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research Isolating subpopulations of human epidermal basal cells based on polyclonal serum against trypsin-resistant CSPG4 epitopes

2 citations , December 2016 in “Experimental cell research”

The research found a way to identify and study skin cells with stem cell traits, revealing they behave differently in culture and questioning current stemness assessment methods.

research Iron Screening in Alopecia Areata Patients May Catch Hereditary Hemochromatosis Early

October 2022 in “Cutis”

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

research Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”

5 citations , January 2002 in “European journal of pediatrics”

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

LSD1 Interacting With HSP90 Promotes Skin Wound Healing by Inducing Metabolic Reprogramming of Hair Follicle Stem Cells Through the c-MYC/LDHA Axis

research LSD1 interacting with HSP90 promotes skin wound healing by inducing metabolic reprogramming of hair follicle stem cells through the c‐MYC/LDHA axis

1 citations , June 2023 in “The FASEB journal”

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

research The molecular basis of human keratin disorders

79 citations , February 2009 in “Human Genetics”

research HHV-6A and HHV-6B in Drug-Induced Hypersensitivity Syndrome/Drug Reaction with Eosinophilia and Systemic Symptoms

2 citations , January 2014 in “Elsevier eBooks”

The document concludes that reactivation of herpesviruses, especially HHV-6, is linked to severe symptoms and complications in drug-induced hypersensitivity syndrome.

research Novel RNF113A Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother

January 2026 in “American Journal of Medical Genetics Part A”

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

research Lower prostate cancer risk in Swedish men with the androgen receptor E213 A-allele

February 2017 in “Cancer Causes & Control”

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

research A Complex Clinical Situation in Polycystic Ovary Syndrome: HAIR‐AN Syndrome ‘‘Case Report’’

January 2025 in “Case Reports in Medicine”

Early detection, consistent management, and lifestyle changes are crucial for managing HAIR-AN syndrome effectively.

research An endocrinopathy characterized by dysfunction of the pituitary-adrenal axis and alopecia universalis: supporting the entity of a triple H syndrome

1 citations , September 2002 in “European Journal of Endocrinology”

Triple H syndrome exists and can vary in symptoms.

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