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Matthias Hammerschmidt

Showing results (101-110 of 125) with videos related to

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Immunity|October 18, 2015
Interleukin-4 Receptor α Signaling in Myeloid Cells Controls Collagen Fibril Assembly in Skin RepairJohanna A Knipper, Sebastian Willenborg, Jürgen Brinckmann, et al.
Science Advances|May 13, 2021
The SAM domain-containing protein 1 (SAMD1) acts as a repressive chromatin regulator at unmethylated CpG islandsBastian Stielow, Yuqiao Zhou, Yinghua Cao, et al.
Cardiovascular Research|June 22, 2014
Expression of fibulin-6 in failing hearts and its role for cardiac fibroblast migrationArpita Chowdhury, Christine Herzog, Lisa Hasselbach, et al.
Neurology. Genetics|January 31, 2018
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 functionNatalia Mendoza-Ferreira, Marie Coutelier, Eva Janzen, et al.
Annals of Neurology|July 13, 2019
SSBP1 mutations in dominant optic atrophy with variable retinal degenerationNeringa Jurkute, Costin Leu, Hans-Martin Pogoda, et al.
Nature Methods|May 10, 2011
In vivo protein trapping produces a functional expression codex of the vertebrate proteomeKarl J Clark, Darius Balciunas, Hans-Martin Pogoda, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
American Journal of Human Genetics|August 9, 2016
The Power of Human Protective Modifiers: PLS3 and CORO1C Unravel Impaired Endocytosis in Spinal Muscular Atrophy and Rescue SMA PhenotypeSeyyedmohsen Hosseinibarkooie, Miriam Peters, Laura Torres-Benito, et al.
American Journal of Human Genetics|December 7, 2010
Temtamy preaxial brachydactyly syndrome is caused by loss-of-function mutations in chondroitin synthase 1, a potential target of BMP signalingYun Li, Kathrin Laue, Samia Temtamy, et al.
American Journal of Human Genetics|April 10, 2012
Attenuated BMP1 function compromises osteogenesis, leading to bone fragility in humans and zebrafishP V Asharani, Katharina Keupp, Oliver Semler, et al.
Pageof 13

Showing results (101-110 of 125) with videos related to

Sort By:
Pageof 13
Immunity|October 18, 2015
Interleukin-4 Receptor α Signaling in Myeloid Cells Controls Collagen Fibril Assembly in Skin RepairJohanna A Knipper, Sebastian Willenborg, Jürgen Brinckmann, et al.
Science Advances|May 13, 2021
The SAM domain-containing protein 1 (SAMD1) acts as a repressive chromatin regulator at unmethylated CpG islandsBastian Stielow, Yuqiao Zhou, Yinghua Cao, et al.
Cardiovascular Research|June 22, 2014
Expression of fibulin-6 in failing hearts and its role for cardiac fibroblast migrationArpita Chowdhury, Christine Herzog, Lisa Hasselbach, et al.
Neurology. Genetics|January 31, 2018
Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 functionNatalia Mendoza-Ferreira, Marie Coutelier, Eva Janzen, et al.
Annals of Neurology|July 13, 2019
SSBP1 mutations in dominant optic atrophy with variable retinal degenerationNeringa Jurkute, Costin Leu, Hans-Martin Pogoda, et al.
Nature Methods|May 10, 2011
In vivo protein trapping produces a functional expression codex of the vertebrate proteomeKarl J Clark, Darius Balciunas, Hans-Martin Pogoda, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
American Journal of Human Genetics|August 9, 2016
The Power of Human Protective Modifiers: PLS3 and CORO1C Unravel Impaired Endocytosis in Spinal Muscular Atrophy and Rescue SMA PhenotypeSeyyedmohsen Hosseinibarkooie, Miriam Peters, Laura Torres-Benito, et al.
American Journal of Human Genetics|December 7, 2010
Temtamy preaxial brachydactyly syndrome is caused by loss-of-function mutations in chondroitin synthase 1, a potential target of BMP signalingYun Li, Kathrin Laue, Samia Temtamy, et al.
American Journal of Human Genetics|April 10, 2012
Attenuated BMP1 function compromises osteogenesis, leading to bone fragility in humans and zebrafishP V Asharani, Katharina Keupp, Oliver Semler, et al.
Pageof 13