Works matching DE "GENETICS of spermatogenesis"
Results: 70
A Novel Growth Retardation and Abnormal Gonad Morphology, Locus on Mouse Chromosome 4.
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- Journal of Heredity, 2009, v. 100, n. 3, p. 380, doi. 10.1093/jhered/esn106
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CAG-repeat polymorphisms in the polymerase γ gene and male infertility: a meta-analysis.
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- Andrologia, 2016, v. 48, n. 9, p. 882, doi. 10.1111/and.12526
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Analysis of partial azoospermia factor c deletion and DAZ copy number in azoospermia and severe oligozoospermia.
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- Andrologia, 2016, v. 48, n. 9, p. 890, doi. 10.1111/and.12527
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DNA methylation levels of imprinted and nonimprinted genes DMRs associated with defective human spermatozoa.
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- Andrologia, 2016, v. 48, n. 9, p. 939, doi. 10.1111/and.12535
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Association of G/T(rs222859) polymorphism in Exon 1 of YBX2 gene with azoospermia, among Iranian infertile males.
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- Andrologia, 2016, v. 48, n. 9, p. 956, doi. 10.1111/and.12537
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Mammalian phospholipase D physiological and pathological roles.
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- Acta Physiologica, 2012, v. 204, n. 2, p. 219, doi. 10.1111/j.1748-1716.2011.02298.x
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Chimaeric mice with disruption of the gene coding for phosphatidylinositol glycan class A (Pig-a) were defective in embryogenesis and spermatogenesis.
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- British Journal of Haematology, 2000, v. 110, n. 3, p. 682, doi. 10.1046/j.1365-2141.2000.02209.x
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Epigenetic Alterations in Sperm DNA Associated with Testicular Cancer Treatment.
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- Toxicological Sciences, 2012, v. 125, n. 2, p. 532, doi. 10.1093/toxsci/kfr307
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HLA-DPB1*04:01 allele is associated with non-obstructive azoospermia in Japanese patients.
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- Human Genetics, 2013, v. 132, n. 12, p. 1405, doi. 10.1007/s00439-013-1347-7
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Examination of Idiopathic Infertility in the Presence of Normal FSH Levels.
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- Fertility Weekly, 2002, p. 16
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Histone H1t is not replaced by H1.1 or H1.2 in pachytene spermatocytes or spermatids of H1t-deficient mice.
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- Cytogenetic & Genome Research, 2003, v. 103, n. 3/4, p. 307, doi. 10.1159/000076818
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The Azoospermia region AZFa: An evolutionar y view.
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- Cytogenetic & Genome Research, 2002, v. 99, n. 1-4, p. 146, doi. 10.1159/000071586
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β-nerve growth factor participates in an auto/paracrine pathway of regulation of the meiotic differentiation of rat spermatocytes.
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- Journal of Cellular Physiology, 2007, v. 210, n. 1, p. 51, doi. 10.1002/jcp.20805
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Study of AZFc partial deletion gr/gr in fertile and infertile Japanese males.
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- Journal of Human Genetics, 2006, v. 51, n. 9, p. 794, doi. 10.1007/s10038-006-0024-2
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Spermatogenic ability is different among males in different Y chromosome lineage.
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- Journal of Human Genetics, 1999, v. 44, n. 5, p. 289, doi. 10.1007/s100380050162
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A Complex Suite of Forces Drives Gene Traffic from Drosophila X Chromosomes.
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- Genome Biology & Evolution, 2009, v. 1, p. 176, doi. 10.1093/gbe/evp018
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A New Role of the Mosquito Complement-like Cascade in Male Fertility in Anopheles gambiae.
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- PLoS Biology, 2015, v. 13, n. 9, p. 1, doi. 10.1371/journal.pbio.1002255
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4-Nonylphenol induces disruption of spermatogenesis associated with oxidative stress-related apoptosis by targeting p53-Bcl-2/Bax-Fas/FasL signaling.
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- Environmental Toxicology, 2017, v. 32, n. 3, p. 739, doi. 10.1002/tox.22274
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Prenatal bisphenol a exposure leads to reproductive hazards on male offspring via the Akt/mTOR and mitochondrial apoptosis pathways.
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- Environmental Toxicology, 2017, v. 32, n. 3, p. 1007, doi. 10.1002/tox.22300
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Cytological evaluation of spermatogenesis: a novel and simple diagnostic method to assess spermatogenesis in non-obstructive azoospermia using testicular sperm extraction specimens.
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- Andrology, 2015, v. 3, n. 3, p. 481, doi. 10.1111/andr.12023
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Congenital bilateral absence of the vas deferens: the impact of spermatogenesis quality on intracytoplasmic sperm injection outcomes in 108 men.
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- Andrology, 2015, v. 3, n. 3, p. 473, doi. 10.1111/andr.12019
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The Roles of Testicular C-kit Positive Cells in De novo Morphogenesis of Testis.
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- Scientific Reports, 2014, p. 1, doi. 10.1038/srep05936
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New Research Grants Awarded in AY 2016-2017 at the John A. Burns School of Medicine.
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- Hawaii Journal of Medicine & Public Health, 2018, v. 77, n. 4, p. 89
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Testicular Stem Cells Express Follicle-Stimulating Hormone Receptors and Are Directly Modulated by FSH.
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- Reproductive Sciences, 2016, v. 23, n. 11, p. 1493, doi. 10.1177/1933719116643593
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Sperm competition-induced plasticity in the speed of spermatogenesis.
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- BMC Evolutionary Biology, 2016, v. 16, p. 1, doi. 10.1186/s12862-016-0629-9
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Evidence that sex chromosome asynapsis, rather than excess Y gene dosage, is responsible for the meiotic impairment of XYY mice.
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- Cytogenetics & Cell Genetics, 2000, v. 89, n. 1/2, p. 38, doi. 10.1159/000015559
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Type 2 cannabinoid receptor contributes to the physiological regulation of spermatogenesis.
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- FASEB Journal, 2016, v. 30, n. 4, p. 1453, doi. 10.1096/fj.15-279034
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Novel Gene Acquisition on Carnivore<br /> Y Chromosomes.
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- PLoS Genetics, 2006, v. 2, n. 3, p. e43, doi. 10.1371/journal.pgen.0020043
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miRNA and mammalian male germ cells.
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- Human Reproduction Update, 2012, v. 18, n. 1, p. 44, doi. 10.1093/humupd/dmr041
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Genetic analysis of a Y-chromosome region that induces triposterile phenotypes and is essential....
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- Genetics, 2000, v. 155, n. 1, p. 179, doi. 10.1093/genetics/155.1.179
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Regulatory elements required for development of Caenorhabditis elegans hermaphrodites are....
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- Genetics, 2000, v. 155, n. 1, p. 105, doi. 10.1093/genetics/155.1.105
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The fog-3 gene and regulation of cell fate in the germ line of Caenorhabditis elegans.
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- Genetics, 1995, v. 139, n. 2, p. 561, doi. 10.1093/genetics/139.2.561
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Toward a molecular genetic analysis of spermatogenesis in Drosophila melanogaster:...
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- Genetics, 1993, v. 135, n. 2, p. 489, doi. 10.1093/genetics/135.2.489
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Hybrid male sterility and genome-wide misexpression of male reproductive proteases.
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- Scientific Reports, 2015, p. 11976, doi. 10.1038/srep11976
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Evolution of the DAZ gene family suggests that Y-linked DAZ plays little, or a limited, role in spermatogenesis but underlines a recent African origin for human populations.
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- Human Molecular Genetics, 1998, v. 7, n. 9, p. 1371, doi. 10.1093/hmg/7.9.1371
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The role of USP9Y and DBY in infertile patients with severely impaired spermatogenesis.
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- Molecular Human Reproduction, 2001, v. 7, n. 7, doi. 10.1093/molehr/7.7.691
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The role of USP9Y and DBY in infertile patients with severely impaired spermatogenesis.
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- Molecular Human Reproduction, 2001, v. 7, n. 7, doi. 10.1093/molehr/7.7.692
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Developmental expression of Y-box protein 1 mRNA and alternatively spliced Y-box protein 3 mRNAs in spermatogenic cells in mice.
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- Molecular Human Reproduction, 2000, v. 6, n. 9, p. 779, doi. 10.1093/molehr/6.9.779
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Diagnosing genetic disease. Screening for cystic fibrosis transmembrane conductance regulator gene mutations in men included in an intracytoplasmic sperm injection programme.
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- Molecular Human Reproduction, 1999, v. 5, n. 6, p. 587, doi. 10.1093/molehr/5.6.587
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Expression of DAZ (deleted in azoospermia), DAZL1 (DAZ -like) and protamine-2 in testis and its application for diagnosis of spermatogenesis in non-obstructive azoospermia.
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- Molecular Human Reproduction, 1998, v. 4, n. 9, doi. 10.1093/molehr/4.9.827
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Meiotic failure in cyclin A1-deficient mouse spermatocytes triggers apoptosis through intrinsic and extrinsic signaling pathways and 14-3-3 proteins.
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- PLoS ONE, 2017, v. 12, n. 3, p. 1, doi. 10.1371/journal.pone.0173926
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An azoospermic man with a de novo point mutation in the Y-chromosomal gene USP9Y.
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- Nature Genetics, 1999, v. 23, n. 4, p. 429, doi. 10.1038/70539
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Embryological Results of Couples Undergoing ICSI-ET Treatments with Males Carrying the Single Nucleotide Polymorphism rs175080 of the MLH3 Gene.
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- International Journal of Molecular Sciences, 2017, v. 18, n. 2, p. 314, doi. 10.3390/ijms18020314
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Genetic, structural, and chemical insights into the dual function of GRASP55 in germ cell Golgi remodeling and JAM-C polarized localization during spermatogenesis.
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- PLoS Genetics, 2017, v. 13, n. 6, p. 1, doi. 10.1371/journal.pgen.1006803
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Zhang, Y., Luo, F., Wu, S., Yu, B., Liu, T. and Wu, Y. (2014), Tribbles homolog 3 expression in spermatogonial stem cells of rat testes. Cell Biology International, 38: 1403-1407. doi: 10.1002/cbin.10338.
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- Cell Biology International, 2016, v. 40, n. 2, p. 240, doi. 10.1002/cbin.10560
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Possible lack of association between E469K polymorphism of ICAM-1 and non-obstructive azoospermia in south-east Turkey.
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- Biotechnology & Biotechnological Equipment, 2017, v. 31, n. 1, p. 143, doi. 10.1080/13102818.2016.1261635
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Gene-Level, but Not Chromosome-Wide, Divergence between a Very Young House Fly Proto-Y Chromosome and Its Homologous Proto-X Chromosome.
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- Molecular Biology & Evolution, 2021, v. 38, n. 2, p. 606, doi. 10.1093/molbev/msaa250
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Influence of mesh materials on the integrity of the vas deferens following Lichtenstein hernioplasty: an experimental model.
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- Hernia, 2008, v. 12, n. 6, p. 621, doi. 10.1007/s10029-008-0400-2
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Ring chromosome 21 and monosomy 21 mosaicism in a patient with azoospermia.
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- Andrologia, 2015, v. 47, n. 1, p. 112, doi. 10.1111/and.12232
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Decrease of anti-Mullerian hormone in genetic spermatogenic failure.
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- Andrologia, 2012, v. 44, n. 5, p. 349, doi. 10.1111/j.1439-0272.2010.01092.x
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