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Institut für Humangenetik

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Siuda, D.; Wu, Z.; Chen, Y. et al.

SOCIAL ISOLATION-INDUCED EPIGENETIC CHANGES IN MIDBRAIN OF ADULT MICE

JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY. Bd. 65. H. 2. 2014 S. 247-255


Vona, Barbara; Mueller, Tobias; Nanda, Indrajit et al.

Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations

GENETICS IN MEDICINE. Bd. 16. H. 12. 2014 S. 945-953


Schweiger, Susann; Dorn, Stephanie; Fuchs, Melanie et al.

The E3 Ubiquitin Ligase MID1 Catalyzes Ubiquitination and Cleavage of Fu

JOURNAL OF BIOLOGICAL CHEMISTRY. Bd. 289. H. 46. 2014 S. 31805-31817


Braeutigam, C.; Rago, L.; Rolke, A. et al.

The RNA-binding protein Rbfox2: an essential regulator of EMT-driven alternative splicing and a mediator of cellular invasion

ONCOGENE. Bd. 33. H. 9. 2014 S. 1082-1092


Schroeder, Julia C.; Laessig, Anne K.; Galetzka, Danuta et al.

A boy with homozygous microdeletion of NEUROG1 presents with a congenital cranial dysinnervation disorder [Moebius syndrome variant]

BEHAVIORAL AND BRAIN FUNCTIONS. Bd. 9. 2013


Lehnen, Harald; Zechner, Ulrich; Haaf, Thomas

Epigenetics of gestational diabetes mellitus and offspring health: the time for action is in early stages of life

MOLECULAR HUMAN REPRODUCTION. Bd. 19. H. 7. 2013 S. 415-422


Burgdörfer, E; Korenkov, M; Jonas, D et al.

FTO and INSIG2 genotyping combined with metabolic and anthropometric phenotyping of morbidly obese patients

Mol Syndromol. Bd. 4. H. 6. 2013 S. 273-279


Miederer, Matthias; Fottner, Christian; Rossmann, Heidi et al.

High incidence of extraadrenal paraganglioma in families with SDHx syndromes detected by functional imaging with [F-18]fluorodihydroxyphenylalanine PET

EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING. Bd. 40. H. 6. 2013 S. 889-896


Follmann, Johannes; Macchiella, Doris; Whybra, Catharina et al.

Identification of novel mutations in the ABCA12 gene, c.1857delA and c.5653-5655delTAT, causing harlequin ichthyosis

GENE. Bd. 531. H. 2. 2013 S. 510-513


Raker, V.; Bacher, N.; Hofmann, C. et al.

IFN-alpha abrogates the regulatory function of human CD4+CD25+FOXP+Treg via MAPK/PDE4 pathway-regulated cAMP repression

JOURNAL OF INVESTIGATIVE DERMATOLOGY. Bd. 133. 2013 S. S2-S2