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Dr James R. McMillan B.Sc. M.Sc. M.B.A.  Ph.D.
Dr James R. McMillan B.Sc. M.Sc. M.B.A. Ph.D.
Email yang diverifikasi di cam.ac.uk - Beranda
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Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome
JA McGrath, JR McMillan, CS Shemanko, SK Runswick, IM Leigh, ...
Nature genetics 17 (2), 240-244, 1997
4961997
Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer
M Akiyama, Y Sugiyama-Nakagiri, K Sakai, JR McMillan, M Goto, K Arita, ...
The Journal of clinical investigation 115 (7), 1777-1784, 2005
4922005
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
FJD Smith, RAJ Eady, IM Leigh, JR McMillan, EL Rugg, DP Kelsell, ...
Nature genetics 13 (4), 450-457, 1996
4591996
Mutations in the 180–kD bullous pemphigoid antigen (BPAG2), a hemidesmosomal transmembrane collagen (COL17A1), in generalized atrophic benign epidermolysis bullosa
JA McGrath, B Gatalica, AM Christiano, K Si, K Owaribe, JR McMillan, ...
Nature genetics 11 (1), 83-86, 1995
4111995
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization.
WH McLean, L Pulkkinen, FJ Smith, EL Rugg, EB Lane, F Bullrich, ...
Genes & development 10 (14), 1724-1735, 1996
4051996
Humanization of autoantigen
W Nishie, D Sawamura, M Goto, K Ito, A Shibaki, JR McMillan, K Sakai, ...
Nature medicine 13 (3), 378-383, 2007
3482007
Hair follicle stem cells provide a functional niche for melanocyte stem cells
S Tanimura, Y Tadokoro, K Inomata, NT Binh, W Nishie, S Yamazaki, ...
Cell stem cell 8 (2), 177-187, 2011
3382011
Intercellular signaling and the polarization of body axes during Drosophila oogenesis 1711
RP Ray, T Schiipbach, WHI McLean, L Pulkkinen, FJD Smith, EL Rugg, ...
DEVELOPMENT 10 (14), 1711-1844, 1996
2551996
A review of first aid treatments for burn injuries
L Cuttle, J Pearn, JR McMillan, RM Kimble
Burns 35 (6), 768-775, 2009
2372009
A functional" knockout" of human keratin 14.
EL Rugg, WH McLean, EB Lane, R Pitera, JR McMillan, ...
Genes & development 8 (21), 2563-2573, 1994
2141994
A homozygous nonsense mutation in the α3 chain gene of laminin 5 (LAMA3) in lethal (Herlitz) junctional epidermolysis bullosa
S Kivirikko, JA McGrath, C Baudoin, D Aberdam, S Ciatti, MGS Dunnill, ...
Human molecular genetics 4 (5), 959-962, 1995
2071995
Epidermal basement membrane zone components: ultrastructural distribution and molecular interactions
JR McMillan, M Akiyama, H Shimizu
Journal of dermatological science 31 (3), 169-177, 2003
1892003
Bullous pemphigoid and cicatricial pemphigoid autoantibodies react with ultrastructurally separable epitopes on the BP180 ectodomain: evidence that BP180 spans the lamina lucida
C Bedane, JR McMillan, SD Balding, P Bernard, C Prost, JM Bonnetblanc, ...
Journal of investigative dermatology 108 (6), 901-907, 1997
1881997
Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress
Swensson, Langbein, Mcmillan, Stevens, Leigh, Mclean, Lane, Eady
British Journal of Dermatology 139 (5), 767-775, 1998
1521998
Compound heterozygosity for a dominant glycine substitution and a recessive internal duplication mutation in the type XVII collagen gene results in junctional epidermolysis …
JA McGrath, B Gatalica, K Li, MG Dunnill, JR McMillan, AM Christiano, ...
The American journal of pathology 148 (6), 1787, 1996
1271996
CTACK/CCL27 accelerates skin regeneration via accumulation of bone marrow‐derived keratinocytes
D Inokuma, R Abe, Y Fujita, M Sasaki, A Shibaki, H Nakamura, ...
Stem cells 24 (12), 2810-2816, 2006
1262006
Mutations in the rod 1A domain of keratins 1 and 10 in Bullous Congenital Ichthyosiform Erythoderma (BCIE)
WHI McLean, RAJ Eady, PJC Dopping-Hepenstal, JR McMillan, IM Leigh, ...
Journal of investigative dermatology 102 (1), 24-30, 1994
1191994
Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1
JA McGrath, PH Hoeger, AM Christiano, JR McMillan, JE Mellerio, ...
British Journal of Dermatology 140 (2), 297-307, 1999
1141999
Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1)
H Nakamura, D Sawamura, M Goto, H Nakamura, JR McMillan, S Park, ...
The Journal of Molecular Diagnostics 7 (1), 28-35, 2005
1072005
A denatured collagen microfiber scaffold seeded with human fibroblasts and keratinocytes for skin grafting
M Kempf, Y Miyamura, PY Liu, ACH Chen, H Nakamura, H Shimizu, ...
Biomaterials 32 (21), 4782-4792, 2011
1032011
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