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KIAA1841
Supporting Information for Proteomics DOI 10.1002/Pmic.200400896
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
PRODUCT SPECIFICATION Product Datasheet
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Microduplication in the 2P16.1P15 Chromosomal Region Linked To
Fundamental Differences in Cell Cycle Deregulation in Human Papillomavirus–Positive and Human Papillomavirus–Negative Head/Neck and Cervical Cancers
Molecular Update and Evolving Classification of Large B-Cell Lymphoma
Content Based Search in Gene Expression Databases and a Meta-Analysis of Host Responses to Infection
Exploring the Role of Rapgef6 in Neuropsychiatric Disorders
Supplemental Solier
1 Supplementary Table 1
Deep RNA Sequencing Analysis of Readthrough Gene Fusions in Human
Detection of H3k4me3 Identifies Neurohiv Signatures, Genomic
Elucidating the Genetic Architecture of Familial Schizophrenia Using Rare Copy Number Variant and Linkage Scans
KIAA1841, a Novel SANT and BTB Domain-Containing Protein, Inhibits Class Switch
Identification and Characterization Of
Unravelling Pathobiological Molecular Mechanisms of T-Cell Acute Lymphoblastic Leukemia
Mice Completely Lacking Immunoproteasomes Display Major Alterations in Antigen Presentation
Top View
Comparison of Dorsal Root Ganglion Gene Expression in Rat Models of Traumatic and HIV-Associated Neuropathic Pain
Genetic Regulation of Disease Risk and Endometrial Gene Expression
The Role of Nanos3 in Tumor Progression
KIAA1841 (T-14): Sc-168354
UC Irvine UC Irvine Electronic Theses and Dissertations
Monoallelic and Biallelic Deletions of 13Q14 in a Group of CLL/SLL
Supplementary File 1
Phosphatidylinositol-3 Kinase/Akt and Fos Like Protein 1
Potential Functional Variants of KIAA Genes Are Associated with Breast Cancer Risk in a Case Control Study
Identification and Characterisation of the Underlying Defects in Patients with Inherited Platelet Bleeding Disorders
Ancestry-Based Stratified Analysis of Immunochip Data Identifies Novel
Functional Genomic Analysis of Novel Microdeletions And
Regulation of Cellular Metabolism by Protein Lysine Acetylation Shimin Zhao, Et Al
P16.1 Microdeletion Syndrome: Molecular Characterization and Association of the OTX1 and XPO1 Genes with Autism Spectrum Disorders
A Combined Systemic Strategy for Overcoming Cisplatin Resistance in Head and Neck Cancer: from Target Identification to Drug Discovery
Brief Report
Hnrnp K Co-Immunoprecipitated Transcripts Regulated by BDNF
Testing for Ancient Selection Using Cross-Population Allele Frequency Differentiation