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FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

The document concludes that understanding hair biology is key to treating hair disorders, with gene therapy showing potential as a future treatment.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Hair follicle stem cells are crucial for touch sensation and proper nerve structure in mice.

The gene for slick hair in Senepol cattle is located on chromosome 20 and may involve the SRD5A2 gene.

Researchers successfully grew horse skin cells that produce pigment from hair follicle samples.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

Coloring shampoos for gray hair may cause gene mutation, reproductive issues, and skin damage, needing stricter regulation and expert consultation.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The G60S Connexin43 mutation causes hair growth issues and poor hair quality in mice, similar to human ODDD patients.

Chicken feather gene mutation helps understand human hair disorders.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

A mouse gene mutation increases the risk of skin cancer.

Some viruses can cause cancer by changing cell processes and avoiding the immune system; vaccines and targeted treatments help reduce these cancers.

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