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A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

The study identified and characterized new keratin genes linked to hair follicles and epithelial tissues.

Scientists found a gene in mice that causes early hearing loss.

Two mouse mutations cause similar hair loss despite different skin changes.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

The scraggly mutation causes hair loss and skin defects in mice.

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

Chromosomal differences affect how muscle cells respond to testosterone.

Certain genes and X chromosome patterns may significantly contribute to the development of hair loss.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

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

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

The study found that variations in hair protein genes are likely due to evolutionary deletions or duplications.

Researchers found a genetic region that influences the number of coat layers in dogs.

A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

The document concludes that current treatments for androgenic alopecia are not fully effective, but new therapies like botulinum toxin and PRP show promise, and future gene therapy could be beneficial.

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.

Alopecia areata is likely caused by a combination of genetic factors and immune system dysfunction, and may represent different diseases with various causes.

Genes and hormones cause hair loss, with four genes contributing equally.

Genes play a significant role in male-pattern baldness, and understanding them could lead to new treatments and insights into related health issues.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.