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Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Women with AGA have higher lipid levels, increasing heart disease risk.

JAGGED1 could help regenerate tissues for bone loss and heart damage if delivered correctly.

Scientists turned mouse stem cells into skin cells that can grow into skin layers and structures.

SHISA6 helps maintain certain stem cells in mouse testes by blocking signals that would otherwise cause them to differentiate.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Pioglitazone usually doesn't effectively treat or cure lichen planopilaris.

Meis1 is crucial for skin health and tumor development.

The research explains how a human enzyme binds and processes its substrate, which could relate to its role in biological functions and hair loss.

Proper diet management is crucial for phenylketonuria patients to avoid severe health issues.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

The document is a detailed medical reference on skin and genetic disorders.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Post-implantation erythema is a red skin condition after medical device implantation that sometimes goes away on its own.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Scientists created MUSIi010-A, a stem cell line from a balding man's scalp, to study hair loss and develop potential treatments.

Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

A gene mutation in Lama3 is linked to a common type of hair loss.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

Certain gene variations are linked to the thickness of cashmere goat hair.