** Look at all the research that has been published on DYRK1A**

DYRK1A Patient Research

Published articles that include data collected on patients.

Featured
DYRK1A Patient Research
Neurocognitive and neurobehavioral characterization of two frequent forms of neurodevelopmental disorders: the DYRK1A and the Wiedemann–Steiner syndromes
DYRK1A Patient Research

Abstract

DYRK1A Patient Research
DYRK1A Patient Research
Clinical and genetic analysis of a child with mental retardation autosomal dominant 7
DYRK1A Patient Research

Chinese Artical / Click Enlish Abstract

DYRK1A Patient Research
DYRK1A Patient Research
Social motivation a relative strength in DYRK1A syndrome on a background of significant speech and language impairments
DYRK1A Patient Research

Abstract

DYRK1A Patient Research
DYRK1A Patient Research
Characterization of phenotypic range in DYRK1A haploinsufficiency syndrome using standardized behavioral measures
DYRK1A Patient Research

Abstract

DYRK1A Patient Research
DYRK1A Patient Research
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Patient Research
Clinical course of epilepsy and white matter abnormality linked to a novel DYRK1A variant
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Patient Research
Sleep Problems in Children with ASD and Gene Disrupting Mutations
DYRK1A Patient Research

Abstract

DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line
DYRK1A Gene Research, DYRK1A Patient Research

Full Article

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Patient Research
Ocular Phenotype Associated with DYRK1A Variants
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Patient Research
Genetic diagnosis of infantile-onset epilepsy in the clinic: Application of whole-exome sequencing following epilepsy gene panel testing
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Patient Research
Description of neurodevelopmental phenotypes associated with 10 genetic neurodevelopmental disorders: A scoping review
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Patient Research
DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Patient Research
Ocular findings of albinism in DYRK1A-related intellectual disability syndrome
DYRK1A Patient Research

Abstract

DYRK1A Patient Research
DYRK1A Patient Research
A novel de novo heterozygous DYRK1A mutation causes complete loss of DYRK1A function and developmental delay
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Patient Research
Impact of DYRK1A Haploinsufficiency on Facial Morphology using Three-Dimensional Morphometric Analysis
DYRK1A Patient Research

Full Article

DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Patient Research, DYRK1A Gene Research
Clinical phenotype of ASD-associated DYRK1A haploinsufficiency
DYRK1A Patient Research, DYRK1A Gene Research

Read Full

DYRK1A Patient Research, DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies.
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A mutations in two unrelated patients
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
A de novo 1.4-Mb deletion at 21q22.11 in a boy with developmental delay
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
 

Archives

DYRK1A Gene Research

Published articles that help us understand the role of the DYRK1A Gene.

Featured
DYRK1A Gene Research
Deep learning is widely applicable to phenotyping embryonic development and disease
DYRK1A Gene Research

Full Article

DYRK1A Gene Research
DYRK1A Gene Research
Dyrk1a gene dosage in glutamatergic neurons has key effects in cognitive deficits observed in mouse models of MRD7 and Down syndrome
DYRK1A Gene Research

Full Article

DYRK1A Gene Research
DYRK1A Gene Research
Global kinome profiling reveals DYRK1A as critical activator of the human mitochondrial import machinery
DYRK1A Gene Research

Full Article

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC line
DYRK1A Gene Research, DYRK1A Patient Research

Full Article

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research
Dyrk1a Mutations Cause Undergrowth of Cortical Pyramidal Neurons via Dysregulated Growth Factor Signaling
DYRK1A Gene Research

Full Article

DYRK1A Gene Research
DYRK1A Gene Research
Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder
DYRK1A Gene Research

Full Article

DYRK1A Gene Research
DYRK1A Gene Research
Altered age‐linked regulation of plasma DYRK1A in elderly cognitive complainers (INSIGHT‐preAD study) with high brain amyloid load
DYRK1A Gene Research

Full Article

DYRK1A Gene Research
DYRK1A Gene Research
Neurodevelopmental disorder risk gene DYRK1A is required for ciliogenesis and brain size in Xenopus embryos
DYRK1A Gene Research

Full Article

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tract
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research
Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Vascular defects of DYRK1A knockouts are ameliorated by modulating calcium signaling in zebrafish
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
The nuclear interactome of DYRK1A reveals a functional role in DNA damage repair
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
A comprehensive proteomics-based interaction screen that links DYRK1A to RNF169 and to the DNA damage response
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Functional characterization of DYRK1A missense variants associated with a syndromic form of intellectual deficiency and autism
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Patient Research, DYRK1A Gene Research
Clinical phenotype of ASD-associated DYRK1A haploinsufficiency
DYRK1A Patient Research, DYRK1A Gene Research

Read Full

DYRK1A Patient Research, DYRK1A Gene Research
DYRK1A Gene Research
Zebrafish knockout of Down syndrome gene, DYRK1A, shows social impairments relevant to autism
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Structural analysis of pathogenic mutations in the DYRK1A gene in patients with developmental disorders
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Association of DYRK1A polymorphisms with sporadic Parkinson’s disease in Chinese Han population
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research
The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients.
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research
Characterizing autism spectrum disorders by key biochemical pathways
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
The Kinase DYRK1A Reciprocally Regulates the Differentiation of Th17 and Regulatory T Cells
DYRK1A Gene Research

Read Full / Video Presentation

DYRK1A Gene Research
DYRK1A Gene Research
Dyrk1A Phosphorylates Parkin at Ser-131 and Negatively Regulates its Ubiquitin E3 Ligase Activity.
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A haploinsufficiency causes a new recognizable syndrome with microcephaly, intellectual disability, speech impairment, and distinct facies.
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A mutations in two unrelated patients
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID.
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
 
Featured
DYRK1A Gene Research
Synaptic, transcriptional and chromatin genes disrupted in autism Associated with Submicroscopic 21q22 Deletion Including DYRK1A
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson's disease.
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Excitation/inhibition balance and learning are modified by Dyrk1a gene dosage
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research
Dyrk1a haploinsufficiency induces diabetes in mice through decreased pancreatic beta cell mass.
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
A de novo 1.4-Mb deletion at 21q22.11 in a boy with developmental delay
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research
Design and Synthesis of Thiazolo[5,4-f]quinazolines as DYRK1A Inhibitors
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Dosage of Dyrk1a Shifts Cells within a p21-Cyclin D1 Signaling Map to Control the Decision to Enter the Cell Cycle
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Inhibition of DYRK1A destabilizes EGFR and reduces EGFR-dependent glioblastoma growth.
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disord
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research
Dyrk1A, a serine/threonine kinase, is involved in ERK and Akt activation in the brain of hyperhomocysteinemic mice.
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research
Minibrain/Dyrk1a regulates food intake through the Sir2-FOXO-sNPF/NPY pathway in Drosophila and mammals
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
De Novo Gene Disruptions in Children on the Autistic Spectrum
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
DYRK1A: a master regulatory protein controlling brain growth.
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research
Phosphorylation of Munc18-1 by DYRK1A regulates its interaction with Syntaxin 1 and X11a
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Transient expression of Mnb/Dyrk1a couples cell cycle exit and differentiation of neuronal precursors by inducing p27KIP1 expression and suppressing NOTCH signaling
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly
DYRK1A Gene Research, DYRK1A Patient Research

Read Abstract

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research, DYRK1A Patient Research
Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research
Function and regulation of DYRK1A: towards understanding down syndrome
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research
Impaired Spatial Learning Strategies and Novel Object Recognition in Mice Haploinsufficient for the Dual Specificity Tyrosine-Regulated Kinase-1A (Dyrk1A)
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research, DYRK1A Patient Research
Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly
DYRK1A Gene Research, DYRK1A Patient Research

Read Full

DYRK1A Gene Research, DYRK1A Patient Research
DYRK1A Gene Research
DYRK1A BAC transgenic mice show altered synaptic plasticity with learning and memory defects
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
DYRK1A Gene Research
DYRK1A enhances the mitogen-activated protein kinase cascade in PC12 cells by forming a complex with Ras, B-Raf, and MEK1.
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
DYRK1A accumulates in splicing speckles through a novel targeting signal and induces speckle disassembly
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice.
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
Possible narrowed assignment of the loci of monosomy 21-associated microcephaly and intrauterine growth retardation to a 1.2-Mb segment at 21q22.2.
DYRK1A Gene Research

Read Full

DYRK1A Gene Research
DYRK1A Gene Research
A human homologue of Drosophila minibrain (MNB) is expressed in the neuronal regions affected in Down syndrome and maps to the critical region
DYRK1A Gene Research

Read Abstract

DYRK1A Gene Research
 

Archives