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Institut für Humangenetik

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Lorenzini, Tiziana; Fliegauf, Manfred; Klammer, Nils et al.

Characterization of the Clinical and Immunological Phenotype and Management of 157 Individuals with 56 Distinct Heterozygous NFKB1 Mutations

JOURNAL OF CLINICAL IMMUNOLOGY. Bd. 40. H. SUPPL 1. 2020 S. S57-S59


Ruffini, Nicolas; Klingenberg, Susanne; Schweiger, Susann et al.

Common Factors in Neurodegeneration: A Meta-Study Revealing Shared Patterns on a Multi-Omics Scale

CELLS. Bd. 9. H. 12. 2020



Beheshtian, Maryam; Akhtarkhavari, Tara; Mehvari, Sepideh et al.

Comprehensivegenotype-phenotypecorrelation inAP-4 deficiency syndrome; Adding data from a large cohort of Iranian patients

CLINICAL GENETICS. 2020


Wendelmuth, M.; Wiliam, M.; Todorov, H. et al.

Dynamic longitudinal behavior in animals exposed to chronic social defeat stress

PLOS ONE. Bd. 15. H. 7. 2020


Gerber, Susanne; Wendelmuth, Marlon; Willam, Michael et al.

Dynamic longitudinal behaviour in animals exposed to chronic social defeat stress

Plos One. Bd. 15. 2020 S. 7


Gomez, R.; Hafezi, N.; Amrani, M. et al.

Genetic findings in miscarriages and their relation to the number of previous miscarriages

ARCHIVES OF GYNECOLOGY AND OBSTETRICS. 2020


Kiouptsi, Klytaimnistra; Pontarollo, Giulia; Todorov, Hristo et al.

Germ-free housing conditions do not affect aortic root and aortic arch lesion size of late atherosclerotic low-density lipoprotein receptor-deficient mice

GUT MICROBES. Bd. 11. H. 6. 2020 S. 1809-1823


Gucev, Zoran; Tasic, Velibor; Bogevska, Ivona et al.

Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation

EUROPEAN JOURNAL OF MEDICAL GENETICS. Bd. 63. H. 1. 2020


Guilherme, Malena dos Santos; Todorov, Hristo; Osterhof, Carina et al.

Impact of Acute and Chronic Amyloid-beta Peptide Exposure on Gut Microbial Commensals in the Mouse

FRONTIERS IN MICROBIOLOGY. Bd. 11. 2020