American_Journal  

Documents (145) JSON TSV

source DB source ID text size updated at # proj. # Ann. updated_at
PMC 1271393 The Heritage of Pathogen Pressures and Ancient Demography in the Human Innate-Immunity CD209/CD209L Region Abstract The innate immunity system constitutes the first line of host defense against patho 64.3 KB 2020-12-30 4
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PMC 1852721 Mendelian Inheritance in Man and Its Online Version, OMIM Last year marked the 40th anniversary of the publication of the first print edition of Mendelian Inheritance in Man (MIM).1 This seems an app 77.9 KB 2020-12-30 4
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PMC 2427286 Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events Abstract Lebanon is an eastern Mediterranean country inhabited by approximately four million people with a wide variety of 30.7 KB 2021-02-10 3
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PMC 2495064 Pathogenic Mitochondrial DNA Mutations Are Common in the General Population Abstract Mitochondrial DNA (mtDNA) mutations are a major cause of genetic disease, but their prevalence in the general popu 17.4 KB 2020-12-30 4
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PMC 2495071 HLA-DRB1∗0401 and HLA-DRB1∗0408 Are Strongly Associated with the Development of Antibodies against Interferon-β Therapy in Multiple Sclerosis Abstract The formation of antibodies to interferon-beta ( 36.8 KB 2020-12-30 4
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PMC 2668026 Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta Abstract The combination of recessively inherited cone-rod dystrophy (CRD) 15.9 KB 2020-09-15 5
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PMC 2668061 The Genetic Legacy of Religious Diversity and Intolerance: Paternal Lineages of Christians, Jews, and Muslims in the Iberian Peninsula Abstract Most studies of European genetic diversity have focused 32.7 KB 2020-12-30 4
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PMC 2681008 Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice Abstract Cone-rod dystrophy (CRD) is an inherited progressive retinal dystrophy affecting the 14.6 KB 2025-10-02 8
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PMC 2694971 Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations Abstract Alveolar capillary dysplasia wi 25.8 KB 2025-10-02 8
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PMC 2725236 CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment Abstract Specific language impairment (SLI) is a common developmental disorder characterized by difficulties in language 31.4 KB 2025-10-02 7
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