引用次数
引用: 4,795
H-指数: 30
I10-指数 : 55
出版物: 141
Genetic and functional analysis of connexin 26 and 30 in skin disease and deafness
IM Leigh , E O'Toole , WL Di , DP Kelsel
In: BRITISH JOURNAL OF DERMATOLOGY. (pp. 849 - 849). BLACKWELL PUBLISHING LTD (2003)
2003
Genetic and functional analysis of connexins in skin disease and deafness.
IM Leigh , DP Kelsell , W Di , Jea Common
In: EUROPEAN JOURNAL OF HUMAN GENETICS. (pp. 68 - 68). NATURE PUBLISHING GROUP (2002)
2002
Functional analyses of connexin mutations in keratinocytes
IM Leigh , DP Kelsell , W Di , Jea Common
Journal of Investigative Dermatology
2001
Defective trafficking and cell death are characteristic of skin disease-associated connexin 31 mutations in keratinocytes
D Zicha , IM Leigh , DP Kelsell , KA Holland
Journal of Investigative Dermatology
2002
Performing Skin Microbiome Research: A Method to the Madness.
Heidi H. Kong , Björn Andersson , Thomas Clavel , John E. Common
Journal of Investigative Dermatology 137 ( 3) 561 -568
179
2017
Human reconstructed skin xenografts on mice to model skin physiology.
Giorgiana Salgado , Yi Zhen Ng , Li Fang Koh , Christabelle S.M. Goh
Differentiation 98 14 -24
15
2017
Tiled array-based sequencing identifies enrichment of loss-of-function variants in the highly homologous filaggrin gene in African-American children with severe atopic dermatitis.
Mary Elizabeth Mathyer , Ashley M. Quiggle , X. F. Colin C. Wong , Simon L. I. J. Denil
Experimental Dermatology 27 ( 9) 989 -992
6
2018
Associating filaggrin copy number variation and atopic dermatitis in African-Americans: Challenges and opportunities.
David J Margolis , Nandita Mitra , Ron Berna , Ole Hoffstad
Journal of Dermatological Science 98 ( 1) 58 -60
2
2020
Identification and elucidation of miRNA's role in atopic dermatitis
Zacharias AD Pramono , Xuejun Mo , Emily Y Gan , Ellen B Lane
Journal of Dermatological Science 69 ( 2)
2013
Plau and Tgfbr3 are YAP-regulated genes that promote keratinocyte proliferation.
Susan M. Corley , Veronica Mendoza-Reinoso , Nichole Giles , Emma Suwanun Singer
Cell Death and Disease 9 ( 11) 1106
3
2018
In vivo Raman spectroscopy discriminates between FLG loss-of-function carriers vs wild-type in day 1-4 neonates.
Carol Ní Chaoimh , Claudio Nico , Gerwin J. Puppels , Peter J. Caspers
Annals of Allergy Asthma & Immunology 124 ( 5) 500 -504
7
2020
Keratinocytes maintain compartmentalization between dermal papilla and fibroblasts in 3D heterotypic tri-cultures.
Justin J. Y. Tan , John E. Common , Chunyong Wu , Paul C. L. Ho
Cell Proliferation 52 ( 5)
17
2019
Low-dose calcipotriol can elicit wound closure, anti-microbial, and anti-neoplastic effects in epidermolysis bullosa keratinocytes.
Christina Guttmann-Gruber , Birgit Tockner , Cornelia Scharler , Clemens Hüttner
Scientific Reports 8 ( 1) 13430
13
2018
Lamin B1 fluctuations have differential effects on cellular proliferation and senescence
Oliver Dreesen , Alexandre Chojnowski , Peh Fern Ong , Tian Yun Zhao
Journal of Cell Biology 200 ( 5) 605 -617
139
2013
Cover Image, Volume 52, Issue 5
Justin J. Y. Tan , John E. Common , Chunyong Wu , Paul C. L. Ho
Cell Proliferation 52 ( 5)
2019
What does acne genetics teach us about disease pathogenesis
J.E.A. Common , J.N. Barker , M.A.M. Steensel
British Journal of Dermatology 181 ( 4) 665 -676
40
2019
Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high‐performance liquid chromatography
E.L. Rugg , J.E.A. Common , A. Wilgoss , H.P. Stevens
British Journal of Dermatology 146 ( 6) 952 -957
14
2002
Wide spectrum of filaggrin‐null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populations
H. Chen , J.E.A. Common , R.L. Haines , A. Balakrishnan
British Journal of Dermatology 165 ( 1) 106 -114
101
2011
Filaggrin mutations are associated with recurrent skin infection in Singaporean Chinese patients with atopic dermatitis
S.C.S. Cai , H. Chen , W.-P. Koh , J.E.A. Common
British Journal of Dermatology 166 ( 1) 200 -203
45
2012
A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndrome.
Ching Yin Neoh , Huijia Chen , See Ket Ng , Ellen Birgitte Lane
International Journal of Dermatology 48 ( 10) 1078 -1081
11
2009
Prof David Kelsell Edel O'Toole Irwin McLean Simon L.I.J. Denil Florent Ginhoux Fook Tim CHEW Niranjan Nagarajan Bernett Lee Alan D. Irvine Sri Anusha Matta Bani Kaur Suri Paola Florez de Sessions Jia Nee Foo Leah A. Vardy Chenhao Li Chng Kern Rei Andreas Wilm baptiste janela Ildikó Szeverényi Jianjun Liu