Identification of a familial cleidocranial dysplasia with a novel RUNX2 mutation and establishment of patient-derived induced pluripotent stem cells
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1618-1255
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Identification of a familial cleidocranial dysplasia with a novel RUNX2 mutation and establishment of patient-derived induced pluripotent stem cells ; day:15 ; month:11 ; year:2021 ; pages:1-8
Odontology ; (15.11.2021), 1-8
- Creator
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Hamada, Atsuko
Mukasa, Hanae
Taguchi, Yuki
Akagi, Eri
Obayashi, Fumitaka
Yamasaki, Sachiko
Kanda, Taku
Koizumi, Koichi
Toratani, Shigeaki
Okamoto, Tetsuji
- Contributor
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SpringerLink (Online service)
- DOI
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10.1007/s10266-021-00674-5
- URN
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urn:nbn:de:101:1-2022012522153665581240
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:40 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Hamada, Atsuko
- Mukasa, Hanae
- Taguchi, Yuki
- Akagi, Eri
- Obayashi, Fumitaka
- Yamasaki, Sachiko
- Kanda, Taku
- Koizumi, Koichi
- Toratani, Shigeaki
- Okamoto, Tetsuji
- SpringerLink (Online service)
Other Objects (12)
Identification of RUNX2 variants associated with cleidocranial dysplasia
A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia
Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia
Modelling neurological diseases using patientderived induced pluripotent stem cells
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review
Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cells
Current advancements of modelling schizophrenia using patient-derived induced pluripotent stem cells
Investigation of immune-related diseases using patient-derived induced pluripotent stem cells
Die Untersuchung des Transkriptionsfaktors RUNX2, insbesondere die RUNX2-Cbfβ-Interaktion [RUNX2-Cbf-Beta-Interaktion] in der Pathogenese der cleidocranialen Dysplasie
Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases
Evaluation of Therapeutic Oligonucleotides for Familial Amyloid Polyneuropathy in Patient-Derived Hepatocyte-Like Cells
Identification of RUNX2 variants associated with cleidocranial dysplasia
A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia
Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia
Modelling neurological diseases using patientderived induced pluripotent stem cells
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review
Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cells
Current advancements of modelling schizophrenia using patient-derived induced pluripotent stem cells
Investigation of immune-related diseases using patient-derived induced pluripotent stem cells
Die Untersuchung des Transkriptionsfaktors RUNX2, insbesondere die RUNX2-Cbfβ-Interaktion [RUNX2-Cbf-Beta-Interaktion] in der Pathogenese der cleidocranialen Dysplasie
Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases
Evaluation of Therapeutic Oligonucleotides for Familial Amyloid Polyneuropathy in Patient-Derived Hepatocyte-Like Cells
Identification of RUNX2 variants associated with cleidocranial dysplasia
A novel, complex RUNX2 gene mutation causes cleidocranial dysplasia
Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia
Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia
Modelling neurological diseases using patientderived induced pluripotent stem cells
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review
Modeling CADASIL vascular pathologies with patient-derived induced pluripotent stem cells
Current advancements of modelling schizophrenia using patient-derived induced pluripotent stem cells
Investigation of immune-related diseases using patient-derived induced pluripotent stem cells
Die Untersuchung des Transkriptionsfaktors RUNX2, insbesondere die RUNX2-Cbfβ-Interaktion [RUNX2-Cbf-Beta-Interaktion] in der Pathogenese der cleidocranialen Dysplasie
Application of patient-derived induced pluripotent stem cells and organoids in inherited retinal diseases