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	41.	Perrault syndrome: further evidence for genetic heterogeneity. [electronic resource] by Jenkinson, Emma M Clayton-Smith, Jill Mehta, Sarju Bennett, Christopher Reardon, Willie Green, Andrew Pearce, Simon H S De Michele, Giuseppe Conway, Gerard S Cilliers, Deirdre Moreton, Natalie Davis, Julian R E Trump, Dorothy Newman, William G Producer: 20121017 In: Journal of neurology vol. 259 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	[Relationship between the increase of hepatic D-bifunctional protein activity and bile acid biosynthesis in rats]. [electronic resource] by Shi, Ru-ling Zhao, Chao-xian Zhu, Hai-bao Yang, Yuan Wang, Su-ling Jiang, Ling-ling Producer: 20060428 In: Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae vol. 27 Availability: No items available. Save to lists Add to cart (remove)
	43.	Pathological complete response of HER2-positive breast cancer to trastuzumab and chemotherapy can be predicted by HSD17B4 methylation. [electronic resource] by Fujii, Satoshi Yamashita, Satoshi Yamaguchi, Takeshi Takahashi, Masato Hozumi, Yasuo Ushijima, Toshikazu Mukai, Hirofumi Producer: 20170920 In: Oncotarget vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis. [electronic resource] by van Grunsven, E G van Berkel, E Mooijer, P A Watkins, P A Moser, H W Suzuki, Y Jiang, L L Hashimoto, T Hoefler, G Adamski, J Wanders, R J Producer: 19990310 In: American journal of human genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Identification of a chronic non-neurodegenerative microglia activation state in a mouse model of peroxisomal β-oxidation deficiency. [electronic resource] by Verheijden, Simon Beckers, Lien Casazza, Andrea Butovsky, Oleg Mazzone, Massimiliano Baes, Myriam Producer: 20160413 In: Glia vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	46.	A homozygous missense variant in HSD17B4 identified in a consanguineous Chinese Han family with type II Perrault syndrome. [electronic resource] by Chen, Kui Yang, Ke Luo, Su-Shan Chen, Chen Wang, Ying Wang, Yi-Xuan Li, Da-Ke Yang, Yu-Jie Tang, Yi-Lin Liu, Feng-Tao Wang, Jian Wu, Jian-Jun Sun, Yi-Min Producer: 20170905 In: BMC medical genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	Structure of the gene for the human 17beta-hydroxysteroid dehydrogenase type IV. [electronic resource] by Leenders, F Dolez, V Begue, A Möller, G Gloeckner, J C de Launoit, Y Adamski, J Producer: 19990216 In: Mammalian genome : official journal of the International Mammalian Genome Society vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	Sensitive analysis of serum 3alpha, 7alpha, 12alpha,24-tetrahydroxy- 5beta-cholestan-26-oic acid diastereomers using gas chromatography-mass spectrometry and its application in peroxisomal D-bifunctional protein deficiency. [electronic resource] by Vreken, P van Rooij, A Denis, S van Grunsven, E G Cuebas, D A Wanders, R J Producer: 19990211 In: Journal of lipid research vol. 39 Availability: No items available. Save to lists Add to cart (remove)
	49.	Normal very-long-chain fatty acids in peroxisomal D-bifunctional protein deficiency: a diagnostic pitfall. [electronic resource] by Soorani-Lunsing, R J van Spronsen, F J Stolte-Dijkstra, I Wanders, R J Ferdinandusse, S Waterham, H R Poll-The, B T Rake, J P Producer: 20060705 In: Journal of inherited metabolic disease vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	Typical cMRI pattern as diagnostic clue for D-bifunctional protein deficiency without apparent biochemical abnormalities in plasma. [electronic resource] by Grønborg, Sabine Krätzner, Ralph Spiegler, Juliane Ferdinandusse, Sacha Wanders, Ronald J A Waterham, Hans R Gärtner, Jutta Producer: 20110204 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Developing antineoplastic agents that target peroxisomal enzymes: cytisine-linked isoflavonoids as inhibitors of hydroxysteroid 17-beta-dehydrogenase-4 (HSD17B4). [electronic resource] by Frasinyuk, Mykhaylo S Zhang, Wen Wyrebek, Przemyslaw Yu, Tianxin Xu, Xuehe Sviripa, Vitaliy M Bondarenko, Svitlana P Xie, Yanqi Ngo, Huy X Morris, Andrew J Mohler, James L Fiandalo, Michael V Watt, David S Liu, Chunming Producer: 20180501 In: Organic & biomolecular chemistry vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Identification of a substrate-binding site in a peroxisomal beta-oxidation enzyme by photoaffinity labeling with a novel palmitoyl derivative. [electronic resource] by Kashiwayama, Yoshinori Tomohiro, Takenori Narita, Kotomi Suzumura, Miyuki Glumoff, Tuomo Hiltunen, J Kalervo Van Veldhoven, Paul P Hatanaka, Yasumaru Imanaka, Tsuneo Producer: 20100930 In: The Journal of biological chemistry vol. 285 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	HSD17B4 overexpression, an independent biomarker of poor patient outcome in prostate cancer. [electronic resource] by Rasiah, Krishan K Gardiner-Garden, Margaret Padilla, Emma J D Möller, Gabriele Kench, James G Alles, M Chehani Eggleton, Sarah A Stricker, Phillip D Adamski, Jerzy Sutherland, Robert L Henshall, Susan M Hayes, Vanessa M Producer: 20090504 In: Molecular and cellular endocrinology vol. 301 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	Bile acid profiles in a peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency. [electronic resource] by Une, M Konishi, M Suzuki, Y Akaboshi, S Yoshii, M Kuramoto, T Fujimura, K Producer: 19980211 In: Journal of biochemistry vol. 122 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Hydratase activities of green fluorescent protein tagged human multifunctional enzyme type 2 hydratase domain and its variants. [electronic resource] by Tsuchida, Shirou Kawamoto, Koutarou Endo, Noriko Nunome, Kana Hamaue, Naoya Aoki, Takashi Producer: 20130326 In: Journal of oleo science vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	Peroxisomal straight-chain Acyl-CoA oxidase and D-bifunctional protein are essential for the retroconversion step in docosahexaenoic acid synthesis. [electronic resource] by Su, H M Moser, A B Moser, H W Watkins, P A Producer: 20011204 In: The Journal of biological chemistry vol. 276 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Steroids, fatty acyl-CoA, and sterols are substrates of 80-kDa multifunctional protein. [electronic resource] by Adamski, J Leenders, F Carstensen, J F Kaufmann, M Markus, M M Husen, B Tesdorpf, J G Seedorf, U de Launoit, Y Jakob, F Producer: 19970529 In: Steroids vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	58.	Thiolase involved in bile acid formation. [electronic resource] by Bun-ya, M Maebuchi, M Kamiryo, T Kurosawa, T Sato, M Tohma, M Jiang, L L Hashimoto, T Producer: 19980818 In: Journal of biochemistry vol. 123 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	59.	Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency. [electronic resource] by van Grunsven, E G Mooijer, P A Aubourg, P Wanders, R J Producer: 19990914 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	60.	Molecular analysis of genomic DNA allows rapid, and accurate, prenatal diagnosis of peroxisomal D-bifunctional protein deficiency. [electronic resource] by Paton, B C Solly, P B Nelson, P V Pollard, A N Sharp, P C Fietz, M J Producer: 20020412 In: Prenatal diagnosis vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 131 results.