Application of NBD-labeled lipids in Membrane and Cell Biology
Springer Series on Fluorescence (Mely, Y., Duportail, G., Eds.), Springer, Heidelberg, vol. 13, pp. 37-50.
2013
Application of NBD-labeled lipids in Membrane and Cell Biology
Springer Series on Fluorescence (Mely, Y., Duportail, G., Eds.), Springer, Heidelberg, vol. 13, pp. 37-50.
2013
Application of Quantitative Fluorescence Microscopic approaches to Monitor Organization and Dynamics of the Serotonin1A Receptor
Springer Series on Fluorescence (Mely, Y., Duportail, G., Eds.), Springer, Heidelberg, vol. 13, pp. 417-437.
2013
Differential Effect of Sterols on Dipole Potential in Hippocampal Membranes: Implications for Receptor Function
Biochim. Biophys. Acta (Biomembranes) 1828: 917-923.
2013
Organization and Dynamics of the N-terminal Domain of Chemokine Receptor CXCR1 in Reverse Micelles: Effect of Graded Hydration
J. Phys. Chem. B 117: 1225-1233.
2013
Cholesterol Biosynthesis and Homeostasis in Regulation of the Cell Cycle
PLoS One 8: e58833.
2013
A Toolbox of Fluorescence Microscopic Approaches Reveals Dynamics and Assembly of a Membrane Associated Protein
Biophys. J. (New and Notable) 104: 1844-1845.
2013
A rare non-synonymous c.102C>G SNP in the IFNB1 gene might be a risk factor for cerebral malaria in Indian populations.
Infect Genet Evol. Jan 16. doi:pii: S1567-1348
2013
The \\\"Double Panda\\\" Sign in Leigh Disease
J Child Neurol. Apr 18. [Epub ahead of print]
2013
Genetic evidence of TAP1 gene variant as a susceptibility factor in Indian leprosy patients
Hum Immunol. Feb 5 [Epub ahead of print]
2013
Mitochondrial DNA variations in Madras motor neuron disease
Mitochondrion. Feb 15 [Epub ahead of print]
2013
Mitochondrial DNA variations in myelodysplastic syndrome
Ann Hematol. Mar 9. [Epub ahead of print]
2013
Association between Neuropeptide Y Gene Polymorphisms and Alcohol Dependence: A Case-Control Study in Two Independent Populations
Eur Addict Res. 19(6): 307-313
2013
Haplogroup heterogeneity of LHON patients carrying m.14484T>C mutation in India
Invest. Ophthalmol. Vis. Sci. May 14 [Epub ahead of print]
2013
Co-occurrence of m.1555A>G and m.11778G>A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy.
Mol Vis. 19:1282-1289
2013
This will close in 0 seconds