Works by George, Aman

Results: 7

Epithelial phenotype restoring drugs suppress macular degeneration phenotypes in an iPSC model.

Published in:

Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27488-x

By:

Sharma, Ruchi;
George, Aman;
Nimmagadda, Malika;
Ortolan, Davide;
Karla, Barbosa-Sabanero;
Qureshy, Zoya;
Bose, Devika;
Dejene, Roba;
Liang, Genqing;
Wan, Qin;
Chang, Justin;
Jha, Balendu Shekhar;
Memon, Omar;
Miyagishima, Kiyoharu Joshua;
Rising, Aaron;
Lal, Madhu;
Hanson, Eric;
King, Rebecca;
Campos, Mercedes Maria;
Ferrer, Marc

Publication type:

Article

Cloning and Characterization of Buffalo NANOG Gene: Alternative Transcription Start Sites, Splicing, and Polyadenylation in Embryonic Stem Cell-Like Cells.

Published in:

DNA & Cell Biology, 2012, v. 31, n. 5, p. 721, doi. 10.1089/dna.2011.1410

By:

Singh, Natwar;
Sharma, Ruchi;
George, Aman;
Singla, Suresh K.;
Palta, Prabhat;
Manik, Radhaysham;
Chauhan, Manmohan S.;
Singh, Dheer

Publication type:

Article

Deep learning predicts function of live retinal pigment epithelium from quantitative microscopy.

Published in:

2020

By:

Schaub, Nicholas J.;
Hotaling, Nathan A.;
Manescu, Petre;
Padi, Sarala;
Wan, Qin;
Sharma, Ruchi;
George, Aman;
Chalfoun, Joe;
Simon, Mylene;
Ouladi, Mohamed;
Simon Jr., Carl G.;
Bajcsy, Peter;
Bharti, Kapil;
Simon, Carl G Jr

Publication type:

journal article

Zebrafish model of RERE syndrome recapitulates key ophthalmic defects that are rescued by small molecule inhibitor of shh signaling.

Published in:

Developmental Dynamics, 2023, v. 252, n. 4, p. 495, doi. 10.1002/dvdy.561

By:

George, Aman;
Lee, Jerry;
Liu, James;
Kim, Suzie;
Brooks, Brian P.

Publication type:

Article

AMPK modulation ameliorates dominant disease phenotypes of CTRP5 variant in retinal degeneration.

Published in:

Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02872-x

By:

Miyagishima, Kiyoharu J.;
Sharma, Ruchi;
Nimmagadda, Malika;
Clore-Gronenborn, Katharina;
Qureshy, Zoya;
Ortolan, Davide;
Bose, Devika;
Farnoodian, Mitra;
Zhang, Congxiao;
Fausey, Andrew;
Sergeev, Yuri V.;
Abu-Asab, Mones;
Jun, Bokkyoo;
Do, Khanh V.;
Kautzman Guerin, Marie-Audrey;
Calandria, Jorgelina;
George, Aman;
Guan, Bin;
Wan, Qin;
Sharp, Rachel C.

Publication type:

Article

A novel variant affecting the cytoplasmic tail of the FAT1 protocadherin causing coloboma and renal failure: A case report.

Published in:

Ophthalmic Genetics, 2023, v. 44, n. 2, p. 182, doi. 10.1080/13816810.2022.2089360

By:

Vieta-Ferrer, Emile R.;
Ullah, Ehsan;
Blain, Delphine;
Christensen, Julie A.;
Brewer, Carmen C.;
Balow, James E.;
George, Aman;
Hufnagel, Robert B.;
Cogliati, Tiziana;
Brooks, Brian P.

Publication type:

Article

Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.

Published in:

Nature Communications, 2019, v. 10, n. 1, p. 1, doi. 10.1038/s41467-019-08547-w

By:

Lahrouchi, Najim;
George, Aman;
Ratbi, Ilham;
Schneider, Ronen;
Elalaoui, Siham C.;
Moosa, Shahida;
Bharti, Sanita;
Sharma, Ruchi;
Abu-Asab, Mones;
Onojafe, Felix;
Adadi, Najlae;
Lodder, Elisabeth M.;
Laarabi, Fatima-Zahra;
Lamsyah, Yassine;
Elorch, Hamza;
Chebbar, Imane;
Postma, Alex V.;
Lougaris, Vassilios;
Plebani, Alessandro;
Altmueller, Janine

Publication type:

Article