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The compound (NH4)2Mn0.17Cu0.83Cl4.2H₂O has a specific structure, shows weak magnetism at low temperatures, and undergoes phase changes at high temperatures.

Disruptions in mammary stem cell division can lead to cancer, but targeting these processes might help treat breast cancer.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A new mouse mutation causes skin and hair issues, influenced by another gene.

CD10 helps distinguish between basal cell carcinoma and benign hair follicle tumors.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

The LMNA mutation affects skin structure even in asymptomatic carriers.

SCD1 is crucial for skin health and overall energy balance.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A girl with Crohn's disease had a hairball causing bowel obstruction, which was removed, and she recovered well.

CD34+ and CD34- melanocyte stem cells have different regenerative abilities.

MSUD patients need careful monitoring of amino acids and zinc to prevent severe symptoms.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Certain genes are linked to the risk of developing Alopecia Areata.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Diagonal earlobe crease and lipoprotein(a) together help diagnose coronary heart disease.

16-MHA can restore the barrier and moisture of damaged hair, making it similar to undamaged hair.

Different enzymes are active in different parts of developing mouse organs.

TCDD speeds up skin barrier formation by increasing certain gene expressions.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

LDE225 is a promising skin-applied treatment for basal cell carcinoma with good skin penetration and effectiveness.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

Anti-Müllerian hormone is a specific marker for ovarian issues in women with conditions like PCOS.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

Deleting the MAD2L1 gene is tolerated in certain mouse cancer models.

Adalimumab significantly improves quality of life for patients with moderate to severe hidradenitis suppurativa.

The lentiviral array can monitor and predict gene activity during stem cell differentiation.

Combining DHT and EDC improves the strength and stability of PADM scaffolds for tissue engineering.