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పేపర్లు ప్రచురించబడ్డాయి

సమీక్షా వ్యాసం

Genetics of Epilepsy

Oluwayemi Joshua Bamikole, Miles-Dei Benedict Olufeagba, Samuel Temitope Soge, Noah Olamide Bukoye, Taiwo Habeeb Olajide, Subulade Abigail Ademola and Olukemi Kehinde Amodu

Genetics is a branch of the human biology which provides insights about basic and vital processes which arises from birth till death, development to Apoptosis (cell death), and ..మరిన్ని చూడండి»

అభిప్రాయం

Overcoming Barriers to Diabetes Technology in Youth with Type 1 Diabetes and Public Insurance

Hazel Scarlett

Continuous Glucose Monitoring (CGM), insulin pumps, and automated insulin administration are all examples of advances in diabetes technology that can help type 1 diabetes patien..మరిన్ని చూడండి»

పరిశోధన వ్యాసం

A Pilot Investigation of Natural Killer Cell Function and Phenotypes in Stable and Active Multiple Sclerosis Patients

Helene Cabanas, Natalie Eaton, Ellie Khalilidehkordi, Simon Broadly, Cassandra Balinas, Stanley Du Preez, Rebekah Maksoud, Donald Staines and Sonya Marshall-Gradisnik

Background: Previous studies have reported impaired cytotoxic activity in Natural Killer (NK) CD56Dim and CD56Bright cell phenotypes in peripheral blood associa..మరిన్ని చూడండి»

పరిశోధన వ్యాసం

Retrospective Analysis of Anterior Interosseous Nerve Lesions and Motor Nerve Conduction Measurements

Shingo Nobuta, Katsumi Sato and Eiji Itoi

Objective: Anterior interosseous nerve (AIN) lesions are rare and a few nerve conduction measurements have been reported. The purpose of this retrospective study was to assess t..మరిన్ని చూడండి»

నైరూప్య

Antibacterial Potentials of Pentacyclic Triterpenoidal Sapogenins from Bligha sapida Seed Pods

Fadipe, L. A

Background: Bligha sapida (family Sapindaceae) is a plant
widely used in ethnomedicine for the treatment of dysentery,
dental decay and whitlow. Qualitative and qu..మరిన్ని చూడండి»

కేసు నివేదిక

A Novel Mutation in the SCN4A Gene in a Japanese Family with Paramyotonia Congenita

Satoru Takahashi, Shiho Yamamoto, Ryosuke Tanaka, Akie Okayama, Akiko Araki, Hiroki Kajino and Hiroshi Azuma

Paramyotoniacongenita is an autosomal-dominant muscle disease caused by missense mutations in SCN4A, the
gene enconding the alpha subunit of skeletal muscle sodium channe..మరిన్ని చూడండి»

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