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Elif Uz

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

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Clinical Immunology (Orlando, Fla.)|June 29, 2015
STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutationSevil Oskay Halacli, Deniz Cagdas Ayvaz, Cagman Sun-Tan, et al.
European Journal of Human Genetics : EJHG|April 6, 2006
Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunityTayfun Ozcelik, Elif Uz, Cemaliye B Akyerli, et al.
Nature Genetics|May 15, 2012
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Carine Bonnard, Anna C Strobl, Mohammad Shboul, et al.
Autonomic Neuroscience : Basic & Clinical|April 26, 2020
Intracerebroventricularly injected nesfatin-1 activates central cyclooxygenase and lipoxygenase pathwaysGokcen Guvenc-Bayram, Burcin Altinbas, Awais Iqbal, et al.
American Journal of Medical Genetics. Part A|November 7, 2013
TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasiaYasemin Alanay, Bekir Ergüner, Eda Utine, et al.
American Journal of Human Genetics|May 11, 2010
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasiaElif Uz, Yasemin Alanay, Dilek Aktas, et al.
Human Molecular Genetics|August 21, 2009
ALX4 dysfunction disrupts craniofacial and epidermal developmentHulya Kayserili, Elif Uz, Carien Niessen, et al.
American Journal of Human Genetics|August 2, 2016
Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 SignalingArda Cetinkaya, Jingwei Rachel Xiong, İbrahim Vargel, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosisKatharina Keupp, Yun Li, Ibrahim Vargel, et al.
Nature Genetics|May 10, 2011
KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromesAudrey Putoux, Sophie Thomas, Karlien L M Coene, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Clinical Immunology (Orlando, Fla.)|June 29, 2015
STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutationSevil Oskay Halacli, Deniz Cagdas Ayvaz, Cagman Sun-Tan, et al.
European Journal of Human Genetics : EJHG|April 6, 2006
Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunityTayfun Ozcelik, Elif Uz, Cemaliye B Akyerli, et al.
Nature Genetics|May 15, 2012
Mutations in IRX5 impair craniofacial development and germ cell migration via SDF1Carine Bonnard, Anna C Strobl, Mohammad Shboul, et al.
Autonomic Neuroscience : Basic & Clinical|April 26, 2020
Intracerebroventricularly injected nesfatin-1 activates central cyclooxygenase and lipoxygenase pathwaysGokcen Guvenc-Bayram, Burcin Altinbas, Awais Iqbal, et al.
American Journal of Medical Genetics. Part A|November 7, 2013
TMCO1 deficiency causes autosomal recessive cerebrofaciothoracic dysplasiaYasemin Alanay, Bekir Ergüner, Eda Utine, et al.
American Journal of Human Genetics|May 11, 2010
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasiaElif Uz, Yasemin Alanay, Dilek Aktas, et al.
Human Molecular Genetics|August 21, 2009
ALX4 dysfunction disrupts craniofacial and epidermal developmentHulya Kayserili, Elif Uz, Carien Niessen, et al.
American Journal of Human Genetics|August 2, 2016
Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 SignalingArda Cetinkaya, Jingwei Rachel Xiong, İbrahim Vargel, et al.
Molecular Genetics & Genomic Medicine|February 6, 2014
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosisKatharina Keupp, Yun Li, Ibrahim Vargel, et al.
Nature Genetics|May 10, 2011
KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromesAudrey Putoux, Sophie Thomas, Karlien L M Coene, et al.
Pageof 2