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Bioorganic & Medicinal Chemistry Letters
|
December 26, 2006
Thienopyridine urea inhibitors of KDR kinase
H Robin Heyman, Robin R Frey, Peter F Bousquet, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Additional EFNB1 mutations in craniofrontonasal syndrome
Deeann Wallis, Felicitas Lacbawan, Mahim Jain, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation
Nathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
American Journal of Human Genetics
|
August 23, 2016
De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive
Mari J Tokita, Alicia A Braxton, Yunru Shao, et al.
American Journal of Human Genetics
|
March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
M Muenke, K W Gripp, D M McDonald-McGinn, et al.
Molecular Cancer Therapeutics
|
May 5, 2017
Discovery and Characterization of Novel Nonsubstrate and Substrate NAMPT Inhibitors
Julie L Wilsbacher, Min Cheng, Dong Cheng, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 15, 2017
SAR and characterization of non-substrate isoindoline urea inhibitors of nicotinamide phosphoribosyltransferase (NAMPT)
Michael L Curtin, H Robin Heyman, Richard F Clark, et al.
Molecular Psychiatry
|
June 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autism
Bin Yu, Shimeng Zhu, Linhu Xiao, et al.
American Journal of Human Genetics
|
August 4, 2023
HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder
Eva Niggl, Arjan Bouman, Lauren C Briere, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 20, 2020
JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome
Eline A Verberne, Shuxiang Goh, Jade England, et al.
Page
of 30
Search research articles
Search
Showing results (281-290 of 297) with videos related to
Sort By:
Page
of 30
Bioorganic & Medicinal Chemistry Letters
|
December 26, 2006
Thienopyridine urea inhibitors of KDR kinase
H Robin Heyman, Robin R Frey, Peter F Bousquet, et al.
American Journal of Medical Genetics. Part A
|
July 16, 2008
Additional EFNB1 mutations in craniofrontonasal syndrome
Deeann Wallis, Felicitas Lacbawan, Mahim Jain, et al.
American Journal of Medical Genetics. Part A
|
October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation
Nathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
American Journal of Human Genetics
|
August 23, 2016
De Novo Truncating Variants in SON Cause Intellectual Disability, Congenital Malformations, and Failure to Thrive
Mari J Tokita, Alicia A Braxton, Yunru Shao, et al.
American Journal of Human Genetics
|
March 1, 1997
A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
M Muenke, K W Gripp, D M McDonald-McGinn, et al.
Molecular Cancer Therapeutics
|
May 5, 2017
Discovery and Characterization of Novel Nonsubstrate and Substrate NAMPT Inhibitors
Julie L Wilsbacher, Min Cheng, Dong Cheng, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 15, 2017
SAR and characterization of non-substrate isoindoline urea inhibitors of nicotinamide phosphoribosyltransferase (NAMPT)
Michael L Curtin, H Robin Heyman, Richard F Clark, et al.
Molecular Psychiatry
|
June 15, 2026
Evidence supporting the role of GIGYF2 in synapse development and autism
Bin Yu, Shimeng Zhu, Linhu Xiao, et al.
American Journal of Human Genetics
|
August 4, 2023
HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder
Eva Niggl, Arjan Bouman, Lauren C Briere, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 20, 2020
JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome
Eline A Verberne, Shuxiang Goh, Jade England, et al.
Page
of 30