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research Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.

30 citations , June 1993 in “The Journal of Cell Biology”

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

Characterization, Genomic Organization, Expression, and Function of the mEphA1 Receptor Tyrosine Kinase

research Characterisation, genomic organisation, expression and function of the mEphA1 receptor Tyrosine Kinase

April 2007

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.

research BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin

117 citations , August 1999 in “Nature Genetics”

research Association between TLR1 polymorphisms and alopecia areata

20 citations , April 2014 in “Autoimmunity”

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

research A BIOCHEMICAL MARKER IN A DOMINANT MOUSE TRAIT

April 1974 in “Pediatric Research”

The Naked (N) trait in mice is linked to lower glycine and tyrosine in hair proteins.

research 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility

April 2017 in “Journal of Investigative Dermatology”

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

research A computationally inferred regulatory heart aging model including post-transcriptional regulations

1 citations , December 2016

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

research The calcium-binding protein calretinin is a marker of the companion cell layer of the human hair follicle

26 citations , June 2005 in “British Journal of Dermatology”

Calretinin identifies the companion cell layer in human hair follicles.

research Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency

24 citations , July 2014 in “Journal of Investigative Dermatology”

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

research Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis

59 citations , November 2011 in “Development”

Trps1 is essential for proper hair follicle development.

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