Search details
1.
Cornichon protein CNIH4 is not essential for mice gametogenesis and fertility.
Dev Biol
; 496: 15-23, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36657507
2.
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Am J Hum Genet
; 108(2): 324-336, 2021 02 04.
Article
in English
| MEDLINE | ID: mdl-33508233
3.
Epidemiology of Pediatric Ocular Surface Inflammatory Diseases in the United States Using the Optum Labs Data Warehouse.
Ophthalmology
; 131(5): 568-576, 2024 May.
Article
in English
| MEDLINE | ID: mdl-38092080
4.
A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella.
J Assist Reprod Genet
; 41(1): 109-120, 2024 Jan.
Article
in English
| MEDLINE | ID: mdl-37831349
5.
Corneal Neurotization: Essentials for The Facial Paralysis Surgeon.
Facial Plast Surg
; 2024 Mar 18.
Article
in English
| MEDLINE | ID: mdl-38378042
6.
The Role of Sensory Innervation in Homeostatic and Injury-Induced Corneal Epithelial Renewal.
Int J Mol Sci
; 24(16)2023 Aug 09.
Article
in English
| MEDLINE | ID: mdl-37628793
7.
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.
Am J Hum Genet
; 104(3): 422-438, 2019 03 07.
Article
in English
| MEDLINE | ID: mdl-30773277
8.
Evaluation of IOL power calculation with the Kane formula for pediatric cataract surgery.
Graefes Arch Clin Exp Ophthalmol
; 260(9): 2877-2885, 2022 Sep.
Article
in English
| MEDLINE | ID: mdl-35895106
9.
Estimation of nitrous oxide emissions from rice paddy fields using the DNDC model: a case study of South Korea.
Water Sci Technol
; 86(6): 1308-1324, 2022 Sep.
Article
in English
| MEDLINE | ID: mdl-36178808
10.
Novel loss-of-function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice.
Clin Genet
; 99(1): 176-186, 2021 01.
Article
in English
| MEDLINE | ID: mdl-33070343
11.
MOF influences meiotic expansion of H2AX phosphorylation and spermatogenesis in mice.
PLoS Genet
; 14(5): e1007300, 2018 05.
Article
in English
| MEDLINE | ID: mdl-29795555
12.
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Am J Hum Genet
; 109(7): 1343, 2022 Jul 07.
Article
in English
| MEDLINE | ID: mdl-35803236
13.
Histone acetyltransferase KAT8 is essential for mouse oocyte development by regulating reactive oxygen species levels.
Development
; 144(12): 2165-2174, 2017 06 15.
Article
in English
| MEDLINE | ID: mdl-28506985
14.
Npat-dependent programmed Sertoli cell proliferation is indispensable for testis cord development and germ cell mitotic arrest.
FASEB J
; 33(8): 9075-9086, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31084574
15.
Development of a pediatric ophthalmology academic partnership between Canada and Ethiopia: a situational analysis.
BMC Med Educ
; 20(1): 438, 2020 Nov 16.
Article
in English
| MEDLINE | ID: mdl-33198727
16.
The Interplay between Toxic and Essential Metals for Their Uptake and Translocation Is Likely Governed by DNA Methylation and Histone Deacetylation in Maize.
Int J Mol Sci
; 21(18)2020 Sep 22.
Article
in English
| MEDLINE | ID: mdl-32971934
17.
Ocular Graft-versus-Host Disease after Hematopoietic Cell Transplantation: Expert Review from the Late Effects and Quality of Life Working Committee of the Center for International Blood and Marrow Transplant Research and Transplant Complications Working Party of the European Society of Blood and Marrow Transplantation.
Biol Blood Marrow Transplant
; 25(2): e46-e54, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30481594
18.
Non-Graft-versus-Host Disease Ocular Complications after Hematopoietic Cell Transplantation: Expert Review from the Late Effects and Quality of Life Working Committee of the Center for International Blood and Marrow Transplant Research and the Transplant Complications Working Party of the European Society for Blood and Marrow Transplantation.
Biol Blood Marrow Transplant
; 25(5): e145-e154, 2019 05.
Article
in English
| MEDLINE | ID: mdl-30521975
19.
A homozygous FANCM frameshift pathogenic variant causes male infertility.
Genet Med
; 21(1): 62-70, 2019 01.
Article
in English
| MEDLINE | ID: mdl-29895858
20.
Correction: A homozygous FANCM frameshift pathogenic variant causes male infertility.
Genet Med
; 21(1): 266, 2019 01.
Article
in English
| MEDLINE | ID: mdl-30158692