1. 4′-Phosphopantetheine and long acyl chain-dependent interactions are integral to human mitochondrial acyl carrier protein function. Issue 2 (29th January 2019) Authors: Majmudar, Jaimeen D.; Feng, Xidong; Fox, Nicholas G.; Nabhan, Joseph F.; Towle, Theresa; Ma, Tiffany; Gooch, Renea; Bulawa, Christine; Yue, Wyatt W.; Martelli, Alain Journal: MedChemComm Issue: Volume 10:Issue 2(2019) Page Start: 209 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Single‐Stranded DNA‐Encoded Chemical Library Based on a Stereoisomeric Scaffold Enables Ligand Discovery by Modular Assembly of Building Blocks. Issue 22 (14th October 2020) Authors: Bassi, Gabriele; Favalli, Nicholas; Vuk, Miriam; Catalano, Marco; Martinelli, Adriano; Trenner, Anika; Porro, Antonio; Yang, Su; Tham, Chuin Lean; Moroglu, Mustafa; Yue, Wyatt W.; Conway, Stuart J.; Vogt, Peter K.; Sartori, Alessandro A.; Scheuermann, Jörg; Neri, Dario Journal: Advanced science Issue: Volume 7:Issue 22(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A structural mapping of mutations causing succinyl‐CoA:3‐ketoacid CoA transferase (SCOT) deficiency. Issue 6 (19th February 2013) Authors: Shafqat, Naeem; Kavanagh, Kate L.; Sass, Jörn Oliver; Christensen, Ernst; Fukao, Toshiyuki; Lee, Wen Hwa; Oppermann, Udo; Yue, Wyatt W. Journal: Journal of inherited metabolic disease Issue: Volume 36:Issue 6(2013) Page Start: 983 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Expanding the genetic and phenotypic spectrum of branched‐chain amino acid transferase 2 deficiency. Issue 5 (1st August 2019) Authors: Knerr, Ina; Colombo, Roberto; Urquhart, Jill; Morais, Ana; Merinero, Begona; Oyarzabal, Alfonso; Pérez, Belén; Jones, Simon A.; Perveen, Rahat; Preece, Mary A.; Rogers, Yvonne; Treacy, Eileen P.; Mayne, Philip; Zampino, Giuseppe; MacKinnon, Sabrina; Wassmer, Evangeline; Yue, Wyatt W.; Robinson, I... Journal: Journal of inherited metabolic disease Issue: Volume 42:Issue 5(2019) Page Start: 809 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. From structural biology to designing therapy for inborn errors of metabolism. Issue 4 (30th May 2016) Authors: Yue, Wyatt W. Journal: Journal of inherited metabolic disease Issue: Volume 39:Issue 4(2016) Page Start: 489 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Functional Characterization and Categorization of Missense Mutations that Cause Methylmalonyl‐CoA Mutase (MUT) Deficiency. Issue 12 (December 2014) Authors: Forny, Patrick; Froese, D. Sean; Suormala, Terttu; Yue, Wyatt W.; Baumgartner, Matthias R. Journal: Human mutation Issue: Volume 35:Issue 12(2014:Dec.) Page Start: 1449 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification of a novel biomarker for pyridoxine‐dependent epilepsy: Implications for newborn screening. Issue 3 (11th March 2019) Authors: Wempe, Michael F.; Kumar, Amit; Kumar, Vijay; Choi, Yu J.; Swanson, Michael A.; Friederich, Marisa W.; Hyland, Keith; Yue, Wyatt W.; Van Hove, Johan L. K.; Coughlin, Curtis R. Journal: Journal of inherited metabolic disease Issue: Volume 42:Issue 3(2019) Page Start: 565 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Novel homozygous variant of carbonic anhydrase 8 gene expanding the phenotype of cerebellar ataxia, mental retardation, and disequilibrium syndrome subtype 3. Issue 11 (18th August 2020) Authors: Paternoster, Lionel; Soblet, Julie; Aeby, Alec; De Tiège, Xavier; Goldman, Serge; Yue, Wyatt W.; Coppens, Sandra; Smits, Guillaume; Vilain, Catheline; Deconinck, Nicolas Journal: American journal of medical genetics Issue: Volume 182:Issue 11(2020) Page Start: 2685 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Protein destabilization and loss of protein‐protein interaction are fundamental mechanisms in cblA‐type methylmalonic aciduria. Issue 8 (6th June 2017) Authors: Plessl, Tanja; Bürer, Céline; Lutz, Seraina; Yue, Wyatt W.; Baumgartner, Matthias R.; Froese, D. Sean Journal: Human mutation Issue: Volume 38:Issue 8(2017) Page Start: 988 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Role of reverse phenotyping in interpretation of next generation sequencing data and a review of INPP5E related disorders. (March 2016) Authors: de Goede, Christian; Yue, Wyatt W.; Yan, Guanhua; Ariyaratnam, Shyamala; Chandler, Kate E.; Downes, Laura; Khan, Nasaim; Mohan, Meyyammai; Lowe, Martin; Banka, Siddharth Journal: European journal of paediatric neurology Issue: Volume 20:Number 2(2016:Mar.) Page Start: 286 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗