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The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

Blood tests can help understand the genetic differences in people with alopecia areata, including how severe it is and if it's inherited.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

The gene Foxq1, controlled by Hoxc13, is crucial for hair follicle differentiation.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Machine learning is effective in predicting gene functions and their relationships with diseases.

HOXC13 is essential for hair and nail development by regulating Foxn1.

The OVOL1 gene, controlled by β-catenin, is crucial for creating hair follicles.

Certain gene variations increase male hair loss risk, influenced by hormone levels.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

The research found that a complex gene network, controlled by microRNAs, is important for hair growth in cashmere goats.

SOX9 is essential for the development of various organs and hair follicles.

Narrowband UVB treatment increases certain gene expressions in psoriasis skin and improves symptoms.

Finasteride may help treat childhood brain tumors by activating certain genes.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

The SbbHLH85 protein helps sweet sorghum grow more root hairs but makes the plant more sensitive to salt.

Mutant mice help researchers understand hair growth and related genetic factors.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Genetic research has advanced our understanding of skin diseases, but complex conditions require an integrative approach for deeper insight.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

Disrupting Notch signaling in blood vessels increases scarring during wound healing in mice.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.