المؤلفون: Chiu, F. P.C., Wessagowit, V., Cakmak, M. F., Doolan, B. J., Kootiratrakarn, T., Chaowalit, P., Bunnag, T., Simpson, M. A., McGrath, J. A., Onoufriadis, A.

المصدر: Chiu , F P C , Wessagowit , V , Cakmak , M F , Doolan , B J , Kootiratrakarn , T , Chaowalit , P , Bunnag , T , Simpson , M A , McGrath , J A & Onoufriadis , A 2020 , ' Molecular basis and inheritance patterns of amyloidosis cutis dyschromica ' , Clinical and Experimental Dermatology , vol. 45 , no. 5 , pp. 650-653 . https://doi.org/10.1111/ced.14183

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/b5db22e8-86c0-4795-b5b1-5d0a478e3732
https://doi.org/10.1111/ced.14183
http://www.scopus.com/inward/record.url?scp=85085960398&partnerID=8YFLogxK

المؤلفون: Epstein, EH, McGrath, JA, McLean, WHI, Eady, RAJ, Mallipeddi, R, Hamada, T, Zaghloul, AB, Wojnarowska, F, Wiebe, CB, Tsuchiya, K, Tadini, G, Suga, Y, Shimizu, H, Sahin, S, Ogawa, H, Mallory, SB, Kitajima, Y, Harada, T, Haber, RM, Fuchs, E, Frieden, IJ, Fine, JD, Caputo, R, Atherton, DJ, Al-Suwaid, R, Al Ismaily, A, Al Hawsawi, K, Al Githami, A, Al Aboud, K, Al Aboud, D, Akiyama, M, Oyama, N, Wessagowit, V, Prescott, AR, Smith, FJD, South, AP, Wilhelmsen, KC, Feiler, HS, Lee, JV, Penagos, HG, Ashton, GHS, Siegel, DH

الاتاحة: https://doi.org/10.1086/376609
https://avesis.hacettepe.edu.tr/publication/details/9e4bbe55-a068-498f-b96d-92e351a5d1d3/oai

المؤلفون: South, A.P., Ashton, G.H.S., Willoughby, C., Ellis, I.H., Bleck, O., Hamada, T., Mannion, G., Wessagowit, V., Hashimoto, T., Eady, R.A.J., Mcgrath, J.A.

المصدر: British Journal of Dermatology ; volume 146, issue 2, page 216-220 ; ISSN 0007-0963 1365-2133

الاتاحة: https://doi.org/10.1046/j.1365-2133.2002.04638.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2133.2002.04638.x
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2133.2002.04638.x/fullpdf

المؤلفون: Wessagowit, V., South, A. P.

المصدر: Clinical and Experimental Dermatology ; volume 27, issue 6, page 485-492 ; ISSN 0307-6938

الاتاحة: https://doi.org/10.1046/j.1365-2230.2002.01117.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1046%2Fj.1365-2230.2002.01117.x
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2230.2002.01117.x/fullpdf

المؤلفون: Oyama, N, Chan, I, Neill, S, South, A, Hamada, T, Wessagowit, V, Black, M, Wojnarowska, F, McGrath, J

Relation: https://ora.ox.ac.uk/objects/uuid:fceadb82-ae82-4c5d-b975-d6016f79a108

الاتاحة: https://ora.ox.ac.uk/objects/uuid:fceadb82-ae82-4c5d-b975-d6016f79a108

المؤلفون: Chiu, F. P. C., Wessagowit, V., Cakmak, M. F., Doolan, B. J., Kootiratrakarn, T., Chaowalit, P., Bunnag, T., Simpson, M. A., McGrath, J. A., Onoufriadis, A.

المصدر: Clinical & Experimental Dermatology; Jul2020, Vol. 45 Issue 5, p650-653, 4p, 1 Color Photograph

مصطلحات موضوعية: ASIANS, ONCOSTATIN M, AMINO acid residues

المؤلفون: Oyama, N, Chan, I, Neill, S, Hamada, T, South, A, Wessagowit, V, Wojnarowska, F, D'Cruz, D, Hughes, G, Black, M, McGrath, J

Relation: https://ora.ox.ac.uk/objects/uuid:39c179df-d595-41f4-b085-97e723030ab9; https://doi.org/10.1016/s0140-6736(03)13863-9

الاتاحة: https://doi.org/10.1016/s0140-6736(03)13863-9
https://ora.ox.ac.uk/objects/uuid:39c179df-d595-41f4-b085-97e723030ab9

المؤلفون: Arita, K, Nanda, A, Wessagowit, V, Akiyama, M, Alsaleh, Q A, McGrath, J A

المصدر: Arita , K , Nanda , A , Wessagowit , V , Akiyama , M , Alsaleh , Q A & McGrath , J A 2008 , ' A novel mutation in the VDR gene in hereditary vitamin D-resistant rickets ' , British Journal of Dermatology , vol. 158 , no. 1 , pp. 168 - 171 . https://doi.org/10.1111/j.1365-2133.2007.08232.x

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/f5231425-e229-4991-a76b-d7f3c750b416

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/f5231425-e229-4991-a76b-d7f3c750b416
https://doi.org/10.1111/j.1365-2133.2007.08232.x

المؤلفون: Clements, S E, Wessagowit, V, Lai-Cheong, J E, Arita, K, McGrath, J A

المصدر: Clements , S E , Wessagowit , V , Lai-Cheong , J E , Arita , K & McGrath , J A 2008 , ' Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN gene ' , Journal of Dermatological Science , vol. 49 , no. 1 , pp. 39 - 42 . https://doi.org/10.1016/j.jdermsci.2007.09.004

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/149090e8-09a7-42a0-a1e6-d74ef74da8ec
https://doi.org/10.1016/j.jdermsci.2007.09.004

المؤلفون: Sercu, S., Poumay, Yves, Herphelin, F., Liekens, J., Beek, L., Zwijsen, A., Wessagowit, V., Huylebroeck, D., McGrath, J. A., Merregaert, J.

المساهمون: FUNDP

المصدر: British Journal of Dermatology, Vol. 157, no. 4, p. 771-775 (2007)

مصطلحات موضوعية: epidermal differentiation, extracellular matrix protein 1, lipoid proteinosis, transgenic mice

Relation: boreal:101481; http://hdl.handle.net/2078.2/101481; urn:ISSN:0007-0963; urn:EISSN:1365-2133

الاتاحة: http://hdl.handle.net/2078.2/101481
https://doi.org/10.1111/j.1365-2133.2007.08114.x

المؤلفون: Sercu, Sandy, Poumay, Y., Herphelin, F., Liekens, J., Beek, L., Zwijsen, A., Wessagowit, V., Huylebroeck, D., McGrath, J.A., Merregaert, Joseph

المصدر: 0007-0963 ; British journal of dermatology

Relation: info:eu-repo/semantics/altIdentifier/isi/000249376900021

الاتاحة: https://hdl.handle.net/10067/665960151162165141

المؤلفون: Arita, K, Wessagowit, V, Inamadar, A C, Palit, A, Fassihi, H, Lai-Cheong, J E, Pourreyron, C, South, A P, McGrath, J A

المصدر: Arita , K , Wessagowit , V , Inamadar , A C , Palit , A , Fassihi , H , Lai-Cheong , J E , Pourreyron , C , South , A P & McGrath , J A 2007 , ' Unusual molecular findings in Kindler syndrome ' , British Journal of Dermatology , vol. 157 , no. 6 , pp. 1252 - 1256 . https://doi.org/10.1111/j.1365-2133.2007.08159.x

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/46e0822d-2975-45c7-a313-6d254c2a00e9

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/46e0822d-2975-45c7-a313-6d254c2a00e9
https://doi.org/10.1111/j.1365-2133.2007.08159.x

المؤلفون: Wessagowit, V, Chunharas, A, Wattanasirichaigoon, D, McGrath, J

المصدر: Wessagowit , V , Chunharas , A , Wattanasirichaigoon , D & McGrath , J 2007 , ' Globalization of DNA-based prenatal diagnosis for recessive dystrophic epidermolysis bullosa. ' , Clinical and Experimental Dermatology , vol. 32 , no. 6 , pp. 687 - 689 . https://doi.org/10.1111/j.1365-2230.2007.02510.x

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/25895a4c-a624-449b-83b2-4b6b2913ec1b
https://doi.org/10.1111/j.1365-2230.2007.02510.x

المؤلفون: Arita, K, Jacyk, W K, Wessagowit, V, van Rensburg, E J, Chaplin, T, Mein, C A, Akiyama, M, Shimizu, H, Happle, R, McGrath, J A

المصدر: Arita , K , Jacyk , W K , Wessagowit , V , van Rensburg , E J , Chaplin , T , Mein , C A , Akiyama , M , Shimizu , H , Happle , R & McGrath , J A 2007 , ' The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1 ' , Journal of Investigative Dermatology , vol. 127 , no. 2 , pp. 490 - 493 . https://doi.org/10.1038/sj.jid.5700550

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/05df2c3f-e1b9-4073-aadb-4e5666159e91
https://doi.org/10.1038/sj.jid.5700550

المؤلفون: Lai-Cheong, J E, Liu, L, Sethuraman, G, Kumar, R, Sharma, V K, Reddy, S R, Vahlquist, A, Pather, S, Arita, K, Wessagowit, V, McGrath, J A

المصدر: Lai-Cheong , J E , Liu , L , Sethuraman , G , Kumar , R , Sharma , V K , Reddy , S R , Vahlquist , A , Pather , S , Arita , K , Wessagowit , V & McGrath , J A 2007 , ' Five new homozygous mutations in the KIND1 gene in Kindler syndrome ' , Journal of Investigative Dermatology , vol. 127 , no. 9 , pp. 2268 - 2270 . https://doi.org/10.1038/sj.jid.5700830

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/five-new-homozygous-mutations-in-the-kind1-gene-in-kindler-syndrome(b6ab3cd2-8bc2-4f97-a421-6cd6b5afad8a).html
https://doi.org/10.1038/sj.jid.5700830

المؤلفون: Arita, K, Wessagowit, V, Inamadar, A C, Lai-Cheong, J E, McGrath, J A

المصدر: Arita , K , Wessagowit , V , Inamadar , A C , Lai-Cheong , J E & McGrath , J A 2007 , ' Unusual clinical and molecular findings in Kindler syndrome ' , British Journal of Dermatology , vol. 156 , no. 5 , pp. 1106 - 1106 .

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/3672703a-7dc6-4eb6-9089-69dae77c6dfc

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/3672703a-7dc6-4eb6-9089-69dae77c6dfc

المؤلفون: Wong, T, Liu, L, Ozoemena, L, Wessagowit, V, Fassihi, H, Dopping-Hepenstal, P J, Jones, C, Mellerio, J E, McGrath, J A

المصدر: Wong , T , Liu , L , Ozoemena , L , Wessagowit , V , Fassihi , H , Dopping-Hepenstal , P J , Jones , C , Mellerio , J E & McGrath , J A 2006 , ' Pathogenic nonglycine substitution missense mutations in the type VII collagen triple helix: implications for genotype-phenotype correlation in recessive dystrophic epidermolysis bullosa. ' , British Journal of Dermatology , vol. 155 , P-18 , pp. 28 - 28 .

Relation: https://kclpure.kcl.ac.uk/portal/en/publications/7dc19517-e053-4bdc-9908-09b5c5716d6b

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/7dc19517-e053-4bdc-9908-09b5c5716d6b

المؤلفون: Liu, L, Choy, Y S, Wessagowit, V, Ozoemena, L, Dopping-Hepenstal, P J C, Fassihi, H, McGrath, J A

المصدر: Liu , L , Choy , Y S , Wessagowit , V , Ozoemena , L , Dopping-Hepenstal , P J C , Fassihi , H & McGrath , J A 2006 , ' Single nucleotide polymorphism in a commonly utilized LAMB3 primer sequence: Implications for mutation detection and haplotype analysis in junctional epidermolysis bullosa ' , Journal of Dermatological Science , vol. 44 , no. 1 , pp. 48 - 51 . https://doi.org/10.1016/j.jdermsci.2006.05.009

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/b594789f-49c4-4958-8ed1-a3ed844a586c
https://doi.org/10.1016/j.jdermsci.2006.05.009

المؤلفون: Has, C, Wessagowit, V, Pascucci, M, Baer, C, Didona, B, Wilhelm, C, Pedicelli, C, Locatelli, A, Kohlhase, J, Ashton, GHS, Tadini, G, Zambruno, G, Bruckner-Tuderman, L, McGrath, JA, Castiglia, D

المصدر: Has , C , Wessagowit , V , Pascucci , M , Baer , C , Didona , B , Wilhelm , C , Pedicelli , C , Locatelli , A , Kohlhase , J , Ashton , GHS , Tadini , G , Zambruno , G , Bruckner-Tuderman , L , McGrath , JA & Castiglia , D 2006 , ' Molecular basis of Kindler syndrome in Italy: Novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene. ' , Journal of Investigative Dermatology , vol. 126 , no. 8 , pp. 1776 ....

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/a96d7f58-650e-491c-8b50-ca3405218859
https://doi.org/10.1038/sj.jid.5700339

المؤلفون: Fassihi, H, Lu, L, Wessagowit, V, Ozoemena, LC, Jones, CA, Dopping-Hepenstal, PJ, Foster, L, Atherton, DJ, Mellerio, JE, McGrath, JA

المصدر: Fassihi , H , Lu , L , Wessagowit , V , Ozoemena , LC , Jones , CA , Dopping-Hepenstal , PJ , Foster , L , Atherton , DJ , Mellerio , JE & McGrath , JA 2006 , ' Complete maternal isodisomy of chromosome 3 in a child with recessive dystrophic epidermolysis bullosa but no other phenotype abnormalities. ' , Journal of Investigative Dermatology , vol. 126 , no. 9 , pp. 2039 - 2043 . https://doi.org/10.1038/sj.jid.5700348

الاتاحة: https://kclpure.kcl.ac.uk/portal/en/publications/b2a98ee4-266a-4fd3-8b07-38a686feae82
https://doi.org/10.1038/sj.jid.5700348