Suchergebnisse - "SCLT1 protein, human"

PubPharm (12)

1

Reduced cone photoreceptor function and subtle systemic manifestations in two siblings with loss of SCLT1

enthalten in: Ophthalmic genetics | 2024

von Grudzinska Pechhacker, M. | Molnar, A. | Pekkola Pacheco, N. | +5

2

Genes whose expressions in the primary lung squamous cell carcinoma are able to accurately predict the progression of metastasis through lymphatic system, inferred from a bioinformatics analyses

enthalten in: Scientific reports | 2023

von Khashei Varnamkhasti, K. | Moghanibashi, M. | Naeimi, S.

3

Bardet-Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations

enthalten in: CEN case reports | 2020

von Morisada, N. | Hamada, R. | Miura, K. | +4

4

The morbid genome of ciliopathies : an update

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2020

von Shamseldin, H. | Shaheen, R. | Ewida, N. | +38

ErratumIn: Genet Med. 2022 Apr;24(4):966. - PMID 35394428

5

KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling

enthalten in: The Journal of cell biology | 2020

von Pejskova, P. | Reilly, M. | Bino, L. | +6

6

Bardet-Biedl Syndrome Caused by Skipping of SCLT1 Complicated by Microvesicular Steatohepatitis

enthalten in: Internal medicine (Tokyo, Japan) | 2020

von Horiuchi, K. | Kogiso, T. | Sagawa, T. | +7

7

Compound heterozygous splice site variants in the SCLT1 gene highlight an additional candidate locus for Senior-Løken syndrome

enthalten in: Scientific reports | 2018

von Katagiri, S. | Hayashi, T. | Yoshitake, K. | +11

8

Problematic alcohol use associates with sodium channel and clathrin linker 1 (SCLT1) in trauma-exposed populations

enthalten in: Addiction biology | 2018

von Almli, L. | Lori, A. | Meyers, J. | +18

9

Super-resolution architecture of mammalian centriole distal appendages reveals distinct blade and matrix functional components

enthalten in: Nature communications | 2018

von Yang, T. | Chong, W. | Wang, W. | +10

10

Sclt1 deficiency causes cystic kidney by activating ERK and STAT3 signaling

enthalten in: Human molecular genetics | 2017

von Li, J. | Lu, D. | Liu, H. | +5