Results
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81.
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Developmental roles of D-bifunctional protein-A zebrafish model of peroxisome dysfunction. [electronic resource] by
- Kim, Yong-Il
- Bhandari, Sushil
- Lee, Joon No
- Yoo, Kyeong-Won
- Kim, Se-Jin
- Oh, Gi-Su
- Kim, Hyung-Jin
- Cho, Meyoung
- Kwak, Jong-Young
- So, Hong-Seob
- Park, Raekil
- Choe, Seong-Kyu
Producer: 20141205
In:
Molecules and cells vol. 37
Availability: No items available.
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82.
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Peroxisomes can oxidize medium- and long-chain fatty acids through a pathway involving ABCD3 and HSD17B4. [electronic resource] by
- Violante, Sara
- Achetib, Nihad
- van Roermund, Carlo W T
- Hagen, Jacob
- Dodatko, Tetyana
- Vaz, Frédéric M
- Waterham, Hans R
- Chen, Hongjie
- Baes, Myriam
- Yu, Chunli
- Argmann, Carmen A
- Houten, Sander M
Producer: 20200511
In:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology vol. 33
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83.
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84.
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85.
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Mutations in the DBP-deficiency protein HSD17B4 cause ovarian dysgenesis, hearing loss, and ataxia of Perrault Syndrome. [electronic resource] by
- Pierce, Sarah B
- Walsh, Tom
- Chisholm, Karen M
- Lee, Ming K
- Thornton, Anne M
- Fiumara, Agata
- Opitz, John M
- Levy-Lahad, Ephrat
- Klevit, Rachel E
- King, Mary-Claire
Producer: 20100901
In:
American journal of human genetics vol. 87
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86.
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87.
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Genomic evidence sheds light on the genetic mechanisms of musk secretion in muskrats. [electronic resource] by
- Zhou, Chuang
- Zhang, Yifan
- Qiu, Shi
- Yu, Haoran
- Tu, Hongmei
- Wen, Qinchao
- George James, Jake
- Meng, Yang
- Wu, Yongjie
- Yang, Nan
- Yue, Bisong
Producer: 20201207
In:
International journal of biological macromolecules vol. 145
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88.
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89.
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Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency. [electronic resource] by
- Suzuki, Y
- Zhang, Z
- Shimozawa, N
- Muro, M
- Shono, H
- Toda, S
- Miyahara, S
- Hashimoto, T
- Usuda, N
- Ito, M
- Takashima, S
- Kondo, N
Producer: 19990608
In:
Journal of human genetics vol. 44
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90.
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91.
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92.
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D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder. [electronic resource] by
- Suzuki, Y
- Jiang, L L
- Souri, M
- Miyazawa, S
- Fukuda, S
- Zhang, Z
- Une, M
- Shimozawa, N
- Kondo, N
- Orii, T
- Hashimoto, T
Producer: 19971212
In:
American journal of human genetics vol. 61
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93.
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94.
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95.
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Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency. [electronic resource] by
- van Grunsven, E G
- van Berkel, E
- Ijlst, L
- Vreken, P
- de Klerk, J B
- Adamski, J
- Lemonde, H
- Clayton, P T
- Cuebas, D A
- Wanders, R J
Producer: 19980409
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 95
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96.
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98.
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99.
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[Altered expression of the HSD17B4 gene in esophageal squamous cell carcinoma and loss of heterozygosity analysis]. [electronic resource] by
- Li, Xiao-dong
- Liu, Xiang-yang
- Huang, Xiao-ping
- Fu, Jian-hua
- Hu, Yi
- Xu, Xin
- Cai, Yan
- Han, Ya-ling
- Rong, Tie-hua
- Wu, Min
- Zhan, Qi-min
- Wang, Ming-rong
Producer: 20060428
In:
Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae vol. 27
Availability: No items available.
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