Dana Landgraf
Dresden, SN 01307, Germany
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
A Humanized and Viable Animal Model for Congenital Adrenal Hyperplasia-CYP21A2-R484Q Mutant Mouse.
Journal: International journal of molecular sciences
Published: March 15, 2024
CYP21A2 Gene Expression in a Humanized 21-Hydroxylase Mouse Model Does Not Affect Adrenocortical Morphology and Function.
Journal: Journal of the Endocrine Society
Published: December 15, 2021
Homozygous mutation in murine retrovirus integration site 1 gene associated with a non-syndromic form of isolated familial achalasia.
Journal: Neurogastroenterology and motility
Published: March 18, 2020
Homozygous deletion of the entire AAAS gene in a triple A syndrome patient.
Journal: European journal of medical genetics
Published: December 05, 2018
Compensation for chronic oxidative stress in ALADIN null mice.
Journal: Biology open
Published: January 25, 2018
Identification of a novel putative interaction partner of the nucleoporin ALADIN.
Journal: Biology open
Published: November 02, 2016
A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima.
Journal: Journal of medical genetics
Published: June 16, 2016
Triple A syndrome with a novel indel mutation in the AAAS gene and delayed puberty.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: September 29, 2014
Changes in differential gene expression in fibroblast cells from patients with triple A syndrome under oxidative stress.
Journal: Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme
Published: January 15, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026