SALL3 expression balance underlies lineage biases in human induced pluripotent stem cell differentiation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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2041-1723
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
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SALL3 expression balance underlies lineage biases in human induced pluripotent stem cell differentiation ; volume:10 ; number:1 ; day:15 ; month:5 ; year:2019 ; pages:1-13 ; date:12.2019
Nature Communications ; 10, Heft 1 (15.5.2019), 1-13, 12.2019
- Classification
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Biowissenschaften, Biologie
- Creator
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Kuroda, Takuya
Yasuda, Satoshi
Tachi, Shiori
Matsuyama, Satoko
Kusakawa, Shinji
Tano, Keiko
Miura, Takumi
Matsuyama, Akifumi
Sato, Yoji
- Contributor
-
SpringerLink (Online service)
- DOI
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10.1038/s41467-019-09511-4
- URN
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urn:nbn:de:101:1-2019090203414650919662
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:32 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kuroda, Takuya
- Yasuda, Satoshi
- Tachi, Shiori
- Matsuyama, Satoko
- Kusakawa, Shinji
- Tano, Keiko
- Miura, Takumi
- Matsuyama, Akifumi
- Sato, Yoji
- SpringerLink (Online service)
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A splicing factor switch controls hematopoietic lineage specification of pluripotent stem cells
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Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
All-trans retinoic acid promotes neural lineage entry by pluripotent embryonic stem cells via multiple pathways
Role of YAP in hematopoietic differentiation and erythroid lineage specification of human-induced pluripotent stem cells
Rapid functional genetics of the oligodendrocyte lineage using pluripotent stem cells
Endocrine lineage biases arise in temporally distinct endocrine progenitors during pancreatic morphogenesis
Brd4‐Brd2 isoform switching coordinates pluripotent exit and Smad2‐dependent lineage specification
Lineage- and developmental stage-specific mechanomodulation of induced pluripotent stem cell differentiation
A splicing factor switch controls hematopoietic lineage specification of pluripotent stem cells
Master regulators of skeletal muscle lineage development and pluripotent stem cells differentiation
Platelet and myeloid lineage biases of transplanted single perinatal mouse hematopoietic stem cells
The role of Cdx2 as a lineage specific transcriptional repressor for pluripotent network during the first developmental cell lineage segregation
HAND factors regulate cardiac lineage commitment and differentiation from human pluripotent stem cells
Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
All-trans retinoic acid promotes neural lineage entry by pluripotent embryonic stem cells via multiple pathways
Role of YAP in hematopoietic differentiation and erythroid lineage specification of human-induced pluripotent stem cells
Rapid functional genetics of the oligodendrocyte lineage using pluripotent stem cells
Endocrine lineage biases arise in temporally distinct endocrine progenitors during pancreatic morphogenesis
Brd4‐Brd2 isoform switching coordinates pluripotent exit and Smad2‐dependent lineage specification
Lineage- and developmental stage-specific mechanomodulation of induced pluripotent stem cell differentiation
A splicing factor switch controls hematopoietic lineage specification of pluripotent stem cells
Master regulators of skeletal muscle lineage development and pluripotent stem cells differentiation
Platelet and myeloid lineage biases of transplanted single perinatal mouse hematopoietic stem cells
The role of Cdx2 as a lineage specific transcriptional repressor for pluripotent network during the first developmental cell lineage segregation
HAND factors regulate cardiac lineage commitment and differentiation from human pluripotent stem cells
Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy
All-trans retinoic acid promotes neural lineage entry by pluripotent embryonic stem cells via multiple pathways