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SEPT5
Diminished Dosage of 22Q11 Genes Disrupts Neurogenesis and Cortical Development in a Mouse Model of 22Q11 Deletion/Digeorge Syndrome
Nº Ref Uniprot Proteína Péptidos Identificados Por MS/MS 1 P01024
A Catalog of Hemizygous Variation in 127 22Q11 Deletion Patients
Supplementary Table S1. List of Differentially Expressed
SEPT5 Antibody (N-Term) Affinity Purified Rabbit Polyclonal Antibody (Pab) Catalog # Ap14767a
Parkin Promotes Degradation of the Mitochondrial Pro- Apoptotic ARTS Protein
Mirna and Parkinson's Disease Protein PARK2
Parkin and Relatives: the RBR Family of Ubiquitin Ligases
Expression of Sept3, Sept5a and Sept5b in the Developing and Adult Nervous System of the Zebrafish (Danio Rerio)
Rabbit Polyclonal Antibody – AP53853PU-N
PRODUCT SPECIFICATION Product Datasheet
Interplay of Placental DNA Methylation and Maternal Insulin Sensitivity in Pregnancy
Structural Studies on Mammalian Septins – New Insights Into Filament Formation
MLL-SEPT5 Fusion Transcript in Two De Novo Acute Myeloid Leukemia Patients with T(11;22)(Q23;Q11)
The MLL Recombinome of Acute Leukemias in 2017
Research Article Mir-185 and SEPT5 Genes May Contribute to Parkinson’S Disease Pathophysiology
Rabbit Anti-Phospho-Parkin-SL19881R-FITC
PARK2 / Parkin 2 Antibody (Aa1-50) Rabbit Polyclonal Antibody Catalog # ALS14772
Top View
Cytogenomic SNP Microarray Abnormal * Patient: Patient
Essay Mammalian Septins Nomenclature Ian G
Analyses of the Associations Between the Genes of 22Q11 Deletion Syndrome and Schizophrenia
Interaction of Recombinant Gallus Gallus SEPT5 and Brain Proteins of H5N1-Avian Influenza Virus-Infected Chickens
Interplay of Placental DNA Methylation and Maternal Insulin Sensitivity in Pregnancy Short Title
Anti-Parkin Antibody (ARG58151)
DNA Methylation Signature of Human Hippocampus in Alzheimer's
A Catalog of Hemizygous Variation in 127 22Q11 Deletion Patients
SNP Array Pathogenic
Copy Number Variation at 22Q11.2: from Rare Variants to Common Mechanisms of Developmental Neuropsychiatric Disorders
Atlas Journal
Viewed As a Transcription Silencing Mechanism [11, 12]
Emerging Roles for Septins Julia Gilden and Matthew F
21 (1), 2018 87-92 Acute Pre-B Lymphoblastic Leukemia And
Modeling Chromosomes in Mouse to Explore the Function of Genes
Mouse Models of 22Q11.2-Associated Autism Spectrum Disorder Noboru Hiroi1,2,3*, Takeshi Hiramoto1, Kathryn M
The Septin Cytoskeleton in Heart Development and Disease
From Benign Inflammatory Dermatosis to Cutaneous Lymphoma. DNA Copy Number Imbalances in Mycosis Fungoides Versus Large Plaque P
Linking F-Box Protein 7 and Parkin to Neuronal Degeneration in Parkinson’S Disease (PD) Zhi Dong Zhou1,3*†, Sushmitha Sathiyamoorthy1†, Dario C
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22Q11.2 Deletion Syndrome
The Organization of Human Septin Heterooligomers
Septins Guide Microtubule Protrusions Induced by Actin-Depolymerizing Toxins Like Clostridium Difficile Transferase (CDT)
SEPT5 (SEPTIN5) (NM 002688) Human Tagged ORF Clone Product Data