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A gene mutation in mice causes permanent hair loss and skin issues.

The document concludes that accurate diagnosis of ichthyosis is crucial for treatment and genetic advice, and ongoing research is needed for better therapies.

Most hair follicle stem cells do not protect their DNA by dividing it unevenly.

Chromosomal differences affect how muscle cells respond to testosterone.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Identical twins had different symptoms because one had more cells with an extra chromosome fragment in different tissues.

Hair samples can be used to create stem cells easily and non-invasively.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

Taking Propecia might lead to the development of cataracts.

Multiple eye conditions were studied, highlighting the importance of various imaging methods for diagnosis, the vision side effects of drugs tamoxifen and Propecia, and the usefulness of optical coherence tomography for diagnosing and monitoring macular and retinal diseases.

Using a combination of specific cell cycle regulators is better for safely keeping hair root cells alive indefinitely compared to cancer-related methods.

SHED-CM can reduce hair graying and protect against damage from X-rays.

ALA-PDT is effective and safe for chronic X-ray dermatitis, providing complete or partial remission.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

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

Finasteride, often used for hair loss, can potentially cause cataracts.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Genetic variation in the KRTAP15-1 gene affects wool yield in sheep.

IFN-γ and IL-2 are important for T cell activation in hair loss in mice.

L-PGDS has specific binding sites for its functions and could help in drug delivery system design.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.