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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.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Certain gene variations in the Vitamin D receptor may increase the risk of chronic hair loss.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Adult esophageal cells can start to become like skin cells, with a key pathway influencing this change.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

Sp6 promotes tooth development by reducing follistatin levels.

Allopregnanolone increases growth and changes gene activity in human brain cancer cells.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

The research suggests that the ZP4 gene is linked to egg development in women with PCOS but requires more study to understand its role in infertility.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

Chinese medicine may help treat hair loss by affecting genes and enzyme activity.

SCDSFs from zebrafish embryos are beneficial for treating cancer, regenerating tissues, and improving conditions like psoriasis and alopecia.

Ritlecitinib effectively improves hair growth in alopecia areata patients, regardless of hair loss pattern.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

A blood pressure drug, diltiazem, may also help treat influenza.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Finasteride causes lasting fertility decrease in rats.

Vitamin D receptor helps control hair growth genes in skin cells.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

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

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

ELL is crucial for gene transcription related to skin cell growth.

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

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

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.