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Publication of Dr. Surya Prakash G. Ponnam

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Publication

  1. Indrani Chetia, Thoithoi Tongbram, Surya Prakash Goud Ponnam , Laxmikant S. Badwaik, Alginate-based encapsulation of edible flower extract: Process optimization, characterization and in vitro release kinetics, International Journal of Biological Macromolecules, 333(Pt 2):148877, 2025, 8.7, Click Here (DOI)
  2. Tobias Wimmer, Anthony Lorenz, Lars Thomas Hossfeld, Surya Prakash Goud Ponnam, Lyubomyr Lytvynchuk, Knut Stieger, Evaluation of CRISPR-Cas9 mismatch activity using a BRET-based reporter system, Microchemical Journal, 208 (2025) 112256, 2024, 4.9, Click Here (DOI)
  3. Surya Prakash Goud Ponnam , Narayan Bardoloi , Subhash Kumar , Amit Prakash , Knut Stieger, Clinical Profiles, Topographic Grading, and Assessment of Keratoconus Patients from Assam, India, International Journal of Keratoconus and Ectatic Corneal Diseases, 11 (1):35-40, 2024, 0, Click Here (DOI)
  4. Mrigyanka Chakravarty, Surya Prakash Goud Ponnam, Narayan Bardoloi , Subhash Kumar, Prasanta Saikia, A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India, European Journal of Ophthalmology, 32 (3) (1361-1369), 2022, 1.4, Click Here (DOI)
  5. Yanik M, Ponnam SPG, Wimmer T, Trimborn L, Müller C, Gambert I, Ginsberg J, Janise A, Domicke J, Wende W, Lorenz B, Stieger K., Development of a Reporter System to Explore MMEJ in the Context of Replacing Large Genomic Fragments., Molecular Therapy - Nucleic Acids, 11, 407-415, 2018, 11, 407-415, Click Here (DOI)
  6. Ponnam SP,Ramesha K, Matalia J, Tejwani S, Ramamurthy B, Kannabiran C., Mutational screening of Indian families with hereditary congenital cataract, Molecular Vision, 19: 1141–1148, 2013, 2.245, Click Here (DOI)
  7. Somaraju Chalasani ML, Muppirala M, G Ponnam SP, Kannabiran C, Swarup G. , A cataract-causing connexin 50 mutant is mislocalized to the ER due to loss of the fourth transmembrane domain and cytoplasmic domain., FEBS Open Bio, 3:22-9, 2012, 2.231, Click Here (DOI)
  8. Ponnam SP,Ramesha K, Tejwani S, Ramamurthy B, Kannabiran C, Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract, BMJ Case Rep, bcr06.2009.1995, 2009, , Click Here (DOI)
  9. Ponnam SP,Ramesha K, Tejwani S, Matalia J, Kannabiran C., A missense mutation in LIM2 causes autosomal recessive congenital cataract. , Molecular Vision, 14:1204-8, 2008, 2.245, Click Here (DOI)
  10. Ponnam SP, Ramesha K, Tejwani S, Ramamurthy B, Kannabiran C. , Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract., Journal of Medical Genetics, 44(7): e85, 2007, 5.751, Click Here (DOI)