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Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation ...
Autosomal recessive, homozygous IFIH1 mutation in the proband. (A ...
| Molecular findings. (A) Family tree. (B) A de novo IFIH1 mutation ...
A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten ...
Ifih1 ΔHel1 mutation enhances MDSC populations. Flow cytometry analysis ...
Ifih1 ΔHel1 mutation reduces MDA5-mediated ATP hydrolysis ...
(PDF) Gain-of-function mutation in IFIH1 can cause both aicardi ...
Ifih1 ΔHel1 mutation leads to reduced MDA5 expression following ...
Further evidence for specific IFIH1 mutation as a cause of Singleton ...
(PDF) A Specific IFIH1 Gain-of-Function Mutation Causes Singleton ...
(PDF) Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation
Brief Report: IFIH1 Mutation Causes Systemic Lupus Erythematosus With ...
Severe viral respiratory infections in children with IFIH1 loss-of ...
Three risk variants of IFIH1 and the proposed functional model. (A ...
Genetic and phenotypic spectrum associated with IFIH1 gain‐of‐function ...
Effects of Type 1 Diabetes-Associated IFIH1 Polymorphisms on MDA5 ...
Loss-of-function IFIH1 mutation. (A, C, and D) Relative increase in ...
Biallelic TLR3 or IFIH1 mutations in two patients with EVE. (A) Family ...
IFIH1 (MDA5) is required for innate immune detection of intron ...
IFIH1 effect on plasma levels of IL-6 and IP-10. Exon map of IFIH1 is ...
Aicardi-Goutières Syndrome Is Caused by IFIH1 Mutations: The American ...
Ancestry and sequence alterations in IFIH1 mutation-positive families ...
(PDF) Genetic and phenotypic spectrum associated with IFIH1 gain‐of ...
Sequence analysis of the IFIH1 gene. DNA samples were provided for ...
(PDF) Gain-of-function mutations in IFIH1 cause a spectrum of human ...
(PDF) Hereditary spastic paraplegia associated with a rare IFIH1 ...
Gain-of-function mutations in IFIH1 cause a spectrum of human disease ...
IFIH1 Gene - GeneCards | IFIH1 Protein | IFIH1 Antibody
Mutations in Ifih1 lead to reduced pancreatic proinflammatory ...
Increased IFIH1 expression in the PF_EPN_B subtype (by Anova, F ...
IFIH1 gene: MedlinePlus Genetics
Ifih1 | Taconic Biosciences
Mouse IFIH1 T946 displays increased basal and ligand-dependent ...
PRMT7 regulates Ddx58 and Ifih1 transcription levels by promoting ...
Binding assay for rs13023380 and molecular model of IFIH1 . (A) EMSA ...
Estimated haplotype tree for the IFIH1 gene region we resequenced ...
Visual summary of the IFIH1 variants identified in the seven children ...
Genome-Wide Association Study Identifies IFIH1 and HLA-DQB1*05:02 Loci ...
Genetic variants of IFIH1 and DHX58 affect the chronicity of hepatitis ...
抗体|Rabbit体内培养的Homo sapiens (Human) IFIH1 Antibody –华美生物
IFIH1 Gene - Somatic Mutations in Cancer
(PDF) IFIH1 loss-of-function predisposes to inflammatory and SARS-CoV-2 ...
IFIH1 restricts HRV and RSV replication. Related to SI Appendix, Figs ...
IFIH1 loss of function predisposes to inflammatory and SARS‐CoV‐2 ...
Expression of IFIH1 gene in type 1 diabetes (T1D) and control group ...
Map of human IFIH1 locus on chromosome 2 (region 2q24.3). The sixteen ...
Figure 2 from Genetic variants of IFIH1 and DHX58 affect the chronicity ...
Human IFIH1 knockout Jurkat cell line (ab305280) | Abcam
Frontiers | Recurrent and Prolonged Infections in a Child with a ...
Antiviral signaling by IFIH1. Double-stranded RNA (dsRNA) derived from ...
| Genetic evaluation of Aicardi-Goutières syndrome. (A) Identification ...
The IFIH1-A946T risk variant promotes diabetes in a sex-dependent ...
Scandinavian Journal of Immunology - Wiley Online Library
Lethal Interstitial Lung Disease Associated with a Gain-of-Function ...
Frontiers | A zebrafish model of Ifih1-driven Aicardi–Goutières ...
Primary Immunodeficiencies and Inflammatory Disease: A Growing Genetic ...
Unusual cutaneous features associated with a heterozygous gain-of ...
(PDF) Singleton-Merten Syndrome: a rare autoimmune disorder caused by a ...
(PDF) Neurological findings and a brief review of the current ...
Pangolins Lack IFIH1/MDA5, a Cytoplasmic RNA Sensor That Initiates ...
(PDF) Case Report: Aicardi-Goutières Syndrome and Singleton-Merten ...
Aberrant RNA sensing in regulatory T cells causes systemic autoimmunity ...
(PDF) Recurrent and Prolonged Infections in a Child with a Homozygous ...
Frontiers | Multifactor dimensionality reduction reveals the effect of ...
The role of interferons in systemic lupus erythematosus - Clinical Tree
The IFIH1/MDA5 rs1990760 Gene Variant (946Thr) Differentiates Early- vs ...
Evaluation of Impact of Interferon-Induced Helicase C Domain-Containing ...
Mouse Monoclonal Antibody to IFIH1_IFIH1-远泰生物抗体定制
Frontiers | Case Report: Aicardi-Goutières Syndrome and Singleton ...
(PDF) Generation of three isogenic induced Pluripotent Stem Cell lines ...
(PDF) IRF1 Is Required for MDA5 (IFIH1) Induction by IFN-α, LPS, and ...
(PDF) Case report: Pneumocystis jirovecii pneumonia in a severe case of ...
IFIH1/MDA5 antibody (21775-1-AP) | Proteintech | 武汉三鹰生物技术有限公司
Specific and overlapping features of monogenic type I... | Download ...
Molar Root Incisor Malformation | PPTX
(PDF) A zebrafish model of Ifih1-driven Aicardi–Goutières syndrome ...
MDA5-autoimmunity and interstitial pneumonitis contemporaneous with the ...
Hepatocyte-macrophage crosstalk via the PGRN-EGFR axis modulates ADAR1 ...
