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Biochemical and Biophysical Research Communications|February 16, 2000
Cathepsin Q, a novel lysosomal cysteine protease highly expressed in placentaK Sol-Church, J Frenck, R W MasonThe Biochemical Journal|April 18, 1998
Amino acid substitutions in the N-terminal segment of cystatin C create selective protein inhibitors of lysosomal cysteine proteinasesR W Mason, K Sol-Church, M AbrahamsonBiochimica Et Biophysica Acta|April 13, 2000
Mouse cathepsin M, a placenta-specific lysosomal cysteine protease related to cathepsins L and PK Sol-Church, J Frenck, R W MasonThe Biochemical Journal|October 8, 1999
Cathepsin P, a novel protease in mouse placentaK Sol-Church, J Frenck, D Troeber, et al.Biochimica Et Biophysica Acta|September 27, 2000
Characterization of mouse cathepsin R, a new member of a family of placentally expressed cysteine proteasesK Sol-Church, J Frenck, G Bertenshaw, et al.Archives of Biochemistry and Biophysics|December 22, 1999
Expression of cysteine proteases in extraembryonic tissues during mouse embryogenesisK Sol-Church, J Shipley, D A Beckman, et al.Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|July 4, 2008
High resolution linkage and linkage disequilibrium analyses of chromosome 1p36 SNPs identify new positional candidate genes for low bone mineral densityH Zhang, K Sol-Church, H Rydbeck, et al.Otolaryngology Case Reports|July 25, 2022
Mutations in LOXHD1 gene can cause auditory neuropathy spectrum disorderT Morlet, K M Robbins, D Stabley, et al.Clinical Genetics|May 12, 2015
Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotypeM Koenighofer, C Y Hung, J L McCauley, et al.Pageof 1