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A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

Nature genetics, 1996-05, Vol.13 (1), p.35-42

1996

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The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Nature genetics, 2000-11, Vol.26 (3), p.324-327

2000

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Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

Nature genetics, 1998-10, Vol.20 (2), p.129-135

1998

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X-linked Retinitis Pigmentosa: RPGR Mutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15

Investigative ophthalmology & visual science, 2003-04, Vol.44 (4), p.1458-1463

2003

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X-linked ocular albinism (Nettleship-Falls): a novel 29-bp deletion in exon 1. Carrier detection by ophthalmic examination and DNA analysis

Graefe's archive for clinical and experimental ophthalmology, 2001-03, Vol.239 (3), p.167-172

2001

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Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity

International journal of molecular medicine, 2001-02, Vol.7 (2), p.155

2001

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Generating several solutions for the scheduling problem in high-level synthesis

Proceedings of EURO-DAC. European Design Automation Conference, 1995, p.66-71

Achatz, H.

1995

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Extended 0/1 LP formulation for the scheduling problem in high-level synthesis

Euro-DAC '93, European Design Automation Conference with Euro-VHDL '93 : proceedings, CCH Hamburg, Germany, September 20-24, 1993, 1993, p.226-231

Achatz, H.

1993

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Isolation and fine mapping of (CA)n repeats from the Xp11.23 and Xp11.4 region

Human molecular genetics, 1994-06, Vol.3 (6), p.1027-1027

1994

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Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins

Nature genetics, 1992-10, Vol.2 (2), p.139-143

1992

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Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome

Human genetics, 1992-11, Vol.90 (3), p.243-246

1992

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Missense mutations in the NDP gene in patients with a less severe course of Norrie disease

Human molecular genetics, 1995-03, Vol.4 (3), p.489-490

1995

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A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa

Human molecular genetics, 1995-12, Vol.4 (12), p.2339-2346

1995

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Sensitivity Analysis of the Bipartite Weighted Matching Problem

Operations Research Proceedings 1998, p.135-141

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UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2

European journal of human genetics : EJHG, 1998-09, Vol.6 (5), p.459-466

1998

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Three novel mutations (I506S, S466X, 1651A→T) in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) detected in patients of Southern German Descent

Human mutation, 1994, Vol.3 (1), p.64-66

1994

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Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins

Nature genetics, 1992-01, Vol.2 (10), p.139-143

1992

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A PCR based X-chromosome inactivation assay for carrier detection in X-linked immunodeficiencies using differential methylation of the androgen receptor gene

Immunodeficiency, 1995, Vol.5 (3), p.187

1995

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Luminescent Sensing of Oxygen Using a Quenchable Probe and Upconverting Nanoparticles

Angewandte Chemie (International ed.), 2011-01, Vol.50 (1), p.260-263

International ed. in English, 2011

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Photon upconverting nanoparticles for luminescent sensing of temperature

Nanoscale, 2012-11, Vol.4 (22), p.79-796

2012

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Photon upconverting nanoparticles for luminescent sensing of temperature

Nanoscale, 2012, Vol.4 (22), p.7090

2012

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Luminescent Sensing of Oxygen Using a Quenchable Probe and Upconverting Nanoparticles

Angewandte Chemie International Edition, 2011-01, Vol.50 (1), p.260-263

International ed. in English, 2011

Volltextzugriff (PDF)

endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (38), p.13386-13391

2005

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Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients

Journal of the European Academy of Dermatology and Venereology, 2020-10, Vol.34 (10), p.2392-2401

2020

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Crucial role of obliquely propagating gravity waves in the quasi-biennial oscillation dynamics

Atmospheric chemistry and physics, 2024-03, Vol.24 (5), p.3297-3308

2024

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A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene

X-linked Retinitis Pigmentosa: RPGR Mutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15

X-linked ocular albinism (Nettleship-Falls): a novel 29-bp deletion in exon 1. Carrier detection by ophthalmic examination and DNA analysis

Complete form of X-linked congenital stationary night blindness: refined mapping and evidence of genetic homogeneity

Generating several solutions for the scheduling problem in high-level synthesis

Extended 0/1 LP formulation for the scheduling problem in high-level synthesis

Isolation and fine mapping of (CA)n repeats from the Xp11.23 and Xp11.4 region

Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins

Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome

Missense mutations in the NDP gene in patients with a less severe course of Norrie disease

A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa

Sensitivity Analysis of the Bipartite Weighted Matching Problem

UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1-p11.2

Three novel mutations (I506S, S466X, 1651A→T) in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) detected in patients of Southern German Descent

Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins

A PCR based X-chromosome inactivation assay for carrier detection in X-linked immunodeficiencies using differential methylation of the androgen receptor gene

Luminescent Sensing of Oxygen Using a Quenchable Probe and Upconverting Nanoparticles

Photon upconverting nanoparticles for luminescent sensing of temperature

Photon upconverting nanoparticles for luminescent sensing of temperature

Luminescent Sensing of Oxygen Using a Quenchable Probe and Upconverting Nanoparticles

endophytic fungus Piriformospora indica reprograms barley to salt-stress tolerance, disease resistance, and higher yield

Comprehensive germline mutation analysis and clinical profile in a large cohort of Brazilian xeroderma pigmentosum patients

Crucial role of obliquely propagating gravity waves in the quasi-biennial oscillation dynamics

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