Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Wilfred Wu"'
Autor:
Chen-Han Wilfred Wu, Alicja Tomaszewski, Louisa Stark, Fernando Scaglia, Ewa Elenberg, Fredrick R. Schumaker
Publikováno v:
Frontiers in Genetics, Vol 15 (2024)
Genetic variability persists across diverse populations, and it may impact the characterization of heritable diseases in different ancestral groups. Cystinosis is a metabolic disease caused by pathogenic variants in the CTNS gene causing the cellular
Externí odkaz:
https://doaj.org/article/8fae72ba3cf744279b4ad06a791a86ad
Autor:
Wilfred Wu, Chen-Han, Patel, Ishita, Lovrenert, Katreya, Eisner, Brian, Meeks, Naomi, Chun-Hui Tsai, Anne, Baum, Michelle, Berry, Gerard, Schumacher, Fredrick R.
Publikováno v:
In Genetics in Medicine January 2025 27(1)
Autor:
Ishita Patel, Ethan Su, Katreya Lovrenert, Donald Bodner, Fredrick Schumacher, Chen-Han Wilfred Wu
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101165- (2024)
Externí odkaz:
https://doaj.org/article/22b1733dcfb14598990b749932a88fd1
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101158- (2024)
Externí odkaz:
https://doaj.org/article/21af165f755a435aac99331ac0aed318
Autor:
Isali, Ilaha, McClellan, Phillip, Wong, Thomas R., Sun, Clara, Stout, Amber Catherine, Schumacher, Fredrick R., Markt, Sarah, Wilfred Wu, Chen-Han, Penney, Kathryn L., El-Nashar, Sherif, Hijaz, Adonis, Sheyn, David
Publikováno v:
In American Journal of Obstetrics and Gynecology January 2023 228(1):36-47
Autor:
Chen-Han Wilfred Wu, Tze Y. Lim, Chunyan Wang, Steve Seltzsam, Bixia Zheng, Luca Schierbaum, Sophia Schneider, Nina Mann, Dervla M. Connaughton, Makiko Nakayama, Amelie T. van der Ven, Rufeng Dai, Caroline M. Kolvenbach, Franziska Kause, Isabel Ottlewski, Natasa Stajic, Neveen A. Soliman, Jameela A. Kari, Sherif El Desoky, Hanan M. Fathy, Danko Milosevic, Daniel Turudic, Muna Al Saffar, Hazem S. Awad, Loai A. Eid, Aravind Ramanathan, Prabha Senguttuvan, Shrikant M. Mane, Richard S. Lee, Stuart B. Bauer, Weining Lu, Alina C. Hilger, Velibor Tasic, Shirlee Shril, Simone Sanna-Cherchi, Friedhelm Hildebrandt
Publikováno v:
European Urology Open Science, Vol 44, Iss , Pp 106-112 (2022)
Background: Congenital anomalies of the kidneys and urinary tract (CAKUT) are the most common cause of chronic kidney disease among children and adults younger than 30 yr. In our previous study, whole-exome sequencing (WES) identified a known monogen
Externí odkaz:
https://doaj.org/article/3efb0bd1ab7841249ffc6b6938766552
Autor:
Joshua Chang, Jad Badreddine, Euhun Eam, Katreya Lovrenert, Donald Bodner, Friedhelm Hildebrandt, Fredrick Schumacher, Chen-Han Wilfred Wu
Publikováno v:
Genetics in Medicine Open, Vol 1, Iss 1, Pp 100019- (2023)
Externí odkaz:
https://doaj.org/article/8253c9df2a964bd6b20aaea2cd714fe0
Autor:
Ching-Shuen Wang, Shen-Dean Luo, Shihai Jia, Wilfred Wu, Shwu-Fen Chang, Sheng-Wei Feng, Chieh-Hsiang Yang, Jiann-Her Lin, Yinshen Wee
Publikováno v:
Antioxidants, Vol 11, Iss 12, p 2351 (2022)
Uncontrolled and sustained inflammation disrupts the wound-healing process and produces excessive reactive oxygen species, resulting in chronic or impaired wound closure. Natural antioxidants such as plant-based extracts and natural polysaccharides h
Externí odkaz:
https://doaj.org/article/e37c0ba23bc04504b3531cecd6ebda1f
Autor:
Patel, Ishita, Su, Ethan, Lovrenert, Katreya, Bodner, Donald, Schumacher, Fredrick, Wilfred Wu, Chen-Han
Publikováno v:
In Genetics in Medicine Open 2024 2 Supplement 1
Publikováno v:
In Genetics in Medicine Open 2024 2 Supplement 1