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The plant hormone auxin activates the TOR pathway, affecting gene expression related to growth and cell size.

The scraggly mutation causes hair loss and skin defects in mice.

The document concludes that dermal papilla cells are key for hair growth and could be used in new hair loss treatments.

Skin healing from blisters can delay hair growth as stem cells focus on repairing skin over developing hair.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

Wnt signaling is crucial for skin development and hair growth.

Tectoridin helps human hair cells grow and makes mouse hair longer, suggesting it could treat hair loss.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

The AUTS2 gene is linked to neurological disorders and may affect human brain development and cognition.

Defects in certain proteins cause major heart abnormalities during early development.

Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

Alginate spheres help maintain hair growth potential in human cells for hair loss treatment.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

Hair papilla cells can create and regenerate hair bulbs under the right conditions.

Drosha and Dicer are essential for hair follicle health and preventing DNA damage in skin cells.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

The document summarizes recent dermatological treatments and advances in areas like pediatric care, wound healing, skin closure, light-based therapies, pigment disorders, hair loss, immunotherapy, infection management, melanoma, drug reactions, and facial rejuvenation.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

Skin symptoms can indicate endocrine disorders and have various treatments.

Melatonin makes cashmere grow earlier and more by increasing certain gene activity in goats.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Melatonin can increase cashmere yield by altering gene expression and restarting the growth cycle early.

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

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

The conclusion suggests that PCOS may persist due to genetic traits that, while harmful for female fertility, could have provided survival and reproductive benefits to males.

Ten miRNAs may play key roles in starting secondary hair follicle development in sheep foetuses.

Flavonoids and Nod factors are key for legume plant growth and could help in sustainable farming.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.