Search

everythinglearnresearchcommunity

for

Search:↓

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Hair keratin-associated proteins are essential for strong hair, with over 80 genes showing specific patterns and variations among people.

Oestrogens help maintain healthy skin, heal wounds, and may protect against skin aging and cancer.

Lamins are vital for cell survival, organ development, and preventing premature aging.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

Type 3 5α-reductase is more common and finasteride and dutasteride strongly inhibit it.

The conclusion suggests that prostate cancer should be classified by castration status and that new therapies targeting androgen receptor signaling show promise.

The document concludes that identifying the cause of amenorrhea is crucial for proper treatment.

Amenorrhea is when a woman doesn't have periods, with primary amenorrhea starting by age 15 or within five years of breast development, and secondary amenorrhea when periods stop for three months. It affects 3-4% of women not pregnant, breastfeeding, or in menopause, mainly due to polycystic ovary syndrome, hypothalamic amenorrhea, hyperprolactinemia, and ovarian failure.

DNA methylation changes are linked to hair growth cycles in goats.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

Mutations in certain receptors can cause diseases and offer new treatment options.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Amenorrhea, or the absence of periods, should be evaluated by age 15 or within five years of early breast development, and is most commonly caused by conditions like polycystic ovary syndrome and hypothalamic amenorrhea.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

The extract from Bacillus/Trapa japonica fruit helps increase hair growth and could be a potential treatment for hair loss.

Stem cell therapies show promise for treating various diseases but face challenges in clinical use and require better monitoring techniques.

Selective breeding caused the unique curly hair in Mangalitza pigs.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

The document explains the difficulty in diagnosing and treating brain diseases caused by the immune system and stresses the need for quick and accurate tests.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Different types of skin stem cells can change and adapt, which is important for developing new treatments.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.