PubMed

Plant DNA barcodes and a community phylogeny of a tropical forest dynamics plot in Panama.

Kress WJ, Erickson DL, Jones FA, Swenson NG, Perez R, Sanjur O, Bermingham E.

Proc Natl Acad Sci U S A. 2009 Nov 3;106(44):18621-6. Epub 2009 Oct 19.PMID: 19841276 [PubMed - in process]Related articlesFree article

The evolution of bat pollination: a phylogenetic perspective.

Fleming TH, Geiselman C, Kress WJ.

Ann Bot. 2009 Nov;104(6):1017-43. Epub 2009 Sep 29.PMID: 19789175 [PubMed - in process]Related articles

DNA BARCODING IN LAND PLANTS: DEVELOPING STANDARDS TO QUANTIFY AND MAXIMIZE SUCCESS.

Erickson DL, Spouge J, Resch A, Weigt LA, Kress WJ.

Taxon. 2008 Nov 1;57(4):1304-1316.PMID: 19779570 [PubMed]Related articlesFree article

The alternating power stroke of a 6-cylinder AAA protease chaperone engine.

Kress W, Weber-Ban E.

Mol Cell. 2009 Sep 11;35(5):545-7.PMID: 19748349 [PubMed - indexed for MEDLINE]Related articles

Clp chaperone-proteases: structure and function.

Kress W, Maglica Z, Weber-Ban E.

Res Microbiol. 2009 Nov;160(9):618-28. Epub 2009 Sep 2.PMID: 19732826 [PubMed - in process]Related articles

Both ATPase domains of ClpA are critical for processing of stable protein structures.

Kress W, Mutschler H, Weber-Ban E.

J Biol Chem. 2009 Nov 6;284(45):31441-52. Epub 2009 Sep 2.PMID: 19726681 [PubMed - in process]Related articles

Studying chaperone-proteases using a real-time approach based on FRET.

Kolygo K, Ranjan N, Kress W, Striebel F, Hollenstein K, Neelsen K, Steiner M, Summer H, Weber-Ban E.

J Struct Biol. 2009 Nov;168(2):267-77. Epub 2009 Jul 8.PMID: 19591940 [PubMed - indexed for MEDLINE]Related articles

Effect of flower shape and size on foraging performance and trade-offs in a tropical hummingbird.

Temeles EJ, Koulouris CR, Sander SE, Kress WJ.

Ecology. 2009 May;90(5):1147-61.PMID: 19537537 [PubMed - indexed for MEDLINE]Related articles

Boy with pseudohypoparathyroidism type 1a caused by GNAS gene mutation (deltaN377), Crouzon-like craniosynostosis, and severe trauma-induced bleeding.

Graul-Neumann LM, Bach A, Albani M, Ringe H, Weimann A, Kress W, Hiort O, Bartsch O.

Am J Med Genet A. 2009 Jul;149A(7):1487-93.PMID: 19530187 [PubMed - indexed for MEDLINE]Related articles

Controlled destruction: AAA+ ATPases in protein degradation from bacteria to eukaryotes.

Striebel F, Kress W, Weber-Ban E.

Curr Opin Struct Biol. 2009 Apr;19(2):209-17. Epub 2009 Apr 10. Review.PMID: 19362814 [PubMed - indexed for MEDLINE]Related articles

Intersubunit cross-talk in pyridoxal 5'-phosphate synthase, coordinated by the C terminus of the synthase subunit.

Raschle T, Speziga D, Kress W, Moccand C, Gehrig P, Amrhein N, Weber-Ban E, Fitzpatrick TB.

J Biol Chem. 2009 Mar 20;284(12):7706-18. Epub 2008 Dec 14.PMID: 19074821 [PubMed - indexed for MEDLINE]Related articles

PTHR1 loss-of-function mutations in familial, nonsyndromic primary failure of tooth eruption.

Decker E, Stellzig-Eisenhauer A, Fiebig BS, Rau C, Kress W, Saar K, Rüschendorf F, Hubner N, Grimm T, Weber BH.

Am J Hum Genet. 2008 Dec;83(6):781-6.PMID: 19061984 [PubMed - indexed for MEDLINE]Related articlesFree article

Sustained platelet-derived growth factor receptor alpha signaling in osteoblasts results in craniosynostosis by overactivating the phospholipase C-gamma pathway.

Moenning A, Jäger R, Egert A, Kress W, Wardelmann E, Schorle H.

Mol Cell Biol. 2009 Feb;29(3):881-91. Epub 2008 Dec 1.PMID: 19047372 [PubMed - indexed for MEDLINE]Related articlesFree article

Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants of COH1.

Seifert W, Holder-Espinasse M, Kühnisch J, Kahrizi K, Tzschach A, Garshasbi M, Najmabadi H, Walter Kuss A, Kress W, Laureys G, Loeys B, Brilstra E, Mancini GM, Dollfus H, Dahan K, Apse K, Hennies HC, Horn D.

Hum Mutat. 2009 Feb;30(2):E404-20.PMID: 19006247 [PubMed - indexed for MEDLINE]Related articles

High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany.

Suominen T, Schoser B, Raheem O, Auvinen S, Walter M, Krahe R, Lochmüller H, Kress W, Udd B.

J Neurol. 2008 Nov;255(11):1731-6. Epub 2008 Sep 24.PMID: 18807109 [PubMed - indexed for MEDLINE]Related articles

Distinct muscle imaging patterns in myofibrillar myopathies.

Fischer D, Kley RA, Strach K, Meyer C, Sommer T, Eger K, Rolfs A, Meyer W, Pou A, Pradas J, Heyer CM, Grossmann A, Huebner A, Kress W, Reimann J, Schröder R, Eymard B, Fardeau M, Udd B, Goldfarb L, Vorgerd M, Olivé M.

Neurology. 2008 Sep 2;71(10):758-65.PMID: 18765652 [PubMed - indexed for MEDLINE]Related articlesFree article

Becker's muscular dystrophy aggravating facioscapulohumeral muscular dystrophy--double trouble as an explanation for an atypical phenotype.

Rudnik-Schöneborn S, Weis J, Kress W, Häusler M, Zerres K.

Neuromuscul Disord. 2008 Nov;18(11):881-5. Epub 2008 Aug 5.PMID: 18684626 [PubMed - indexed for MEDLINE]Related articles

Late onset in dysferlinopathy widens the clinical spectrum.

Klinge L, Dean AF, Kress W, Dixon P, Charlton R, Müller JS, Anderson LV, Straub V, Barresi R, Lochmüller H, Bushby K.

Neuromuscul Disord. 2008 Apr;18(4):288-90.PMID: 18396043 [PubMed - indexed for MEDLINE]Related articles

The flexible attachment of the N-domains to the ClpA ring body allows their use on demand.

Cranz-Mileva S, Imkamp F, Kolygo K, Maglica Z, Kress W, Weber-Ban E.

J Mol Biol. 2008 Apr 25;378(2):412-24. Epub 2008 Feb 29.PMID: 18358489 [PubMed - indexed for MEDLINE]Related articles

Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy.

Zirn B, Kress W, Grimm T, Berthold LD, Neubauer B, Kuchelmeister K, Müller U, Hahn A.

Am J Med Genet A. 2008 Apr 15;146A(8):1049-54.PMID: 18348272 [PubMed - indexed for MEDLINE]Related articles

Novel RYR1 missense mutation causes core rod myopathy.

von der Hagen M, Kress W, Hahn G, Brocke KS, Mitzscherling P, Huebner A, Müller-Reible C, Stoltenburg-Didinger G, Kaindl AM.

Eur J Neurol. 2008 Apr;15(4):e31-2. Epub 2008 Feb 26. No abstract available. PMID: 18312400 [PubMed - indexed for MEDLINE]Related articles

DNA barcodes: genes, genomics, and bioinformatics.

Kress WJ, Erickson DL.

Proc Natl Acad Sci U S A. 2008 Feb 26;105(8):2761-2. Epub 2008 Feb 19. No abstract available. PMID: 18287050 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.

Schulz AL, Albrecht B, Arici C, van der Burgt I, Buske A, Gillessen-Kaesbach G, Heller R, Horn D, Hübner CA, Korenke GC, König R, Kress W, Krüger G, Meinecke P, Mücke J, Plecko B, Rossier E, Schinzel A, Schulze A, Seemanova E, Seidel H, Spranger S, Tuysuz B, Uhrig S, Wieczorek D, Kutsche K, Zenker M.

Clin Genet. 2008 Jan;73(1):62-70. Epub 2007 Nov 27.PMID: 18042262 [PubMed - indexed for MEDLINE]Related articles

The phenotype and long-term follow-up in 11 patients with juvenile selenoprotein N1-related myopathy.

Schara U, Kress W, Bönnemann CG, Breitbach-Faller N, Korenke CG, Schreiber G, Stoetter M, Ferreiro A, von der Hagen M.

Eur J Paediatr Neurol. 2008 May;12(3):224-30. Epub 2007 Oct 22.PMID: 17951086 [PubMed - indexed for MEDLINE]Related articles

Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.

Wieland I, Weidner C, Ciccone R, Lapi E, McDonald-McGinn D, Kress W, Jakubiczka S, Collmann H, Zuffardi O, Zackai E, Wieacker P.

Clin Genet. 2007 Dec;72(6):506-16. Epub 2007 Oct 16.PMID: 17941886 [PubMed - indexed for MEDLINE]Related articles

Endocardial cushion defect in a patient with Crouzon syndrome carrying a mutation in the fibroblast growth factor receptor (FGFR)-2 gene.

Schulz C, Kress W, Schömig A, Wessely R.

Clin Genet. 2007 Oct;72(4):305-7.PMID: 17850625 [PubMed - indexed for MEDLINE]Related articles

Orthostatic tremor in three brothers.

Fischer M, Kress W, Reiners K, Rieckmann P.

J Neurol. 2007 Dec;254(12):1759-60. Epub 2007 Jul 31. No abstract available. PMID: 17657402 [PubMed - indexed for MEDLINE]Related articles

Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disorders.

Michel P, Sternberg D, Jeannet PY, Dunand M, Thonney F, Kress W, Fontaine B, Fournier E, Kuntzer T.

Muscle Nerve. 2007 Nov;36(5):643-50.PMID: 17654559 [PubMed - indexed for MEDLINE]Related articles

A two-locus global DNA barcode for land plants: the coding rbcL gene complements the non-coding trnH-psbA spacer region.

Kress WJ, Erickson DL.

PLoS One. 2007 Jun 6;2(6):e508.PMID: 17551588 [PubMed]Related articlesFree article

Assembly pathway of an AAA+ protein: tracking ClpA and ClpAP complex formation in real time.

Kress W, Mutschler H, Weber-Ban E.

Biochemistry. 2007 May 29;46(21):6183-93. Epub 2007 May 4.PMID: 17477547 [PubMed - indexed for MEDLINE]Related articles

Scapuloperoneal syndrome type Kaeser and a wide phenotypic spectrum of adult-onset, dominant myopathies are associated with the desmin mutation R350P.

Walter MC, Reilich P, Huebner A, Fischer D, Schröder R, Vorgerd M, Kress W, Born C, Schoser BG, Krause KH, Klutzny U, Bulst S, Frey JR, Lochmüller H.

Brain. 2007 Jun;130(Pt 6):1485-96. Epub 2007 Apr 17.PMID: 17439987 [PubMed - indexed for MEDLINE]Related articlesFree article

Encephalomyopathy and optic atrophy with tall stature and mitochondrial dysfunction: a new syndrome.

Morava E, Bongers EM, Kress W, Sie L, Rodenburg R, van den Heuvel L, Brunner HG.

Clin Dysmorphol. 2007 Apr;16(2):131-4. No abstract available. PMID: 17351361 [PubMed - indexed for MEDLINE]Related articles

A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene.

Schoser BG, Schröder JM, Grimm T, Sternberg D, Kress W.

Muscle Nerve. 2007 May;35(5):599-606.PMID: 17212350 [PubMed - indexed for MEDLINE]Related articles

Variability of the recessive oculopharyngeal muscular dystrophy phenotype.

Semmler A, Kress W, Vielhaber S, Schröder R, Kornblum C.

Muscle Nerve. 2007 May;35(5):681-4.PMID: 17206657 [PubMed - indexed for MEDLINE]Related articles

Tandem duplication of DMD exon 18 associated with epilepsy, macroglossia, and endocrinologic abnormalities.

Weiss C, Jakubiczka S, Huebner A, Klopocki E, Kress W, Voit T, Hübner C, Schuelke M.

Muscle Nerve. 2007 Mar;35(3):396-401.PMID: 17143888 [PubMed - indexed for MEDLINE]Related articles

Why a positive genetic test for myotonic dystrophy type I does not always imply the right diagnosis.

Meuth SG, Kleinschnitz C, Frank M, Wessig C, Bendszus M, Kress W, Wiendl H.

J Neurol Neurosurg Psychiatry. 2006 Dec;77(12):1381-2. No abstract available. PMID: 17110752 [PubMed - indexed for MEDLINE]Related articles

Genetic investigations of Saethre-Chotzen syndrome presenting with renal cell carcinoma.

Seifert G, Kress W, Meisel C, Henze G, Seeger K.

Cancer Genet Cytogenet. 2006 Nov;171(1):76-8.PMID: 17074596 [PubMed - indexed for MEDLINE]Related articles

Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.

Hiller A, Hagenah JM, Djarmati A, Hedrich K, Reetz K, Schneider-Gold C, Kress W, Münchau A, Klein C.

Mov Disord. 2007 Jan;22(1):145-7.PMID: 17013904 [PubMed - indexed for MEDLINE]Related articles

Extreme phenotypic variability in a German family with X-linked myotubular myopathy associated with E404K mutation in MTM1.

Hoffjan S, Thiels C, Vorgerd M, Neuen-Jacob E, Epplen JT, Kress W.

Neuromuscul Disord. 2006 Nov;16(11):749-53. Epub 2006 Sep 26.PMID: 17005396 [PubMed - indexed for MEDLINE]Related articles

Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?

Hedrich K, Hagenah J, Djarmati A, Hiller A, Lohnau T, Lasek K, Grünewald A, Hilker R, Steinlechner S, Boston H, Kock N, Schneider-Gold C, Kress W, Siebner H, Binkofski F, Lencer R, Münchau A, Klein C.

Arch Neurol. 2006 Jun;63(6):833-8.PMID: 16769864 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel missense mutation in ALS2 gene results in infantile ascending hereditary spastic paralysis.

Eymard-Pierre E, Yamanaka K, Haeussler M, Kress W, Gauthier-Barichard F, Combes P, Cleveland DW, Boespflug-Tanguy O.

Ann Neurol. 2006 Jun;59(6):976-80.PMID: 16718699 [PubMed - indexed for MEDLINE]Related articles

Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding.

Wenzel K, Carl M, Perrot A, Zabojszcza J, Assadi M, Ebeling M, Geier C, Robinson PN, Kress W, Osterziel KJ, Spuler S.

Hum Mutat. 2006 Jun;27(6):599-600.PMID: 16705711 [PubMed - indexed for MEDLINE]Related articles

140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management.

Udd B, Meola G, Krahe R, Thornton C, Ranum LP, Bassez G, Kress W, Schoser B, Moxley R.

Neuromuscul Disord. 2006 Jun;16(6):403-13. Epub 2006 May 8. No abstract available. PMID: 16684600 [PubMed - indexed for MEDLINE]Related articles

Outcome and effect of pregnancy in myotonic dystrophy type 2.

Rudnik-Schöneborn S, Schneider-Gold C, Raabe U, Kress W, Zerres K, Schoser BG.

Neurology. 2006 Feb 28;66(4):579-80.PMID: 16505316 [PubMed - indexed for MEDLINE]Related articles

Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosis.

von der Hagen M, Schallner J, Kaindl AM, Koehler K, Mitzscherling P, Abicht A, Grieben U, Korinthenberg R, Kress W, von Moers A, Müller JS, Schara U, Vorgerd M, Walter MC, Müller-Reible C, Hübner C, Lochmüller H, Huebner A.

Neuromuscul Disord. 2006 Jan;16(1):4-13. Epub 2005 Dec 27.PMID: 16378727 [PubMed - indexed for MEDLINE]Related articles

Balanced translocation in a patient with craniosynostosis disrupts the SOX6 gene and an evolutionarily conserved non-transcribed region.

Tagariello A, Heller R, Greven A, Kalscheuer VM, Molter T, Rauch A, Kress W, Winterpacht A.

J Med Genet. 2006 Jun;43(6):534-40. Epub 2005 Oct 28.PMID: 16258006 [PubMed - indexed for MEDLINE]Related articlesFree article

Saethre-Chotzen syndrome caused by TWIST 1 gene mutations: functional differentiation from Muenke coronal synostosis syndrome.

Kress W, Schropp C, Lieb G, Petersen B, Büsse-Ratzka M, Kunz J, Reinhart E, Schäfer WD, Sold J, Hoppe F, Pahnke J, Trusen A, Sörensen N, Krauss J, Collmann H.

Eur J Hum Genet. 2006 Jan;14(1):39-48.PMID: 16251895 [PubMed - indexed for MEDLINE]Related articlesFree article

Repeated evolution of net venation and fleshy fruits among monocots in shaded habitats confirms a priori predictions: evidence from an ndhF phylogeny.

Givnish TJ, Pires JC, Graham SW, McPherson MA, Prince LM, Patterson TB, Rai HS, Roalson EH, Evans TM, Hahn WJ, Millam KC, Meerow AW, Molvray M, Kores PJ, O'Brien HE, Hall JC, Kress WJ, Sytsma KJ.

Proc Biol Sci. 2005 Jul 22;272(1571):1481-90.PMID: 16011923 [PubMed - indexed for MEDLINE]Related articlesFree article

Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS).

Wieland I, Reardon W, Jakubiczka S, Franco B, Kress W, Vincent-Delorme C, Thierry P, Edwards M, König R, Rusu C, Schweiger S, Thompson E, Tinschert S, Stewart F, Wieacker P.

Hum Mutat. 2005 Aug;26(2):113-8.PMID: 15959873 [PubMed - indexed for MEDLINE]Related articles

Use of DNA barcodes to identify flowering plants.

Kress WJ, Wurdack KJ, Zimmer EA, Weigt LA, Janzen DH.

Proc Natl Acad Sci U S A. 2005 Jun 7;102(23):8369-74. Epub 2005 May 31.PMID: 15928076 [PubMed - indexed for MEDLINE]Related articlesFree article