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Page 1
Zebrafish: A Resourceful Vertebrate Model to Investigate Skeletal Disorders.
Tonelli F, Bek JW, Besio R, De Clercq A, Leoni L, Salmon P, Coucke PJ, Willaert A, Forlino A. Tonelli F, et al. Among authors: salmon p. Front Endocrinol (Lausanne). 2020 Jul 31;11:489. doi: 10.3389/fendo.2020.00489. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32849280 Free PMC article. Review.
b3galt6 Knock-Out Zebrafish Recapitulate β3GalT6-Deficiency Disorders in Human and Reveal a Trisaccharide Proteoglycan Linkage Region.
Delbaere S, De Clercq A, Mizumoto S, Noborn F, Bek JW, Alluyn L, Gistelinck C, Syx D, Salmon PL, Coucke PJ, Larson G, Yamada S, Willaert A, Malfait F. Delbaere S, et al. Front Cell Dev Biol. 2020 Dec 10;8:597857. doi: 10.3389/fcell.2020.597857. eCollection 2020. Front Cell Dev Biol. 2020. PMID: 33363150 Free PMC article.
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.
Pottie L, Adamo CS, Beyens A, Lütke S, Tapaneeyaphan P, De Clercq A, Salmon PL, De Rycke R, Gezdirici A, Gulec EY, Khan N, Urquhart JE, Newman WG, Metcalfe K, Efthymiou S, Maroofian R, Anwar N, Maqbool S, Rahman F, Altweijri I, Alsaleh M, Abdullah SM, Al-Owain M, Hashem M, Houlden H, Alkuraya FS, Sips P, Sengle G, Callewaert B. Pottie L, et al. Among authors: salmon pl. Am J Hum Genet. 2021 Jun 3;108(6):1095-1114. doi: 10.1016/j.ajhg.2021.04.016. Epub 2021 May 14. Am J Hum Genet. 2021. PMID: 33991472 Free PMC article.
Editorial: Putting the "Why" Back into Bone "Archytecture".
Salmon P. Salmon P. Front Endocrinol (Lausanne). 2016 Feb 11;7:14. doi: 10.3389/fendo.2016.00014. eCollection 2016. Front Endocrinol (Lausanne). 2016. PMID: 26903950 Free PMC article. No abstract available.
Low-Dose Imaging in a New Preclinical Total-Body PET/CT Scanner.
Molinos C, Sasser T, Salmon P, Gsell W, Viertl D, Massey JC, Mińczuk K, Li J, Kundu BK, Berr S, Correcher C, Bahadur A, Attarwala AA, Stark S, Junge S, Himmelreich U, Prior JO, Laperre K, Van Wyk S, Heidenreich M. Molinos C, et al. Among authors: salmon p. Front Med (Lausanne). 2019 May 3;6:88. doi: 10.3389/fmed.2019.00088. eCollection 2019. Front Med (Lausanne). 2019. PMID: 31131277 Free PMC article.
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.
Pottie L, Adamo CS, Beyens A, Lütke S, Tapaneeyaphan P, De Clercq A, Salmon PL, De Rycke R, Gezdirici A, Gulec EY, Khan N, Urquhart JE, Newman WG, Metcalfe K, Efthymiou S, Maroofian R, Anwar N, Maqbool S, Rahman F, Altweijri I, Alsaleh M, Abdullah SM, Al-Owain M, Hashem M, Houlden H, Alkuraya FS, Sips P, Sengle G, Callewaert B. Pottie L, et al. Among authors: salmon pl. Am J Hum Genet. 2021 Dec 2;108(12):2386-2388. doi: 10.1016/j.ajhg.2021.11.009. Am J Hum Genet. 2021. PMID: 34861177 Free PMC article. No abstract available.
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