9 Einträge gefunden

1. Octa-repeat domain of the mammalian prion protein mRNA forms stable A-helical hairpin structure rather than G-quadruplexes

   1. Czech, Andreas
   2. Konarev, Petr V.
   3. Goebel, Ingrid
   4. Svergun, Dmitri I.
   5. Wills, Peter R.
   6. Ignatova, Zoya

   2019 - Forschungsinformationssystem der UHH - frei zugänglich
2. Zellkulturen : Labormethoden der Biochemie

   1. Goebel, Ingrid

   2018 - Lecture2Go UHH - frei zugänglich
3. AUNA2: A Novel Type of Non-Syndromic Slowly Progressive Auditory Synaptopathy/Auditory Neuropathy with Autosomal-Dominant Inheritance

   1. Lang-Roth, Ruth
   2. Fischer-Krall, Eva
   3. Kornblum, Cornelia
   4. Nürnberg, Gudrun
   5. Meschede, Dieter
   6. Goebel, Ingrid
   7. Nürnberg, Peter

   2017 - Forschungsinformationssystem des UKE
4. Dysfunction of the MDM2/p53 axis is linked to premature aging

   1. Lessel, Davor
   2. Wu, Danyi
   3. Trujillo, Carlos
   4. Ramezani, Thomas
   5. Lessel, Ivana
   6. Alwasiyah, Mohammad K
   7. Saha, Bidisha

   2017 - Forschungsinformationssystem des UKE
5. Identification of two novel ALS2 mutations in infantile-onset ascending hereditary spastic paraplegia

   1. Daud, Shakeela
   2. Kakar, Naseebullah
   3. Goebel, Ingrid
   4. Hashmi, Abu Saeed
   5. Yaqub, Tahir
   6. Nürnberg, Gudrun
   7. Nürnberg, Peter

   2016 - Forschungsinformationssystem des UKE
6. A post GWAS association study of SNPs associated with cleft lip with or without cleft palate in submucous cleft palate

   1. Reiter, Rudolf
   2. Brosch, Sibylle
   3. Goebel, Ingrid
   4. Ludwig, Kerstin U
   5. Pickhard, Anja
   6. Högel, Josef
   7. Schlömer, Guido

   2015 - Forschungsinformationssystem des UKE
7. Interactive effects of citalopram and serotonin transporter genotype on neural correlates of response inhibition and attentional orienting

   1. Fischer, Adrian G
   2. Endrass, Tanja
   3. Goebel, Ingrid
   4. Reuter, Martin
   5. Montag, Christian
   6. Kubisch, Christian
   7. Ullsperger, Markus

   2015 - Forschungsinformationssystem des UKE
8. De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients

   1. Hübers, Annemarie
   2. Just, Walter
   3. Rosenbohm, Angela
   4. Müller, Kathrin
   5. Marroquin, Nicolai
   6. Goebel, Ingrid
   7. Högel, Josef

   2015 - Forschungsinformationssystem des UKE
9. A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephaly.

   1. Kakar, Naseebullah
   2. Goebel, Ingrid
   3. Daud, Shakeela
   4. Nürnberg, Gudrun
   5. Agha, Noor
   6. Ahmad, Adeel
   7. Nürnberg, Peter

   2012 - Forschungsinformationssystem des UKE