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The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

C-scores can help predict gain-of-function and loss-of-function mutations.

Genetic counselors should be culturally skilled and aware of transgender patients' unique health risks and needs.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

Large data can lead to new medical discoveries and personalized medicine.

A genetic mutation in the LIPH gene causes tightly curled hair that stops growing in some Japanese individuals.

Different genes cause Female Pattern Hair Loss compared to male hair loss, and treatments vary, but more research is needed to understand it fully.

New treatments like nanotechnology show promise in improving skin cancer therapy.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Researchers found 63 genes linked to male-pattern baldness, which could help in understanding its biology and developing new treatments.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

Women look young for their age due to larger lips, less sun damage, and genes that prevent gray hair and wrinkles.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

The study suggests that hypothyroidism may cause alopecia areata.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Young HS patients often have other physical and mental health issues, and research on HS covers a wide range of topics including genetics, triggers, treatments, and the need for more data.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Both gene and non-gene areas of DNA evolved to make some mammals hairless.

Genetic screening can help diagnose and manage infertility in Slovenian couples.

Female cuckoo color differences are linked to their unique genes and help avoid male harassment.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.