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1 . Academic Journal
Deciphering the impacts of modulating the Wnt-planar cell polarity (PCP) pathway on alveolar repair
저자
by
Sally Yunsun Kim
;
David McTeague
;
Sek-Shir Cheong
;
Matthew Hind
;
Charlotte H. Dean
.
소스
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
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7 . Academic Journal
A method for TAT-Cre recombinase-mediated floxed allele modification in ex vivo tissue slices
저자
by
Sek-Shir Cheong
;
Tiago C. Luis
;
Michelle Stewart
;
Rosie Hillier
;
Matthew Hind
, et al.
소스
Disease Models & Mechanisms, Vol 16, Iss 11 (2023)
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7 . Academic Journal
The Planar Polarity Component VANGL2 Is a Key Regulator of Mechanosignaling
저자
by
Sek-Shir Cheong
;
Khondoker M. Akram
;
Carlos Matellan
;
Sally Yunsun Kim
;
David C. A. Gaboriau
, et al.
소스
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Open Access (DOAJ)
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7 . Academic Journal
Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness.
저자
by
Alice E Davidson
;
Sek-Shir Cheong
;
Pirro G Hysi
;
Cristina Venturini
;
Vincent Plagnol
, et al.
소스
PLoS ONE, Vol 9, Iss 8, p e104163 (2014)
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7 . Academic Journal
Deciphering the impacts of modulating the Wnt-planar cell polarity (PCP) pathway on alveolar repair.
저자
by
Yunsun Kim, Sally
;
McTeague, David
;
Sek-Shir Cheong
;
Hind, Matthew
;
Dean, Charlotte H.
.
소스
Frontiers in Cell & Developmental Biology; 2024, p1-18, 18p
Web of Science
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7 . Academic Journal
Current progress and prospects for G protein-coupled estrogen receptor in triple-negative breast cancer.
저자
by
Kim, Sally Yunsun
;
McTeague, David
;
Sek-Shir Cheong
;
Hind, Matthew
;
Dean, Charlotte H.
.
소스
Frontiers in Cell & Developmental Biology; 2024, p1-17, 17p
Web of Science
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7 .
Simple Models of Lung Development
저자
by
Charlotte H. Dean
;
Sek-Shir Cheong
.
소스
Advances in Experimental Medicine and Biology ISBN: 9783031266249
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4 .
Novel disease-causing variants and phenotypic features of X-linked megalocornea
저자
by
Alice E. Davidson
;
Manuela Vaneckova
;
Stephen J. Tuft
;
Jana Jedlickova
;
Martin Hlozanek
, et al.
소스
Acta ophthalmologicaReferences
. 100(4)
Full Text (Wiley)
Scopus
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7 .
Familial Limbal Stem Cell Deficiency: Clinical, Cytological and Genetic Characterization
저자
by
James D. Lauderdale
;
Viera Vesela
;
Michalis Palos
;
Stanislava Merjava
;
Pavlina Skalicka
, et al.
소스
Stem cell reviews and reports
. 14(1)
Open Access (OpenAIRE)
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7 .
Pleiotropic effect of a novel mutation in GCNT2 causing congenital cataract and a rare adult i blood group phenotype
저자
by
Sek-Shir Cheong
;
Anthony T. Moore
;
Benjamin Jones
;
Ravinder K. Chana
;
Sarah Hull
, et al.
소스
Human genome variation, vol 4, iss 1
Open Access (OpenAIRE)
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