Search

everythinglearnresearchcommunity

for

Search:↓

The VDR gene polymorphism does not affect BDNF levels in autoimmune thyroiditis and hypothyroidism patients.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Targeting protein S-palmitoylation could lead to new skin disease treatments.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

A goat's skin infection was cured with itraconazole and D-biotin.

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

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

Untreated epidermolysis bullosa acquisita can cause total hair and nail loss.

A gene mutation causes monilethrix in a Chinese family.

Using both minoxidil and biotin together increased hair growth more than using either one alone.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Mutations in the DSG4 gene cause specific hair and scalp issues.

The patient's hair has unique structural differences with alternating bright and dark bands.

A Thai Bangkaew dog with diabetes and pancreatic issues improved with insulin, enzymes, and vitamins.

Alopecia Areata patients have too many Firmicutes and too few Bacteroides in their gut.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps due to a gene mutation.

Zinc deficiency causes skin issues and hair loss, treatable with zinc supplements.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

The enzyme system in hair follicles is similar to the liver's and is inhibited by certain substances.

Certain genetic variants in keratins increase the risk of tooth decay.

Immunological treatment improved both neuropathy and alopecia.

A gene mutation in mice causes severe skin disorder similar to a human condition.

A rare case of severe scalp hair loss and nail issues in keratosis follicularis was observed.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.