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Molecular Biology of the Cell|August 2, 2013
Nuclear-localized Asunder regulates cytoplasmic dynein localization via its role in the integrator complexJeanne N Jodoin, Poojitha Sitaram, Todd R Albrecht, et al.African Journal of Paediatric Surgery : AJPS|August 3, 2021
Infantile systemic hyalinosis: Variable grades of severityAli Al Kaissi, Marwa Hilmi, Zulfiya Betadolova, et al.Calcified Tissue International|May 18, 2021
Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus SyndromeAli Al Kaissi, Barbara M Misof, Franco Laccone, et al.Frontiers in Pediatrics|May 7, 2020
Clinical and Genetic Heterogeneity in Six Tunisian Families With Horizontal Gaze Palsy With Progressive Scoliosis: A Retrospective Study of 13 CasesSami Bouchoucha, Asma Chikhaoui, Dorra Najjar, et al.Human Molecular Genetics|February 26, 2015
Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defectsCalista K L Ng, Mohammad Shboul, Valerio Taverniti, et al.Nature Genetics|May 15, 2012
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Carine Bonnard, Anna C Strobl, Mohammad Shboul, et al.Diagnostics (Basel, Switzerland)|October 27, 2022
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic EntitiesAli Al Kaissi, Sergey Ryabykh, Nabil Nassib, et al.Bone Reports|July 26, 2016
Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralizationCorey J Cain, Nathalie Gaborit, Wint Lwin, et al.American Journal of Human Genetics|December 7, 2010
Loss of CHSY1, a secreted FRINGE enzyme, causes syndromic brachydactyly in humans via increased NOTCH signalingJing Tian, Ling Ling, Mohammad Shboul, et al.Nature Communications|March 20, 2026
IVNS1ABP mutation drives cellular senescence in newly identified progeroid neuropathyFang Yuan, Ye Sing Tan, Haofei Wang, et al.Pageof 5