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PTEN was identified as a specific marker for the skin disease cutaneous lupus erythematosus, and it helps increase the expression of harmful type I interferons.

Scientists created a detailed map of gene activity in different parts of human hair follicles.

Atopic dermatitis shows a link between skin layers in inflammation, detectable with detailed gene analysis.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Testosterone raises blood pressure by affecting kidney function and brain gene regulation over time.

R-spondin2 may help treat hair loss, gene differences could explain baldness, a peptide's regulation is linked to psoriasis, B-defensin gene copies may affect a skin condition's risk and severity, and potential markers and targets for alopecia areata were identified.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Exosomes from skin cells can boost hair growth by stimulating a gene called LEF1.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

The analysis of a large pilomatricoma revealed five distinct areas with different gene activity related to hair growth and tumor development.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Certain gene patterns in breast cancer are linked to how active hormone receptors are and could affect patient survival.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Certain gene mutations can weaken the skin barrier and, when combined with environmental factors, lead to eczema and severe itching.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

FOXN1 gene variants cause low T cells and immune issues from birth.

FGF13 gene changes cause excessive hair growth in a rare condition.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

The E2 protein affects gene activity in hair follicles of mice.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Adding Triamcinolone to the anesthetic can reduce swelling after hair transplants, and using Platelet-Rich Plasma can improve hair thickness and patient satisfaction. The SRD5A2 gene also plays a key role in the success of hair transplants.

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