Motazacker, M. M.: search on Z-Library

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1

Proteome of human plasma very low-density lipoprotein and low-density lipoprotein exhibits a link with coagulation and lipid metabolism

Dashty, Monireh, Motazacker, Mohammad, Levels, Johannes, Vries, Marcel de, Mahmoudi, Morteza, Peppelenbosch, Maikel, Rezaee, Farhad

Journal:

Thrombosis and Haemostasis

Year:

2014

Language:

english

File:

PDF, 22.86 MB

english, 2014

2

ST3GAL3 Mutations Impair the Development of Higher Cognitive Functions

Hao Hu, Katinka Eggers, Wei Chen, Masoud Garshasbi, M. Mahdi Motazacker, Klaus Wrogemann, Kimia Kahrizi, Andreas Tzschach, Masoumeh Hosseini, Ideh Bahman, Tim Hucho, Martina Mühlenhoff, Rita Gerardy-S

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 511 KB

english, 2011

3

Significance of surface charge and shell material of superparamagnetic iron oxide nanoparticle (SPION) based core/shell nanoparticles on the composition of the protein corona

Sakulkhu, Usawadee, Mahmoudi, Morteza, Maurizi, Lionel, Coullerez, Geraldine, Hofmann-Amtenbrink, Margarethe, Vries, Marcel, Motazacker, Mahdi, Rezaee, Farhad, Hofmann, Heinrich

Journal:

Biomaterials Science

Year:

2015

Language:

english

File:

PDF, 5.28 MB

english, 2015

4

Superparamagnetic iron oxide nanoparticles alter expression of obesity and T2D-associated risk genes in human adipocytes

Sharifi, S., Daghighi, S., Motazacker, M. M., Badlou, B., Sanjabi, B., Akbarkhanzadeh, A., Rowshani, A. T., Laurent, S., Peppelenbosch, M. P., Rezaee, F.

Journal:

Scientific Reports

Year:

2013

Language:

english

File:

PDF, 2.24 MB

english, 2013

5

ABCA1 mutation carriers with low high-density lipoprotein cholesterol are characterized by a larger atherosclerotic burden

Bochem, A. E., van Wijk, D. F., Holleboom, A. G., Duivenvoorden, R., Motazacker, M. M., Dallinga-Thie, G. M., de Groot, E., Kastelein, J. J. P., Nederveen, A. J., Hovingh, G. K., Stroes, E. S. G.

Journal:

European Heart Journal

Year:

2013

Language:

english

File:

PDF, 214 KB

english, 2013

6

Genetic defects in protein glycosylation as a cause of dyslipidemia

van den Boogert, M.A.W., Kuil, S.D., Hovingh, G.K., Motazacker, M.M., Levels, J.H.M., Dallinga-Thie, G., Kuivenhoven, J.A., Wevers, R., Stroes, E.S.G., Lefeber, D.J., Holleboom, A.G.

Journal:

Atherosclerosis

Year:

2014

Language:

english

File:

PDF, 51 KB

english, 2014

7

Evidence of a Polygenic Origin of Extreme High-Density Lipoprotein Cholesterol Levels

Motazacker, M. M., Peter, J., Treskes, M., Shoulders, C. C., Kuivenhoven, J. A., Hovingh, G. K.

Journal:

Arteriosclerosis Thrombosis and Vascular Biology

Year:

2013

Language:

english

File:

PDF, 796 KB

english, 2013

8

Lipoprotein distribution and serum concentrations of 7α-hydroxy-4-cholesten-3-one and bile acids: effects of monogenic disturbances in high-density lipoprotein metabolism

Steiner, Carine, Holleboom, Adriaan G., Karuna, Ratna, Motazacker, Mohammad M., Kuivenhoven, Jan Albert, Frikke‑Schmidt, Ruth, Tybjaerg‑Hansen, Anne, Rohrer, Lucia, Rentsch, Katharina M., von Eckardst

Journal:

Clinical Science

Year:

2012

Language:

english

File:

PDF, 384 KB

english, 2012

9

The Cypriot and Iranian National Mutation Frequency Databases

Marina Kleanthous, Philippos C. Patsalis, Anthi Drousiotou, Mehdi Motazacker, Kyproula Christodoulou, Marios Cariolou, Erol Baysal, Kimia Khrizi, Babak Moghimi, Farzin Pourfarzad, Sjozef van Baal, Con

Journal:

Year:

2006

Language:

english

File:

PDF, 203 KB

english, 2006

10

Heterozygosity for a Loss-of-Function Mutation in GALNT2 Improves Plasma Triglyceride Clearance in Man

Adriaan G. Holleboom, Helen Karlsson, Ruei-Shiuan Lin, Thomas M. Beres, Jeroen A. Sierts, Daniel S. Herman, Erik S.G. Stroes, Johannes M. Aerts, John J.P. Kastelein, Mohammad M. Motazacker, Geesje M.

Journal:

Cell Metabolism

Year:

2011

Language:

english

File:

PDF, 485 KB

english, 2011

11

Advances in genetics show the need for extending screening strategies for autosomal dominant hypercholesterolaemia

Motazacker, M. M., Pirruccello, J., Huijgen, R., Do, R., Gabriel, S., Peter, J., Kuivenhoven, J. A., Defesche, J. C., Kastelein, J. J. P., Hovingh, G. K., Zelcer, N., Kathiresan, S., Fouchier, S. W.

Journal:

European Heart Journal

Year:

2012

Language:

english

File:

PDF, 259 KB

english, 2012

12

Genome-Wide Association Studies in Atherosclerosis

S. Sivapalaratnam, M. M. Motazacker, S. Maiwald, G. K. Hovingh, J. J. P. Kastelein, M. Levi, M. D. Trip, G. M. Dallinga-Thie

Journal:

Current Atherosclerosis Reports

Year:

2011

Language:

english

File:

PDF, 276 KB

english, 2011

13

Exome Sequencing in Suspected Monogenic Dyslipidemias

Stitziel, N. O., Peloso, G. M., Abifadel, M., Cefalu, A. B., Fouchier, S., Motazacker, M. M., Tada, H., Larach, D. B., Awan, Z., Haller, J. F., Pullinger, C. R., Varret, M., Rabes, J.-P., Noto, D., Ta

Journal:

Circulation Cardiovascular Genetics

Year:

2015

Language:

english

File:

PDF, 2.70 MB

english, 2015

14

High prevalence of mutations in LCAT in patients with low HDL cholesterol levels in the Netherlands: Identification and characterization of eight novel mutations

Adriaan G. Holleboom, Jan A. Kuivenhoven, Frank Peelman, Alinda W. Schimmel, Jorge Peter, Joep C. Defesche, John J.P. Kastelein, G. Kees Hovingh, Erik S. Stroes, Mohammad Mahdi Motazacker

Journal:

Year:

2011

Language:

english

File:

PDF, 337 KB

english, 2011

15

Characterization of antioxidant/anti-inflammatory properties and apoA-I-containing subpopulations of HDL from family subjects with monogenic low HDL disorders

Georgios Daniil, Alexia A.P. Phedonos, Adriaan G. Holleboom, Mohammad Mahdi Motazacker, Letta Argyri, Jan Albert Kuivenhoven, Angeliki Chroni

Journal:

Clinica Chimica Acta

Year:

2011

Language:

english

File:

PDF, 629 KB

english, 2011

16

Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability

Lia Abbasi-Moheb, Sara Mertel, Melanie Gonsior, Leyla Nouri-Vahid, Kimia Kahrizi, Sebahattin Cirak, Dagmar Wieczorek, M. Mahdi Motazacker, Sahar Esmaeeli-Nieh, Kirsten Cremer, Robert Weißmann, Andreas

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 567 KB

english, 2012

17

Genetics of HDL-C: A Causal Link to Atherosclerosis?

Capelleveen, Julian C., Bochem, Andrea E., Motazacker, M. Mahdi, Hovingh, G. Kees, Kastelein, John J. P.

Journal:

Current Atherosclerosis Reports

Year:

2013

Language:

english

File:

PDF, 218 KB

english, 2013

18

Erratum to: The Aggregation Potential of the 1–15- and 1–16-Fragments of the Amyloid β Peptide and Their Influence on the Aggregation of Aβ40

Hashemi Shabestari, M., Plug, T., Motazacker, M. M., Meeuwenoord, N. J., Filippov, D. V., Meijers, J. C. M., Huber, M.

Journal:

Applied Magnetic Resonance

Year:

2013

Language:

english

File:

PDF, 109 KB

english, 2013

19

Ex situ evaluation of the composition of protein corona of intravenously injected superparamagnetic nanoparticles in rats

Sakulkhu, Usawadee, Maurizi, Lionel, Mahmoudi, Morteza, Motazacker, Mahdi, Vries, Marcel, Gramoun, Azza, Ollivier Beuzelin, Marie-Gabrielle, Vallée, Jean-Paul, Rezaee, Farhad, Hofmann, Heinrich

Journal:

Year:

2014

Language:

english

File:

PDF, 940 KB

english, 2014

20

Proteome of human plasma very low-density lipoprotein and low-density lipoprotein exhibits a link with coagulation and lipid metabolism

Dashti, M., Levels, J., Motazacker, M., Vries, M. Marcel, Mahmoudi, M., Peppelenbosch, M., Rezaee, F.

Journal:

Atherosclerosis

Year:

2014

Language:

english

File:

PDF, 133 KB

english, 2014

21

Investigation of multiple dyslipidemias in a large Austrian pedigree by genetic risk scores and exome sequencing

Nikkola, E., Ko, A., Cantor, R.M., Muxel, R., Matikainen, N., Söderlund, S., Motazacker, M.M., Kuivenhoven, J.A., Boren, J., Kronenberg, F., Schneider, W., Palotie, A., Laakso, M., Taskinen, M.R., Paj

Journal:

Atherosclerosis

Year:

2016

Language:

english

File:

PDF, 57 KB

english, 2016

22

A loss-of-function variant in OSBPL1A predisposes to low plasma HDL cholesterol levels and impaired cholesterol efflux capacity

van Capelleveen, J., Pirhonen, J., Motazacker, M.M., Weber-Boyvat, M., Jauhiainen, M., Hovingh, G.K., Dallinga-Thie, G.M., Olkkonen, V.

Journal:

Atherosclerosis

Year:

2016

Language:

english

File:

PDF, 134 KB

english, 2016

23

Adrenal Function in Females with Low Plasma HDL-C Due to Mutations in ABCA1 and LCAT

Bochem, Andrea E., Holleboom, Adriaan G., Romijn, Johannes A., Hoekstra, Menno, Dallinga, Geesje M., Motazacker, Mahdi M., Hovingh, G. Kees, Kuivenhoven, Jan A., Stroes, Erik S. G., Kocher, Olivier

Journal:

Year:

2014

Language:

english

File:

PDF, 310 KB

english, 2014

24

CO-SEGREGATION OF EL AND HL VARIANTS WITH HIGH PLASMA HDL-C LEVELS IN FAMILIES WITH HYPERALPHALIPOPROTAEINEMIA

M.M. Motazacker, A.G. Holleboom, R. Franssen, J. Azevedo, G.K. Hovingh, J.J.P. Kastelein, J.A. Kuivenhoven

Journal:

Atherosclerosis

Year:

2009

Language:

english

File:

PDF, 55 KB

english, 2009

25

Expanding the spectrum of CEP55 âassociated disease to viable phenotypes

Barrie, Elizabeth S., Overwater, Eline, Haelst, Mieke M., Motazacker, M. Mahdi, Truxal, Kristen V., Crist, Erin, Mostafavi, Roya, Pivnick, Eniko K., Choudhri, Asim F., Narumanchi, TaraChandra, Castell

Journal:

American Journal of Medical Genetics Part A

Year:

2020

Language:

english

File:

PDF, 1.36 MB

english, 2020

26

Identification of Mutations in TRAPPC9, which Encodes the NIK- and IKK-β-Binding Protein, in Nonsyndromic Autosomal-Recessive Mental Retardation

Asif Mir, Liana Kaufman, Abdul Noor, Mahdi M. Motazacker, Talal Jamil, Matloob Azam, Kimia Kahrizi, Muhammad Arshad Rafiq, Rosanna Weksberg, Tanveer Nasr, Farooq Naeem, Andreas Tzschach, Andreas W. Ku

Journal:

The American Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 650 KB

english, 2009

27

Genetic Variant of the Scavenger Receptor BI in Humans

Vergeer, Menno, Korporaal, Suzanne J.A., Franssen, Remco, Meurs, Illiana, Out, Ruud, Hovingh, G. Kees, Hoekstra, Menno, Sierts, Jeroen A., Dallinga-Thie, Geesje M., Motazacker, Mohammad Mahdi, Hollebo

Journal:

Boston Medical and Surgical Journal

Year:

2011

Language:

english

File:

PDF, 1.10 MB

english, 2011

28

Zeolite Nanoparticles for Selective Sorption of Plasma Proteins

Rahimi, M., Ng, E.-P., Bakhtiari, K., Vinciguerra, M., Ahmad, H. Ali, Awala, H., Mintova, S., Daghighi, M., Bakhshandeh Rostami, F., de Vries, M., Motazacker, M. M., Peppelenbosch, M. P., Mahmoudi, M.

Journal:

Scientific Reports

Year:

2015

Language:

english

File:

PDF, 1.16 MB

english, 2015

29

Abstract: S3-21 FINDING NOVEL HDL GENES

Motazacker, M, Peter, J, Azevedo, J, Stroes, E, Hovingh, K, Kastelein, J, Kuivenhoven, J

Journal:

Atherosclerosis Supplements

Year:

2009

Language:

english

File:

PDF, 71 KB

english, 2009

30

A rare variant in MCF2L identified using exclusion linkage in a pedigree with premature atherosclerosis

Maiwald, Stephanie, Motazacker, Mahdi M, van Capelleveen, Julian C, Sivapalaratnam, Suthesh, van der Wal, Allard C, van der Loos, Chris, Kastelein, John J P, Ouwehand, Willem H, Hovingh, G Kees, Trip,

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.55 MB

english, 2015

31

Regulation of HDL-c levels via ABCA1: A role for Lrp1

Oldoni, F., van Capelleveen, J., Motazacker, M.M., Heeren, J., Sinke, R., Dallinga-Thie, G., Hui, D., Hovingh, K., Kuivenhoven, J.A.

Journal:

Atherosclerosis

Year:

2016

Language:

english

File:

PDF, 46 KB

english, 2016

32

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

Hossein Najmabadi, Mohammad Mahdi Motazacker, Masoud Garshasbi, Kimia Kahrizi, Andreas Tzschach, Wei Chen, Farkhondeh Behjati, Valeh Hadavi, Sahar Esmaeeli Nieh, Seyedeh Sedigheh Abedini, Reza Vazifeh

Journal:

Year:

2007

Language:

english

File:

PDF, 307 KB

english, 2007

33

Alopecia–mental retardation syndrome: clinical and molecular characterization of four patients

A. Tzschach, B. Bozorgmehr, V. Hadavi, K. Kahrizi, M. Garshasbi, M.M. Motazacker, H.-H. Ropers, A.W. Kuss, H. Najmabadi

Journal:

British Journal of Dermatology

Year:

2008

Language:

english

File:

PDF, 355 KB

english, 2008

34

A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation

Mohammad Mahdi Motazacker, Benjamin Rainer Rost, Tim Hucho, Masoud Garshasbi, Kimia Kahrizi, Reinhard Ullmann, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saeid Hosseini Amini, Chandan Goswami, And

Journal:

The American Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 6.13 MB

english, 2007

35

The Aggregation Potential of the 1–15- and 1–16-Fragments of the Amyloid β Peptide and Their Influence on the Aggregation of Aβ40

M. Shabestari, T. Plug, M. M. Motazacker, N. J. Meeuwenoord…

Journal:

Applied Magnetic Resonance

Year:

2013

Language:

english

File:

PDF, 339 KB

english, 2013

36

A loss-of-function variant in OSBPL1A predisposes to low plasma HDL cholesterol levels and impaired cholesterol efflux capacity

Motazacker, Mahdi M., Pirhonen, Juho, van Capelleveen, Julian C., Weber-Boyvat, Marion, Kuivenhoven, Jan Albert, Shah, Saundarya, Hovingh, G. Kees, Metso, Jari, Li, Shiqian, Ikonen, Elina, Jauhiainen,

Journal:

Atherosclerosis

Year:

2016

Language:

english

File:

PDF, 1.44 MB

english, 2016

37

603 COMBINING EXOME SEQUENCING WITH EXCLUSION LINKAGE ANALYSIS AS A TOOL TO UNRAVEL THE MOLECULAR BASIS OF A COMMON GENETIC DISEASE

Motazacker, M.M., Huijgen, R., Peter, J., Defesche, J.C., Kastelein, J.J.R, Hovingh, G.K., Kathiresan, S., Zelcer, N., Fouchier, S.W.

Journal:

Atherosclerosis Supplements

Year:

2011

Language:

english

File:

PDF, 45 KB

english, 2011

38

High density lipoprotein as a source of cholesterol for adrenal steroidogenesis: a study in individuals with low plasma HDL-C

Bochem, A. E., Holleboom, A. G., Romijn, J. A., Hoekstra, M., Dallinga-Thie, G. M., Motazacker, M. M., Hovingh, G. K., Kuivenhoven, J. A., Stroes, E. S. G.

Journal:

The Journal of Lipid Research

Year:

2013

Language:

english

File:

PDF, 635 KB

english, 2013

39

Family-specific aggregation of lipid GWAS variants confers the susceptibility to familial hypercholesterolemia in a large Austrian family

Nikkola, Elina, Ko, Arthur, Alvarez, Marcus, Cantor, Rita M., Garske, Kristina, Kim, Elliot, Gee, Stephanie, Rodriguez, Alejandra, Muxel, Reinhard, Matikainen, Niina, Söderlund, Sanni, Motazacker, Mah

Journal:

Atherosclerosis

Year:

2017

Language:

english

File:

PDF, 5.23 MB

english, 2017

40

Two novel mutations in apolipoprotein C3 underlie atheroprotective lipid profiles in families

Bochem, A.E., van Capelleveen, J.C., Dallinga-Thie, G.M., Schimmel, A.W.M., Motazacker, M.M., Tietjen, I., Singaraja, R.R., Hayden, M.R., Kastelein, J.J.P., Stroes, E.S.G., Hovingh, G.K.

Journal:

Clinical Genetics

Year:

2014

Language:

english

File:

PDF, 739 KB

english, 2014

41

Identification of a loss-of-function inducible degrader of the low-density lipoprotein receptor variant in individuals with low circulating low-density lipoprotein

V. Sorrentino, S. W. Fouchier, M. M. Motazacker, J. K. Nelson, J. C. Defesche, G. M. Dallinga-thie, J. J. P. Kastelein, G. Kees Hovingh, N. Zelcer

Year:

2013

Language:

english

File:

PDF, 254 KB

english, 2013

42

RELN rare variants in myoclonus-dystonia

Groen, Justus L., Ritz, Katja, Jalalzadeh, Hamid, van der Salm, Sandra M.A., Jongejan, Aldo, Mook, Olaf R., Haagmans, Martin A., Zwinderman, Aeilko H., Motazacker, Mahdi M., Hennekam, Raoul C., Baas,

Journal:

Movement Disorders

Year:

2015

Language:

english

File:

PDF, 323 KB

english, 2015

43

Are high-density lipoprotein genes and their products targets for therapy?

Motazacker, Mohammad Mahdi, Kastelein, John J, Kuivenhoven, Jan Albert

Journal:

Current Opinion in Lipidology

Year:

2010

Language:

english

File:

PDF, 243 KB

english, 2010

44

The role of ABCA1 in glycosphingolipid trafficking and efflux

Karen Ghauharali, Wouter Kallemeijn, Menno Vergeer, M. Motazacker, Marco van Eijk, Hans Aerts, Ans Groener

Journal:

Chemistry and Physics of Lipids

Year:

2009

Language:

english

File:

PDF, 56 KB

english, 2009

45

SNP array-based homozygosity mapping revealsMCPH1deletion in family with autosomal recessive mental retardation and mild microcephaly

Masoud Garshasbi, Mohammad Mahdi Motazacker, Kimia Kahrizi, Farkhondeh Behjati, Seyedeh Sedigheh Abedini, Sahar Esmaeeli Nieh, Saghar Ghasemi Firouzabadi, Christian Becker, Franz Rüschendorf, Peter Nü

Journal:

Year:

2006

Language:

english

File:

PDF, 380 KB

english, 2006

46

Corona protein composition and cytotoxicity evaluation of ultra-small zeolites synthesized from template free precursor suspensions

Laurent, S., Ng, E.-P., Thirifays, C., Lakiss, L., Goupil, G.-M., Mintova, S., Burtea, C., Oveisi, E., Hébert, C., de Vries, M., Motazacker, M. M., Rezaee, F., Mahmoudi, M.

Journal:

Toxicology Research

Year:

2013

Language:

english

File:

PDF, 3.80 MB

english, 2013

47

Plasma levels of sphingosine-1-phosphate and apolipoprotein M in patients with monogenic disorders of HDL metabolism

Ratna Karuna, Rebekka Park, Alaa Othman, Adriaan G. Holleboom, Mohammad Mahdi Motazacker, Iryna Sutter, Jan Albert Kuivenhoven, Lucia Rohrer, Hugues Matile, Thorsten Hornemann, Markus Stoffel, Kathari

Journal:

Atherosclerosis

Year:

2011

Language:

english

File:

PDF, 555 KB

english, 2011

48

Plasma levels of 27-hydroxycholesterol in humans and mice with monogenic disturbances of high density lipoprotein metabolism

Ratna Karuna, Adriaan G. Holleboom, Mohammad M. Motazacker, Jan Albert Kuivenhoven, Ruth Frikke-Schmidt, Anne Tybjaerg-Hansen, Spiros Georgopoulos, Miranda van Eck, Theo J.C. van Berkel, Arnold von Ec

Journal:

Atherosclerosis

Year:

2011

Language:

english

File:

PDF, 226 KB

english, 2011

49

P218 TWO NOVEL GENETIC LOCI FOR HIGH AND LOW PLASMA HDL-C LEVELS IN 2 LARGE FAMILIES FROM DUTCH ANCESTRY

Mahdi Motazacker, Mo., Tietjen, I., Hayden, M., Kastelein, J.P.P., Stroes, E.S.G., Hovingh, G.K., Kuivenhoven, J.A.

Journal:

Atherosclerosis Supplements

Year:

2010

Language:

english

File:

PDF, 60 KB

english, 2010

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