Search

everythinglearnresearchcommunity

for

Search:↓

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

The Korean study found that twenty-nail dystrophy mainly affects adults, more often women, and has five distinct types with different clinical progressions.

The human scalp has different types of pigment cells in hair follicles with varying abilities to produce pigment.

Small white dots on the scalp seen with a dermoscope correspond to sweat ducts and vary with different hair disorders.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

Onychomatricoma is a unique nail tumor, not related to other hair-related tumors.

A keratin hHb6 mutation causes a hair disorder with varying severity, influenced by other factors.

Cystic panfolliculoma resembles hair follicle tumors due to specific cell interactions.

New findings suggest potential treatments for melanoma, hyperpigmentation, hair defects, and multiple sclerosis, and show skin microbiome changes don't cause atopic dermatitis.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

MicroRNA-200 prevents sebaceous gland development by inhibiting SOX9 and cell cycle progression.

A person had two different benign skin tumors, a trichoadenoma and melanocytic naevi, at the same time but in different places on the face.

Specific miRNA profiles can help diagnose and treat alopecia areata.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

The nodule on the woman's back was a benign hair follicle tumor, not cancer, but needed removal.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Certain microRNAs may protect against hair loss in alopecia areata and could be potential treatment targets.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Multiple perifollicular fibromas may actually be unrecognized cases of Birt-Hogg-Dubé syndrome.

Vigorous rubbing of herbal powder on the scalp caused hair damage and loss.

Researchers found a gene mutation responsible for a rare hair loss condition.

A woman had a rare, non-cancerous skin growth on her face, which was removed and did not come back after a year.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

Sentinel lymph node biopsy is recommended for all types of desmoplastic melanoma due to higher rates of nodal metastasis.

A woman with severe hypothyroidism had a rare skin condition usually linked to a different thyroid disease.

Different types of female pattern hair loss have unique characteristics and are associated with various 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.

A new type of alopecia areata, called the "confetti variant," causes small bald spots that often heal on their own in a few months.

Lower MC2R expression may contribute to alopecia areata.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.