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research Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood

12 citations , March 2012 in “JEADV. Journal of the European Academy of Dermatology and Venereology/Journal of the European Academy of Dermatology and Venereology”

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

research A Founder Mutation in the POMC 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA

4 citations , July 2022 in “The Journal of Clinical Endocrinology & Metabolism”

A specific genetic mutation causes POMC deficiency, leading to symptoms like weight gain and red hair.

research FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis

17 citations , June 2017 in “Gene”

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Novel Splice Site Mutation in the LIPH Gene in a Patient with Autosomal Recessive Woolly Hair/Hypotrichosis: Case Report and Published Work Review

research Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review

9 citations , February 2018 in “The Journal of Dermatology”

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

research Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review

3 citations , January 2013 in “Dermatology”

New genetic mutations causing hair loss were found in a Chinese family.

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community Solving Hair Loss with Research at MIT

in Research/Science 595 upvotes 1 year ago

Hair loss treatments like minoxidil, finasteride, TDM-105795, and PP405. MIT is hosting a hackathon to find innovative hair loss solutions.

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research Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood

research A Founder Mutation in the POMC 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA

research FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis

research Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review

research Atrichia with Papular Lesions in a Chinese Family Caused by Novel Compound Heterozygous Mutations and Literature Review

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community Solving Hair Loss with Research at MIT

community CRISPR Is Curing People Right Now. Genetic Hair Loss is Next?

community Alright boys, who’s willing to burn their scalp for science?

community Hope Medicine's HMI-115 could be out in 2027 per Company Founder

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