PMC Links for Protein (Select 52486194) - PMC

Select item 66782821.

Possible Involvement of Intracellular Calcium-Independent Phospholipase A₂ in the Release of Secretory Phospholipases from Mast Cells—Increased Expression in Ileal Mast Cells of Crohn’s Disease

Ulrika Christerson, Åsa V. Keita, Martin E. Winberg, Johan D. Söderholm, Christina Gustafson-Svärd

Cells. 2019 Jul; 8(7): 672. Published online 2019 Jul 3. doi: 10.3390/cells8070672

PMCID:: PMC6678282

Abstract Article PDF–3.7M

Select item 37159972.

Human Pancreatic Islets Express mRNA Species Encoding Two Distinct Catalytically Active Isoforms of Group VI Phospholipase A₂ (iPLA₂) That Arise from an Exon-skipping Mechanism of Alternative Splicing of the Transcript from the iPLA₂ Gene on Chromosome 22q13.1

Zhongmin Ma, Xiying Wang, William Nowatzke, Sasanka Ramanadham, John Turk

J Biol Chem. Author manuscript; available in PMC 2013 Jul 19.

Published in final edited form as: J Biol Chem. 1999 Apr 2; 274(14): 9607–9616. doi: 10.1074/jbc.274.14.9607

PMCID:: PMC3715997

Abstract Article PDF–1.4M

Select item 21173283.

PLA2G6, encoding a phospholipase A₂, is mutated in neurodegenerative disorders with high brain iron

Neil V Morgan, Shawn K Westaway, Jenny E V Morton, Allison Gregory, Paul Gissen, Scott Sonek, Hakan Cangul, Jason Coryell, Natalie Canham, Nardo Nardocci, Giovanna Zorzi, Shanaz Pasha, Diana Rodriguez, Isabelle Desguerre, Amar Mubaidin, Enrico Bertini, Richard C Trembath, Alessandro Simonati, Carolyn Schanen, Colin A Johnson, Barbara Levinson, C Geoffrey Woods, Beth Wilmot, Patricia Kramer, Jane Gitschier, Eamonn R Maher, Susan J Hayflick

Nat Genet. Author manuscript; available in PMC 2007 Dec 5.

Published in final edited form as: Nat Genet. 2006 Jul; 38(7): 752–754. Published online 2006 Jun 18. doi: 10.1038/ng1826

Correction in:: volume 38 on page 957

PMCID:: PMC2117328

Abstract Article PDF–452K

Select item 67129224.

Atypical Childhood-onset Neuroaxonal Dystrophy in an Indian Girl

Sakshi Jain, Himani Bhasin, Marta Romani, Enza maria valente, Suvasini Sharma

J Pediatr Neurosci. 2019 Apr-Jun; 14(2): 90–93. doi: 10.4103/jpn.JPN_91_18

PMCID:: PMC6712922

Abstract Article

Select item 60482715.

Heterozygous PLA2G6 Mutation Leads to Iron Accumulation Within Basal Ganglia and Parkinson's Disease

Rosangela Ferese, Simona Scala, Francesca Biagioni, Emiliano Giardina, Stefania Zampatti, Nicola Modugno, Claudio Colonnese, Marianna Storto, Francesco Fornai, Giuseppe Novelli, Stefano Ruggieri, Stefano Gambardella

Front Neurol. 2018; 9: 536. Published online 2018 Jul 10. doi: 10.3389/fneur.2018.00536

PMCID:: PMC6048271

Abstract Article PDF–1.0M

Select item 55974576.

PLA2G6 MUTATIONS ASSOCIATED WITH A CONTINUOUS CLINICAL SPECTRUM FROM NEUROAXONAL DYSTROPHY TO HEREDITARY SPASTIC PARAPLEGIA

Burcak Ozes, Nazan Karagoz, Rebecca Schüle, Adriana Rebelo, María-Jesús Sobrido, Florian Harmuth, Matthis Synofzik, Samuel Ignacio Pascual Pascual, Melek Colak, Beyza Ciftci-Kavaklioglu, Batuhan Kara, Andrés Ordóñez-Ugalde, Beatriz Quintáns, Michael A. Gonzalez, Aysun Soysal, Stephan Zuchner, Esra Battaloglu

Clin Genet. Author manuscript; available in PMC 2018 Nov 1.

Published in final edited form as: Clin Genet. 2017 Nov; 92(5): 534–539. Published online 2017 Apr 19. doi: 10.1111/cge.13008

PMCID:: PMC5597457

Abstract Article PDF–549K

Select item 47855357.

Novel PLA2G6 mutations associated with an exonic deletion due to non-allelic homologous recombination in a patient with infantile neuroaxonal dystrophy

Toshiyuki Yamamoto, Keiko Shimojima, Takashi Shibata, Mari Akiyama, Makio Oka, Tomoyuki Akiyama, Harumi Yoshinaga, Katsuhiro Kobayashi

Hum Genome Var. 2015; 2: 15048. Published online 2015 Nov 19. doi: 10.1038/hgv.2015.48

PMCID:: PMC4785535

Abstract Article PDF–1.4M

Select item 43144158.

Phylogenetic and structural analysis of the phospholipase A2 gene family in vertebrates

QI HUANG, YUAN WU, CHAO QIN, WENWU HE, XING WEI

Int J Mol Med. 2015 Mar; 35(3): 587–596. Published online 2014 Dec 23. doi: 10.3892/ijmm.2014.2047

PMCID:: PMC4314415

Abstract Article PDF–2.0M

Select item 16985589.

PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy

Shareef Khateeb, Hagit Flusser, Rivka Ofir, Ilan Shelef, Ginat Narkis, Gideon Vardi, Zamir Shorer, Rachel Levy, Aharon Galil, Khalil Elbedour, Ohad S. Birk

Am J Hum Genet. 2006 Nov; 79(5): 942–948. Published online 2006 Sep 19. doi: 10.1086/508572

PMCID:: PMC1698558

Abstract Article PDF–2.4M

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