Expression and Role of Ubiquitin-Specific Peptidases in Osteoblasts
Hariri, Hadla, St-Arnaud, René
Published in International journal of molecular sciences (20.07.2021)
Published in International journal of molecular sciences (20.07.2021)
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Journal Article
Deficiency of glucocorticoid receptor in bone marrow adipocytes has mild effects on bone and hematopoiesis but does not influence expansion of marrow adiposity with caloric restriction
Schill, Rebecca L, Visser, Jack, Ashby, Mariah L, Li, Ziru, Lewis, Kenneth T, Morales-Hernandez, Antonio, Hoose, Keegan S, Maung, Jessica N, Uranga, Romina M, Hariri, Hadla, Hermsmeyer, Isabel D K, Mori, Hiroyuki, MacDougald, Ormond A
Published in Frontiers in endocrinology (Lausanne) (03.06.2024)
Published in Frontiers in endocrinology (Lausanne) (03.06.2024)
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Journal Article
Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis
Hariri, Hadla, Kurban, Mazen, Al-Haddad, Christiane, Fahed, Akl C., Poladian, Sarin, Khalil, Athar, Abbas, Oussama, Arabi, Mariam, Bitar, Fadi, Nemer, Georges
Published in Journal of dermatological science (01.12.2018)
Published in Journal of dermatological science (01.12.2018)
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Journal Article
A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
Khalil, Athar, Al-Haddad, Christiane, Hariri, Hadla, Shibbani, Kamel, Bitar, Fadi, Kurban, Mazen, Nemer, Georges, Arabi, Mariam
Published in Frontiers in cardiovascular medicine (20.09.2017)
Published in Frontiers in cardiovascular medicine (20.09.2017)
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Journal Article
New PTH Signals Mediating Bone Anabolism
Hariri, Hadla, Pellicelli, Martin, St-Arnaud, René
Published in Current molecular biology reports (2017)
Published in Current molecular biology reports (2017)
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Journal Article
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient
Kassab, Kameel, Hariri, Hadla, Gharibeh, Lara, Fahed, Akl C., Zein, Manal, El‐Rassy, Inaam, Nemer, Mona, El‐Rassi, Issam, Bitar, Fadi, Nemer, Georges
Published in Molecular genetics & genomic medicine (01.03.2016)
Published in Molecular genetics & genomic medicine (01.03.2016)
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Journal Article
GATA 5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient
Kassab, Kameel, Hariri, Hadla, Gharibeh, Lara, Fahed, Akl C., Zein, Manal, El‐Rassy, Inaam, Nemer, Mona, El‐Rassi, Issam, Bitar, Fadi, Nemer, Georges
Published in Molecular genetics & genomic medicine (01.03.2016)
Published in Molecular genetics & genomic medicine (01.03.2016)
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Journal Article