Dagan Jenkins
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Explore the profile of Dagan Jenkins including associated specialties, affiliations and a list of published articles.
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33
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1108
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Recent Articles
1.
Beyer T, Diwan G, Leonhard T, Dahlke K, Klose F, Stehle I, et al.
Mol Cell Proteomics
. 2025 Jan;
24(3):100916.
PMID: 39880085
Genotype-phenotype correlations of rare diseases are complicated by low patient number, high phenotype variability, and compound heterozygosity. Mutations may cause instability of single proteins, and affect protein complex formation or...
2.
Mukhopadhyay A, Toropova K, Daly L, Wells J, Vuolo L, Mladenov M, et al.
EMBO J
. 2024 Mar;
43(7):1257-1272.
PMID: 38454149
Dynein-2 is a large multiprotein complex that powers retrograde intraflagellar transport (IFT) of cargoes within cilia/flagella, but the molecular mechanism underlying this function is still emerging. Distinctively, dynein-2 contains two...
3.
Jenkins D, Chubb J, Galea G
Philos Trans R Soc Lond B Biol Sci
. 2024 Mar;
379(1900):20230043.
PMID: 38432319
No abstract available.
4.
Jenkins D
Philos Trans R Soc Lond B Biol Sci
. 2024 Mar;
379(1900):20230045.
PMID: 38432317
Incomplete penetrance is the rule rather than the exception in Mendelian disease. In syndromic monogenic disorders, phenotypic variability can be viewed as the combination of incomplete penetrance for each of...
5.
Freke G, Martins T, Davies R, Beyer T, Seda M, Peskett E, et al.
Cells
. 2023 Nov;
12(22).
PMID: 37998397
Bardet-Biedl syndrome (BBS) is an archetypal ciliopathy caused by dysfunction of primary cilia. BBS affects multiple tissues, including the kidney, eye and hypothalamic satiety response. Understanding pan-tissue mechanisms of pathogenesis...
6.
Beyer T, Martins T, Jeyabalan Srikaran J, Seda M, Peskett E, Klose F, et al.
Methods Mol Biol
. 2023 Oct;
2725:199-212.
PMID: 37856026
Biological complexity is achieved through elaborate interactions between relatively few individual components. Affinity purification (AP) has allowed these networks of protein-protein interactions that regulate key biological processes to be interrogated...
7.
Seda M, Crespo B, Corcelli M, Osborn D, Jenkins D
Sci Rep
. 2023 Apr;
13(1):6783.
PMID: 37100808
Idiopathic scoliosis (IS) is the deformation and/or abnormal curvature of the spine that develops progressively after birth. It is a very common condition, affecting approximately 4% of the general population,...
8.
Lam W, Tang C, So M, Yue H, Hsu J, Chung P, et al.
EBioMedicine
. 2021 Aug;
71:103530.
PMID: 34455394
Background: Biliary atresia (BA) is the most common obstructive cholangiopathy in neonates, often progressing to end-stage cirrhosis. BA pathogenesis is believed to be multifactorial, but the genetic contribution, especially for...
9.
Bryant D, Seda M, Peskett E, Maurer C, Pomeranz G, Ghosh M, et al.
Sci Rep
. 2020 Aug;
10(1):13763.
PMID: 32792680
Mutations in the SNX14 gene cause spinocerebellar ataxia, autosomal recessive 20 (SCAR20) in both humans and dogs. Studies implicating the phenotypic consequences of SNX14 mutations to be consequences of subcellular...
10.
Manole A, Efthymiou S, OConnor E, Mendes M, Jennings M, Maroofian R, et al.
Am J Hum Genet
. 2020 Aug;
107(2):311-324.
PMID: 32738225
Aminoacyl-tRNA synthetases (ARSs) are ubiquitous, ancient enzymes that charge amino acids to cognate tRNA molecules, the essential first step of protein translation. Here, we describe 32 individuals from 21 families,...