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Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Further testing of paclitaxel poliglumex for this cancer treatment is not justified.

Benzo[c]quinolizin-3-ones are effective nonsteroidal inhibitors of human steroid 5α-reductase 1.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

New LSS gene variants help understand congenital hypotrichosis 14 better.

Using both DLQI and Skindex-16 together gives a better understanding of quality of life in skin disease patients.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.

SQSTM1 gene issues may increase the risk of alopecia areata.

The Dermatology Life Quality Index is reliable and consistent but needs more diverse participant studies.

The document's conclusion cannot be provided because the document is not available or cannot be read.

The Hair660™ light therapy device effectively and safely improves hair density in people with androgenetic alopecia.

Certain genetic variants in PRLR and PCCA genes may lead to shorter hair in cattle, which could help with heat tolerance.

A specific genetic variation affects wool quality in sheep.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.