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Muse cells keep their special features and can become different cell types even after being frozen and thawed three times.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

Ruxolitinib helped a woman with a genetic mutation regrow her hair and improved her health.

Gene variations may increase oxidative stress in male pattern baldness.

Consider NF1 in newborns with rare congenital anomalies.

The trial aims to understand how obesity and lifestyle affect circadian rhythms in people with schizophrenia and bipolar disorder.

KRTAP6 genes affect wool quality in sheep.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Acne patients have higher mTOR gene expression.

Reticulocyte hemoglobin content is the best indicator of iron deficiency causing hair loss in women.

Removing REDD1 in mice increases skin fat by making fat cells larger and more numerous.

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Hair follicles can be used to quickly assess drug effects in cancer treatment.

An 86-year-old man with prostate cancer was diagnosed with a rare, low-grade breast cancer and underwent surgery but declined additional hormone therapy.

ANp63 is crucial for skin integrity, new filaggrin gene mutations link to eczema, hair can regrow from non-stem cells, sunburns are increasing, and glucocorticoids help treat skin allergies by affecting immune cells.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Mutations in the hairless gene cause a rare form of permanent hair loss.

A new DSG4 gene mutation causes hair defects in a young girl.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

Researchers found a new mutation in the HR gene causing hair loss and skin bumps in a Pakistani family.

Early diagnosis and comprehensive management improve life quality for Netherton syndrome patients.

Sweat glands and hair follicles are determined by opposing signals, with BMPs promoting sweat glands and blocking BMPs leading to hair follicles.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

PTCH gene mutations contribute to basal cell carcinoma development.

TGF-β signaling is crucial for stem cell maintenance, differentiation, and has implications for cancer treatment.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Researchers developed a method to grow hair follicles using special beads that could help with hair loss treatment.

Researchers developed a 3D model of human hair follicle cells that can help understand hair growth and test new hair loss treatments.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.