Lutz B. Giebel - Concepedia

Author

Lutz B. Giebel

University of Wisconsin–Madison

Also Known As

L B Giebel, L. B. Giebel, L.B. Giebel, Lutz B Giebel, Lutz B. Giebel

Publications

2.3K

Citations

H-Index

Concepts

All Affiliations

University of Wisconsin–Madison Heidelberg University Sunesis (United States)

About

Lutz B. Giebel is an author at University of Wisconsin–Madison specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	18	1.7K
2	Natural Sciences	7	7	519
3	Biology	5	5	298
4	Biochemistry	4	4	356
5	Engineering	1	1	22

Lutz B. Giebel

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism. Lutz B. Giebel, Richard A. Spritz Proceedings of the National Academy of Sciences Cell LineageDevelopmental BiologyCytogeneticsDevelopmental GeneticsGenetics	1991	384
Screening of cyclic peptide phage libraries identifies ligands that bind streptavidin with high affinities Lutz B. Giebel, Robert Cass, Daniel L. Milligan, Biochemistry Peptide EngineeringHigh AffinitiesMolecular BiologyChemical BiologyProtein Folding	1995	206
Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segment Lutz B. Giebel, Kathleen M. Strunk, Richard A. Spritz Genomics GeneticsNucleotide SequencesMolecular BiologyTruncated Tyrosinase-related SegmentHuman Tyrosinase Gene	1991	181
Dominant negative and loss of function mutations of the c-kit (mast/stem cell growth factor receptor) proto-oncogene in human piebaldism. Richard A. Spritz, Lutz B. Giebel, Stuart A. Holmes PubMed	1992	159
Developmental regulation of a constitutively expressed mouse mRNA encoding a 72-kDa heat shock-like protein Lutz B. Giebel, Bernd P. Dworniczak, E. K. F. Bautz Developmental Biology Protein FunctionDevelopmental BiologyProtein ExpressionMouse MrnaGene Regulation	1988	119
A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse. Lutz B. Giebel, R. K. Tripathi, Richard A. King, Journal of Clinical Investigation BiologyTemperature-sensitive TypeOculocutaneous AlbinismTyrosinase PolypeptideDevelopmental Biology	1991	100
Detection of Mutations in the Tyrosinase Gene in a Patient with Type IA Oculocutaneous Albinism Richard A. Spritz, Kathleen M. Strunk, Lutz B. Giebel, New England Journal of Medicine Oculocutaneous AlbinismOcular DiseaseMendelian DisorderOphthalmologyGenetic Disorder	1990	94
Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinism. Lutz B. Giebel, R. K. Tripathi, Kathleen M. Strunk, PubMed	1991	92
Crystal Structure of an Antagonist Mutant of Human Growth Hormone, G120R, in Complex with Its Receptor at 2.9 Å Resolution M. Sundström, T. Lundqvist, Joakim Rödin, Journal of Biological Chemistry	1996	88
Tyrosinase gene mutations in type I (tyrosinase‐deficient) oculocutaneous albinism define two clusters of missense substitutions Ram K. Tripathi, Kathleen M. Strunk, Lutz B. Giebel, American Journal of Medical Genetics BiologyTyrosinase PolypeptideAllelic VariantOca Tyrosinase ActivityTyrosinase Gene Mutations	1992	83

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