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

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Advances in genetics may lead to targeted treatments for hair disorders.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

PCOS is a hormonal disorder causing symptoms like irregular periods and acne, and increases the risk of diabetes and heart disease.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Neutrophil extracellular traps slow down hair follicle healing after injury.

Hair graying is caused by the loss of pigment cells due to poor maintenance of stem cells in the hair follicle.

People with early onset hair loss (Androgenetic Alopecia) in Ile-Ife, Nigeria, have significantly lower iron levels compared to those with adult-onset hair loss.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.

A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

TRPV3 could be a target for treating pain, skin disorders, and hair problems, but more research is needed to create effective drugs.

Different processes create patterns in skin and things like hair and feathers.

Msx2 and Foxn1 are both crucial for hair growth and health.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

Humans lost body hair relatively recently in evolution.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

The document concludes that careful design of genetic fate mapping experiments is crucial for accurate cell lineage tracing in mice.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

Using special RNA to target a mutant gene fixed hair problems in mice.

Removing Sprouty genes in mice causes various hormone-related issues but does not increase cancer risk by one year of age.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Hormones and their receptors, especially androgens, play a key role in hair growth and disorders like baldness.

The method quickly analyzes hair growth genes and shows that blocking Smo in skin cells stops hair growth.

Defective mink guard hairs have split tips and missing cuticle cells, causing a metallic sheen.