Unfavorable switching of skewed X chromosome inactivation leads to Menkes disease in a female infant
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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1 Online-Ressource.
- Language
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Englisch
- Bibliographic citation
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Unfavorable switching of skewed X chromosome inactivation leads to Menkes disease in a female infant ; volume:14 ; number:1 ; day:3 ; month:1 ; year:2024 ; pages:1-9 ; date:12.2024
Scientific reports ; 14, Heft 1 (3.1.2024), 1-9, 12.2024
- Creator
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Matsumoto, Ayumi
Kano, Shintaro
Kobayashi, Natsumi
Matsuki, Mitsuru
Furukawa, Rieko
Yamagishi, Hirokazu
Yoshinari, Hiroki
Nakata, Waka
Wakabayashi, Hiroko
Tsuda, Hidetoshi
Watanabe, Kazuhisa
Takahashi, Hironori
Yamagata, Takanori
Matsumura, Takayoshi
Osaka, Hitoshi
Mori, Harushi
Iwamoto, Sadahiko
- Contributor
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SpringerLink (Online service)
- DOI
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10.1038/s41598-023-50668-2
- URN
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urn:nbn:de:101:1-2024031814035363881903
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:59 AM CEST
Data provider
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Matsumoto, Ayumi
- Kano, Shintaro
- Kobayashi, Natsumi
- Matsuki, Mitsuru
- Furukawa, Rieko
- Yamagishi, Hirokazu
- Yoshinari, Hiroki
- Nakata, Waka
- Wakabayashi, Hiroko
- Tsuda, Hidetoshi
- Watanabe, Kazuhisa
- Takahashi, Hironori
- Yamagata, Takanori
- Matsumura, Takayoshi
- Osaka, Hitoshi
- Mori, Harushi
- Iwamoto, Sadahiko
- SpringerLink (Online service)
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Skewed X-chromosome inactivation in patients with esophageal carcinoma
A new sex-specific underlying mechanism for female schizophrenia: accelerated skewed X chromosome inactivation
Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
Association of skewed X-chromosome inactivation with FMR1 CGG repeat length and anti-Mullerian hormone levels: a cohort study
A Statistical Testing Strategy Accounting for Random and Nonrandom (Skewed) X-Chromosome Inactivation Identifies Lung Cancer Susceptibility Loci among Smokers
Skewed X-chromosomal inactivation impacts T regulatory cell function in systemic sclerosis
Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation
High-resolution chromosomal microarray analysis of early-stage human embryonic stem cells reveals an association between X chromosome instability and skewed X inactivation
Skewed X-inactivation is associated with retinal dystrophy in female carriers of RPGR mutations
Transcriptome regulation during the X chromosome inactivation process
The complex story of human X chromosome inactivation
Skewed X-chromosome inactivation in patients with esophageal carcinoma
A new sex-specific underlying mechanism for female schizophrenia: accelerated skewed X chromosome inactivation
Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases
Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease
Association of skewed X-chromosome inactivation with FMR1 CGG repeat length and anti-Mullerian hormone levels: a cohort study
A Statistical Testing Strategy Accounting for Random and Nonrandom (Skewed) X-Chromosome Inactivation Identifies Lung Cancer Susceptibility Loci among Smokers
Skewed X-chromosomal inactivation impacts T regulatory cell function in systemic sclerosis
Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation
High-resolution chromosomal microarray analysis of early-stage human embryonic stem cells reveals an association between X chromosome instability and skewed X inactivation
Skewed X-inactivation is associated with retinal dystrophy in female carriers of RPGR mutations
Transcriptome regulation during the X chromosome inactivation process