DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» Atlastin
Atlastin
The N-Cadherin Interactome in Primary Cardiomyocytes As Defined Using Quantitative Proximity Proteomics Yang Li1,*, Chelsea D
A Missense Mutation in SLC33A1, Which Encodes the Acetyl-Coa Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42)
220 Patients with Autosomal Dominant Spastic
Genetic Mapping of a Susceptibility Locus for Disc Herniation and Spastic
Hereditary Spastic Paraplegia: from Genes, Cells and Networks to Novel Pathways for Drug Discovery
A Gain-Of-Function Screen to Identify Genes That Reduce Lifespan in The
A Sleeping Beauty Transposon-Mediated Screen Identifies Murine Susceptibility Genes for Adenomatous Polyposis Coli (Apc)-Dependent Intestinal Tumorigenesis
Atlastin-Mediated Membrane Tethering Is Critical for Cargo Mobility and Exit from the Endoplasmic Reticulum
Circadian Clock-Dependent and -Independent Rhythmic Proteomes Implement Distinct Diurnal Functions in Mouse Liver
Relationship Between Domains of the ER Membrane Protein Atlastin
Comparison of Human and Drosophila Atlastin Gtpases
12728 Atlastin-1 (D2E6) Rabbit Mab
Structures of the Atlastin Gtpase Provide Insight Into Homotypic Fusion of Endoplasmic Reticulum Membranes
Alu-Specific Microhomology-Mediated Deletion of the Final Exon of SPAST in Three Unrelated Subjects with Hereditary Spastic Paraplegia Philip M
Evidence for Autosomal Recessive Inheritance in SPG3A Caused by Homozygosity for a Novel ATL1 Missense Mutation
FARE2015 WINNERS Sorted by Study Section
Modelling Hereditary Spastic Paraplegias Using Human Pluripotent Stem Cells Kyle Denton University of Connecticut - Storrs,
[email protected]
Effects of Cold Exposure Revealed by Global Transcriptomic Analysis In
Top View
Mutations in the ER-Shaping Protein Reticulon 2 Cause the Axon- Degenerative Disorder Hereditary Spastic Paraplegia Type 12
Platform Abstracts
Common Molecular Pathological Themes Emerge in the Hereditary Spastic Paraplegias E Reid
NDKB and Atlastin Structure Endoplasmic Reticulum Membranes
Clinical and Genetic Analysis of a Korean Family with Hereditary Spastic Paraplegia Type 3
The 15Q11.2 BP1-BP2 Microdeletion
Atlastin-1 Antibody
De Novo Occurrence of Novel SPG3A/Atlastin Mutation Presenting As Cerebral Palsy
Atlastin-Mediated Membrane Tethering Is Critical for Cargo Mobility and Exit from the Endoplasmic Reticulum
ATL1 Gene Atlastin Gtpase 1
The 2020 Version of the Gene Table of Neuromuscular Disorders (Nuclear Genome) Louise Benarroch, Gisèle Bonne, Francois Rivier, Dalil Hamroun
Integrated Computational Analysis of Genes Associated with Human Hereditary Insensitivity to Pain
University of Florida Thesis Or Dissertation Formatting
Rabbitmab Severe Progressivespasticityofthelowerlimbs(5,6)
Clinical and Genetic Heterogeneity in Hereditary Spastic Paraplegias: from SPG1 to SPG72 and Still Counting Stephan Klebe, Giovanni Stevanin, Christel Depienne
Integrated Analysis of Proteomics Data to Assess and Improve the Scope of Mass Spectrometry Based Genome Annotation
Weighted Gene Co-Expression Network Analysis Identi Es Speci C
Atlastin-2 (D-12): Sc-109213