11 Einträge gefunden

1. Mice heterozygous for an osteogenesis imperfecta-linked MBTPS2 variant display a compromised subchondral osteocyte lacunocanalicular network associated with abnormal articular cartilage

   1. Danyukova, Tatyana
   2. Alimy, Assil Ramin
   3. Velho, Renata Voltolini
   4. Yorgan, Timur A.
   5. Di Lorenzo, Giorgia
   6. von Kroge, Simon
   7. Tidow, Henning

   2023 - Forschungsinformationssystem der UHH
2. A homozygous hypomorphic BNIP1 variant causes an increase in autophagosomes and reduced autophagic flux and results in a spondylo-epiphyseal dysplasia

   1. Holling, Tess
   2. Bhavani, Gandham S
   3. von Elsner, Leonie
   4. Shah, Hitesh
   5. Kausthubham, Neethukrishna
   6. Bhattacharyya, Shaila S
   7. Shukla, Anju

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
3. Site-1 and site-2 proteases: A team of two in regulated proteolysis

   1. Danyukova, Tatyana
   2. Schöneck, Kenneth
   3. Pohl, Sandra

   2022 - Forschungsinformationssystem des UKE - frei zugänglich
4. Transgenic inhibition of interleukin-6 trans-signaling does not prevent skeletal pathologies in mucolipidosis type II mice

   1. Westermann, Lena Marie
   2. Baranowsky, Anke
   3. Di Lorenzo, Giorgia
   4. Danyukova, Tatyana
   5. Soul, Jamie
   6. Schwartz, Jean-Marc
   7. Hendrickx, Gretl

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
5. Enzyme replacement therapy in mice lacking arylsulfatase B targets bone remodeling cells, but not chondrocytes

   1. Hendrickx, Gretl
   2. Danyukova, Tatyana
   3. Baranowsky, Anke
   4. Rolvien, Tim
   5. Angermann, Alexandra
   6. Schweizer, Michaela
   7. Keller, Johannes

   2020 - Forschungsinformationssystem des UKE
6. Combined in-vitro and in-silico analyses of missense mutations in GNPTAB provide new insights into the molecular bases of mucolipidosis II and III alpha/beta

   1. Danyukova, Tatyana
   2. Ludwig, Nataniel F
   3. Velho, Renata Voltolini
   4. Harms, Frederike L
   5. Güneş, Nilay
   6. Tidow, Henning
   7. Schwartz, Ida V

   2020 - Forschungsinformationssystem des UKE - frei zugänglich
7. The lysosomal storage disorders mucolipidosis type II, type III alpha/beta and type III gamma: Update on GNPTAB and GNPTG mutations

   1. Velho, Renata Voltolini
   2. Harms, Frederike L
   3. Danyukova, Tatyana
   4. Ludwig, Nataniel F
   5. Friez, Michael J
   6. Cathey, Sara S
   7. Filocamo, Mirella

   2019 - Forschungsinformationssystem des UKE
8. Mice deficient in the lysosomal enzyme palmitoyl-protein thioesterase 1 (PPT1) display a complex retinal phenotype

   1. Atiskova, Yevgeniya
   2. Bartsch, Susanne
   3. Danyukova, Tatyana
   4. Becker, Elke
   5. Hagel, Christian
   6. Storch, Stephan
   7. Bartsch, Udo

   2019 - Forschungsinformationssystem des UKE - frei zugänglich
9. A newly generated neuronal cell model of CLN7 disease reveals aberrant lysosome motility and impaired cell survival.

   1. von Kleist, Lisa
   2. Ariunbat, Khandsuren
   3. Braren, Ingke
   4. Stauber, Tobias
   5. Storch, Stephan
   6. Danyukova, Tatyana

   2019 - Forschungsinformationssystem des UKE
10. Toward Engineering the Mannose 6-Phosphate Elaboration Pathway in Plants for Enzyme Replacement Therapy of Lysosomal Storage Disorders

    1. Zeng, Ying
    2. He, Xu
    3. Danyukova, Tatyana
    4. Pohl, Sandra
    5. Kermode, Allison R

    2019 - Forschungsinformationssystem des UKE - frei zugänglich
11. Loss of CLN7 results in depletion of soluble lysosomal proteins and impaired mTOR reactivation

    1. Danyukova, Tatyana
    2. Ariunbat, Khandsuren
    3. Thelen, Melanie
    4. Brocke-Ahmadinejad, Nahal
    5. Mole, Sara E
    6. Storch, Stephan

    2018 - Forschungsinformationssystem des UKE