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A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus

Journal of molecular medicine (Berlin, Germany), 2007-05, Vol.85 (5), p.531-537

2007

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Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p

American journal of human genetics, 2006-10, Vol.79 (4), p.731-737

2006

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Babbling opens the sensory phase for imitative vocal learning

Proceedings of the National Academy of Sciences - PNAS, 2024-04, Vol.121 (18), p.e2312323121

2024

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Androgen and estrogen sensitivity of bird song: a comparative view on gene regulatory levels

Journal of Comparative Physiology, 2018-01, Vol.204 (1), p.113-126

2018

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Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment options

Clinical rheumatology, 2011-02, Vol.30 (2), p.275-283

2011

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Defective removal of ribonucleotides from DNA promotes systemic autoimmunity

The Journal of clinical investigation, 2015-01, Vol.125 (1), p.413-424

2015

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Rapid and sustained remission of systemic juvenile idiopathic arthritis-associated macrophage activation syndrome through treatment with anakinra and corticosteroids

Journal of clinical rheumatology, 2011-01, Vol.17 (1), p.23

2011

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Five years of experience with biochemical cystic fibrosis newborn screening based on IRT/PAP in Germany

Pediatric pulmonology, 2015-07, Vol.50 (7), p.655-664

2015

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Evaluating the predictive value of doublecortin as a marker for adult neurogenesis in canaries (Serinus canaria)

Journal of comparative neurology (1911), 2014-04, Vol.522 (6), p.1299-1315

2014

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Professional politicians speak positively of a federal ombudsman for children

Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege, 2015-06, Vol.34 (6), p.230

Gahr, Manfred

2015

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What makes a marker a good marker?. Commentary on Balthazart J and Ball G (2014): Doublecortin is a highly valuable endogenous marker of adult neurogenesis in canaries. Brain Behav Evol 84:1-4

Brain, behavior and evolution, 2014, Vol.84 (1), p.5-7

2014

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The Stem Cell Marker Prominin‐1/CD133 on Membrane Particles in Human Cerebrospinal Fluid Offers Novel Approaches for Studying Central Nervous System Disease

Stem cells (Dayton, Ohio), 2008-03, Vol.26 (3), p.698-705

2008

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Presentations and Treatment of Childhood Scleroderma: Localized Scleroderma, Eosinophilic Fasciitis, Systemic Sclerosis, and Graft-Versus-Host Disease

Clinical pediatrics, 2011-07, Vol.50 (7), p.604-614

2011

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Unsere Petion fur die Einsetzung einer/eines Kinderbeauftragten des Bundestages - Petiton 57180

Kinderkrankenschwester : Organ der Sektion Kinderkrankenpflege, 2016-09, Vol.35 (7), p.268

Gahr, Manfred

2016

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Long-term follow-up and outcome of 39 patients with chronic granulomatous disease

The Journal of pediatrics, 2000-11, Vol.137 (5), p.687-693

2000

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Reptilian sex steroid receptors: Amplification, sequence and expression analysis

The Journal of steroid biochemistry and molecular biology, 1995-11, Vol.55 (2), p.261-269

1995

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Melatonin affects the temporal organization of the song of the zebra finch

The FASEB journal, 2005-05, Vol.19 (7), p.848-850

2005

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Autologous stem cell transplantation in refractory paediatric Wegener's granulomatosis

Clinical and experimental rheumatology, 2011-09, Vol.29 (5), p.897

2011

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Haploinsufficiency, rather than the effect of an excessive production of soluble CD95 (CD95ΔTM), is the basis for ALPS Ia in a family with duplicated 3′ splice site AG in CD95 intron 5 on one allele

Blood, 2005-09, Vol.106 (5), p.1652-1659

2005

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Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD)

Human mutation, 2010-02, Vol.31 (2), p.151-158

2010

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Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-γ-receptor (IFNγR1) deficiency : Mutational analysis and evaluation of therapeutic options

Experimental hematology, 1999-09, Vol.27 (9), p.1368-1374

1999

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P-glycoprotein expression increases ATP release in respiratory cystic fibrosis cells

Journal of cystic fibrosis, 2005-09, Vol.4 (3), p.157-168

2005

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A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD)

Gene, 2006-04, Vol.371 (2), p.174-181

2006

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A mutation in TREX1 that impairs susceptibility to granzyme A-mediated cell death underlies familial chilblain lupus

Familial Chilblain Lupus, a Monogenic Form of Cutaneous Lupus Erythematosus, Maps to Chromosome 3p

Babbling opens the sensory phase for imitative vocal learning

Androgen and estrogen sensitivity of bird song: a comparative view on gene regulatory levels

Early onset systemic lupus erythematosus: differential diagnoses, clinical presentation, and treatment options

Defective removal of ribonucleotides from DNA promotes systemic autoimmunity

Rapid and sustained remission of systemic juvenile idiopathic arthritis-associated macrophage activation syndrome through treatment with anakinra and corticosteroids

Five years of experience with biochemical cystic fibrosis newborn screening based on IRT/PAP in Germany

Evaluating the predictive value of doublecortin as a marker for adult neurogenesis in canaries (Serinus canaria)

Cultural bias in the AAP's 2012 Technical Report and Policy Statement on male circumcision

Professional politicians speak positively of a federal ombudsman for children

What makes a marker a good marker?. Commentary on Balthazart J and Ball G (2014): Doublecortin is a highly valuable endogenous marker of adult neurogenesis in canaries. Brain Behav Evol 84:1-4

The Stem Cell Marker Prominin‐1/CD133 on Membrane Particles in Human Cerebrospinal Fluid Offers Novel Approaches for Studying Central Nervous System Disease

Naturally Occurring Genetic Variants of Human Caspase-1 Differ Considerably in Structure and the Ability to Activate Interleukin-1β

Presentations and Treatment of Childhood Scleroderma: Localized Scleroderma, Eosinophilic Fasciitis, Systemic Sclerosis, and Graft-Versus-Host Disease

Unsere Petion fur die Einsetzung einer/eines Kinderbeauftragten des Bundestages - Petiton 57180

Long-term follow-up and outcome of 39 patients with chronic granulomatous disease

Reptilian sex steroid receptors: Amplification, sequence and expression analysis

Melatonin affects the temporal organization of the song of the zebra finch

Autologous stem cell transplantation in refractory paediatric Wegener's granulomatosis

Haploinsufficiency, rather than the effect of an excessive production of soluble CD95 (CD95ΔTM), is the basis for ALPS Ia in a family with duplicated 3′ splice site AG in CD95 intron 5 on one allele

Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD)

Listeria monocytogenes and recurrent mycobacterial infections in a child with complete interferon-γ-receptor (IFNγR1) deficiency : Mutational analysis and evaluation of therapeutic options

P-glycoprotein expression increases ATP release in respiratory cystic fibrosis cells

A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD)

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