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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

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