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Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Most dogs with alopecia had higher than normal levels of certain hormones, but hair loss might not always be linked to these hormone changes.

The document concludes that new treatments for skin conditions are complex but effective, including spironolactone for female hair loss and propranolol for infantile hemangiomas.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

The reviews critique three psychology books, noting skepticism about a personality inventory for teens, praising a practical guide on body image issues, and recommending a book on grief therapy.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

The document concludes that treating skin conditions should include psychological care and a multidisciplinary approach is essential for effective management.

The document suggests that Alopecia X in dogs is mainly a cosmetic issue and might be better left untreated.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

In June 2019, the stem cell research field saw major progress, including new clinical trials, FDA approvals, and industry collaborations.

Hyperadrenocorticism in ferrets is linked to neutering and indoor housing, and is best treated with surgery and a deslorelin implant.

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

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Children with scalp fungal infections need proper diagnosis and treatment, usually with antifungal medications, and newer drugs may offer quicker recovery.

The document suggests medicine should integrate biological and cultural factors and focus on holistic, equitable care.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Choline and biotin are important for liver health and preventing certain deficiencies in animals, and more research is needed to understand their benefits in humans.

Children with cancer had slightly more unusual facial shapes than healthy kids, but not enough to easily tell them apart.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

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

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

IL-1 family cytokines are crucial for skin defense and healing, but their imbalance can cause skin diseases.

Researchers found genes and genetic variants linked to sheep wool and skin wrinkles.

Geriatric Julia Creek dunnarts often suffer from reproductive and skin diseases, impacting conservation efforts.

Tet2 and Tet3 enzymes are important for controlling hair growth and shape by affecting gene activity and DNA structure in hair follicles.

A 9-year-old Hispanic girl has Uncombable Hair Syndrome, which may improve with age and biotin treatment.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.