Suchergebnisse - "Ki, Chang-Seok"

PubPharm (875)

1

Familial chylomicronemia syndrome : case reports of siblings with deletions of the GPIHBP1 gene

enthalten in: BMC endocrine disorders | 2024

von Kim, K. | Heo, Y. | Ko, J. | +4

2

Familial chylomicronemia syndrome: case reports of siblings with deletions of the GPIHBP1 gene

enthalten in: BMC endocrine disorders | 2024

von Kim, K. | Heo, Y. | Ko, J. | +4

3

KCNJ3 is a novel candidate gene for autosomal dominant pure hereditary spastic paraplegia identified using whole genome sequencing

enthalten in: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2024

von Lee, W. | Lee, C. | Ki, C.

4

Differentiation, maturation, and collection of THP-1-derived dendritic cells based on a PEG hydrogel culture platform

enthalten in: Biotechnology letters | 2024

von Choi, J. | Ki, C.

5

Effect of Matrix Stiffness and Hepatocyte Growth Factor on Small Cell Lung Cancer Cells in Decellularized Extracellular Matrix-Based Hydrogels

enthalten in: Macromolecular bioscience | 2024

von Han, Y. | Ki, C.

6

Progranulin haploinsufficiency mediates cytoplasmic TDP-43 aggregation with lysosomal abnormalities in human microglia

enthalten in: Journal of neuroinflammation | 2024

von Sung, W. | Noh, M. | Nahm, M. | +5

7

Novel In-Frame Deletion CNOT3 Variant in a Family With Intellectual Developmental Disorder With Speech Delay and Dysmorphic Facies

enthalten in: Neurology. Genetics | 2024

von Lee, C. | Kim, H. | Seol, C. | +1

8

Differentiation, maturation, and collection of THP-1-derived dendritic cells based on a PEG hydrogel culture platform

enthalten in: Biotechnology letters | 2024

von Choi, J. | Ki, C.

9

A case of type A insulin resistance syndrome in a 14-year-old adolescent girl without common clinical features

enthalten in: Annals of pediatric endocrinology & metabolism | 2023

von Lee, N. | Jeong, J. | Kim, Y. | +2

10

Carrier frequency and incidence of aromatic L-amino acid decarboxylase deficiency : a gnomAD-based study

enthalten in: Pediatric research | 2023

von Park, J. | Lee, T. | Ha, K. | +2

1
2
3
4
5
6
7
8
9
10
11
Nächster »
[88]