Matthias Wolf

Follow-up of five patients with FHHNC due to mutations in the Paracellin-1 gene.

A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution.

Pulmonary re-occurrence of post-transplant lymphoproliferative disease with hypogammaglobulinaemia.

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.

Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis.

Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination.

Refinement of the critical region for MCKD1 by detection of transcontinental haplotype sharing.

Mutations of the Uromodulin gene in MCKD type 2 patients cluster in exon 4, which encodes three EGF-like domains.

Phylogeny of Firmicutes with special reference to Mycoplasma (Mollicutes) as inferred from phosphoglycerate kinase amino acid sequence data.

Accurate and robust phylogeny estimation based on profile distances: a study of the Chlorophyceae (Chlorophyta).

Telomeric refinement of the MCKD1 locus on chromosome 1q21.

Remote computing environment compensating for brain shift.

Medullary cystic kidney disease type 1 in a large Native-American kindred.

Expression and phenotype analysis of the nephrocystin-1 and nephrocystin-4 homologs in Caenorhabditis elegans.

ProfDist: a tool for the construction of large phylogenetic trees based on profile distances.

Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2-q34.2 by total genome search for linkage.

A common core of secondary structure of the internal transcribed spacer 2 (ITS2) throughout the Eukaryota.

ITS-2 and 18S rRNA gene phylogeny of Aplysinidae (Verongida, Demospongiae).

CBCAnalyzer: inferring phylogenies based on compensatory base changes in RNA secondary structures.

Homology modeling revealed more than 20,000 rRNA internal transcribed spacer 2 (ITS2) secondary structures.

Ewald sphere correction for single-particle electron microscopy.

Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing.

The internal transcribed spacer 2 database--a web server for (not only) low level phylogenetic analyses.

A java applet for exploring the new higher level classification of eukaryotes with emphasis on the taxonomy of protists.

4SALE--a tool for synchronous RNA sequence and secondary structure alignment and editing.

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome.

Distinguishing species.

Deep metazoan phylogeny.

Calcitonin gene-related peptide: a marker for putative primary afferent neurons in the pig small intestinal myenteric plexus?

Evidence of oligogenic inheritance in nephronophthisis.

The ITS2 Database II: homology modelling RNA structure for molecular systematics.

A new method for spherical object detection and its application to computer aided detection of pulmonary nodules in CT images.

Mutation analysis in nephronophthisis using a combined approach of homozygosity mapping, CEL I endonuclease cleavage, and direct sequencing.

Subpicosecond midinfrared spectroscopy of the Pfr reaction of phytochrome Agp1 from Agrobacterium tumefaciens.

Computer-aided detection of pulmonary embolism: influence on radiologists' detection performance with respect to vessel segments.

Sub-picosecond time resolved infrared spectroscopy of high-spin state formation in Fe(ii) spin crossover complexes.

ITS2 data corroborate a monophyletic chlorophycean DO-group (Sphaeropleales).

ProfDistS: (profile-) distance based phylogeny on sequence--structure alignments.

Ultrafast infrared spectroscopy of riboflavin: dynamics, electronic structure, and vibrational mode analysis.

Mutation analysis of the Uromodulin gene in 96 individuals with urinary tract anomalies (CAKUT).

Synchronous visual analysis and editing of RNA sequence and secondary structure alignments using 4SALE.

5.8S-28S rRNA interaction and HMM-based ITS2 annotation.

A systematic approach to mapping recessive disease genes in individuals from outbred populations.

A probabilistic model of cell size reduction in Pseudo-nitzschia delicatissima (Bacillariophyta).

Ultrafast protein conformational alterations in bacteriorhodopsin and its locked analogue BR5.12.

ITS2 sequence-structure analysis in phylogenetics: a how-to manual for molecular systematics.

Evolutionary diversification indicated by compensatory base changes in ITS2 secondary structures in a complex fungal species, Rhizoctonia solani.

Compensatory base changes illuminate morphologically difficult taxonomy.

Methanogenic archaeal community in the sediment of an artificially partitioned acidic bog lake.

Primary photoinduced protein response in bacteriorhodopsin and sensory rhodopsin II.

The ITS2 Database III--sequences and structures for phylogeny.

Microevolution and speciation in Thalassiosira weissflogii (Bacillariophyta).

Structure of clathrin coat with bound Hsc70 and auxilin: mechanism of Hsc70-facilitated disassembly.

ITS2 secondary structure improves phylogeny estimation in a radiation of blue butterflies of the subgenus Agrodiaetus (Lepidoptera: Lycaenidae: Polyommatus ).

Including RNA secondary structures improves accuracy and robustness in reconstruction of phylogenetic trees.

Uromodulin is expressed in renal primary cilia and UMOD mutations result in decreased ciliary uromodulin expression.

Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy.

Subunit interactions in bovine papillomavirus.

A two-level approach towards semantic colon segmentation: removing extra-colonic findings.

Nephronophthisis.

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy.

A molecular phylogeny of Hypnales (Bryophyta) inferred from ITS2 sequence-structure data.

Excited-state dynamics of protochlorophyllide revealed by subpicosecond infrared spectroscopy.

Evolutionary distances in the twilight zone--a rational kernel approach.

Internal transcribed spacer 2 (nu ITS2 rRNA) sequence-structure phylogenetics: towards an automated reconstruction of the green algal tree of life.

Modelling cross-hybridization on phylogenetic DNA microarrays increases the detection power of closely related species.

Vibrational mode analysis of isotope-labeled electronically excited riboflavin.

Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKD.

Computer-aided detection of colorectal polyps in CT colonography with and without fecal tagging: a stand-alone evaluation.

Robust large scale prone-supine polyp matching using local features: a metric learning approach.

Phylogeny of Oedogoniales, Chaetophorales and Chaetopeltidales (Chlorophyceae): inferences from sequence-structure analysis of ITS2.

ITS2 Database IV: Interactive taxon sampling for internal transcribed spacer 2 based phylogenies.