Search

everythinglearnresearchcommunity

for

Search:↓

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

The conclusion is that a certain test might help find cancer spread in lymph nodes for melanoma patients, but more research is needed due to false positives.

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

Six new genetic regions linked to early hair loss also connect to Parkinson's disease and prostate cancer, possibly leading to new treatments.

Four genetic risk spots found for hair loss, with WNT signaling involved and a link to curly hair.

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

Keratin 79 marks a new group of cells that are key for creating and repairing the hair follicle's structure.

New cells are added to the hair's dermal papilla during the active growth phase.

The document concludes that there is a significant lack of reporting on the sex and age of cells in skin research, which could affect clinical trials and treatments.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Researchers found that certain RNA molecules might play a role in the growth of Cashmere goat hair.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

AGA progression involves increased lipid synthesis, electron transport, and hair follicle miniaturization.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

The treatment was ineffective in humans.

Activating β-catenin increases melanocytes and decreases Schwann cells.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Gray hair can potentially be reversed, leading to new treatments.

Activating TERT in mice skin boosts hair growth by waking up hair follicle stem cells.

Mutations in the KRT85 gene cause hair and nail problems.

Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Dermatologists are essential in helping transgender and gender diverse patients with skin and hair issues related to gender affirmation and hormone therapy.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Edar signaling is crucial for proper hair follicle development and function.

A mouse gene mutation increases the risk of skin cancer.