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Three different methods were compared for creating Titan cells, a type of fungus cell. The OZ method made the most cells initially, but the number dropped quickly. The EB method also made a lot of cells, but the number also dropped. The AA method made fewer cells, but the number stayed steady. The methods also affected which genes were active in the cells.

Connexin-26 gene mutations may increase cancer risk in KID syndrome patients.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

Vitamin E with oral contraceptives helps reduce PCOS symptoms by affecting hormone levels and stress.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

CEP135 may predict cancer outcomes, and targeting PLK1 could help treat certain sarcomas.

A DNA aptamer helps promote hair growth by enhancing a key cell growth signal in hair follicle cells.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

TICE salvage chemotherapy is effective for treating germ-cell tumors with poor prognosis.

TCDD changes skin cell growth and keratin production in mice.

Scientists found new and known long non-coding RNAs in mouse hair follicle stem cells that may be important for stem cell function and could be targets for cancer treatment.

Genetically modified sheep with more β-catenin grew more wool without changing the wool's length or thickness.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

ACOD1 deficiency worsens hair loss by causing cell aging and mitochondrial problems, but 4-OI may help.

A specific gene variant is linked to severe insulin resistance and hormone imbalance in a teenage girl.

The KRTAP36-1 gene affects wool quality in Chinese Tan lambs.

Longer CAG repeats in gene linked to more severe hair loss in females.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Four circRNAs were found to be significantly different in cashmere goat skin, affecting cashmere fineness.

Certain long non-coding RNAs are important for controlling hair growth cycles in sheep.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

Created large amounts of grape seed compounds using a new method.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

OCT can non-invasively diagnose follicular keratosis and other hair follicle disorders.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Ornithine decarboxylase is crucial for hair growth regulation in mice.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

TCDD reduces EGF receptors in the liver, affecting growth and development.