Induced dedifferentiation of barley (Hordeum vulgare L.) embryonic cells and its relationship with agronomic traits von Naseri, R., Cheghamirza, K., Zarei, L., Saroei, E.

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Genetic diversity of characteristics in barley cultivars von Saroei, Elahe, Cheghamirza, Kianoosh, Zarei, Leila

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CYP1B1 Mutation Profile of Iranian Primary Congenital Glaucoma Patients and Associated Haplotypes von Chitsazian, Fereshteh, Tusi, Betsabeh Khoramian, Elahi, Elahe, Saroei, Heidar Amini, Sanati, Mohammad H, Yazdani, Shahin, Pakravan, Mohammad, Nilforooshan, Navid, Eslami, Yadollah, Mehrjerdi, Mohammad Ali Zare, Zareei, Reza, Jabbarvand, Mahmood, Abdolahi, Ali, Lasheyee, Ali R, Etemadi, Arash, Bayat, Behnaz, Sadeghi, Mehdi, Banoei, Mohammad M, Ghafarzadeh, Behnam, Rohani, Mohammad R, Rismanchian, Akram, Thorstenson, Yvonne, Sarfarazi, Mansoor

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Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazil von de Melo, Mônica Barbosa, Mandal, Anil K, Tavares, Ivan M, Ali, Mohammed Hasnat, Kabra, Meha, de Vasconcellos, José Paulo Cabral, Senthil, Sirisha, Sallum, Juliana M F, Kaur, Inderjeet, Betinjane, Alberto J, Moura, Christiane R, Paula, Jayter S, Costa, Karita A, Sarfarazi, Mansoor, Paolera, Mauricio Della, Finzi, Simone, Ferraz, Victor E F, Costa, Vital P, Belfort, Jr, Rubens, Chakrabarti, Subhabrata

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Exome sequencing identifies novel genes underlying primary congenital glaucoma in the National Birth Defects Prevention Study von Blue, Elizabeth E., Moore, Kristin J., North, Kari E., Desrosiers, Tania A., Carmichael, Suzan L., White, Janson J., Chong, Jessica X., Bamshad, Michael J., Jenkins, Mary M., Almli, Lynn M., Brody, Lawrence C., Freedman, Sharon F., Reefhuis, Jennita, Romitti, Paul A., Shaw, Gary M., Werler, Martha, Kay, Denise M., Browne, Marilyn L., Feldkamp, Marcia L., Finnell, Richard H., Nembhard, Wendy N., Pangilinan, Faith, Olshan, Andrew F.

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Determination of genetic diversity in Acacia modesta germplasm using SDS-PAGE von Zahoor, M., Nisar, M., Rahman, A. Ur, Bari, W. Ul

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Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patients von Shojaee, Seyedmehdi, Fazlali, Zeinab, Ghazavi, Farzaneh, Banihosseini, Setareh Sadat, Kazemi, Mohammad Hossein, Parsa, Khosro, Sadeghi, Homa, Sina, Farzad, Shahidi, Gholam-Ali, Ronaghi, Mostafa, Elahi, Elahe

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Overview of Cytochrome P450 1B1 gene mutations in patients with primary congenital glaucoma von Li, Ni, Zhou, Yong, Du, Liang, Wei, Maoling, Chen, Xiaoming

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Sex Bias in Primary Congenital Glaucoma Patients with and without CYP1B1 Mutations von Suri, Fatemeh, Chitsazian, Fereshteh, Khoramian-Tusi, Betsabeh, Amini, Heidar, Yazdani, Shahin, Nilforooshan, Naveed, Zargar, S Jalal, Elahi, Elahe

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Genome diversity and population structure analysis of Iranian landrace and improved barley (Hordeum vulgare L.) genotypes using arbitrary functional gene-based molecular markers von Ahmed, Diyar Abubakr, Tahir, Nawroz Abdul-razzak, Salih, Sirwan Hassan, Talebi, Reza

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Glaucoma in iran and contributions of studies in iran to the understanding of the etiology of glaucoma von Suri, Fatemeh, Yazdani, Shahin, Elahi, Elahe

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P.Gly61Glu and P.Arg368His mutations in CYP1B1 that cause congenital glaucoma may be relatively frequent in certain regions of Gilan province, Iran von Qashqai, Mansoure, Suri, Fatemeh, Yaseri, Mehdi, Elahi, Elahe

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Mapping fractional woody cover in an extensive semi-arid woodland area at different spatial grains with Sentinel-2 and very high-resolution data von Shafeian, Elham, Fassnacht, Fabian Ewald, Latifi, Hooman

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Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma von Narooie-Nejad, Mehrnaz, Paylakhi, Seyed Hassan, Shojaee, Seyedmehdi, Fazlali, Zeinab, Rezaei Kanavi, Mozhgan, Nilforushan, Naveed, Yazdani, Shahin, Babrzadeh, Farbod, Suri, Fatemeh, Ronaghi, Mostafa, Elahi, Elahe, Paisán-Ruiz, Coro

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Genetic changes and testing associated with childhood glaucoma: A systematic review von Kumar, Anika, Han, Ying, Oatts, Julius T

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Genetic analysis of patients with primary congenital glaucoma von Ava, Sedat, Demirtaş, Atılım Armağan, Karahan, Mine, Erdem, Seyfettin, Oral, Diclehan, Keklikçi, Uğur

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Exploring the Genetic Landscape of Childhood Glaucoma von Pan, Yang, Iwata, Takeshi

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First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype-Genotype Association von Stingl, Julia V, Diederich, Stefan, Diel, Heidi, Schuster, Alexander K, Wagner, Felix M, Chronopoulos, Panagiotis, Aghayeva, Fidan, Grehn, Franz, Winter, Jennifer, Schweiger, Susann, Hoffmann, Esther M

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Role of CYP1B1, p.E229K and p.R368H mutations among 120 families with sporadic juvenile onset open-angle glaucoma von Gupta, Viney, Somarajan, Bindu I., Walia, Gagandeep Kaur, Kaur, Jasbir, Kumar, Sunil, Gupta, Shikha, Chaurasia, Abadh K., Gupta, Dinesh, Kaushik, Abhinav, Mehta, Aditi, Gupta, Vipin, Sharma, Arundhati

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Novel gene mutations causing primary congenital glaucoma von Feizi, Sepehr

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