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Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

The 190-kbp domain contains all human type I hair keratin genes, showing their organization and evolution.

Conductive hydrogels show promise for medical uses like healing wounds and tissue regeneration but need improvements in safety and stability.

The document concludes that while there are promising methods to control CRISPR/Cas9 gene editing, more research is needed to overcome challenges related to safety and effectiveness for clinical use.

Exosomes can improve skin health and offer new treatments for skin repair and rejuvenation.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

pH, calcium, and reactive oxygen species regulate plant cell growth, with key roles for NADPH oxidases and plasma membrane H+-ATPases.

Steroid Sulfatase inhibitors show promise in treating hormone-dependent disorders like cancers, hair loss, and acne, with 667COUMATE being a potential candidate for breast cancer treatment trials.

New androgen receptor modulators show promise for treating diseases like prostate cancer and muscle wasting.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Minoxidil mixed with 2-hydroxypropyl-β-cyclodextrin in water can improve hair growth more than minoxidil alone.

The study found new details about human hair growth and suggests that preventing a specific biological pathway could potentially treat hair graying.

Researchers found two new genetic variants linked to Alzheimer's disease.

Pantothenic acid helps mink hair follicles grow by affecting certain cell signals.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

Mice genetically modified to produce more Del1 protein had faster hair regrowth.

Adjusting estradiol-ANGPT2 levels can promote hair growth in female pattern hair loss.

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

Inducing ferroptosis in hepatic stellate cells is crucial for treating liver fibrosis.

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

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

A new mutation in the TMEM173 gene and a risk allele in IFIH1 cause a unique set of immune-related symptoms.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

ZDHHC13 is important for normal liver function and metabolism, affecting mitochondrial activity.

Researchers found 15 new genetic links to skin traits in Japanese women.

Different types of androgens bind differently to two receptors, AR1 and AR2, in Atlantic croaker's brain and ovarian tissues, suggesting these receptors may control different androgen actions in fish.

Mice that can regenerate tissue have cells that pause in the cell cycle, which is important for healing, similar to axolotls.