Zobrazeno 1 - 10
of 146
pro vyhledávání: '"Gerd Scherer"'
Autor:
Hans-Heinrich Limbach, Simone Baumgärtner, Roland Franke, Ferdinand Männle, Gerd Scherer, Gleb S. Denisov
Publikováno v:
Molecules, Vol 26, Iss 14, p 4373 (2021)
Using dynamic liquid-state NMR spectroscopy a degenerate double proton tautomerism was detected in tetramethyl reductic acid (TMRA) dissolved in toluene-d8 and in CD2Cl2. Similar to vitamin C, TMRA belongs to the class of reductones of biologically i
Externí odkaz:
https://doaj.org/article/9ed5f8c3d10746daa820b4356342d36c
Autor:
Francisco J Barrionuevo, Alicia Hurtado, Gwang-Jin Kim, Francisca M Real, Mohammed Bakkali, Janel L Kopp, Maike Sander, Gerd Scherer, Miguel Burgos, Rafael Jiménez
Publikováno v:
eLife, Vol 5 (2016)
The new concept of mammalian sex maintenance establishes that particular key genes must remain active in the differentiated gonads to avoid genetic sex reprogramming, as described in adult ovaries after Foxl2 ablation. Dmrt1 plays a similar role in p
Externí odkaz:
https://doaj.org/article/55e4d53a596c4d5dbe487f59661d903b
Autor:
Simone Baumgärtner, Ferdinand Männle, Roland Franke, Gerd Scherer, Hans-Heinrich Limbach, Gleb S. Denisov
Publikováno v:
Molecules, Vol 26, Iss 4373, p 4373 (2021)
Molecules
Volume 26
Issue 14
Molecules
Volume 26
Issue 14
Using dynamic liquid-state NMR spectroscopy a degenerate double proton tautomerism was detected in tetramethyl reductic acid (TMRA) dissolved in toluene-d8 and in CD2Cl2. Similar to vitamin C, TMRA belongs to the class of reductones of biologically i
Autor:
Anna E. von Bohlen, Ralf Stücker, Ramona Pop, Gerd Scherer, Deborah J. Morris-Rosendahl, Diana S. Johnson, John Tolmie, Johann Böhm
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Campomelic dysplasia (CD) is a semilethal developmental disorder caused by mutations in and around SOX9. CD is characterized by multiple skeletal malformations including bending (campomelia) of long bones. Surviving patients frequently hav
Autor:
Gerd Scherer, Susanne Ledig, Ann-Christin Tewes, Judit Horvath, Jan Rehkämper, Peter Wieacker
Publikováno v:
Sexual Development. 11:248-253
46,XY gonadal dysgenesis (46,XY GD) is a disorder of sexual development caused by mutations in genes involved in early gonadal development (bipotential gonads) and testis differentiation. In 46,XY GD individuals, mutations of the SRY gene are detecte
Autor:
Jan, Rehkämper, Ann-Christin, Tewes, Judit, Horvath, Gerd, Scherer, Peter, Wieacker, Susanne, Ledig
Publikováno v:
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 11(5-6)
46,XY gonadal dysgenesis (46,XY GD) is a disorder of sexual development caused by mutations in genes involved in early gonadal development (bipotential gonads) and testis differentiation. In 46,XY GD individuals, mutations of the SRY gene are detecte
The liquid chromatographic behavior of p-tert-butylcalix[n]arene (n = 4,5,6, and 8) for the separation of cis/trans peptide bond isomers of proline-containing peptides is studied to demonstrate the chromatographic selectivity of calixarene stationary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c73babe47413385ede073fd257a25405
http://doc.rero.ch/record/299308/files/36-8-388.pdf
http://doc.rero.ch/record/299308/files/36-8-388.pdf
Autor:
Gerd Scherer, Takashi Nakamura, Yuki Sugimoto, Ralf Kist, Yuji Hiraki, Chisa Shukunami, Haruhiko Akiyama, Aki Takimoto
Publikováno v:
Development. 140:2280-2288
SRY-box containing gene 9 (Sox9) and scleraxis (Scx) regulate cartilage and tendon formation, respectively. Here we report that murine Scx(+)/Sox9(+) progenitors differentiate into chondrocytes and tenocytes/ligamentocytes to form the junction betwee
Autor:
Rafael Jiménez, Maike Sander, Gerd Scherer, Miguel Burgos, Gwang-Jin Kim, Francisca M. Real, Francisco J. Barrionuevo, Alicia Hurtado, Janel L. Kopp, Mohammed Bakkali
Publikováno v:
eLife, Vol 5 (2016)
eLife
eLife
The new concept of mammalian sex maintenance establishes that particular key genes must remain active in the differentiated gonads to avoid genetic sex reprogramming, as described in adult ovaries after Foxl2 ablation. Dmrt1 plays a similar role in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c338cc8042f92d2f827d84655a7182d3
http://edoc.mdc-berlin.de/22493/1/22493oa.pdf
http://edoc.mdc-berlin.de/22493/1/22493oa.pdf
Autor:
Rafael Jiménez, Gwang-Jin Kim, Alicia Hurtado, Francisco J. Barrionuevo, Miguel Burgos, Francisca M. Real, Maike Sander, Mohammed Bakkali, Gerd Scherer, Janel L. Kopp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36e6dcfe7a6476c51d60c7996bcdc913
https://doi.org/10.7554/elife.15635.037
https://doi.org/10.7554/elife.15635.037