Missense mutations in SLC26A8, encoding a sperm-specific activator of CFTR, are associated with human asthenozoospermia
Abstract
Loss-of-function mutations in LRRC6, a gene essential for proper axonemal assembly of inner and outer dynein arms, cause primary ciliary dyskinesia
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[Morphological defects of sperm flagellum implicated in human male infertility]
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Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse
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Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human
Abstract
Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia
Abstract
Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility
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Male Infertility: Genetics, Mechanism, and Therapies
Abstract
Assessment of the frequency of sperm annulus defects in a large cohort of patients presenting asthenozoospermia
Abstract
Effects of environmental cadmium and lead exposure on adults neighboring a discharge: Evidences of adverse health effects
Abstract