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

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

Forensic DNA phenotyping can help generate new leads in cold cases but faces accuracy, legal, and acceptance challenges.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

A specific gene mutation causes long hair in Angora rabbits.

Polycystic ovary syndrome, a disorder causing menstrual issues and infertility, can be treated with lifestyle changes, medication, herbal remedies, surgery, and assisted reproductive techniques like artificial insemination and IVF.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

The skin systems of jawed vertebrates evolved diverse appendages like hair and scales from a common structure over 420 million years ago.

Our microbiome may affect the development of the hair loss condition Alopecia Areata, but more research is needed to understand this relationship.

Too much epidermal growth factor can cause hair loss.

Certain genes are linked to the quality of cashmere in goats.

Androgens and a high-fat diet may increase the risk of severe COVID-19 in women with PCOS by upregulating certain proteins in the heart and kidneys.

Ring Chromosome 11 may be linked to conditions like early puberty, excessive hair growth, hair loss, and type 2 diabetes.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

There is no causal relationship between androgenetic alopecia and serum uric acid.

Mesenchymal stem cells could help treat aging-related diseases better than current methods.

Sons of mothers with polycystic ovary syndrome (PCOS) have a higher risk of obesity and insulin resistance, possibly due to certain genes and factors passed down from their mothers.

Deleting the EDAR gene in Cashmere goats affects genes and proteins related to hair growth.

FGF12 is important for hair growth and could be targeted for hair loss treatment.

Melatonin helps broccoli roots produce anti-cancer compounds by controlling nitric oxide and hydrogen peroxide levels.

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

Gut bacteria may affect hair loss risk.

Chromosomal microarray analysis is important for diagnosing rare genetic variations and guiding treatment.

Key genes and pathways improve wool quality in Zhexi Angora rabbits.

Afro-textured hair needs personalized care due to its unique genetic traits.