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EDA signaling is linked to skin disorders, various cancers, and liver disease.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Fibronectin-attached cell sheets improve wound healing and are safe and effective.

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

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

Edar signaling is crucial for proper hair follicle development and function.

FGF13 gene changes cause excessive hair growth in a rare condition.

Lipocalin-Type Prostaglandin D2 Synthase (L-PGDS) is a protein that plays many roles in the body, including sleep regulation, pain management, food intake, and protection against harmful substances. It also affects fat metabolism, glucose intolerance, cell maturation, and is involved in various diseases like diabetes, cancer, and arthritis. It can influence sex organ development and embryonic cell differentiation, and its levels can be used as a diagnostic marker for certain conditions.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

Overexpression of FGF5s makes Chinese Merino sheep grow longer and heavier wool.

AE can have varied symptoms and genetic causes, but zinc therapy helps.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

Low oxygen areas help maintain and protect blood stem cells by using a simple sugar breakdown process for energy and managing their activity levels.

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

Vitamin D is important for bones, hair, blood pressure, and breast development.

Activating the Sonic hedgehog gene in mice can start the hair growth phase.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Overexpressing follistatin in mice delays wound healing and reduces scar size.

Fibroblast Growth Factors (FGFs) are important for tissue repair and regeneration, influencing cell behavior and other factors involved in healing, and are crucial in processes like wound healing, bone repair, and hair growth.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Bimatoprost is effective for growing longer, thicker, and darker eyelashes.

Loss of OGG1 increases skin inflammation and auto-antibodies in lupus.

Edar signaling is crucial for controlling hair growth and regression.

PPAR-γ helps control skin oil glands and inflammation, and its disruption can cause hair loss diseases.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

Hair becomes gray and thin as we age, and while most hair loss in older people is due to genetics, there's a chance for gray hair to regain color under certain conditions.

Overactivating Hedgehog signaling makes hair follicle cells in mice grow hair faster and create more follicles.