17
results
for author:"Hennig S."
in Literature Citations
| Structural and functional analyses of PAS domain interactions of the clock proteins Drosophila PERIOD and mouse PERIOD2. Hennig S., Strauss H.M., Vanselow K., Yildiz O., Schulze S., Arens J., Kramer A., Wolf E. PLoS Biol. 7:e94-e94(2009) · Mapped (3) |
| Auto-regulation of the circadian slave oscillator component AtGRP7 and regulation of its targets is impaired by a single RNA recognition motif point mutation. Schoning J.C., Streitner C., Page D.R., Hennig S., Uchida K., Wolf E., Furuya M., Staiger D. Plant J. 52:1119-1130(2007) · Mapped (12) |
| A novel photoreaction mechanism for the circadian blue light photoreceptor Drosophila cryptochrome. Berndt A., Kottke T., Breitkreuz H., Dvorsky R., Hennig S., Alexander M., Wolf E. J. Biol. Chem. 282:13011-13021(2007) · UniProtKB (1) |
| The DNA sequence, annotation and analysis of human chromosome 3. Muzny D.M., Scherer S.E., Kaul R., Wang J., Yu J., Sudbrak R., Buhay C.J., Chen R., Cree A., Ding Y. et al. Nature 440:1194-1198(2006) · UniProtKB (2,861) |
| Mutational analysis of the NPHP4 gene in 250 patients with nephronophthisis. Hoefele J., Sudbrak R., Reinhardt R., Lehrack S., Hennig S., Imm A., Muerb U., Utsch B., Attanasio M., O'Toole J.F. et al. |
| The DNA sequence of the human X chromosome. Ross M.T., Grafham D.V., Coffey A.J., Scherer S., McLay K., Muzny D., Platzer M., Howell G.R., Burrows C., Bird C.P. et al. Nature 434:325-337(2005) · UniProtKB (1,199) |
| Crystal structure and interactions of the PAS repeat region of the Drosophila clock protein PERIOD. Yildiz O., Doi M., Yujnovsky I., Cardone L., Berndt A., Hennig S., Schulze S., Urbanke C., Sassone-Corsi P., Wolf E. |
| Crystal structure of narbonin at 1.8 A resolution. Hennig M., Pfeffer-Hennig S., Dauter Z., Wilson K.S., Schlesier B., Nong V.H. Acta Crystallogr. D Biol. Crystallogr. 51:177-189(1995) · Mapped (1) |
| Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region. Sudbrak R., Reinhardt R., Hennig S., Lehrach H., Gunther E., Walter L. Immunogenetics 54:699-704(2003) · UniProtKB (4) |
| Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry. Olbrich H., Haeffner K., Kispert A., Voelkel A., Volz A., Sasmaz G., Reinhardt R., Hennig S., Lehrach H., Konietzko N. et al. Nat. Genet. 30:143-144(2002) · UniProtKB (2) |
| The cytoplasmic domain of the ligand ephrinB2 is required for vascular morphogenesis but not cranial neural crest migration. Adams R.H., Diella F., Hennig S., Helmbacher F., Deutsch U., Klein R. Cell 104:57-69(2001) · Mapped (23) |
| Triple A syndrome is caused by mutations in AAAS, a new WD-repeat protein gene. Handschug K., Sperling S., Yoon S.-J.K., Hennig S., Clark A.J.L., Huebner A. Hum. Mol. Genet. 10:283-290(2001) · UniProtKB (1) |
| The DNA sequence of human chromosome 21. Hattori M., Fujiyama A., Taylor T.D., Watanabe H., Yada T., Park H.-S., Toyoda A., Ishii K., Totoki Y., Choi D.-K. et al. Nature 405:311-319(2000) · UniProtKB (510) |
| Analysis of the spermine synthase gene region in Fugu rubripes, Tetraodon fluviatilis, and Danio rerio. Boeddrich A., Burgtorf C., Roest Crollius H., Hennig S., Bernot A., Clark M., Reinhardt R., Lehrach H., Francis F. Genomics 57:164-168(1999) · UniProtKB (3) |
| An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains. Aaltonen J., Bjoerses P., Perheentupa J., Horelli-Kuitunen N., Palotie A., Peltonen L., Lee Y.S., Francis F., Hennig S., Thiel C. et al. Nat. Genet. 17:399-403(1997) · UniProtKB (1) |
| Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets. Francis F., Strom T.M., Hennig S., Boeddrich A., Lorenz B., Brandau O., Mohnike K.L., Cagnoli M., Steffens C., Klages S. et al. Genome Res. 7:573-585(1997) · UniProtKB (2) |
| A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP consortium |
