Ponnam SP[au] - Search Results

Year	Number of Results
2007	1
2008	1
2009	1
2013	1
2018	1
2022	1
2023	0

1

A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India.

Chakravarty M, Ponnam SPG, Bardoloi N, Kumar S, Saikia P. Chakravarty M, et al. Among authors: ponnam spg. Eur J Ophthalmol. 2022 May;32(3):1361-1369. doi: 10.1177/11206721221087551. Epub 2022 Mar 16. Eur J Ophthalmol. 2022. PMID: 35296157

2

Development of a Reporter System to Explore MMEJ in the Context of Replacing Large Genomic Fragments.

Yanik M, Ponnam SPG, Wimmer T, Trimborn L, Müller C, Gambert I, Ginsberg J, Janise A, Domicke J, Wende W, Lorenz B, Stieger K. Yanik M, et al. Among authors: ponnam spg. Mol Ther Nucleic Acids. 2018 Jun 1;11:407-415. doi: 10.1016/j.omtn.2018.03.010. Epub 2018 Mar 22. Mol Ther Nucleic Acids. 2018. PMID: 29858075 Free PMC article.

3

Mutational screening of Indian families with hereditary congenital cataract.

Ponnam SP, Ramesha K, Matalia J, Tejwani S, Ramamurthy B, Kannabiran C. Ponnam SP, et al. Mol Vis. 2013 May 29;19:1141-8. Print 2013. Mol Vis. 2013. PMID: 23734083 Free PMC article.

4

A missense mutation in LIM2 causes autosomal recessive congenital cataract.

Ponnam SP, Ramesha K, Tejwani S, Matalia J, Kannabiran C. Ponnam SP, et al. Mol Vis. 2008 Jun 23;14:1204-8. Mol Vis. 2008. PMID: 18596884 Free PMC article.

5

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract.

Ponnam SP, Ramesha K, Tejwani S, Ramamurthy B, Kannabiran C. Ponnam SP, et al. BMJ Case Rep. 2009;2009:bcr06.2009.1995. doi: 10.1136/bcr.06.2009.1995. Epub 2009 Jun 30. BMJ Case Rep. 2009. PMID: 21720542 Free PMC article.

6

Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract.

Ponnam SP, Ramesha K, Tejwani S, Ramamurthy B, Kannabiran C. Ponnam SP, et al. J Med Genet. 2007 Jul;44(7):e85. doi: 10.1136/jmg.2007.050138. J Med Genet. 2007. PMID: 17601931 Free PMC article.

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