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Site of Beige and Leaden Pigment Gene Expression Determined by Recombinant Embryonic Skin Grafts and Aggregation Mouse Chimaeras Employing Sash Homozygotes

research Site of beige (bg) and leaden (ln) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (W^sh) homozygotes

7 citations , October 1985 in “Genetics Research”

Beige and leaden pigment genes act within melanocytes, affecting pigment patterns.

research scINSIGHT for interpreting single-cell gene expression from biologically heterogeneous data

24 citations , March 2022 in “Genome biology”

scINSIGHT accurately identifies cell clusters and gene patterns in complex data.

research 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages

April 2023 in “The journal of investigative dermatology/Journal of investigative dermatology”

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

research Molecular basis of androgen insensitivity

309 citations , June 2001 in “Molecular and Cellular Endocrinology”

Mutations in the androgen receptor gene cause androgen insensitivity, leading to female traits in genetically male individuals.

Non-Steroidal Modulation of the 5-Alpha Reductase Axis: A Dual Therapeutic Strategy for Prostatic Chemoprevention and Androgenetic Alopecia

research Non-Steroidal Modulation of the 5-Alpha Reductase Axis: A Dual Therapeutic Strategy for Prostatic Chemoprevention and Androgenetic Alopecia

January 2026 in “Zenodo (CERN European Organization for Nuclear Research)”

LX-38 is a safer drug option for hair loss and prostate issues without hormonal side effects.

research Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing

99 citations , October 2008 in “Journal of Investigative Dermatology”

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

research 322 Upregulation of SERPINB3/B4 and S100A7-9 in hidradenitis suppurativa/acne inversa

September 2019 in “The journal of investigative dermatology/Journal of investigative dermatology”

Certain proteins are significantly increased in the skin of people with hidradenitis suppurativa.

research The Role of Pannexin 3 in Bone Biology

32 citations , November 2016 in “Journal of Dental Research”

Pannexin 3 is important for bone formation and the development of bone cells.

research Trans glutaminase-mediated cross-linking in mammalian epidermis

44 citations , January 1984 in “Molecular and Cellular Biochemistry”

research Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA

9 citations , September 2023 in “Viruses”

The XBB lineage of the Omicron variant spread rapidly in Southeastern Wisconsin.

research FORMULATION AND EVALUATION OF CONTROLLED RELEASE MATRIX TABLETS OF FINASTERIDE

1 citations , January 2014

The F9 formulation of Finasteride tablets, using Eudragit, successfully controlled drug release.

research NUDT15,FTO, andRUNX1genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases

40 citations , January 2017 in “Intestinal Research”

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

research 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy

April 2017 in “Journal of Investigative Dermatology”

Deep phenotyping helps distinguish between xeroderma pigmentosum and trichothiodystrophy, aiding in diagnosis and treatment.

Novel Splice Site Mutation in the LIPH Gene in a Patient with Autosomal Recessive Woolly Hair/Hypotrichosis: Case Report and Published Work Review

research Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review

9 citations , February 2018 in “The Journal of Dermatology”

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

research Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis

41 citations , January 2022 in “Clinical Immunology”

Females are more prone to lupus and arthritis due to X chromosome factors.

research Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis

74 citations , January 2006 in “The journal of investigative dermatology/Journal of investigative dermatology”

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

research Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A

5 citations , December 2017 in “The Journal of Dermatology”

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

research The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)

July 2021 in “Advances in laboratory medicine”

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

research XV Italian Society of Hair Restoration International Meeting June 27- 28, 2014 • Siracusa, Italy

September 2014 in “Hair transplant forum international”

I'm sorry, but there's no conclusion provided to summarize.

research Matrix effects and application of matrix effect factor

323 citations , November 2017 in “Bioanalysis”

Matrix effects in LC-MS can be managed but not completely avoided.

research Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients

November 2025 in “Clinical Cosmetic and Investigational Dermatology”

LIPH mutations cause woolly hair in some Chinese people.

research Reformulando a pasta de enxofre: tratamentos mais eficazes

August 2018 in “Cadernos de Agroecologia”

The new sulfur paste effectively treats rabbit scabies, promoting healing and hair growth.

research Non-Steroidal Modulation of the 5-Alpha Reductase Axis: A Dual Therapeutic Strategy for Prostatic Chemoprevention and Androgenetic Alopecia

January 2026 in “Zenodo (CERN European Organization for Nuclear Research)”

LX-38 is a safer drug option for treating prostate issues and hair loss without hormonal side effects.

research miR‐203a‐3p promotes loureirin A‐induced hair follicle stem cells differentiation by targeting Smad1

12 citations , June 2020 in “The anatomical record”

miR-203a-3p helps hair follicle stem cells become specialized by targeting Smad1.

research X linked mental retardation.

79 citations , June 1991 in “Journal of Medical Genetics”

X-linked mental retardation includes various syndromes with both mental and physical abnormalities.

research Preclinical Development and Phase I Study of ZSYY001, a Polymeric Micellar Paclitaxel for Advanced Solid Tumor

6 citations , July 2025 in “Cancer Medicine”

The study investigated ZSYY001, a polymeric micellar paclitaxel formulation, in preclinical and phase I trials for advanced solid tumors. Preclinical tests on xenograft models showed significant tumor growth inhibition without weight loss. In the phase I trial, involving 18 patients, ZSYY001 was administered at doses up to 390 mg/m² without premedication, and no dose-limiting toxicities were observed. Common side effects included anemia and hair loss, but no acute hypersensitivity reactions occurred. The study found two partial responses and seven cases of stable disease, indicating promising antitumor activity. ZSYY001 was deemed safe, well-tolerated, and exhibited non-linear pharmacokinetics, suggesting it as a potential treatment option.

research A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report

18 citations , January 2018 in “BMC dermatology”

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

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research Site of beige (bg) and leaden (ln) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (W^sh) homozygotes

research scINSIGHT for interpreting single-cell gene expression from biologically heterogeneous data

research 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages

research Molecular basis of androgen insensitivity

research Non-Steroidal Modulation of the 5-Alpha Reductase Axis: A Dual Therapeutic Strategy for Prostatic Chemoprevention and Androgenetic Alopecia

research Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing

research 322 Upregulation of SERPINB3/B4 and S100A7-9 in hidradenitis suppurativa/acne inversa

research The Role of Pannexin 3 in Bone Biology

research Trans glutaminase-mediated cross-linking in mammalian epidermis

research Genomic Surveillance Reveals the Rapid Expansion of the XBB Lineage among Circulating SARS-CoV-2 Omicron Lineages in Southeastern Wisconsin, USA

research FORMULATION AND EVALUATION OF CONTROLLED RELEASE MATRIX TABLETS OF FINASTERIDE

research NUDT15,FTO, andRUNX1genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases

research 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy

research Novel splice site mutation in the LIPH gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review

research Long non-coding RNA Xist contribution in systemic lupus erythematosus and rheumatoid arthritis

research Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis

research Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A

research The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)

research XV Italian Society of Hair Restoration International Meeting June 27- 28, 2014 • Siracusa, Italy

research Matrix effects and application of matrix effect factor

research Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients

research Reformulando a pasta de enxofre: tratamentos mais eficazes

research Non-Steroidal Modulation of the 5-Alpha Reductase Axis: A Dual Therapeutic Strategy for Prostatic Chemoprevention and Androgenetic Alopecia

research miR‐203a‐3p promotes loureirin A‐induced hair follicle stem cells differentiation by targeting Smad1

research X linked mental retardation.

research Preclinical Development and Phase I Study of ZSYY001, a Polymeric Micellar Paclitaxel for Advanced Solid Tumor

research A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report

research 132 Design of an in vitro skin 3D model mimicking a disruption of the barrier function

research INNOVATIVE APPROACH TO CRC PREVENTION: THE ROLE OF LOW-PENETRATION GENES

research A doxycycline- and light-inducible Cre recombinase mouse model for optogenetic genome editing