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A new mutation in the hairless gene causes hair loss and skin wrinkling in mice.

Low birthweight and rapid weight gain after birth may increase the risk of developing polycystic ovary syndrome.

Diagnosing PCOS in teenage girls is tricky and requires careful evaluation and management.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

HPV genes and estradiol increase a cancer-related signaling pathway, which may be targeted for cervical cancer treatment.

MC4R gene variants not linked to female hair loss.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

Astrotactin proteins are important for brain and skin development and are linked to several neurodevelopmental disorders.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

White piedra, a rare fungal infection, was diagnosed in two women in a northern climate.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

A specific group of slow-growing stem cells marked by Thy1 is crucial for skin maintenance and healing in mice.

Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Genetic variants affect minoxidil hair loss treatment success.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

The document concludes that patients with skin of color need specialized dermatological care and education to manage unique skin conditions effectively.

Two mouse mutations cause similar hair loss despite different skin changes.

Certain bacteria can boost lentil growth and improve soil used for farming.

STAT3 signaling is important for healthy skin and hair follicles, and its disruption can lead to skin conditions like atopic dermatitis.

Dermal EZH2 controls skin cell development and hair growth in mice.

3D culture helps maintain hair growth cells better than 2D culture and identifies key genes for potential hair loss treatments.

Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

Adding yeast extract and methyl jasmonate to Eclipta alba cell cultures increased the production of the compound wedelolactone.

Notch1 signaling is crucial for improving wound healing and skin regeneration by affecting stem cell behavior.