Mutations in PRSS56 are Associated with Primary Congenital Glaucoma

被引：0

作者：

Chakrabarti, Subhabrata ^{[1
]}

Pyatla, Goutham ^{[1
]}

Labelle-Dumais, Cassandre ^{[2
]}

Koli, Swanand ^{[2
]}

Mandal, Anil K. ^{[3
]}

Senthil, Sirisha ^{[3
]}

Kabra, Meha ^{[1
]}

Tolman, Nicholas ^{[4
]}

Hameed, Syed ^{[1
]}

Khanna, Rohit Chandramohan ^{[5
]}

Kaur, Inderjeet ^{[1
]}

John, Simon ^{[4
]}

Nair, Saidas ^{[2
,6
]}

机构：

[1] LV Prasad Eye Inst, Brien Holden Eye Res Ctr, Hyderabad, Telangana, India

[2] Univ Calif San Francisco, Ophthalmol, San Francisco, CA 94143 USA

[3] LV Prasad Eye Inst, Jasti V Ramanamma Childrens Eye Care Ctr, Hyderabad, Telangana, India

[4] Jackson Lab, Howard Hughes Med Inst, 600 Main St, Bar Harbor, ME 04609 USA

[5] LV Prasad Eye Inst, Gullapalli Pratibha Rao Int Ctr Adv Rural Eye Car, Hyderabad, Telangana, India

[6] Univ Calif San Francisco, Anat, San Francisco, CA 94143 USA

来源：

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE | 2019年 / 60卷 / 09期

关键词：

D O I：

暂无

中图分类号：

R77 [眼科学];

学科分类号：

100212 ;

摘要：

2834

引用

页数：4

共 50 条

[41] Visual outcomes and associated factors of primary congenital glaucoma in children
Lee, Haeng-Jin
Kim, Young Kook
Jeoung, Jin Wook
Park, Ki Ho
Kim, Seong-Joon
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2021, 259 (11) : 3445 - 3451
[42] Choroidal neovascular membrane associated with primary congenital glaucoma and buphthalmos
Wang, Ye Elaine
Ramirez, Dhariana Acon
Hussain, Rehan M.
Berrocal, Audina M.
Chang, Ta Chen
JOURNAL OF AAPOS, 2020, 24 (01): : 53 - 56
[43] CYP1B1 mutations in patients with primary congenital glaucoma
Sitorus, RS
Preising, MN
Ardjo, SM
Lorenz, B
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 : U961 - U961
[44] Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees
Panicker, SG
Reddy, ABM
Mandal, AK
Ahmed, N
Nagarajaram, HA
Hasnain, SE
Balasubramanian, D
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2002, 43 (05) : 1358 - 1366
[45] Screening and Functional Analysis of TEK Mutations in Chinese Children With Primary Congenital Glaucoma
Qiao, Yunsheng
Chen, Yuhong
Tan, Chen
Sun, Xinghuai
Chen, Xueli
Chen, Junyi
FRONTIERS IN GENETICS, 2021, 12
[46] Angiopoietin receptor TEK mutations underlie primary congenital glaucoma with variable expressivity
Souma, Tomokazu
Tompson, Stuart W.
Thomson, Benjamin R.
Siggs, Owen M.
Kizhatil, Krishnakumar
Yamaguchi, Shinji
Feng, Liang
Limviphuvadh, Vachiranee
Whisenhunt, Kristina N.
Maurer-Stroh, Sebastian
Yanovitch, Tammy L.
Kalaydjieva, Luba
Azmanov, Dimitar N.
Finzi, Simone
Mauri, Lucia
Javadiyan, Shahrbanou
Souzeau, Emmanuelle
Zhou, Tiger
Hewitt, Alex W.
Kloss, Bethany
Burdon, Kathryn P.
MacKey, David A.
Allen, Keri F.
Ruddle, Jonathan B.
Lim, Sing-Hui
Rozen, Steve
Tran-Viet, Khanh-Nhat
Liu, Xiaorong
John, Simon
Wiggs, Janey L.
Pasutto, Francesca
Craig, Jamie E.
Jin, Jing
Quaggin, Susan E.
Young, Terri L.
JOURNAL OF CLINICAL INVESTIGATION, 2016, 126 (07): : 2575 - 2587
[47] Identification of MFRP and the secreted serine proteases PRSS56 and ADAMTS19 as part of a molecular network involved in ocular growth regulation
Koli, Swanand
Labelle-Dumais, Cassandre
Zhao, Yin
Paylakhi, Seyyedhassan
Nair, K. Saidas
PLOS GENETICS, 2021, 17 (03):
[48] Gene Profiling of Postnatal Mfrprd6 Mutant Eyes Reveals Differential Accumulation of Prss56, Visual Cycle and Phototransduction mRNAs
Soundararajan, Ramani
Won, Jungyeon
Stearns, Timothy M.
Charette, Jeremy R.
Hicks, Wanda L.
Collin, Gayle B.
Naggert, Juergen K.
Krebs, Mark P.
Nishina, Patsy M.
PLOS ONE, 2014, 9 (10):
[49] PRIMARY TRABECULECTOMY IN CONGENITAL GLAUCOMA
BURKE, JP
BOWELL, R
BRITISH JOURNAL OF OPHTHALMOLOGY, 1989, 73 (03) : 186 - 190
[50] An Insight into Primary Congenital Glaucoma
Khan, Muhammad Umer
Zia, Musabih ul Qayyum
Tabassum, Wajeeha
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 2020, 30 (01): : 39 - 43

← 1 2 3 4 5 →