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Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

The research found that certain microRNAs are important for human hair growth and health.

DHT reduces a cell's ability to promote hair growth, while 3D culture without DHT improves it.

The endocannabinoid system affects oil production and inflammation in skin cells.

Zinc deficiency disrupts hair growth and cycle, but zinc supplements can fix this.

Tissue from dog stem cells helped grow hair in mice.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Parthenolide promotes hair growth in mice and may influence pathways related to male pattern baldness.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Mouse profilaggrin helps in skin cell differentiation and may be involved in calcium signaling.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

Crataegi Fructus water extract may help treat hair loss.

Corneous beta-proteins evolved uniquely in reptiles and birds, forming scales, claws, beaks, and feathers.

Fatp4 is crucial for healthy skin development and function.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Foxn1 gene regulation is crucial for thymus development but not for hair growth.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Changes in KRT17 gene activity linked to wool production in Angora rabbits.

Certain skin proteins can form anchoring structures without the protein AMACO.

Certain gene variations may increase the risk of hair loss in Egyptians.

Certain genetic variants and pathways are linked to hair loss.

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