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research Sequence analyses of Type I and Type II chains in human hair and epithelial keratin intermediate filaments: Promiscuous obligate heterodimers, Type II template for molecule formation and a rationale for heterodimer formation

19 citations , December 2006 in “Journal of Structural Biology”

Type I and Type II keratin chains can form heterodimers despite sequence differences.

research Selection signatures in goats reveal a novel deletion mutant underlying cashmere yield and diameter

November 2022 in “Gigascience”

A specific genetic deletion in goats affects cashmere yield and thickness.

research Structure and expression of the ovine Hoxc-13 gene

12 citations , December 2003 in “Gene”

The ovine Hoxc-13 gene is crucial for hair formation and may have other skin functions.

research 891 Comparison of phenotypes and transcriptomes of mouse skin-derived precursors and dermal mesenchymal stem cells

April 2019 in “Journal of Investigative Dermatology”

The search scheme SMRI is faster and more secure for retrieving encrypted data from the cloud.

research Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA

6 citations , June 2018 in “bioRxiv (Cold Spring Harbor Laboratory)”

Humans have ancient DNA from Neanderthals and other lineages in their chromosomes, affecting traits and evolution.

research Different phenotypes in a family with androgen insensitivity caused by the same M780I point mutation in the androgen receptor gene.

78 citations , August 1996 in “The Journal of Clinical Endocrinology & Metabolism”

The same gene mutation can cause different symptoms in family members.

research Mesenchymal Meis2 controls whisker development independently from trigeminal sensory innervation

November 2024

Meis2 is essential for whisker development, independent of nerve involvement.

research Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants

6 citations , June 2021 in “The journal of investigative dermatology/Journal of investigative dermatology”

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

research Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia

14 citations , July 2001 in “American Journal of Human Genetics”

Haplogroup X found in Altaian population supports Amerindian origin.

research miR-133a-3p and miR-145-5p co-promote goat hair follicle stem cell differentiation by regulating NANOG and SOX9 expression

November 2023 in “Animal Bioscience”

miR-133a-3p and miR-145-5p help goat hair follicle stem cells differentiate by controlling NANOG and SOX9.

research Faculty Opinions recommendation of Stem cell niche exit in C. elegans via orientation and segregation of daughter cells by a cryptic cell outside the niche.

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

Stem cell niche exit in C. elegans is influenced by Sh1 cell membrane protrusions.

research Par3–mInsc and Gαi3 cooperate to promote oriented epidermal cell divisions through LGN

July 2021

Par3–mInsc and Gαi3 work together to ensure proper cell division orientation in skin development.

A Case of MBTPS1-Related Disorder Due to Compound Heterozygous Variants in MBTPS1 Gene: Genotype-Phenotype Expansion and the Emergence of a Novel Syndrome

research A case of MBTPS1‐related disorder due to compound heterozygous variants in MBTPS1 gene: Genotype–phenotype expansion and the emergence of a novel syndrome

December 2023 in “American journal of medical genetics. Part A”

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

research Identification de 2 polymorphismes génétiques (SNPs) associés aux spondylarthropathies (SpA) dans le locus SPA2 (9q31-34)

October 2007 in “Revue du Rhumatisme”

research Structure and Expression of a New Complementary DNA Encoding the almost Exclusive 3β-Hydroxysteroid Dehydrogenase/Δ⁵-Δ⁴-lsomerase in Human Adrenals and Gonads

354 citations , August 1991 in “Molecular Endocrinology”

Human adrenals and gonads have a unique enzyme for steroid hormone production.

research The Fraser Complex Proteins (Frem1, Frem2, and Fras1) Can Form Anchoring Cords in the Absence of AMACO at the Dermal–Epidermal Junction of Mouse Skin

1 citations , April 2023 in “International journal of molecular sciences”

Certain skin proteins can form anchoring structures without the protein AMACO.

research Genetic Polymorphisms of the 3'-Untranslated Regions (3'-UTR) of the HSP 70 Gene in Moa Buffalo (Bubalus bubalis)

September 2025 in “Jurnal Penelitian Pendidikan IPA”

Two genetic variations in Moa buffalo help them adapt to heat.

research 689 Cell-type-specific nascent transcriptomics through PRECISE-seq reveal molecular principles of tissue dynamics

July 2024 in “Journal of Investigative Dermatology”

research Supplementary figure S2

August 2020 in “OPAL (Open@LaTrobe) (La Trobe University)”

research AXR3andSHY2interact to regulate root hair development

157 citations , October 2003 in “Development”

AXR3 and SHY2 genes control the growth and timing of root hair development in plants.

research Dicer- and BSC-dependent miRNAs during murine anagen development

1 citations , January 2020 in “bioRxiv (Cold Spring Harbor Laboratory)”

Dicer is crucial for hair growth in mice.

research Identification and expression of the target gene SLC24A2 of oar-miR-377 and its novel SNPs effects on wool traits in sheep

March 2024 in “Research Square (Research Square)”

The TT genotype of a specific SNP in sheep is linked to better wool quality.

research Sequence Analysis of mtDNA NADH-Ubiquinone Oxidoreductase Chain 1 Gene (ND1) of the Asian Black Bear Sichuan Subspecies (Ursus thibetanus mupinensis)

January 2007 in “Journal of Southwest University”

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

research Structure of human type II 5 alpha-reductase gene

76 citations , September 1992 in “Endocrinology”

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

research Bioinformatics analysis of EST segment from goat

1 citations , January 2008 in “China Journal of Bioinformatics”

Goat skin has more keratin genes, while the mammary gland has more immunity-related genes.

research Haplotypes spanning centromeric regions reveal persistence of large blocks of archaic DNA

49 citations , June 2019 in “eLife”

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

research A Ca ²⁺ /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning

477 citations , March 2004 in “Proceedings of the National Academy of Sciences”

The DMI3 gene is essential for nodule development and symbiosis in certain plants.

research A novel human type I hair keratin gene: evidence for two keratin hHa3 isoforms

21 citations , January 1995 in “Molecular Biology Reports”

Scientists discovered two versions of a new human hair keratin gene.

research Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection

August 2025 in “Biomedicines”

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

research Two siblings with uncombable hair syndrome: A new pathogenic variant

2 citations , March 2024 in “Pediatric Dermatology”

Two siblings have a rare hair condition caused by a new genetic variant.

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