LENZ Therapeutics, Inc. SAN DIEGO, April 30, 2025 (GLOBE NEWSWIRE) -- LENZ Therapeutics, Inc. (Nasdaq: LENZ or “LENZ” or the “Company”), a pre-commercial stage biopharmaceutical company ...

Bartter syndrome is a group of similar rare conditions that affect the kidneys. It's genetic, meaning it's caused by a problem with a gene. If you have this condition, too much salt and calcium ...

ucl.ac.uk Background/aims Microphthalmia, anophthalmia and coloboma (MAC ... six bilateral and two unilateral. Patient 9–1 with Kabuki syndrome, 22–1 with learning difficulties and 22–1 with ...

People who are born female usually have two X chromosomes. Triple X syndrome (also called trisomy X syndrome, XXX syndrome, or 47,XXX) is a rare genetic condition where females inherit an extra X ...

CDC42 controls actin remodeling, apicobasal polarity, and junction assembly. Here we identify a novel essential function for Cdc42 during eye morphogenesis in mouse; in Cdc42 mutant eyes expansion of ...

Here we show the functional interaction of MITF‐M and LEF‐1 using the DCT gene promoter, which represents a novel mechanism by which Wnt signaling leads to transcriptional activation of target genes.

DINNER FOR VAMPIRES: Life on a Cult TV Show (While Also in an Actual Cult!), by Bethany Joy Lenz Bethany Joy Lenz knows cults have gone a little mainstream. “When I tell someone I was in a cult ...

Bosma Arhinia Microphthalmia Syndrome is a rare condition caused by SMCHD1 gene mutations, leading to distinctive facial abnormalities and developmental issues. Epidemiology Bosma arhinia ...

Bosma arhinia microphthalmia syndrome or BAMS is an extremely rare condition associated with facial abnormalities, mainly of the nose and the eye. Mutations in the SMCHD1 gene are the most common ...

What is Usher syndrome in children? Usher syndrome is a disorder that is passed down through families (inherited). A syndrome is a group of recognizable symptoms that happen together. Usher syndrome ...