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A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

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

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

Loss of the Y chromosome and UTY gene activity increases cancer risk in men.

Chromosomal differences affect how muscle cells respond to testosterone.

A patient with a rare chromosome condition also had a rare type of hair loss.

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

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

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

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

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

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.

Certain genetic markers on chromosome 20 are linked to hair loss in the Han Chinese from Yunnan.

The research concluded that selection significantly shaped the genetic variation of the X chromosome, with certain regions affected by past selective events.

Infertile men are more likely to produce sperm with abnormal chromosome numbers, which can affect pregnancy success and embryo health.

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.

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

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.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

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.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

The document concludes that more multidisciplinary research is needed to understand and treat PCOS, a condition that significantly affects women's health and quality of life.