Study provides new insights into the molecular causes of rare, fatal hereditary disease

A study entitled “IER3IP1-mutations cause microcephaly by selective inhibition of ER-Golgi transport”, now published in the open access journal “Cellular and Molecular Life Sciences”, provides new insights into the molecular causes of a rare and usually fatal hereditary disease called MEDS1.

Opinion | All Specialties Struggle With ‘Moral Injury’

Emily Hutto is an Associate Video Producer & Editor for MedPage Today. She is based in Manhattan. In this exclusive Instagram Live clip, Jeremy Faust,

September 30, 2023

Analysts expect a reimbursement boost for Shockwave coronary artery-clearing device

Dive Brief: The Centers for Medicare and Medicaid Services is set to propose outpatient reimbursement that will increase sales of Shockwave Medical’s heart disease device,

July 11, 2023

WHO Links Sweetener to Cancer; Younger-Age CRC Risk; PCOS and Ovarian Cancer

The World Health Organization’s cancer research arm has concluded that the widely used artificial sweetener aspartame is “possibly carcinogenic to humans.” (Reuters) A large matched

June 30, 2023

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