Publikationen von Ralf Sudbrak
Alle Typen
Zeitschriftenartikel (38)
21.
Zeitschriftenartikel
343 (7031), S. 325 - 337 (2005)
The DNA sequence of the human X chromosome. Nature 22.
Zeitschriftenartikel
343 (7031), S. 325 - 337 (2005)
The DNA sequence of the human X chromosome. Nature 23.
Zeitschriftenartikel
151 (4), S. 521 - 529 (2004)
Mono-allelic expression of the IGF-I receptor does not affect IGF responses in human fibroblasts. European Journal of Endocrinology 24.
Zeitschriftenartikel
14 (4), S. 631 - 639 (2004)
The genomic sequence and comparative analysis of the rat major histocompatibility complex. Genome Research 25.
Zeitschriftenartikel
83 (2), S. 193 - 202 (2004)
Plasticity of human chromosome 3 during primate evolution. Genomics 26.
Zeitschriftenartikel
2004 (1), S. 17 - 19 (2004)
Vergleichende Sequenzierung von Kandidatengenen: die Resequencing-Plattform am MPI-MG. GenomXPress: Informationen aus der Deutschen Genomforschung 27.
Zeitschriftenartikel
14 (Suppl. S), S. 359A - 359A (2003)
Mutational analysis in nephronophthisis type 4. Journal of the American Society of Nephrology 28.
Zeitschriftenartikel
34 (4), S. 455 - 459 (2003)
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis. Nature Genetics 29.
Zeitschriftenartikel
54 (10), S. 699 - 704 (2003)
Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region. Immunogenetics 30.
Zeitschriftenartikel
54 (10), S. 699 - 704 (2002)
Comparative and evolutionary analysis of the rhesus macaque extended MHC class II region. Immunogenetics 31.
Zeitschriftenartikel
71 (5), S. 1161 - 1167 (2002)
A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution. American Journal of Human Genetics 32.
Zeitschriftenartikel
71 (5), S. 1161 - 1167 (2002)
A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution. American Journal of Human Genetics 33.
Zeitschriftenartikel
54 (4), S. 268 - 275 (2002)
Physical mapping of the major histocompatibility complex class II and class III regions of the rat. Immunogenetics 34.
Zeitschriftenartikel
118 (2), S. 338 - 343 (2002)
Hailey-Hailey Disease: Molecular and Clinical Characterization of Novel Mutations in the ATP2C1 Gene. Journal of Investigative Dermatology 35.
Zeitschriftenartikel
30 (2), S. 143 - 144 (2002)
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry. Nature Genetics 36.
Zeitschriftenartikel
30 (2), S. 143 - 144 (2002)
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry. Nature Genetics 37.
Zeitschriftenartikel
30 (2), S. 143 - 144 (2002)
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry. Nature Genetics 38.
Zeitschriftenartikel
80 (2), S. 169 - 176 (2002)
Gene for integrin-associated protein (IAP, CD47): physical mapping, genomic structure, and expression studies in skeletal muscle. Biochemistry and Cell Biology Buchkapitel (1)
39.
Buchkapitel
133, S. 15 - 33 (Hg. Seitz, H.; Schuhmacher, S.). Springer, Berlin Heidelberg (2013)
Future of Medicine: Models in Predictive Diagnostics and Personalized Medicine. In: Advances in Biochemical Engineering/Biotechnology, Bd. Konferenzbeitrag (1)
40.
Konferenzbeitrag
IT Future of Medicine (ITFoM). In: Proceedings Iwbbio 2013: International Work-Conference on Bioinformatics and Biomedical Engineering, S. 335 - 335. International Work-Conference on Bioinformatics and Biomedical Engineering, IWBBIO 2013, Granada, Spain, March 18-20, 2013. Proceedings. , Grenada, 18. März 2013 - 20. März 2013. (2013)