20 results on '"Wooding, Carol"'
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2. The Human Scavenger Receptor CD36: GLYCOSYLATION STATUS AND ITS ROLE IN TRAFFICKING AND FUNCTION
3. Repacking of the transmembrane domains of P‐glycoprotein during the transport ATPase cycle
4. Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1
5. Linkage studies in a kindred from Oklahoma, with familial benign (hypocalciuric) hypercalcaemia (FBH) and developmental elevations in serum parathyroid hormone levels, indicate a third locus for FBH
6. Mapping the Gene Causing X-Linked Recessive Nephrolithiasis to Xp11.22 by Linkage Studies
7. Taxation.
8. KDM2A integrates DNA and histone modification signals through a CXXC/PHD module and direct interaction with HP1
9. KDM2A integrates DNA and histone modification signals through a CXXC/PHD module and direct interaction with HP1
10. Association of parathyroid tumors in multiple endocrine neoplasia type 1 with loss of alleles on chromosome 11
11. Cd36, a class B scavenger receptor, functions as a monomer to bind acetylated and oxidized low-density lipoproteins
12. Evidence for a Sav1866‐like architecture for the human multidrug transporter P‐glycoprotein
13. Membrane phosphatidylserine distribution as a non-apoptotic signalling mechanism in lymphocytes
14. Renal Chloride Channel, CLCN5, Mutations in Dent's Disease
15. Mutational Analysis of PHEX Gene in X-Linked Hypophosphatemia1
16. Linkage Studies of a Missouri Kindred with Autosomal Dominant Spondyloepimetaphyseal Dysplasia (SEMD) Indicate Genetic Heterogeneity
17. Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of Ì-calpain as the multiple endocrine neoplasia type 1 gene
18. Dent's disease, a renal Fanconi syndrome with nephrocalcinosis and kidney stones, is associated with a microdeletion involving DXS255 and maps to Xp11.22
19. Mothers' speech to young children: variation in context.
20. KDM2A integrates DNA and histone modification signals through a CXXC/PHD module and direct interaction with HP1.
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