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Huiqing Zhou

Showing results (111-120 of 123) with videos related to

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Plos Genetics|June 13, 2017
p63 exerts spatio-temporal control of palatal epithelial cell fate to prevent cleft palateRose Richardson, Karen Mitchell, Nigel L Hammond, et al.
Nature Communications|November 1, 2019
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signalingMonica Frega, Katrin Linda, Jason M Keller, et al.
The Journal of Allergy and Clinical Immunology|May 23, 2025
Dissecting key contributions of T<sub>H</sub>2 and T<sub>H</sub>17 cytokines to atopic dermatitis pathophysiologyLuca D Meesters, Janou A Y Roubroeks, Aranka Gerritsen, et al.
Plos Genetics|October 26, 2017
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorderTom S Koemans, Tjitske Kleefstra, Melissa C Chubak, et al.
American Journal of Human Genetics|June 26, 2012
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disabilityTjitske Kleefstra, Jamie M Kramer, Kornelia Neveling, et al.
Plos Genetics|September 3, 2010
Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locusEvelyn N Kouwenhoven, Simon J van Heeringen, Juan J Tena, et al.
Developmental Biology|December 24, 2013
Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome miceMonique C M Balemans, Muhammad Ansar, Astrid R Oudakker, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
American Journal of Human Genetics|May 2, 2017
Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian FamiliesThandiswa Ngcungcu, Martin Oti, Jan C Sitek, et al.
Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
Pageof 13

Showing results (111-120 of 123) with videos related to

Sort By:
Pageof 13
Plos Genetics|June 13, 2017
p63 exerts spatio-temporal control of palatal epithelial cell fate to prevent cleft palateRose Richardson, Karen Mitchell, Nigel L Hammond, et al.
Nature Communications|November 1, 2019
Neuronal network dysfunction in a model for Kleefstra syndrome mediated by enhanced NMDAR signalingMonica Frega, Katrin Linda, Jason M Keller, et al.
The Journal of Allergy and Clinical Immunology|May 23, 2025
Dissecting key contributions of T<sub>H</sub>2 and T<sub>H</sub>17 cytokines to atopic dermatitis pathophysiologyLuca D Meesters, Janou A Y Roubroeks, Aranka Gerritsen, et al.
Plos Genetics|October 26, 2017
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorderTom S Koemans, Tjitske Kleefstra, Melissa C Chubak, et al.
American Journal of Human Genetics|June 26, 2012
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disabilityTjitske Kleefstra, Jamie M Kramer, Kornelia Neveling, et al.
Plos Genetics|September 3, 2010
Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locusEvelyn N Kouwenhoven, Simon J van Heeringen, Juan J Tena, et al.
Developmental Biology|December 24, 2013
Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome miceMonique C M Balemans, Muhammad Ansar, Astrid R Oudakker, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
American Journal of Human Genetics|May 2, 2017
Duplicated Enhancer Region Increases Expression of CTSB and Segregates with Keratolytic Winter Erythema in South African and Norwegian FamiliesThandiswa Ngcungcu, Martin Oti, Jan C Sitek, et al.
Human Mutation|June 20, 2019
Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humansTimothy C Cox, Andrew C Lidral, Jason C McCoy, et al.
Pageof 13