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Carcinogenesis|November 7, 2002
Human melanomas of fibroblast and epithelial morphology differ widely in their ability to synthesize retinyl estersDenise Perry Simmons, Fausto Andreola, Luigi M De Luca
Nanomaterials (Basel, Switzerland)|July 2, 2020
Single-Step Photochemical Formation of Near-Infrared-Absorbing Gold Nanomosaic within PNIPAm Microgels: Candidates for Photothermal Drug DeliverySreekar Babu Marpu, Brian Leon Kamras, Nooshin MirzaNasiri, et al.
Carcinogenesis|October 20, 2005
Evidence that sequence homologous region in LRAT-like proteins possesses anti-proliferative activity and DNA binding properties: translational implications and mechanism of actionDenise Perry Simmons, Megan L Peach, Jonathan R Friedman, et al.
American Journal of Medical Genetics. Part A|March 26, 2018
Congenital sodium diarrhea and chorioretinal coloboma with optic disc coloboma in a patient with biallelic SPINT2 mutations, including p.(Tyr163Cys)Kristin E Hirabayashi, Anthony T Moore, Bryce A Mendelsohn, et al.
Molecular Syndromology|March 29, 2021
Expanding the Phenotype of <i>TUBB2A</i>-Related Tubulinopathy: Three Cases of a Novel, Heterozygous <i>TUBB2A</i> Pathogenic Variant p.Gly98ArgLindsey Schmidt, Karen E Wain, Catherine Hajek, et al.
Annals of Human Genetics|May 16, 2025
First Insights Into the Phenotype and Genotype of Inherited Retinal Disorders in the Democratic Republic of Congo (DRC)Nadine Nsiangani Lusambo, Patrick Fuanani, Gerrye Mubungu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrumLisa T Emrick, Jill A Rosenfeld, Seema R Lalani, et al.
American Journal of Medical Genetics. Part A|August 8, 2022
Wide range of phenotypic severity in individuals with late truncations unique to the predominant CDKL5 transcript in the brainLaura Keehan, Isabel Haviland, Yoel Gofin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a changeHeidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
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