PMC Links for OMIM (Select 603331) - PMC - NCBI

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Items: 4

Select item 65569081.

Bi-allelic Variants in DYNC1I2 Cause Syndromic Microcephaly with Intellectual Disability, Cerebral Malformations, and Dysmorphic Facial Features

Muhammad Ansar, Farid Ullah, Sohail A. Paracha, Darius J. Adams, Abbe Lai, Lynn Pais, Justyna Iwaszkiewicz, Francisca Millan, Muhammad T. Sarwar, Zehra Agha, Sayyed Fahim Shah, Azhar Ali Qaisar, Emilie Falconnet, Vincent Zoete, Emmanuelle Ranza, Periklis Makrythanasis, Federico A. Santoni, Jawad Ahmed, Nicholas Katsanis, Christopher Walsh, Erica E. Davis, Stylianos E. Antonarakis

Am J Hum Genet. 2019 Jun 6; 104(6): 1073–1087. Published online 2019 May 9. doi: 10.1016/j.ajhg.2019.04.002

PMCID:: PMC6556908

Abstract Article PDF–1.7M

Select item 25930242.

Identification of predicted human outer dynein arm genes: candidates for primary ciliary dyskinesia genes

G J Pazour, N Agrin, B L Walker, G B Witman

J Med Genet. 2006 Jan; 43(1): 62–73. Published online 2005 Jun 3. doi: 10.1136/jmg.2005.033001

PMCID:: PMC2593024

Abstract Article PDF–509K

Select item 22895963.

Homology of the 74-kD cytoplasmic dynein subunit with a flagellar dynein polypeptide suggests an intracellular targeting function

J Cell Biol. 1992 Sep 1; 118(5): 1133–1143. doi: 10.1083/jcb.118.5.1133

PMCID:: PMC2289596

Summary PDF–1.6M

Select item 21206894.

Cytoplasmic dynein binds dynactin through a direct interaction between the intermediate chains and p150Glued

J Cell Biol. 1995 Dec 2; 131(6): 1507–1516. doi: 10.1083/jcb.131.6.1507

PMCID:: PMC2120689

Summary PDF–1.4M

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