Search

everythinglearnresearchcommunity

for

Search:↓

FGF13 gene changes cause excessive hair growth in a rare condition.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Some families have a genetic condition where they are born with irregular scalp defects.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

Human fetal placental stromal cell injections speed up healing and improve skin and hair recovery after radiation damage.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

Understanding hair growth involves complex interactions between molecules and could help treat hair disorders.

The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

Keratin is crucial for keeping skin cells healthy and its changes can lead to diseases and affect cell behavior.

Scientists have improved 3D models of human skin for research and medical uses, but still face challenges in perfectly replicating real skin.

Certain genes and pathways are linked to the production of finer and denser wool in Hetian sheep.

Researchers identified specific genes that are important for mouse skin cell development and healing.

Bone Morphogenetic Proteins (BMPs) help control skin health, hair growth, and color, and could potentially be used to treat skin and hair disorders.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

A protein found in safflower seeds can stimulate hair growth and speed up wound healing in mice.

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.

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

The document concludes that parathyroid diseases have a range of clinical features and outcomes, with some conditions being treatable and others having a high risk of mortality.

Adrenal disorders can cause lasting brain and behavior issues in children.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Mouse zigzag hair bends form due to a 3-day cycle of changes in hair progenitors and their environment.

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

CD61 is important for mouse tooth cell growth and works through Lgr5.