Showing results (141-150 of 209) with videos related to

Sort By:
Pageof 21
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 29, 2016
Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burdenMohamed Abouelhoda, Turki Sobahy, Mohamed El-Kalioby, et al.
Scientific Reports|February 22, 2018
Aberrant Regulation of Notch3 Signaling Pathway in Polycystic Kidney DiseaseJessica Idowu, Trisha Home, Nisha Patel, et al.
Scientific Reports|December 1, 2025
Africa's booming rice cultivation is fueling regional warmingBasudev Swain, Marco Vountas, Aishwarya Singh, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 18, 2022
Interactome of Aiolos/Ikaros Reveals Combination Rationale of Cereblon Modulators with HDAC Inhibitors in DLBCLPatrick R Hagner, Hsiling Chiu, Vivek S Chopra, et al.
AIDS (London, England)|April 30, 2021
Prevalence of HIV/hepatitis B and HIV/hepatitis C coinfection among people of East, South, Central and West African ancestry in the United KingdomRachel Hung, Nisha Patel, Julie Fox, et al.
American Journal of Physiology. Heart and Circulatory Physiology|November 1, 2024
Early pathological mechanisms in a mouse model of heart failure with preserved ejection fractionPaola C Rosas, Liomar A A Neves, Nisha Patel, et al.
The American Journal of Emergency Medicine|February 5, 2015
The relationship of intravenous fluid chloride content to kidney function in patients with severe sepsis or septic shockFaheem W Guirgis, Deborah J Williams, Matthew Hale, et al.
Epigenetics|November 25, 2021
An integrative epi-transcriptomic approach identifies the human cartilage chitinase 3-like protein 2 (CHI3L2) as a potential mediator of B12 deficiency in adipocytesB William Ogunkolade, Antonysunil Adaikalakoteswari, Shirleny Romualdo Cardoso, et al.
Dementia (London, England)|November 24, 2025
Recognizing Structural and Social Determinants of Health in the Diagnosis and Care of DementiaShana D Stites, Sharnita Midgett, Nisha Patel, et al.
American Journal of Human Genetics|April 29, 2014
Mutations in ASPH cause facial dysmorphism, lens dislocation, anterior-segment abnormalities, and spontaneous filtering blebs, or Traboulsi syndromeNisha Patel, Arif O Khan, Ahmad Mansour, et al.
Pageof 21