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Compression of morbidity in a progeroid mouse model through the attenuation of myostatin/activin signalling

Vertaisarvioitu
Avoin saatavuus
DOI
10.1002/jcsm.12404
Alyodawi, Khalid; Vermeij, Wilbert P.; Omairi, Saleh; Kretz, Oliver; Hopkinson, Mark; Solagna, Franc...
Journal of cachexia, sarcopenia and muscle2019

Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice

Vertaisarvioitu
DOI
10.1016/j.cmet.2011.11.012
Ahlqvist, Kati J.; Hämäläinen, Riikka; Yatsuga, Shuichi; Uutela, Marko; Terzioglu, Mugen; Gotz, Alex...
Cell metabolism2012

Improved health by combining dietary restriction and promoting muscle growth in DNA repair-deficient progeroid mice

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Avoin saatavuus
DOI
10.1002/jcsm.13570
Vermeij, Wilbert P.; Alyodawi, Khalid; van Galen, Ivar; von der Heide, Jennie L.; Birkisdóttir, Marí...
Journal of cachexia, sarcopenia and muscle2024

Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa

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Fischer-Zirnsak B; Escande-Beillard N; Ganesh J; Tan YXuan; Al Bughaili M; Lin AE; Sahai I; Bahena P...
American Journal of Human Genetics2015

Recurrent De Novo Mutations Affecting Residue Arg1 38 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa

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DOI
10.1016/j.ajhg.2015.08.001
Fischer-Zirnsak, Bjoern; Escande-Beillard, Nathalie; Ganesh, Jaya; Tan, Yu Xuan; Al Bughaili, Mohamm...
American journal of human genetics2015

Abnormal Proteoglycan Synthesis Due to Gene Defects Causes Skeletal Diseases with Overlapping Phenotypes

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DOI
10.1055/s-0042-118706
Taylan, F.; Makitie, O.
Hormone and metabolic research2016

Compression of morbidity in a progeroid mouse model through the attenuation of myostatin/activin signalling

Vertaisarvioitu
Avoin saatavuus
DOI
10.1002/jcsm.12404
2019

Somatic Progenitor Cell Vulnerability to Mitochondrial DNA Mutagenesis Underlies Progeroid Phenotypes in Polg Mutator Mice

Vertaisarvioitu
DOI
10.1016/j.cmet.2011.11.012
2012

Improved health by combining dietary restriction and promoting muscle growth in DNA repair-deficient progeroid mice

Vertaisarvioitu
Avoin saatavuus
DOI
10.1002/jcsm.13570
2024

Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa

Vertaisarvioitu
2015

Recurrent De Novo Mutations Affecting Residue Arg1 38 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa

Vertaisarvioitu
DOI
10.1016/j.ajhg.2015.08.001
2015

Abnormal Proteoglycan Synthesis Due to Gene Defects Causes Skeletal Diseases with Overlapping Phenotypes

Vertaisarvioitu
DOI
10.1055/s-0042-118706
2016