Tina Ho | Medical Services
Specialties
Programs & Services
Tina Ho | Education
Undergraduate School
Yale University
2009, New Haven, CT
Graduate School
University of Pennsylvania
2015, Philadelphia, PA
Medical School
University of Pennsylvania
2017, Philadelphia, PA
Internship
Pediatrics
Children's Hospital of Philadelphia
2018, Philadelphia, PA
Residency
Dermatology
University of Cincinnati
2021, Cincinnati, OH
Fellowship
Pediatric Dermatology
Boston Children's Hospital
2022, Boston, MA
Tina Ho | Publications
Medicaid coverage for nonsteroidal topical atopic dermatitis treatment is often restrictive and variable across the United States. Arch Dermatol Res. 2024 Jun 15; 316(7):406. View Medicaid coverage for nonsteroidal topical atopic dermatitis treatment is often restrictive and variable across the United States. Abstract
Most common pediatric skin conditions managed in outpatient dermatology clinics in the United States stratified by race and ethnicity. Pediatr Dermatol. 2021 Nov; 38 Suppl 2:129-131. View Most common pediatric skin conditions managed in outpatient dermatology clinics in the United States stratified by race and ethnicity. Abstract
Participation of keratinocyte- and fibroblast-derived factors in melanocyte homeostasis, the response to UV, and pigmentary disorders. Pigment Cell Melanoma Res. 2021 07; 34(4):762-776. View Participation of keratinocyte- and fibroblast-derived factors in melanocyte homeostasis, the response to UV, and pigmentary disorders. Abstract
Trends in coal tar use in the United States. J Am Acad Dermatol. 2021 11; 85(5):1338-1339. View Trends in coal tar use in the United States. Abstract
SLC45A2 protein stability and regulation of melanosome pH determine melanocyte pigmentation. Mol Biol Cell. 2020 11 15; 31(24):2687-2702. View SLC45A2 protein stability and regulation of melanosome pH determine melanocyte pigmentation. Abstract
The enigma and challenges of vitiligo pathophysiology and treatment. Pigment Cell Melanoma Res. 2020 11; 33(6):778-787. View The enigma and challenges of vitiligo pathophysiology and treatment. Abstract
Clinical course of porokeratosis ptychotropica over 7 years in an otherwise healthy child. Pediatr Dermatol. 2020 Jan; 37(1):248-250. View Clinical course of porokeratosis ptychotropica over 7 years in an otherwise healthy child. Abstract
Cutaneous Small-Vessel Vasculitis in Two Children with Inflammatory Bowel Disease: Case Series and Review of the Literature. Pediatr Dermatol. 2017 Sep; 34(5):e235-e240. View Cutaneous Small-Vessel Vasculitis in Two Children with Inflammatory Bowel Disease: Case Series and Review of the Literature. Abstract
Including Langerhans cell histiocytosis in the differential diagnosis of skin tumors with osteoclast-like multinucleated giant cells. J Cutan Pathol. 2017 Jul; 44(7):659-661. View Including Langerhans cell histiocytosis in the differential diagnosis of skin tumors with osteoclast-like multinucleated giant cells. Abstract
The Kringle-like Domain Facilitates Post-endoplasmic Reticulum Changes to Premelanosome Protein (PMEL) Oligomerization and Disulfide Bond Configuration and Promotes Amyloid Formation. J Biol Chem. 2016 Feb 12; 291(7):3595-612. View The Kringle-like Domain Facilitates Post-endoplasmic Reticulum Changes to Premelanosome Protein (PMEL) Oligomerization and Disulfide Bond Configuration and Promotes Amyloid Formation. Abstract
NK cell lytic granules are highly motile at the immunological synapse and require F-actin for post-degranulation persistence. J Immunol. 2012 Nov 15; 189(10):4870-80. View NK cell lytic granules are highly motile at the immunological synapse and require F-actin for post-degranulation persistence. Abstract
Mutagenesis identifies the critical amino acid residues of human endonuclease G involved in catalysis, magnesium coordination, and substrate specificity. J Biomed Sci. 2009 Jan 15; 16:6. View Mutagenesis identifies the critical amino acid residues of human endonuclease G involved in catalysis, magnesium coordination, and substrate specificity. Abstract
Histidine residue at position 226 is critical for iodide uptake activity of human sodium/iodide symporter. J Endocrinol. 2008 Nov; 199(2):213-9. View Histidine residue at position 226 is critical for iodide uptake activity of human sodium/iodide symporter. Abstract