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The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

New hair regrowth model proposed, imiquimod found to kill skin cancer cells, T-cadherin loss linked to invasive skin cancer, no clear gene link to skin cancer after transplant, and study on children's hair loss shows male dominance and genetic ties.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

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

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

EDA2R gene linked to hair loss.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

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

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Mutations in the androgen receptor gene cause Androgen Insensitivity Syndrome, affecting sexual development.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

A new gene mutation linked to a skin condition was found in a Spanish family.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

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.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

Nanog gene boosts stem cells, helps hair growth, and may treat hair loss.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.