Hereditary disorders affecting the lacrimal system
RC Allen - Current opinion in ophthalmology, 2014 - journals.lww.com
Hereditary disorders affecting the lacrimal system : Current Opinion in Ophthalmology
Hereditary disorders affecting the lacrimal system : Current Opinion in Ophthalmology Log in or …
Hereditary disorders affecting the lacrimal system : Current Opinion in Ophthalmology Log in or …
Renal progenitors and childhood: from development to disorders
Nephropathies arise from conditions that alter nephron development or trigger nephron
damage during neonatal, juvenile, and adult stages of life. Much evidence suggests that a …
damage during neonatal, juvenile, and adult stages of life. Much evidence suggests that a …
[HTML][HTML] Gene4HL: an integrated genetic database for hearing loss
S Huang, G Zhao, J Wu, K Li, Q Wang, Y Fu… - Frontiers in …, 2021 - frontiersin.org
Hearing loss (HL) is one of the most common disabilities in the world. In industrialized
countries, HL occurs in 1–2/1,000 newborns, and approximately 60% of HL is caused by …
countries, HL occurs in 1–2/1,000 newborns, and approximately 60% of HL is caused by …
The PAX-SIX-EYA-DACH network modulates GATA-FOG function in fly hematopoiesis and human erythropoiesis
TM Creed, R Baldeosingh, CL Eberly… - …, 2020 - journals.biologists.com
ABSTRACT The GATA and PAX-SIX-EYA-DACH transcriptional networks (PSEDNs) are
essential for proper development across taxa. Here, we demonstrate novel PSEDN roles in …
essential for proper development across taxa. Here, we demonstrate novel PSEDN roles in …
[HTML][HTML] Genome-wide association between EYA1 and aspirin-induced peptic ulceration
S Bourgeois, DF Carr, CO Musumba, A Penrose… - …, 2021 - thelancet.com
Background Low-dose aspirin can cause gastric and duodenal ulceration, hereafter called
peptic ulcer disease (PUD). Predisposition is thought to be related to clinical and genetic …
peptic ulcer disease (PUD). Predisposition is thought to be related to clinical and genetic …
Noise exposure and distortion product otoacoustic emission suprathreshold amplitudes: a genome-wide association study
J Lavinsky, G Kasperbauer, RF Bento… - Audiology and …, 2021 - karger.com
Background: Although several candidate-gene association studies have been conducted to
investigate noise-induced hearing loss (NIHL) in humans, most are underpowered …
investigate noise-induced hearing loss (NIHL) in humans, most are underpowered …
Environmental factors for the development of fetal urinary malformations
MY Hei, ZW Yi - World Journal of Pediatrics, 2014 - Springer
Background The development of the kidneys and other organs of the urinary tract also follow
the natural rule of gene-environment-lifestyle interaction. Both intrinsic and extrinsic factors …
the natural rule of gene-environment-lifestyle interaction. Both intrinsic and extrinsic factors …
Congenital Anomalies of the Kidneys
Congenital kidney anomalies are the result of embryonic maldevelopment that dates back to
the fifth gestational week in humans. At this time-point, the metanephric mesenchyme, which …
the fifth gestational week in humans. At this time-point, the metanephric mesenchyme, which …
[HTML][HTML] Redundant functions of Rac GTPases in inner ear morphogenesis
Development of the mammalian inner ear requires coordination of cell proliferation, cell fate
determination and morphogenetic movements. While significant progress has been made in …
determination and morphogenetic movements. While significant progress has been made in …
[HTML][HTML] Recurrent 8q13. 2-13.3 microdeletions associated with branchio-oto-renal syndrome are mediated by human endogenous retroviral (HERV) sequence blocks
X Chen, J Wang, E Mitchell, J Guo, L Wang… - BMC medical …, 2014 - Springer
Background Human endogenous retroviral (HERV) sequences are the remnants of ancient
retroviral infection and comprise approximately 8% of the human genome. The high …
retroviral infection and comprise approximately 8% of the human genome. The high …