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Nabil Moghrabi

University of Texas Southwestern Medical Center

15

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871

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Cystic fibrosis gene mutations and polymorphisms in Saudi men with infertility.

2020 Annals of Saudi Medicine
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MP38-02 CFTR GENE MUTATIONS IN SAUDI INFERTILE MEN WITH AZOOSPERMIA OR OLIGOASTHENOTERATOZOOSPERMIA

2020 The Journal of Urology
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Double homozygous Cystic Fibrosis Transmembrane Regulator gene (CFTR) mutation: A case series and review of the literature

2020
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Homozygous loss‐of‐function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies

2019 Human Mutation
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A Role for the deep orange and carnation Eye Color Genes in Lysosomal Delivery in Drosophila

1999 Molecular Cell
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17β-hydroxysteroid dehydrogenases : Physiological roles in health and disease

1998 Trends in Endocrinology and Metabolism
- Nabil Moghrabi
- Stefan Andersson
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Deficient 17β-hydroxysteroid dehydrogenase type 2 expression in endometriosis: Failure to metabolize 17β-estradiol

1998 The Journal of Clinical Endocrinology and Metabolism
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Deleterious Missense Mutations and Silent Polymorphism in the Human 17β-Hydroxysteroid Dehydrogenase 3 Gene (HSD17B3)

1998 The Journal of Clinical Endocrinology and Metabolism
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Cell Type-Specific Expression of 17β-Hydroxysteroid Dehydrogenase Type 2 in Human Placenta and Fetal Liver1

1997 The Journal of Clinical Endocrinology and Metabolism
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Assignment of the human peroxisomal branched-chain acyl-CoA oxidase gene to chromosome 3p21.1-p14.2 by rodent/human somatic cell hybridization

1997 Biochemical and Biophysical Research Communications
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Citations (3)