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

Fat cells are important for healthy skin, hair growth, and healing, and changes in these cells can affect skin conditions and aging.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Wild African goats have genetic adaptations for surviving harsh desert conditions.

FGF18 treatment during hair's resting phase can protect against hair loss from radiation.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

The skin and thymus develop similarly to protect and support immunity.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

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

Understanding how cells die in the skin is important for treating skin diseases and preventing hair loss.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Pannexin 3 helps skin and hair growth by controlling a protein called Epiprofin.

Wnt-10b is important for keeping mouse skin cells healthy for hair growth.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Long scalp hair evolved for cooling and social signaling.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

The mTurq2-Col4a1 mouse model shows that cells can divide while attached to stable basement membranes during development.

Dermatologists diagnose and manage melanoma more effectively than general practitioners.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A new EDA gene mutation was found in a Chinese family with a specific skin disorder.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.