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Genetic variations greatly affect individual metabolism and can impact health and disease risk.

Increasing research diversity is key for better understanding and treating Parkinson's Disease.

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

Air Vice-Marshal Sir Ralph Jackson significantly advanced dialysis technology in the UK.

Addressing underrepresentation in Parkinson's research is crucial for better treatments and understanding.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

A new gene, JMJD1C, may affect testosterone levels in men.

New genetic locations explain much of hair color variation in Europeans.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Identified genes linked to male-pattern baldness may help develop new treatments.

The DNA of ancient Koreans from the Three Kingdoms period shows a mix of northern Chinese and Japanese-Jomon ancestry, revealing two distinct genetic groups.

The research suggests that the global distribution of PCOS is likely due to historical human migration and that genes affecting PCOS may have different impacts on males and females.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

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

Better hair loss models needed for research.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

PCOS has a strong genetic basis, but more research is needed to fully understand it.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

A scarring hair loss condition mainly affects middle-aged women of African descent, impacting their quality of life, with treatments more effective when started early.

Hair diameter and curvature are mostly determined by genetics.

Men with high genetic risk for Polycystic Ovary Syndrome (PCOS) have increased chances of obesity, type 2 diabetes, heart disease, and hair loss, showing PCOS risk factors can affect both genders.

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

The study found that certain genes are important for hedgehog skin appendage development and immunity, with spines possibly evolving for protection and infection resistance.

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.

Genetic testing is crucial before giving azathioprine to avoid severe side effects.

Xiangdong black goats have moderate genetic diversity, minimal inbreeding, and important genes for reproduction, immunity, and other traits.