Rachid Tazi-Ahnini

Rachid Tazi-Ahnini

UNVERIFIED PROFILE

Are you Rachid Tazi-Ahnini?   Register this Author

Register author
Rachid Tazi-Ahnini

Rachid Tazi-Ahnini

Publications by authors named "Rachid Tazi-Ahnini"

Are you Rachid Tazi-Ahnini?   Register this Author

27Publications

594Reads

29Profile Views

Epigallocatechin-3 Gallate Inhibits and Reduces CD8 MKG2D Lymphocytes of Alopecia Areata Patients.

Int J Environ Res Public Health 2018 12 15;15(12). Epub 2018 Dec 15.

Department of Infection, Immunity and Cardiovascular disease, The Medical School, University of Sheffield, Sheffield S10 2RX, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3390/ijerph15122882DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6313664PMC
December 2018

Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle East.

Dermatol Res Pract 2018 7;2018:1284568. Epub 2018 Aug 7.

Department of Infection, Immunity and Cardiovascular Disease, The Medical School, University of Sheffield, Sheffield S10 2RX, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2018/1284568DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6106946PMC
August 2018

First report of SLC39A4 mutation in acrodermatitis enteropathica family from the Middle East.

Int J Dermatol 2017 May 10;56(5):e97-e100. Epub 2017 Feb 10.

Infection and Immunity Department, Medical school, University of Sheffield, Sheffield, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/ijd.13463DOI Listing
May 2017

A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.

Biomed Res Int 2016 20;2016:3460234. Epub 2016 Jun 20.

Research Team on Neurodegenerative Diseases, Medical School and Pharmacy, Mohammed V University, 10100 Rabat, Morocco; Department of Neurology and Neurogenetics, Specialties Hospital, CHU Ibn Sina, 10100 Rabat, Morocco.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2016/3460234DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931068PMC
March 2017

CLN6 p.I154del mutation causing late infantile neuronal ceroid lipofuscinosis in a large consanguineous Moroccan family.

Indian J Pediatr 2013 Aug 22;80(8):694-6. Epub 2012 Nov 22.

Service de Neurologie et de Neurogénétique, Hôpital des Spécialités, BP, 6402 Al Irfane, Rabat, Morocco.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s12098-012-0889-3DOI Listing
August 2013

HLA-C, CSTA and DS12346 susceptibility alleles confer over 100-fold increased risk of developing psoriasis: evidence of gene interaction.

J Hum Genet 2011 Jun 17;56(6):423-7. Epub 2011 Mar 17.

The Medical School, University of Sheffield, Sheffield, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/jhg.2011.33DOI Listing
June 2011

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

Nat Genet 2010 Nov 17;42(11):985-90. Epub 2010 Oct 17.

Wellcome Trust Centre for Human Genetics, Oxford, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/ng.694DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749730PMC
November 2010

Epidermal barrier dysfunction in atopic dermatitis.

J Invest Dermatol 2009 Aug 4;129(8):1892-908. Epub 2009 Jun 4.

The Paediatric Dermatology Clinic, Sheffield Children's Hospital, Sheffield, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/jid.2009.133DOI Listing
August 2009

Association analysis of the skin barrier gene cystatin A at the PSORS5 locus in psoriatic patients: evidence for interaction between PSORS1 and PSORS5.

Eur J Hum Genet 2008 Aug 26;16(8):1002-9. Epub 2008 Mar 26.

School of Medicine and Biomedical Sciences, University of Sheffield, Sheffield, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/ejhg.2008.40DOI Listing
August 2008

New perspectives on epidermal barrier dysfunction in atopic dermatitis: gene-environment interactions.

J Allergy Clin Immunol 2006 Jul 9;118(1):3-21; quiz 22-3. Epub 2006 Jun 9.

Pediatric Dermatology Clinic, Children's Hospital, Sheffield S10 2RX, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jaci.2006.04.042DOI Listing
July 2006

The non-synonymous C1858T substitution in the PTPN22 gene is associated with susceptibility to the severe forms of alopecia areata.

Hum Immunol 2006 Jul 4;67(7):535-9. Epub 2006 May 4.

Division of Clinical Sciences (North), University of Sheffield, Sheffield, S5 7AU, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.humimm.2006.04.006DOI Listing
July 2006

Predisposition to sensitive skin and atopic eczema.

Community Pract 2005 Dec;78(12):440-2

Division of Genomic Medicine, University of Sheffield Medical School.

View Article

Download full-text PDF

Source
December 2005

Genome-wide studies of psoriasis susceptibility loci: a review.

J Dermatol Sci 2004 Sep;35(3):171-9

Biomedical Genetics Project, Division of Genomic Medicine, D Floor Medical School, Royal Hallamshire Hospital, University of Sheffield, Beech Hill Road, Sheffield S10 2RX, UK.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jdermsci.2004.02.009DOI Listing
September 2004

Identification of known and novel genes whose expression is regulated by endogenous retinoic acid during early embryonic development of the mouse.

Mech Dev 2002 Jun;114(1-2):205-12

Program of Nutritional Sciences and the Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX 78721, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0925-4773(02)00066-7DOI Listing
June 2002