Results 111 to 120 of about 1,816 (142)

Bioinformatics Analysis of Peroxisomal Biogenesis Factor Proteins in Breast Malignancy for Introducing Potential Prognostic Biomarkers. [PDF]

Iran J Pathol
Mahdei Nasirmahalleh N, Hemmati M, Parsamanesh N.   +2 more
europepmc   +1 more source

Engineering yeast peroxisome assembly enables the increased production of acetyl-CoA and its derived 5-deoxyflavonoids. [PDF]

Nat Commun
Li Y, Du B, Li C, Feng X.
europepmc   +1 more source

Pigmentary retinal dystrophy associated with peroxisome biogenesis disorder-Zellweger syndrome spectrum. [PDF]

Oxf Med Case Reports
Zou H, Sutherland L, Geddie B.
europepmc   +1 more source

Zebrafish Mib Promotes Long-Distance Transport of Jagged2 Via Extracellular Vesicles. [PDF]

Dev Reprod
Hong JY, Won SY, Lee JJ, Ryu JH, Park Y, Kim SH, Cho HJ, Yeo SY.   +7 more
europepmc   +1 more source

Wide transcriptional outlook to uncover Penicillium expansum genes underlying fungal incompatible infection. [PDF]

Heliyon
de Ramón-Carbonell M, Sánchez-Torres P.   +1 more
europepmc   +1 more source

Jalili syndrome: Sibling cases with variable phenotypes. [PDF]

Indian J Ophthalmol
Sharda S, Bharti N.
europepmc   +1 more source

Long non-coding SINEUP RNA enhancing BDNF translation prevents dendritic atrophy following an Aβ-peptide challenge. [PDF]

Cell Mol Life Sci
Atzori M, Fabbretti E, Ciraci V, Zucchelli S, Bon C, Mikašinović S, Baj G, Gustincich S, Tongiorgi E.   +8 more
europepmc   +1 more source

Mammalian pexophagy at a glance.

J Cell Sci
Bajdzienko J, Bremm A.
europepmc   +1 more source

Structural Mapping of Missense Mutations in the Pex1/Pex6 Complex [PDF]

International Journal of Molecular Sciences, 2019
Peroxisome biogenesis disorders (PBDs) are nontreatable hereditary diseases with a broad range of severity. Approximately 65% of patients are affected by mutations in the peroxins Pex1 and Pex6.
Petra Wendler
exaly   +7 more sources

PEX1mutations in the Zellweger spectrum of the peroxisome biogenesis disorders

Human Mutation, 2005
Diseases of the Zellweger spectrum represent a major subgroup of the peroxisome biogenesis disorders, a group of autosomal-recessive diseases that are characterized by widespread tissue pathology, including neurodegeneration.
Denis Crane
exaly   +6 more sources