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Differential transgene expression in brain cells in vivo and in vitro from AAV-2 vectors with small transcriptional control units

Virology (New York, N.Y.), 2003-06, Vol.311 (1), p.89-95

2003

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An Update on Familial Hyperaldosteronism

Hormone and metabolic research, 2015-12, Vol.47 (13), p.941-946

2015

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Potentiation of in vivo neuroprotection by BclXL and GDNF co-expression depends on post-lesion time in deafferentiated CNS neurons

Gene therapy, 2006-11, Vol.13 (22), p.1569-1578

2006

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Hyperaldosteronism

Der Internist (Berlin), 2021-03, Vol.62 (3), p.245-251

Scholl, U I

2021

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Comprehensive genomic analysis of adrenocortical carcinoma reveals genetic profiles associated with patient survival

ESMO open, 2024-07, Vol.9 (7), p.103617, Article 103617

2024

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Evaluation of epitope tags for protein detection after in vivo CNS gene transfer

The European journal of neuroscience, 2006-04, Vol.23 (8), p.1961-1969

2006

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Characterization of the human T cell response against the neuronal protein synapsin in patients with multiple sclerosis

Journal of neuroimmunology, 2001-04, Vol.115 (1), p.176-181

2001

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Primary aldosteronism : Genetics and pathology

Der Pathologe, 2019-12, Vol.40 (Suppl 3), p.369-372

Scholl, U

2019

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Maritime history at maritime museums

International journal of maritime history, 2020-05, Vol.32 (2), p.434-443

Scholl, Lars U.

2020

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Matrix metalloproteinase-9 (MMP-9) in human cerebrospinal fluid (CSF): elevated levels are primarily related to CSF cell count

Journal of neuroimmunology, 2000-10, Vol.110 (1), p.244-251

2000

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Simulationsgestützte Optimierung von partiell gehärteten Automobilteilen aus Mehrphasen-Stahl

Journal of heat treatment and materials : HTM = Zeitschrift für Werkstoffe, Wärmebehandlung, Fertigung, 2022-04, Vol.63 (4), p.213-221

2022

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Primärer Hyperaldosteronismus: Genetik und Pathologie

Der Pathologe, 2019-12, Vol.40 (Suppl 3), p.369-372

Scholl, U.

2019

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Hyperaldosteronismus

Der Internist (Berlin), 2021-03, Vol.62 (3), p.245-251

Scholl, U. I.

2021

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Glatiramer acetate (Copolymer-1)-specific, human T cell lines: cytokine profile and suppression of T cell lines reactive against myelin basic protein

Neuroscience letters, 2000-08, Vol.289 (3), p.205-208

2000

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26O Comprehensive genomic analysis of adrenocortical carcinoma reveals genetic profiles associated with patient survival

ESMO open, 2024-03, Vol.9, p.102415, Article 102415

2024

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Potentiation of in vivo neuroprotection by BclX(L) and GDNF co-expression depends on post-lesion time in deafferentiated CNS neurons

Gene therapy, 2006-11, Vol.13 (22), p.1569-1578

2006

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The "point of no return" and the rate of progression in the natural history of IgA nephritis

Clinical nephrology, 1999-11, Vol.52 (5), p.285

1999

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Development of an ultrasensitive enzyme immunoassay for the determination of matrix metalloproteinase-9 (MMP-9) levels in normal human cerebrospinal fluid

Journal of neuroimmunology, 2001-06, Vol.116 (2), p.233-237

2001

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Migration of human granulocytes through reconstituted basement membrane is not dependent on matrix metalloproteinase-9 (MMP-9)

Journal of neuroimmunology, 2001-05, Vol.116 (1), p.49-55

2001

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Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

eLife, 2015-04, Vol.4, p.e06315-e06315

2015

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Transfection of “naked” siRNA results in endosomal uptake and metabolic impairment in cultured neurons

Biochemical and biophysical research communications, 2004-03, Vol.315 (4), p.1126-1133

2004

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Whole-Exome Sequencing Characterizes the Landscape of Somatic Mutations and Copy Number Alterations in Adrenocortical Carcinoma

The journal of clinical endocrinology and metabolism, 2015-03, Vol.100 (3), p.E493-E502

2015

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Major German Shipping Lines during the 1920s and 1930s

International journal of maritime history, 2009-06, Vol.21 (1), p.27-54

2009

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Diagnosis and treatment of primary aldosteronism

Yearbook of Paediatric Endocrinology, 2022-09

2022

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P23.4 Seizures, sensori-neural deafness, ataxia, mental retardation and electrolyte imbalance (SeSAME syndrome) caused by KCNJ10 mutation

European journal of paediatric neurology, 2011-05, Vol.15, p.S124-S124

2011

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Differential transgene expression in brain cells in vivo and in vitro from AAV-2 vectors with small transcriptional control units

An Update on Familial Hyperaldosteronism

Potentiation of in vivo neuroprotection by BclXL and GDNF co-expression depends on post-lesion time in deafferentiated CNS neurons

Hyperaldosteronism

Comprehensive genomic analysis of adrenocortical carcinoma reveals genetic profiles associated with patient survival

Evaluation of epitope tags for protein detection after in vivo CNS gene transfer

Characterization of the human T cell response against the neuronal protein synapsin in patients with multiple sclerosis

Primary aldosteronism : Genetics and pathology

Maritime history at maritime museums

Matrix metalloproteinase-9 (MMP-9) in human cerebrospinal fluid (CSF): elevated levels are primarily related to CSF cell count

Simulationsgestützte Optimierung von partiell gehärteten Automobilteilen aus Mehrphasen-Stahl

Primärer Hyperaldosteronismus: Genetik und Pathologie

Hyperaldosteronismus

Glatiramer acetate (Copolymer-1)-specific, human T cell lines: cytokine profile and suppression of T cell lines reactive against myelin basic protein

26O Comprehensive genomic analysis of adrenocortical carcinoma reveals genetic profiles associated with patient survival

Potentiation of in vivo neuroprotection by BclX(L) and GDNF co-expression depends on post-lesion time in deafferentiated CNS neurons

The "point of no return" and the rate of progression in the natural history of IgA nephritis

Development of an ultrasensitive enzyme immunoassay for the determination of matrix metalloproteinase-9 (MMP-9) levels in normal human cerebrospinal fluid

Migration of human granulocytes through reconstituted basement membrane is not dependent on matrix metalloproteinase-9 (MMP-9)

Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism

Transfection of “naked” siRNA results in endosomal uptake and metabolic impairment in cultured neurons

Whole-Exome Sequencing Characterizes the Landscape of Somatic Mutations and Copy Number Alterations in Adrenocortical Carcinoma

Major German Shipping Lines during the 1920s and 1930s

Diagnosis and treatment of primary aldosteronism

P23.4 Seizures, sensori-neural deafness, ataxia, mental retardation and electrolyte imbalance (SeSAME syndrome) caused by KCNJ10 mutation

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