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The study found that certain mutations in the vitamin D receptor can cause rickets and potentially affect hair growth.

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.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

MED1 is essential for normal hair growth and maintaining hair follicle stem cells.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

Too much prolactin can cause menstrual problems, infertility, and sexual issues in women.

Some skin medications can harm male fertility, but they don't seem to cause birth defects from father's exposure.

The Itpr3 gene causes a specific hair pattern in mice.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

The topical finasteride spray was safe and well-tolerated with stable effects.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

Six new risk spots for early hair loss were found, which also link to Parkinson's disease and lower fertility. Two genes, FOXA2 and HDAC4, could be new treatment targets. Hair loss might also be connected to heart disease, metabolic syndrome, and prostate cancer.

People with Myotonic Dystrophy type 1 are more likely to have certain skin conditions, but not more likely to get skin cancer.

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

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Knocking out certain genes in mice helps understand skin and hair growth problems.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.

Porphyra-334 may help reduce wrinkles and promote hair growth.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

A rare genetic disease caused severe, worsening hair loss from early childhood with poor treatment results.

Histone modification is key in treating chronic inflammatory skin diseases.