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You searched for: Author/Creator Hammerschmidt, Matthias

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1. Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function. (February 2018)

2. Expression of fibulin-6 in failing hearts and its role for cardiac fibroblast migration. (20th June 2014)

3. FAM96A is a novel pro‐apoptotic tumor suppressor in gastrointestinal stromal tumors. Issue 6 (12th March 2015)

4. FAM96A is a novel pro‐apoptotic tumor suppressor in gastrointestinal stromal tumors. Issue 6 (12th March 2015)

6. Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon‐like craniosynostosis. Issue 4 (19th August 2013)

7. SSBP1 mutations in dominant optic atrophy with variable retinal degeneration. Issue 3 (31st July 2019)

8. TGS1 impacts snRNA 3′-end processing, ameliorates survival motor neuron-dependent neurological phenotypes in vivo and prevents neurodegeneration. Issue 21 (10th August 2022)