ArticleMammalian genome : official journal of the International Mammalian Genome Society1998
Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains.
Article in Mammalian genome : official journal of the International Mammalian Genome Society, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
22 citing papers in PubMed, 1 synthesis or guideline pooled it, 69 citations in OpenAlex.
- ATR-X syndrome: genetics, clinical spectrum, and management.Human genetics · 2021Pooled it
- The Multiple Facets of ATRX Protein.Cancers · 2021Review
- Dynamic Activity of Histone H3-Specific Chaperone Complexes in Oncogenesis.Frontiers in oncology · 2021Review
- Molecular effects of dADD1 misexpression in chromatin organization and transcription.BMC molecular and cell biology · 2020Article
- Neurodevelopmental Disorders Caused by Defective Chromatin Remodeling: Phenotypic Complexity Is Highlighted by a Review of ATRX Function.Frontiers in genetics · 2020Review
- Syndromic disorder of sex development due to a novel hemizygous mutation in the carboxyl-terminal domain ofHuman genome variation · 2017Article
- Analysis of neonatal brain lacking ATRX or MeCP2 reveals changes in nucleosome density, CTCF binding and chromatin looping.Nucleic acids research · 2014Article
- Structure and Mechanisms of SF1 DNA Helicases.Advances in experimental medicine and biology · 2013Article
- Compromised genomic integrity impedes muscle growth after Atrx inactivation.The Journal of clinical investigation · 2012Article
- α-Thalassemia, mental retardation, and myelodysplastic syndrome.Cold Spring Harbor perspectives in medicine · 2012Article
- Loss of Atrx sensitizes cells to DNA damaging agents through p53-mediated death pathways.PloS one · 2012Article
- Role of ATRX in chromatin structure and function: implications for chromosome instability and human disease.Reproduction (Cambridge, England) · 2011Review
- Comparative analysis of the ATRX promoter and 5' regulatory region reveals conserved regulatory elements which are linked to roles in neurodevelopment, alpha-globin regulation and testicular function.BMC research notes · 2011Article
- ATRX has a critical and conserved role in mammalian sexual differentiation.BMC developmental biology · 2011Article
- The ATRX-ADD domain binds to H3 tail peptides and reads the combined methylation state of K4 and K9.Human molecular genetics · 2011Article
- Defining the cause of skewed X-chromosome inactivation in X-linked mental retardation by use of a mouse model.American journal of human genetics · 2007Article
- Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues.PLoS genetics · 2006Article
- The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.The Journal of clinical investigation · 2005Article
- A missense mutation in the coiled-coil motif of the HP1-interacting domain of ATR-X in a family with X-linked mental retardation.Neurogenetics · 2005Article
- The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies.Proceedings of the National Academy of Sciences of the United States of America · 2003Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 2 institutions in 2 countries.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.