Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

More PDCD4 is linked to obesity, insulin problems, and cell death in ovaries for those with polycystic ovary syndrome.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Sex steroids affect the MafB gene differently in male and female hamsters.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

Lhx2 helps retinal cells respond to signals for eye development.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

PDCD4 protein levels, affected by genetics and breastfeeding, may predict breast cancer treatment response.

Overexpression of hurpin in mice leads to abnormal skin and higher skin cancer risk.

GMG-43AC may help reduce unwanted hair growth and treat certain hair loss conditions.

Miz1 is essential for proper hair structure and growth.

Liver damage in PCOS is linked to iron overload and cell death due to the miR-761-hepcidin/GPX4 pathway.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

PPAR-γ helps control skin oil glands and inflammation, and its disruption can cause hair loss diseases.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

A specific mutation in PA-PLA1α causes abnormal hair growth.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Mitf plays a key role in melanoma progression and is linked to disease stage.

CAP1 decreases the expression of a hair-related protein in young Tan sheep's skin.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

α-MSH may help treat skin inflammation and fibrosis.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.