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Chapter 7: Monogenic Forms of Diabetes
Abstracts from the 9Th Biennial Scientific Meeting of The
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
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Myopathy Genes (HGNC) Neuropathy (HGNC) Neuromuscular Disease
ASAH1 Variant Causing a Mild SMA Phenotype with No Myoclonic Epilepsy: a Clinical, Biochemical and Molecular Study
Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival In
Full Disclosure Forms
Supplementary Table 2
A Peripheral Blood Gene Expression Signature to Diagnose Subclinical Acute Rejection
Genetic Testing Policy Number: PG0041 ADVANTAGE | ELITE | HMO Last Review: 04/11/2021
Autosomal Dominant Late-Onset Spinal Motor Neuronopathy Is Linked to a New Locus on Chromosome 22Q11.2-Q13.2
BSCL2-Gene-Related): Current Understanding
BSCL2 Gene BSCL2, Seipin Lipid Droplet Biogenesis Associated
Impact of Low-Intensity Pulsed Ultrasound on Transcription
Amygdala Gene Expression Correlates of Social Behavior in Monkeys Experiencing Maternal Separation
Exploring the Pathophysiology Behind the More Common Genetic and Acquired Lipodystrophies
Perkinelmer Genomics to Request the Saliva Swab Collection Kit for Patients That Cannot Provide a Blood Sample As Whole Blood Is the Preferred Sample
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(B6;129.Cg-Gt(ROSA)26Sor Tm20(CAG-Ctgf-GFP)Jsd) Were Crossed with Female Foxd1cre/+ Heterozygote Mice 1, and Experimental Mice Were Selected As Foxd1cre/+; Rs26cig/+
NGS Panel Portfolio Bene T from Our Medical Expertise and Streamlined Genetic Testing
A Case of Congenital Generalized Lipodystrophy Type 2 with Novel
Seipin Deletion in Mice Enhances Phosphorylation and Aggregation Of
Autocrine IFN Signaling Inducing Profibrotic Fibroblast Responses By
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
A Yeast-Based Model for Hereditary Motor and Sensory Neuropathies: a Simple System for Complex, Heterogeneous Diseases
The Protective Effect of Club Cell Secretory Protein (CC-16) on COPD Risk And
Novel BSCL2 Gene Mutation E189X in Chinese Congenital Generalized Lipodystrophy Child with Early Onset Diabetes Mellitus
Single-Cell Transcriptional Atlas of the Chinese Horseshoe Bat
Multi-Tissue Probabilistic Fine-Mapping of Transcriptome-Wide Association Study Identifies Cis-Regulated Genes for Miserableness
SUPPLEMENTARY DATA Supplementary Table 1. Characteristics of the Organ Donors and Human Islet Preparations Used for RNA-Seq
(A) Information on Patients Whose Tumors Were Used for Establishing PDX Models
Table 8. 341 Human Cdnas Used for Hierarchical Clustering of DNA
S41467-019-13144-Y.Pdf
Supplemental Material Deletions of Specific Exons of FHOD3 Detected
Supplementary Appendix
Lipodystrophy Information Sheet 6-13-19
Peripheral Neuropathy in Mitochondrial Disorders
You Can Check If Genes Are Captured by the Agilent Sureselect V5 Exome
Supplementary Materials Table S1. List of 63 Evaluated Genes Related to Dyslipidemia and Premature Atherosclerosis with Associated Phenotypes
Screening and Verification of Hub Genes Involved in Osteoarthritis Using Bioinformatics
Differential Phosphorylation of Perilipin 1A at the Initiation of Lipolysis Revealed by Novel Monoclonal Antibodies and High Content Analysis
Ncomms4657.Pdf
Whole Genome Sequence Data Provides Novel Insights Into the Genetic Architecture of Meat Quality Traits in Beef
Signature Redacted
RNA-Sequencing Identifies Dysregulation of the Human Pancreatic Islet Transcriptome
Exploring Seipin: from Biochemistry to Bioinformatics Predictions
Bscl2 Deficiency Does Not Directly Impair the Innate Immune Response in a Murine Model of Generalized Lipodystrophy
Supplementary Table 4. Gene-Set Differential Expression Analysis of TKI Resistance Sample (R2) Versus Pre-TKI Sample (R1) Using Rnaseq Exon Expression Data
Neural Innervation As a Potential Trigger of Morphological Color Change and Sexual Dimorphism in Cichlid Fsh Yipeng Liang, Axel Meyer* & Claudius F
RUNX1-EVI1 Disrupts Lineage Determination and the Cell Cycle by Interfering with RUNX1 and EVI1 Driven Gene Regulatory Networks
A Systematic Inventory of the Causative Genes
The Human Lipodystrophy Gene BSCL2/Seipin May Be Essential for Normal Adipocyte Differentiation Victoria A
Overview of Genes Derived from Possum Database in the Category and Subcategories of Skin Vascular Changes (N=139)
Probe List HTG Transcriptome Panel