المؤلفون: Weng P. L., Majmundar A. J., Khan K., Lim T. Y., Shril S., Jin G., Musgrove J., Wang M., Ahram D. F., Aggarwal V. S., Bier L. E., Heinzen E. L., Onuchic-Whitford A. C., Mann N., Buerger F., Schneider R., Deutsch K., Kitzler T. M., Klambt V., Kolb A., Mao Y., Moufawad El Achkar C., Mitrotti A., Martino J., Beck B. B., Altmuller J., Benz M. R., Yano S., Mikati M. A., Gunduz T., Cope H., Shashi V., Trachtman H., Bodria M., Caridi G., Pisani I., Fiaccadori E., AbuMaziad A. S., Martinez-Agosto J. A., Yadin O., Zuckerman J., Kim A., John-Kroegel U., Tyndall A. V., Parboosingh J. S., Innes A. M., Bierzynska A., Koziell A. B., Muorah M., Saleem M. A., Hoefele J., Riedhammer K. M., Gharavi A. G., Jobanputra V., Pierce-Hoffman E., Seaby E. G., O'Donnell-Luria A., Rehm H. L., Mane S., D'Agati V. D., Pollak M. R., Ghiggeri G. M., Lifton R. P., Goldstein D. B., Davis E. E., Hildebrandt F., Sanna-Cherchi S.

المساهمون: Weng, P. L., Majmundar, A. J., Khan, K., Lim, T. Y., Shril, S., Jin, G., Musgrove, J., Wang, M., Ahram, D. F., Aggarwal, V. S., Bier, L. E., Heinzen, E. L., Onuchic-Whitford, A. C., Mann, N., Buerger, F., Schneider, R., Deutsch, K., Kitzler, T. M., Klambt, V., Kolb, A., Mao, Y., Moufawad El Achkar, C., Mitrotti, A., Martino, J., Beck, B. B., Altmuller, J., Benz, M. R., Yano, S., Mikati, M. A., Gunduz, T., Cope, H., Shashi, V., Trachtman, H., Bodria, M., Caridi, G., Pisani, I., Fiaccadori, E., Abumaziad, A. S., Martinez-Agosto, J. A., Yadin, O., Zuckerman, J., Kim, A., John-Kroegel, U., Tyndall, A. V., Parboosingh, J. S., Innes, A. M., Bierzynska, A., Koziell, A. B., Muorah, M., Saleem, M. A., Hoefele, J., Riedhammer, K. M., Gharavi, A. G., Jobanputra, V., Pierce-Hoffman, E., Seaby, E. G., O'Donnell-Luria, A., Rehm, H. L., Mane, S., D'Agati, V. D., Pollak, M. R., Ghiggeri, G. M., Lifton, R. P., Goldstein, D. B., Davis, E. E., Hildebrandt, F., Sanna-Cherchi, S.

مصطلحات موضوعية: epilepsy, FSGS, genomic, monogenic, nuclear body, SRNS, TRIM8, Adult, Animal, Carrier Protein, Cell Line, Child, Preschool, Codon, Nonsense, Developmental Disabilitie, Female, Glomerulosclerosis, Focal Segmental, Human, Intranuclear Space, Kidney, Male, Mice, Mutation, Nephrotic Syndrome, Nerve Tissue Protein, Phenotype, Podocyte, Whole Exome Sequencing

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000629135400014; volume:108; issue:2; firstpage:357; lastpage:367; numberofpages:11; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11381/2911490

الاتاحة: http://hdl.handle.net/11381/2911490
https://doi.org/10.1016/j.ajhg.2021.01.008

المؤلفون: Mohan, D., Aggarwal, V. S., Tolia, D. S.

المصدر: Géotechnique ; volume 21, issue 4, page 423-423 ; ISSN 0016-8505 1751-7656

الاتاحة: http://dx.doi.org/10.1680/geot.1971.21.4.423
https://www.icevirtuallibrary.com/doi/pdf/10.1680/geot.1971.21.4.423

المؤلفون: Tolia, D. S., Mohan, D., Aggarwal, V. S.

المصدر: Géotechnique; Sep1970, Vol. 20 Issue 3, p315-319, 5p

المؤلفون: Mohan, D., Aggarwal, V. S., Tolia, D. S.

المصدر: Géotechnique ; volume 20, issue 3, page 315-319 ; ISSN 0016-8505 1751-7656

الاتاحة: http://dx.doi.org/10.1680/geot.1970.20.3.315
https://www.icevirtuallibrary.com/doi/pdf/10.1680/geot.1970.20.3.315

المؤلفون: Groopman, E. E.¹, Marasa, M.¹, Cameron-Christie, S.², Petrovski, S.², Aggarwal, V. S.³, Milo-Rasouly, H.¹, Li, Y.¹, Zhang, J.¹, Nestor, J.¹, Krithivasan, P.¹, Lam, W. Y.¹, Mitrotti, A.¹, Piva, S.¹, Kil, B. H.¹, Chatterjee, D.¹, Reingold, R.¹, Bradbury, D.¹, DiVecchia, M.¹, Snyder, H.¹, Mu, X.¹

المصدر: New England Journal of Medicine. 1/10/2019, Vol. 380 Issue 2, p142-151. 10p.

مصطلحات موضوعية: *CHRONIC kidney failure, *COMPARATIVE studies, *DISEASE susceptibility, *GENETICS, *GENOMES, *LONGITUDINAL method, *RESEARCH methodology, *MEDICAL cooperation, *GENETIC mutation, *RESEARCH, *RESEARCH funding, *EVALUATION research, *SEQUENCE analysis