Pages that link to "Q24312391"
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The following pages link to Mutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia (Q24312391):
Displaying 50 items.
- Zinc finger MYND-type containing 10 (Q21115625) (← links)
- Leucine rich repeat containing 6 (Q21136260) (← links)
- CCDC151 mutations cause primary ciliary dyskinesia by disruption of the outer dynein arm docking complex formation (Q24303570) (← links)
- HEATR2 plays a conserved role in assembly of the ciliary motile apparatus (Q24304187) (← 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)
- Genetic factors contributing to human primary ciliary dyskinesia and male infertility (Q26748534) (← links)
- Diverse Roles of Axonemal Dyneins in Drosophila Auditory Neuron Function and Mechanical Amplification in Hearing. (Q27305175) (← links)
- Unexpected genetic heterogeneity for primary ciliary dyskinesia in the Irish Traveller population. (Q27324715) (← links)
- Mutations in PIH1D3 Cause X-Linked Primary Ciliary Dyskinesia with Outer and Inner Dynein Arm Defects (Q28975778) (← links)
- Zinc finger MYND-type containing 10 Dmel_CG11253 (Q29819486) (← links)
- Novel roles for the radial spoke head protein 9 in neural and neurosensory cilia. (Q30372862) (← links)
- Hearing in Drosophila (Q30400378) (← links)
- Targeted NGS gene panel identifies mutations in RSPH1 causing primary ciliary dyskinesia and a common mechanism for ciliary central pair agenesis due to radial spoke defects. (Q30580167) (← links)
- Systematic discovery of novel ciliary genes through functional genomics in the zebrafish. (Q30592941) (← links)
- X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3. (Q30838646) (← links)
- The "omics" of human male infertility: integrating big data in a systems biology approach (Q31031878) (← links)
- Comparative expression profiling of testis-enriched genes regulated during the development of spermatogonial cells. (Q33570597) (← links)
- The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesia (Q33640482) (← links)
- Nonsense mutation in coiled-coil domain containing 151 gene (CCDC151) causes primary ciliary dyskinesia. (Q34438841) (← links)
- Recent advances in primary ciliary dyskinesia genetics. (Q34852544) (← links)
- Characterizing the ultrastructure of primary ciliary dyskinesia transposition defect using electron tomography. (Q35116940) (← links)
- Chlamydomonas axonemal dynein assembly locus ODA8 encodes a conserved flagellar protein needed for cytoplasmic maturation of outer dynein arm complexes (Q35181562) (← links)
- Unique among ciliopathies: primary ciliary dyskinesia, a motile cilia disorder (Q35210996) (← links)
- The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathies (Q35229307) (← links)
- Genetic Testing in the Diagnosis of Primary Ciliary Dyskinesia: State-of-the-Art and Future Perspectives (Q35667275) (← links)
- ZMYND10--Mutation Analysis in Slavic Patients with Primary Ciliary Dyskinesia (Q35908459) (← links)
- Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia. (Q35926452) (← links)
- The ciliary inner dynein arm, I1 dynein, is assembled in the cytoplasm and transported by IFT before axonemal docking (Q36001191) (← links)
- Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels (Q36267724) (← links)
- Simultaneous identification and prioritization of variants in familial, de novo, and somatic genetic disorders with VariantMaster. (Q37550264) (← links)
- Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype (Q37698245) (← links)
- Gene mutations in primary ciliary dyskinesia related to otitis media (Q38181444) (← links)
- A mutation study of sperm head shape and motility in the mouse: lessons for the clinic (Q38289619) (← links)
- Identification of FOXJ1 effectors during ciliogenesis in the foetal respiratory epithelium and embryonic left-right organiser of the mouse (Q38439569) (← links)
- Genetic basis of human left-right asymmetry disorders (Q38563680) (← links)
- Primary ciliary dyskinesia: mechanisms and management (Q42364406) (← links)
- Impact of Natural Compounds on DNA Methylation Levels of the Tumor Suppressor Gene RASSF1A in Cancer (Q45814721) (← links)
- Exome sequencing and genotyping identify a rare variant in NLRP7 gene associated with ulcerative colitis. (Q46248987) (← links)
- Sperm dysfunction and ciliopathy. (Q47171971) (← links)
- Axonemal dynein assembly requires the R2TP complex component Pontin. (Q47428760) (← links)
- Loss of zinc finger MYND-type containing 10 (zmynd10) affects cilia integrity and axonemal localization of dynein arms, resulting in ciliary dysmotility, polycystic kidney and scoliosis in medaka (Oryzias latipes). (Q47929915) (← links)
- Live birth after Laser Assisted Viability Assessment (LAVA) to detect pentoxifylline resistant ejaculated immotile spermatozoa during ICSI in a couple with male Kartagener's syndrome. (Q48103854) (← links)
- The need to improve patient care through discriminate use of intracytoplasmic sperm injection (ICSI) and improved understanding of spermatozoa, oocyte and embryo biology (Q48580312) (← links)
- Clinical phenotype and current diagnostic criteria for primary ciliary dyskinesia (Q50315572) (← links)
- ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms. (Q51730557) (← links)
- Genetics of male infertility. (Q52330584) (← links)
- Whole-Exome Sequencing Identified a Novel Compound Heterozygous Mutation of LRRC6 in a Chinese Primary Ciliary Dyskinesia Patient. (Q52670785) (← links)
- C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia (Q54850008) (← links)
- Expression of the onconeural protein CDR1 in cerebellum and ovarian cancer. (Q54936358) (← links)
- Ciliary dynein motor preassembly is regulated by Wdr92 in association with HSP90 co-chaperone, R2TP. (Q55517564) (← links)