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Disease Models & Mechanisms
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March 9, 2013
Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome
Fahad Mahmood, Monika Mozere, Anselm A Zdebik, et al.
American Journal of Human Genetics
|
December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees
N Katsanis, R A Lewis, D W Stockton, et al.
American Journal of Medical Genetics. Part A
|
August 17, 2013
Intellectual disability, unusual facial morphology and hand anomalies in sibs
Sérgio B Sousa, Margarida Venâncio, Estelle Chanudet, et al.
Kidney360
|
November 26, 2024
Cell Catcher: A New Method to Extract and Preserve Live Renal Cells from Urine
Katia Nazmutdinova, Cheuk Yan Man, Martyn Carter, et al.
Mechanisms of Development
|
January 31, 2016
Non-essential role for cilia in coordinating precise alignment of lens fibres
Yuki Sugiyama, Elizabeth J Shelley, Bradley K Yoder, et al.
Human Molecular Genetics
|
January 10, 2012
The Lowe syndrome protein OCRL1 is involved in primary cilia assembly
Brian G Coon, Victor Hernandez, Kayalvizhi Madhivanan, et al.
Journal of Cell Science
|
June 22, 2012
Heat shock induces rapid resorption of primary cilia
Natalia V Prodromou, Clare L Thompson, Daniel P S Osborn, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 19, 2023
Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG Tags
Tina Beyer, Tiago Martins, Jeshmi Jeyabalan Srikaran, et al.
American Journal of Human Genetics
|
May 23, 2002
BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance
Nicholas Katsanis, Erica R Eichers, Stephen J Ansley, et al.
European Journal of Haematology
|
October 16, 2016
Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia
Motasem Melhem, Mohamed Abu-Farha, Dinu Antony, et al.
Page
of 20
Search research articles
Search
Showing results (101-110 of 194) with videos related to
Sort By:
Page
of 20
Disease Models & Mechanisms
|
March 9, 2013
Generation and validation of a zebrafish model of EAST (epilepsy, ataxia, sensorineural deafness and tubulopathy) syndrome
Fahad Mahmood, Monika Mozere, Anselm A Zdebik, et al.
American Journal of Human Genetics
|
December 1, 1999
Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees
N Katsanis, R A Lewis, D W Stockton, et al.
American Journal of Medical Genetics. Part A
|
August 17, 2013
Intellectual disability, unusual facial morphology and hand anomalies in sibs
Sérgio B Sousa, Margarida Venâncio, Estelle Chanudet, et al.
Kidney360
|
November 26, 2024
Cell Catcher: A New Method to Extract and Preserve Live Renal Cells from Urine
Katia Nazmutdinova, Cheuk Yan Man, Martyn Carter, et al.
Mechanisms of Development
|
January 31, 2016
Non-essential role for cilia in coordinating precise alignment of lens fibres
Yuki Sugiyama, Elizabeth J Shelley, Bradley K Yoder, et al.
Human Molecular Genetics
|
January 10, 2012
The Lowe syndrome protein OCRL1 is involved in primary cilia assembly
Brian G Coon, Victor Hernandez, Kayalvizhi Madhivanan, et al.
Journal of Cell Science
|
June 22, 2012
Heat shock induces rapid resorption of primary cilia
Natalia V Prodromou, Clare L Thompson, Daniel P S Osborn, et al.
Methods in Molecular Biology (Clifton, N.J.)
|
October 19, 2023
Affinity Purification of Intraflagellar Transport (IFT) Proteins in Mice Using Endogenous Streptavidin/FLAG Tags
Tina Beyer, Tiago Martins, Jeshmi Jeyabalan Srikaran, et al.
American Journal of Human Genetics
|
May 23, 2002
BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance
Nicholas Katsanis, Erica R Eichers, Stephen J Ansley, et al.
European Journal of Haematology
|
October 16, 2016
Novel G6B gene variant causes familial autosomal recessive thrombocytopenia and anemia
Motasem Melhem, Mohamed Abu-Farha, Dinu Antony, et al.
Page
of 20