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The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Hidradenitis Suppurativa has genetic links, with certain gene mutations more common in patients and a third of cases having a family history.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Genetic marker rs12558842 strongly linked to male hair loss.

Heparan sulfate is important for hair growth, preventing new hair formation in mature skin, and controlling oil gland development.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Activin activation in skin cells speeds up wound healing without affecting scar quality.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

The rs6152 allele is not a good marker for baldness in the Indonesian population, but family history, age, gender, high blood pressure, and body weight are linked to the risk.

Certain gene variations may increase the risk of hair loss in Egyptians.

Certain gene variations and different levels of BDNF and CRH hormones are linked to vitiligo.

Some blood-thinning medications can increase the risk of bleeding, and certain factors like genetics and other health conditions affect their safety and effectiveness.

The absence of functional sebaceous glands causes hair follicle destruction and scarring alopecia.

Metformin works better for adolescent girls with PCOS who have certain genetic variations.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Using special RNA to target a mutant gene fixed hair problems in mice.

Oral contraceptive use may increase the risk of frontal fibrosing alopecia in women with a specific CYP1B1 gene variant.

The Orenburg goat breed has unique genetics that require more detailed research and careful breeding.

Certain variations of the HDAC9 gene can increase or decrease stroke risk in the Chinese population.

The STRIPAK complex is crucial for skin cell organization and creating a functional skin barrier.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The VEGF +405G allele may increase the risk of PCOS in South Indian women.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.