Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jesse Barnes"'
Autor:
Alvaro Quintanal-Villalonga, Kenta Kawasaki, Esther Redin, Fathema Uddin, Swanand Rakhade, Vidushi Durani, Amin Sabet, Moniquetta Shafer, Wouter R. Karthaus, Samir Zaidi, Yingqian A. Zhan, Parvathy Manoj, Harsha Sridhar, Dennis Kinyua, Hong Zhong, Barbara P. Mello, Metamia Ciampricotti, Umesh K. Bhanot, Irina Linkov, Juan Qiu, Radhika A. Patel, Colm Morrissey, Sanjoy Mehta, Jesse Barnes, Michael C. Haffner, Nicholas D. Socci, Richard P. Koche, Elisa de Stanchina, Sonia Molina-Pinelo, Sohrab Salehi, Helena A. Yu, Joseph M. Chan, Charles M. Rudin
Publikováno v:
Signal Transduction and Targeted Therapy, Vol 9, Iss 1, Pp 1-14 (2024)
Abstract Neuroendocrine (NE) transformation is a mechanism of resistance to targeted therapy in lung and prostate adenocarcinomas leading to poor prognosis. Up to date, even if patients at high risk of transformation can be identified by the occurren
Externí odkaz:
https://doaj.org/article/501fe4c8a5e9423ca573e0d9f455d0b2
Autor:
Hequn Liu, Jesse Barnes, Erika Pedrosa, Nathaniel S. Herman, Franklin Salas, Ping Wang, Deyou Zheng, Herbert M. Lachman
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-16 (2020)
Abstract Background Lowe syndrome (LS) is caused by loss-of-function mutations in the X-linked gene OCRL, which codes for an inositol polyphosphate 5-phosphatase that plays a key role in endosome recycling, clathrin-coated pit formation, and actin po
Externí odkaz:
https://doaj.org/article/dd11e8258a334c02b7c31968977e764c
Autor:
Jesse Barnes, Franklin Salas, Ryan Mokhtari, Hedwig Dolstra, Erika Pedrosa, Herbert M. Lachman
Publikováno v:
Molecular Autism, Vol 9, Iss 1, Pp 1-16 (2018)
Abstract Background Lowe syndrome (LS) is a rare genetic disorder caused by loss of function mutations in the X-linked gene, OCRL, which codes for inositol polyphosphate 5-phosphatase. LS is characterized by the triad of congenital cataracts, neurode
Externí odkaz:
https://doaj.org/article/a6a0abed191741b99fa95e9f9cd235fa
Publikováno v:
PLoS ONE, Vol 11, Iss 12, p e0168256 (2016)
Perineuronal nets (PNNs) are aggregates of extracellular matrix that form structures surrounding a subset of GABAergic interneurons. The staining intensity of PNNs appears to be related to plasticity. Environmental enrichment (EE) influences plastici
Externí odkaz:
https://doaj.org/article/074bbe991f664db4af2aa9c802aede69
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e54164 (2013)
Environmental enrichment (EE) reduces drug and sucrose cue-reactivity in rats. In a previous study we reported that 1 month of EE (large cage, toys, and social cohorts) significantly reduced sucrose cue-reactivity. In the present study, we examined w
Externí odkaz:
https://doaj.org/article/6eb33402aa3a4b61bac588ab2c57c722
Autor:
Theresa H. Cruz, Courtney A. FitzGerald, Valerie Quintana, Jesse Barnes, Kenny E. Sanchez, Meta Hirschl, Amy Lavender, Leigh Caswell
Publikováno v:
Health Promotion Practice. 23:153S-163S
Linking clinical services to community-based resources is a promising strategy for assisting patients with chronic disease prevention and management. However, there remains a gap in understanding how to effectively develop and implement community–c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c07321b0b90b17c27f26fefe2019593
https://doi.org/10.1177/15248399221111192
https://doi.org/10.1177/15248399221111192
Publikováno v:
Journal of Business Research. 158:113655
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54a0f5d400406bd0de0b5f6ef5d53c15
https://doi.org/10.1016/j.jbusres.2023.113655
https://doi.org/10.1016/j.jbusres.2023.113655
Autor:
Nathaniel S. Herman, Deyou Zheng, Hequn Liu, Jesse Barnes, Ping Wang, Herbert M. Lachman, Franklin Salas, Erika Pedrosa
Publikováno v:
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-16 (2020)
Journal of Neurodevelopmental Disorders, Vol 12, Iss 1, Pp 1-16 (2020)
Background Lowe syndrome (LS) is caused by loss-of-function mutations in the X-linked gene OCRL, which codes for an inositol polyphosphate 5-phosphatase that plays a key role in endosome recycling, clathrin-coated pit formation, and actin polymerizat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02d04277f0ff387b1b52bc7eb6f736ef
https://doi.org/10.1186/s11689-020-09317-2
https://doi.org/10.1186/s11689-020-09317-2
Autor:
Franklin Salas, Erika Pedrosa, Hedwig Dolstra, Herbert M. Lachman, Ryan Mokhtari, Jesse Barnes
Publikováno v:
Molecular Autism
Molecular Autism, Vol 9, Iss 1, Pp 1-16 (2018)
Molecular Autism, Vol 9, Iss 1, Pp 1-16 (2018)
Background Lowe syndrome (LS) is a rare genetic disorder caused by loss of function mutations in the X-linked gene, OCRL, which codes for inositol polyphosphate 5-phosphatase. LS is characterized by the triad of congenital cataracts, neurodevelopment
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f3633f02a177fc07bbbaf962aaa0480
http://europepmc.org/articles/PMC6094927
http://europepmc.org/articles/PMC6094927
Publikováno v:
Behavioural Pharmacology. 24:633-639
Dopamine receptors are implicated in the reinforcing effects of food and drug reinforcement. The purpose of this study was to evaluate whether blocking D2 dopamine receptors during extinction (secondary reinforcement) would affect reacquisition of re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f8d623271d78461607a5c28c3a99a1a
https://doi.org/10.1097/fbp.0000000000000002
https://doi.org/10.1097/fbp.0000000000000002