Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lanikea B King"'
Autor:
Aaron Stahl, Nathaniel C Noyes, Tamara Boto, Valentina Botero, Connor N Broyles, Miao Jing, Jianzhi Zeng, Lanikea B King, Yulong Li, Ronald L Davis, Seth M Tomchik
Publikováno v:
eLife, Vol 11 (2022)
Anatomical and physiological compartmentalization of neurons is a mechanism to increase the computational capacity of a circuit, and a major question is what role axonal compartmentalization plays. Axonal compartmentalization may enable localized, pr
Externí odkaz:
https://doaj.org/article/dec195defa834890b9033a0c335f44a0
Autor:
Lanikea B King, Tamara Boto, Valentina Botero, Ari M Aviles, Breanna M Jomsky, Chevara Joseph, James A Walker, Seth M Tomchik
Publikováno v:
PLoS Genetics, Vol 16, Iss 7, p e1008920 (2020)
Neurofibromatosis type 1 is a monogenetic disorder that predisposes individuals to tumor formation and cognitive and behavioral symptoms. The neuronal circuitry and developmental events underlying these neurological symptoms are unknown. To better un
Externí odkaz:
https://doaj.org/article/ae8d234fbaca46dda88aec55e54dde36
Autor:
Valentina Botero, Bethany A. Stanhope, Elizabeth B. Brown, Eliza C. Grenci, Tamara Boto, Scarlet J. Park, Lanikea B. King, Keith R. Murphy, Kenneth J. Colodner, James A. Walker, Alex C. Keene, William W. Ja, Seth M. Tomchik
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Neurofibromatosis type 1 (NF1) is a genetic disorder caused by mutations in neurofibromin and associated with disruptions in physiology and behavior. Here the authors show that neurofibromin regulates metabolic homeostasis via a discrete brain circui
Externí odkaz:
https://doaj.org/article/9bdfedfd53ef4415959b9f694b37b1af
Autor:
Aaron Stahl, Nathaniel C Noyes, Tamara Boto, Valentina Botero, Connor N Broyles, Miao Jing, Jianzhi Zeng, Lanikea B King, Yulong Li, Ronald L Davis, Seth M Tomchik
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4501d1ac00269bd3c752b46a22af60be
https://doi.org/10.7554/elife.76712.sa2
https://doi.org/10.7554/elife.76712.sa2
Autor:
Seth M. Tomchik, Chevara Joseph, Breanna M. Jomsky, Tamara Boto, James A. Walker, Ari M. Aviles, Valentina Botero, Lanikea B. King
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 16, Iss 7, p e1008920 (2020)
PLoS Genetics, Vol 16, Iss 7, p e1008920 (2020)
Neurofibromatosis type 1 is a monogenetic disorder that predisposes individuals to tumor formation and cognitive and behavioral symptoms. The neuronal circuitry and developmental events underlying these neurological symptoms are unknown. To better un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20fddb39df7532ade4b9d915e8363eb1
https://pubmed.ncbi.nlm.nih.gov/32697780
https://pubmed.ncbi.nlm.nih.gov/32697780
Autor:
Tamara Boto, Alex C. Keene, Seth M. Tomchik, Scarlet J. Park, Kenneth J. Colodner, James A. Walker, Eliza C. Grenci, William W. Ja, Lanikea B. King, Valentina Botero, Keith R. Murphy, Bethany A. Stahl
Neurofibromatosis type 1 (NF1) is a genetic disorder predisposing patients to a range of features, the most characteristic of which include areas of abnormal skin pigmentation and benign tumors associated with peripheral nerves, termed neurofibromas.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6147cd113a736d370679420c4375934d
Autor:
Eliza C. Grenci, William W. Ja, Seth M. Tomchik, Scarlet J. Park, Keith R. Murphy, Elizabeth B. Brown, Valentina Botero, Bethany A. Stanhope, Tamara Boto, Kenneth J. Colodner, James A. Walker, Lanikea B. King, Alex C. Keene
Publikováno v:
Nature Communications
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Nature Communications, Vol 12, Iss 1, Pp 1-13 (2021)
Neurofibromatosis type 1 is a chronic multisystemic genetic disorder that results from loss of function in the neurofibromin protein. Neurofibromin may regulate metabolism, though the underlying mechanisms remain largely unknown. Here we show that ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbe5c8b19861167fc69d59486e1bfc57
https://pubmed.ncbi.nlm.nih.gov/34257279
https://pubmed.ncbi.nlm.nih.gov/34257279
Publikováno v:
Biological Psychiatry. 80:160-169
Background Oxytocin (OXT) modulates several aspects of social behavior. Intranasal OXT is a leading candidate for treating social deficits in patients with autism spectrum disorder, and common genetic variants in the human OXTR gene are associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1957af4a77c0377f2bc81203a2d5b8ee
https://doi.org/10.1016/j.biopsych.2015.12.008
https://doi.org/10.1016/j.biopsych.2015.12.008
Autor:
Lanikea B. King
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience. 36(32)
Oxytocin is a member of a neuropeptide family with a well established role modulating reproductive and social behaviors ([Donaldson and Young, 2008][1]). Oxytocin is expressed in conserved populations of neurons that release oxytocin broadly througho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dca455ac615912a0126b71edc3e3d11e
https://pubmed.ncbi.nlm.nih.gov/27511002
https://pubmed.ncbi.nlm.nih.gov/27511002
Autor:
Yoheilly Velazquez, Keith R. Murphy, Seth M. Tomchik, Lanikea B. King, William W. Ja, Marta Koch
Publikováno v:
G3: Genes|Genomes|Genetics
G3: Genes, Genomes, Genetics, Vol 6, Iss 4, Pp 1083-1093 (2016)
G3: Genes, Genomes, Genetics, Vol 6, Iss 4, Pp 1083-1093 (2016)
Neurofibromatosis I is a common genetic disorder that results in tumor formation, and predisposes individuals to a range of cognitive/behavioral symptoms, including deficits in attention, visuospatial skills, learning, language development, and sleep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f05b9eea6d5a3c9bcb0d61c0ede05cb0
https://pubmed.ncbi.nlm.nih.gov/26896440
https://pubmed.ncbi.nlm.nih.gov/26896440