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DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson’s disease

Cell death & disease, 2014-06, Vol.5 (6), p.e1289-e1289

2014

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Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/− mouse

Neurobiology of disease, 2005-10, Vol.20 (1), p.115-122

2005

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Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

Human genetics, 2000-01, Vol.106 (1), p.40-44

2000

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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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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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Expression of the Type VI Secretion System 1 Component Hcp1 Is Indirectly Repressed by OpaR in Vibrio parahaemolyticus

TheScientificWorld, 2012-01, Vol.2012 (2012), p.1-7

2012

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Alu-splice cloning of human Intersectin (ITSN), a putative multivalent binding protein expressed in proliferating and differentiating neurons and overexpressed in Down syndrome

European journal of human genetics : EJHG, 1999-09, Vol.7 (6), p.704-712

1999

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Dyrk1A Haploinsufficiency Affects Viability and Causes Developmental Delay and Abnormal Brain Morphology in Mice

Molecular and Cellular Biology, 2002-09, Vol.22 (18), p.6636-6647

2002

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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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Mutations in the Mitochondrial tRNA Ser(UCN) and in the GJB2 (Connexin 26) Gene Are Not Modifiers of the Age at Onset or Severity of Hearing Loss in Spanish Patients with the 12S rRNA A1555G Mutation

American journal of human genetics, 2000-04, Vol.66 (4), p.1465-1467

2000

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Plasma DYRK1A as a novel risk factor for Alzheimer’s disease

Translational psychiatry, 2014-08, Vol.4 (8), p.e425-e425

2014

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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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MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

American journal of human genetics, 2001-09, Vol.69 (3), p.635-640

2001

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Gene targeting in normal somatic cells: inactivation of the interferon-γ receptor in myoblasts

Nature genetics, 1994-01, Vol.6 (1), p.90-97

1994

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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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Functional genomics of Down syndrome: a multidisciplinary approach

Journal of neural transmission. Supplementum, 2001 (61), p.131

2001

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Connexin mutations in hearing loss, dermatological and neurological disorders

Trends in Molecular Medicine, 2002-05, Vol.8 (5), p.205-212

2002

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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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R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?

European journal of human genetics : EJHG, 2001-01, Vol.9 (1), p.70-70

2001

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IFN-γR -/- mice show an enhanced liver and brain metallothionein I+II response to endotoxin but not to immobilization stress

Journal of endotoxin research, 1997-10, Vol.4 (5), p.363-370

1997

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DYRK1A (dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A)

Atlas of genetics and cytogenetics in oncology and haematology, 2011-11 (5)

2011

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DYRK1A promotes dopaminergic neuron survival in the developing brain and in a mouse model of Parkinson’s disease

Alterations in the phenotype of neocortical pyramidal cells in the Dyrk1A+/− mouse

Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene

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

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

Expression of the Type VI Secretion System 1 Component Hcp1 Is Indirectly Repressed by OpaR in Vibrio parahaemolyticus

Alu-splice cloning of human Intersectin (ITSN), a putative multivalent binding protein expressed in proliferating and differentiating neurons and overexpressed in Down syndrome

Dyrk1A Haploinsufficiency Affects Viability and Causes Developmental Delay and Abnormal Brain Morphology in Mice

Characteristics of nitric oxide synthase type I of rat cerebellar astrocytes

Mutations in the Mitochondrial tRNA Ser(UCN) and in the GJB2 (Connexin 26) Gene Are Not Modifiers of the Age at Onset or Severity of Hearing Loss in Spanish Patients with the 12S rRNA A1555G Mutation

Plasma DYRK1A as a novel risk factor for Alzheimer’s disease

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

MYO6, the Human Homologue of the Gene Responsible for Deafness in Snell’s Waltzer Mice, Is Mutated in Autosomal Dominant Nonsyndromic Hearing Loss

Gene targeting in normal somatic cells: inactivation of the interferon-γ receptor in myoblasts

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

Functional genomics of Down syndrome: a multidisciplinary approach

Connexin mutations in hearing loss, dermatological and neurological disorders

[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+

R32W variant in Connexin 31: mutation or polymorphism for deafness and skin disease?

IFN-γR -/- mice show an enhanced liver and brain metallothionein I+II response to endotoxin but not to immobilization stress

DYRK1A (dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A)

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