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Autor/in
- Kubisch, Christian
- Lessel, Davor 11
- Borck, Guntram 10
- Volk, Alexander E 8
- Nürnberg, Peter 7
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Sprache
- Englisch 46
46 Einträge gefunden
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Involvement of astrocyte and oligodendrocyte gene sets in migraine
- Eising, Else
- de Leeuw, Christiaan
- Min, Josine L
- Anttila, Verneri
- Verheijen, Mark Hg
- Terwindt, Gisela M
- Dichgans, Martin
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Interactive effects of citalopram and serotonin transporter genotype on neural correlates of response inhibition and attentional orienting
- Fischer, Adrian G
- Endrass, Tanja
- Goebel, Ingrid
- Reuter, Martin
- Montag, Christian
- Kubisch, Christian
- Ullsperger, Markus
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STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly
- Kakar, Naseebullah
- Ahmad, Jamil
- Morris-Rosendahl, Deborah J
- Altmüller, Janine
- Friedrich, Katrin
- Barbi, Gotthold
- Nürnberg, Peter
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Carpal tunnel syndrome is associated with high fibrinogen and fibrinogen deposits
- Utrobičić, Ivan
- Novak, Ivana
- Marinović-Terzić, Ivana
- Matić, Katarina
- Lessel, Davor
- Salamunić, Ilza
- Babić, Mirna Saraga
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A rare missense variant abrogates the signaling activity of tetherin/BST-2 without affecting its effect on virus release
- Sauter, Daniel
- Hotter, Dominik
- Engelhart, Susanne
- Giehler, Fabian
- Kieser, Arnd
- Kubisch, Christian
- Kirchhoff, Frank
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Exon skipping and severe childhood-onset obesity caused by a leptin receptor mutation
2013 - Forschungsinformationssystem des UKE -
Spectrum of novel mutations found in Waardenburg syndrome types 1 and 2: implications for molecular genetic diagnostics
- Wildhardt, Gabriele
- Zirn, Birgit
- Graul-Neumann, Luitgard M
- Wechtenbruch, Juliane
- Suckfüll, Markus
- Buske, Annegret
- Bohring, Axel
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Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry
- Saha, Bidisha
- Lessel, Davor
- Nampoothiri, Sheela
- Rao, Anuradha S
- Hisama, Fuki M
- Peter, Dincy
- Bennett, Chris
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A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly.
- Kakar, Naseebullah
- Goebel, Ingrid
- Daud, Shakeela
- Nürnberg, Gudrun
- Agha, Noor
- Ahmad, Adeel
- Nürnberg, Peter
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Rare hereditary diseases with defects in DNA-repair.
2012 - Forschungsinformationssystem des UKE -
A phenotype map for 14q32.3 terminal deletions.
- Engels, Hartmut
- Schüler, Herdit M
- Zink, Alexander M
- Wohlleber, Eva
- Brockschmidt, Antje
- Hoischen, Alexander
- Drechsler, Matthias