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Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

Mutations in the Sgk3 gene cause fuzzy hair in mice.

miR-29 is a key factor that accelerates aging.

Changing the amount of PLC5 in Arabidopsis affects root growth and drought resistance, with less PLC5 slowing root growth and more PLC5 improving drought tolerance but hindering root hair growth.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Mouse Scube3 affects teeth, tongue, vibrissae, and eye development, but not facial structure or limb growth.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The CUBIC protocol allows detailed 3D visualization of proteins in mouse skin biopsies.

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

Changing YBX1 protein activity affects skin stem cell function and aging.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

A specific protein complex increases the activity of a plant enzyme, but this action is not required for plant root hair growth.

The Dfl mutation in mice causes poor sebaceous gland function and complete hair loss.

miRNA-24 affects goat coat color by controlling proteins involved in pigment production.

The 4C32 gene may help in mouse skin development and differentiation.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

Blocking Rab27a slows hair growth, while blocking Rab27b encourages it.

XMU-MP-1 stops cell growth in a human mini-organ and reduces the effectiveness of the chemotherapy drug paclitaxel.

Mice with CBS deficiency are healthier on a low-methionine diet.

MPA increases cancer spread by boosting Eph A2 activity.

A specific gene mutation causes complete hair loss without other health issues.

The -866G/A polymorphism in the UCP2 gene is not linked to polycystic ovary syndrome.

Mice can correct hair follicle orientation without certain genes, but proper overall alignment needs those genes.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

A new therapy for a skin blistering condition has not been developed yet.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.