СИНДРОМЫ.
НАСЛЕДСТВЕННЫЕ БОЛЕЗНИ
LANGUAGE DISORDER
GENETIC AND MOLECULAR BASIS
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The Genetic and Molecular Basis of Developmental Language Disorder
LAMINOPATHIES
LAMINS A-TYPE
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Description
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Role of stem cells
LEIGH SYNDROME
FRENCH CANADIAN VARIANT
Defects PGC-1a/LRP130 complex
MODELS
Disease models of Leigh syndrome: From yeast to organoids
LEUKEMIA
INTERACTIONS CELLS
Niche Interactions Lock Down Leukemia Cells
LIMB DISORDERS
GENETIC CONTROL
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Genetic cold cases: lessons from solving complex congenital limb disorders
LIPIDEMIA
REDUCED BLOOD LIPID LEVELS
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CRISPR-Cas9 Base Editing of ANGPTL3
LISSENCEPHALY
Описание
Reln+Pafah1
Molecular Mechanisms
Mutations in α-tubulin
LIVER DISEASE
SUPPRESSION AND IMPAIRMENT IN AUTOIMMUNE
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Regulatory T cells
GENETICS
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the role of TRAIL in liver diseases
HEPATOTOXICITY
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model system to study liver diseases and related drug discovery
LYMPHANGIOGENESIS ANOMALY
PRIMARY LYMPHATIC DYSPLASIA
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Genetics
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Genetics
LYNCH SYNDROME
PATHOGENESIS
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Epigenetic mutations
LUNG DISEASES
CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD)
Getenics
GENETICS
Lung Developmental Biology and Adult Lung Function
LYMPHANGIOGENESIS
Anomaly
LYMPHEDEMA
Genes involved in endothelial cell apoptosis by their implication in lymphedema
LYSOSOMAL STORAGE DISORDERS
LYSOSOME BIOGENESIS
Lysosome biogenesis in health and disease