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Results for
""Craniofacial Dysostosis""[mesh_terms]

6 Results

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Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome.

Tracy Lester, A Jeannette M Hoogeboom, Ans M W van den Ouweland, Steven A Wall, Irene M J Mathijssen, Andrew O M Wilkie, Helen Lord, Julia Rankin, Aimee L Fenwick, Jacqueline A C Goos

BMC medical genetics 2014;15():95

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The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

C A Francomano, D J Wilkin, Z Vajo

Endocrine reviews 2000;21(1):23-39

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Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix.

Francesco Carinci, Furio Pezzetti, Paola Locci, Ennio Becchetti, Friedrick Carls, Anna Avantaggiato, Alessio Becchetti, Paolo Carinci, Tiziano Baroni, Maria Bodo

The Journal of craniofacial surgery 2005;16(3):361-8

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Characterization of membrane protein interactions in plasma membrane derived vesicles with quantitative imaging Förster resonance energy transfer.

Sarvenaz Sarabipour, Nuala Del Piccolo, Kalina Hristova

Accounts of chemical research 2016;48(8):2262-9

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Syndromic craniosynostosis: from history to hydrogen bonds.

Machael L Cunningham, Marianne L Seto, Chootima Ratisoontorn, Carrie L Heike, Anne V Hing

Orthodontics & craniofacial research 2007;10(2):67-81

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Conventional transarterial chemoembolization combined with systemic therapy versus systemic therapy alone as second-line treatment for unresectable colorectal liver metastases: randomized clinical trial.

W Chang, Y Liu, B Zhou, Y Wei, W Tang, F Liang, Y Chen, Z Yan, M Lv, L Ren, J Xu

The British journal of surgery 2021;108(4):373-379

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Results for ""Craniofacial Dysostosis""[mesh_terms]

Apparently synonymous substitutions in FGFR2 affect splicing and result in mild Crouzon syndrome.

The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix.

Characterization of membrane protein interactions in plasma membrane derived vesicles with quantitative imaging Förster resonance energy transfer.

Syndromic craniosynostosis: from history to hydrogen bonds.

Conventional transarterial chemoembolization combined with systemic therapy versus systemic therapy alone as second-line treatment for unresectable colorectal liver metastases: randomized clinical trial.

Results for
""Craniofacial Dysostosis""[mesh_terms]