Detalhe da pesquisa
1.
Cornichon protein CNIH4 is not essential for mice gametogenesis and fertility.
Dev Biol
; 496: 15-23, 2023 04.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| MEDLINE | ID: mdl-37831349
5.
Corneal Neurotization: Essentials for The Facial Paralysis Surgeon.
Facial Plast Surg
; 2024 Mar 18.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| MEDLINE | ID: mdl-33070343
11.
MOF influences meiotic expansion of H2AX phosphorylation and spermatogenesis in mice.
PLoS Genet
; 14(5): e1007300, 2018 05.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| MEDLINE | ID: mdl-30521975
19.
Correction: A homozygous FANCM frameshift pathogenic variant causes male infertility.
Genet Med
; 21(1): 266, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30158692
20.
A homozygous FANCM frameshift pathogenic variant causes male infertility.
Genet Med
; 21(1): 62-70, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29895858