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research LB1777 A novel ex vivo model of human hair follicle immune privilege collapse reveals the potential of farudodstat, a DHODH inhibitor, as a therapeutic for alopecia areata treatment

1 citations , August 2023 in “Journal of Investigative Dermatology”

Farudodstat may help treat alopecia areata by protecting hair follicles.

research AI06 ALUDWIG: an automated artificial intelligence-based assessment of female androgenic alopecia

June 2025 in “British Journal of Dermatology”

ALUDWIG can help standardize female hair loss assessment from a single image.

research A Case of Hair Change and Acneiform Eruption Induced by ZD1839 (Iressa$^{(R)}$)

2 citations , January 2004 in “Linchuang pifuke zazhi”

ZD1839 can cause skin issues like acne and hair changes.

research L-Ornithine ketoacid-transaminase assay in hair roots of homozygotes and heterozygotes for gyrate atrophy

8 citations , June 1981 in “Clinica Chimica Acta”

research ORLANDO LIVE SURGERY WORKSHOP XIV: ADVANCING THE INDUSTRY OF HAIR RESTORATION APRIL 3-5 2008 ORLANDO

July 2008 in “Hair transplant forum international”

research Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets

107 citations , March 2014 in “BoneKEy Reports”

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

research ISIDLB1777 - A novel ex vivo model of human hair follicle immune privilege collapse reveals the potential of farudodstat, a DHODH inhibitor, as a therapeutic for alopecia areata treatment

May 2023

Farudodstat may effectively treat alopecia areata by protecting hair follicles without harmful effects.

research Reply by Authors

May 2020 in “The Journal of Urology”

research Farmácia D'Arrábida, Vila Nova de Gaia

October 2023 in “Open Repository of the University of Porto (University of Porto)”

research Cyberspace Chat

January 2007 in “International Society of Hair Restoration Surgery”

research Birt-Hogg-Dube Syndrome with a Novel Mutation in the FLCN Gene

7 citations , August 2017 in “Genetic testing and molecular biomarkers”

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

research Finasteride < Rec INN; BAN; USAN >

5 citations , January 1991 in “Drugs of The Future”

research Decision letter: Plant Trans-Golgi Network/Early Endosome pH regulation requires Cation Chloride Cotransporter (CCC1)

September 2021

CCC1 is essential for ion balance and proper plant cell function.

research Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population

September 2024 in “Frontiers in Genetics”

A specific genetic marker is linked to male pattern baldness in Han Chinese men.

research 42005 Sustained scalp, eyebrow, and eyelash hair regrowth with ritlecitinib through Week 48 in patients with alopecia areata: post hoc analysis of the ALLEGRO phase 2b/3 study

1 citations , September 2023 in “Journal of the American Academy of Dermatology”

Ritlecitinib effectively regrows and maintains scalp, eyebrow, and eyelash hair in alopecia areata patients.

research Correction to ‘Long‐term safety and efficacy of ritlecitinib in adults and adolescents with alopecia areata and at least 25% scalp hair loss: Results from the ALLEGRO‐LT phase 3, open‐label study’

July 2025 in “Journal of the European Academy of Dermatology and Venereology”

research Ligand Based 3D-QSAR Study on a Series of Steroidal Human 5α-Reductase Inhibitors

3 citations , August 2010 in “Letters in Drug Design & Discovery”

research A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome

11 citations , December 2017 in “Orphanet Journal of Rare Diseases”

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

research Identification of a Rare Variant in the SRD5A2 Gene in Siblings With 46,XY Disorders of Sexual Development

January 2025 in “Case Reports in Genetics”

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

research Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA

3 citations , February 2018 in “Experimental and Molecular Medicine/Experimental and molecular medicine”

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.