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The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

MOF controls skin development by regulating genes for mitochondria and cilia.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Minoxidil treatment improves heart defects in a DiGeorge syndrome model.

The document concludes that inflammation markers can be used in diabetes, vitamin D3 affects immune pathways, hyperthyroidism changes hormone levels, androgen levels help diagnose Adrenocortical Carcinoma, erectile dysfunction is linked to diabetes, hypogonadism is common in HIV-infected males, and hormones can be biomarkers for various conditions.

The mesenchyme can start hair growth, but the exact signal that causes this is still unknown.

The gene Ascl4 is not necessary for the development of hair, teeth, or mammary glands.

The conclusion is that analyzing RNA from skin oils is a promising way to understand skin diseases.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

Primary cilia affect the size and oil production of eye glands but not the oil's makeup.

A protein called EGFR protects hair follicle stem cells, and when it's disrupted, hair follicles can be damaged, but blocking certain pathways can restore hair growth.

Different fish use the same genes to regrow teeth.

Alopecia Areata is an autoimmune condition causing hair loss, influenced by genetics, environment, and possibly improved by anti-MIF therapy, with many patients experiencing regrowth within a year.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

HAIR may cause fetal loss by triggering different cell death processes in the uterus and placenta.

Rapamycin may help treat Leigh syndrome by targeting protein kinase C.

The gene Prss53 affects hair shape and bone development in rabbits.

Early regulatory T cells are crucial for normal skin pigmentation.

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

Gene therapy in mice increased lifespan and improved health without causing cancer.

Too much β-catenin activity can mess up the development of mammary glands and make them more like hair follicles.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Climate-related nutritional stress may cause hair loss in juvenile male Guadalupe fur seals.

Many hair transplant patients are unhappy due to clinical mistakes and the need for better training of surgical assistants is crucial.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.