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SPTB
A Computational Approach for Defining a Signature of Β-Cell Golgi Stress in Diabetes Mellitus
Neurodegeneration Induces a Developmental RNA Processing Program by Calpain
High Constitutive Cytokine Release by Primary Human Acute Myeloid Leukemia Cells Is Associated with a Specific Intercellular Communication Phenotype
Transcriptome Profiling of the Lungs Reveals Molecular Clock Genes Expression Changes After Chronic Exposure to Ambient Air Particles
SCIENCE CHINA Spectrin: Structure, Function and Disease
The Trans KCNMA1-M744T and Cis ANXA11-I457V and DYDC2-P123R Variants Are Associated with Familial Dilated Cardiomyopathy
Clinical, Molecular, and Immune Analysis of Dabrafenib-Trametinib
270 Genes Genetic Insights Panel
A Novel SPTB Gene Mutation in Neonatal Hereditary Spherocytosis: a Case Report and Literature Review
Novel Protein Pathways in Development and Progression of Pulmonary Sarcoidosis Maneesh Bhargava1*, K
Novel Mutation in SPTA1 Gene Associated with Severe Hemolytic Anemia
Aagab S00002 Aars S00003 Aars2 S00004 Aass S02483
ADX609 3301 Athena Newborndx Gene Panel Update 3-30-20.Indd
Molecular Genetics Lab Requisition
Next Gen Sequencing Panels
SUPPLEMENTARY DATA Retinoic Acid Mediates Visceral-Specific
Identification of Proteins Implicated in the Increased Heart Rate in Shensongyangxin-Treated Bradycardia Rabbits by Itraq-Based Quantitative Proteomics
Proteomics Profiling of Neuron-Derived Small
Top View
Decoding Transcriptional Regulation Via a Human Gene Expression Predictor
Alsaai Udel 0060D 14351.Pdf
For Personal Use. Only Reproduce with Permission from the Lancet Publishing Group
Hereditary Spherocytosis, Elliptocytosis, and Other Red Cell Membrane Disorders☆
Accounting for Diverse Evolutionary Forces Reveals Mosaic Patterns of Selection on Human Preterm Birth Loci
Proteomic Analysis Identifies Distinct Glomerular Extracellular Matrix In
Table S1 (Revised)
Next Generation Sequencing (V10)
The Spectrin Family of Proteins
Membranes of Human Neutrophils Secretory Vesicle Membranes And
Proteomic Landscape of the Human Choroid–Retinal Pigment Epithelial Complex
Accounting for Diverse Evolutionary Forces Reveals the Mosaic Nature of Selection on Genomic 2 Regions Associated with Human Preterm Birth
Table S3 Gene List of Panel Classification Gene OMIM ID
Supplementary Appendix
Somatic Mutations and T-Cell Clonality in Patients with Immunodeficiency
ANNUAL NEWSLETTER 2020 - 2021 Dear Colleagues
Figure S1. GO and KEGG Pathways, Protein Domains and Cluster Analysis of Crotonylated Proteins in Immunoglobulin a Nephropathy
Research Article Alzheimer's Disease