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Items: 1 to 20 of 87

1.

Characterization of genetic diversity in the nematode Pristionchus pacificus from population-scale resequencing data.

Rödelsperger C, Neher RA, Weller AM, Eberhardt G, Witte H, Mayer WE, Dieterich C, Sommer RJ.

Genetics. 2014 Apr;196(4):1153-65. doi: 10.1534/genetics.113.159855.

2.

Description of three Pristionchus species (Nematoda: Diplogastridae) from Japan that form a cryptic species complex with the model organism P. pacificus.

Kanzaki N, Ragsdale EJ, Herrmann M, Mayer WE, Sommer RJ.

Zoolog Sci. 2012 Jun;29(6):403-17. doi: 10.2108/zsj.29.403.

PMID:
22639812
3.

Horizontal gene transfer of microbial cellulases into nematode genomes is associated with functional assimilation and gene turnover.

Mayer WE, Schuster LN, Bartelmes G, Dieterich C, Sommer RJ.

BMC Evol Biol. 2011 Jan 13;11:13. doi: 10.1186/1471-2148-11-13.

4.

Quantitative assessment of the nematode fauna present on Geotrupes dung beetles reveals species-rich communities with a heterogeneous distribution.

Weller AM, Mayer WE, Rae R, Sommer RJ.

J Parasitol. 2010 Jun;96(3):525-31. doi: 10.1645/GE-2319.1.

PMID:
20557197
5.

Molecular phylogeny of beetle associated diplogastrid nematodes suggests host switching rather than nematode-beetle coevolution.

Mayer WE, Herrmann M, Sommer RJ.

BMC Evol Biol. 2009 Aug 24;9:212. doi: 10.1186/1471-2148-9-212.

6.

The Strongyloides (Nematoda) of sheep and the predominant Strongyloides of cattle form at least two different, genetically isolated populations.

Eberhardt AG, Mayer WE, Bonfoh B, Streit A.

Vet Parasitol. 2008 Oct 20;157(1-2):89-99. doi: 10.1016/j.vetpar.2008.07.019.

PMID:
18760537
7.
9.
10.

The free-living generation of the nematode Strongyloides papillosus undergoes sexual reproduction.

Eberhardt AG, Mayer WE, Streit A.

Int J Parasitol. 2007 Jul;37(8-9):989-1000.

PMID:
17324432
11.

Sex, bugs and Haldane's rule: the nematode genus Pristionchus in the United States.

Herrmann M, Mayer WE, Sommer RJ.

Front Zool. 2006 Sep 12;3:14.

12.
13.

Organization, alternative splicing, polymorphism, and phylogenetic position of lamprey CD45 gene.

Uinuk-Ool T, Nikolaidis N, Sato A, Mayer WE, Klein J.

Immunogenetics. 2005 Sep;57(8):607-17.

PMID:
16078081
14.

Prototypic T cell receptor and CD4-like coreceptor are expressed by lymphocytes in the agnathan sea lamprey.

Pancer Z, Mayer WE, Klein J, Cooper MD.

Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13273-8.

15.

The Ig-like domain of tapasin influences intermolecular interactions.

Turnquist HR, Petersen JL, Vargas SE, McIlhaney MM, Bedows E, Mayer WE, Grandea AG 3rd, Van Kaer L, Solheim JC.

J Immunol. 2004 Mar 1;172(5):2976-84.

16.

Clustering of C-type lectin natural killer receptor-like loci in the bony fish Oreochromis niloticus.

Kikuno R, Sato A, Mayer WE, Shintani S, Aoki T, Klein J.

Scand J Immunol. 2004 Feb;59(2):133-42.

17.

Phylogenetic relationships among East African haplochromine fish as revealed by short interspersed elements (SINEs).

Terai Y, Takezaki N, Mayer WE, Tichy H, Takahata N, Klein J, Okada N.

J Mol Evol. 2004 Jan;58(1):64-78.

PMID:
14743315
18.

Phylogeny of antigen-processing enzymes: cathepsins of a cephalochordate, an agnathan and a bony fish.

Uinuk-Ool TS, Takezaki N, Kuroda N, Figueroa F, Sato A, Samonte IE, Mayer WE, Klein J.

Scand J Immunol. 2003 Oct;58(4):436-48.

19.

A molecule bearing an immunoglobulin-like V region of the CTX subfamily in amphioxus.

Sato A, Mayer WE, Klein J.

Immunogenetics. 2003 Sep;55(6):423-7.

PMID:
12898067
20.

Genes encoding putative natural killer cell C-type lectin receptors in teleostean fishes.

Sato A, Mayer WE, Overath P, Klein J.

Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7779-84.

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