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Poplar seed hairs grow from the placenta at the ovary base, with endoreduplication playing a key role in their development, and share similar cellulose synthesis processes with cotton fibers.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

Found different proteins in balding and non-balding cells, giving insight into hair loss causes.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

A specific RNA molecule, circCOL1A1, affects the growth and quality of goat hair by interacting with miR-149-5p and influencing cell growth pathways.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

A 19-year-old male had two rare skin conditions causing scarring and permanent hair loss.

Recent selection on immune response genes was identified across seven ethnicities.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

The peach gene pCTG134 helps control the interaction between auxin and ethylene hormones during fruit ripening.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

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 protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Autism's genetics are linked with early age of puberty and less hair loss, but not with hormone levels or polycystic ovary syndrome.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The vitamin D receptor can work without its usual activating molecule.

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

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

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

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

New genetic mutations linked to rare skin disorders were found in three newborns.

hsa-miR-193a-5p may help diagnose and treat alopecia areata.

Lhx2 is a crucial regulator of the Sonic Hedgehog signaling in early mouse retinal development.

Hair follicles may soon be used more for targeted and systemic drug delivery.

The best method for transplanting skin cells to regenerate hair follicles is the Hemi-vascularized sandwich method, as it produces more mature follicles and promotes hair growth.

Tissue-derived extracellular vesicles are crucial for cancer diagnosis, prognosis, and treatment.