Search Results - "Pyatla G"

Potential Involvements of Cilia-Centrosomal Genes in Primary Congenital Glaucoma.

Authors: Pyatla, Goutham Kabra, Meha Mandal, Anil K. et al.

Source: International Journal of Molecular Sciences. Sep2024, Vol. 25 Issue 18, p10028. 14p.

The Increased Burden of Rare Variants in Four Matrix Metalloproteinase-Related Genes in Childhood Glaucoma Suggests a Complex Genetic Inheritance of the Disease.

Authors: Tevar, Angel Aroca-Aguilar, José-Daniel Bonet-Fernández, Juan-Manuel et al.

Source: International Journal of Molecular Sciences. Jun2024, Vol. 25 Issue 11, p5757. 21p.

Genetic changes and testing associated with childhood glaucoma: A systematic review.

Authors: Kumar, Anika Han, Ying Oatts, Julius T.

Source: PLoS ONE. 2/22/2024, Vol. 19 Issue 2, p1-23. 23p.

Inhibition of VE-PTP rejuvenates Schlemm's canal in aged mice and acts via Tie2.

Authors: Mishra, Sarthak Ipe, Ute Nottebaum, Astrid F. et al.

Source: PLoS ONE. 5/16/2025, Vol. 20 Issue 5, p1-15. 15p.

Exome sequencing identifies procollagen-lysine 2-oxoglutarate 5-dioxygenase 2 mutations in primary congenital and juvenile glaucoma.

Authors: Gupta, Viney Somarajan, Bindu Kaur, Gagandeep et al.

Source: Indian Journal of Ophthalmology. Oct2021, Vol. 69 Issue 10, p2710-2716. 7p.

Serine protease PRSS56, a novel cancer-testis antigen activated by DNA hypomethylation, promotes colorectal and gastric cancer progression via PI3K/AKT axis.

Authors: Li, Dandan Xia, Lingyun Huang, Pan et al.

Source: Cell & Bioscience. 7/3/2023, Vol. 13 Issue 1, p1-15. 15p.

Whole-exome sequencing identifies PRSS56 variants in Chinese patients with microphthalmia.

Authors: Luo J Li K Yang R et al.

Source: BMC medical genomics [BMC Med Genomics] 2026 Apr 21; Vol. 19 (1). Date of Electronic Publication: 2026 Apr 21.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101319628 Publication Model: Electronic Cited Medium: Internet ISSN: 1755-8794 (Electronic) Linking ISSN: 17558794 NLM ISO Abbreviation: BMC Med Genomics Subsets: MEDLINE

Loss of PRSS56 function leads to ocular angle defects and increased susceptibility to high intraocular pressure.

Authors: Labelle-Dumais C Pyatla G Paylakhi S et al.

Source: Disease models & mechanisms [Dis Model Mech] 2020 May 29; Vol. 13 (5). Date of Electronic Publication: 2020 May 29.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Company of Biologists Ltd Country of Publication: England NLM ID: 101483332 Publication Model: Electronic Cited Medium: Internet ISSN: 1754-8411 (Electronic) Linking ISSN: 17548403 NLM ISO Abbreviation: Dis Model Mech Subsets: MEDLINE

Whole-exome screening for primary congenital glaucoma in Lebanon.

Authors: Makhoul, Nadine J. Wehbi, Zahi El Hadi, Dalia et al.

Source: Ophthalmic Genetics. Jun2023, Vol. 44 Issue 3, p234-245. 12p.

Anterior segment dysgenesis: Insights into the genetics and pathogenesis.

Authors: Kaushik, Sushmita Dubey, Suneeta Choudhary, Sandeep et al.

Source: Indian Journal of Ophthalmology. Jul2022, Vol. 70 Issue 7, p2293-2303. 11p.

Potential Involvements of Anterior Segment Dysgenesis-Associated Genes in Primary Congenital Glaucoma.

Authors: Pyatla G Bera S Mishra A et al.

Source: Seminars in ophthalmology [Semin Ophthalmol] 2025 Nov; Vol. 40 (8), pp. 733-742. Date of Electronic Publication: 2024 Dec 09.

Publication Type: Journal Article; Review

Journal Info: Publisher: Informa Healthcare Country of Publication: England NLM ID: 8610759 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5205 (Electronic) Linking ISSN: 08820538 NLM ISO Abbreviation: Semin Ophthalmol Subsets: MEDLINE

Research progress on human genes involved in the pathogenesis of glaucoma.

Authors: Wang, Hong-Wei Sun, Peng Chen, Yao et al.

Source: Molecular Medicine Reports. Jul2018, Vol. 18 Issue 1, p656-674. 19p.

First Results from the Prospective German Registry for Childhood Glaucoma: Phenotype–Genotype Association.

Authors: Stingl, Julia V. Diederich, Stefan Diel, Heidi et al.

Source: Journal of Clinical Medicine. Jan2022, Vol. 11 Issue 1, p16. 1p.

Retinal Detachment After Primary Congenital Glaucoma Surgery.

Authors: Bayoumi NHL Khalifa NAE Moustafa M et al.

Source: Journal of pediatric ophthalmology and strabismus [J Pediatr Ophthalmol Strabismus] 2026 Jan-Feb; Vol. 63 (1), pp. 23-27. Date of Electronic Publication: 2025 Jul 30.

Publication Type: Journal Article

Journal Info: Publisher: Slack Country of Publication: United States NLM ID: 7901143 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1938-2405 (Electronic) Linking ISSN: 01913913 NLM ISO Abbreviation: J Pediatr Ophthalmol Strabismus Subsets: MEDLINE

Identification of immune-related biomarkers for glaucoma using gene expression profiling.

Authors: Wang D Pu Y Tan S et al.

Source: Frontiers in genetics [Front Genet] 2024 Apr 17; Vol. 15, pp. 1366453. Date of Electronic Publication: 2024 Apr 17 (Print Publication: 2024).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE

Angiopoietin receptor TEK interacts with CYP1B1 in primary congenital glaucoma.

Authors: Kabra M Zhang W Rathi S et al.

Source: Human genetics [Hum Genet] 2017 Aug; Vol. 136 (8), pp. 941-949. Date of Electronic Publication: 2017 Jun 15.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE

A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia.

Authors: Jiang C Melles RB Yin J et al.

Corporate Authors: Jiang C Melles RB Yin J et al.

Source: Frontiers in genetics [Front Genet] 2023 Jun 07; Vol. 14, pp. 1113058. Date of Electronic Publication: 2023 Jun 07 (Print Publication: 2023).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE

Screening and Functional Analysis of TEK Mutations in Chinese Children With Primary Congenital Glaucoma.

Authors: Qiao Y Chen Y Tan C et al.

Source: Frontiers in genetics [Front Genet] 2021 Dec 10; Vol. 12, pp. 764509. Date of Electronic Publication: 2021 Dec 10 (Print Publication: 2021).

Publication Type: Journal Article

Journal Info: Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101560621 Publication Model: eCollection Cited Medium: Print ISSN: 1664-8021 (Print) Linking ISSN: 16648021 NLM ISO Abbreviation: Front Genet Subsets: PubMed not MEDLINE

TEK gene-related primary congenital glaucoma: Phenotypic features and mutational spectrum in a Mexican cohort of 10 unrelated families.

Authors: Chacon-Camacho OF Ordaz-Robles T Cid-García MA et al.

Source: American journal of medical genetics. Part A [Am J Med Genet A] 2024 Oct; Vol. 194 (10), pp. e63716. Date of Electronic Publication: 2024 Jun 07.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Familial Paget's disease of bone with ocular manifestations and a novel TNFRSF11A duplication variant (72dup27).

Authors: Saito-Hakoda A Kikuchi A Takahashi T et al.

Source: Journal of bone and mineral metabolism [J Bone Miner Metab] 2023 Mar; Vol. 41 (2), pp. 193-202. Date of Electronic Publication: 2022 Dec 15.

Publication Type: Review; Journal Article

Journal Info: Publisher: Japanese Society of Bone and Mineral Metabolism Country of Publication: Japan NLM ID: 9436705 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1435-5604 (Electronic) Linking ISSN: 09148779 NLM ISO Abbreviation: J Bone Miner Metab Subsets: MEDLINE