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Steroid Sulfatase inhibitors show promise in treating hormone-dependent disorders like cancers, hair loss, and acne, with 667COUMATE being a potential candidate for breast cancer treatment trials.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

The African spiny mouse can fully regenerate its muscle without scarring, unlike the common house mouse.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

The spiny mouse is a unique menstruating rodent that can help us understand menstruation and reproductive disorders.

Treg dysfunction is linked to various autoimmune skin diseases, and understanding Treg properties is key for new treatments.

Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

NFIC helps human dental stem cells grow and become tooth-like cells.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

A new gene mutation linked to a skin condition was found in a Spanish family.

KLF4 is important for maintaining skin stem cells and helps heal wounds.

VEGF stimulates hair cell growth and increases growth receptor levels through a specific signaling pathway.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Nested PCR can reliably identify fungal infections when traditional methods fail.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Tissue stiffness affects hair follicle regeneration, and Twist1 is a key regulator.

Changthangi goats have specific genes that help produce Pashmina wool.

The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

A specific protein in chicken embryos links early skin layers to feather development.

Hoxc13 is linked to seasonal hair growth in Cashmere goats and is affected by melatonin.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.