Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Yujuan, Hou"'
Publikováno v:
Shipin Kexue, Vol 44, Iss 20, Pp 20-27 (2023)
Glutenin (Glu) was modified by pH-shifting to improve its properties. The effect of pH-shifting treatment on the structure and micromorphology of glutenin was investigated by dynamic light scattering (DLS), transmission electron microscopy (TEM), flu
Externí odkaz:
https://doaj.org/article/235daf9888804e01af1c4b7345095446
Autor:
Tahereh Mohammadian Gol, Guillermo Ureña-Bailén, Yujuan Hou, Ralph Sinn, Justin S. Antony, Rupert Handgretinger, Markus Mezger
Publikováno v:
Frontiers in Genome Editing, Vol 4 (2023)
Blood disorders are a group of diseases including hematological neoplasms, clotting disorders and orphan immune deficiency diseases that affects human health. Current improvements in genome editing based therapeutics demonstrated preclinical and clin
Externí odkaz:
https://doaj.org/article/af6536b6e18e46e6acc0fbb918946857
Autor:
Mezger, Yujuan Hou, Guillermo Ureña-Bailén, Tahereh Mohammadian Gol, Paul Gerhard Gratz, Hans Peter Gratz, Alicia Roig-Merino, Justin S. Antony, Andrés Lamsfus-Calle, Alberto Daniel-Moreno, Rupert Handgretinger, Markus
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2348
X-linked severe combined immunodeficiency (X-SCID) is a primary immunodeficiency that is caused by mutations in the interleukin-2 receptor gamma (IL2RG) gene. Some patients present atypical X-SCID with mild clinical symptoms due to somatic revertant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::496e7a39b5708de395302caf9566ef15
Somatic Reversion of a Novel IL2RG Mutation Resulting in Atypical X-Linked Combined Immunodeficiency
Autor:
Yujuan Hou, Hans Peter Gratz, Guillermo Ureña-Bailén, Paul G. Gratz, Karin Schilbach-Stückle, Tina Renno, Derya Güngör, Daniel A. Mader, Elke Malenke, Justin S. Antony, Rupert Handgretinger, Markus Mezger
Publikováno v:
Genes, Vol 13, Iss 35, p 35 (2022)
Mutations of the IL2RG gene, which encodes for the interleukin-2 receptor common gamma chain (γC, CD132), can lead to X-linked severe combined immunodeficiency (X-SCID) associated with a T−B+NK− phenotype as a result of dysfunctional γC-JAK3-ST
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::bf9941b84e0ef1f1a485ae4de657f54a
https://www.mdpi.com/2073-4425/13/1/35
https://www.mdpi.com/2073-4425/13/1/35
Autor:
Yujuan, Hou, Guillermo, Ureña-Bailén, Tahereh, Mohammadian Gol, Paul Gerhard, Gratz, Hans Peter, Gratz, Alicia, Roig-Merino, Justin S, Antony, Andrés, Lamsfus-Calle, Alberto, Daniel-Moreno, Rupert, Handgretinger, Markus, Mezger
Publikováno v:
Genes. 13(12)
X-linked severe combined immunodeficiency (X-SCID) is a primary immunodeficiency that is caused by mutations in the interleukin-2 receptor gamma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e5c03504dfa2bd5a07bdc0ca50e9cf1
https://pubmed.ncbi.nlm.nih.gov/36553615
https://pubmed.ncbi.nlm.nih.gov/36553615
Preclinical Evaluation of CRISPR-Edited CAR-NK-92 Cells for Off-the-Shelf Treatment of AML and B-ALL
Autor:
Mezger, Guillermo Ureña-Bailén, Jérôme-Maurice Dobrowolski, Yujuan Hou, Alicia Dirlam, Alicia Roig-Merino, Sabine Schleicher, Daniel Atar, Christian Seitz, Judith Feucht, Justin S. Antony, Tahereh Mohammadian Gol, Rupert Handgretinger, Markus
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 21; Pages: 12828
Acute myeloid leukemia (AML) and B-cell acute lymphocytic leukemia (B-ALL) are severe blood malignancies affecting both adults and children. Chimeric antigen receptor (CAR)-based immunotherapies have proven highly efficacious in the treatment of leuk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::5d61e5d78e26b851856f1e0efb3e894d
Preclinical Evaluation of CRISPR-Edited CAR-NK-92 Cells for Off-the-Shelf Treatment of AML and B-ALL
Autor:
Guillermo, Ureña-Bailén, Jérôme-Maurice, Dobrowolski, Yujuan, Hou, Alicia, Dirlam, Alicia, Roig-Merino, Sabine, Schleicher, Daniel, Atar, Christian, Seitz, Judith, Feucht, Justin S, Antony, Tahereh, Mohammadian Gol, Rupert, Handgretinger, Markus, Mezger
Publikováno v:
International journal of molecular sciences. 23(21)
Acute myeloid leukemia (AML) and B-cell acute lymphocytic leukemia (B-ALL) are severe blood malignancies affecting both adults and children. Chimeric antigen receptor (CAR)-based immunotherapies have proven highly efficacious in the treatment of leuk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e701d1b7c93b60df3f3de9658c0f89c1
https://pubmed.ncbi.nlm.nih.gov/36361619
https://pubmed.ncbi.nlm.nih.gov/36361619
Somatic Reversion of a Novel IL2RG Mutation Resulting in Atypical X-Linked Combined Immunodeficiency
Autor:
Mezger, Yujuan Hou, Hans Peter Gratz, Guillermo Ureña-Bailén, Paul G. Gratz, Karin Schilbach-Stückle, Tina Renno, Derya Güngör, Daniel A. Mader, Elke Malenke, Justin S. Antony, Rupert Handgretinger, Markus
Publikováno v:
Genes; Volume 13; Issue 1; Pages: 35
Mutations of the IL2RG gene, which encodes for the interleukin-2 receptor common gamma chain (γC, CD132), can lead to X-linked severe combined immunodeficiency (X-SCID) associated with a T−B+NK− phenotype as a result of dysfunctional γC-JAK3-ST
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::e1453bce5afeaba8a3ac49e581eb908c
Autor:
Guillermo Ureña-Bailén, Justin S. Antony, Yujuan Hou, Janani Raju, Andres Lamsfus-Calle, Alberto Daniel-Moreno, Rupert Handgretinger, Markus Mezger
Publikováno v:
CRISPR-/Cas9 Based Genome Editing for Treating Genetic Disorders and Diseases ISBN: 9781003088516
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8279a845175e1eb8f593456c1f2e1d2d
https://doi.org/10.1201/9781003088516-11
https://doi.org/10.1201/9781003088516-11
Autor:
Justin S. Antony, Alberto Daniel-Moreno, Andrés Lamsfus-Calle, Janani Raju, Merve Kaftancioglu, Guillermo Ureña-Bailén, Jennifer Rottenberger, Yujuan Hou, Vidiyaah Santhanakumaran, Jun-Hoe Lee, Lukas Heumos, Judith Böhringer, Ingeborg Krägeloh-Mann, Rupert Handgretinger, Markus Mezger
Publikováno v:
The CRISPR journal. 5(1)
Metachromatic leukodystrophy (MLD) is a rare genetic disorder caused by mutations in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76ca4189a348c009f112f420bcb8eb38
https://pubmed.ncbi.nlm.nih.gov/34882002
https://pubmed.ncbi.nlm.nih.gov/34882002