Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Katerina Zorina-Lichtenwalter"'
Autor:
Katerina Zorina-Lichtenwalter, Carmen I. Bango, Lukas Van Oudenhove, Marta Čeko, Martin A. Lindquist, Andrew D. Grotzinger, Matthew C. Keller, Naomi P. Friedman, Tor D. Wager
Publikováno v:
Pain.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2128fb64a5f8d1c42ed23987645dd24f
https://doi.org/10.1097/j.pain.0000000000002922
https://doi.org/10.1097/j.pain.0000000000002922
Autor:
Katerina Zorina-Lichtenwalter, Carmen I. Bango, Lukas Van Oudenhove, Marta Čeko, Martin A. Lindquist, Andrew D. Grotzinger, Matthew C. Keller, Naomi P. Friedman, Tor D. Wager
Chronic pain is attributable to both local and systemic pathology. To investigate the latter, we focused on genetic risk shared among 24 chronic pain conditions in the UK Biobank. We conducted genome-wide association studies (GWAS) on all conditions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45ea0b54b295242ed12e1382590b792d
https://doi.org/10.1101/2022.06.28.22277025
https://doi.org/10.1101/2022.06.28.22277025
Publikováno v:
Pain
Genetic variation in melanocortin-1 receptor (MC1R) has a known role in red hair. Studies on responses to noxious stimuli in red-haired individuals have also been conducted, with mixed findings. To investigate a possible divergence between variants r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd07d83bec9144d8205425d62b75f328
https://europepmc.org/articles/PMC7202363/
https://europepmc.org/articles/PMC7202363/
Publikováno v:
Genomics of Pain and Co-Morbid Symptoms ISBN: 9783030216566
Neuropathic pain stems from a lesion or disease of the somatosensory system. Disorders characterised by neuropathic pain vary considerably in their etiology and frequency. Hereditary conditions are usually monogenic, and their causal genetic variants
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b42132382d4f36a7e80f374d1b01b6aa
https://doi.org/10.1007/978-3-030-21657-3_12
https://doi.org/10.1007/978-3-030-21657-3_12
Publikováno v:
Pain
A comprehensive overview of published associations between genetic variants and human neuropathic pain conditions with validation of reported findings in the U.K. Biobank.
Numerous studies have shown associations between genetic variants and neu
Numerous studies have shown associations between genetic variants and neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e55c9a7081656f6a4f1d178ec3944a79
https://doi.org/10.1097/j.pain.0000000000001099
https://doi.org/10.1097/j.pain.0000000000001099
Autor:
John Jacobs, Emma Frost, Mark A. Suckow, Shahriar Mobashery, Kiran V. Mahasenan, Derong Ding, William R. Wolter, Katerina Zorina-Lichtenwalter, Mayland Chang, Valerie A. Schroeder, Ming Gao, Maria Bastian
Publikováno v:
ACS Medicinal Chemistry Letters. 8:654-659
Matrix metalloproteinases (MMPs) have numerous physiological functions and share a highly similar catalytic domain. Differential dynamical information on the closely related human MMP-8, -13, and -14 was integrated onto the benzoxazinone molecular te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8295158ed7f8b1d255d132612f7a5bc
https://doi.org/10.1021/acsmedchemlett.7b00130
https://doi.org/10.1021/acsmedchemlett.7b00130
Autor:
Dima V Zaykin, Luda Diatchenko, Katerina Zorina-Lichtenwalter, Marc Parisien, Simon Gravel, Ryan N. Lichtenwalter, Andrey V. Bortsov
Publikováno v:
Hum Mol Genet
Genetic variation in melanocortin-1 receptor (MC1R) is a known contributor to disease-free red hair in humans. Three loss-of-function single-nucleotide variants (rs1805007, rs1805008 and rs1805009) have been established as strongly correlated with re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db022bf679dfd33ce22406e6245a2d84
https://europepmc.org/articles/PMC6548228/
https://europepmc.org/articles/PMC6548228/
Autor:
Marc Parisien, Luda Diatchenko, Stefano Cattaneo, Marjo Piltonen, Richard Klares, Ryan N. Lichtenwalter, Anne-Julie Chabot-Doré, Nicol Tugarinov, Katerina Zorina-Lichtenwalter, Xia Wen, Samar Khoury, Carolina B. Meloto, Rodrigo Benavides, Vivek Verma
Publikováno v:
Pain. 159(4)
The Human Pain Genetics Database (HPGDB) is a comprehensive variant-focused inventory of genetic contributors to human pain. After curation, the HPGDB currently includes 294 studies reporting associations between 434 distinct genetic variants and var
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11e71e04a292bfd740c8eb05dff3f729
https://pubmed.ncbi.nlm.nih.gov/29300278
https://pubmed.ncbi.nlm.nih.gov/29300278
Publikováno v:
Advances in Databases and Information Systems ISBN: 9783319669168
ADBIS
ADBIS
As technologies to produce genotypic data have become less expensive, the widths and depths of such data have sharply increased. Relational databases have performed poorly in this domain. Data storage and retrieval is now mostly conducted by highly c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9ebb35c1553d73199be2840d9ecc011
https://doi.org/10.1007/978-3-319-66917-5_27
https://doi.org/10.1007/978-3-319-66917-5_27