Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD033013-01A1
Application #
2206357
Study Section
General Medicine B Study Section (GMB)
Project Start
1996-02-12
Project End
1999-01-31
Budget Start
1996-02-12
Budget End
1997-01-31
Support Year
1
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Washington University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Whyte, Michael P; Tau, Cristina; McAlister, William H et al. (2014) Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK. Bone 68:153-61
Andrew Nesbit, M; Bowl, Michael R; Harding, Brian et al. (2004) X-linked hypoparathyroidism region on Xq27 is evolutionarily conserved with regions on 3q26 and 13q34 and contains a novel P-type ATPase. Genomics 84:1060-70
Whyte, Michael P; Obrecht, Sara E; Finnegan, Patrick M et al. (2002) Osteoprotegerin deficiency and juvenile Paget's disease. N Engl J Med 347:175-84
Vacca, M; Matarazzo, M R; Jones, J et al. (1999) Evolution of the X-specific block embedded in the human Xq21.3/Yp11.1 homology region. Genomics 62:293-6
Redolfi, E; Pizzuti, A; Di Bacco, A et al. (1999) Mapping of the MYCL2 processed gene to Xq22-23 and identification of an additional L MYC-related sequence in Xq27.2. FEBS Lett 446:273-7
Zucchi, I; Jones, J; Affer, M et al. (1999) Transcription map of Xq27: candidates for several X-linked diseases. Genomics 57:209-18
Redolfi, E; Montagna, C; Mumm, S et al. (1998) Identification of CXorf1, a novel intronless gene in Xq27.3, expressed in human hippocampus. DNA Cell Biol 17:1009-16
Mumm, S; Whyte, M P; Thakker, R V et al. (1997) mtDNA analysis shows common ancestry in two kindreds with X-linked recessive hypoparathyroidism and reveals a heteroplasmic silent mutation. Am J Hum Genet 60:153-9
Grieff, M; Mumm, S; Waeltz, P et al. (1997) Expression and cloning of the human X-linked hypophosphatemia gene cDNA. Biochem Biophys Res Commun 231:635-9