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3. Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy

7. N -acetylneuraminate pyruvate lyase controls sialylation of muscle glycoproteins essential for muscle regeneration and function

19. Maternal anti-platelet β3 integrins impair angiogenesis and cause intracranial hemorrhage

20. Activated NK cells cause placental dysfunction and miscarriages in fetal alloimmune thrombocytopenia

21. Plasma obtained following murine hindlimb ischemic conditioning protects against oxidative stress in zebrafish models through activation of nrf2a and downregulation of duox

22. Financing and investment efficiency, information quality, and accounting biases

27. Correction to: The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis

33. Building the vertebrate codex using the gene breaking protein trap library

34. A deficiency in the region homologous to human 17q21.33-q23.2 causes heart defects in mice

41. ndufa7plays a critical role in cardiac hypertrophy

42. Building the vertebrate codex using the gene breaking protein trap library

43. Author response: Building the vertebrate codex using the gene breaking protein trap library

44. The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms

48. Fetal bovine serum impacts the observed N‐glycosylation defects in TMEM165 KO HEK cells

49. Glutaminase Deficiency Caused by Short Tandem Repeat Expansion in GLS

50. Bi-allelic GOT2 Mutations Cause a Treatable Malate-Aspartate Shuttle-Related Encephalopathy

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