СИНДРОМЫ.
НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ
И
IDIOPATHIC PULMONARY FIBROSIS
FIBROGENESIS
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FoxO3 an important player in fibrogenesis for idiopathic pulmonary fibrosis.
HARLEQUIN
ICHTHYOSIS
CLINICAL, PATHOLOGICAL and THERAPEUTIC
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Harlequin Ichthyosis: A Comprehensive Clinical, Pathological, and Therapeutic of the Most Severe Form of Congenital Ichthyosis
IMPRINTING IN HUMAN DISEASE
DYSREGULATION IMPRINTED GENE
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Disease
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Advances in Imprinting Disorders
INFARCTION of MYOCARDE
RISK
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Factors
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Role of ALOX5AP
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Role of Period 2
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‘telomerasing’ for cardioprotection
INFANTILE-ONSET MULTISYSTEM NEUROLOGIC ENDOCRINE AND PANCREATIC DISEASE (IMNEPD)
PTRH2 GENE
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PTRH2 Gene Variants: infantile-onset multisystem neurologic endocrine and pancreatic disease (IMNEPD)
INFERTILITY
GENES
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Loss-of-function mutations in CEP78 cause male infertility in humans and mice
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heritable gain-of-function chk1 mutations impair human fertility
MALES
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Role of Endoplasmic Reticulum Stress in The Male Reproductive System
INFLAMMATION DISEASE
Neutrophilic Inflammation
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Dampen Neutrophilic Inflammation with MicroRNA-223
INFLAMMATORY BOWEL DISEASE
INNATE IMMUNE RESPONSE GENES
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Genes polymorphisms
MITOCHONDRIAL DNA
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Mitochondrial DNA Is a Pro-Inflammatory Damage-Associated During Active IBD
monogenic INTESTINAL EPITHELIAL DISORDERS
GENETICS
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The genetics of monogenic intestinal epithelial disorders
INTELLECTUAL DISABILITY
NEW GENES
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26 novel candidate genes
INTELLECTUAL/DEVELOPMENTAL DISABILITY
DNA METHYLATION BIOMARKERS
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DNA methylation biomarkers of intellectual/developmental disability across the lifespan
Intestinal Neuronal Dysplasia B
INTRAUTERINE DEVELOPMENTAL ABNORMALITIES
MATERNAL ENVIRONMENT
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Glucose and oxygen in the early intrauterine environment and their role in developmental abnormalities
IRON DISABILITY
NEURODEGENERATIONS
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Iron Accumulation: neurodegenerations
IRON-DEFICIENCY ANEMIA
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Scribble-mediated control of the erythropoietin receptor
IVF