Congenital malformations of hands and feet in Smith-Lemli-Opitz syndrome
Smith-Lemli-Opitz syndrome is rare genetic disorder with multiple limb malformations and neurological manifestation, caused by inborn defect of cholesterol metabolism.
N. A. Kovalenko-Klychkova +2 more
doaj +1 more source
A Forgotten Victory: Courcelette, 15 September 1916 [PDF]
The 2nd Canadian Division, which landed in France on 15 September 1915, had established an uncertain operational record by the summer of 1916. As part of the Canadian Corps, the division had spent virtually all of its time in or near Belgium’s notorious ...
Campbell, David
core +1 more source
Disordered but rhythmic—the role of intrinsic protein disorder in eukaryotic circadian timing
Unstructured domains known as intrinsically disordered regions (IDRs) are present in nearly every part of the eukaryotic core circadian oscillator. IDRs enable many diverse inter‐ and intramolecular interactions that support clock function. IDR conformations are highly tunable by post‐translational modifications and environmental conditions, which ...
Emery T. Usher, Jacqueline F. Pelham
wiley +1 more source
Subluxation and dislocation of the hip in children with spina bifida (review)
Subluxation or dislocation of the hip joint develops in 30-50% children with spina bifida during the first 2-3 years of life. These problems results from force disbalance between muscle group and other structural changes of the hip and pelvis components ...
A. G. Baindurashvili +2 more
doaj +1 more source
Protein pyrophosphorylation by inositol pyrophosphates — detection, function, and regulation
Protein pyrophosphorylation is an unusual signaling mechanism that was discovered two decades ago. It can be driven by inositol pyrophosphate messengers and influences various cellular processes. Herein, we summarize the research progress and challenges of this field, covering pathways found to be regulated by this posttranslational modification as ...
Sarah Lampe +3 more
wiley +1 more source
Surgical treatment of diastematomyelia using ct-based navigation system (case report)
The authors presented the clinical observation of the patient 14 years old with congenital malformation of the spinal canal associated with congenital scoliosis and multiple vertebral malformations.
S. V. Vissarionov +2 more
doaj +1 more source
Holotype of Agathymus escalantei Stallings, Turner, and Stallings, 1966 (Lepidoptera: Hesperiidae: Megathyminae) [PDF]
Agathymus escalantei Stallings, Turner, and Stallings, 1966 (Lepidoptera: Hesperiidae) is the only described species of Megathyminae known from a single collected individual.
Boyd, Bret M.
core
Determining the sample size for a cluster-randomised trial: Bayesian hierarchical modelling of the ICC estimate [PDF]
In common with many cluster-randomised trials, it was difficult to determine the appropriate sample size for the planned trial of the effectiveness of a systematic voiding programme for post-stroke incontinence due to the lack of a robust estimate of the
Leathley, Michael John +4 more
core +1 more source
The role of histone modifications in transcription regulation upon DNA damage
This review discusses the critical role of histone modifications in regulating gene expression during the DNA damage response (DDR). By modulating chromatin structure and recruiting repair factors, these post‐translational modifications fine‐tune transcriptional programmes to maintain genomic stability.
Angelina Job Kolady, Siyao Wang
wiley +1 more source
Introduction: axial deformities in the lower extremities of children lead to an uneven distribution of the load in different compartments of the knee joint, which can contribute to the development of osteoarthritis.
E. S. Morenko +2 more
doaj +1 more source

