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As skin cells mature, vitamin D receptor levels decrease while retinoid X receptor α levels increase.

KLHL24-mutant stem cells help understand skin and heart disease.

Pmg-1 and Pmg-2 are new genes important for skin and mammary gland development.

Sdr16c5 and Sdr16c6 genes regulate a key point in lipid production that affects eye and skin gland function.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Radiation damages hair stem cells and changes keratin expression, with Krt5 as a potential marker for radiation effects.

Dermal EZH2 controls skin cell development and hair growth in mice.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

SGK1 is important in cancer growth and treatment resistance, and targeting it could improve therapies.

Alpha-ketoglutarate protects rabbit skin cells from oxidative damage by activating a specific cell pathway.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

New treatments targeting specific genes show promise for treating keratin disorders.

Egfl6 is not needed for zebrafish face development.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe symptoms and organ damage in mice.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

SMR-2 and SMR-6 are much more toxic than retinoic acid, causing severe side effects.

The newborn with Klippel-Trénaunay syndrome was healthy but needed regular check-ups for possible complications.

A gene variation is linked to hair thickness in Asians.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

p2y5, now called LPA6, is a receptor important for human hair growth.

Keratin 17 is crucial for normal hair growth by regulating hair cycle transitions with TNFα.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.