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CLEC16A
Genome-Scale Single-Cell Mechanical Phenotyping Reveals Disease-Related Genes Involved in Mitotic Rounding
Clec16a, Nrdp1, and USP8 Form a Ubiquitin-Dependent
Genome-Wide DNA Methylation Dynamics During Epigenetic
POGLUT1, the Putative Effector Gene Driven by Rs2293370 in Primary
Full-Text.Pdf
A CLEC16A Variant Confers Risk for Juvenile Idiopathic Arthritis and Anti
Sji.13050.Pdf
CLEC16A Regulates Splenocyte and NK Cell Function in Part Through MEK Signaling
Inducible Knockout of Clec16a in Mice Results in Sensory Neurodegeneration Heather S
Schizophrenia-Associated Differential DNA Methylation in the Superior Temporal
NIH Public Access Author Manuscript Nat Genet
Table S1. 103 Ferroptosis-Related Genes Retrieved from the Genecards
Clarifying the Function of Genes at the Chromosome 16P13 Locus in Type 1 Diabetes: CLEC16A and DEXI
The Diabetes Susceptibility Gene Clec16a Regulates Mitophagy
Genomics of Asthma, Allergy and Chronic Rhinosinusitis
Exploring the CLEC16A Gene Reveals a MS-Associated Variant with Correlation to the Relative Expression of CLEC16A Isoforms in Thymus
The Human Disease Gene CLEC16A Encodes an Intrinsically Disordered Protein Region
From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A
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Multiple Sclerosis-Associated Single-Nucleotide Polymorphisms in CLEC16A Correlate with Reduced SOCS1 and DEXI Expression in the Thymus
Clec16a Is Critical for Autolysosome Function and Purkinje Cell Survival Veronika Redmann Washington University School of Medicine
Transcriptome Profiling of NIH3T3 Cell Lines Expressing Opsin and The
Diabetes Susceptibility Genes Pdx1 and Clec16a Function in a Pathway Regulating Mitophagy in B-Cells
Polymorphisms of CLEC16A Region and Autoimmune Thyroid Diseases
Genome-Wide Copy Number Variation (CNV)
The Correlation Between the CLEC16A Gene and Genetic Susceptibility to Type 1 Diabetes in Chinese Children
Rabbit Anti-CLEC16A/FITC Conjugated Antibody
Diabetes Susceptibility Genes Pdx1 and Clec16a Function in a Pathway Regulating Mitophagy in B-Cells
Variation Within the CLEC16A Gene Shows Consistent Disease Association with Both Multiple Sclerosis and Type 1 Diabetes in Sardinia
Association of CLEC16A with Human Common Variable Immunodeficiency Disorder and Role in Murine B Cells
9Q34 & 16P13 Chromosome Duplications in Autism
SUPPLEMENTARY MATERIAL FOR: Vascular Pathology in Multiple
Multiple Sclerosis Risk Allele in CLEC16A Acts As an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells
Clec16a, Nrdp1, and USP8 Form a Ubiquitin-Dependent Tripartite Complex That Regulates B-Cell Mitophagy
Genetic Alterations on Chromosome 16 And
How CLEC16A Modifies the Function of Thymic Epithelial Cells - Wie CLEC16A Die Funktion Von Thymus-Epithelzellen Beeinflusst