Publications by authors named "Alexandra Neller"

Claim this Profile
M
Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease.
Nikoletta Nagy, Margit Pal, Jozsef Kun, Bence Galik, Peter Urban, Alexandra Neller

Int J Mol Sci· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients.
Margit Pál, Dóra Nagy, Alexandra Neller, Katalin Farkas, Dóra Leprán-Török

Int J Mol Sci· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Acetylation State of Lysine 14 of Histone H3.3 Affects Mutant Huntingtin Induced Pathogenesis.
Anikó Faragó, Nóra Zsindely, Anita Farkas, Alexandra Neller, Fruzsina Siági

Int J Mol Sci· December 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hat1 acetylates histone H4 and modulates the transcriptional program in Drosophila embryogenesis.
Júlia Varga, Szabina Korbai, Alexandra Neller, Nóra Zsindely, László Bodai

Sci Rep· November 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis