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Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Zebrafish need MYC and FGF to regenerate inner ear hair cells.

Skin organoids from stem cells could better mimic real skin but face challenges.

PRX01, PRX44, and PRX73 are essential for root hair growth in Arabidopsis thaliana.

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.

Vitamin D and calcium are essential for normal hair growth.

Activating Nrf2 can help protect against hearing loss.

Cutaneous gene therapy could become a viable treatment for skin and hair disorders with improved vector development and gene expression control.

Mice without certain skin enzymes have faster hair growth and bigger eye glands.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

The document concludes that a systematic approach is crucial to identify causes of androgen excess in women beyond the most common cause, Polycystic ovary syndrome (PCOS).

A specific gene mutation causes Olmsted syndrome.

The workshop discussed the role of a protein called calreticulin in health and disease, its potential as a treatment target, and its possible use as a disease marker.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

SOX9 is essential for the development of various organs and hair follicles.

Adding a second method to PROTACs could improve cancer treatment.

When skin blisters, healing the wound is more important than growing hair, and certain stem cells mainly fix the blisters without helping hair growth.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

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

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

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

GDNF helps grow hair and heal skin wounds by acting on hair stem cells.