S-P Lin - JoVE Visualize

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Advanced Healthcare Materials|February 22, 2023

Engineering of an Osteoinductive and Growth Factor-Free Injectable Bone-Like Microgel for Bone RegenerationRamesh Subbiah, Edith Y Lin, Avathamsa Athirasala, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 9, 2004

Estrogen prevents bone loss through transforming growth factor beta signaling in T cellsYuhao Gao, Wei-Ping Qian, Kimberly Dark, et al.

Investigative Ophthalmology & Visual Science|October 29, 2000

Growth and differentiation of human lens epithelial cells in vitro on matrixE A Blakely, K A Bjornstad, P Y Chang, et al.

Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000

Molecular diagnosis of Apert syndrome in Chinese patientsF J Tsai, C H Tsai, C T Peng, et al.

Osteoarthritis and Cartilage|June 11, 2013

Localized 3D analysis of cartilage composition and morphology in small animal models of joint degenerationT Thote, A S P Lin, Y Raji, et al.

Human Genetics|October 28, 1997

Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parentsJ G Chang, Y J Jong, S P Lin, et al.

Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000

An R248C mutation of FGFR3 leading to thanatophoric dysplasia type IF J Tsai, L P Tsai, S P Lin, et al.

Genetic Counseling (Geneva, Switzerland)|October 18, 2012

Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delayC P Chen, S P Lin, M R Chen, et al.

Experimental and Clinical Immunogenetics|June 10, 1998

DQA1*Arg52,DQB1*nonAsp57, and DRB1*04 genotypes in Chinese children with insulin-dependent diabetes mellitusF Y Huang, Y J Lee, F S Lo, et al.

Pageof 16

Showing results (121-130 of 154) with videos related to

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Pageof 16

Advanced Healthcare Materials|February 22, 2023

Engineering of an Osteoinductive and Growth Factor-Free Injectable Bone-Like Microgel for Bone RegenerationRamesh Subbiah, Edith Y Lin, Avathamsa Athirasala, et al.

Genetic Counseling (Geneva, Switzerland)|February 26, 2013

De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delayC-P Chen, S-P Lin, Y-L Huang, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 9, 2004

Estrogen prevents bone loss through transforming growth factor beta signaling in T cellsYuhao Gao, Wei-Ping Qian, Kimberly Dark, et al.

Investigative Ophthalmology & Visual Science|October 29, 2000

Growth and differentiation of human lens epithelial cells in vitro on matrixE A Blakely, K A Bjornstad, P Y Chang, et al.

Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000

Molecular diagnosis of Apert syndrome in Chinese patientsF J Tsai, C H Tsai, C T Peng, et al.

Osteoarthritis and Cartilage|June 11, 2013

Localized 3D analysis of cartilage composition and morphology in small animal models of joint degenerationT Thote, A S P Lin, Y Raji, et al.

Human Genetics|October 28, 1997

Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parentsJ G Chang, Y J Jong, S P Lin, et al.

Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi|July 27, 2000

An R248C mutation of FGFR3 leading to thanatophoric dysplasia type IF J Tsai, L P Tsai, S P Lin, et al.

Genetic Counseling (Geneva, Switzerland)|October 18, 2012

Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delayC P Chen, S P Lin, M R Chen, et al.

Experimental and Clinical Immunogenetics|June 10, 1998

DQA1*Arg52,DQB1*nonAsp57, and DRB1*04 genotypes in Chinese children with insulin-dependent diabetes mellitusF Y Huang, Y J Lee, F S Lo, et al.

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