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Arthritis & Rheumatology (Hoboken, N.J.)|April 23, 2019
Identification of Novel Adenosine Deaminase 2 Gene Variants and Varied Clinical Phenotype in Pediatric VasculitisKristen M Gibson, Kimberly A Morishita, Paul Dancey, et al.
The Journal of Clinical Endocrinology and Metabolism|March 22, 2017
Phenotypic Spectrum in Osteogenesis Imperfecta Due to Mutations in TMEM38B: Unraveling a Complex Cellular DefectEmma A Webb, Meena Balasubramanian, Nadja Fratzl-Zelman, et al.
Hypertension in Pregnancy|February 25, 2016
MYC-induced nuclear antigen (MINA) and preeclampsiaMargarita L Martinez-Fierro, Edwin A Reyes-Oliva, Griselda A Cabral-Pacheco, et al.
Fitoterapia|August 14, 2024
[1-7-NαC]-Crocaorb A1 and A2, orbitides from the latex of Croton campanulatusSuzana A S Queiroz, Ana Letícia P Dos Santos, Antonio F Bobey, et al.
Anais Da Academia Brasileira De Ciencias|March 7, 2024
Intraoperative thermal mapping of mammary tumors in dogsSilvia Maria R Cadena, Paula G A Cabral, Scarlath O P Dos Santos, et al.
Nature Communications|July 7, 2016
MBTPS2 mutations cause defective regulated intramembrane proteolysis in X-linked osteogenesis imperfectaUschi Lindert, Wayne A Cabral, Surasawadee Ausavarat, et al.
Genes|June 2, 2021
Whole-Exome Sequencing, Proteome Landscape, and Immune Cell Migration Patterns in a Clinical Context of Menkes DiseaseMargarita L Martinez-Fierro, Griselda A Cabral-Pacheco, Idalia Garza-Veloz, et al.
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