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The Possible Implication of the S250C Variant of the Autoimmune Regulator Protein in a Patient with Autoimmunity and Immunodeficiency: In Silico Analysis Suggests a Molecular Pathogenic Mechanism for the Variant

research The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant

11 citations , July 2014 in “Gene”

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

research 10.1063/5.0132123.1

February 2023 in “Default Digital Object Group”

research Serine-rich ultra high sulfur protein gene expression in murine hair and skin during the hair cycle

1 citations , February 1991 in “Journal of Biological Chemistry”

research Exomic Sequencing of Immune-Related Genes Reveals Novel Candidate Variants Associated with Alopecia Universalis

18 citations , January 2013 in “PLoS ONE”

HLA-DRB5 and other genes may be linked to alopecia universalis.

research Computer physics communications instructions to authors (third revision)

1 citations , January 1980 in “Computer Physics Communications”

research Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology

January 2013 in “Faculty of Health; Institute of Health and Biomedical Innovation”

Four genetic risk areas related to male-pattern baldness were identified, with WNT signaling playing a role in its development.

research Finding bald spots on chromosome 20p11

1 citations , February 2009 in “Clinical Genetics”

New genes linked to male pattern baldness were found on chromosome 20p11.

research 085 Coordinate expressions of cyclin-dependent kinase inhibitors and high sulfur protein in human hair follicles

June 1996 in “Journal of Dermatological Science”

research A randomized evaluator blinded study of effect of microneedling in androgenetic alopecia: A pilot study

136 citations , January 2013 in “International Journal of Trichology”

research 42008 Long Term Hematologic Laboratory Safety of Dupilumab in Patients Aged 6 Months to 5 Years With Moderate-to-Severe Atopic Dermatitis

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

research Adiponectin serum levels and ADIPOQ (rs2241766) polymorphism in alopecia areata Egyptian patients

1 citations , November 2023 in “Anais Brasileiros de Dermatologia”

Certain gene variations and low adiponectin levels may increase the risk of hair loss in Egyptians.

research Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened

63 citations , May 2011 in “Clinical cancer research”

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

research Regulation of Hair Follicle Growth and Development by Different Alternative Spliceosomes of FGF5 in Rabbits

March 2024 in “Genes”

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

research LncRNA NEAT1 and miRNA 101 as potential diagnostic biomarkers in patients with alopecia areata

4 citations , August 2024 in “Non-coding RNA Research”

research A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.

89 citations , March 1996 in “Proceedings of the National Academy of Sciences”

CD18-deficient mice developed psoriasis-like skin disease, useful for studying inflammatory skin disorders.

research RGB video microscopic system for in-vitro monitoring of optical properties of hair shaft and follicle

1 citations , May 2001 in “Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE”

The system helps monitor hair properties using RGB video microscopy.

research 712 A small molecule modulator of the wnt pathway (SM04554) as a potential topical treatment for androgenetic alopecia (AGA)

1 citations , April 2017 in “Journal of Investigative Dermatology”

SM04554 may increase hair growth as a topical treatment for androgenetic alopecia.

Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets (HVDRR): Clinical Heterogeneity and Long-Term Efficacious Management of Eight Patients from Four Unrelated Arab Families with a Loss of Function VDR Mutation

research Hereditary 1,25-dihydroxyvitamin D-resistant rickets (HVDRR): clinical heterogeneity and long-term efficacious management of eight patients from four unrelated Arab families with a loss of function VDR mutation

6 citations , June 2018 in “Journal of pediatric endocrinology & metabolism/Journal of pediatric endocrinology and metabolism”

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

research Novel de novo pathogenic variant in the ODC1 gene in a girl with developmental delay, alopecia, and dysmorphic features

39 citations , September 2018 in “American Journal of Medical Genetics Part A”

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

The Evaluation of IL-4 VNTR Intron 3 and TNF-α (rs1799964) Gene Polymorphisms in Egyptian Patients with Alopecia Areata: A Case–Control Study

research The evaluation of IL-4 VNTR intron 3 and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with alopecia areata: a case–control study

July 2024 in “Egyptian Journal of Medical Human Genetics”

These gene variations are not linked to alopecia areata in Egyptians.

research Itpr3 Is Responsible for the Mouse Tufted (tf) Locus

6 citations , October 2012 in “Journal of Heredity”

The Itpr3 gene causes a specific hair pattern in mice.

research Faculty Opinions recommendation of Identification of drug-specific public TCR driving severe cutaneous adverse reactions.

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

Researchers found a specific T cell receptor linked to severe drug reactions like Stevens-Johnson syndrome when patients take carbamazepine.

research Linkage of Monilethrix to the Trichocyte and Epithelial Keratin Gene Cluster on 12q11-q13

43 citations , April 1996 in “Journal of Investigative Dermatology”

research 112 Post-Finasteride Syndrome – Outcomes of FDA Database

April 2016 in “The Journal of Sexual Medicine”

research Chapter 26 Scalp Micropigmentation

January 2021 in “Thieme Medical and Scientific Publishers Private Limited eBooks”

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research 1565 nm laser and topical drugs for hair regeneration in patients with alopecia areata

April 2025 in “Asian Journal of Surgery”

research ABHRS Profile

May 2018 in “Hair transplant forum international”

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research Characterization and functional analysis of Krtap11-1 during hair follicle development in Angora rabbits (Oryctolagus cuniculus)

8 citations , September 2020 in “Genes & Genomics”

The Influence of ESR1 Polymorphisms on Hormonal, Metabolic, and Mineral Balance Markers in Women with Hyperandrogenism

research The influence of ESR1 polymorphisms on selected hormonal, metabolic and mineral balance markers in women with hyperandrogenism

November 2022 in “Scientific Reports”

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

research Cell‐free transcriptomic profiles and mechanism insights in female androgenetic alopecia

November 2025 in “Clinical and Translational Medicine”

DNAJB9 cfRNA could help diagnose and treat female hair loss.

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