PMC Links for Nucleotide (Select 1676319451) - PMC

Select item 59184161.

A Neurodegenerative Mitochondrial Disease Phenotype Due to Biallelic Loss-of-function Variants in PNPLA8 Encoding Calcium-independent Phospholipase A2γ

Anju Shukla, Russell P Saneto, Malavika Hebbar, Ghayda Mirzaa, Katta M Girisha

Am J Med Genet A. Author manuscript; available in PMC 2019 May 1.

Published in final edited form as: Am J Med Genet A. 2018 May; 176(5): 1232–1237. doi: 10.1002/ajmg.a.38687

PMCID:: PMC5918416

Article PDF–659K

Select item 57669132.

Heart failure–induced activation of phospholipase iPLA₂γ generates hydroxyeicosatetraenoic acids opening the mitochondrial permeability transition pore

Sung Ho Moon, Xinping Liu, Ari M. Cedars, Kui Yang, Michael A. Kiebish, Susan M. Joseph, John Kelley, Christopher M. Jenkins, Richard W. Gross

J Biol Chem. 2018 Jan 5; 293(1): 115–129. Published online 2017 Nov 20. doi: 10.1074/jbc.RA117.000405

PMCID:: PMC5766913

Article PDF–1.1M

Select item 43613073.

Loss of function variants in human PNPLA8 encoding calcium-independent phospholipase A₂γ recapitulate the mitochondriopathy of the homologous null mouse

Carol J. Saunders, Sung Ho Moon, Xinping Liu, Isabelle Thiffault, Keith Coffman, Jean-Baptiste LePichon, Eugenio Taboada, Laurie D. Smith, Emily G. Farrow, Neil Miller, Margaret Gibson, Melanie Patterson, Stephen F. Kingsmore, Richard W. Gross

Hum Mutat. Author manuscript; available in PMC 2016 Mar 1.

Published in final edited form as: Hum Mutat. 2015 Mar; 36(3): 301–306. doi: 10.1002/humu.22743

Correction in:: volume 36 on page 656

PMCID:: PMC4361307

Article PDF–506K

Select item 41969024.

Group VIB Calcium-Independent Phospholipase A₂ (iPLA₂γ) Regulates Platelet Activation, Hemostasis and Thrombosis in Mice

Emiko Yoda, Kohmi Rai, Mai Ogawa, Yuki Takakura, Hiroshi Kuwata, Hidenori Suzuki, Yoshihito Nakatani, Makoto Murakami, Shuntaro Hara

PLoS One. 2014; 9(10): e109409. Published online 2014 Oct 14. doi: 10.1371/journal.pone.0109409

PMCID:: PMC4196902

Article PDF–1.2M

Select item 36039895.

Fine Mapping for Weaver Syndrome in Brown Swiss Cattle and the Identification of 41 Concordant Mutations across NRCAM, PNPLA8 and CTTNBP2

Matthew McClure, Euisoo Kim, Derek Bickhart, Daniel Null, Tabatha Cooper, John Cole, George Wiggans, Paolo Ajmone-Marsan, Licia Colli, Enrico Santus, George E. Liu, Steve Schroeder, Lakshmi Matukumalli, Curt Van Tassell, Tad Sonstegard

PLoS One. 2013; 8(3): e59251. Published online 2013 Mar 20. doi: 10.1371/journal.pone.0059251

PMCID:: PMC3603989

Article PDF–923K

Select item 10837326.

Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing

Jeremy C. Simpson, Ruth Wellenreuther, Annemarie Poustka, Rainer Pepperkok, Stefan Wiemann

EMBO Rep. 2000 Sep 15; 1(3): 287–292. doi: 10.1093/embo-reports/kvd058

PMCID:: PMC1083732

Article PDF–375K

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