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Items: 1 to 20 of 48

1.
Regulation of Axon Guidance by Slit2 and Netrin-1 Signaling in the Lacrimal Gland of Aqp5 Knockout Mice
Ying Bai, Guohu Di, Huanhuan Ge, Bin Li, Kaier Zhang, Di Zhang, Dianqiang Wang, Peng Chen
Invest Ophthalmol Vis Sci. 2023 Sep; 64(12): 27. Published online 2023 Sep 14. doi: 10.1167/iovs.64.12.27
PMCID:
PMC10506685
ArticlePDF–12M
2.
Screening marker genes of type 2 diabetes mellitus in mouse lacrimal gland by LASSO regression
Xiaoting Pei, Di Qi, Jiangman Liu, Hongli Si, Shenzhen Huang, Sen Zou, Dingli Lu, Zhijie Li
Sci Rep. 2023; 13: 6862. Published online 2023 Apr 26. doi: 10.1038/s41598-023-34072-4
PMCID:
PMC10133337
ArticlePDF–3.9M
3.
Conjunctival sac microbiome in anophthalmic patients: Flora diversity and the impact of ocular prosthesis materials
Hejia Zhao, Yanjun Chen, Yixu Zheng, Jing Xu, Chenyu Zhang, Min Fu, Ke Xiong
Front Cell Infect Microbiol. 2023; 13: 1117673. Published online 2023 Mar 7. doi: 10.3389/fcimb.2023.1117673
PMCID:
PMC10027910
ArticlePDF–2.8M
4.
Common Neuroimaging Findings in Bosch-Boonstra-Schaaf Optic Atrophy Syndrome
N.K. Desai, S.F. Kralik, J.C. Edmond, V. Shah, T.A.G.M. Huisman, M. Rech, C.P. Schaaf
AJNR Am J Neuroradiol. 2023 Feb; 44(2): 212–217. doi: 10.3174/ajnr.A7758
PMCID:
PMC9891320
ArticlePDF–1.4M
5.
The Role of Ectodysplasin A on the Ocular Surface Homeostasis
Shangkun Ou, Mani Vimalin Jeyalatha, Yi Mao, Junqi Wang, Chao Chen, Minjie Zhang, Xiaodong Liu, Minghui Liang, Sijie Lin, Yiming Wu, Yixuan Li, Wei Li
Int J Mol Sci. 2022 Dec; 23(24): 15700. Published online 2022 Dec 10. doi: 10.3390/ijms232415700
PMCID:
PMC9779463
ArticlePDF–1.5M
6.
Phenotypic spectrum of FGF10-related disorders: a systematic review
Katarzyna Bzdega, Justyna A. Karolak
PeerJ. 2022; 10: e14003. Published online 2022 Sep 14. doi: 10.7717/peerj.14003
PMCID:
PMC9482362
ArticlePDF–761K
7.
Abnormal Epigenetic Regulations in the Immunocytes of Sjögren’s Syndrome Patients and Therapeutic Potentials
Peng Li, Mengwei Han, Xingyu Zhao, Guanqun Ren, Si Mei, Chao Zhong
Cells. 2022 Jun; 11(11): 1767. Published online 2022 May 27. doi: 10.3390/cells11111767
PMCID:
PMC9179300
ArticlePDF–2.0M
8.
Unraveling Human AQP5-PIP Molecular Interaction and Effect on AQP5 Salivary Glands Localization in SS Patients
Clara Chivasso, Veronika Nesverova, Michael Järvå, Anne Blanchard, Kristie L Rose, Fredrik Kryh Öberg, Zhen Wang, Maud Martin, Florent Lhotellerie, Egor Zindy, Bruna Junqueira, Karelle Leroy, Benoit Vanhollebeke, Valérie Delforge, Nargis Bolaky, Jason Perret, Muhammad Shahnawaz Soyfoo, Stefania Moscato, Chiara Baldini, François Chaumont, Letizia Mattii, Kevin L Schey, Yvonne Myal, Susanna Törnroth-Horsefield, Christine Delporte
Cells. 2021 Aug; 10(8): 2108. Published online 2021 Aug 17. doi: 10.3390/cells10082108
PMCID:
PMC8391295
ArticlePDF–4.0M
9.
Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasia
Emma M. Wade, Padmini Parthasarathy, Jingyi Mi, Tim Morgan, Bernd Wollnik, Stephen P. Robertson, Tim Cundy
Eur J Hum Genet. 2022 Apr; 30(4): 480–484. Published online 2021 May 9. doi: 10.1038/s41431-021-00902-0
PMCID:
PMC8106901
ArticlePDF–739K
10.
Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations
M. Elmaleh-Bergès, C. Baumann, N. Noël-Pétroff, A. Sekkal, V. Couloigner, K. Devriendt, M. Wilson, S. Marlin, G. Sebag, V. Pingault
AJNR Am J Neuroradiol. 2013 Jun; 34(6): 1257–1263. doi: 10.3174/ajnr.A3367
PMCID:
PMC7964579
ArticlePDF–897K
11.
IRGM1 links mitochondrial quality control to autoimmunity
Prashant Rai, Kyathanahalli S. Janardhan, Julie Meacham, Jennifer H. Madenspacher, Wan-Chi Lin, Peer W.F. Karmaus, Jennifer Martinez, Quan-Zhen Li, Mei Yan, Jialiu Zeng, Mark W. Grinstaff, Orian S. Shirihai, Gregory A. Taylor, Michael B. Fessler
Nat Immunol. Author manuscript; available in PMC 2021 Jul 28.
Published in final edited form as: Nat Immunol. 2021 Mar; 22(3): 312–321. Published online 2021 Jan 28. doi: 10.1038/s41590-020-00859-0
PMCID:
PMC7906953
ArticlePDF–6.5M
12.
The expression of miRNA‐146a‐5p and its mechanism of treating dry eye syndrome
Liang Yin, Mingxue Zhang, Tiangeng He, Song Chen
J Clin Lab Anal. 2021 Jan; 35(1): e23571. Published online 2020 Sep 16. doi: 10.1002/jcla.23571
PMCID:
PMC7843290
ArticlePDF–758K
13.
Identification of KRAS mutation in a patient with linear nevus sebaceous syndrome: a case report
Chun Pan, Xiaowei Zhou, Anlan Hong, Fang Fang, Yan Wang
BMC Med Genomics. 2020; 13: 188. Published online 2020 Dec 12. doi: 10.1186/s12920-020-00847-1
PMCID:
PMC7733249
ArticlePDF–1.1M
14.
Malformation of Tear Ducts Underlies the Epiphora and Precocious Eyelid Opening in Prickle 1 Mutant Mice: Genetic Implications for Tear Duct Genesis
Jiali Ru, Dianlei Guo, Jiaying Fan, Jiao Zhang, Rong Ju, Hong Ouyang, Lai Wei, Yizhi Liu, Chunqiao Liu
Invest Ophthalmol Vis Sci. 2020 Nov; 61(13): 6. Published online 2020 Nov 3. doi: 10.1167/iovs.61.13.6
PMCID:
PMC7645213
ArticlePDF–35M
15.
Lacrimo‐auriculo‐dento‐digital syndrome: A novel mutation in a Korean family and review of literature
Young Hye Ryu, Jong Kyun Chae, Jung‐Wook Kim, Soyoung Lee
Mol Genet Genomic Med. 2020 Oct; 8(10): e1412. Published online 2020 Jul 26. doi: 10.1002/mgg3.1412
PMCID:
PMC7549548
ArticlePDF–833K
16.
Ocular findings in Fabry disease in Colombian patients
Katherine Rothstein, Jubby M. Gálvez, Ángela M. Gutiérrez, Laura Rico, Eveling Criollo, Alejandra de-la-Torre
Biomedica. 2019 Sep; 39(3): 434–439. Published online 2019 Sep 1. doi: 10.7705/biomedica.3841
PMCID:
PMC7357367
ArticlePDF–678K
17.
Ngly1−/− rats develop neurodegenerative phenotypes and pathological abnormalities in their peripheral and central nervous systems
Makoto Asahina, Reiko Fujinawa, Sayuri Nakamura, Kotaro Yokoyama, Ryuichi Tozawa, Tadashi Suzuki
Hum Mol Genet. 2020 Jun 27; 29(10): 1635–1647. Published online 2020 Apr 7. doi: 10.1093/hmg/ddaa059
PMCID:
PMC7322575
ArticlePDF–1.4M
18.
Lacrimal Sac Malignant Melanoma in 15 Japanese Patients: Case Report and Literature Review
Toshihiko Matsuo, Takehiro Tanaka, Osamu Yamasaki
J Investig Med High Impact Case Rep. 2019 Jan-Dec; 7: 2324709619888052. Published online 2019 Nov 20. doi: 10.1177/2324709619888052
PMCID:
PMC6873277
ArticlePDF–822K
19.
A Novel Claudinopathy Based on Claudin-10 Mutations
Susanne Milatz
Int J Mol Sci. 2019 Nov; 20(21): 5396. Published online 2019 Oct 30. doi: 10.3390/ijms20215396
PMCID:
PMC6862131
ArticlePDF–1.1M
20.
A requirement for Fgfr2 in middle ear development
Diana Rigueur, Ryan R. Roberts, Lauren Bobzin, Amy E. Merrill
Genesis. Author manuscript; available in PMC 2020 Jan 1.
Published in final edited form as: Genesis. 2019 Jan; 57(1): e23252. Published online 2018 Oct 4. doi: 10.1002/dvg.23252
PMCID:
PMC6349551
ArticlePDF–4.4M

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