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1

Natural Antimicrobials in the Dental Pulp

Lundy, Fionnuala T., Irwin, Christopher R., McLean, Denise F., Linden, Gerard J., El Karim, Ikhlas A.

Journal:

Journal of Endodontics

Year:

2020

File:

PDF, 542 KB

2020

2

K15 Expression Implies Lateral Differentiation within Stratified Epithelial Basal Cells

Porter, Rebecca M, Lunny, Declan P, Ogden, Patricia H, Morley, Susan M, McLean, W H Irwin, Evans, Alan, Harrison, Dolores L, Rugg, Elizabeth L, Lane, E Birgitte

Journal:

Laboratory Investigation

Year:

2000

Language:

english

File:

PDF, 1.83 MB

english, 2000

3

Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis

Sandilands, Aileen, O'Regan, Gráinne M, Liao, Haihui, Zhao, Yiwei, Terron-Kwiatkowski, Ana, Watson, Rosemarie M, Cassidy, Andrew J, Goudie, David R, Smith, Frances J D, McLean, W H Irwin

Journal:

The Journal of Investigative Dermatology

Year:

2006

Language:

english

File:

PDF, 185 KB

english, 2006

4

Broken bricks and cracked mortar – epidermal diseases resulting from genetic abnormalities

E. Birgitte Lane, W.H. Irwin McLean

Journal:

Drug Discovery Today: Disease Mechanisms

Year:

2008

Language:

english

File:

PDF, 1.02 MB

english, 2008

5

Human periplakin: cDNA and genomic cloning, chromosomal mapping, mRNA expression, and a paraneoplastic antigen

Aho, Sirpa, McLean, W.H.Irwin, Mahoney, My, Stanley, John R., Uitto, Jouni

Journal:

Journal of Dermatological Science

Year:

1998

Language:

english

File:

PDF, 210 KB

english, 1998

6

Filaggrin Mutations Associated with Skin and Allergic Diseases

Irvine, Alan D., McLean, W.H. Irwin, Leung, Donald Y.M.

Journal:

Boston Medical and Surgical Journal

Year:

2011

Language:

english

File:

PDF, 1.82 MB

english, 2011

7

The Association between Domestic Water Hardness, Chlorine and Atopic Dermatitis Risk in Early Life: A Population-Based Cross-Sectional Study

Perkin, Michael R., Craven, Joanna, Logan, Kirsty, Strachan, David, Marrs, Tom, Radulovic, Suzana, Campbell, Linda E., MacCallum, Stephanie F., McLean, W.H. Irwin, Lack, Gideon, Flohr, Carsten

Journal:

Journal of Allergy and Clinical Immunology

Year:

2016

Language:

english

File:

PDF, 1.40 MB

english, 2016

8

Cloning of multiple keratin 16 genes facilitates prenatal diagnosis of pachyonychia congenita type 1

Frances J. D. Smith, Victor A. McKusick, Karl Nielsen, Ellen Pfendner, Jouni Uitto, W. H. Irwin McLean

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 409 KB

english, 1999

9

Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex

Laura D. Corden, Jemima E. Mellerio, Matthew J. Gratian, Robin A. J. Eady, John I. Harper, Marc Lacour, Gareth Magee, E. Birgitte Lane, John A. McGrath, W. H. Irwin McLean

Journal:

Year:

1998

Language:

english

File:

PDF, 304 KB

english, 1998

10

Identification of a novel C16orf57 mutation in Athabaskan patients with Poikiloderma with Neutropenia

Carol Clericuzio, Karine Harutyunyan, Weidong Jin, Robert P. Erickson, Alan D. Irvine, W.H. Irwin McLean, Yaran Wen, Rochelle Bagatell, Thomas A. Griffin, Tor A. Shwayder, Sharon E. Plon, Lisa L. Wang

Journal:

American Journal of Medical Genetics Part A

Year:

2011

Language:

english

File:

PDF, 204 KB

english, 2011

11

Characterization of human skin fibroblast extracellular proteins by two-dimensional polyacrylamide gel electrophoresis

Dr. Colin A. Graham, W. H. Irwin McLean, Anne E. Hughes, Norman C. Nevin

Journal:

ELECTROPHORESIS

Year:

1988

Language:

english

File:

PDF, 900 KB

english, 1988

12

Compound Heterozygosity for Non-Sense and Mis-Sense Mutations in Desmoplakin Underlies Skin Fragility/Woolly Hair Syndrome

Whittock, Neil V., Wan, Hong, Eady, Robin A.J., Morley, Susan M., Garzon, Maria C., Kristal, Leonard, Hyde, Patrice, Irwin McLean, W.H., Pulkkinen, Leena, Uitto, Juoni, Christiano, Angela M., McGrath,

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 439 KB

english, 2002

13

A Novel Connexin 30 Mutation in Clouston Syndrome

Smith, Frances J.D., Irwin McLean, W.H., Morley, Susan M.

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 115 KB

english, 2002

14

Recurrent Mutations in Kindlin-1, a Novel Keratinocyte Focal Contact Protein, in the Autosomal Recessive Skin Fragility and Photosensitivity Disorder, Kindler Syndrome

Ashton, Gabrielle H.S., Irwin Mclean, W.H., South, Andrew P., Oyama, Noritaka, Smith, Frances J.D., Al-Suwaid, Raouf, Al Ismaily, Abla, Atherton, David J., Harwood, Catherine A., Leigh, Irene M., Moss

Journal:

The Journal of Investigative Dermatology

Year:

2004

Language:

english

File:

PDF, 2.08 MB

english, 2004

15

Novel Mechanism of Revertant Mosaicism in Dowling–Meara Epidermolysis Bullosa Simplex

Smith, Frances J.D., Irwin McLean, W.H., Morley, Susan M.

Journal:

The Journal of Investigative Dermatology

Year:

2004

Language:

english

File:

PDF, 1.22 MB

english, 2004

16

Genetic disorders of palm skin and nail

W. H. Irwin McLean

Journal:

Journal of Anatomy

Year:

2003

Language:

english

File:

PDF, 205 KB

english, 2003

17

Genomic Organization and Fine Mapping of the Keratin 2e Gene (KRT2E): K2e V1 Domain Polymorphism and Novel Mutations in Ichthyosis Bullosa of Siemens

Smith, Frances J D, Maingi, Chetan, Covello, Seana P, Higgins, Caroline, Schmidt, Maike, Lane, E Birgitte, Uitto, Jouni, Leigh, Irene M, McLean, W H Irwin

Journal:

The Journal of Investigative Dermatology

Year:

1998

Language:

english

File:

PDF, 364 KB

english, 1998

18

An Atypical Form of Bullous Congenital Ichthyosiform Erythroderma is Caused by a Mutation in the L12 Linker Region of Keratin 1

Kremer, Hannie, Lavrijsen, Adriana P M, McLean, W H Irwin, Lane, E Birgitte, Melchers, Diana, Ruiter, Dirk J, Mariman, Edwin C M, Steijlen, Peter M

Journal:

The Journal of Investigative Dermatology

Year:

1998

Language:

english

File:

PDF, 337 KB

english, 1998

19

Mutations in Keratin K9 in Kindreds with Epidermolytic Palmoplantar Keratoderma and Epidemiology in Northern Ireland

Covello, Seana P, Irvine, Alan D, McKenna, Kevin E, Munro, Colin S, Nevin, Norman C, Smith, Frances J D, Uitto, Jouni, McLean, W H Irwin

Journal:

The Journal of Investigative Dermatology

Year:

1998

Language:

english

File:

PDF, 228 KB

english, 1998

20

The Gene for Naegeli-Franceschetti-Jadassohn Syndrome Maps to 17q21

Whittock, Neil V., Coleman, Carrie M., McLean, W. H. Irwin, Ashton, Gabrielle H. S., Acland, K. M., Eady, Robin A. J., McGrath, John A.

Journal:

The Journal of Investigative Dermatology

Year:

2000

Language:

english

File:

PDF, 271 KB

english, 2000

21

A Mutation in the V1 Domain of K16 is Responsible for Unilateral Palmoplantar Verrucous Nevus

Terrinoni, Alessandro, Puddu, Pietro, Didona, Biagio, De Laurenzi, Vincenzo, Candi, Eleonora, Smith, Frances J. D., McLean, W. H. Irwin, Melino, Gerry

Journal:

The Journal of Investigative Dermatology

Year:

2000

Language:

english

File:

PDF, 519 KB

english, 2000

22

Novel Keratin 17 Mutations in Pachyonychia Congenita Type 2

Smith, Frances J D, Coleman, Carrie M, Bayoumy, Nagy M, Tenconi, Romano, Nelson, John, David, Albert, McLean, W H Irwin

Journal:

The Journal of Investigative Dermatology

Year:

2001

Language:

english

File:

PDF, 140 KB

english, 2001

23

Two Cases of Primarily Palmoplantar Keratoderma Associated with Novel Mutations in Keratin 1

Terron-Kwiatkowski, Ana, Paller, Amy S., Compton, John, Atherton, David J., McLean, W. H. Irwin, Irvine, Alan D.

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 201 KB

english, 2002

24

Frameshift Mutation in the V2 Domain of Human Keratin 1 Results in Striate Palmoplantar Keratoderma

Whittock, Neil V., Smith, Frances J., Wan, Hong, Mallipeddi, Rajeev, Griffiths, W. Andrew, Dopping-Hepenstal, Patricia, Ashton, Gabrielle H., Eady, Robin A., McLean, W. H. Irwin, McGrath, John A.

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 267 KB

english, 2002

25

Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles

Porter, Rebecca M., Jahoda, Colin A. B., Lunny, Declan P., Henderson, Gayle, Ross, Jane, Irwin McLean, W. H., Whittock, Neil V., Wilson, Neil J., Reichelt, Julia, Magin, Thomas M., Lane, E. Birgitte

Journal:

The Journal of Investigative Dermatology

Year:

2002

Language:

english

File:

PDF, 289 KB

english, 2002

26

Long-Range Polymerase Chain Reaction for Specific Full-Length Amplification of the Human Keratin 14 Gene and Novel Keratin 14 Mutations in Epidermolysis Bullosa Simplex Patients

Wood, Pamela, Baty, David U, Lane, E Birgitte, McLean, W H Irwin

Journal:

The Journal of Investigative Dermatology

Year:

2003

Language:

english

File:

PDF, 276 KB

english, 2003

27

Clouston Syndrome Can Mimic Pachyonychia Congenita

van Steensel, Maurice A.M., Jonkman, Marcel F., van Geel, Michel, Steijlen, Peter M., Irwin McLean, W.H., Smith, Frances J.D.

Journal:

The Journal of Investigative Dermatology

Year:

2003

Language:

english

File:

PDF, 922 KB

english, 2003

28

Genomic localization, organization and amplification of the human zinc transporter protein gene,ZNT4, and exclusion as a candidate gene in different clinical variants of acrodermatitis enteropathica

Oliver Bleck, Gabrielle H. S. Ashton, Rajeev Mallipeddi, Andrew P. South, Neil V. Whittock, W. H. Irwin McLean, David J. Atherton, J. A. McGrath

Journal:

Archives of Dermatological Research

Year:

2001

Language:

english

File:

PDF, 68 KB

english, 2001

29

Effects of Keratin 14 Ablation on the Clinical and Cellular Phenotype in a Kindred with Recessive Epidermolysis Bullosa Simplex.

Jonkman, Marcel F., Heeres, Klaas, Pas, Hendri H., van Luyn, Marja J. A., Elema, Job D., Corden, Laura D., Smith, Frances J. D., McLean, W. H. Irwin, Ramaekers, Frans C. S., Burton, Margaret, Scheffer

Journal:

The Journal of Investigative Dermatology

Year:

1996

File:

PDF, 2.47 MB

1996

30

Close Shave for a Keratin Disorder-K6hf Polymorphism Linked to Pseudofolliculitis Barbae

McLean, W.H.Irwin

Journal:

The Journal of Investigative Dermatology

Year:

2004

Language:

english

File:

PDF, 623 KB

english, 2004

31

Mapping of two genetic loci for autosomal dominant hidradenitis suppurativa

W. H. Irwin McLean, Pam Wood, Alan D. Irvine, Jan Von Der Werth

Journal:

Experimental Dermatology

Year:

2006

Language:

english

File:

PDF, 127 KB

english, 2006

32

Clinical and Pathological Features of Pachyonychia Congenita

Leachman, Sancy A., Kaspar, Roger L., Fleckman, Philip, Florell, Scott R., Smith, Frances J. D., McLean, W. H. Irwin, Lunny, Declan P., Milstone, Leonard M., Steensel, Maurice A. M., Munro, Colin S.,

Journal:

JID Symposium Proceedings

Year:

2005

Language:

english

File:

PDF, 6.56 MB

english, 2005

33

Preface to Pachyonychia Congenita Symposium Proceedings

Leachman, Sancy A., McLean, W. H. Irwin, Schwartz, Janice N., Schwartz, Mary E.

Journal:

JID Symposium Proceedings

Year:

2005

Language:

english

File:

PDF, 36 KB

english, 2005

34

Insights into Genotype-Phenotype Correlation in Pachyonychia Congenita from the Human Intermediate Filament Mutation Database

McLean, W. H. Irwin, Smith, Frances J. D., Cassidy, Andrew J.

Journal:

JID Symposium Proceedings

Year:

2005

Language:

english

File:

PDF, 1.05 MB

english, 2005

35

Filaggrin null mutations are associated with increased asthma exacerbations in children and young adults

K. Basu, C. N. A. Palmer, B. J. Lipworth, W. H. Irwin McLean, A. Terron-Kwiatkowski, Y. Zhao, H. Liao, F. J. D. Smith, A. Mitra, S. Mukhopadhyay

Journal:

Year:

2008

Language:

english

File:

PDF, 110 KB

english, 2008

36

Levels of filaggrin degradation products are influenced by both filaggrin genotype and atopic dermatitis severity

S. Kezic, G. M. O’Regan, N. Yau, A. Sandilands, H. Chen, L. E. Campbell, K. Kroboth, R. Watson, M. Rowland, W. H. Irwin McLean, A. D. Irvine

Journal:

Year:

2011

Language:

english

File:

PDF, 249 KB

english, 2011

37

Human keratin diseases: : Hereditary fragility of specific epithelial tissues

Laura D. Cordon, W H. Irwin McLean

Journal:

Experimental Dermatology

Year:

1996

Language:

english

File:

PDF, 10.71 MB

english, 1996

38

Plectin and human genetic disorders of the skin and muscle : The paradigm of epidermolysis bullosa with muscular dystrophy

Jouni Uitto, Leena Pulkkinen, Frances J. D. Smith, W H Irwin McLean

Journal:

Experimental Dermatology

Year:

1996

Language:

english

File:

PDF, 8.91 MB

english, 1996

39

Missing C-terminal filaggrin expression, NFkappaB activation and hyperproliferation identify the dog as a putative model to study epidermal dysfunction in atopic dermatitis

Ludovic Chervet, Arnaud Galichet, W. H. Irwin McLean, Huijia Chen, Maja M. Suter, Petra J. Roosje, Eliane J. Müller

Journal:

Experimental Dermatology

Year:

2010

Language:

english

File:

PDF, 705 KB

english, 2010

40

Unique and Recurrent Mutations in the Filaggrin Gene in Singaporean Chinese Patients with Ichthyosis Vulgaris

Chen, Huijia, Ho, Jean C C, Sandilands, Aileen, Chan, Yuin Chew, Giam, Yoke Chin, Evans, Alan T, Lane, E Birgitte, McLean, W H Irwin

Journal:

The Journal of Investigative Dermatology

Year:

2008

Language:

english

File:

PDF, 4.98 MB

english, 2008

41

Association of Skin Barrier Genes within the PSORS4 Locus Is Enriched in Singaporean Chinese with Early-Onset Psoriasis

Chen, Huijia, Toh, Terry K L, Szeverenyi, Ildiko, Ong, Rick T H, Theng, Colin T S, McLean, W H Irwin, Seielstad, Mark, Lane, E Birgitte

Journal:

The Journal of Investigative Dermatology

Year:

2008

Language:

english

File:

PDF, 1.30 MB

english, 2008

42

Clinical Severity Correlates with Impaired Barrier in Filaggrin-Related Eczema

Nemoto-Hasebe, Ikue, Akiyama, Masashi, Nomura, Toshifumi, Sandilands, Aileen, McLean, WH Irwin, Shimizu, Hiroshi

Journal:

The Journal of Investigative Dermatology

Year:

2008

Language:

english

File:

PDF, 1.08 MB

english, 2008

43

Loss-of-Function Mutations in the Filaggrin Gene Lead to Reduced Level of Natural Moisturizing Factor in the Stratum Corneum

Kezic, Sanja, Kemperman, Patrick M J H, Koster, Ellen S, de Jongh, Cindy M, Thio, Hok Bing, Campbell, Linda E, Irvine, Alan D, McLean, Irwin W H, Puppels, Gerwin J, Caspers, Peter J

Journal:

The Journal of Investigative Dermatology

Year:

2008

Language:

english

File:

PDF, 108 KB

english, 2008

44

Heterozygous Null Alleles in Filaggrin Contribute to Clinical Dry Skin in Young Adults and the Elderly

Campbell, Linda E, Hull, Peter R, Porter, Martin, Palmer, Colin N A, Smith, Frances J D, Sergeant, Ann, McLean, W H Irwin, Munro, Colin S

Journal:

The Journal of Investigative Dermatology

Year:

2008

Language:

english

File:

PDF, 167 KB

english, 2008

45

Prevalent and Rare Mutations in the Gene Encoding Filaggrin in Japanese Patients with Ichthyosis Vulgaris and Atopic Dermatitis

Nomura, Toshifumi, Akiyama, Masashi, Sandilands, Aileen, Nemoto-Hasebe, Ikue, Sakai, Kaori, Nagasaki, Akari, Palmer, Colin N A, Smith, Frances J D, McLean, W H Irwin, Shimizu, Hiroshi

Journal:

The Journal of Investigative Dermatology

Year:

2008

Language:

english

File:

PDF, 2.60 MB

english, 2008

46

Eczema Genetics: Current State of Knowledge and Future Goals

Brown, Sara J, McLean, W H Irwin

Journal:

The Journal of Investigative Dermatology

Year:

2009

Language:

english

File:

PDF, 317 KB

english, 2009

47

Achieving Successful Delivery of Nucleic Acids to Skin: 6th Annual Meeting of the International Pachyonychia Congenita Consortium

Kaspar, Roger L, McLean, W H Irwin, Schwartz, Mary E

Journal:

The Journal of Investigative Dermatology

Year:

2009

Language:

english

File:

PDF, 66 KB

english, 2009

48

Combing the genome for the root cause of baldness

McLean, W H Irwin

Journal:

Nature Genetics

Year:

2008

Language:

english

File:

PDF, 413 KB

english, 2008

49

Mutation S233L in the 1B Domain of Keratin 1 Causes Epidermolytic Palmoplantar Keratoderma with “Tonotubular” Keratin

Terron-Kwiatkowski, Ana, van Steensel, Maurice A M, van Geel, Michel, Lane, E Birgitte, McLean, W H Irwin, Steijlen, Peter M

Journal:

The Journal of Investigative Dermatology

Year:

2006

Language:

english

File:

PDF, 206 KB

english, 2006

50

Breaking the (Un)Sound Barrier: Filaggrin Is a Major Gene for Atopic Dermatitis

McLean, W H Irwin, Irvine, Alan D

Journal:

The Journal of Investigative Dermatology

Year:

2006

Language:

english

File:

PDF, 140 KB

english, 2006

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