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2005 Mar . 102(12), 4608-4612.
Externí odkaz:
https://www.jstor.org/stable/3375029
Akademický článek
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Publikováno v:
In Physiology & Behavior 22 April 2014 129:287-296
Publikováno v:
In Brain Research 5 September 2013 1529:74-82
Akademický článek
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Autor:
Pooja Jain, Ranjini Kudwa
Publikováno v:
Annals of Pathology and Laboratory Medicine. 7:C51-54
Epithelioid sarcoma is a rare highly aggressive soft tissue sarcoma with a high incidence of local recurrence and metastasis. It is a tumor of uncertain histogenesis & poses a diagnostic difficulty as it is often misdiagnosed as other benign or malig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5469db235d9b48c36d824b422a8c5692
https://doi.org/10.21276/apalm.2678
https://doi.org/10.21276/apalm.2678
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 381(2)
Antipsychotic medications function by blocking postsynaptic dopaminergic signaling in the central nervous system. Dopamine transmission can also be modulated presynaptically by inhibitors of vesicular monoamine transporter 2 (VMAT2), which inhibit lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbf73fa36242bdc0b6b57e69a665b9ff
https://pubmed.ncbi.nlm.nih.gov/35197321
https://pubmed.ncbi.nlm.nih.gov/35197321
Autor:
Pooja Jain, Ranjini Kudwa
Epithelioid sarcoma is a rare highly aggressive soft tissue sarcoma with a high incidence of local recurrence and metastasis. It is a tumor of uncertain histogenesis & poses a diagnostic difficulty as it is often misdiagnosed as other benign or malig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfc3bc8deb9d989c9029c50da940d96b
https://doi.org/10.9734/bpi/rdmmr/v2/4275f
https://doi.org/10.9734/bpi/rdmmr/v2/4275f
Autor:
Yasaman Ataei, Larry Park, D. James Surmeier, B. Joseph Vu, Seung Kwak, Richard T. Surosky, Anand Narayanan, David A. Shivak, Josee Laganiere, Christer Halldin, Andrea Varrone, Matthew C. Mendel, Karsten Tillack, Lei Zhang, Bryan Zeitler, Dmitry Guschin, Lexi Kopan, Sarah J. Hinkley, Kimberly Marlen, Jocelynn R. Pearl, Qi Yu, Taneli Heikkinen, Annette Gärtner, Yalda Sedaghat, Christina Thiede, Miklós Tóth, Jennifer M. Cherone, David Paschon, Jyothisri Kondapalli, Andrea E. Kudwa, Ladislav Mrzljak, Rainier Amora, Kimmo Lehtimäki, Edward J. Rebar, Lenke Tari, Ignacio Munoz-Sanjuan, Jeffrey C. Miller, Sylvie Ramboz, Marie Svedberg, Steven Froelich, Irina Ankoudinova, Philip D. Gregory, Stephen Lam, Michelle Day, Jonathan Bard, Hoang Oanh B. Nguyen, Fyodor D. Urnov, Davis Li, Jenny Haggkvist, H. Steve Zhang, Guijuan Qiao
Publikováno v:
Nature Medicine. 25:1131-1142
Huntington’s disease (HD) is a dominantly inherited neurodegenerative disorder caused by a CAG trinucleotide expansion in the huntingtin gene (HTT), which codes for the pathologic mutant HTT (mHTT) protein. Since normal HTT is thought to be importa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d19307c1ae395108f0cf1b74fb590fb6
https://doi.org/10.1038/s41591-019-0478-3
https://doi.org/10.1038/s41591-019-0478-3