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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.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

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

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

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

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

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

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 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 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.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

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.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

New treatments for alopecia areata may target specific immune cells and pathways involved in hair loss.

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

The mouse hairy ears mutation causes longer ear hair due to changes in gene expression.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

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

Two specific genetic markers increase the risk of hair loss in Asian populations.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

A teenager's hair with alternating white and dark bands, known as Pili annulati, is a genetic condition that is usually harmless and often considered attractive.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

The meeting discussed various skin conditions, treatments, and unusual cases, highlighting the effectiveness of tetracycline in treating rosacea.

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

A person with Turner Syndrome showed severe schizophrenia that didn't respond to treatment and had brain shrinkage.

AGA is caused by genetics and androgens, treatable with finasteride and minoxidil.