Search Results - "Stelzer, Christiane"

Expression profile of Papss2 (3′‐phosphoadenosine 5′‐phosphosulfate synthase 2) during cartilage formation and skeletal development in the mouse embryo by Stelzer, Christiane, Brimmer, Annette, Hermanns, Pia, Zabel, Bernhard, Dietz, Uwe H.

“…Sulfation of proteoglycans is a very important posttranslational modification in chondrocyte growth and development. The enzyme 3′‐phosphoadenosine…”
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A novel mutation in FGFR-3 disrupts a putative N-glycosylation site and results in hypochondroplasia by WINTERPACHT, ANDREAS, HILBERT, KATJA, STELZER, CHRISTIANE, SCHWEIKARDT, THORSTEN, DECKER, HEINZ, SEGERER, HUGO, SPRANGER, JURGEN, ZABEL, BERNHARD

“…1 Children's Hospital, University of Mainz, D-55101 Mainz 2 Institute of Human Genetics, University of Hamburg, D-22529 Hamburg 3 Institute for Molecular…”
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Grebe Dysplasia And The Spectrum Of CDMP1 Mutations by Stelzer, Christiane, Winterpacht, Andreas, Spranger, Jürgen, Zabel, Bernhard

“…We report on a 4-year-old boy with the typical phenotype of Grebe dysplasia born to consanguineous parents. The father seems to be unaffected; the mother…”
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SPOC1, a novel PHD‐finger protein: Association with residual disease and survival in ovarian cancer by Mohrmann, Gerrit, Hengstler, Jan G., Hofmann, Thomas G., Endele, Sabine U., Lee, Brendan, Stelzer, Christiane, Zabel, Bernhard, Brieger, Juergen, Hasenclever, Dirk, Tanner, Berno, Sagemueller, Jens, Sehouli, Jalid, Will, Hans, Winterpacht, Andreas

“…We report the identification of a novel human gene (SPOC1) which encodes a protein with a PHD‐finger domain. The gene is located in chromosomal region 1p36.23,…”
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Expression profiling of human fetal growth plate cartilage by EST sequencing by Tagariello, Andreas, Schlaubitz, Silke, Hankeln, Thomas, Mohrmann, Gerrit, Stelzer, Christiane, Schweizer, Anja, Hermanns, Pia, Lee, Brendan, Schmidt, Erwin R., Winterpacht, Andreas, Zabel, Bernhard

“…The differentiation of mesenchymal stem cells into hypertrophic chondrocytes is an integral and multistep process important in pattern formation, endochondral…”
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Grebe dysplasia and the spectrum of CDMP1 mutations by Stelzer, Christiane, Winterpacht, Andreas, Spranger, Jürgen, Zabel, Bernhard

“…We report on a 4-year-old boy with the typical phenotype of Grebe dysplasia born to consanguineous parents. The father seems to be unaffected; the mother…”
Get full text