Search

everythinglearnresearchcommunity

for

Search:↓

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

The study created hair-bearing skin models that lack a key protein for skin layer attachment, limiting their use for certain skin disease research.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

C-tactile afferents are linked to emotional touch and social bonding through hair movement.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Stem cell differentiation involves gradual chromatin changes and dynamic gene activity.

E6/E7 oncogenes in hair follicles cause continuous hair growth by skipping the resting phase.

Basal cell carcinoma shows keratin patterns similar to hair follicle structures.

Two new gene mutations cause a rare hair disorder.

Scientists created keratinocyte cell lines from human hair that can differentiate similarly to normal skin cells, offering a new way to study skin biology and diseases.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

Lentiviral vector effectiveness in skin is influenced by external factors, not receptor availability.

Stem cells compete for space using cell adhesion, and mutations can affect their competitive success, with implications for tissue health and disease.

TB and BCC tumors show similar follicular differentiation patterns.

Blocking α1-integrin makes adult fibroblasts more like foetal ones, improving their movement and aiding wound healing.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

CD4+ skin cells may be precursors to basal cell carcinoma.

CD200 is not a reliable marker for identifying stem cells in all skin types.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Researchers found a specific T cell receptor linked to severe drug reactions like Stevens-Johnson syndrome when patients take carbamazepine.

Touch sensitivity in mouse skin decreases during hair growth due to changes in touch receptors.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Skin cells might help spread prion diseases like Creutzfeldt-Jakob disease.

Different people show different symptoms for genetic diseases because of how sensitive their bodies are to small changes in important factors.

The keratin 5 mutation in a family with epidermolysis bullosa simplex was due to mosaicism, not a new mutation.

A unique skin cell similar to hair bulb melanocytes was identified, with better preservation using permanganate fixation.