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Gerd Scherer

Free University of Berlin

58H指数
183论文数
1.2W被引数
收录论文 44
发表时间
Direct interaction of SRY-related protein SOX9 and steroidogenic factor 1 regulates transcription of the human anti-Mullerian hormone gene
err2023-03-28
err562
errOAAI
errDe Santa Barbara, P; Bonneaud, N; Boizet, B; Desclozeaux, M; Moniot, B; Sudbeck, P; Scherer, G; Poulat, F; Berta, P
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Sox9 and Sox8 protect the adult testis from male-to-female genetic reprogramming and complete degeneration
err2016-06-21
err81
errOAAI
errBarrionuevo, Francisco J.; Hurtado, Alicia; Kim, Gwang-Jin; Real, Francisca M.; Bakkali, Mohammed; Kopp, Janel L.; Sander, Maike; Scherer, Gerd; Burgos, Miguel; Jimenez, Rafael
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FGFR2 mutation in 46, XY sex reversal with craniosynostosis
err2015-09-11
err42
errOAAI
errBagheri-Fam, Stefan; Ono, Makoto; Li, Li; Zhao, Liang; Ryan, Janelle; Lai, Raymond; Katsura, Yukako; Rossello, Fernando J.; Koopman, Peter; Scherer, Gerd; Bartsch, Oliver; Eswarakumar, Jacob V. P.; Harley, Vincent R.
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Copy number variation of two separate regulatory regions upstream of SOX9 causes isolated 46,XY or 46,XX disorder of sex development
err2015-01-20
err90
PREAI
errKim, Gwang-Jin; Sock, Elisabeth; Buchberger, Astrid; Just, Walter; Denzer, Friederike; Hoepffner, Wolfgang; German, James; Cole, Trevor; Mann, Jillian; Seguin, John H.; Zipf, William; Costigan, Colm; Schmiady, Hardi; Rostasy, Moritz; Kramer, Mildred; Kaltenbach, Simon; Roesler, Bernd; Georg, Ina; Troppmann, Elke; Teichmann, Anne-Christin; Salfelder, Anika; Widholz, Sebastian A.; Wieacker, Peter; Hiort, Olaf; Camerino, Giovanna; Radi, Orietta; Wegner, Michael; Arnold, Hans-Henning; Scherer, Gerd
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Scx+/Sox9+ progenitors contribute to the establishment of the junction between cartilage and tendon/ligament
err2013-06-01
err251
errOAAI
errSugimoto, Yuki; Takimoto, Aki; Akiyama, Haruhiko; Kist, Ralf; Scherer, Gerd; Nakamura, Takashi; Hiraki, Yuji; Shukunami, Chisa
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Genome-wide identification of Sox8-, and Sox9-dependent genes during early post-natal testis development in the mouse
err2013-01-13
err14
PREAI
errChalmel, F.; Lardenois, A.; Georg, I.; Barrionuevo, F.; Demougin, P.; Jegou, B.; Scherer, G.; Primig, M.
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Tyrosinemia Type III detected via neonatal screening: Management and outcome
err2012-11-01
err26
PREAI
errHeylen, Evelyne; Scherer, Gerd; Vincent, Marie-Francoise; Marie, Sandrine; Fischer, Judith; Nassogne, Marie-Cecile
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Clinical Utility Gene Card for: campomelic dysplasia
err2012-10-10
err5
errOAAI
errScherer, Gerd; Zabel, Bernhard; Nishimura, Gen
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L-Sox5 and Sox6 Proteins Enhance Chondrogenic miR-140 MicroRNA Expression by Strengthening Dimeric Sox9 Activity
err2012-06-01
err83
errOAAI
errYamashita, Satoshi; Miyaki, Shigeru; Kato, Yoshio; Yokoyama, Shigetoshi; Sato, Tempei; Barrionuevo, Francisco; Akiyama, Haruhiko; Scherer, Gerd; Takada, Shuji; Asahara, Hiroshi
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A large TAT deletion in a tyrosinaemia type II patient
err2011-11-01
err6
PREAI
errLegarda, Maria; Wlodarczyk, Katarzyna; Lage, Sergio; Andrade, Fernando; Kim, Gwang-Jin; Bausch, Elke; Scherer, Gerd; Jose Aldamiz-Echevarria, Luis
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Profiling spermatogenic failure in adult testes bearing Sox9-deficient Sertoli cells identifies genes involved in feminization, inflammation and stress
err2010-12-23
err15
errOAAI
errLardenois, Aurelie; Chalmel, Frederic; Barrionuevo, Francisco; Demougin, Philippe; Scherer, Gerd; Primig, Michael
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Hydroureternephrosis due to loss of Sox9-regulated smooth muscle cell differentiation of the ureteric mesenchyme
err2010-09-29
err52
errOAAI
errAirik, Rannar; Trowe, Mark-Oliver; Foik, Anna; Farin, Henner F.; Petry, Marianne; Schuster-Gossler, Karin; Schweizer, Michaela; Scherer, Gerd; Kist, Ralf; Kispert, Andreas
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Response to: Extremely Low Risk of Pheochromocytomas in Complete VHL Gene Deletion Cases
err2009-09-01
err0
errOAAI
errFranke, Gerlind; Scherer, Gerd; Neumann, Hartmut P. H.
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The PGD2 pathway, independently of FGF9, amplifies SOX9 activity in Sertoli cells during male sexual differentiation
err2009-06-01
err160
errOAAI
errMoniot, Brigitte; Declosmenil, Faustine; Barrionuevo, Francisco; Scherer, Gerd; Aritake, Kosuke; Malki, Safia; Marzi, Laetitia; Cohen-Solal, Anne; Georg, Ina; Klattig, Juergen; Englert, Christoph; Kim, Yuna; Capel, Blanche; Eguchi, Naomi; Urade, Yoshihiro; Boizet-Bonhoure, Brigitte; Poulat, Francis
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Alu-Alu Recombination Underlies the Vast Majority of Large VHL Germline Deletions: Molecular Characterization and Genotype-Phenotype Correlations in VHL Patients
err2009-03-11
err95
errOAAI
errFranke, Gerlind; Bausch, Birke; Hoffmann, Michael M.; Cybulla, Markus; Wilhelm, Christian; Kohlhase, Juergen; Scherer, Gerd; Neumann, Hartmut P. H.
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