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A Frameshift Insertion in SGK3 Leads to Recessive Hairlessness in Scottish Deerhounds: A Candidate Gene for Human Alopecia Conditions

research A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions

10 citations , March 2019 in “Human Genetics”

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

research Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS

6 citations , December 2021 in “International Journal of Endocrinology”

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

research Lecture Synopsis: Critical and Non-critical Factors in Recipient Site Creation and Graft Placement

January 2016 in “Hair transplant forum international”

The key points for successful grafting are how the recipient site is prepared and how the graft is placed.

research Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor

50 citations , September 2009 in “Molecular Genetics and Metabolism”

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

research Genetic association of HLA‐DQB1 and HLA‐DRB1 polymorphisms with alopecia areata in the Italian population

35 citations , June 2011 in “British Journal of Dermatology”

The DQB1*03 allele is linked to higher alopecia areata risk in Italians.

research Faculty Opinions recommendation of Association of topical minoxidil with autosomal recessive woolly hair/hypotrichosis caused by LIPH pathogenic variants.

July 2020 in “Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature”

research The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis

11 citations , April 2012 in “Journal of Investigative Dermatology”

A specific mutation in PA-PLA1α causes abnormal hair growth.

research Close Shave for a Keratin Disorder—K6hf Polymorphism Linked to Pseudofolliculitis Barbae

12 citations , March 2004 in “Journal of Investigative Dermatology”

research 96 Hair Restoration

January 2015

The document cannot be summarized as it is not provided or is unclear.

research Correction to: Efficacy assessment for low‑level laser therapy in the treatment of androgenetic alopecia: a real‑world study on 1383 patients

March 2022 in “Lasers in Medical Science”

research Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family

1 citations , September 2021 in “Frontiers in genetics”

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

research Genetic variations associated with response to dutasteride in the treatment of male subjects with androgenetic alopecia

3 citations , September 2019 in “PLOS ONE”

Genetic variations affect dutasteride treatment response for male pattern hair loss.

research Navigating Rhupus Complexity

January 2024 in “Ankara City Hospital Medical Journal”

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

research ISID1394 - Long non-coding RNA AL136131.3 inhibits hair growth through mediating glycolysis in androgenetic alopecia

May 2023

The RNA AL136131.3 slows down hair growth and speeds up hair loss by affecting sugar breakdown in hair follicles.

Taking Advantage of Phenotype Variability in a Local Animal Genetic Resource: Identification of Genomic Regions Associated with the Hairless Phenotype in Casertana Pigs

research Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs

16 citations , April 2018 in “Animal Genetics”

Researchers found two genes that may explain why some Casertana pigs don't have hair.

research A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population

21 citations , March 2015 in “Neurological Sciences”

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

research Genome-Wide Associations with Body and Fleece Weight in United States Sheep

June 2025 in “Genes”

Certain genetic markers can help predict wool production in U.S. sheep.

research 44179 Characterization of subclinical atherosclerosis in chronic severe alopecia areata.

September 2023 in “Journal of the American Academy of Dermatology”

research Suppression of mammary tumorigenesis in transgenic mice by the RXR-selective retinoid, LGD1069.

143 citations , May 2002 in “PubMed”

LGD1069 effectively prevents breast tumors in mice without toxicity.

research Reply by Authors

May 2020 in “The Journal of Urology”

research Farmácia da Ponte, Mirandela

February 2021 in “Open Repository of the University of Porto (University of Porto)”

research 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing

July 2024 in “Journal of Investigative Dermatology”

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

research The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene

50 citations , February 2004 in “Genomics”

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

research Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing

5 citations , November 2022 in “Genetics selection evolution”

Low-coverage sequencing is a cost-effective way to find genetic factors affecting rabbit wool traits.

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