Search

everythinglearnresearchcommunity

for

Search:↓

A new compound slows cancer cell growth and causes cell death by blocking cell cycle progression and increasing cell-damaging molecules.

The protein p21 is more abundant in normal skin cells than in melanoma cells and may help protect against melanoma, with UVB light affecting its levels.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

Deleting MED1 in skin cells causes hair loss and skin changes.

Edar signaling is crucial for controlling hair growth and regression.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

Increasing calcium sensing receptor speeds up skin and hair development in mice.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

EGF receptors are crucial for skin cell growth and decrease with age.

SVpgC2a cells show abnormal growth and keratin changes, modeling early cancer development.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

Keratinocyte cytokines and genetic variations influence the development of moles and skin pigmentation.

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Researchers found a non-functional sheep keratin gene due to mutations.

Deleting a specific protein in skin cells disrupts normal hair growth and development.

Lichen Planopilaris and Frontal Fibrosing Alopecia may help us understand hair follicle stem cell disorders and suggest new treatments.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Too much parathyroid hormone-related protein in skin disrupts hair growth in mice.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

Cholesteatoma shows abnormal and increased EGF receptor expression, indicating its rapid growth.

The gene Prss53 affects hair shape and bone development in rabbits.

EGF–FGF2 helps mouse stem cells grow and become more like nerve cells.

A new mutation in the XEDAR gene might cause a rare skin condition called hypohidrotic ectodermal dysplasia.

WNT10A and EBF1 interaction affects hair growth in male-pattern baldness.

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