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1. Publisher Correction: A postnatal network of co-hepato/pancreatic stem/progenitors in the biliary trees of pigs and humans

2. A postnatal network of co-hepato/pancreatic stem/progenitors in the biliary trees of pigs and humans

3. Patch grafting of organoids of stem/progenitors into solid organs can correct genetic-based disease states

4. The clinical significance of adenomatous polyposis coli (APC) and catenin Beta 1 (CTNNB1) genetic aberrations in patients with melanoma

5. TDP-43 pathology links innate and adaptive immunity in amyotrophic lateral sclerosis

6. RNA-binding deficient TDP-43 drives cognitive decline in a mouse model of TDP-43 proteinopathy

7. Increased Tryptophan, But Not Increased Glucose Metabolism, Predict Resistance of Pembrolizumab in Stage III/IV Melanoma

8. A TDP-43 acetylation-mimic mutation that disrupts RNA-binding drives FTLD-like neurodegeneration in a mouse model of sporadic TDP-43 proteinopathy

9. Additional file 1 of The clinical significance of adenomatous polyposis coli (APC) and catenin Beta 1 (CTNNB1) genetic aberrations in patients with melanoma

11. Increased tryptophan, but not increased glucose metabolism, predict resistance of pembrolizumab in stage III/IV melanoma.

12. Patch Grafting of Stem/Progenitor Organoids, Strategies for Cell Therapies for Solid Organs, and Exemplified in Liver and Pancreas

13. High intratumoral tryptophan metabolism is a poor predictor of response to pembrolizumab (pembro) in metastatic melanoma (MM): Results from a prospective trial using baseline C11-labeled alpha-methyl tryptophan (C11-AMT) PET imaging for response prediction.

14. Patch Grafting of Cells into Solid Organs Such as Liver and Pancreas

15. Expression of tryptophan metabolizing enzymes (TMEs) and its transporter, LAT1, in metastatic melanoma (MM): Prognostic and therapeutic implications.

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