ArticleAmerican journal of human genetics1997
Possible narrowed assignment of the loci of monosomy 21-associated microcephaly and intrauterine growth retardation to a 1.2-Mb segment at 21q22.2.
Article in American journal of human genetics, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
What it found
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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
16 citing papers in PubMed.
- Down syndrome and DYRK1A overexpression: relationships and future therapeutic directions.Frontiers in molecular neuroscience · 2024Review
- Over-expression of Dyrk1A affects bleeding by modulating plasma fibronectin and fibrinogen level in mice.Journal of cellular and molecular medicine · 2023Article
- Identification of two novel and one rare mutation inFrontiers in genetics · 2023Article
- Ocular Phenotype Associated withGenes · 2021Article
- DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature.Molecular genetics & genomic medicine · 2020Review
- A novel de novo heterozygous DYRK1A mutation causes complete loss of DYRK1A function and developmental delay.Scientific reports · 2020Article
- Abnormalities of DYRK1A-Cytoskeleton Complexes in the Blood Cells as Potential Biomarkers of Alzheimer's Disease.Journal of Alzheimer's disease : JAD · 2019Article
- Clinical phenotype of ASD-associatedMolecular autism · 2017Article
- Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature.BMC medical genetics · 2016Review
- Concurrent psu dic(21)(q22.3) and t(13;17)(q14.1;p12) in a mosaic Down's syndrome patient: review of thirty-one similar dicentrics.Journal of genetics · 2014Article
- One-carbon cycle alterations induced by Dyrk1a dosage.Molecular genetics and metabolism reports · 2014Article
- Gene dosage-dependent association of DYRK1A with the cytoskeleton in the brain and lymphocytes of down syndrome patients.Journal of neuropathology and experimental neurology · 2012Article
- Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case report.Molecular cytogenetics · 2010Article
- Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A.Molecular syndromology · 2010Article
- Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.American journal of human genetics · 2008Article
- Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice.Molecular and cellular biology · 2002Article
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Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
9106547PMC1712454What 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.