Strategies for improving the transduction efficiency of single-stranded adeno-associated virus vectors in vitro and in vivo von Jayandharan, G R, Zhong, L, Li, B, Kachniarz, B, Srivastava, A

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Nuclear factor (NF)‐κB and its associated pathways are major molecular regulators of blood‐induced joint damage in a murine model of hemophilia von Sen, D., Chapla, A., Walter, N., Daniel, V., Srivastava, A., Jayandharan, G. R.

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Molecular basis of quantitative fibrinogen disorders in 27 patients from India von Sumitha, E., Jayandharan, G. R., Arora, N., Abraham, A., David, S., Devi, G. S., Shenbagapriya, P., Nair, S. C., George, B., Mathews, V., Chandy, M., Viswabandya, A., Srivastava, A.

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Nuclear factor (NF)-[kappa]B and its associated pathways are major molecular regulators of blood-induced joint damage in a murine model of hemophilia von Sen, D, Chapla, A, Walter, N, Daniel, V, Srivastava, A, Jayandharan, G. R

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Molecular basis of Bernard–Soulier syndrome in 27 patients from India von SUMITHA, E., JAYANDHARAN, G. R., DAVID, S., JACOB, R. R., SANKARI DEVI, G., BARGAVI, B., SHENBAGAPRIYA, S., NAIR, S. C., ABRAHAM, A., GEORGE, B., VISWABANDYA, A., MATHEWS, V., CHANDY, M., SRIVASTAVA, A.

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Molecular basis of hereditary factor V deficiency in India: Identification of four novel mutations and their genotype-phenotype correlation von Chapla, Aaron, Jayandharan, Giridhara Rao, Sumitha, Elayaperumal, Devi, Govindanattar Sankari, Shenbagapriya, Paneerselvam, Nair, Sukesh Chandran, Viswabandya, Auro, George, Biju, Mathews, Vikram, Srivastava, Alok

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Quality issues in laboratory haemostasis von PRESTON, F. E., LIPPI, G., FAVALORO, E. J., JAYANDHARAN, G. R., EDISON, E. S., SRIVASTAVA, A.

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Fluorescent PCR-based gene dose analysis for detection of deletion mutations in carriers of haemophilia von Devi, G. Sankari, Arora, N., Rajkumar, S. V., Edison, E. S., Srivastava, A., Jayandharan, G. R.

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Genetics of haemostasis von GOODEVE, A. C., PERRY, D. J., CUMMING, T., HILL, M., JENNINGS, I., KITCHEN, S., WALKER, I., GRAY, E., JAYANDHARAN, G. R., TUDDENHAM, E.

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Molecular basis of hereditary factor VII deficiency in India: five novel mutations including a double missense mutation (Ala191Glu; Trp364Cys) in 11 unrelated patients von Jayandharan, Giridhara Rao, Viswabandya, Auro, Nair, Sukesh C, Chandy, Mammen, Srivastava, Alok

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Polymorphism in factor VII gene modifies phenotype of severe haemophilia von JAYANDHARAN, G. R., NAIR, S. C., POONNOOSE, P. M., THOMAS, R., JOHN, J., KESHAV, S. K., CHERIAN, R. S., DEVADARISHINI, M., LAKSHMI, K. M., SHAJI, R. V., VISWABANDYA, A., GEORGE, B., MATHEWS, V., CHANDY, M., SRIVASTAVA, A.

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High-Efficiency Transduction of Fibroblasts and Mesenchymal Stem Cells by Tyrosine-Mutant AAV2 Vectors for Their Potential Use in Cellular Therapy von MENGXIN LI, JAYANDHARAN, Giridhara R, BAOZHENG LI, CHEN LING, WENQIN MA, SRIVASTAVA, Arun, LI ZHONG

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Human Hepatocyte Growth Factor Receptor Is a Cellular Coreceptor for Adeno-Associated Virus Serotype 3 von CHEN LING, YUAN LU, LI ZHONG, AGBANDJE-MCKENNA, Mavis, SRIVASTAVA, Arun, KALSI, Jasmine K, JAYANDHARAN, Giridhara R, BAOZHENG LI, WENQIN MA, BINBIN CHENG, GEE, Samantha W. Y, MCGOOGAN, Katherine E, GOVINDASAMY, Lakshmanan

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Adeno-Associated Virus Serotype 6 Capsid Tyrosine-to-Phenylalanine Mutations Improve Gene Transfer to Skeletal Muscle von CHUNPING QIAO, WEI ZHANG, ZHENHUA YUAN, SHIN, Jin-Hong, JIANBIN LI, JAYANDHARAN, Giridhara R, LI ZHONG, SRIVASTAVA, Arun, XIAO XIAO, DONGSHENG DUAN

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Optimized Adeno-Associated Virus (AAV)-Protein Phosphatase-5 Helper Viruses for Efficient Liver Transduction by Single-Stranded AAV Vectors: Therapeutic Expression of Factor IX at... von JAYANDHARAN, Giridhara R, LI ZHONG, SACK, Brandon K, RIVERS, Angela E, MENGXIN LI, BAOZHENG LI, HERZOG, Roland W, SRIVASTAVA, Arun

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The Adeno-Associated Virus Genome Packaging Puzzle von Ling, Chen, Wang, Yuan, Lu, Yuan, Wang, Lina, Jayandharan, Giridhara R, Aslanidi, George V, Li, Baozheng, Cheng, Binbin, Ma, Wenqin, Lentz, Thomas, Ling, Changquan, Xiao, Xiao, Samulski, R Jude, Muzyczka, Nicholas, Srivastava, Arun

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Molecular basis of quantitative fibrinogen disorders in 27 patients from I ndia von Sumitha, E., Jayandharan, G. R., Arora, N., Abraham, A., David, S., Devi, G. S., Shenbagapriya, P., Nair, S. C., George, B., Mathews, V., Chandy, M., Viswabandya, A., Srivastava, A.

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Mutations in coagulation factor XIII A gene in eight unrelated Indians Five novel mutations identified by a novel PCR-CSGE approach von JAYANDHARAN, Giridhara R, VISWABANDYA, Auro, BAIDYA, Shoma, NAIR, Sukesh C, GEORGE, Biju, MATHEWS, Vikram, CHANDY, Mammen, SRIVASTAVA, Alok

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Molecular characterization of factor IX gene mutations in 53 patients with haemophilia B in India von Jayandharan, Giridhara Rao, Shaji, Ramachandran V, Baidya, Shoma, Nair, Sukesh Chandran, Chandy, Mammen, Srivastava, Alok

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In Vitro Study of ATP7B (Wilson's Disease) Protein Function von Kumar, SS, Yadav, P, Balasubramanian, KA, Oommen, A, Kurian, G, Chandy, G, Jayandharan, GR, Eapen, CE, Mazumdar, S

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