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Plos One|June 30, 2010
Oncoproteomic analysis reveals co-upregulation of RELA and STAT5 in carboplatin resistant ovarian carcinomaNatini Jinawath, Chanont Vasoontara, Artit Jinawath, et al.
Ophthalmic Genetics|May 6, 2026
Evaluating gene-disease relationship strength in crystallin genes in association with pediatric cataractsAlexander Ing, Allison Goetsch Weisman, Andy Drackley, et al.
Genes|August 28, 2025
GPR143-Associated Ocular Albinism in a Hispanic Family and Review of the LiteratureAnushree Aneja, Brenda L Bohnsack, Valerie Allegretti, et al.
Plos One|August 8, 2013
Loss of NAC1 expression is associated with defective bony patterning in the murine vertebral axisKai Lee Yap, Polina Sysa-Shah, Brad Bolon, et al.
Cell Reports. Medicine|May 26, 2022
Genetic changes associated with relapse in favorable histology Wilms tumor: A Children's Oncology Group AREN03B2 studySamantha Gadd, Vicki Huff, Andrew D Skol, et al.
Journal of Human Genetics|May 23, 2018
The era of immunogenomics/immunopharmacogenomicsMakda Zewde, Kazuma Kiyotani, Jae-Hyun Park, et al.
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society|November 20, 2022
Transitional care and clinical management of adolescents, young adults, and suspected new adult patients with congenital central hypoventilation syndromeSusan M Slattery, Iris A Perez, Isabella Ceccherini, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 7, 2021
Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype-phenotype correlation in congenital central hypoventilation syndrome (CCHS)Amy Zhou, Casey M Rand, Sara M Hockney, et al.
JAMA Cardiology|August 11, 2021
Genomic Autopsy of Sudden Deaths in Young IndividualsGregory Webster, Megan J Puckelwartz, Lorenzo L Pesce, et al.
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