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Keratinocytes in hair follicles differentiate similarly to skin cells, with specific patterns in different regions.

Lack of TrkC receptor delays hair follicle development.

Reduced matriptase activity causes skin and hair issues in both humans and mice.

A specific type II hair keratin was identified and found in hair cortex and tongue cells.

Short-term treatment with ROCKi increases skin cell growth without changing stem cell features.

LHX2, with other markers, can identify hair placodes in rats.

Hair germ cells differ from epidermal cells in keratin expression, and specific keratins form after hair differentiation.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

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

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

A man with a rare skin condition and a new gene mutation developed high calcium levels due to his treatment.

Terbinafine effectively treated kerion celsi despite disrupted immune responses.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

Upadacitinib effectively treats pyoderma gangrenosum.

The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

The protein p53 directly reduces the production of Keratin 17, a skin and hair protein, in rats with radiation dermatitis.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

AGD1 is important for root hair development in Arabidopsis, working with phosphoinositide signaling and the actin cytoskeleton.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

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

mTORC2 is crucial for healthy skin barrier by regulating lipids and filaggrin.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

Mutant MK6a transgenes in mice cause blistering, hair loss, and potential human alopecia.

Wnt7a helps corneal cells grow and stick together, aiding in repair.

BLTP1 and KIF27 gene mutations can help breed better wool sheep.

Combining hair transplantation with PRP is more effective for treating hair loss than hair transplantation alone.

The gene Prss53 affects hair shape and bone development in rabbits.

ROOT HAIR SPECIFIC 10 (RHS10) reduces the length of root hairs in Arabidopsis plants.

TRP channels in the skin are important for sensation and health, and targeting them could help treat skin disorders.

PEG and keratin scaffolds can effectively deliver protein drugs by controlling release based on pH levels.