Proteintech

IFT88 Polyclonal antibody

#13967-1-AP

143

Citing papers

3.9k

Combined citations

Supplier page Find this product

Research areas

Genetic and Kidney Cyst Diseases44 Hedgehog Signaling Pathway Studies17 Microtubule and mitosis dynamics14 Renal and related cancers11 Protist diversity and phylogeny10 Genetic Syndromes and Imprinting7 Epigenetics and DNA Methylation5 Cerebrospinal fluid and hydrocephalus4

Papers citing this product

1

Nek2 activation of Kif24 ensures cilium disassembly during the cell cycle

Nature Communications·2015·173 cit.·DOI

2

Superresolution Pattern Recognition Reveals the Architectural Map of the Ciliary Transition Zone

Scientific Reports·2015·159 cit.·DOI

3

Exome sequencing identifies <i>DYNC2H1</i> mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement

Journal of Medical Genetics·2013·145 cit.·DOI

4

Crystal structures of IFT70/52 and IFT52/46 provide insight into intraflagellar transport B core complex assembly

The Journal of Cell Biology·2014·127 cit.·DOI

5

Transition fibre protein FBF1 is required for the ciliary entry of assembled intraflagellar transport complexes

Nature Communications·2013·124 cit.·DOI

6

ICK is essential for cell type‐specific ciliogenesis and the regulation of ciliary transport

The EMBO Journal·2014·120 cit.·DOI

7

Primary cilia sensitize endothelial cells to BMP and prevent excessive vascular regression

The Journal of Cell Biology·2018·110 cit.·DOI

8

Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome

Nature Communications·2015·100 cit.·DOI

9

Unraveling cellular complexity with transient adapters in highly multiplexed super-resolution imaging

Cell·2024·98 cit.·DOI

10

Centriolar satellites are required for efficient ciliogenesis and ciliary content regulation

EMBO Reports·2019·98 cit.·DOI

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