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3. Personalized Stem Cell Therapy to Correct Corneal Defects Due to a Unique Homozygous-Heterozygous Mosaicism of Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome. (5th May 2016)

4. Personalized Stem Cell Therapy to Correct Corneal Defects Due to a Unique Homozygous‐Heterozygous Mosaicism of Ectrodactyly‐Ectodermal Dysplasia‐Clefting Syndrome. (5th May 2016)

6. SAMHD1 restricts the deoxyguanosine triphosphate pool contributing to telomere stability in telomerase‐positive cells. Issue 4 (19th March 2023)

7. SAMHD1‐deficient fibroblasts from Aicardi‐Goutières Syndrome patients can escape senescence and accumulate mutations. Issue 1 (26th November 2019)

8. SAMHD1‐deficient fibroblasts from Aicardi‐Goutières Syndrome patients can escape senescence and accumulate mutations. Issue 1 (26th November 2019)

9. Separase prevents genomic instability by controlling replication fork speed. Issue 1 (20th November 2017)

10. The displacement of frataxin from the mitochondrial cristae correlates with abnormal respiratory supercomplexes formation and bioenergetic defects in cells of Friedreich ataxia patients. Issue 3 (25th February 2021)