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Gene variation affects prostate issues and hair loss.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

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

Anti-Desmocollin 3 antibodies can cause pemphigus-like symptoms in mice.

Loss of Desmocollin 3 in mice causes skin blisters and hair loss.

Hair follicle-derived IL-7 and IL-15 are crucial for maintaining skin-resident memory T cells and could be targeted for treating skin diseases and lymphoma.

The document concludes that recent research has improved understanding of skin diseases and the balance between cell growth and differentiation in the epidermis.

Intestinal intraepithelial lymphocytes are crucial for gut immunity and maintaining the mucosal barrier.

PROTO1 and PROTO2 protect against hearing damage.

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

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Scientists created a functional 3D skin system from stem cells that can be transplanted into wounds.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

New mouse models of Pemphigus show severe symptoms and need better treatments.

Different types of resting melanocyte stem cells have unique characteristics and vary in their potential to become other cells.

Meibomian glands are highly specialized and differ significantly from other sebaceous glands in structure and function.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Herpes simplex virus infections should be considered in pemphigus patients to avoid unnecessary changes in treatment.

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

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Activating c-Myc in skin causes rapid cell growth and changes, but these effects are reversible.

Phosphorylation controls TFEB's location in the cell, affecting cell metabolism and stress response.

TGF-β2 helps activate hair follicle stem cells by counteracting BMP signals.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

YAP and TAZ are crucial for skin cell growth and repair.

Notch signalling helps skin cells differentiate and prevents tumors.

Colorectal cancer development involves both genetic changes and epigenetic alterations like DNA methylation and microRNA changes.