Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Anas M Khanshour"'
Autor:
Hao Yu, Anas M Khanshour, Aki Ushiki, Nao Otomo, Yoshinao Koike, Elisabet Einarsdottir, Yanhui Fan, Lilian Antunes, Yared H Kidane, Reuel Cornelia, Rory R Sheng, Yichi Zhang, Jimin Pei, Nick V Grishin, Bret M Evers, Jason Pui Yin Cheung, John A Herring, Chikashi Terao, You-qiang Song, Christina A Gurnett, Paul Gerdhem, Shiro Ikegawa, Jonathan J Rios, Nadav Ahituv, Carol A Wise
Publikováno v:
eLife, Vol 12 (2024)
Adolescent idiopathic scoliosis (AIS) is a common and progressive spinal deformity in children that exhibits striking sexual dimorphism, with girls at more than fivefold greater risk of severe disease compared to boys. Despite its medical impact, the
Externí odkaz:
https://doaj.org/article/008395c97b104a1f9a8bdc58a295796f
Autor:
Elisabet Einarsdottir, Anna Grauers, Jingwen Wang, Hong Jiao, Stefan A Escher, Aina Danielsson, Ane Simony, Mikkel Andersen, Steen Bach Christensen, Kristina Åkesson, Ikuyo Kou, Anas M Khanshour, Acke Ohlin, Carol Wise, Shiro Ikegawa, Juha Kere, Paul Gerdhem
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189591 (2017)
A Swedish pedigree with an autosomal dominant inheritance of idiopathic scoliosis was initially studied by genetic linkage analysis, prioritising genomic regions for further analysis. This revealed a locus on chromosome 1 with a putative risk haploty
Externí odkaz:
https://doaj.org/article/9574148f9bf84766ab16c3ef7fd66273
Autor:
Chandreshkumar Patel, Anas M. Khanshour, David Wilkes, Jonathan J. Rios, Kelly W. Sheff, Lorien Nassi, Carol A. Wise
Publikováno v:
Clinical Case Reports, Vol 8, Iss 8, Pp 1452-1457 (2020)
Abstract We present the use of whole‐genome sequencing to correctly diagnose progressive pseudorheumatoid dysplasia in patients with atypical clinical and radiologic findings and prior diagnosis of juvenile idiopathic arthritis.
Externí odkaz:
https://doaj.org/article/76be860ad0644cd09a25ceb24f6f4175
Autor:
Hao Yu, Anas M. Khanshour, Aki Ushiki, Nao Otomo, Yoshinao Koike, Elisabet Einarsdottir, Yanhui Fan, Lilian Antunes, Yared H. Kidane, Reuel Cornelia, Rory Sheng, Yichi Zhang, Jimin Pei, Nick V. Grishin, Bret M. Evers, Jason Pui Yin Cheung, John A. Herring, Chikashi Terao, You-Qiang Song, Christina A. Gurnett, Paul Gerdhem, Shiro Ikegawa, Jonathan J. Rios, Nadav Ahituv, Carol A. Wise
Publikováno v:
bioRxiv
Adolescent idiopathic scoliosis (AIS) is a common and progressive spinal deformity in children that exhibits striking sexual dimorphism, with girls at more than five-fold greater risk of severe disease compared to boys. Despite its medical impact, th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1b6873f64125c5187cc4cbcfa6d92a0
https://europepmc.org/articles/PMC10245954/
https://europepmc.org/articles/PMC10245954/
Autor:
Jakub Cieslak, Lukasz Wodas, Alicja Borowska, Ernest G. Cothran, Anas M. Khanshour, Mariusz Mackowski
Publikováno v:
PeerJ, Vol 5, p e3714 (2017)
The Polish Primitive Horse (PPH, Konik) is a Polish native horse breed managed through a conservation program mainly due to its characteristic phenotype of a primitive horse. One of the most important goals of PPH breeding strategy is the preservatio
Externí odkaz:
https://doaj.org/article/edf6db9e78ba4cc2bd231e89c4f4b9b1
Autor:
Anas M. Khanshour, Yongbo Lu, Xudong Xie, Stephen Aplin Lyon, Jamie Russell, Bruce Beutler, Eva Marie Y. Moresco, Aysha B. Khalid, Yang Li, Nandina Paria, Qian Xu, Jian Q. Feng, Joshua E. Mayfield, Kristin Denton, Xiaohong Li, Julia Kozlitina, Robert E. Hammer, Sara Ludwig, Jonathan J. Rios, Amy F Lewanda, Carol Wise, Carlos Ferreira, Miao Tang
Publikováno v:
J Bone Miner Res
Proper embryonic and postnatal skeletal development require coordination of myriad complex molecular mechanisms. Disruption of these processes, through genetic mutation, contributes to variation in skeletal development. We developed a high-throughput
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1ad0a0b1f88f6e3ac5156b58cc85e92
https://doi.org/10.1002/jbmr.4323
https://doi.org/10.1002/jbmr.4323
Publikováno v:
Diversity, Vol 11, Iss 10, p 174 (2019)
The Cleveland Bay (CB) is the United Kingdom’s oldest established horse breed. In this study we analyzed the genetic variability in CB horses and investigated its genetic relationships with other horse breeds. We examined the genetic variability am
Externí odkaz:
https://doaj.org/article/9f0df94651304763bbb78af85317a6cd
Autor:
Jennifer E. Posey, Yu Zheng, V. Reid Sutton, Yipeng Wang, Jia Liu, Hong Zhao, Yuan Xu, Jiachen Lin, Yuchen Niu, Jianxiong Shen, Xiaoxin Li, Weisheng Chen, Lichao Jin, Zhihong Wu, Zefu Chen, Shugang Li, Brandon A. Ramo, Yingzhao Huang, Yong Wu, Yongyu Ye, Sen Zhao, Jianzhong Su, James R. Lupski, Zhe Liu, Shuyang Zhang, Ying Liu, Guanfeng Lin, Na Zhang, Zhen Zhang, Jianhua Hu, Zihui Yan, Anas M. Khanshour, Bin Yu, Nan Wu, Yu Zhao, Yuanqiang Zhang, Zhaoyang Wang, Lianlei Wang, Hengqiang Zhao, Yared H. Kidane, Sen Liu, Mao Lin, Feng Zhang, Ying Yang, Na Gao, Guixing Qiu, Wenli Li, Yanxue Zhao, Weiyu Li, Pengfei Liu, Xu Yang, Jonathan J. Rios, Jingdan Chen, Jianguo Zhang, Renqian Du, Ye Tian, Carol Wise, Jiaqi Liu, Shengru Wang, Keyi Yu, Yongxin Yang
Publikováno v:
J Med Genet
BackgroundEarly-onset scoliosis (EOS), defined by an onset age of scoliosis less than 10 years, conveys significant health risk to affected children. Identification of the molecular aetiology underlying patients with EOS could provide valuable inform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08b7224b1ec51c0e87bdde1c1f2f2584
https://doi.org/10.1136/jmedgenet-2019-106823
https://doi.org/10.1136/jmedgenet-2019-106823
Autor:
Jonathan J. Rios, Carlos Ferreira, Stephen Aplin Lyon, Robert E. Hammer, Amy F Lewanda, Sara Ludwig, Jian Q. Feng, Julia Kozlitina, Anas M. Khanshour, Joshua E. Mayfield, Bruce Beutler, Yang Li, Yongbo Lu, Aysha B. Khalid, Kristin Denton, Xiaohong Li, Qian Xu, Xudong Xie, Carol Wise, Nandina Paria, Miao Tang, Eva Marie Y Moresco, Jamie Russell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ff410a54d9f2df68bc9d204dc324329
https://doi.org/10.1002/jbmr.4323/v2/response1
https://doi.org/10.1002/jbmr.4323/v2/response1
Autor:
Yared H. Kidane, F. Kent Hamra, Alexandra J Rafipay, Jacqueline T. Hecht, Mitchell K. Weston, Jonathan J. Rios, Matthew B. Dobbs, B. Stephens Richards, Nandina Paria, Anas M. Khanshour, Megan J. Wilson, Vanessa De Mello, Aysha B. Khalid, Julia Kozlitina, Neil Vargesson, Christina A. Gurnett, Carol Wise, Reuel Cornelia
Publikováno v:
Hum Mol Genet
Talipes equinovarus (clubfoot, TEV) is a congenital rotational foot deformity occurring in 1 per 1000 births with increased prevalence in males compared with females. The genetic etiology of isolated clubfoot (iTEV) remains unclear. Using a genome-wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9b6ad8a6eb81a1ad80e7c555814e2d9
https://europepmc.org/articles/PMC7823076/
https://europepmc.org/articles/PMC7823076/