Adriana A. De Jesus Rasheed
Pediatric Rheumatology
2000 Longmead Rd
Silver Spring, MD 20906
Silver Spring, MD 20906
Last Updated: 09/26/2026
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Found 7 publications
Human induced pluripotent stem cells (NIHTVBi029-A and NIHTVBi030-A) generated from two patients with a heterozygous mutation in the CDC42 gene.
Journal: Stem cell research
Published: July 19, 2024
Establishment of a human induced pluripotent stem cell line (NIHTVBi031-A) derived from a COPA syndrome patient with a heterozygous p.Ala239Pro mutation.
Journal: Stem cell research
Published: July 05, 2024
Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stress.
Journal: Nature communications
Published: January 26, 2024
Corrigendum to "Human induced pluripotent stem cells generated from a patient with a homozygous mutation in the Lyn kinase gene" [Stem Cell Res. 64 (2022) 102933].
Journal: Stem cell research
Published: March 15, 2023
Human induced pluripotent stem cells generated from a patient with a homozygous mutation in the Lyn kinase gene.
Journal: Stem cell research
Published: September 21, 2022
Human induced pluripotent stem cells generated from STING-associated vasculopathy with onset in infancy (SAVI) patients with a heterozygous mutation in the STING gene.
Journal: Stem cell research
Published: August 09, 2022
Human induced pluripotent stem cells generated from Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome patients with a homozygous mutation in the PSMB8 gene (NIHTVBi016-A, NIHTVBi017-A, NIHTVBi018-A).
Journal: Stem cell research
Published: April 18, 2022
Showing 1-7 of 7
Last Updated: 09/26/2026