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People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

Understanding hair follicle development can help treat hair loss, skin regeneration, and certain skin cancers.

EDA2R gene linked to hair loss.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

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

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

TNF family proteins are crucial for the development of skin features like hair, teeth, and mammary glands.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Some women with PCOS have rare genetic variants linked to the condition.

FGF5 gene mutations cause long hair in domestic cats.

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.

Androgens contribute to common male hair loss; more research needed for hair growth medication.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Aromatase gene variation may increase female hair loss risk.

Systemic diseases can cause hair loss, which is often reversible with treatment.

Retinoids can prevent skin cancer in high-risk people but have side effects and require more research on dosing and effectiveness.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

Changes to the Foxp3 protein affect how well regulatory T cells can control the immune system, which could help treat immune diseases and cancer.

Chemokine signaling is important for hair development.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

Disrupting the FGF5 gene in rabbits leads to longer hair by extending the hair growth phase.