| Elevated tumor necrosis factor in serum is associated with increased retinal ischemia in proliferative eales' disease. Saxena S., Khanna V.K., Pant A.B., Meyer C.H., Singh V.K.
Pathobiology 78:261-265(2011) · Mapped (6) |
| Association of polymorphism in cytochrome P450 2D6 and N-acetyltransferase-2 with Parkinson's disease. Singh M., Khanna V.K., Shukla R., Parmar D.
Dis. Markers 28:87-93(2010) · Mapped (36) |
| Polymorphism in environment responsive genes and association with Parkinson disease. Singh M., Khan A.J., Shah P.P., Shukla R., Khanna V.K., Parmar D.
Mol. Cell. Biochem. 312:131-138(2008) · Mapped (64) |
| Temporal and spatial expression analysis of gamma kafirin promoter from Sorghum (Sorghum bicolor L. moench) var. M 35-1. Mishra A., Tomar A., Bansal S., Khanna V.K., Garg G.K.
Mol. Biol. Rep. 35:81-88(2008) · UniProtKB (1) |
| Role of the sequence surrounding predicted transmembrane helix M4 in membrane association and function of the Ca(2+) release channel of skeletal muscle sarcoplasmic reticulum (ryanodine receptor isoform 1). Du G.G., Avila G., Sharma P., Khanna V.K., Dirksen R.T., MacLennan D.H.
J. Biol. Chem. 279:37566-37574(2004) · Mapped (6) |
| Topology of the Ca2+ release channel of skeletal muscle sarcoplasmic reticulum (RyR1). Du G.G., Sandhu B., Khanna V.K., Guo X.H., MacLennan D.H.
Proc. Natl. Acad. Sci. U.S.A. 99:16725-16730(2002) · UniProtKB (1) |
| The mutation of Pro(789) to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca(2+) ATPase (SERCA1) and is associated with Brody disease. Odermatt A., Barton K., Khanna V.K., Mathieu J., Escolar D., Kuntzer T., Karpati G., MacLennan D.H.
Hum. Genet. 106:482-491(2000) · UniProtKB (1) |
| Sarcolipin regulates the activity of SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+-ATPase. Odermatt A., Becker S., Khanna V.K., Kurzydlowski K., Leisner E., Pette D., MacLennan D.H.
J. Biol. Chem. 273:12360-12369(1998) |
| Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody disease. Odermatt A., Taschner P.E.M., Scherer S.W., Beatty B., Khanna V.K., Cornblath D.R., Chaudhry V., Yee W.-C., Schrank B., Karpati G. et al.
Genomics 45:541-553(1997) · UniProtKB (1) · Mapped (5) |
| Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease. Odermatt A., Taschner P.E., Khanna V.K., Busch H.F., Karpati G., Jablecki C.K., Breuning M.H., MacLennan D.H.
Nat. Genet. 14:191-194(1996) · Mapped (2) |
| The structural organization of the human skeletal muscle ryanodine receptor (RYR1) gene. Phillips M.S., Fujii J., Khanna V.K., de Leon S., Yokobata K., de Jong P.J., McLennan D.H.
Genomics 34:24-41(1996) · UniProtKB (1) |
| A mutation in the human ryanodine receptor gene associated with central core disease. Zhang Y., Chen H.S., Khanna V.K., de Leon S., Phillips M.S., Schappert K.T., Britt B.A., Brownell A.K.W., McLennan D.H.
Nat. Genet. 5:46-50(1993) · UniProtKB (1) |
| The substitution of Arg for Gly2433 in the human skeletal muscle ryanodine receptor is associated with malignant hyperthermia. Phillips M.S., Khanna V.K., de Leon S., Frodis W., Britt B.A., McLennan D.H.
Hum. Mol. Genet. 3:2181-2186(1994) · UniProtKB (1) · Mapped (5) |
| Amino acid sequence of rabbit fast-twitch skeletal muscle calsequestrin deduced from cDNA and peptide sequencing. Fliegel L., Ohnishi M., Carpenter M.R., Khanna V.K., Reithmeier R.A.F., McLennan D.H.
Proc. Natl. Acad. Sci. U.S.A. 84:1167-1171(1987) · UniProtKB (1) |
| Molecular cloning of cDNA encoding the Ca2+ release channel (ryanodine receptor) of rabbit cardiac muscle sarcoplasmic reticulum. Otsu K., Willard H.F., Khanna V.K., Zorzato F., Green N.M., Maclennan D.H.
J. Biol. Chem. 265:13472-13483(1990) · UniProtKB (1) |
| Identification of a mutation in porcine ryanodine receptor associated with malignant hyperthermia. Fujii J., Otsu K., Zorzato F., de Leon S., Khanna V.K., Weiler J.E., O'Brien P.J., MacLennan D.H.
Science 253:448-451(1991) · UniProtKB (2) |
| A substitution of cysteine for arginine 614 in the ryanodine receptor is potentially causative of human malignant hyperthermia. Gillard E.F., Otsu K., Fujii J., Khanna V.K., de Leon S., Derdemezi J., Britt B.A., Duff C.L., Worton R.G., MacLennan D.H.
Genomics 11:751-755(1991) · UniProtKB (1) |
| Cosegregation of porcine malignant hyperthermia and a probable causal mutation in the skeletal muscle ryanodine receptor gene in backcross families. Otsu K., Khanna V.K., Archibald A.L., MacLennan D.H.
Genomics 11:744-750(1991) · Mapped (2) |
| Refinement of diagnostic assays for a probable causal mutation for porcine and human malignant hyperthermia. Otsu K., Phillips M.S., Khanna V.K., de Leon S., McLennan D.H.
Genomics 13:835-837(1992) · UniProtKB (2) |
| Polymorphisms and deduced amino acid substitutions in the coding sequence of the ryanodine receptor (RYR1) gene in individuals with malignant hyperthermia. Gillard E.F., Otsu K., Fujii J., Duff C.L., de Leon S., Khanna V.K., Britt B.A., Worton R.G., McLennan D.H.
Genomics 13:1247-1254(1992) · UniProtKB (1) |
