Zobrazeno 1 - 10
of 156
pro vyhledávání: '"Simon Chang"'
Autor:
Amin Hassanzadeh‐Barforoushi, Simon Chang‐Hao Tsao, Audrey Nadalini, David W. Inglis, Yuling Wang
Publikováno v:
Advanced Sensor Research, Vol 3, Iss 7, Pp n/a-n/a (2024)
Abstract Circulating tumor cells (CTCs) have garnered special attention as promising cancer biomarkers. Phenotypic changes of CTCs reveal invaluable information for oncologists in disease prognosis and adjusting their treatment options. Microfluidic
Externí odkaz:
https://doaj.org/article/65ff5fb93c344019bc6fa32a4abf84c7
Publikováno v:
Endocrine Connections, Vol 12, Iss 5, Pp 1-13 (2023)
Context: Klinefelter syndrome (KS, 47,XXY) and 47,XYY syndrome are genetic conditions characterized by a supernumerary sex chromosome. The conditions share many traits, but considerable phenotypic differences are seen between the two. Focusing on mor
Externí odkaz:
https://doaj.org/article/c4c445c1f0684e1f917e3b462dbbc0f8
Autor:
Mette Viuff, Anne Skakkebæk, Emma B. Johannsen, Simon Chang, Steen Bønlykke Pedersen, Katrine Meyer Lauritsen, Mette Glavind Bülow Pedersen, Christian Trolle, Jesper Just, Claus H. Gravholt
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-19 (2023)
Abstract Background Sex chromosome aneuploidies (SCAs) give rise to a broad range of phenotypic traits and diseases. Previous studies based on peripheral blood samples have suggested the presence of ripple effects, caused by altered X chromosome numb
Externí odkaz:
https://doaj.org/article/db4f75ab2f61487782271ccbb0b67421
Autor:
Johannes Wirth, Nina Huber, Kelvin Yin, Sophie Brood, Simon Chang, Celia P. Martinez-Jimenez, Matthias Meier
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Examining the spatially resolved transcriptome of tissue sections promises advances in biomedical research. Here, the authors present xDBiT, a versatile, microfluidics-based approach to cost-effectively measure the spatial transcriptome of multiple t
Externí odkaz:
https://doaj.org/article/59a2142557544a51b045d3e617e358bd
Publikováno v:
IBRO Neuroscience Reports, Vol 15, Iss , Pp S758- (2023)
Externí odkaz:
https://doaj.org/article/233b4fb8c8ef4fe79b9f623ee1d50529
Autor:
Simon Chang-Hao Tsao, Wei Zhang, Cao Hoang Long Nao, Jerresa Jabson, Katherine Wongtrakul-Kish, David Inglis, Yuling Wang
Publikováno v:
Breast, Vol 68, Iss , Pp 242- (2023)
Externí odkaz:
https://doaj.org/article/e55718211f274f4cadc0b3a5d7c194fd
Autor:
Simon Chang, Arkadiusz J Goszczak, Anne Skakkebæk, Jens Fedder, Anders Bojesen, M Vakur Bor, Moniek P M de Maat, Claus H Gravholt, Anna-Marie B Münster
Publikováno v:
Endocrine Connections, Vol 11, Iss 5, Pp 1-9 (2022)
Objective: Klinefelter syndrome (KS) is associated with increased risk of thrombosis. Hypogonadism and accumulating body fat in KS have a potential i mpact on fibrinolysis. In this study, we assessed the fibrinolytic system and the assoc iation with
Externí odkaz:
https://doaj.org/article/3810e98b37cb4a0f898c426e0977c44c
Autor:
Emma B. Johannsen, Jesper Just, Mette H. Viuff, Trine Line Hauge Okholm, Steen B. Pedersen, Katrine Meyer Lauritsen, Christian Trolle, Mette Glavind Bülow Pedersen, Simon Chang, Jens Fedder, Anne Skakkebæk, Claus H. Gravholt
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Purpose: The landscape of circular RNAs (circRNAs), an important class of non-coding RNAs that regulate gene expression, has never been described in human disorders of sex chromosome aneuploidies. We profiled circRNAs in Turner syndrome females (45,X
Externí odkaz:
https://doaj.org/article/09f4c95916ff4bb38d3bc3b60b89e920
Autor:
Simon Chang, Christian Fynbo Christiansen, Anders Bojesen, Svend Juul, Anna-Marie B Münster, Claus H Gravholt
Publikováno v:
Endocrine Connections, Vol 9, Iss 1, Pp 34-43 (2020)
Objectives: Klinefelter syndrome (KS), 47,XXY, can be viewed as a disease model for investigating the risk of thrombosis in male hypogonadism and the subsequent risk related to testosterone treatment. We describe rates of thrombotic risk factors, thr
Externí odkaz:
https://doaj.org/article/bbc8de585ce04f8a9c503874e7feac67
Autor:
Agnethe Berglund, Mette Hansen Viuff, Anne Skakkebæk, Simon Chang, Kirstine Stochholm, Claus Højbjerg Gravholt
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-9 (2019)
Abstract Background Knowledge on the prevalence of sex chromosome abnormalities (SCAs) is limited, and delayed diagnosis or non-diagnosis of SCAs are a continuous concern. We aimed to investigate change over time in incidence, prevalence and age at d
Externí odkaz:
https://doaj.org/article/93f8ffcb071a40398958f745c4fa04fe