Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
BMC Medical Genetics|November 19, 2008
A novel HSF4 gene mutation (p.R405X) causing autosomal recessive congenital cataracts in a large consanguineous family from PakistanNaheed Sajjad, Ingrid Goebel, Naseebullah Kakar, et al.
Scientific Reports|February 23, 2019
Octa-repeat domain of the mammalian prion protein mRNA forms stable A-helical hairpin structure rather than G-quadruplexesAndreas Czech, Petr V Konarev, Ingrid Goebel, et al.
Nucleic Acids Research|June 14, 2021
smORFer: a modular algorithm to detect small ORFs in prokaryotesAlexander Bartholomäus, Baban Kolte, Ayten Mustafayeva, et al.
Human Genetics|January 20, 2009
New genetic evidence for involvement of the dopamine system in migraine with auraUnda Todt, Christian Netzer, Mohammad Toliat, et al.
Life Science Alliance|November 21, 2018
Dynamic m<sup>6</sup>A methylation facilitates mRNA triaging to stress granulesMaximilian Anders, Irina Chelysheva, Ingrid Goebel, et al.
European Journal of Medical Genetics|September 20, 2012
A homozygous splice site mutation in TRAPPC9 causes intellectual disability and microcephalyNaseebullah Kakar, Ingrid Goebel, Shakeela Daud, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 2, 2006
Haplotype-based systematic association studies of ATP1A2 in migraine with auraChristian Netzer, Unda Todt, Axel Heinze, et al.
Pageof 3