The lymphatic system is comprised of a network of vessels interrelated with lymphoid tissue,
which has the holistic function to maintain the local physiologic environment for every cell in …

The lymphatic vascular system develops from the pre-existing blood vasculature of the
vertebrate embryo. New insights into lymphatic vascular development have recently been …

Clinical interpretation of DNA sequence variants is a critical step in reporting clinical genetic
testing results. Application of next‐generation sequencing technology in molecular genetic …

Importance Retinal detachment with avascularity of the peripheral retina, typically
associated with familial exudative vitreoretinopathy (FEVR), can result from mutations …

Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation
(MCLMR)(MIM No. 152950) is a rare autosomal dominant condition for which a causative …

KIF11 gene mutations cause a rare autosomal dominant inheritable disease called
microcephaly with or without chorioretinopathy, lymphedema, or mental retardation …

During mitosis, Kif11, a kinesin motor protein, promotes bipolar spindle formation and
chromosome movement, and during interphase, Kif11 mediates diverse trafficking …

The microcephaly‐lymphedema‐chorioretinal dysplasia (MLCRD) syndrome is a distinct
microcephaly syndrome. The hallmark features, microcephaly, chorioretinopathy, and …

The present study aimed to clarify the association between kinesin family member 11
(KIF11) and human breast cancer, and the effect of KIF11 on breast cancer cell progression …

UFMylation is a highly conserved ubiquitin-like post-translational modification that catalyzes
the covalent linkage of UFM1 to its target proteins. This modification plays a critical role in …