Search

Your search keyword '"Mansfield, Brian C."' showing total 13 results

Search Constraints

Start Over You searched for: Author "Mansfield, Brian C." Remove constraint Author: "Mansfield, Brian C." Topic glycogen storage disease Remove constraint Topic: glycogen storage disease
13 results on '"Mansfield, Brian C."'

Search Results

2. Downregulation of SIRT1 signaling underlies hepatic autophagy impairment in glycogen storage disease type Ia.

3. The glucose-6-phosphate transporter is a phosphate-linked antiporter deficient in glycogen storage disease type Ib and Ic.

4. The signature motif in human glucose-6-phosphate transporter is essential for microsomal transport of glucose-6-phosphate.

5. Glycogen storage disease type I and G6Pase-β deficiency: etiology and therapy.

6. Gene therapy using a novel G6PC-S298C variant enhances the long-term efficacy for treating glycogen storage disease type Ia.

7. Inhibition of Wnt/β-catenin signaling reduces renal fibrosis in murine glycogen storage disease type Ia.

8. Glycogen storage disease type Ia mice with less than 2% of normal hepatic glucose-6-phosphatase-α activity restored are at risk of developing hepatic tumors.

9. Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type lb.

10. The upstream enhancer elements of the G6PC promoter are critical for optimal G6PC expression in murine glycogen storage disease type Ia.

11. Complete Normalization of Hepatic G6PC Deficiency in Murine Glycogen Storage Disease Type Ia Using Gene Therapy.

12. Normoglycemia alone is insufficient to prevent long-term complications of hepatocellular adenoma in glycogen storage disease type Ib mice

13. Bone Marrow-derived Cells Require a Functional Glucose 6-Phosphate Transporter for Normal Myeloid Functions.

Catalog

Books, media, physical & digital resources