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The transition from growth to regression in Cashmere goat hair follicles involves changes in expression of genes related to keratin and cell differentiation.

Keratin-associated proteins are part of the developing hair fiber cuticle.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

Human hair keratin can be used in many medical applications.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Scientists successfully created mouse hair proteins in the lab, which are stable and similar to natural hair.

Disulfide bonds make keratin in hair stronger and tougher.

Blocking the FGF5 gene in sheep leads to more fine wool and active hair follicles due to changes in certain cell signaling pathways.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

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

Cutaneous gene therapy could become a viable treatment for skin and hair disorders with improved vector development and gene expression control.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Human hair-derived particles can effectively carry and release the cancer drug Paclitaxel in a pH-sensitive manner, potentially targeting cancer cells while sparing healthy ones.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.