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Congenital heart disease in children: Orofacial myofunctional aspects, eating behavior and facial temperature. , Barbosa MDG, Castelo PM, Ferreira CLP, Haddad DS, Chiari BM, Santana MV, Bommarito S., Int J Pediatr Otorhinolaryngol. April 1, 2020; 131 109883.
Xenbase: Facilitating the Use of Xenopus to Model Human Disease. , Nenni MJ , Fisher ME , James-Zorn C , Pells TJ , Ponferrada V , Chu S , Fortriede JD , Burns KA , Wang Y , Lotay VS , Wang DZ, Segerdell E, Chaturvedi P, Karimi K , Vize PD , Zorn AM ., Front Physiol. February 26, 2019; 10 154.
WDR5 regulates left-right patterning via chromatin-dependent and -independent functions. , Kulkarni SS, Khokha MK., Development. November 28, 2018; 145 (23):
RPSA, a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in Xenopus. , Griffin JN, Sondalle SB, Robson A, Mis EK, Griffin G, Kulkarni SS, Deniz E, Baserga SJ, Khokha MK., Development. October 18, 2018; 145 (20):
Single nucleotide editing without DNA cleavage using CRISPR/Cas9-deaminase in the sea urchin embryo. , Shevidi S, Uchida A, Schudrowitz N, Wessel GM , Yajima M ., Dev Dyn. December 1, 2017; 246 (12): 1036-1046.
Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography. , Deniz E, Jonas S, Hooper M, N Griffin J, Choma MA, Khokha MK., Sci Rep. February 14, 2017; 7 42506.
Proteolytic processing of von Willebrand factor by adamts13 and leukocyte proteases. , Lancellotti S, Basso M, De Cristofaro R., Mediterr J Hematol Infect Dis. September 2, 2013; 5 (1): e2013058.
Shells and heart: are human laterality and chirality of snails controlled by the same maternal genes? , Oliverio M, Digilio MC, Versacci P, Dallapiccola B, Marino B., Am J Med Genet A. October 1, 2010; 152A (10): 2419-25.
Starfish-assisted off-pump obliteration of massive coronary arteriovenous fistulae. , Sun S, Li JY, Hu PY, Wu SJ., Tex Heart Inst J. January 1, 2005; 32 (4): 595-7.
Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein ( EMAP) from the Usher syndrome type 1a locus at 14q32. , Eudy JD, Ma-Edmonds M, Yao SF, Talmadge CB, Kelley PM, Weston MD, Kimberling WJ, Sumegi J., Genomics. July 1, 1997; 43 (1): 104-6.
Keratoderma hereditarium mutilans (Vohwinkel''s syndrome) associated with congenital deaf-mutism. , Peris K, Salvati EF, Torlone G, Chimenti S., Br J Dermatol. April 1, 1995; 132 (4): 617-20.