(Q56804273)

1

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Evan E. Eichler

2

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Stephanie M. Fullerton

3

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Douglas Carrell

Systems Biology in Reproductive Medicine

4

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publication date

January 2010

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published in

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volume

56

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issue

1

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page(s)

18-26

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cites work

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The genetics of male infertility: a field of study whose time is now.

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Genetic causes of male infertility

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Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk

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The gr/gr deletion(s): a new genetic test in male infertility?

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Mapping and sequencing of structural variation from eight human genomes

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The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile men.

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Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

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Gene copy number variations in Asian patients with congenital bilateral absence of the vas deferens

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Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan

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Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

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Cytogenetic determinants of male fertility

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Proteomic identification of human sperm proteins

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Expression of SPANX proteins in human-ejaculated spermatozoa and sperm precursors.

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Expression of SpanX proteins in normal testes and in testicular germ cell tumours

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CCL3L1 and CCL4L1: variable gene copy number in adolescents with and without human immunodeficiency virus type 1 (HIV-1) infection

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Segmental duplications and copy-number variation in the human genome

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Genome architecture, rearrangements and genomic disorders

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Spermatid-specific expression of the novel X-linked gene product SPAN-X localized to the nucleus of human spermatozoa

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Genomic organization, incidence, and localization of the SPAN-x family of cancer-testis antigens in melanoma tumors and cell lines

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Hominoid-specific SPANXA/D genes demonstrate differential expression in individuals and protein localization to a distinct nuclear envelope domain during spermatid morphogenesis

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Gene copy-number variation and associated polymorphisms of complement component C4 in human systemic lupus erythematosus (SLE): low copy number is a risk factor for and high copy number is a protective factor against SLE susceptibility in European A

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The human SPANX multigene family: genomic organization, alignment and expression in male germ cells and tumor cell lines.

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Partial AZFc deletions and duplications: clinical correlates in the Italian population

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