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2023
Mark From Epistemic Norms to Logical Rules : Epistemic Models for Logical Expressivists
Dahl, Niklas ^LU (2023) In Journal of Philosophical Logic 52(6). p.1517-1533
- Contribution to journal › Article
Mark Heredity of pregnancy-related pelvic girdle pain in Sweden
Kristiansson, Per ; Zöller, Bengt ^LU ; Dahl, Niklas ; Kalliokoski, Paul ; Hallqvist, Johan and Li, Xinjun ^LU (2023) In Acta Obstetricia et Gynecologica Scandinavica 102(10). p.1250-1258
- Contribution to journal › Article
2022
Mark A Fixed-Point Problem for Theories of Meaning
Dahl, Niklas ^LU (2022) In Synthese 200(1). p.1-15
- Contribution to journal › Article
Mark Att prata om saker
Dahl, Niklas ^LU (2022) In Svensk Filosofi
- Contribution to specialist publication or newspaper › Specialist publication article
Mark Partial Monosomy 21 Mirrors Gene Expression of Trisomy 21 in a Patient-Derived Neuroepithelial Stem Cell Model
Schuy, Jakob ; Eisfeldt, Jesper ; Pettersson, Maria ; Shahrokhshahi, Niloofar ; Moslem, Mohsen ; Nilsson, Daniel ; Dahl, Niklas ; Shahsavani, Mansoureh ; Falk, Anna ^LU and Lindstrand, Anna (2022) In Frontiers in Genetics 12.
- Contribution to journal › Article
2020
Mark DNA methylation changes in Down syndrome derived neural iPSCs uncover co-dysregulation of ZNF and HOX3 families of transcription factors
Laan, Loora ; Klar, Joakim ; Sobol, Maria ; Hoeber, Jan ; Shahsavani, Mansoureh ; Kele, Malin ; Fatima, Ambrin ; Zakaria, Muhammad ; Annerén, Göran and Falk, Anna ^LU , et al. (2020) In Clinical Epigenetics 12(1).
- Contribution to journal › Article
2019
Mark Transcriptome and Proteome Profiling of Neural Induced Pluripotent Stem Cells from Individuals with Down Syndrome Disclose Dynamic Dysregulations of Key Pathways and Cellular Functions
Sobol, Maria ; Klar, Joakim ; Laan, Loora ; Shahsavani, Mansoureh ; Schuster, Jens ; Annerén, Göran ; Konzer, Anne ; Mi, Jia ; Bergquist, Jonas and Nordlund, Jessica , et al. (2019) In Molecular Neurobiology 56(10). p.7113-7127
- Contribution to journal › Article
Mark Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186
Kvarnung, Malin ; Shahsavani, Mansoureh ; Taylan, Fulya ; Moslem, Mohsen ; Breeuwsma, Nicole ; Laan, Loora ; Schuster, Jens ; Jin, Zhe ^LU ; Nilsson, Daniel ^LU and Lieden, Agne , et al. (2019) In Frontiers in Genetics 10.
- Contribution to journal › Article
Mark Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality
Lam, Matti ^LU ; Moslem, Mohsen ; Bryois, Julien ; Pronk, Robin J ; Uhlin, Elias ; Ellström, Ivar Dehnisch ; Laan, Loora ; Olive, Jessica ; Morse, Rebecca and Rönnholm, Harriet , et al. (2019) In Experimental Cell Research 383(1).
- Contribution to journal › Article
2016
Mark Generation of human iPS cell line CTL07-II from human fibroblasts, under defined and xeno-free conditions
Kele, Malin ; Day, Kelly ; Rönnholm, Harriet ; Schuster, Jens ; Dahl, Niklas and Falk, Anna ^LU (2016) In Stem Cell Research 17(3). p.474-478
- Contribution to journal › Article

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