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Human Genetics|April 27, 2017
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidismNir Pillar, Oren Pleniceanu, Mingyan Fang, et al.
Nature Communications|December 9, 2023
RAAS-deficient organoids indicate delayed angiogenesis as a possible cause for autosomal recessive renal tubular dysgenesisNaomi Pode-Shakked, Megan Slack, Nambirajan Sundaram, et al.
Stem Cells Translational Medicine|December 22, 2017
Lung Injury Repair by Transplantation of Adult Lung Cells Following Preconditioning of Recipient MiceIrit Milman Krentsis, Chava Rosen, Elias Shezen, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 5, 2003
In situ activation pattern of Met docking site following renal injury and hypertrophyBenjamin Dekel, Sharon Biton, Gil M Yerushalmi, et al.
Prenatal Diagnosis|October 27, 2019
Prenatal diagnosis and postnatal outcome of anterior urethral anomaliesSharon Perlman, Yael Borovitz, David Ben-Meir, et al.
Stem Cells Translational Medicine|May 15, 2023
Correction of T-Cell Repertoire and Autoimmune Diabetes in NOD Mice by Non-myeloablative T-Cell Depleted Allogeneic HSCTRakefet Sidlik Muskatel, Bar Nathansohn-Levi, Shlomit Reich-Zeliger, et al.
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