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Adolescent sexual development should focus on positive aspects, including biological, psychological, and contextual factors, and recognize individual differences and the role of pleasure.

New genetic variants linked to albinism were found in Pakistani families.

A specific gene variant may increase the risk of developing Alopecia Areata.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

Computer vision techniques can help detect and assess skin conditions like vitiligo, alopecia areata, and dermatitis.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

A botanical extract blend improved skin and scalp health in women working outdoors.

MicroRNAs and AI can improve cashmere goat hair quality and aid in hair disorder diagnosis.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Some women with PCOS have rare genetic variants linked to the condition.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Cancer prevention is crucial, with a focus on research and improved screening methods.

Dihydroartemisinin could be a versatile cosmetic ingredient but needs more research and development.

A genetic variant in "Blonde d'Aquitaine" calves causes death at birth due to a missing protein.

Genetic variants in specific genes cause central centrifugal cicatricial alopecia.

New LSS gene variants help understand congenital hypotrichosis 14 better.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Iron deficiency can cause psychiatric symptoms that improve with proper treatment.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

A single robotic system can accurately harvest and implant hair grafts, showing promise for real-world use.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.