Periodontitis treatment and microbiome in a patient with FAM20A mutation: Case study of 1.5 years
Abstract Background Enamel‐renal‐gingival syndrome (ERGS) is an autosomal recessive disorder caused by mutations in the FAMily with sequence similarity 20A (FAM20A) gene, and is characterized by amelogenesis imperfecta, delayed or failed tooth eruption, and periodontitis.
John Rong Hao Tay +2 more
wiley +1 more source
Homozygous <i>Myo7A</i> mutation associations teratozoospermia and intracytoplasmic sperm injection failure in humans and mice. [PDF]
Liao H +13 more
europepmc +1 more source
Graphical representation of nanorobotic platforms for targeted drug delivery. Abstract Background Nanorobotic systems represent an emerging and disruptive paradigm in nanomedicine for precision drug delivery, controlled therapeutic release, and minimally invasive biomedical interventions.
Mohd Shoab Ali +5 more
wiley +1 more source
CFAP251 Deficiency Induces Male Infertility and PCD-like Ciliary Defects by Disrupting TUBB4B and SLC25A4 Recruitment in Humans and Mice. [PDF]
Liu L +12 more
europepmc +1 more source
From Plate to Patient: A Systematic Review of Food‐Related Campylobacteriosis Case Reports
ABSTRACT Background and Aims Campylobacteriosis, primarily caused by Campylobacter jejuni, C. coli, and C. fetus, remains the leading bacterial cause of foodborne gastroenteritis globally, with increasing incidence in both developed and developing nations.
Minoo Moghimani +3 more
wiley +1 more source
Light-Dependent Switching of Circling Handedness in Microswimmer Navigation. [PDF]
Wang Z +4 more
europepmc +1 more source
Low‐Head Dam Removal Restores Biofilm Structure but Not Function in a Temperate Stream
ABSTRACT Barrier removal is a common stream restoration practice aimed at restoring longitudinal connectivity, yet its effects on biofilm structure and function, through alteration of near‐bed hydrodynamics, remain unclear. Using a space‐for‐time substitution approach, we assessed how the presence and removal of a low‐head dam affect biofilm structure ...
Julia Pasqualini +9 more
wiley +1 more source
Novel loss-of-function <i>SPAG</i>17 homozygous variant segregated in a family with severe asthenozoospermia: upgrading gene-disease validity to strong. [PDF]
Wang L +9 more
europepmc +1 more source

