Fatty Acid Oxidation-Driven Src Links Mitochondrial Energy Reprogramming and Oncogenic Properties in Triple-Negative Breast Cancer
Park, Jun Hyoung, Vithayathil, Sajna, Kumar, Santosh, Sung, Pi-Lin, Dobrolecki, Lacey Elizabeth, Putluri, Vasanta, Bhat, Vadiraja B., Bhowmik, Salil Kumar, Gupta, Vineet, Arora, Kavisha, Wu, Danli, Tsouko, Efrosini, Zhang, Yiqun, Maity, Suman, Donti, Taraka R., Graham, Brett H., Frigo, Daniel E., Coarfa, Cristian, Yotnda, Patricia, Putluri, Nagireddy, Sreekumar, Arun, Lewis, Michael T., Creighton, Chad J., Wong, Lee-Jun C., Kaipparettu, Benny Abraham
Published in Cell reports (Cambridge) (08.03.2016)
Published in Cell reports (Cambridge) (08.03.2016)
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Biparental Inheritance of Mitochondrial DNA in Humans
Luo, Shiyu, Valencia, C. Alexander, Zhang, Jinglan, Lee, Ni-Chung, Slone, Jesse, Gui, Baoheng, Wang, Xinjian, Li, Zhuo, Dell, Sarah, Brown, Jenice, Chen, Stella Maris, Chien, Yin-Hsiu, Hwu, Wuh-Liang, Fan, Pi-Chuan, Wong, Lee-Jun, Atwal, Paldeep S., Huang, Taosheng
Published in Proceedings of the National Academy of Sciences - PNAS (18.12.2018)
Published in Proceedings of the National Academy of Sciences - PNAS (18.12.2018)
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Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA
Zhang, Jinglan, Li, Jianli, Saucier, Jennifer B, Feng, Yanming, Jiang, Yanjun, Sinson, Jefferson, McCombs, Anne K, Schmitt, Eric S, Peacock, Sandra, Chen, Stella, Dai, Hongzheng, Ge, Xiaoyan, Wang, Guoli, Shaw, Chad A, Mei, Hui, Breman, Amy, Xia, Fan, Yang, Yaping, Purgason, Anne, Pourpak, Alan, Chen, Zhao, Wang, Xia, Wang, Yue, Kulkarni, Shashikant, Choy, Kwong Wai, Wapner, Ronald J, Van den Veyver, Ignatia B, Beaudet, Arthur, Parmar, Sheetal, Wong, Lee-Jun, Eng, Christine M
Published in Nature medicine (01.03.2019)
Published in Nature medicine (01.03.2019)
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Hepatocellular carcinoma associated with tight‐junction protein 2 deficiency
Zhou, Shengmei, Hertel, Paula M., Finegold, Milton J., Wang, Larry, Kerkar, Nanda, Wang, Jing, Wong, Lee‐Jun C., Plon, Sharon E., Sambrotta, Melissa, Foskett, Pierre, Niu, Zhiyv, Thompson, Richard J., Knisely, A.S.
Published in Hepatology (Baltimore, Md.) (01.12.2015)
Published in Hepatology (Baltimore, Md.) (01.12.2015)
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Clinical and laboratory interpretation of mitochondrial mRNA variants
Wong, Lee‐Jun C., Chen, Ting, Schmitt, Eric S., Wang, Jing, Tang, Sha, Landsverk, Megan, Li, Fangyuan, Zhang, Shulin, Wang, Yue, Zhang, Victor W., Craigen, William J.
Published in Human mutation (01.10.2020)
Published in Human mutation (01.10.2020)
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Small heterodimer partner deletion prevents hepatic steatosis and when combined with farnesoid X receptor loss protects against type 2 diabetes in mice
Akinrotimi, Oludemilade, Riessen, Ryan, VanDuyne, Philip, Park, Jung Eun, Lee, Yoon Kwang, Wong, Lee‐Jun, Zavacki, Ann M., Schoonjans, Kristina, Anakk, Sayeepriyadarshini
Published in Hepatology (Baltimore, Md.) (01.12.2017)
Published in Hepatology (Baltimore, Md.) (01.12.2017)
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Crosstalk from non-cancerous mitochondria can inhibit tumor properties of metastatic cells by suppressing oncogenic pathways
Kaipparettu, Benny Abraham, Ma, Yewei, Park, Jun Hyoung, Lee, Tin-Lap, Zhang, Yiqun, Yotnda, Patricia, Creighton, Chad J, Chan, Wai-Yee, Wong, Lee-Jun C
Published in PloS one (09.05.2013)
Published in PloS one (09.05.2013)
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MPV17‐related mitochondrial DNA maintenance defect: New cases and review of clinical, biochemical, and molecular aspects
El‐Hattab, Ayman W., Wang, Julia, Dai, Hongzheng, Almannai, Mohammed, Staufner, Christian, Alfadhel, Majid, Gambello, Michael J., Prasun, Pankaj, Raza, Saleem, Lyons, Hernando J., Afqi, Manal, Saleh, Mohammed A. M., Faqeih, Eissa A., Alzaidan, Hamad I., Alshenqiti, Abduljabbar, Flore, Leigh Anne, Hertecant, Jozef, Sacharow, Stephanie, Barbouth, Deborah S., Murayama, Kei, Shah, Amit A., Lin, Henry C., Wong, Lee‐Jun C.
Published in Human mutation (01.04.2018)
Published in Human mutation (01.04.2018)
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Interpretation of mitochondrial tRNA variants
Wong, Lee-Jun C, Chen, Ting, Wang, Jing, Tang, Sha, Schmitt, Eric S, Landsverk, Megan, Li, Fangyuan, Wang, Yue, Zhang, Shulin, Zhang, Victor Wei, Craigen, William J
Published in Genetics in medicine (01.05.2020)
Published in Genetics in medicine (01.05.2020)
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ADIPOR1 Is Mutated in Syndromic Retinitis Pigmentosa
Xu, Mingchu, Eblimit, Aiden, Wang, Jing, Li, Jianli, Wang, Feng, Zhao, Li, Wang, Xia, Xiao, Ningna, Li, Yumei, Wong, Lee-Jun C., Lewis, Richard A., Chen, Rui
Published in Human mutation (01.03.2016)
Published in Human mutation (01.03.2016)
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Quantitative Evaluation of the Mitochondrial DNA Depletion Syndrome
DIMMOCK, David, TANG, Lin-Ya, SCHMITT, Eric S, WONG, Lee-Jun C
Published in Clinical chemistry (Baltimore, Md.) (01.07.2010)
Published in Clinical chemistry (Baltimore, Md.) (01.07.2010)
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Detection and Quantification of Mosaic Mutations in Disease Genes by Next-Generation Sequencing
Qin, Lan, Wang, Jing, Tian, Xia, Yu, Hui, Truong, Cavatina, Mitchell, John J, Wierenga, Klaas J, Craigen, William J, Zhang, Victor Wei, Wong, Lee-Jun C
Published in The Journal of molecular diagnostics : JMD (01.05.2016)
Published in The Journal of molecular diagnostics : JMD (01.05.2016)
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Dependable and efficient clinical utility of target capture-based deep sequencing in molecular diagnosis of retinitis pigmentosa
Wang, Jing, Zhang, Victor W, Feng, Yanming, Tian, Xia, Li, Fang-Yuan, Truong, Cavatina, Wang, Guoli, Chiang, Pei-Wen, Lewis, Richard A, Wong, Lee-Jun C
Published in Investigative ophthalmology & visual science (06.10.2014)
Published in Investigative ophthalmology & visual science (06.10.2014)
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Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States
Miller, Marcus J., Burrage, Lindsay C., Gibson, James B., Strenk, Meghan E., Lose, Edward J., Bick, David P., Elsea, Sarah H., Sutton, V. Reid, Sun, Qin, Graham, Brett H., Craigen, William J., Zhang, Victor Wei, Wong, Lee-Jun C.
Published in Molecular genetics and metabolism (01.11.2015)
Published in Molecular genetics and metabolism (01.11.2015)
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Molecular and clinical genetics of mitochondrial diseases due to POLG mutations
Wong, Lee-Jun C, Naviaux, Robert K, Brunetti-Pierri, Nicola, Zhang, Qing, Schmitt, Eric S, Truong, Cavatina, Milone, Margherita, Cohen, Bruce H, Wical, Beverly, Ganesh, Jaya, Basinger, Alice A, Burton, Barbara K, Swoboda, Kathryn, Gilbert, Donald L, Vanderver, Adeline, Saneto, Russell P, Maranda, Bruno, Arnold, Georgianne, Abdenur, Jose E, Waters, Paula J, Copeland, William C
Published in Human mutation (01.09.2008)
Published in Human mutation (01.09.2008)
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Antimicrobial mitochondrial reactive oxygen species induction by lung epithelial immunometabolic modulation
Wang, Yongxing, Kulkarni, Vikram V, Pantaleón García, Jezreel, Leiva-Juárez, Miguel M, Goldblatt, David L, Gulraiz, Fahad, Vila Ellis, Lisandra, Chen, Jichao, Longmire, Michael K, Donepudi, Sri Ramya, Lorenzi, Philip L, Wang, Hao, Wong, Lee-Jun, Tuvim, Michael J, Evans, Scott E
Published in PLoS pathogens (11.09.2023)
Published in PLoS pathogens (11.09.2023)
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