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1 PURA gene purine rich element binding protein A Normal Function The PURA gene provides instructions for making a protein called Puralpha Pur a binda molecular cousin of DNAa molecular cousin. & the . NLM Web Site. . Loren Frant. Loren.Frant@nih.gov. 2. m.medlineplus.gov. Screen captures of the MedlinePlus English homepages. before and after the redesign.. 3. Screen capture of the MedlinePlus English asthma health topic page. Helping Consumers To Professionals With Good Health Information. (Your health wins!). Jacqueline Leskovec, MLIS, MA, RN. NNLM . GMR. Network Librarian. Objectives. Participants will:. Learn how to access MedlinePlus and PubMed. 1 Generalized arterial calcification of infancy Description GACIGACI system that becomes apparent before birth or within the first few months of life. It is calcificationcalcification walls of the bl 1 PIGO gene phosphatidylinositol glycan anchor biosynthesis class O Normal Function The PIGO gene provides instructions for making one part of an enzyme called GPI GPI-ET3GPI-ET3 produced from a ge 1RARA generetinoic acid receptor alphaNormal FunctionThe RARA gene provides instructions for making a transcription factor called the retinoic acid receptor alpha RARa A transcription factor is a prot Who can implement MedlinePlus ConnectMedlinePlus Connect can be implemented as a quick onetime change by Health IT EHRor patient portalvendorswho offer MedlinePlus Connect as a feature to their client 1MelanomaDescriptionMelanoma is a type of skin cancer that begins in pigment-producing cells called melanocytes This cancer typically occurs in areas that are only occasionally sun-exposed tumors are 1 Ankylosing spondylitis Description Ankylosing spondylitis is a form of painful, ongoing joint inflammation (chronic inflammatory arthritis) that primarily affects the spine. Early symptoms of anky 1 Atopic dermatitis Description also known as atopic eczemaalso known as atopic eczema dermatitisdermatitis often disappears before adolescence. However, in some affected individuals the condition co 1 Dupuytren contracture Description Dupuytren contracture is characterized by a deformity of the hand in which the joints of extendedextended flexedflexed supports the body's muscles, joints, organs, 1 Hereditary hyperekplexia Description Hereditary hyperekplexia is a condition in which affected infants have increased muscle hypertoniahypertonia loud noises. Following the startle reaction, infant 1 FBLN5 gene fibulin 5 Normal Function The FBLN5 gene provides instructions for making a protein called fibulin-5. This protein is part of a group of proteins called fibulins. Fibulins have a varie 1 Sandhoff disease Description Sandhoff disease is a rare inherited disorder that progressively destroys nerve cells ( central nervous systemcentral nervous system classified into three major types ba 1 Horner syndrome Description Horner syndrome is a disorder that affects the eye and surrounding tissues on one side of the face and results from paralysis of certain nerves. Horner syndrome can appe