Pages that link to "Q34619343"
Jump to navigation
Jump to search
The following pages link to Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility. (Q34619343):
Displaying 50 items.
- teratospermia (Q2161625) (← links)
- In vitro expression of the HIV-2 genomic RNA is controlled by three distinct internal ribosome entry segments that are regulated by the HIV protease and the Gag polyprotein (Q22241577) (← links)
- DEAD-box protein DDX3 associates with eIF4F to promote translation of selected mRNAs (Q24295198) (← links)
- A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation (Q24296542) (← links)
- Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella (Q24315743) (← links)
- Single nucleotide polymorphisms in the SEPTIN12 gene may be associated with azoospermia by meiotic arrest in Japanese men (Q24614084) (← links)
- Small-molecule inhibition of BRDT for male contraception (Q24616901) (← links)
- Functions of Aurora kinase C in meiosis and cancer (Q26782717) (← links)
- Possible Role of Aurora-C in Meiosis (Q26795739) (← links)
- Sexual polyploidization in plants--cytological mechanisms and molecular regulation (Q26827323) (← links)
- Aurora at the pole and equator: overlapping functions of Aurora kinases in the mitotic spindle (Q27021024) (← links)
- A Cell Biologist's Field Guide to Aurora Kinase Inhibitors (Q27308125) (← links)
- Disruption of dmc1 Produces Abnormal Sperm in Medaka (Oryzias latipes) (Q27320526) (← links)
- Aurora-C Interactions with Survivin and INCENP Reveal Shared and Distinct Features Compared with Aurora-B Chromosome Passenger Protein Complex (Q28771757) (← links)
- Chromosomal passengers: conducting cell division (Q29620468) (← links)
- Aurora-C kinase deficiency causes cytokinesis failure in meiosis I and production of large polyploid oocytes in mice (Q30495481) (← links)
- Genome-wide expression of azoospermia testes demonstrates a specific profile and implicates ART3 in genetic susceptibility (Q33319281) (← links)
- The power of mouse genetics to study spermatogenesis (Q33956928) (← links)
- Overexpression of active Aurora-C kinase results in cell transformation and tumour formation (Q34064502) (← links)
- The aurora kinases in cell cycle and leukemia (Q34203062) (← links)
- Array comparative genomic hybridization in male infertility (Q34246420) (← links)
- Comprehensive 5-year study of cytogenetic aberrations in 668 infertile men (Q34263804) (← links)
- The chromosome passenger complex is required for fidelity of chromosome transmission and cytokinesis in meiosis of mouse oocytes (Q34371416) (← links)
- Genetic aspects of monomorphic teratozoospermia: a review (Q34464318) (← links)
- Exome sequencing reveals a nonsense mutation in TEX15 causing spermatogenic failure in a Turkish family (Q34486302) (← links)
- HIV-2 genomic RNA accumulates in stress granules in the absence of active translation. (Q34489574) (← links)
- The Wilms tumor gene, Wt1, is critical for mouse spermatogenesis via regulation of sertoli cell polarity and is associated with non-obstructive azoospermia in humans (Q34917167) (← links)
- Mutations of the aurora kinase C gene causing macrozoospermia are the most frequent genetic cause of male infertility in Algerian men. (Q34927993) (← links)
- Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest. (Q35205846) (← links)
- Male infertility and its causes in human (Q35419590) (← links)
- CANDID: a flexible method for prioritizing candidate genes for complex human traits. (Q35571604) (← links)
- Association of mutations in the zona pellucida binding protein 1 (ZPBP1) gene with abnormal sperm head morphology in infertile men. (Q35630465) (← links)
- Aurora kinase-C-T191D is constitutively active mutant (Q35883353) (← links)
- Expression and characterization of three Aurora kinase C splice variants found in human oocytes (Q35897954) (← links)
- The genetics of human infertility by functional interrogation of SNPs in mice (Q35989784) (← links)
- A novel role for TPX2 as a scaffold and co-activator protein of the Chromosomal Passenger Complex (Q35996051) (← links)
- Macrozoospermia: screening for the homozygous c.144delC mutation in AURKC gene in infertile men and estimation of its heterozygosity frequency in the Tunisian population (Q36297234) (← links)
- Australin: a chromosomal passenger protein required specifically for Drosophila melanogaster male meiosis (Q36446618) (← links)
- A new AURKC mutation causing macrozoospermia: implications for human spermatogenesis and clinical diagnosis. (Q36804447) (← links)
- Major spliceosome defects cause male infertility and are associated with nonobstructive azoospermia in humans (Q36821514) (← links)
- Mendelian genetics of male infertility (Q36846121) (← links)
- UBE2B mRNA alterations are associated with severe oligozoospermia in infertile men. (Q36849131) (← links)
- Single-nucleotide polymorphisms in HORMAD1 may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients (Q37037508) (← links)
- Genetic causes of spermatogenic failure. (Q37074590) (← links)
- Cell cycle-dependent ciliogenesis and cancer (Q37125352) (← links)
- The biology of infertility: research advances and clinical challenges (Q37206451) (← links)
- Quantitative phosphoproteomics identifies substrates and functional modules of Aurora and Polo-like kinase activities in mitotic cells (Q37254703) (← links)
- The Genetics of Infertility: Current Status of the Field (Q37450892) (← links)
- ENMD-2076 for hematological malignancies (Q37991379) (← links)
- Mitotic failures in cancer: Aurora B kinase and its potential role in the development of aneuploidy. (Q38030445) (← links)