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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.

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

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Male hormones and their receptors play a key role in hair loss and skin health, with potential new treatments being explored.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Exosomes from dermal papilla cells help hair growth by making hair follicle stem cells multiply and change.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

GmMAX3b gene in soybeans boosts nodulation and affects hormone levels.

Researchers found a way to create cells from stem cells that act like human cells important for hair growth and could be used for hair regeneration treatments.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Wnt proteins from certain skin cells are crucial for normal hair growth and renewal.

New treatments targeting the Hedgehog pathway can help treat advanced skin cancer but may have side effects and their effectiveness in early stages is unknown.

Cannabinoid receptor-1 signaling is essential for the survival and growth of human hair follicle stem cells.

Lack of cystatin M/E causes thin hair and dry skin.

Scientists found genes linked to hair length in Brangus cattle that could help breed heat-tolerant cattle.

A specific thyroid hormone resistance mutation may be linked to different types of hair loss.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

Tianeptine, an antidepressant, may prevent stress-induced hair loss in mice.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Activated ras can protect kidney cells from a certain substance that causes cell death.

Some domesticated animals have the same genetic skin diseases as humans, which can help doctors understand human genetic mutations.

Different amounts of daylight affect cashmere growth in goats by changing the activity of certain genes and molecules.