Giovana B. Bampi

Hamburg, HH, Germany

Last Updated: 09/26/2026

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Found 11 publications

Rational design of a modular mRNA vaccine platform for rapid adaptation to SARS-CoV-2 variants.

Rational design of a modular mRNA vaccine platform for rapid adaptation to SARS-CoV-2 variants.

Journal: Scientific reports

Published: September 27, 2025

Large variations in total and allele-specific transcript expression in a disease mutation-independent manner.

Large variations in total and allele-specific transcript expression in a disease mutation-independent manner.

Journal: Scientific reports

Published: August 03, 2025

Positive epistasis between disease-causing missense mutations and silent polymorphism with effect on mRNA translation velocity.

Positive epistasis between disease-causing missense mutations and silent polymorphism with effect on mRNA translation velocity.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: January 20, 2021

The Effect of Synonymous Single-Nucleotide Polymorphisms on an Atypical Cystic Fibrosis Clinical Presentation.

The Effect of Synonymous Single-Nucleotide Polymorphisms on an Atypical Cystic Fibrosis Clinical Presentation.

Journal: Life (Basel, Switzerland)

Published: November 30, 2020

Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

Correction to: Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

Journal: Cerebellum (London, England)

Published: January 16, 2020

Global assessment of the integrated stress response in CF patient-derived airway and intestinal tissues.

Global assessment of the integrated stress response in CF patient-derived airway and intestinal tissues.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: January 16, 2020

Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

Genetic Analysis of Hereditary Ataxias in Peru Identifies SCA10 Families with Incomplete Penetrance.

Journal: Cerebellum (London, England)

Published: January 05, 2020

Fine-tuning the metabolic rewiring and adaptation of translational machinery during an epithelial-mesenchymal transition in breast cancer cells.

Fine-tuning the metabolic rewiring and adaptation of translational machinery during an epithelial-mesenchymal transition in breast cancer cells.

Journal: Cancer & metabolism

Published: September 13, 2019

ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.

ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.

Journal: Cerebellum (London, England)

Published: July 26, 2019

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.

Exome sequencing and network analysis identifies shared mechanisms underlying spinocerebellar ataxia.

Journal: Brain : a journal of neurology

Published: March 20, 2017

Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.

Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.

Journal: Neuromolecular medicine

Published: September 26, 2016

Showing 1-11 of 11

Last Updated: 09/26/2026