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A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

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

A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Activating β-catenin in mammary cells leads to changes that cause early-stage abnormal growths similar to skin structures.

Different forms of FGF5 either promote or inhibit hair growth.

High doses of Lepidium sativum seed extract are toxic and should be used with caution.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

AP-2α and AP-2β proteins are essential for healthy adult skin and hair.

Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

Hutchinson-Gilford Progeria Syndrome causes rapid aging from a genetic mutation, with no cure but ongoing research into potential treatments.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Plant roots respond to fungus smells by possibly using certain proteins and a plant hormone to change root growth, but more research is needed.

Personalized treatment based on detailed tumor analysis successfully managed and reduced the patient's aggressive hair follicle cancer.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

The document tests knowledge and decision-making in hematology through multiple-choice questions.

The document provides 70 multiple choice questions to improve haematology skills.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Specialized ribosomes affect aging in human skin cells.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.