Winter, J.; Lehmann, T.; Krauß, S.; Trockenbacher, A.; Kijas, Z.; Foerster, J.; Suckow, V.; Yaspo, M.-L.; Kulozik, A.; Kalscheuer, V. M. et al.; Schneider, R.; Schweiger, S.: Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing. Human Genetics 114 (6), S. 541 - 552 (2004)

Winter, J.; Lehmann, T.; Krauß, S.; Trockenbacher, A.; Kijas, Z.; Foerster, J.; Suckow, V.; Yaspo, M.-L.; Kulozik, A.; Kalscheuer, V. M. et al.; Schneider, R.; Schweiger, S.: Regulation of the MID1 protein function is fine-tuned by a complex pattern of alternative splicing. Human Genetics 114 (6), S. 541 - 552 (2004)

Antebi, A.: Tipping the balance toward longevity. Developmental Cell 6 (3), S. 315 - 316 (2004)

Chang, T. H.-T.; Primig, M.; Hadchouel, J.; Tajbakhsh, S.; Rocancourt, D.; Fernandez, A.; Kappler, R.; Scherthan, H.; Buckingham, M.: An enhancer directs differential expression of the linked Mrf4 and Myf5 myogenic regulatory genes in the mouse. Developmental Biology 269 (2), S. 595 - 608 (2004)

Theendakara, V.; Tromp, G.; Kuivaniem, H.; White, P. S.; Panchal, S.; Cox, J.; Winters, R. S.; Riebeling, P.; Tost, F.; Hoeltzenbein, M. et al.; Tervo, T. M.; Henn, W.; Denniger, E.; Krause, M.; Koksal, M.; Kargi, S.; Ugurbas, S. H.; Latvala, T.; Shearman, A. M.; Weiss, J. S.: Fine mapping of the Schnyder's crystalline corneal dystrophy locus. Human Genetics 114 (6), S. 594 - 600 (2004)

Kontou, M.; Will, R. D.; Adelfalk, C.; Wittig, R.; Poustka, A.; Hirsch-Kauffmann, M.; Schweiger, M.: Thioredoxin, a regulator of gene expression. Oncogene 23 (12), S. 2146 - 2152 (2004)

Nuber, U. A.; Tinschert, S.; Mundlos, S.; Hauber, I.: Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation. American Journal of Medical Genetics Part A 125A (3), S. 261 - 266 (2004)

Nuber, U. A.; Tinschert, S.; Mundlos, S.; Hauber, I.: Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation. American Journal of Medical Genetics Part A 125A (3), S. 261 - 266 (2004)

Nuber, U. A.; Tinschert, S.; Mundlos, S.; Hausser, I.: Dyschromatosis universalis hereditaria: Familial case and ultrastructural skin investigation. American Journal of Medical Genetics Part A 125A (3), S. 261 - 266 (2004)

Alsheimer, M.; Liebe, B.; Sewell, L.; Stewart, C. L.; Scherthan, H.; Benavente, R.: Disruption of spermatogenesis in mice lacking A-type lamins. Journal of Cell Science 117 (7), S. 1173 - 1178 (2004)

Klaunick, G.; Ebner, A.; Jochum, F.; Otto, S.; Hoeltzenbein, M.; Würfel, B.; Fusch, C.: Fehlende Gyrierung des Gehirns bei einem SGA-Neugeborenen. Monatsschrift Kinderheilkunde: Organ der Deutschen Gesellschaft für Kinderheilkunde 152 (5), S. 564 - 568 (2004)

Scheich, C.; Leitner, D.; Sievert, V.; Leidert, M.; Schlegel, B.; Simon, B.; Letunic, I.; Büssow, K.; Diehl, A.: Fast identification of folded human protein domains expressed in E. coli suitable for structural analysis. BMC Structural Biology 4, S. 4 - 4 (2004)

Haesler, S.; Wada, K.; Nshdejan, A.; Lints, T.; Jarvis, E. D.; Scharff, C.: FoxP2 expression in avian vocal learners and non-learners. The Journal of Neuroscience 24 (13), S. 3164 - 3175 (2004)

Hertz, J. M.; Sivertsen, B.; Silahtaroglu, A.; Bugge, M.; Kalscheuer, V. M.; Weber, A.; Wirth, J.; Ropers, H.-H.; Tommerup, N.; Tümer, Z.: Early onset, non-progressive, mild cerebellar ataxia cosegregating with a familial balanced translocation t(8;20)(p22;q13). Journal of Medical Genetics 41, S. e25 - e25 (2004)

Mueller, H.; Lehmann, V.; Gustavsson, N.; Gobom, J.; Lange, B. M. H.: Identification and molecular characterisation of centrosomal proteins in Drosophila melanogaster. European Journal of Cell Biology. Supplement 83 (Suppl. 54), S. 76 - 76 (2004)

Patkar, A. A.; Berrettini, W. H.; Mannelli, P.; Gopalakrishnan, R.; Hoehe, M. R.; Bilal, L.; Weinstein, S.; Vergare, M. J.: Relationship between serotonin transporter gene polymorphisms and platelet serotonin transporter sites among African-American cocaine-dependent individuals and healthy volunteers. Psychiatric Genetics 14 (1), S. 25 - 32 (2004)

Thiele, H.; McCann, C.; van't Padje, S.; Schwabe, G. C.; Hennies, H. C.; Camera, G.; Opitz, J.; Laxova, R.; Mundlos, S.; Nurnberg, P.: Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36. Journal of Medical Genetics 41 (3), S. 213 - 218 (2004)

Thiele, H.; McCann, C.; van’t Padje, S.; Schwabe, G. C.; Hennies, H. C.; Camera, G.; Opitz, J.; Laxova, R.; Mundlos, S.; Nürnberg, P.: Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36. Journal of Medical Genetics 41 (3), S. 213 - 218 (2004)

Stuhlmüller, B.; Tandon, N.; Hultschig, C.; Kuban, R. J.; Hernandez, M.; Burmester, G. R.; Häupl, T.: A customized monocyte cDNA microarray for diagnosis of rheumatoid arthritis and prognosis of anti-TNF-α therapy. Arthritis Research & Therapy 6 (Suppl. 1), S. 69 - 69 (2004)

Gunawan, B.; Schulten, H.-J.; von Heydebreck, A.; Schmidt, B.; Enders, C.; Höer, J.; Langer, C.; Schüler, P.; Schindler, C. G.; Kuhlgatz, J. et al.; Füzesi, L.: Site-independent prognostic value of chromosome 9q loss in primary gastrointestinal stromal tumours. The Journal of Pathology: an Official Journal of the Pathological Society of Great Britain and Ireland 202 (4), S. 421 - 429 (2004)