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Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

Low ERCC3 gene activity is linked to non-pigmented hair growth.

Different types of skin stem cells can change and adapt, which is important for developing new treatments.

The timing of when the gene Bmal1 is active affects aging and survival, with its absence during development, not adulthood, leading to premature aging.

Disrupting Smad4 in mouse skin causes early hair follicle stem cell activity that leads to their eventual depletion.

Hair greying is linked to reduced ATM protein in hair cells, which protects against stress and damage.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

MOF controls skin development by regulating genes for mitochondria and cilia.

People's decision-making can be influenced by their internal biological clocks, as shown by gene expression, not just self-reported preferences for morning or evening.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Understanding gene expression in hair follicles can reveal insights into hair growth and disorders.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Cat color patterns are determined early in development by gene expression and epidermal changes, with the Dickkopf 4 gene playing a crucial role.

Researchers found WNT10A to be a key gene in developing goat hair follicles.

ELL is crucial for gene transcription related to skin cell growth.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

The conclusion is that the nuclear lamina and LINC complex in skin cells respond to mechanical signals, affecting gene expression and cell differentiation, which is important for skin health and can impact skin diseases.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

FOXN1 gene variants cause low T cells and immune issues from birth.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

The gene p53 is crucial for removing damaged cells to allow for healthy tissue renewal.

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

FoxN1 gene is essential for proper thymus structure and preventing hair loss.