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Triplication of DYRK1A causes retinal structural and functional alterations in Down syndrome

Human molecular genetics, 2013-07, Vol.22 (14), p.2775-2784

2013

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Regulator of calcineurin 1 mediates pathological vascular wall remodeling

The Journal of experimental medicine, 2011-09, Vol.208 (10), p.2125-2139

2011

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Upregulation of RCAN1 causes Down syndrome-like immune dysfunction

Journal of medical genetics, 2013-07, Vol.50 (7), p.444-454

2013

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Dyrk1a haploinsufficiency induces diabetes in mice through decreased pancreatic beta cell mass

Diabetologia, 2014-05, Vol.57 (5), p.960-969

2014

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Sequential contribution of L- and P-selectin to leukocyte rolling in vivo

The Journal of experimental medicine, 1995-02, Vol.181 (2), p.669-675

1995

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Lymphocyte homing and leukocyte rolling and migration are impaired in L-selectin-deficient mice

Immunity (Cambridge, Mass.), 1994-07, Vol.1 (4), p.247-260

1994

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Over-expression of RCAN1 causes Down syndrome-like hippocampal deficits that alter learning and memory

Human molecular genetics, 2012-07, Vol.21 (13), p.3025-3041

2012

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Gene expression analysis of the embryonic subplate

Cerebral cortex (New York, N.Y. 1991), 2012-06, Vol.22 (6), p.1343-1359

2012

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RCAN1 (DSCR1) increases neuronal susceptibility to oxidative stress: a potential pathogenic process in neurodegeneration

Human molecular genetics, 2007-05, Vol.16 (9), p.1039-1050

2007

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DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease

Human molecular genetics, 2008-04, Vol.17 (7), p.1020-1030

2008

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Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

Human molecular genetics, 2001-04, Vol.10 (9), p.947-952

2001

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DYRK1A and cognition: A lifelong relationship

Pharmacology & therapeutics (Oxford), 2019-02, Vol.194, p.199-221

2019

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Differential expression of members of the RCAN family of calcineurin regulators suggests selective functions for these proteins in the brain

The European journal of neuroscience, 2007-09, Vol.26 (5), p.1213-1226

2007

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DYRK1A modulates c-MET in pancreatic ductal adenocarcinoma to drive tumour growth

Gut, 2019-08, Vol.68 (8), p.1465-1476

2019

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Characteristics of nitric oxide synthase type I of rat cerebellar astrocytes

Glia, 1996-11, Vol.18 (3), p.224-232

1996

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Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

Human mutation, 2001-12, Vol.18 (6), p.548-548

2001

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Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

Human mutation, 2002-07, Vol.20 (1), p.77-78

2002

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Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis

Human molecular genetics, 2003-09, Vol.12 (17), p.2097-2108

2003

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Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndrome

Human mutation, 1999-01, Vol.14 (6), p.520-526

1999

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[P1.27]: Dyrk1A gene dosage controls developmental cell death of the mesencephalic dopaminergic neurons

INTERNATIONAL JOURNAL OF DEVELOPMENTAL NEUROSCIENCE, 2010-12, Vol.28 (8), p.664-665

2010

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Dopaminergic deficiency in mice with reduced levels of the dual‐specificity tyrosine‐phosphorylated and regulated kinase 1A, Dyrk1A+

Genes, brain and behavior, 2007-08, Vol.6 (6), p.569-578

2007

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Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) gene

Human mutation, 2000-05, Vol.15 (5), p.481-482

2000

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Presence and distribution of histaminergic components in rat and bovine retina

Neurochemistry international, 1988, Vol.13 (1), p.97-104

1988

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Abstract P192: MicroRNA-199b Targets the Nuclear Kinase Dyrk1a in an Auto-Amplification Loop Promoting Calcineurin/NFAT Signaling

Circulation research, 2011-12, Vol.109 (suppl_1)

2011

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Psoriasis, metabolic syndrome and cardiovascular risk factors. A population‐based study

Journal of the European Academy of Dermatology and Venereology, 2019-01, Vol.33 (1), p.128-135

2019

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Triplication of DYRK1A causes retinal structural and functional alterations in Down syndrome

Regulator of calcineurin 1 mediates pathological vascular wall remodeling

Upregulation of RCAN1 causes Down syndrome-like immune dysfunction

Dyrk1a haploinsufficiency induces diabetes in mice through decreased pancreatic beta cell mass

Sequential contribution of L- and P-selectin to leukocyte rolling in vivo

Lymphocyte homing and leukocyte rolling and migration are impaired in L-selectin-deficient mice

Over-expression of RCAN1 causes Down syndrome-like hippocampal deficits that alter learning and memory

Gene expression analysis of the embryonic subplate

RCAN1 (DSCR1) increases neuronal susceptibility to oxidative stress: a potential pathogenic process in neurodegeneration

DSCR1/RCAN1 regulates vesicle exocytosis and fusion pore kinetics: implications for Down syndrome and Alzheimer's disease

Connexin 31 (GJB3) is expressed in the peripheral and auditory nerves and causes neuropathy and hearing impairment

DYRK1A and cognition: A lifelong relationship

Differential expression of members of the RCAN family of calcineurin regulators suggests selective functions for these proteins in the brain

DYRK1A modulates c-MET in pancreatic ductal adenocarcinoma to drive tumour growth

Characteristics of nitric oxide synthase type I of rat cerebellar astrocytes

Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

Erratum: Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment

Slc7a9-deficient mice develop cystinuria non-I and cystine urolithiasis

Splice-site mutation in the PDS gene may result in intrafamilial variability for deafness in Pendred syndrome

[P1.27]: Dyrk1A gene dosage controls developmental cell death of the mesencephalic dopaminergic neurons

Dopaminergic deficiency in mice with reduced levels of the dual‐specificity tyrosine‐phosphorylated and regulated kinase 1A, Dyrk1A+

Identification of seven novel SNPS (five nucleotide and two amino acid substitutions) in the connexin31 (GJB3) gene

Presence and distribution of histaminergic components in rat and bovine retina

Abstract P192: MicroRNA-199b Targets the Nuclear Kinase Dyrk1a in an Auto-Amplification Loop Promoting Calcineurin/NFAT Signaling

Psoriasis, metabolic syndrome and cardiovascular risk factors. A population‐based study

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