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searching for primary ciliary dyskinesia 10 found (67 total)

alternate case: Primary ciliary dyskinesia

DNAI1 (798 words) [view diff] exact match in snippet view article find links to article

abnormal ciliary ultrastructure and function associated with primary ciliary dyskinesia (PCD) and Kartagener syndrome. The DNAI1 gene is involved in the

DNAH1 (473 words) [view diff] exact match in snippet view article find links to article

Naturally occurring mutations in this gene are associated with primary ciliary dyskinesia and multiple morphological anomalies of the flagella that result

DNAH9 (622 words) [view diff] exact match in snippet view article find links to article

sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia". Genomics. 72 (1): 21–33. doi:10.1006/geno.2000.6462. hdl:2123/16163

CCDC40 (gene) (426 words) [view diff] case mismatch in snippet view article

Smith RJ, Stephens K, Zariwala MA, Knowles MR, Leigh MW (1993). "Primary Ciliary Dyskinesia". PMID 20301301. {{cite journal}}: Cite journal requires |journal=

SPEF2 (572 words) [view diff] exact match in snippet view article find links to article

SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia". Biology of Reproduction. 85 (4): 690–701. doi:10.1095/biolreprod

Mimiviridae (2,195 words) [view diff] case mismatch in snippet view article find links to article

2020). "Pulmonary Infection Related to Mimivirus in Patient with Primary Ciliary Dyskinesia". Emerging Infectious Diseases. 26 (10): 2524–2526. doi:10.3201/eid2610

Orange ribbon (1,644 words) [view diff] case mismatch in snippet view article find links to article

Week (NIAW) is an annual event during the last week of April. Primary Ciliary Dyskinesia (PCD), a rare lung disease Gun violence protests At-risk animal

FOXJ1 (2,069 words) [view diff] exact match in snippet view article find links to article

deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD)". Cytogenetics and Cell Genetics. 90 (1–2): 119–22. doi:10

Strømme syndrome (2,717 words) [view diff] exact match in snippet view article find links to article

jejunal atresia with microcephaly and ocular anomalies, (formerly) primary ciliary dyskinesia 31 (CILD31) Female infant with Strømme syndrome showing microcephaly

2021 New Year Honours (23,511 words) [view diff] case mismatch in snippet view article find links to article

Copeland. Lately Chair, Primary Ciliary Dyskinesia Family Support Group. For services to Raising Awareness of Primary Ciliary Dyskinesia. (Milton Keynes, Buckinghamshire)