O. Jaka

发表

Effects of Natural Monoamine Oxidase Inhibitors on Anxiety-Like Behavior in Zebrafish

M. Peitsch, J. Hoeng, K. Koshibu, 2021, Frontiers in Pharmacology.

Impaired calcium calmodulin kinase signaling and muscle adaptation response in the absence of calpain 3.

A. López de Munain, E. Kudryashova, M. Spencer, 2012, Human molecular genetics.

A mouse model offers novel insights into the myopathy and tendinopathy often associated with pseudoachondroplasia and multiple epiphyseal dysplasia

R. Boot-Handford, K. Kadler, R. S. Meadows, 2009, Human molecular genetics.

Differentiating the Neuropharmacological Properties of Nicotinic Acetylcholine Receptor-Activating Alkaloids

M. Peitsch, J. Hoeng, K. Koshibu, 2022, Frontiers in Pharmacology.

Human primary skeletal muscle‐derived myoblasts and fibroblasts reveal different senescent phenotypes

S. Harridge, O. Jaka, N. Lazarus, 2022, JCSM Rapid Communications.

Ret function in muscle stem cells points to tyrosine kinase inhibitor therapy for facioscapulohumeral muscular dystrophy

C. Banerji, E. Blanc, Francesco Saverio Tedesco, 2016, eLife.

Active GSK3β and an intact β-catenin TCF complex are essential for the differentiation of human myogenic progenitor cells

C. C. Agley, S. Harridge, P. Francis-West, 2017, Scientific Reports.

in muscle stem cells points to tyrosine kinase inhibitor therapy for facioscapulohumeral muscular dystrophy.

C. Banerji, E. Blanc, Francesco Saverio Tedesco, 2016 .

Altitude exposure and increased heart rate: the role of the parasympathetic nervous system

F. Lewis, Julia Attias, Philip A Carvil, 2017, The Journal of physiology.

Costamere proteins and their involvement in myopathic processes

L. Casas-Fraile, A. López de Munain, A. Sáenz, 2015, Expert Reviews in Molecular Medicine.

VGLL3 operates via TEAD1, TEAD3 and TEAD4 to influence myogenesis in skeletal muscle

D. Matallanas, A. García-Muñoz, A. Pobbati, 2019, Journal of Cell Science.

C3KO mouse expression analysis: downregulation of the muscular dystrophy Ky protein and alterations in muscle aging

A. Sáenz, M. Spencer, O. Jaka, 2012, neurogenetics.

Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients.

A. Aiastui, A. López de Munain, B. Aguado, 2013, Human molecular genetics.

FRZB and melusin, overexpressed in LGMD2A, regulate integrin β1D isoform replacement altering myoblast fusion and the integrin-signalling pathway

A. Aiastui, L. Casas-Fraile, A. López de Munain, 2017, Expert Reviews in Molecular Medicine.

C3KO mouse expression analysis: downregulation of the muscular dystrophy Ky protein and alterations in muscle aging

A. López de Munain, A. Sáenz, M. Spencer, 2012, neurogenetics.

Effects of nicotinic acetylcholine receptor-activating alkaloids on anxiety-like behavior in zebrafish

M. Peitsch, J. Hoeng, K. Koshibu, 2021, Journal of Natural Medicines.

Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients.

A. Aiastui, A. López de Munain, B. Aguado, 2013, Human molecular genetics.

Screening for chemicals with thyroid hormone-disrupting effects using zebrafish embryo.

A. Muriana, O. Jaka, I. Iturria, 2023, Reproductive toxicology.

Altered expression of proteins involved in metabolism in LGMDR1 muscle is lost in cell culture conditions

Garazi Guembelzu, A. Aiastui, Andrea Valls, 2023, Orphanet Journal of Rare Diseases.

Entire CAPN3 gene deletion in a patient with limb‐girdle muscular dystrophy type 2A

N. Lévy, L. Casas-Fraile, A. López de Munain, 2014, Muscle & nerve.