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Find link is a tool written by Edward Betts .
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Oligoasthenozoospermia (view )
searching for Asthenozoospermia 9 found (24 total)
alternate case: asthenozoospermia
DNAH1
(473 words)
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and multiple morphological anomalies of the flagella that result in asthenozoospermia and male infertility. Mice with a homozygous knockout of the orthologous
DNAH11
(1,735 words)
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Zhang G (June 2019). "Association of DNAH11 gene polymorphisms with asthenozoospermia in Northeast Chinese patients". Bioscience Reports. 39 (6). doi:10
Mother's curse
(991 words)
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than females. In mice, a deletion on mtDNA causes oligospermia and asthenozoospermia , resulting in infertility. Taken together, mtDNA mutations pose a
SMCP
(549 words)
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Neesen J, Rieche M, Wolf S, Sancken U, Kleene K, Engel W (May 2002). "Asthenozoospermia in mice with targeted deletion of the sperm mitochondrion-associated
ADCY10
(835 words)
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(June 2019). "ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria". Human Reproduction
Capacitation
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approximately 60 minutes and it is specially indicated in oligozoospermia, asthenozoospermia and abundant debris samples. At the end, all the cells will arrive
Genetics of infertility
(1,468 words)
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count], teratozoospermia [presence of sperm with abnormal shapes], and asthenozoospermia [sperm with reduced motility]); c) band 11 from the short arm of chromosome
Soluble adenylyl cyclase
(1,834 words)
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June 2019). "ADCY10 frameshift variant leading to severe recessive asthenozoospermia and segregating with absorptive hypercalciuria". Human Reproduction
Small supernumerary marker chromosome
(7,172 words)
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teratozoospermia [i.e. presence of sperm with abnormal shapes], and asthenozoospermia [i.e. sperm with reduced motility]). Infertility associated with a