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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A certain genetic variation is linked to a higher risk of polycystic ovarian syndrome.

Marie Antoinette syndrome causes sudden hair whitening, but its exact cause is unknown.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Type 1 diabetes often occurs with other autoimmune diseases, and personalized treatment based on genetics can improve outcomes.

Polycystic Ovary Syndrome (PCOS) is a common but often undiagnosed disorder in women that can cause irregular periods, infertility, and other symptoms, and can be managed with lifestyle changes, medication, and sometimes surgery.

A thorough initial check-up is essential before sperm banking to ensure the best chance of preserving good quality sperm.

Less AgNOR protein production is linked to hair loss.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

A protein found in safflower seeds can stimulate hair growth and speed up wound healing in mice.

The Asiatic lion has very low genetic diversity and unique genetic traits, highlighting the need for its conservation.

High wool density in Rex rabbits is linked to specific gene activity affecting hair follicle development.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

People with Down syndrome have higher rates of certain immune-related conditions and need special medical attention.

The safety and effectiveness of gender-affirming treatments for children are uncertain, with potential long-term risks like infertility.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

A man experienced hair loss from radiotherapy, which can be temporary or permanent depending on radiation dose, with potential treatments available.

Hair loss in men treated best with early medication or transplant, new treatments researched.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

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

Certain genes related to sulfur metabolism are more active during the growth phase of Cashmere goat wool, and melatonin might help this process.

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

Non-classic congenital adrenal hyperplasia is a common disorder causing symptoms like acne and infertility, and it's managed based on symptoms, not just test results. Treatment can improve fertility and reduce miscarriage risk.