OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
The N‐terminal p.(Ser38Cys) TIMP3 mutation underlying Sorsby fundus dystrophy is a founder mutation disrupting an intramolecular disulfide bond
Sarah Naessens, Julie De Zaeytijd, Delfien Syx, et al.
Human Mutation (2019) Vol. 40, Iss. 5, pp. 539-551
Open Access | Times Cited: 12
Sarah Naessens, Julie De Zaeytijd, Delfien Syx, et al.
Human Mutation (2019) Vol. 40, Iss. 5, pp. 539-551
Open Access | Times Cited: 12
Showing 12 citing articles:
The Role of Vitamin A in Retinal Diseases
Jana Sajovic, Andrej Meglič, Damjan Glavač, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 3, pp. 1014-1014
Open Access | Times Cited: 54
Jana Sajovic, Andrej Meglič, Damjan Glavač, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 3, pp. 1014-1014
Open Access | Times Cited: 54
The Diverse Roles of TIMP-3: Insights into Degenerative Diseases of the Senescent Retina and Brain
Jennifer M. Dewing, Roxana O. Carare, Andrew Lotery, et al.
Cells (2019) Vol. 9, Iss. 1, pp. 39-39
Open Access | Times Cited: 38
Jennifer M. Dewing, Roxana O. Carare, Andrew Lotery, et al.
Cells (2019) Vol. 9, Iss. 1, pp. 39-39
Open Access | Times Cited: 38
Distinct structural basis and catalytic classification of matrix metalloproteinases and their endogenous tissue inhibitors with glycosylation issue in cellular and tissue regulation
Hee-Do Kim, Hyunju Choi, Jun‐Young Park, et al.
Archives of Biochemistry and Biophysics (2025), pp. 110436-110436
Closed Access
Hee-Do Kim, Hyunju Choi, Jun‐Young Park, et al.
Archives of Biochemistry and Biophysics (2025), pp. 110436-110436
Closed Access
Macular neovascularization in inherited retinal diseases: A review
Rachael C. Heath Jeffery, Fred K. Chen
Survey of Ophthalmology (2023) Vol. 69, Iss. 1, pp. 1-23
Open Access | Times Cited: 6
Rachael C. Heath Jeffery, Fred K. Chen
Survey of Ophthalmology (2023) Vol. 69, Iss. 1, pp. 1-23
Open Access | Times Cited: 6
In vitro stem cell modelling demonstrates a proof‐of‐concept for excess functional mutant TIMP3 as the cause of S orsby f undus d ystrophy
Heidi Hongisto, Jennifer M. Dewing, David R. Christensen, et al.
The Journal of Pathology (2020) Vol. 252, Iss. 2, pp. 138-150
Open Access | Times Cited: 14
Heidi Hongisto, Jennifer M. Dewing, David R. Christensen, et al.
The Journal of Pathology (2020) Vol. 252, Iss. 2, pp. 138-150
Open Access | Times Cited: 14
Longitudinal phenotypic study of late-onset retinal degeneration due to a founder variant c.562C>A p.(Pro188Thr) in theC1QTNF5gene
Julie De Zaeytijd, Frauke Coppieters, Marieke De Bruyne, et al.
Ophthalmic Genetics (2021) Vol. 42, Iss. 5, pp. 521-532
Closed Access | Times Cited: 10
Julie De Zaeytijd, Frauke Coppieters, Marieke De Bruyne, et al.
Ophthalmic Genetics (2021) Vol. 42, Iss. 5, pp. 521-532
Closed Access | Times Cited: 10
Hidden Relationships between N-Glycosylation and Disulfide Bonds in Individual Proteins
Tania Bakshi, David Pham, Raminderjeet Kaur, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3742-3742
Open Access | Times Cited: 6
Tania Bakshi, David Pham, Raminderjeet Kaur, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 7, pp. 3742-3742
Open Access | Times Cited: 6
Evidence that all Sorsby's fundus dystrophy mutations cause TIMP3 dimerization resulting in impaired inhibition of VEGFR2
Fatimah Alsaffar, Ahmed H. Mujamammi, Mohammed S. Aldughaim, et al.
Genes & Diseases (2022) Vol. 10, Iss. 1, pp. 45-47
Open Access | Times Cited: 3
Fatimah Alsaffar, Ahmed H. Mujamammi, Mohammed S. Aldughaim, et al.
Genes & Diseases (2022) Vol. 10, Iss. 1, pp. 45-47
Open Access | Times Cited: 3
Disease-Causing TIMP3 Variants and Deep Phenotyping of Two Czech Families with Sorsby Fundus Dystrophy Associated with Novel p.(Tyr152Cys) Mutation
Andrea Vergaro, Monika Pankievic, Jana Jedličková, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 7, pp. 3744-3744
Open Access
Andrea Vergaro, Monika Pankievic, Jana Jedličková, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 7, pp. 3744-3744
Open Access
Review: Mechanisms of TIMP-3 accumulation and pathogenesis in Sorsby fundus dystrophy.
Jacob H.J. Betts, Linda Troeberg
PubMed (2024) Vol. 30, pp. 74-91
Closed Access
Jacob H.J. Betts, Linda Troeberg
PubMed (2024) Vol. 30, pp. 74-91
Closed Access
A novel TIMP3 mutation associated with a retinitis pigmentosa-like phenotype
Meghan J. DeBenedictis, Yosef Gindzin, Enrico Glaab, et al.
Ophthalmic Genetics (2020) Vol. 41, Iss. 5, pp. 480-484
Open Access | Times Cited: 2
Meghan J. DeBenedictis, Yosef Gindzin, Enrico Glaab, et al.
Ophthalmic Genetics (2020) Vol. 41, Iss. 5, pp. 480-484
Open Access | Times Cited: 2
Study the expression rate and methylation of TIMP-3 gene in the blood samples of people suffering from gastric cancer
Zahra Karimi Shahrivar, Elham Moslemi
Bionatura (2022) Vol. 7, Iss. 3, pp. 1-4
Open Access
Zahra Karimi Shahrivar, Elham Moslemi
Bionatura (2022) Vol. 7, Iss. 3, pp. 1-4
Open Access
