ISSN: 1933-6896

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Prion Q2 Unclaimed

Landes Bioscience United States

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Prion is a journal indexed in SJR in Cell Biology and Biochemistry with an H index of 50. It has an SJR impact factor of 0,614 and it has a best quartile of Q2. It has an SJR impact factor of 0,614.

Type: Journal

Type of Copyright:

Languages:

Open Access Policy: Open Access

Type of publications:

Publication frecuency: -

Categories: Infectious Diseases (Q2) Biochemistry (Q3) Cell Biology (Q3) Cellular and Molecular Neuroscience (Q4)

Price

- €

Inmediate OA

NPD

Embargoed OA

- €

Non OA

Metrics

0,614

SJR Impact factor

50

H Index

17

Total Docs (Last Year)

70

Total Docs (3 years)

767

Total Refs

156

Total Cites (3 years)

68

Citable Docs (3 years)

1.72

Cites/Doc (2 years)

45.12

Ref/Doc

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Aims and Scope

Best articles by citations

Mouse neuronal cells expressing exogenous bovinePRNPand simultaneous downregulation of endogenous mousePRNPusing siRNAs

Pyrroloquinoline quinone inhibits the fibrillation of amyloid proteins

Fragment molecular orbital calculations reveal that the E200K mutation markedly alters local structural stability in the human prion protein

Interdependence of amyloid formation in yeast

From Molecular Tumors to Protein Genes and Back

Polyglutamine misfolding in yeast: Toxic and protective aggregation

Modeling Huntington disease in yeast: Perspectives and future directions

The yeast prions [PSI+] and [URE3] are molecular degenerative diseases

Amyloid-like assembly of the low complexity domain of yeast Nab3

Flow cytometric quantification and characterization of intracellular protein aggregates in yeast

Influence of prion variant and yeast strain variation on prion-molecular chaperone requirements

beta-amyloid oligomers and prion protein

SHOW MORE ARTICLES

Amyloids and prions in plants: Facts and perspectives

PrP overdrive

Regional distribution of anchorless prion protein, PrP226*, in the human brain

When amyloids become prions

In vitroneutralization of prions with PrPSc-specific antibodies

Nucleic acid-free mutation of prion strains

Countering amyloid polymorphism and drug resistance with minimal drug cocktails

Erratum to: Poster Session PPo1: Protein Misfolding

Metals in obex and retropharyngeal lymph nodes of Illinois white-tailed deer and their variations associated with CWD status

The toxicity of an "artificial" amyloid is related to how it interacts with membranes

A Special focus on Microbial Models for Amyloids and Prions

Yeast prions assembly and propagation: Contributions of the prion and non-prion moieties and the nature of assemblies