The human inactive X chromosome modulates expression of the active X chromosome.

Klinefelter syndrome X chromosome inactivation aneuploidy dosage sensitivity gene expression sex chromosomes sex differences turner syndrome

Journal

Cell genomics
ISSN: 2666-979X
Titre abrégé: Cell Genom
Pays: United States
ID NLM: 9918284260106676

Informations de publication

Date de publication:
08 Feb 2023
Historique:
received: 02 03 2022
revised: 12 08 2022
accepted: 06 01 2023
entrez: 23 2 2023
pubmed: 24 2 2023
medline: 24 2 2023
Statut: epublish

Résumé

The "inactive" X chromosome (Xi) has been assumed to have little impact, in

Identifiants

pubmed: 36819663
doi: 10.1016/j.xgen.2023.100259
pii: S2666-979X(23)00015-0
pmc: PMC9932992
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100259

Informations de copyright

© 2023 The Authors.

Déclaration de conflit d'intérêts

The authors declare no competing interests.

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Auteurs

Adrianna K San Roman (AK)

Whitehead Institute, Cambridge, MA 02142, USA.

Alexander K Godfrey (AK)

Whitehead Institute, Cambridge, MA 02142, USA.
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Helen Skaletsky (H)

Whitehead Institute, Cambridge, MA 02142, USA.
Howard Hughes Medical Institute, Whitehead Institute, Cambridge, MA 02142, USA.

Daniel W Bellott (DW)

Whitehead Institute, Cambridge, MA 02142, USA.

Abigail F Groff (AF)

Whitehead Institute, Cambridge, MA 02142, USA.

Hannah L Harris (HL)

Whitehead Institute, Cambridge, MA 02142, USA.
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Laura V Blanton (LV)

Whitehead Institute, Cambridge, MA 02142, USA.

Jennifer F Hughes (JF)

Whitehead Institute, Cambridge, MA 02142, USA.

Laura Brown (L)

Whitehead Institute, Cambridge, MA 02142, USA.
Howard Hughes Medical Institute, Whitehead Institute, Cambridge, MA 02142, USA.

Sidaly Phou (S)

Whitehead Institute, Cambridge, MA 02142, USA.
Howard Hughes Medical Institute, Whitehead Institute, Cambridge, MA 02142, USA.

Ashley Buscetta (A)

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Paul Kruszka (P)

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Nicole Banks (N)

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

Amalia Dutra (A)

Cytogenetics and Microscopy Core, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Evgenia Pak (E)

Cytogenetics and Microscopy Core, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

Patricia C Lasutschinkow (PC)

Focus Foundation, Davidsonville, MD 21035, USA.

Colleen Keen (C)

Focus Foundation, Davidsonville, MD 21035, USA.

Shanlee M Davis (SM)

Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.

Nicole R Tartaglia (NR)

Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Developmental Pediatrics, eXtraOrdinarY Kids Program, Children's Hospital Colorado, Aurora, CO 80011, USA.

Carole Samango-Sprouse (C)

Focus Foundation, Davidsonville, MD 21035, USA.
Department of Pediatrics, George Washington University, Washington, DC 20052, USA.
Department of Human and Molecular Genetics, Florida International University, Miami, FL 33199, USA.

Maximilian Muenke (M)

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.

David C Page (DC)

Whitehead Institute, Cambridge, MA 02142, USA.
Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Howard Hughes Medical Institute, Whitehead Institute, Cambridge, MA 02142, USA.

Classifications MeSH