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Lef1 helps adult skin cells maintain their ability to heal wounds and regenerate hair, but the study's methods and conclusions have been questioned.

Mitochondrial dysfunction contributes to skin aging and hair loss.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

Aging in one type of stem cell can cause aging-like changes in various organs.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Sebum from sebocytes is important for skin health and linked to conditions like acne and hair loss.

Unconventional lymphocytes are important for quick immune responses and healing of skin and mucosal barriers.

OR2AT4 helps reduce aging and cell damage in human skin cells.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

Using quantitative traits in genetics can improve understanding and management of skin health and conditions.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Understanding genetics is crucial for treating heart and skin diseases.

A child with Olmsted syndrome showed mild improvement in hair and skin issues with treatment.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Different types of stem cells in the skin contribute to the variety of melanoma forms.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Mutations in keratin genes cause cell fragility and various skin disorders.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

ADSCs help in wound healing and skin regeneration but need more research for full understanding.

The study found that polymorphous light eruption varies among patients and can be distinguished from benign summer light eruption by the time it takes for symptoms to appear after sun exposure.

Forensic DNA phenotyping is becoming useful for predicting physical traits in criminal investigations but is limited by ethical concerns and incomplete genetic understanding.

Modulating BMP activity changes the number, size, shape, and type of ectodermal organs.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Stem cells show promise for nerve injury treatment, but more research is needed before human use.

Women with only irregular periods or excess hair have a better hormone profile than those with full PCOS, but both groups are similar, indicating a need for better PCOS diagnosis methods.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.