Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Michael S. Nahorski"'
Autor:
Brittany A. McKelvey, Hillary S. Andrews, Frederick L. Baehner, James Chen, Carin R. Espenschied, David Fabrizio, Vanessa Gorton, Claire Gould, Justin Guinney, Greg Jones, Xiangyang Lv, Michael S. Nahorski, Melanie R. Palomares, Gary A. Pestano, Mark Sausen, Alain Silk, Nicole Zhang, Zhihong Zhang, Mark D. Stewart, Jeff D. Allen
Publikováno v:
Diagnostics, Vol 14, Iss 9, p 912 (2024)
Circulating tumor DNA (ctDNA) holds promise as a biomarker for predicting clinical responses to therapy in solid tumors, and multiple ctDNA assays are in development. However, the heterogeneity in ctDNA levels prior to treatment (baseline) across dif
Externí odkaz:
https://doaj.org/article/6100185e977649be90845d41c4acd4d9
Autor:
Eamonn R. Maher, Farida Latif, Zsuzsanna Nagy, Laurence Seabra, Anne Reiman, Erzsebet Rabai, Michael S. Nahorski, Janine Fenton, Wenbin Wei, Xiaohong Lu
Supplementary Figure 1 from Therapeutic Targeting the Loss of the Birt-Hogg-Dubé Suppressor Gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d63287e8d219e69eb6a8e5d4761be51
https://doi.org/10.1158/1535-7163.22496691
https://doi.org/10.1158/1535-7163.22496691
Autor:
Eamonn R. Maher, Farida Latif, Zsuzsanna Nagy, Laurence Seabra, Anne Reiman, Erzsebet Rabai, Michael S. Nahorski, Janine Fenton, Wenbin Wei, Xiaohong Lu
Supplementary Figure Legend from Therapeutic Targeting the Loss of the Birt-Hogg-Dubé Suppressor Gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89fe3872a9362a14143acc9978c3af04
https://doi.org/10.1158/1535-7163.22496688
https://doi.org/10.1158/1535-7163.22496688
Autor:
Eamonn R. Maher, Farida Latif, Zsuzsanna Nagy, Laurence Seabra, Anne Reiman, Erzsebet Rabai, Michael S. Nahorski, Janine Fenton, Wenbin Wei, Xiaohong Lu
Brit-Hogg-Dubé (BHD) syndrome, an autosomal dominant familial cancer, is associated with increased risk of kidney cancer. BHD syndrome is caused by loss-of-function mutations in the folliculin (FLCN) protein. To develop therapeutic approaches for re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7d65a718810eec0cb86c25e7e910ac83
https://doi.org/10.1158/1535-7163.c.6535368
https://doi.org/10.1158/1535-7163.c.6535368
Autor:
Kalthoum Tlili-Graiess, Hayley J. Sharpe, Susan Lindsay, Emily V. Fletcher, Geoff Woods, Amal Alhashem, Katherine Schon, Ranad Shaheen, Michael S. Nahorski, Ichrak Drissi, Sarah F. Smithson, Fowzan S. Alkuraya, Steve Lisgo, Alberto Fernández-Jaén
Funder: NIHR Cambridge Biomedical Research centre
Background: Holoprosencephaly is a spectrum of developmental disorder of the embryonic forebrain in which there is failed or incomplete separation of the prosencephalon into two cerebral hemisphe
Background: Holoprosencephaly is a spectrum of developmental disorder of the embryonic forebrain in which there is failed or incomplete separation of the prosencephalon into two cerebral hemisphe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f3ebfedaf94b9e49a20e3f6d314a4a
https://www.repository.cam.ac.uk/handle/1810/326540
https://www.repository.cam.ac.uk/handle/1810/326540
Autor:
David K. Menon, Van B. Lu, Frank Reimann, Christopher A. Brown, Daniel W. Wheeler, Michael C. Lee, Gerard Callejo, James R.F. Hockley, C. Geoffrey Woods, Emily V. Fletcher, Michael S. Nahorski, Luke A. Pattison, Ichrak Drissi, Patrik Ernfors, Kaitlin Stouffer, Gillian Ison, Ewan St. John Smith
Publikováno v:
CELL REPORTS
Cell Reports
Cell Reports
Summary By studying healthy women who do not request analgesia during their first delivery, we investigate genetic effects on labor pain. Such women have normal sensory and psychometric test results, except for significantly higher cuff pressure pain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c065c50f304e81604ab566092d75803a
http://livrepository.liverpool.ac.uk/3090310/1/Cell_Reports_2020.pdf
http://livrepository.liverpool.ac.uk/3090310/1/Cell_Reports_2020.pdf
Autor:
Ewan St. John Smith, Patrik Ernfors, David K. Menon, Frank Reimann, Geoffrey Woods, Kaitlin Stouffer, Michael S. Nahorski, Emily V. Fletcher, Van B. Lu, Daniel W. Wheeler, Christopher A. Brown, Ichrak Drissi, James R.F. Hockley, Gill Ison, Michael C. Lee, Luke A. Pattison, Gerard Callejo
Publikováno v:
SSRN Electronic Journal.
We sought genetic effects on labour pain by studying healthy women who did not request analgesia during their first delivery. Extensive sensory and psychometric testing were normal in these women, except for significantly higher cuff-pressure pain. W
Autor:
Michael C. Lee, Michael S. Nahorski, James R.F. Hockley, Van B. Lu, Gillian Ison, Luke A. Pattison, Gerard Callejo, Kaitlin Stouffer, Emily Fletcher, Christopher Brown, Ichrak Drissi, Daniel Wheeler, Patrik Ernfors, David Menon, Frank Reimann, Ewan St John Smith, C. Geoffrey Woods
We sought genetic effects on labour pain by studying healthy women who did not request analgesia during their first delivery. Extensive sensory and psychometric testing were normal in these women, except for significantly higher cuff-pressure pain. W
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8cccd3031016ced653cb344dd0e3ed0
https://doi.org/10.1101/489310
https://doi.org/10.1101/489310
Autor:
Mohnish Suri, Hamish Houston, Alasdair Parker, C. Geoffrey Woods, Sameer M. Zuberi, Manali Chitre, Michael S. Nahorski, Angela F. Brady, Kaitlin Stouffer, Bryony Dunning-Davies, Emma Wakeling
BackgroundProgressive encephalopathy, hypsarrhythmia and optic atrophy (PEHO) has been described as a clinically distinct syndrome. It has been postulated that it is an autosomal recessive condition. However, the aetiology is poorly understood, and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11f3ae89e4413b510b12edbfab7c7319
https://www.repository.cam.ac.uk/handle/1810/285865
https://www.repository.cam.ac.uk/handle/1810/285865
Autor:
Geoff Woods, N. Sarveswaran, S. M. Srinivas, V. K. Gowda, F. Browne, Michael S. Nahorski, Celia Moss
Publikováno v:
The British journal of dermatology. 179(5)
Background Midface toddler excoriation syndrome (MiTES) is a condition recently reported in three unrelated children. Habitual scratching from the first year of life inflicted deep, chronic, scarring wounds around the nose and eyes. One child had a m