Madeleine Durbeej-Hjalt

1 – 10 of 63

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/person/ff1ad48f-2712-4293-9975-afc8e7f9f05f?embed=1&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
2
3
4
…
6
7
next »

2022
Mark Skeletal muscle regeneration is altered in the R6/2 mouse model of Huntington’s disease
Hoque, Sanzana ^LU ; Sjögren, Marie ^LU ; Allamand, Valérie ^LU ; Gawlik, Kinga ^LU ; Franke, Naomi ; Durbeej, Madeleine ^LU ; Björkqvist, Maria ^LU and Soylu Kucharz, Rana ^LU (2022) p.1-23
- Working paper/Preprint › Preprint in preprint archive
2021
Mark A guide to the composition and functions of the extracellular matrix
Karamanos, Nikos K. ; Theocharis, Achilleas D. ; Piperigkou, Zoi ; Manou, Dimitra ; Passi, Alberto ; Skandalis, Spyros S. ; Vynios, Demitrios H. ; Orian-Rousseau, Véronique ; Ricard-Blum, Sylvie and Schmelzer, Christian E.H. , et al. (2021) In The FEBS Journal 288(24). p.6850-6912
- Contribution to journal › Article
Mark Merosin deficient congenital muscular dystrophy type 1A : An international workshop on the road to therapy 15-17 November 2019, Maastricht, the Netherlands
Smeets, Hubert J.M. ; Verbrugge, Bram ; Springuel, Pierre ; Voermans, Nicol C. ; Cossu, Giulio ; de Coo, René ; Diamantidis, Christos ; Dragendorf, Eric ; Durbeej-Hjalt, Madeleine ^LU and Dziewczapolski, Gustavo , et al. (2021) In Neuromuscular Disorders 31(7). p.673-680
- Contribution to journal › Article
2020
Mark Antioxidants reduce muscular dystrophy in the dy^2J/dy^2J mouse model of laminin α2 chain-deficient muscular dystrophy
Harandi, Vahid M. ^LU ; Oliveira, Bernardo Moreira Soares ^LU ; Allamand, Valérie ^LU ; Friberg, Ariana ; Fontes-Oliveira, Cibely C. ^LU and Durbeej, Madeleine ^LU (2020) In Antioxidants 9(3).
- Contribution to journal › Article
Mark A Family of Laminin α2 Chain-Deficient Mouse Mutants : Advancing the Research on LAMA2-CMD
Gawlik, Kinga I. ^LU and Durbeej, Madeleine ^LU (2020) In Frontiers in Molecular Neuroscience 13.
- Contribution to journal › Scientific review
2019
Mark A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene
Kemaladewi, Dwi U ; Bassi, Prabhpreet S ; Erwood, Steven ; Al-Basha, Dhekra ; Gawlik, Kinga I ^LU ; Lindsay, Kyle ; Hyatt, Elzbieta ; Kember, Rebekah ; Place, Kara M and Marks, Ryan M , et al. (2019) In Nature 572(7767). p.125-130
- Contribution to journal › Letter
Mark Effects of N-acetyl-L-cysteine and vitamin E on congenital muscular dystrophy type 1A disease progression in mice
M. Harandi, Vahid ^LU ; Moreira Soares Oliveira, Bernardo ^LU ; Friberg, Ariana ; Gawlik, Kinga ^LU and Durbeej, Madeleine ^LU (2019) 24th International Annual Congress of the World Muscle Society 29. p.163-164
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
2018
Mark Effects of metformin on congenital muscular dystrophy type 1A disease progression in mice: a gender impact study
Fontes Oliveira, Cibely ^LU ; M. Soares Oliveira, Bernardo ^LU ; Körner, Zandra ^LU ; Harandi, Vahid ^LU and Durbeej-Hjalt, Madeleine ^LU (2018) In Scientific Reports
- Contribution to journal › Article
Mark Laminin α1 reduces muscular dystrophy in dy^2Jmice
Gawlik, Kinga I. ^LU ; Harandi, Vahid M. ^LU ; Cheong, Rachel Y. ^LU ; Petersén, Åsa ^LU and Durbeej, Madeleine ^LU (2018) In Matrix Biology 70. p.36-49
- Contribution to journal › Article
Mark Exploratory Profiling of Urine MicroRNAs in the dy2J/dy2J Mouse Model of LAMA2-CMD : Relation to Disease Progression
Moreira Soares Oliveira, Bernardo ^LU ; Gawlik, Kinga I ^LU ; Durbeej, Madeleine ^LU and Holmberg, Johan ^LU (2018) In PLoS Currents 10.
- Contribution to journal › Article

« previous
1
2
3
4
…
6
7
next »