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Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

Cancer treatments targeting specific cells often cause skin, hair, and nail problems, affecting patients' lives and requiring careful management.

Researchers fixed gene mutations causing a skin disease in stem cells, which then improved skin grafts in mice.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Cytochrome P-450 enzymes in the skin help break down various substances and could be targeted to treat skin conditions.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Understanding how EDC genes are regulated can help develop better drugs for skin diseases.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

Porphyra-334 may help reduce wrinkles and promote hair growth.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

Skin issues can indicate immune system problems.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

Alopecia areata involves both innate and adaptive immunity, with specific genes linked to the disease.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Sheep have a unique gene, KAP8-2, that humans don't have, which may affect wool properties.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

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

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

Dehydroepiandrosterone (DHEA) is a prohormone important for producing sex steroids and has potential health benefits.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.