PMC Articles for MedGen (Select 435866) - PMC

Select item 34197301.

NRFL-1, the C. elegans NHERF Orthologue, Interacts with Amino Acid Transporter 6 (AAT-6) for Age-Dependent Maintenance of AAT-6 on the Membrane

Kohei Hagiwara, Shushi Nagamori, Yasuhiro M. Umemura, Ryuichi Ohgaki, Hidekazu Tanaka, Daisuke Murata, Saya Nakagomi, Kazuko H. Nomura, Eriko Kage-Nakadai, Shohei Mitani, Kazuya Nomura, Yoshikatsu Kanai

PLoS One. 2012; 7(8): e43050. Published online 2012 Aug 15. doi: 10.1371/journal.pone.0043050

PMCID:: PMC3419730

Article PDF–2.3M

Select item 30320522.

Genome-wide RNAi screens in African trypanosomes identify the nifurtimox activator NTR and the eflornithine transporter AAT6

Nicola Baker, Sam Alsford, David Horn

Mol Biochem Parasitol. 2011 Mar; 176(1): 55–57. doi: 10.1016/j.molbiopara.2010.11.010

PMCID:: PMC3032052

Article

Select item 96123733.

Systematic Review and Meta-Analysis on Human African Trypanocide Resistance

Keneth Iceland Kasozi, Ewan Thomas MacLeod, Susan Christina Welburn

Pathogens. 2022 Oct; 11(10): 1100. Published online 2022 Sep 25. doi: 10.3390/pathogens11101100

PMCID:: PMC9612373

Article PDF–760K

Select item 62841984.

The Reproduction Rate of Peptide Transporter PEPT-1 Deficient C. elegans Is Dependent on Dietary Glutamate Supply

Britta Spanier, Jacqueline Wallwitz, Despoina Zapoglou, Bio Maria Ghéo Idrissou, Christine Fischer, Martina Troll, Katrin Petzold, Hannelore Daniel

Front Mol Biosci. 2018; 5: 109. Published online 2018 Nov 30. doi: 10.3389/fmolb.2018.00109

PMCID:: PMC6284198

Article PDF–1.9M

Select item 99318275.

Familial acute aortic dissection associated with a novel ACTA2 germline variant

Thomas Strecker, Felix Wiesmueller, Sabine Rudnik-Schöneborn, Juliane Hoyer, André Reis, Michael Weyand, Abbas Agaimy

Virchows Arch. 2023; 482(2): 437–443. Published online 2022 Jul 28. doi: 10.1007/s00428-022-03366-9

PMCID:: PMC9931827

Article PDF–1.1M

Select item 58562136.

Fatal thoracic aortic aneurysm and dissection in a large family with a novel MYLK gene mutation: delineation of the clinical phenotype

Adel Shalata, Mohammad Mahroom, Dianna M. Milewicz, Gong Limin, Fadi Kassum, Khader Badarna, Nader Tarabeih, Nimmer Assy, Rona Fell, Hector Cohen, Munir Nashashibi, Alejandro Livoff, Muhammad Azab, George Habib, Dan Geiger, Omer Weissbrod, William Nseir

Orphanet J Rare Dis. 2018; 13: 41. Published online 2018 Mar 15. doi: 10.1186/s13023-018-0769-7

PMCID:: PMC5856213

Article PDF–2.3M

Select item 55147407.

Vascular disease-causing mutation, smooth muscle α-actin R258C, dominantly suppresses functions of α-actin in human patient fibroblasts

Zhenan Liu, Audrey N. Chang, Frederick Grinnell, Kathleen M. Trybus, Dianna M. Milewicz, James T. Stull, Kristine E. Kamm

Proc Natl Acad Sci U S A. 2017 Jul 11; 114(28): E5569–E5578. Published online 2017 Jun 26. doi: 10.1073/pnas.1703506114

PMCID:: PMC5514740

Article PDF–2.5M

Select item 49502388.

Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm

Tie Ke, Meng Han, Miao Zhao, Qing Kenneth Wang, Huazhi Zhang, Yuanyuan Zhao, Xinlong Ruan, Hui Li, Chengqi Xu, Tucheng Sun

BMC Med Genet. 2016; 17: 45. Published online 2016 Jul 18. doi: 10.1186/s12881-016-0310-6

PMCID:: PMC4950238

Article PDF–2.8M

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