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A Disease-Causing Novel Missense Mutation in the ST14 Gene Underlies Autosomal Recessive Ichthyosis with Hypotrichosis Syndrome in a Consanguineous Family

research A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family

9 citations , March 2018 in “European journal of dermatology/EJD. European journal of dermatology”

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

An Update on Congenital Adrenal Hyperplasia

research An Update of Congenital Adrenal Hyperplasia

151 citations , December 2004 in “Annals of the New York Academy of Sciences”

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

research Synchronous profiling and analysis of mRNAs and ncRNAs in the dermal papilla cells from cashmere goats

17 citations , June 2019 in “BMC genomics”

Non-coding RNAs help control hair growth in cashmere goats.

research An X-Linked Gene Involved in Androgenetic Alopecia: A Lesson to Be Learned from Adrenoleukodystrophy

24 citations , January 2000 in “Dermatology”

Gene linked to common hair loss found, may lead to new treatments.

research Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family

April 2024 in “Anais Brasileiros de Dermatologia”

Hunting the Hair Cycle Clock: Evidence That Mitochondrially Localized MPZL3 Is a Key Element in Murine and Human Hair Follicles

research 715 Hunting the hair cycle clock (HCC): Evidence that mitochondrially localized MPZL3 is a key HCC element in murine and human hair follicles

July 2022 in “The journal of investigative dermatology/Journal of investigative dermatology”

MPZL3 is important for controlling the hair growth cycle in mice and humans.

research The Peripheral Clock Regulates Human Pigmentation

81 citations , October 2014 in “The journal of investigative dermatology/Journal of investigative dermatology”

Certain genes control the color of human hair by affecting pigment production.

research Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation

October 2023 in “Case reports in dermatological medicine”

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

research Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan

August 2020 in “Pakistan Journal of Zoology”

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

research Hairless controls hair fate decision via Wnt/β–catenin signaling

6 citations , July 2017 in “Biochemical and Biophysical Research Communications”

The Hairless gene is crucial for hair cell development, affecting whether skin cells become hair or skin and oil gland cells.

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