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Wei-De Lin

Showing results (11-20 of 93) with videos related to

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Clinical Chemistry and Laboratory Medicine|September 25, 2015
Genetic screening of the makorin ring finger 3 gene in girls with idiopathic central precocious pubertyWei-De Lin, Chung-Hsing Wang, Fuu-Jen Tsai
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: COMP. Disease: pseudoachondroplasiaChung-Hsing Wang, Wei-De Lin, Anne Tsai, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: EXT2. Disease: exostoses (multiple) 2Wei-De Lin, Chang-Hai Tsai, Chih-Ping Chen, et al.
Human Genetics|October 11, 2008
Gene symbol: LMX1B. Disease: Nail-patella syndromeWei-De Lin, Chih-Ping Chen, Der-Yean Wang, et al.
Biotechnology Progress|September 22, 2009
Asymmetrically simultaneous synthesis of L-homophenylalanine and N6-protected-2-oxo-6-amino-hexanoic acid by engineered Escherichia coli aspartate aminotransferaseHsueh-Hsia Lo, Wei-De Lin, Shih-Kuang Hsu, et al.
Acta Ophthalmologica|February 1, 2014
A novel one-base insertion mutation in the retinitis pigmentosa 2 gene in a large X-linked Taiwanese familyWei- De Lin, Chung-Hsing Wang, I-Ching Chou, et al.
Forensic Science, Medicine, and Pathology|February 12, 2024
Identification of the efficacy of parentage testing based on bi-allelic autosomal single nucleotide polymorphism markers in Taiwanese populationYu-Chia Chen, Wei-De Lin, Ting-Yuan Liu, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1Wei-De Lin, Shuan-Pei Lin, Chih-Ping Chen, et al.
Pediatrics and Neonatology|November 23, 2017
Novel mutations in the cartilage oligomeric matrix protein gene identified in two Taiwanese patients with pseudoachondroplasia and multiple epiphyseal dysplasiaWei-De Lin, I-Ching Chou, Chung-Hsing Wang, et al.
Frontiers in Nutrition|June 15, 2026
Preoperative low Geriatric Nutritional Risk Index increases intensive care unit admission risk in patients undergoing gastrointestinal tumor surgeryWei-De Lin, Bi-Xia Lin, Jun-Fan Chen, et al.
Pageof 10

Showing results (11-20 of 93) with videos related to

Sort By:
Pageof 10
Clinical Chemistry and Laboratory Medicine|September 25, 2015
Genetic screening of the makorin ring finger 3 gene in girls with idiopathic central precocious pubertyWei-De Lin, Chung-Hsing Wang, Fuu-Jen Tsai
Human Genetics|March 26, 2009
Novel human pathological mutations. Gene symbol: COMP. Disease: pseudoachondroplasiaChung-Hsing Wang, Wei-De Lin, Anne Tsai, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: EXT2. Disease: exostoses (multiple) 2Wei-De Lin, Chang-Hai Tsai, Chih-Ping Chen, et al.
Human Genetics|October 11, 2008
Gene symbol: LMX1B. Disease: Nail-patella syndromeWei-De Lin, Chih-Ping Chen, Der-Yean Wang, et al.
Biotechnology Progress|September 22, 2009
Asymmetrically simultaneous synthesis of L-homophenylalanine and N6-protected-2-oxo-6-amino-hexanoic acid by engineered Escherichia coli aspartate aminotransferaseHsueh-Hsia Lo, Wei-De Lin, Shih-Kuang Hsu, et al.
Acta Ophthalmologica|February 1, 2014
A novel one-base insertion mutation in the retinitis pigmentosa 2 gene in a large X-linked Taiwanese familyWei- De Lin, Chung-Hsing Wang, I-Ching Chou, et al.
Forensic Science, Medicine, and Pathology|February 12, 2024
Identification of the efficacy of parentage testing based on bi-allelic autosomal single nucleotide polymorphism markers in Taiwanese populationYu-Chia Chen, Wei-De Lin, Ting-Yuan Liu, et al.
Human Genetics|April 4, 2008
Human gene mutations. Gene symbol: EXT1. Disease: exostoses (multiple) 1Wei-De Lin, Shuan-Pei Lin, Chih-Ping Chen, et al.
Pediatrics and Neonatology|November 23, 2017
Novel mutations in the cartilage oligomeric matrix protein gene identified in two Taiwanese patients with pseudoachondroplasia and multiple epiphyseal dysplasiaWei-De Lin, I-Ching Chou, Chung-Hsing Wang, et al.
Frontiers in Nutrition|June 15, 2026
Preoperative low Geriatric Nutritional Risk Index increases intensive care unit admission risk in patients undergoing gastrointestinal tumor surgeryWei-De Lin, Bi-Xia Lin, Jun-Fan Chen, et al.
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