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Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Knocking out certain genes in mice helps understand skin and hair growth problems.

The review highlights the importance of stem cells in hair health and suggests new treatment strategies for hair loss conditions.

Progerin affects cell shape but not hair or skin in mice.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Eating a Mediterranean diet and taking certain supplements may improve symptoms of PCOS.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

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.

The document explains how to identify different hair problems using a microscope.

Ellis van Creveld syndrome, a rare genetic disorder, can cause unexpected abnormalities in various body organs, requiring thorough patient evaluations.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

A 45-year-old woman with autoimmune diseases experienced patchy hair loss due to alopecia areata, which has no cure but can be treated, with varying success.

Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

Androgens can both increase body hair and cause scalp hair loss.

Early recognition and management of skin side effects from new cancer therapies can prevent treatment delays.

ACBP is essential for healthy skin and fur by maintaining the skin's barrier function.

The study found that hair fragility in Pili annulati may be caused by cavities and damage within the hair shafts.

Skin issues can indicate immune system problems.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Eating glucoraphanin can help prevent psychosis in offspring whose mothers had immune system activation.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

The document explains the genetic causes and characteristics of inherited hair disorders.