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Hatice Asuman Ozkara

Showing results (1-10 of 9) with videos related to

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Brain & Development|November 10, 2004
Recent advances in the biochemistry and genetics of sphingolipidosesHatice Asuman Ozkara
Brain & Development|April 12, 2003
A new point mutation (G412 to A) at the last nucleotide of exon 3 of hexosaminidase alpha-subunit gene affects splicingHatice Asuman Ozkara, Konrad Sandhoff
Brain & Development|April 12, 2003
Characterization of two Turkish beta-hexosaminidase mutations causing Tay-Sachs diseaseHatice Asuman Ozkara, Konrad Sandhoff
Brain & Development|July 28, 2004
Sphingolipidoses in TurkeyHatice Asuman Ozkara, Meral Topçu
Clinical Biochemistry|May 17, 2011
Two novel alpha-galactosidase A mutations causing Fabry disease: A missense mutation M11V in a heterozygote woman and a nonsense mutation R190X in a hemizygote manBasak Celtikci, Meral Topçu, Hatice Asuman Ozkara
Clinical Biochemistry|January 12, 2012
Four novel mutations in the β-galactosidase gene identified in infantile type of GM1 gangliosidosisBaşak Celtikçi, Halil İbrahim Aydın, Serap Sivri, et al.
Advances in Protein Chemistry and Structural Biology|January 13, 2019
Inflammatory response and its relation to sphingolipid metabolism proteins: Chaperones as potential indirect anti-inflammatory agentsZ Begum Yagci, Elif Esvap, Hatice Asuman Ozkara, et al.
Paediatric and Perinatal Epidemiology|October 20, 2010
Why are they having infant colic? A nested case-control studyS Songül Yalçin, Emel Orün, Banu Mutlu, et al.
Journal of Neuroimmunology|June 25, 2022
Myelin oligodendrocyte glycoprotein antibodies in genetic leukodystrophiesNesibe Gevher Eroglu-Ertugrul, Mohammadreza Yousefi, Faruk Pekgül, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Brain & Development|November 10, 2004
Recent advances in the biochemistry and genetics of sphingolipidosesHatice Asuman Ozkara
Brain & Development|April 12, 2003
A new point mutation (G412 to A) at the last nucleotide of exon 3 of hexosaminidase alpha-subunit gene affects splicingHatice Asuman Ozkara, Konrad Sandhoff
Brain & Development|April 12, 2003
Characterization of two Turkish beta-hexosaminidase mutations causing Tay-Sachs diseaseHatice Asuman Ozkara, Konrad Sandhoff
Brain & Development|July 28, 2004
Sphingolipidoses in TurkeyHatice Asuman Ozkara, Meral Topçu
Clinical Biochemistry|May 17, 2011
Two novel alpha-galactosidase A mutations causing Fabry disease: A missense mutation M11V in a heterozygote woman and a nonsense mutation R190X in a hemizygote manBasak Celtikci, Meral Topçu, Hatice Asuman Ozkara
Clinical Biochemistry|January 12, 2012
Four novel mutations in the β-galactosidase gene identified in infantile type of GM1 gangliosidosisBaşak Celtikçi, Halil İbrahim Aydın, Serap Sivri, et al.
Advances in Protein Chemistry and Structural Biology|January 13, 2019
Inflammatory response and its relation to sphingolipid metabolism proteins: Chaperones as potential indirect anti-inflammatory agentsZ Begum Yagci, Elif Esvap, Hatice Asuman Ozkara, et al.
Paediatric and Perinatal Epidemiology|October 20, 2010
Why are they having infant colic? A nested case-control studyS Songül Yalçin, Emel Orün, Banu Mutlu, et al.
Journal of Neuroimmunology|June 25, 2022
Myelin oligodendrocyte glycoprotein antibodies in genetic leukodystrophiesNesibe Gevher Eroglu-Ertugrul, Mohammadreza Yousefi, Faruk Pekgül, et al.
Pageof 1