Pages that link to "Q33711147"

The following pages link to A functional SNP in the regulatory region of the decay-accelerating factor gene associates with extraocular muscle pareses in myasthenia gravis. (Q33711147):

Displaying 18 items.

• Semantic prioritization of novel causative genomic variants (Q33620978) (← links)
• Implications of genomic signatures in the differential vulnerability to fetal alcohol exposure in C57BL/6 and DBA/2 mice (Q33735914) (← links)
• dPORE-miRNA: polymorphic regulation of microRNA genes. (Q33822102) (← links)
• Extraocular muscle characteristics related to myasthenia gravis susceptibility (Q34586123) (← links)
• Mutations and binding sites of human transcription factors (Q36001687) (← links)
• Biomarker development for myasthenia gravis (Q36515375) (← links)
• The role of decay accelerating factor in environmentally induced and idiopathic systemic autoimmune disease (Q37579400) (← links)
• Preconditioned mesenchymal stem cells treat myasthenia gravis in a humanized preclinical model. (Q37730809) (← links)
• Complement and cytokine based therapeutic strategies in myasthenia gravis (Q37884228) (← links)
• Characteristics Of acetylcholine-receptor-antibody-negative myasthenia gravis in a South African cohort (Q40786088) (← links)
• The African-387 C>T TGFB1 variant is functional and associates with the ophthalmoplegic complication in juvenile myasthenia gravis. (Q42485842) (← links)
• Analysis of multiple polymorphisms in the bovine neuropeptide Y5 receptor gene and structural modelling of the encoded protein (Q42617704) (← links)
• Association of transforming growth factor β-1 (TGFB1) regulatory region polymorphisms with myasthenia gravis-related ophthalmoparesis. (Q43648490) (← links)
• A unique subphenotype of myasthenia gravis. (Q46527309) (← links)
• Homo sapiens-Specific Binding Site Variants within Brain Exclusive Enhancers Are Subject to Accelerated Divergence across Human Population. (Q55365579) (← links)
• Candidate genes versus genome-wide associations: which are better for detecting genetic susceptibility to infectious disease? (Q55554209) (← links)
• Profiling of patient-specific myocytes identifies altered gene expression in the ophthalmoplegic subphenotype of myasthenia gravis (Q61807485) (← links)
• Using Whole Genome Sequencing in an African Subphenotype of Myasthenia Gravis to Generate a Pathogenetic Hypothesis (Q64076634) (← links)