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The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

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.

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

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.

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.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

Researchers found genes that may explain why some pigs grow winter hair, which could help breed cold-resistant pigs.

Researchers found genes linked to feather growth speed in Shouguang chickens, highlighting two genes that might explain differences in feathering.

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.

The research found specific genes that may cause longer hair in Tianzhu White Yak.

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

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

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

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.

Taking Propecia might lead to the development of cataracts.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Hair samples can be used to create stem cells easily and non-invasively.

Finasteride, often used for hair loss, can potentially cause cataracts.