1 - 25 of 63 results for author:"Scherer G." in Literature citations
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| L-Sox5 and Sox6 proteins enhance chondrogenic miR-140 microRNA expression by strengthening dimeric Sox9 activity. Yamashita S., Miyaki S., Kato Y., Yokoyama S., Sato T., Barrionuevo F., Akiyama H., Scherer G., Takada S., Asahara H. J. Biol. Chem. 287:22206-22215(2012) · Mapped (42) |
| A large TAT deletion in a tyrosinaemia type II patient. Legarda M., Wlodarczyk K., Lage S., Andrade F., Kim G.J., Bausch E., Scherer G., Aldamiz-Echevarria L.J. Mol. Genet. Metab. 104:407-409(2011) · Mapped (3) |
| A novel SOX9 nonsense mutation, q401x, in a case of campomelic dysplasia with XY sex reversal. Stoeva R., Grozdanova L., Scherer G., Krasteva M., Bausch E., Krastev T., Linev A., Stefanova M. Genet. Couns. 22:49-53(2011) · Mapped (2) |
| The phosphatidylcholine-hydrolysing phospholipase C NPC4 plays a role in response of Arabidopsis roots to salt stress. Kocourkova D., Krckova Z., Pejchar P., Veselkova S., Valentova O., Wimalasekera R., Scherer G.F., Martinec J. J. Exp. Bot. 62:3753-3763(2011) · Mapped (1) |
| COPPER AMINE OXIDASE1 (CuAO1) of Arabidopsis thaliana contributes to abscisic acid- and polyamine-induced nitric oxide biosynthesis and abscisic acid signal transduction. Wimalasekera R., Villar C., Begum T., Scherer G.F. Mol Plant 4:663-678(2011) · Mapped (1) |
| The heterozygous abp1/ABP1 insertional mutant has defects in functions requiring polar auxin transport and in regulation of early auxin-regulated genes. Effendi Y., Rietz S., Fischer U., Scherer G.F. Plant J. 65:282-294(2011) · Mapped (1) |
| Novel splice variants of human IKKepsilon negatively regulate IKKepsilon-induced IRF3 and NF-kB activation. Koop A., Lepenies I., Braum O., Davarnia P., Scherer G., Fickenscher H., Kabelitz D., Adam-Klages S. Eur. J. Immunol. 41:224-234(2011) · Mapped (12) |
| Hydroureternephrosis due to loss of Sox9-regulated smooth muscle cell differentiation of the ureteric mesenchyme. Airik R., Trowe M.O., Foik A., Farin H.F., Petry M., Schuster-Gossler K., Schweizer M., Scherer G., Kist R., Kispert A. Hum. Mol. Genet. 19:4918-4929(2010) · Mapped (121) |
| Mutations of the SRY-responsive enhancer of SOX9 are uncommon in XY gonadal dysgenesis. Georg I., Bagheri-Fam S., Knower K.C., Wieacker P., Scherer G., Harley V.R. Sex Dev 4:321-325(2010) · Mapped (2) |
| Roles of Arabidopsis patatin-related phospholipases a in root development are related to auxin responses and phosphate deficiency. Rietz S., Dermendjiev G., Oppermann E., Tafesse F.G., Effendi Y., Holk A., Parker J.E., Teige M., Scherer G.F. Mol Plant 3:524-538(2010) |
| Dicer is required for Sertoli cell function and survival. Kim G.J., Georg I., Scherthan H., Merkenschlager M., Guillou F., Scherer G., Barrionuevo F. Int. J. Dev. Biol. 54:867-875(2010) · Mapped (119) |
| The PGD2 pathway, independently of FGF9, amplifies SOX9 activity in Sertoli cells during male sexual differentiation. Moniot B., Declosmenil F., Barrionuevo F., Scherer G., Aritake K., Malki S., Marzi L., Cohen-Solal A., Georg I., Klattig J. et al. Development 136:1813-1821(2009) · Mapped (50) |
| Alu-Alu recombination underlies the vast majority of large VHL germline deletions: Molecular characterization and genotype-phenotype correlations in VHL patients. Franke G., Bausch B., Hoffmann M.M., Cybulla M., Wilhelm C., Kohlhase J., Scherer G., Neumann H.P. Hum. Mutat. 30:776-786(2009) · Mapped (3) |
| Testis cord differentiation after the sex determination stage is independent of Sox9 but fails in the combined absence of Sox9 and Sox8. Barrionuevo F., Georg I., Scherthan H., Lecureuil C., Guillou F., Wegner M., Scherer G. Dev. Biol. 327:301-312(2009) · Mapped (117) |
| TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome. Lausch E., Hermanns P., Farin H.F., Alanay Y., Unger S., Nikkel S., Steinwender C., Scherer G., Spranger J., Zabel B. et al. Am. J. Hum. Genet. 83:649-655(2008) · UniProtKB (1) · Mapped (4) |
| Interaction with XIAP prevents full caspase-3/-7 activation in proliferating human T lymphocytes. Paulsen M., Ussat S., Jakob M., Scherer G., Lepenies I., Schutze S., Kabelitz D., Adam-Klages S. Eur. J. Immunol. 38:1979-1987(2008) · Mapped (9) |
| The words of the regulatory code are arranged in a variable manner in highly conserved enhancers. Rastegar S., Hess I., Dickmeis T., Nicod J.C., Ertzer R., Hadzhiev Y., Thies W.G., Scherer G., Strahle U. Dev. Biol. 318:366-377(2008) · Mapped (3) |
| Loss of Sox9 function results in defective chondrocyte differentiation of mouse embryonic stem cells in vitro. Hargus G., Kist R., Kramer J., Gerstel D., Neitz A., Scherer G., Rohwedel J. Int. J. Dev. Biol. 52:323-332(2008) · Mapped (22) |
| Extended pedigree with multiple cases of XX sex reversal in the absence of SRY and of a mutation at the SOX9 locus. Temel S.G., Gulten T., Yakut T., Saglam H., Kilic N., Bausch E., Jin W.J., Leipoldt M., Scherer G. Sex Dev 1:24-34(2007) · Mapped (21) |
| Sox9 is required for invagination of the otic placode in mice. Barrionuevo F., Naumann A., Bagheri-Fam S., Speth V., Taketo M.M., Scherer G., Neubuser A. Dev. Biol. 317:213-224(2008) · Mapped (99) |
| Zeatin-induced nitric oxide (NO) biosynthesis in Arabidopsis thaliana mutants of NO biosynthesis and of two-component signaling genes. Tun N.N., Livaja M., Kieber J.J., Scherer G.F. New Phytol. 178:515-531(2008) · Mapped (6) |
| Loss of Fgfr2 leads to partial XY sex reversal. Bagheri-Fam S., Sim H., Bernard P., Jayakody I., Taketo M.M., Scherer G., Harley V.R. Dev. Biol. 314:71-83(2008) · Mapped (91) |
| Sox9 regulates cell proliferation and is required for Paneth cell differentiation in the intestinal epithelium. Bastide P., Darido C., Pannequin J., Kist R., Robine S., Marty-Double C., Bibeau F., Scherer G., Joubert D., Hollande F. et al. J. Cell Biol. 178:635-648(2007) · Mapped (22) |
| A role for phospholipase A in auxin-regulated gene expression. Scherer G.F., Zahn M., Callis J., Jones A.M. FEBS Lett. 581:4205-4211(2007) · Mapped (2) |
| Sox9 is required for precursor cell expansion and extracellular matrix organization during mouse heart valve development. Lincoln J., Kist R., Scherer G., Yutzey K.E. Dev. Biol. 305:120-132(2007) · Mapped (23) |

