UQCRH downregulation promotes Warburg effect in renal cell carcinoma cells

Journal Article published Dec 2020 in Scientific Reports volume 10 issue 1

Research funded by Boler-Parseghian Center for Rare and Neglected Diseases | Mike and Josie Harper Cancer Research Institute | Boler Family Foundation

Authors: Yanting Luo, Louise Medina Bengtsson, Xuechun Wang, Tianhe Huang, Guoqiang Liu, Sean Murphy, Caiqin Wang, John Koren, Zachary Schafer, Xin Lu

Trace element content of Zingiber officinalis and Salvia officinalis medicinal plants from Algeria

Journal Article published Jul 2016 in Journal of Radioanalytical and Nuclear Chemistry volume 309 issue 1 on pages 17 to 22

Research funded by Boler-Parseghian Center for Rare and Neglected Diseases (500 EU) | Comena /Centre de Recherche Nucléaire de Draria (850 EU) | CRND-CRNA (400)

Authors: Z. Lamari, R. Larbi, H. Negache

Algorithmic assessment of missense mutation severity in the Von-Hippel Lindau protein

Journal Article published 5 Nov 2020 in PLOS ONE volume 15 issue 11 on page e0234100

Research funded by Boler-Parseghian Center for Rare and Neglected Diseases (Pilot Study Award)

Authors: Francisco R. Fields, Niraja Suresh, Morgan Hiller, Stefan D. Freed, Kasturi Haldar, Shaun W. Lee

Editors: Ramin Massoumi

Case report: a synonymous VHL mutation (c.414A > G, p.Pro138Pro) causes pathogenic familial hemangioblastoma through dysregulated splicing

Journal Article published Dec 2020 in BMC Medical Genetics volume 21 issue 1

Research funded by Boler Family Foundation | Boler-Parseghian Center for Rare and Neglected Diseases | China Scholarship Council (201708340071) | National Key Research and Development Program of China Stem Cell and Translational Research (2017YFA0103902)

Authors: Fang Liu, Barbara Calhoun, Md. Suhail Alam, Miaomiao Sun, Xuechun Wang, Chao Zhang, Kasturi Haldar, Xin Lu