Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Estera Rintz"'
Autor:
Grzegorz Węgrzyn, Takashi Higuchi, Estera Rintz, Hiroshi Kobayashi, Shunji Tomatsu, Deni S. Galileo
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 24, Iss, Pp 71-87 (2022)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
More than 50 lysosomal storage diseases (LSDs) are associated with lysosomal dysfunctions with the frequency of 1:5,000 live births. As a result of missing enzyme activity, the lysosome dysfunction accumulates undegraded or partially degraded molecul
Publikováno v:
International journal of molecular sciences. 23(11)
The skeletal development process in the body occurs through sequential cellular and molecular processes called endochondral ossification. Endochondral ossification occurs in the growth plate where chondrocytes differentiate from resting, proliferativ
Autor:
Karolina Pierzynowska, Lidia Gaffke, Magdalena Żabińska, Zuzanna Cyske, Estera Rintz, Karolina Wiśniewska, Magdalena Podlacha, Grzegorz Węgrzyn
Publikováno v:
International Journal of Molecular Sciences. 24:3887
The oxytocin receptor (OXTR), encoded by the OXTR gene, is responsible for the signal transduction after binding its ligand, oxytocin. Although this signaling is primarily involved in controlling maternal behavior, it was demonstrated that OXTR also
Publikováno v:
Molecular Genetics and Metabolism. 138:107047
Autor:
Andrés Felipe Leal, Eliana Benincore-Flórez, Estera Rintz, Angélica María Herreño-Pachón, Betul Celik, Yasuhiko Ago, Carlos Javier Alméciga-Díaz, Shunji Tomatsu
Publikováno v:
International Journal of Molecular Sciences. 24:477
Mucopolysaccharidoses (MPSs) constitute a heterogeneous group of lysosomal storage disorders characterized by the lysosomal accumulation of glycosaminoglycans (GAGs). Although lysosomal dysfunction is mainly affected, several cellular organelles such
Autor:
Estera Rintz, Joanna Brokowska, Lidia Gaffke, Grzegorz Węgrzyn, Karolina Pierzynowska, Magdalena Podlacha, Zuzanna Cyske
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 9
International Journal of Molecular Sciences, Vol 21, Iss 3194, p 3194 (2020)
Volume 21
Issue 9
International Journal of Molecular Sciences, Vol 21, Iss 3194, p 3194 (2020)
Although mucopolysaccharidoses (MPS), inherited metabolic diseases from the group of lysosomal storage diseases (LSD), are monogenic disorders, recent studies indicated that their molecular mechanisms are complicated. Storage of glycosaminoglycans (G
Autor:
Joanna Brokowska, Estera Rintz, Zuzanna Cyske, Karolina Pierzynowska, Lidia Gaffke, Magdalena Podlacha, Dżesika Hoinkis, Grzegorz Węgrzyn
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1204 (2020)
Volume 21
Issue 4
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1204 (2020)
Volume 21
Issue 4
Mucopolysaccharidoses (MPS), a group of inherited metabolic disorders caused by deficiency in enzymes involved in degradation of glycosaminoglycans (GAGs), are examples (and models) of monogenic diseases. Accumulation of undegraded GAGs in lysosomes
Autor:
Joanna Brokowska, Karolina Pierzynowska, Grzegorz Węgrzyn, Magdalena Podlacha, Estera Rintz, Zuzanna Cyske, Lidia Gaffke
Publikováno v:
Molecular Genetics and Metabolism. 129:S160-S161
Autor:
S. Lopez-Lugo, D. Pankanin, Zuzanna Cyske, Karolina Pierzynowska, Grzegorz Węgrzyn, Estera Rintz, Lidia Gaffke
Publikováno v:
New Biotechnology. 44:S31-S32