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The HATMSC1 cell line from fat tissue can produce helpful factors for regenerative and immune therapies.

The protein called small nuclear ribonucleoprotein polypeptide E is identified as a cause of a type of hair loss without other symptoms.

Overexpression of sPLA2-IIA in mouse skin reduces hair stem cells and increases cell differentiation through JNK/c-Jun pathway activation.

Two microRNAs in stem cell exosomes help treat hair loss by targeting a specific signaling pathway.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

HSP90 and lamin A/C are crucial for hair growth and could be targets for treating hair loss.

Skin cells can naturally limit the growth of cancerous changes by balancing cell renewal and differentiation.

MicroRNA-148a is crucial for maintaining healthy skin and hair growth by affecting stem cell functions.

JMJD3 and NF-κB activate Notch1, which is essential for skin cell movement and wound healing.

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

Zfp462 deficiency in mice causes anxiety-like behaviors and excessive self-grooming.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Understanding how acne develops in different diseases could lead to new treatments.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

1 alpha,25-dihydroxy-vitamin D3 and calcipotriol speed up cell differentiation in hair follicles.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

New treatments for immune disorders caused by FOXN1 deficiency are promising.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

Replacing defective mesenchymal cells with normal ones fixes thymic growth issues in 22q11.2DS mouse models.

A virus protein can activate a pathway that may lead to abnormal hair follicle development.

A new gene, mrp4, is found in mice and may play a unique role in hair follicle development in tails and ears.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Centipeda minima extract helps hair grow by activating important growth signals and could be a promising hair loss treatment.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

The fuzzy gene is crucial for controlling hair growth cycles.