Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9
- 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
-
Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9 ; volume:9 ; number:1 ; day:14 ; month:12 ; year:2018 ; pages:1-10 ; date:12.2018
Nature Communications ; 9, Heft 1 (14.12.2018), 1-10, 12.2018
- Creator
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Croft, Brittany
Ohnesorg, Thomas
Hewitt, Jacky
Bowles, Josephine
Quinn, Alexander
Tan, Jacqueline
Corbin, Vincent
Pelosi, Emanuele
Bergen, Jocelyn van den
Sreenivasan, Rajini
Knarston, Ingrid
Robevska, Gorjana
Vu, Dung Chi
Hutson, John
Harley, Vincent
Ayers, Katie
Koopman, Peter
Sinclair, Andrew
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41467-018-07784-9
- URN
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urn:nbn:de:101:1-2019012723385394139153
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:58 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
- Croft, Brittany
- Ohnesorg, Thomas
- Hewitt, Jacky
- Bowles, Josephine
- Quinn, Alexander
- Tan, Jacqueline
- Corbin, Vincent
- Pelosi, Emanuele
- Bergen, Jocelyn van den
- Sreenivasan, Rajini
- Knarston, Ingrid
- Robevska, Gorjana
- Vu, Dung Chi
- Hutson, John
- Harley, Vincent
- Ayers, Katie
- Koopman, Peter
- Sinclair, Andrew
- SpringerLink (Online service)
Other Objects (12)
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Mapping of a responsible region for sex reversal upstream of Sox9 by production of mice with serial deletion in a genomic locus
Using Gene Duplication and Gene Deletion in Evolution Strategies
Psychiatric disorders in children with 16p11.2 deletion and duplication
7q36 deletion and 9p22 duplication: effects of a double imbalance
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Differential transactivation of the upstream aggrecan enhancer regulated by PAX1/9 depends on SOX9-driven transactivation
A mutation creating an upstream initiation codon in the SOX9 5′ UTR causes acampomelic campomelic dysplasia
Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Enhancers, enhancers – from their discovery to today’s universe of transcription enhancers
Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter
SOX9 duplication linked to intersex in deer
Epilepsies in Children with 2q24.3 Deletion/Duplication
Mapping of a responsible region for sex reversal upstream of Sox9 by production of mice with serial deletion in a genomic locus
Using Gene Duplication and Gene Deletion in Evolution Strategies
Psychiatric disorders in children with 16p11.2 deletion and duplication
7q36 deletion and 9p22 duplication: effects of a double imbalance
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Differential transactivation of the upstream aggrecan enhancer regulated by PAX1/9 depends on SOX9-driven transactivation
A mutation creating an upstream initiation codon in the SOX9 5′ UTR causes acampomelic campomelic dysplasia
Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Enhancers, enhancers – from their discovery to today’s universe of transcription enhancers
Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter
SOX9 duplication linked to intersex in deer
Epilepsies in Children with 2q24.3 Deletion/Duplication
Mapping of a responsible region for sex reversal upstream of Sox9 by production of mice with serial deletion in a genomic locus
Using Gene Duplication and Gene Deletion in Evolution Strategies
Psychiatric disorders in children with 16p11.2 deletion and duplication
7q36 deletion and 9p22 duplication: effects of a double imbalance
A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review
Differential transactivation of the upstream aggrecan enhancer regulated by PAX1/9 depends on SOX9-driven transactivation
A mutation creating an upstream initiation codon in the SOX9 5′ UTR causes acampomelic campomelic dysplasia
Uncovering missing pieces: duplication and deletion history of arrestins in deuterostomes
Enhancers, enhancers – from their discovery to today’s universe of transcription enhancers