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Variant PADI3 in Central Centrifugal Cicatricial Alopecia

The New England journal of medicine, 2019-02, Vol.380 (9), p.833-841

2019

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Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression

Scientific reports, 2022-04, Vol.12 (1), p.5958-5958, Article 5958

2022

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Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis

Genetics in medicine, 2020-07, Vol.22 (7), p.1227-1234

2020

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Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population

Experimental dermatology, 2021-09, Vol.30 (9), p.1290-1297

2021

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Cutaneous and Developmental Effects of CARD14 Overexpression in Zebrafish

Biomedicines, 2022-12, Vol.10 (12), p.3192

2022

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Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma

British journal of dermatology (1951), 2023-08, Vol.189 (3), p.302-311

2023

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ARCI7 Revisited and Repositioned

Journal of investigative dermatology, 2017-04, Vol.137 (4), p.970-972

2017

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A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes

British journal of dermatology (1951), 2022-11, Vol.187 (5), p.773-777

2022

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Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratoderma

Genetics in medicine, 2022-05, Vol.24 (5), p.1085-1095

2022

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Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar Keratoderma

Journal of investigative dermatology, 2020-11, Vol.140 (11), p.2178-2187

2020

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Epidermolytic epidermal nevus caused by a somatic mutation in KRT2

Pediatric dermatology, 2021-03, Vol.38 (2), p.538-540

2021

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Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis

Journal of allergy and clinical immunology, 2019-01, Vol.143 (1), p.173-181.e10

2019

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Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1

American journal of medical genetics. Part A, 2022-10, Vol.188 (10), p.2879-2887

2022

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Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A

Journal of investigative dermatology, 2018-08, Vol.138 (8), p.1736-1743

2018

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Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4

American journal of medical genetics. Part A, 2023-12, Vol.191 (12), p.2806-2812

2023

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SAM syndrome is characterized by extensive phenotypic heterogeneity

Experimental dermatology, 2018-07, Vol.27 (7), p.787-790

2018

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Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa

Pediatric dermatology, 2023-11, Vol.40 (6), p.1021-1027

2023

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Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions

American journal of human genetics, 2016-08, Vol.99 (2), p.430-436

2016

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Cutaneous and Developmental Effects of ICARD14/I Overexpression in Zebrafish

Biomedicines, 2022-12, Vol.10 (12)

2022

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Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis

Experimental dermatology, 2020-08, Vol.29 (8), p.742-748

2020

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LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION

הרפואה, 2020-01, Vol.159 (1), p.25

2020

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A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes

The British journal of dermatology, 2022, Vol.187 (5), p.773-777

2022

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MODEL OF TEACHING MALAY LANGUAGE TO NON-NATIVE AND FOREIGN SPEAKER

Malaysian journal of learning & instruction, 2024-01, Vol.21 (1), p.1-38

2024

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Content Validity of The Reading Skills Teaching Module Through a Foreign Language Teaching Approach

Malaysian Journal of Social Sciences and Humanities (MJSSH), 2022-12, Vol.7 (12), p.e001990

2022

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Application of Dudley-Evans & St. John Model in Malay Language: The Needs Analysis Phase

Malaysian Journal of Social Sciences and Humanities (MJSSH), 2022-07, Vol.7 (7), p.e001628

2022

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Variant PADI3 in Central Centrifugal Cicatricial Alopecia

Up-regulation of ST18 in pemphigus vulgaris drives a self-amplifying p53-dependent pathomechanism resulting in decreased desmoglein 3 expression

Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis

Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population

Cutaneous and Developmental Effects of CARD14 Overexpression in Zebrafish

Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma

ARCI7 Revisited and Repositioned

A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes

Loss-of-function variants in KLF4 underlie autosomal dominant palmoplantar keratoderma

Loss-of-Function Variants in SERPINA12 Underlie Autosomal Recessive Palmoplantar Keratoderma

Epidermolytic epidermal nevus caused by a somatic mutation in KRT2

Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis

Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1

Filaggrin 2 Deficiency Results in Abnormal Cell-Cell Adhesion in the Cornified Cell Layers and Causes Peeling Skin Syndrome Type A

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4

SAM syndrome is characterized by extensive phenotypic heterogeneity

Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa

Loss-of-Function Mutations in SERPINB8 Linked to Exfoliative Ichthyosis with Impaired Mechanical Stability of Intercellular Adhesions

Cutaneous and Developmental Effects of ICARD14/I Overexpression in Zebrafish

Phenotypic suppression of acral peeling skin syndrome in a patient with autosomal recessive congenital ichthyosis

LINEAR MYCOSIS FUNGOIDES IN A BLASCHKOID DISTRIBUTION

A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes

MODEL OF TEACHING MALAY LANGUAGE TO NON-NATIVE AND FOREIGN SPEAKER

Content Validity of The Reading Skills Teaching Module Through a Foreign Language Teaching Approach

Application of Dudley-Evans & St. John Model in Malay Language: The Needs Analysis Phase

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