Search

everythinglearnresearchcommunity

for

Search:↓

Hirsutism in women is often due to hormone sensitivity and has significant psychological effects.

The Kras mutation changes normal cell signals, leading to disrupted tissue structure and potential cancer.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

The vitamin D receptor helps regulate skin and hair health independently of its usual vitamin D ligand.

Alopecia areata's causes are unclear, treatments exist but relapses are common.

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

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

Caspases are enzymes important for both cell death and various non-lethal cell functions, affecting head development and hair growth, with different caspases playing specific roles.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

The extracellular matrix is crucial for controlling skin stem cell behavior and health.

Zinc oxide nanoparticle biscuits improved growth and health in zinc-deficient rats without toxicity.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Skin changes can indicate starvation and nutritional deficiencies in anorexia nervosa.

Alopecia X in dogs is a cosmetic issue, not a hormonal disorder, and harmful treatments should be avoided.

A new mouse mutation causes skin and hair defects due to a gene change.

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

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

The first in-prison dermatology clinic in the U.S. faced challenges and found certain skin conditions common among inmates, with rare cases of serious skin cancer.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

The conclusion is that women under 35 should start fertility checks after 12 months of trying to conceive, women over 35 after 6 months, and women over 40 should start immediately. The checks should include ovulation status, reproductive tract structure, and male partner's semen evaluation.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Rosacea is a skin condition with unclear causes, classified into four subtypes.

Cancer treatments can cause various eye problems, so eye doctors should know how to diagnose and treat these early.

Msx2 deficiency in mice leads to bone growth and organ development problems.

The woman has a rare, harmless skin condition specific to pregnancy that causes itchy bumps and will go away after she gives birth.