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Cell Reports. Medicine
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May 5, 2021
Preclinical evaluation for engraftment of CD34<sup>+</sup> cells gene-edited at the sickle cell disease locus in xenograft mouse and non-human primate models
Naoya Uchida, Linhong Li, Tina Nassehi, et al.
Science Translational Medicine
|
October 16, 2024
High-fidelity PAMless base editing of hematopoietic stem cells to treat chronic granulomatous disease
Vera Bzhilyanskaya, Linyuan Ma, Siyuan Liu, et al.
Frontiers in Immunology
|
January 23, 2023
CRISPR-Cas9-AAV versus lentivector transduction for genome modification of X-linked severe combined immunodeficiency hematopoietic stem cells
Julie Brault, Taylor Liu, Siyuan Liu, et al.
The Journal of Allergy and Clinical Immunology
|
December 31, 2013
CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation
Clarisa M Buckner, Susan Moir, Lela Kardava, et al.
Nature Communications
|
June 28, 2022
Lentivector cryptic splicing mediates increase in CD34+ clones expressing truncated HMGA2 in human X-linked severe combined immunodeficiency
Suk See De Ravin, Siyuan Liu, Colin L Sweeney, et al.
Nature Biotechnology
|
March 8, 2016
Targeted gene addition in human CD34(+) hematopoietic cells for correction of X-linked chronic granulomatous disease
Suk See De Ravin, Andreas Reik, Pei-Qi Liu, et al.
Blood
|
May 22, 2010
Hypomorphic Rag mutations can cause destructive midline granulomatous disease
Suk See De Ravin, Edward W Cowen, Kol A Zarember, et al.
Blood
|
June 4, 2021
CRISPR-targeted MAGT1 insertion restores XMEN patient hematopoietic stem cells and lymphocytes
Julie Brault, Taylor Liu, Ezekiel Bello, et al.
Blood
|
February 24, 2021
Enhanced homology-directed repair for highly efficient gene editing in hematopoietic stem/progenitor cells
Suk See De Ravin, Julie Brault, Ronald J Meis, et al.
Blood Advances
|
December 10, 2025
Clinical Characteristics, Management, and Hematopoietic Cell Transplantation of Patients with TLR8 Gain-of-Function
Danielle E Arnold, Saara Kaviany, Jahnavi Aluri, et al.
Page
of 7
Search research articles
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Showing results (41-50 of 66) with videos related to
Sort By:
Page
of 7
Cell Reports. Medicine
|
May 5, 2021
Preclinical evaluation for engraftment of CD34<sup>+</sup> cells gene-edited at the sickle cell disease locus in xenograft mouse and non-human primate models
Naoya Uchida, Linhong Li, Tina Nassehi, et al.
Science Translational Medicine
|
October 16, 2024
High-fidelity PAMless base editing of hematopoietic stem cells to treat chronic granulomatous disease
Vera Bzhilyanskaya, Linyuan Ma, Siyuan Liu, et al.
Frontiers in Immunology
|
January 23, 2023
CRISPR-Cas9-AAV versus lentivector transduction for genome modification of X-linked severe combined immunodeficiency hematopoietic stem cells
Julie Brault, Taylor Liu, Siyuan Liu, et al.
The Journal of Allergy and Clinical Immunology
|
December 31, 2013
CXCR4/IgG-expressing plasma cells are associated with human gastrointestinal tissue inflammation
Clarisa M Buckner, Susan Moir, Lela Kardava, et al.
Nature Communications
|
June 28, 2022
Lentivector cryptic splicing mediates increase in CD34+ clones expressing truncated HMGA2 in human X-linked severe combined immunodeficiency
Suk See De Ravin, Siyuan Liu, Colin L Sweeney, et al.
Nature Biotechnology
|
March 8, 2016
Targeted gene addition in human CD34(+) hematopoietic cells for correction of X-linked chronic granulomatous disease
Suk See De Ravin, Andreas Reik, Pei-Qi Liu, et al.
Blood
|
May 22, 2010
Hypomorphic Rag mutations can cause destructive midline granulomatous disease
Suk See De Ravin, Edward W Cowen, Kol A Zarember, et al.
Blood
|
June 4, 2021
CRISPR-targeted MAGT1 insertion restores XMEN patient hematopoietic stem cells and lymphocytes
Julie Brault, Taylor Liu, Ezekiel Bello, et al.
Blood
|
February 24, 2021
Enhanced homology-directed repair for highly efficient gene editing in hematopoietic stem/progenitor cells
Suk See De Ravin, Julie Brault, Ronald J Meis, et al.
Blood Advances
|
December 10, 2025
Clinical Characteristics, Management, and Hematopoietic Cell Transplantation of Patients with TLR8 Gain-of-Function
Danielle E Arnold, Saara Kaviany, Jahnavi Aluri, et al.
Page
of 7