PMC Links for Nucleotide (Select 1519311559) - PMC

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Items: 6

Select item 26499671.

Identification of Novel Mutations and Sequence Variation in the Zellweger Syndrome Spectrum of Peroxisome Biogenesis Disorders

Wing Yan Yik, Steven J. Steinberg, Ann B. Moser, Hugo W. Moser, Joseph G. Hacia

Hum Mutat. Author manuscript; available in PMC 2009 Mar 2.

Published in final edited form as: Hum Mutat. 2009 Mar; 30(3): E467–E480. doi: 10.1002/humu.20932

PMCID:: PMC2649967

Abstract Article PDF–853K

Select item 1090162.

PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p

Kanji Okumoto, Nobuyuki Shimozawa, Atsusi Kawai, Shigehiko Tamura, Toshiro Tsukamoto, Takashi Osumi, Hugo Moser, Ronald J. A. Wanders, Yasuyuki Suzuki, Naomi Kondo, Yukio Fujiki

Mol Cell Biol. 1998 Jul; 18(7): 4324–4336. doi: 10.1128/mcb.18.7.4324

PMCID:: PMC109016

Abstract Article PDF–3.3M

Select item 61438713.

miR-29b affects neurocyte apoptosis by targeting MCL-1 during cerebral ischemia/reperfusion injury

Zhi Huang, Lu Lu, Tianpeng Jiang, Shuai Zhang, Yaping Shen, Zhu Zheng, Ansu Zhao, Rui Gao, Rui Li, Shi Zhou, Jing Liu

Exp Ther Med. 2018 Oct; 16(4): 3399–3404. Published online 2018 Aug 20. doi: 10.3892/etm.2018.6622

PMCID:: PMC6143871

Abstract Article PDF–902K

Select item 57940574.

Whole exome sequencing in neurogenetic odysseys: An effective, cost- and time-saving diagnostic approach

Marta Córdoba, Sergio Alejandro Rodriguez-Quiroga, Patricia Analía Vega, Valeria Salinas, Josefina Perez-Maturo, Hernán Amartino, Cecilia Vásquez-Dusefante, Nancy Medina, Dolores González-Morón, Marcelo Andrés Kauffman

PLoS One. 2018; 13(2): e0191228. Published online 2018 Feb 1. doi: 10.1371/journal.pone.0191228