Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Daniel, Liedtke"'
Autor:
Asuman Koparir, Caroline Lekszas, Kemal Keseroglu, Thalia Rose, Lena Rappl, Aboulfazl Rad, Reza Maroofian, Nakul Narendran, Atefeh Hasanzadeh, Ehsan Ghayoor Karimiani, Felix Boschann, Uwe Kornak, Eva Klopocki, Ertuğrul M. Özbudak, Barbara Vona, Thomas Haaf, Daniel Liedtke
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-13 (2024)
Abstract Background/Objectives Rare genetic disorders causing specific congenital developmental abnormalities often manifest in single families. Investigation of disease-causing molecular features are most times lacking, although these investigations
Externí odkaz:
https://doaj.org/article/4ca8372a9ecd42798f65bafe5883ded4
Autor:
Victoria C. Moris, Lars Podsiadlowski, Sebastian Martin, Jan Philip Oeyen, Alexander Donath, Malte Petersen, Jeanne Wilbrandt, Bernhard Misof, Daniel Liedtke, Markus Thamm, Ricarda Scheiner, Thomas Schmitt, Oliver Niehuis
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-15 (2023)
Transcriptomic and molecular analyses on Hymenoptera facilitated identification of cuticular hydrocarbon (CHC) pathway genes, whose phylogenetic distribution implies that the origin of CHC biosynthesis predates the arthropods’ colonization of land.
Externí odkaz:
https://doaj.org/article/36c7d2e870e54063a9d314cef8e0584b
Publikováno v:
BMC Health Services Research, Vol 21, Iss 1, Pp 1-18 (2021)
Abstract Background A hospitalization phase represents a challenge to medication safety especially for multimorbid patients as acute medical needs might interact with pre-existing medications or evoke adverse drug effects. This project aimed to exami
Externí odkaz:
https://doaj.org/article/3a8e6007fc494a40b3a5543aa06e0193
Autor:
Miriam Zink, Anne Seewald, Mareike Rohrbach, Andreas Brodehl, Daniel Liedtke, Tatjana Williams, Sarah J. Childs, Brenda Gerull
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 17, p 9530 (2022)
Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disease caused by heterozygous missense mutations within the gene encoding for the nuclear envelope protein transmembrane protein 43 (TMEM43). The disease is characterized by myocyte lo
Externí odkaz:
https://doaj.org/article/35d6def1145d4b15abc89c047ae62d2e
Autor:
Stephanie Graser, Sofia Paulus, Elisa Riekert, Franz Jakob, Eva Klopocki, Denitsa Docheva, Theresa Kreuzahler, Maximilian Rudert, Marietta Herrmann, Daniel Liedtke
Publikováno v:
Bone Reports, Vol 14, Iss , Pp 101006- (2021)
Externí odkaz:
https://doaj.org/article/a20e737e612142a7a6c105cd518553c7
Autor:
Angela Borst, Barbara Ohlebusch, Rabea Blümel, Eva Klopocki, Franz Jakob, Daniel Liedtke, Stephanie Graser
Publikováno v:
Bone Reports, Vol 13, Iss , Pp 100593- (2020)
Externí odkaz:
https://doaj.org/article/4cca6957fdb74c9089109fbdb3d381d4
Autor:
Caroline Lekszas, Ombretta Foresti, Ishier Raote, Daniel Liedtke, Eva-Maria König, Indrajit Nanda, Barbara Vona, Peter De Coster, Rita Cauwels, Vivek Malhotra, Thomas Haaf
Publikováno v:
eLife, Vol 9 (2020)
The transport and Golgi organization 1 (TANGO1) proteins play pivotal roles in the secretory pathway. Full length TANGO1 is a transmembrane protein localised at endoplasmic reticulum (ER) exit sites, where it binds bulky cargo within the ER lumen and
Externí odkaz:
https://doaj.org/article/02c70536fc7c43d181bb634c407c75db
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 24, p 13417 (2021)
Prerequisite to any biological laboratory assay employing living animals is consideration about its necessity, feasibility, ethics and the potential harm caused during an experiment. The imperative of these thoughts has led to the formulation of the
Externí odkaz:
https://doaj.org/article/541883e8a4874c58b45aee56434bf2b9
Publikováno v:
PLoS ONE, Vol 14, Iss 6, p e0218286 (2019)
The transcription factor 12 (tcf12) is a basic Helix-Loop-Helix protein (bHLH) of the E-protein family, proven to play an important role in developmental processes like neurogenesis, mesoderm formation, and cranial vault development. In humans, mutat
Externí odkaz:
https://doaj.org/article/4f7e9cc68db6488581054eea5a6ae357
Publikováno v:
Osteologie. 31:89-93
This brief review describes the role of tissue-nonspecific alkaline phosphatase (TNAP) during dental development. Mutations within the ALPL gene, which is encoding the human ectoenzyme TNAP, lead to the rare disease Hypophosphatasia (HPP). Apart from