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CBLC
Upregulation of E3 Ubiquitin Ligase CBLC Enhances EGFR
Downloaded from the App Store and Nucleobase, Nucleotide and Nucleic Acid Metabolism 7 Google Play
An X-Linked Cobalamin Disorder Caused by Mutations in Transcriptional Coregulator HCFC1
Cysteine-Mediated Decyanation of Vitamin B12 by the Predicted Membrane Transporter Btum
A Graph-Theoretic Approach to Model Genomic Data and Identify Biological Modules Asscociated with Cancer Outcomes
Original Article Genetic Analysis of Four Cases of Methylmalonic Aciduria and Homocystinuria, Cblc Type
Mechanistic Models of Signaling Pathways Reveal the Drug Action Mechanisms Behind Gender-Specific Gene Expression for Cancer Treatments
A PRDX1 Mutant Allele Causes a MMACHC Secondary Epimutation in Cblc Patients
Phenotype Informatics
Three New Cases of Late-Onset Cblc Defect and Review of the Literature
Powerful Gene-Based Testing by Integrating Long-Range Chromatin Interactions and Knockoff Genotypes
A PRDX1 Mutant Allele Causes a MMACHC Secondary Epimutation in Cblc Patients
Characterization of the Mouse Cblc/Cbl3 Gene Frédéric Fiore, Vincent Ollendorff, Daniel Birnbaum
Comprehensive Genetic Diagnosis of Acute Myeloid Leukemia by Next-Generation Sequencing
Genome-Wide Analysis of Genetic Predisposition to Alzheimer's
Anti-CBLC Monoclonal Antibody, Clone 4E0 (DCABH-3476) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
CRISPR and Human Fertility
PRDX1 Gene-Related Epi‑Cblc Disease Is a Common Type of Inborn Error of Cobalamin Metabolism with Mono- Or Bi-Allelic MM
Top View
Proteomics of Vitamin B Processing
Cbl C (CBLC) Mouse Monoclonal Antibody [Clone ID: OTI3D9] Product Data
SALL3 Expression Balance Underlies Lineage Biases in Human Induced Pluripotent Stem Cell Differentiation
Cbl C (CBLC) Mouse Monoclonal Antibody [Clone ID: OTI3B4] Product Data
Cblc (NM 023224) Mouse Tagged ORF Clone Lentiviral Particle – MR220739L3V | Origene
(Cobalamin) Metabolism
Schwann Cell Reprogramming and Lung Cancer Progression: a Meta-Analysis of Transcriptome Data
Molecular Genetic Characterization of Cblc Defects in 126 Pedigrees And
Renal Thrombotic Microangiopathy in Patients with Cblc Defect: Review of an Under-Recognized Entity
Transcriptional Alterations During Mammary Tumor Progression in Mice
METHYLMALONIC ACIDURIAS Mut0/Mut- and Cblc Defects in Portuguese Population
2019 NHGRI Symposium
SRC Antibody Purified Mouse Monoclonal Antibody (Mab) Catalog # Am8694b
Characterization of Patients with Combined Methylmalonic Aciduria and Homocystinuria Diagnosed As Cblc
Cblc (NM 023224) Mouse Tagged ORF Clone – MR220739 | Origene
Ruma Banerjee Carmen Gherasim, Michael Lofgren and Delivery, and Disorders of Cobalamin Road: Assimilation, 12 Navigating the B
Methylmalonic Acidemia with Homocystinuria
American Society of Human Genetics 67Th Annual Meeting October 17–21, 2017 in Orlando, Florida
Gene Expression Profiles for Low-Dose Exposure to Diethyl
CBL Mutation-Related Patterns of Phosphorylation and Sensitivity to Tyrosine Kinase Inhibitors
Supplemental Table 2: UC Vs. NL Gene List Gene Name Symbol
Combined Methylmalonic Aciduria and Homocystinuria Cblc Type of a Taiwanese Infant with C.609G>A and C.567Dupt Mutations in the MMACHC Gene
Anti-CBLC Monoclonal Antibody (DCABH-10845) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use