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Institut für Humangenetik

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  25

Dünschede, F; Tybl, E; Kiemer, A et al.

Bcl-2 upregulation after 3-nitropropionic acid preconditioning in warm rat liver ischemia

Shock. Bd. 30. H. 6. 2008 S. 699-704


Tuysuz, B; Demirel, A; Uysal, S et al.

Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.

Genet Couns. Bd. 19. H. 1. 2008 S. 29-35


Pantakani, DV; Zechner, U; Arygriou, L et al.

Compound heterozygosity in the SPG4 gene causes hereditary spastic paraplegia.

Clin Genet. Bd. 73. H. 3. 2008 S. 268-72


Wildhardt, G; Trübenbach, J; Kohlschmidt, N et al.

Familial Beckwith-Wiedemann syndrome caused by novel mutations in the CDKN1C-gene

Medizinische Genetik. Bd. 20. H. 1. 2008 S. 119


Haaf, T

Genetische Beratung von Kinderwunschpaaren

GYN Praktische Gynäkologie. Bd. 13. 2008 S. 193-201


Puusepp, H; Zordania, R; Paal, M et al.

Girl with partial turner syndrome and absence epilepsy.

Pediatr Neurol. Bd. 38. H. 4. 2008 S. 289-92




Galetzka, D; Weis, E; Rittner, G et al.

Microarray mRNA expression analysis of Fanconi anemia fibroblasts

Cytogenet Genome Res. Bd. 121. 2008 S. 10-13


Zovoilis, A; Nolte, J; Drusenheimer, N et al.

Multipotent adult germline stem cells and embryonic stem cells have similar microRNA profiles.

Mol Hum Reprod. Bd. 14. H. 9. 2008 S. 521-9


Hoffarth, S; Zitzer, A; Wiewrodt, R et al.

pp32/PHAPI determines the apoptosis response of non-small-cell lung cancer.

Cell Death Differ. Bd. 15. H. 1. 2008 S. 161-70


Balci, S; Ergun, MA; Yuksel-Konuk, EB et al.

Rubinstein-Taybi syndrome with normal FISH result and CREBBP gene analysis: a case report.

Turk J Pediatr. Bd. 50. H. 3. 2008 S. 265-8


Nanda, I; Schlegelmilch, K; Haaf, T et al.

Synteny conservation of the Z chromosome in 14 avian species (11 families) supports a role for Z dosage in avian sex determination

Cytogenet Genome Res. Bd. 122. 2008 S. 150-156


Korenkov, M; Kohlschmidt, N; Zechner, U et al.

Adipositaschirurgie bei monogenetisch bedingter Adipositas

Zentralbl Chir. Bd. 132. 2007 S. 256-259



Zimmermann, N; Acosta, AM; Kohlhase, J et al.

Confirmation of EP300 gene mutations as a rare cause of Rubinstein-Taybi syndrome

Eur J Hum Genet. Bd. 15. H. 8. 2007 S. 837-842


Dünzinger, U; Haaf, T; Zechner, U

Conserved synteny of mammalian imprinted genes in chicken, frog, and fish genomes

Cytogenet Genome Res. Bd. 117. 2007 S. 78-85




Galetzka, D; Weis, E; Kohlschmidt, N et al.

Expression of somatic DNA repair genes in human testes

J Cell Biochem. Bd. 100. 2007 S. 1232-1239


Nanda, I; Buwe, A; Wizenman, A et al.

Fanconi anemia genes in vertebrates: evolutionary conservation, sex-linkage, and embryonic expression of FANCC and FANCG in avian cells

Schindler D, Hoehn H (Hrsg). Fanconi Anemia. A Paradigmatic Disease for the Understanding of Cancer and Aging. Basel: Karger 2007


Nolte, J; Rathsack, K; Drusenheimer, N et al.

Männliche Keimzellen aus embryonalen Stammzellen

Medizinische Genetik. Bd. 19. 2007 S. 10-17