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Analysis of Hidradenitis Suppurativa-Linked Mutations in Four Genes and the Effects of PSEN1-P242LfsX11 on Cytokine and Chemokine Expression in Macrophages

research Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages

25 citations , December 2018 in “Human Molecular Genetics”

The document concludes that certain mutations may contribute to the inflammation in hidradenitis suppurativa and suggests that targeting TNFα could be a treatment strategy.

research Message from the 2017 Surgical Assistants Program Chair

January 2017 in “Hair transplant forum international”

The document's content could not be processed.

research Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome

71 citations , February 2012 in “The American Journal of Human Genetics”

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

Clinical Description of a Rare Dermatological Disease, Acne Keloidalis Nuchae, and Successful Homeopathic Management: A Case Report

research Clinical description of a rare dermatological disease, acne Keloidalis Nuchae, and successful homoeopathic management: A case report

5 citations , April 2021 in “International Journal of Homoeopathic Sciences”

Homeopathy improved Acne Keloidalis Nuchae in a 14-year-old.

research Frontal hairline design

November 2009 in “Cambridge University Press eBooks”

The document's conclusion cannot be provided because the content is not accessible.

research Current Protocols: Alopecia Areata Mouse Models for Drug Efficacy and Mechanism Studies

August 2024 in “Current Protocols”

The C3H/HeJ mouse model is useful for studying and testing treatments for alopecia areata.

research Quantitative Evaluation of Female Pattern Hair Loss in Chinese Women

September 2015 in “Dermatologic Surgery”

Computer-aided imaging system accurately measures baldness in Chinese women with hair loss.

research FLCN regulates transferrin receptor 1 transport and iron homeostasis

1 citations , January 2021 in “Journal of biological chemistry/The Journal of biological chemistry”

FLCN helps control iron levels in cells.

research FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation

60 citations , July 2014 in “Autophagy”

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

research Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome

44 citations , September 2011 in “Journal of Pediatric Gastroenterology and Nutrition”

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.

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