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

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

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

GABRA2 gene variations impact alcohol response, and hair loss medication finasteride reduces some effects.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

The TRPV3 gene mutation affects hair growth by keeping mice in the growth phase longer, which could help treat hair loss.

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

The length of the CAG repeat in the androgen receptor gene affects the risk and progression of prostate cancer, BPH, infertility, and undermasculinized genitalia.

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

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

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

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Alopecia areata involves immune response and gene changes affecting hair loss.

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.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

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

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

A specific gene mutation causes Olmsted syndrome.

Certain genetic variations in the RAB5B gene are linked to a higher risk of polycystic ovary syndrome in Chinese Han women.

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

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

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

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.