Results 131 to 140 of about 12,282 (232)

Correction to: Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier's disease, causes behavioral abnormalities and a hyper-dopaminergic state [PDF]

, 2023

openalex   +1 more source

Epigenetische Suppression von RASAL1 und ATP2A2 als Biomarker und Therapieansatz bei kardialer Fibrogenese [PDF]

, 2020
Jonas Gosch
openalex   +1 more source

Molecular characterization of human HSPCs with different cell fates in vivo using single‐cell transcriptome analysis and lentiviral barcoding technology

Clinical and Translational Medicine
Hematopoietic stem and progenitor cells (HSPCs) possess the potential to produce all types of blood cells throughout their lives. It is well recognized that HSPCs are heterogeneous, which is of great significance for their clinical applications and the ...
Junnan Hua, Ke Wang, Yue Chen, Xiaojing Xu, Guoyi Dong, Yue Li, Rui Liu, Yecheng Xiong, Jiabin Ding, Tingting Zhang, Xinru Zeng, Yuxi Li, Haixi Sun, Ying Gu, Sixi Liu, Wenjie Ouyang, Chao Liu   +16 more
doaj   +1 more source

Transcriptional Response to Acute Thermal Exposure in Juvenile Chinook Salmon Determined by RNAseq. [PDF]

, 2015
Thermal exposure is a serious and growing challenge facing fish species worldwide. Chinook salmon (Oncorhynchus tshawytscha) living in the southern portion of their native range are particularly likely to encounter warmer water due to a confluence of ...
Baerwald, Melinda R, Fangue, Nann A, May, Bernie P, Meek, Mariah H, Rincón, Gonzalo, Stephens, Molly R, Tomalty, Katharine MH   +6 more
core  

An <i>ATP2A2</i> Missense Mutation in a Japanese Family with Darier Disease: A Case Report and Review of the Japanese Darier Disease Patients with <i>ATP2A2</i> Mutations

, 2017
Min Li, Naoyuki Higashi, Hajime Nakano, Hidehisa Saeki   +3 more
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心筋への直接転換における細胞周期の機能解析 [PDF]

, 2018
筑波大学 (University of Tsukuba ...
BEKTIK EMRE
core   +1 more source

Inflammatory myopathies in a patient with Darier\'s disease, a possible association

Caspian Journal of Internal Medicine, 2018
Background: Darier disease (DD) is an autosomal dominant genetic disorder which develops from a mutation in the ATP2A2 gene. Inflammatory myopathies (IM) are the largest group of potentially treatable myopathies. In this case, we report development of IM
Kaveh Gharaeinejad, Hojat Eftekhari, rana rafiei, Abbas Darjani, Narges Alizadeh   +4 more
doaj  

Identification of mutation c.632G>A (p.G211D) in the ATP2A2 gene and genotype–phenotype correlation in a large Chinese family with Darier’s disease [PDF]

, 2011
Feng‐Yan Lu, Ling Xu, Xun‐Guo Yin, Ping Wan, Xiao‐De Zhang, Weiwen Chen, Shao‐Ping Ding, Yong‐Gang Yao   +7 more
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Brain-specific heterozygous loss-of-function of ATP2A2, endoplasmic reticulum Ca2+ pump responsible for Darier’s disease, causes behavioral abnormalities and a hyper-dopaminergic state [PDF]

, 2021
Kazuo Nakajima, Mizuho Ishiwata, Adam Z. Weitemier, Hirotaka Shoji, Hiromu Monai, Hiroyuki Miyamoto, Kazuhiro Yamakawa, Tsuyoshi Miyakawa, Thomas J. McHugh, Tadafumi Kato   +9 more
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Severe Darier’s disease in a 39-year-old patient

Przegląd Dermatologiczny, 2019
Dorota Kozłowska, Teresa Reduta, Joanna Bacharewicz-Szczerbicka, Iwona Flisiak   +3 more
doaj   +1 more source