Works matching AU Orr-Urtreger, Avi

Results: 87

Estimation of genetic risk function with covariates in the presence of missing genotypes.

Published in:

2017

By:

Lee, Annie J.;
Marder, Karen;
Alcalay, Roy N.;
Mejia‐Santana, Helen;
Orr‐Urtreger, Avi;
Giladi, Nir;
Bressman, Susan;
Wang, Yuanjia;
Mejia-Santana, Helen;
Orr-Urtreger, Avi

Publication type:

journal article

A Possible Modifying Effect of the G2019S Mutation in the LRRK2 Gene on GBA Parkinson's Disease.

Published in:

2020

By:

Omer, Nurit;
Giladi, Nir;
Gurevich, Tanya;
Bar‐Shira, Anat;
Gana‐Weisz, Mali;
Goldstein, Orly;
Kestenbaum, Meir;
Cedarbaum, Jesse M.;
Orr‐Urtreger, Avi;
Mirelman, Anat;
Thaler, Avner;
Bar-Shira, Anat;
Gana-Weisz, Mali;
Orr-Urtreger, Avi

Publication type:

journal article

Tossing and Turning in Bed: Nocturnal Movements in Parkinson's Disease.

Published in:

2020

By:

Mirelman, Anat;
Hillel, Inbar;
Rochester, Lynn;
Del Din, Silvia;
Bloem, Bastiaan R.;
Avanzino, Laura;
Nieuwboer, Alice;
Maidan, Inbal;
Herman, Talia;
Thaler, Avner;
Gurevich, Tanya;
Kestenbaum, Meir;
Orr‐Urtreger, Avi;
Brys, Mirek;
Cedarbaum, Jesse M.;
Giladi, Nir;
Hausdorff, Jeffrey M.;
Orr-Urtreger, Avi

Publication type:

journal article

Survival rates among Parkinson's disease patients who carry mutations in the LRRK2 and GBA genes.

Published in:

2018

By:

Thaler, Avner;
Kozlovski, Tal;
Gurevich, Tanya;
Bar‐Shira, Anat;
Gana‐Weisz, Mali;
Orr‐Urtreger, Avi;
Giladi, Nir;
Mirelman, Anat;
Bar-Shira, Anat;
Gana-Weisz, Mali;
Orr-Urtreger, Avi

Publication type:

journal article

The effect of polygenic risk score on PD risk and phenotype in LRRK2 G2019S and GBA1 carriers.

Published in:

Journal of Parkinson's Disease, 2025, v. 15, n. 2, p. 291, doi. 10.1177/1877718X241310722

By:

Goldstein, Orly;
Shani, Shachar;
Gana-Weisz, Mali;
Elkoshi, Nadav;
Casey, Fergal;
Sun, Yu H;
Chandratre, Khyati;
Cedarbaum, Jesse M;
Blauwendraat, Cornelis;
Bar-Shira, Anat;
Thaler, Avner;
Gurevich, Tanya;
Mirelman, Anat;
Giladi, Nir;
Orr-Urtreger, Avi;
Alcalay, Roy N

Publication type:

Article

P2RX7, an adaptive immune response gene, is associated with Parkinson's disease risk and age at onset.

Published in:

Journal of Parkinson's Disease, 2024, v. 14, n. 8, p. 1575, doi. 10.1177/1877718X241296015

By:

Shani, Shachar;
Gana-Weisz, Mali;
Bar-Shira, Anat;
Thaler, Avner;
Gurevich, Tanya;
Mirelman, Anat;
Giladi, Nir;
Alcalay, Roy N.;
Orr-Urtreger, Avi;
Goldstein, Orly

Publication type:

Article

Mutations in GBA and LRRK2 Are Not Associated with Increased Inflammatory Markers.

Published in:

Journal of Parkinson's Disease, 2021, v. 11, n. 3, p. 1285, doi. 10.3233/JPD-212624

By:

Thaler, Avner;
Omer, Nurit;
Giladi, Nir;
Gurevich, Tanya;
Bar-Shira, Anat;
Gana-Weisz, Mali;
Goldstein, Orly;
Kestenbaum, Meir;
Shirvan, Julia C.;
Cedarbaum, Jesse M.;
Orr-Urtreger, Avi;
Regev, Keren;
Shenhar-Tsarfaty, Shani;
Mirelman, Anat

Publication type:

Article

Homozygosity for the MTX1 c.184T>A (p.S63T) alteration modifies the age of onset in GBA-associated Parkinson's disease.

Published in:

Neurogenetics, 2011, v. 12, n. 4, p. 325, doi. 10.1007/s10048-011-0293-6

By:

Gan-Or, Ziv;
Bar-Shira, Anat;
Gurevich, Tanya;
Giladi, Nir;
Orr-Urtreger, Avi

Publication type:

Article

Ashkenazi Parkinson’s disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries.

Published in:

Neurogenetics, 2009, v. 10, n. 4, p. 355, doi. 10.1007/s10048-009-0186-0

By:

Bar-Shira, Anat;
Hutter, Carolyn M.;
Giladi, Nir;
Zabetian, Cyrus P.;
Orr-Urtreger, Avi

Publication type:

Article

MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome.

Published in:

Human Mutation, 2002, v. 20, n. 4, p. 323, doi. 10.1002/humu.9069

By:

Yaron, Yuval;
Ben Zeev, Bruria;
Shomrat, Ruth;
Bercovich, Dani;
Naiman, Tova;
Orr-Urtreger, Avi

Publication type:

Article

Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations.

Published in:

Human Mutation, 2002, v. 19, n. 6, p. 664, doi. 10.1002/humu.9037

By:

Gavert, Nancy;
Yaron, Yuval;
Naiman, Tova;
Bercovich, Dani;
Rozen, Paul;
Shomrat, Ruth;
Legum, Cyril;
Orr-Urtreger, Avi

Publication type:

Article

Novel mutations in the emerin gene in Israeli families.

Published in:

Human Mutation, 2001, v. 17, n. 6, p. 522, doi. 10.1002/humu.1139

By:

Nevo, Yoram;
Ahituv, Sarit;
Yaron, Yuval;
Kedmi, Merav;
Shomrat, Ruth;
Legum, Cyril;
Orr-Urtreger, Avi

Publication type:

Article

GBA mutations are associated with Rapid Eye Movement Sleep Behavior Disorder.

Published in:

Annals of Clinical & Translational Neurology, 2015, v. 2, n. 9, p. 941, doi. 10.1002/acn3.228

By:

Gan‐Or, Ziv;
Mirelman, Anat;
Postuma, Ronald B.;
Arnulf, Isabelle;
Bar‐Shira, Anat;
Dauvilliers, Yves;
Desautels, Alex;
Gagnon, Jean‐François;
Leblond, Claire S.;
Frauscher, Birgit;
Alcalay, Roy N.;
Saunders‐Pullman, Rachel;
Bressman, Susan B.;
Marder, Karen;
Monaca, Christelle;
Högl, Birgit;
Orr‐Urtreger, Avi;
Dion, Patrick A.;
Montplaisir, Jacques Y.;
Giladi, Nir

Publication type:

Article

Selective deletion of theα5 subunit differentially affects somatic–dendriticversusaxonally targeted nicotinic ACh receptors in mouse.

Published in:

Journal of Physiology, 2005, v. 563, n. 1, p. 119, doi. 10.1113/jphysiol.2004.075788

By:

Fischer, Harald;
Orr-Urtreger, Avi;
Role, Lorna W.;
Huck, Sigismund

Publication type:

Article

Autonomic function in mice lacking α5 neuronal nicotinic acetylcholine receptor subunit.

Published in:

Journal of Physiology, 2002, v. 542, n. 2, p. 347, doi. 10.1113/jphysiol.2001.013456

By:

Wang, Ningshan;
Orr-Urtreger, Avi;
Chapman, Joab;
Rabinowitz, Ruth;
Nachman, Rachel;
Korczyn, Amos D.

Publication type:

Article

Progression in the LRRK2-Asssociated Parkinson Disease Population.

Published in:

JAMA Neurology, 2018, v. 75, n. 3, p. 312, doi. 10.1001/jamaneurol.2017.4019

By:

Saunders-Pullman, Rachel;
Mirelman, Anat;
Alcalay, Roy N.;
Wang, Cuiling;
Ortega, Roberto A.;
Raymond, Deborah;
Mejia-Santana, Helen;
Orbe-Reilly, Martha;
Johannes, Brooke A.;
Thaler, Avner;
Ozelius, Laurie;
Orr-Urtreger, Avi;
Marder, Karen S.;
Giladi, Nir;
Bressman, Susan B.

Publication type:

Article

High Frequency of GBA Gene Mutations in Dementia With Lewy Bodies Among Ashkenazi Jews.

Published in:

JAMA Neurology, 2016, v. 73, n. 12, p. 1448, doi. 10.1001/jamaneurol.2016.1593

By:

Shiner, Tamara;
Mirelman, Anat;
Weisz, Mali Gana;
Bar-Shira, Anat;
Ash, Elissa;
Cialic, Ron;
Nevler, Naomi;
Gurevich, Tanya;
Bregman, Noa;
Orr-Urtreger, Avi;
Giladi, Nir

Publication type:

Article

Higher Frequency of Certain Cancers in LRRK2 G2019S Mutation Carriers With Parkinson Disease A Pooled Analysis.

Published in:

JAMA Neurology, 2015, v. 72, n. 1, p. 58, doi. 10.1001/jamaneurol.2014.1973

By:

Agalliu, Ilir;
San Luciano, Marta;
Mirelman, Anat;
Giladi, Nir;
Waro, Bjorg;
Aasly, Jan;
Inzelberg, Rivka;
Hassin-Baer, Sharon;
Friedman, Eitan;
Ruiz-Martinez, Javier;
Marti-Masso, Jose Felix;
Orr-Urtreger, Avi;
Bressman, Susan;
Saunders-Pullman, Rachel

Publication type:

Article

A novel mutation in TARDBP segregates with amyotrophic lateral sclerosis in a large family with early onset and fast progression.

Published in:

Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2020, v. 21, n. 3/4, p. 280, doi. 10.1080/21678421.2020.1747496

By:

Goldstein, Orly;
Kedmi, Merav;
Gana-Weisz, Mali;
Nefussy, Beatrice;
Vainer, Batel;
Fainmesser, Yaara;
Drory, Vivian E.;
Orr-Urtreger, Avi

Publication type:

Article

MAPT Locus in Parkinson's Disease Patients of Ashkenazi Origin: A Stratified Analysis.

Published in:

Genes, 2024, v. 15, n. 1, p. 46, doi. 10.3390/genes15010046

By:

Shani, Shachar;
Gana-Weisz, Mali;
Bar-Shira, Anat;
Thaler, Avner;
Gurevich, Tanya;
Mirelman, Anat;
Giladi, Nir;
Alcalay, Roy N.;
Goldstein, Orly;
Orr-Urtreger, Avi

Publication type:

Article

C9orf72 -G 4 C 2 Intermediate Repeats and Parkinson's Disease; A Data-Driven Hypothesis.

Published in:

Genes, 2021, v. 12, n. 8, p. 1210, doi. 10.3390/genes12081210

By:

Kobo, Hila;
Goldstein, Orly;
Gana-Weisz, Mali;
Bar-Shira, Anat;
Gurevich, Tanya;
Thaler, Avner;
Mirelman, Anat;
Giladi, Nir;
Orr-Urtreger, Avi

Publication type:

Article

The LRRK2 G2019S mutation as the cause of Parkinson’s disease in Ashkenazi Jews.

Published in:

Journal of Neural Transmission, 2009, v. 116, n. 11, p. 1473, doi. 10.1007/s00702-009-0303-0

By:

Thaler, Avner;
Ash, Elissa;
Gan-Or, Ziv;
Orr-Urtreger, Avi;
Giladi, Nir

Publication type:

Article

Variable PARK2 Mutations Cause Early-Onset Parkinson's Disease in a Small Restricted Population.

Published in:

Journal of Molecular Neuroscience, 2017, v. 63, n. 2, p. 216, doi. 10.1007/s12031-017-0972-3

By:

Ben-Shachar, Shay;
Afawi, Zaid;
Masalha, Rafik;
Badarny, Samih;
Neiman, Tova;
Pavzner, Dina;
Bar-Shira, Anat;
Orr-Urtreger, Avi

Publication type:

Article

SEPT14 Is Associated with a Reduced Risk for Parkinson's Disease and Expressed in Human Brain.

Published in:

Journal of Molecular Neuroscience, 2016, v. 59, n. 3, p. 343, doi. 10.1007/s12031-016-0738-3

By:

Rozenkrantz, Liron;
Gan-Or, Ziv;
Gana-Weisz, Mali;
Mirelman, Anat;
Giladi, Nir;
Bar-Shira, Anat;
Orr-Urtreger, Avi

Publication type:

Article

The Age at Motor Symptoms Onset in LRRK2-Associated Parkinson's Disease is Affected by a Variation in the MAPT Locus: A Possible Interaction.

Published in:

Journal of Molecular Neuroscience, 2012, v. 46, n. 3, p. 541, doi. 10.1007/s12031-011-9641-0

By:

Gan-Or, Ziv;
Bar-Shira, Anat;
Mirelman, Anat;
Gurevich, Tanya;
Giladi, Nir;
Orr-Urtreger, Avi

Publication type:

Article

FGFR1 over-expression in primary rhabdomyosarcoma tumors is associated with hypomethylation of a 5′ CpG Island and abnormal expression of the AKT1, NOG, and BMP4 genes.

Published in:

Genes, Chromosomes & Cancer, 2007, v. 46, n. 11, p. 1028, doi. 10.1002/gcc.20489

By:

Goldstein, Myriam;
Meller, Isaac;
Orr-Urtreger, Avi

Publication type:

Article

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.

Published in:

Movement Disorders, 2015, v. 30, n. 7, p. 981, doi. 10.1002/mds.26213

By:

Mirelman, Anat;
Alcalay, Roy N.;
Saunders‐Pullman, Rachel;
Yasinovsky, Kira;
Thaler, Avner;
Gurevich, Tanya;
Mejia‐Santana, Helen;
Raymond, Deborah;
Gana‐Weisz, Mali;
Bar‐Shira, Anat;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Urtreger, Avi;
Bressman, Susan;
Marder, Karen;
Giladi, Nir

Publication type:

Article

A voxel-based morphometry and diffusion tensor imaging analysis of asymptomatic Parkinson's disease-related G2019S LRRK2 mutation carriers.

Published in:

Movement Disorders, 2014, v. 29, n. 6, p. 823, doi. 10.1002/mds.25827

By:

Thaler, Avner;
Artzi, Moran;
Mirelman, Anat;
Jacob, Yael;
Helmich, Rick C.;
Nuenen, Bart F.L.;
Gurevich, Tanya;
Orr‐Urtreger, Avi;
Marder, Karen;
Bressman, Susan;
Bloem, Bastiaan R.;
Hendler, Talma;
Giladi, Nir;
Ben Bashat, Dafna

Publication type:

Article

Fall risk and gait in Parkinson's disease: The role of the LRRK2 G2019S mutation.

Published in:

Movement Disorders, 2013, v. 28, n. 12, p. 1683, doi. 10.1002/mds.25587

By:

Mirelman, Anat;
Heman, Talia;
Yasinovsky, Kira;
Thaler, Avner;
Gurevich, Tanya;
Marder, Karen;
Bressman, Susan;
Bar‐Shira, Anat;
Orr‐Urtreger, Avi;
Giladi, Nir;
Hausdorff, Jeffrey M.

Publication type:

Article

Multiplex Nested PCR for Preimplantation Genetic Diagnosis of Spinal Muscular Atrophy.

Published in:

Fetal Diagnosis & Therapy, 2004, v. 19, n. 2, p. 199, doi. 10.1159/000075151

By:

Malcov, Mira;
Schwartz, Tamar;
Mei-Raz, Nava;
Yosef, Dalit Ben;
Amit, Ami;
Lessing, Joseph B.;
Shomrat, Ruth;
Orr-Urtreger, Avi;
Yaron, Yuval

Publication type:

Article

A Comparison between Maternal Serum Free β-Human Chorionic Gonadotrophin and Pregnancy-Associated Plasma Protein A Levels in First-Trimester Twin and Singleton Pregnancies.

Published in:

Fetal Diagnosis & Therapy, 2004, v. 19, n. 2, p. 174, doi. 10.1159/000075145

By:

Mashiach, Roy;
Orr-Urtreger, Avi;
Yaron, Yuval

Publication type:

Article

First trimester maternal serum free human chorionic gonadotropin as a predictor of adverse pregnancy outcome.

Published in:

2002

By:

Yaron, Yuval;
Ochshorn, Yifat;
Heifetz, Sigal;
Lehavi, Ofer;
Sapir, Yaron;
Orr-Urtreger, Avi

Publication type:

journal article

Radiological markers of CSF α-synuclein aggregation in Parkinson's disease patients.

Published in:

NPJ Parkinson's Disease, 2025, v. 11, n. 1, p. 1, doi. 10.1038/s41531-024-00854-4

By:

Droby, Amgad;
Yoffe-Vasiliev, Avital;
Atias, Daniel;
Fraser, Kyle B.;
Mabrouk, Omar S.;
Omer, Nurit;
Bar-Shira, Anat;
Gana-Weisz, Mali;
Goldstein, Orly;
Artzi, Moran;
Ben Bashat, Dafna;
Alcalay, Roy N.;
Orr-Urtreger, Avi;
Shirvan, Julia C.;
Cedarbaum, Jesse M.;
Giladi, Nir;
Mirelman, Anat;
Thaler, Avner

Publication type:

Article

TMEM16F regulates pathologic α‐synuclein secretion and spread in cellular and mouse models of Parkinson's disease.

Published in:

Aging Cell, 2025, v. 24, n. 2, p. 1, doi. 10.1111/acel.14387

By:

Cohen‐Adiv, Stav;
Amer‐Sarsour, Fatima;
Berdichevsky, Yevgeny;
Boxer, Emily;
Goldstein, Orly;
Gana‐Weisz, Mali;
Tripathi, Utkarsh;
Rike, Wote Amelo;
Prag, Gali;
Gurevich, Tanya;
Giladi, Nir;
Stern, Shani;
Orr‐Urtreger, Avi;
Friedmann‐Morvinski, Dinorah;
Ashkenazi, Avraham

Publication type:

Article

Hierarchical Data-Driven Analysis of Clinical Symptoms Among Patients With Parkinson's Disease.

Published in:

Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00531

By:

Kozlovski, Tal;
Mitelpunkt, Alexis;
Thaler, Avner;
Gurevich, Tanya;
Orr-Urtreger, Avi;
Gana-Weisz, Mali;
Shachar, Netta;
Galili, Tal;
Marcus-Kalish, Mira;
Bressman, Susan;
Marder, Karen;
Giladi, Nir;
Benjamini, Yoav;
Mirelman, Anat

Publication type:

Article

Network abnormalities among non‐manifesting Parkinson disease related LRRK2 mutation carriers.

Published in:

Human Brain Mapping, 2019, v. 40, n. 8, p. 2546, doi. 10.1002/hbm.24543

By:

Jacob, Yael;
Rosenberg‐Katz, Keren;
Gurevich, Tanya;
Helmich, Rick C.;
Bloem, Bastiaan R.;
Orr‐Urtreger, Avi;
Giladi, Nir;
Mirelman, Anat;
Hendler, Talma;
Thaler, Avner

Publication type:

Article

The effects of aging vs. α7 nAChR subunit deficiency on the mouse brain transcriptome: aging beats the deficiency.

Published in:

Age (0161-9152), 2011, v. 33, n. 1, p. 1, doi. 10.1007/s11357-010-9155-7

By:

Kedmi, Merav;
Orr-Urtreger, Avi

Publication type:

Article

Cytogenetic analysis of sinonasal carcinomas

Published in:

Otolaryngology-Head & Neck Surgery, 2006, v. 134, n. 4, p. 654, doi. 10.1016/j.otohns.2005.10.055

By:

Gil, Ziv;
Orr-Urtreger, Avi;
Voskoboinik, Nadia;
Trejo-Leider, Leonor;
Spektor, Sergey;
Shomrat, Ruth;
Fliss, Dan M.

Publication type:

Article

The homozygous P582S mutation in the oxygen?dependent degradation domain of HIF?1? is associated with increased risk for prostate cancer.

Published in:

Prostate, 2007, v. 67, n. 1, p. 8, doi. 10.1002/pros.20433

By:

Avi Orr?Urtreger;
Anat Bar?Shira;
Haim Matzkin;
Nicola J. Mabjeesh

Publication type:

Article

Mutation screening and association study of the candidate prostate cancer susceptibility genes MSR1, PTEN, and KLF6.

Published in:

Prostate, 2006, v. 66, n. 10, p. 1052, doi. 10.1002/pros.20425

By:

Anat Bar‐Shira;
Noa Matarasso;
Serena Rosner;
Dani Bercovich;
Haim Matzkin;
Avi Orr‐Urtreger

Publication type:

Article

HIF1A C1772T polymorphism leads to HIF-1α mRNA overexpression in prostate cancer patients.

Published in:

Cancer Biology & Therapy, 2012, v. 13, n. 9, p. 720, doi. 10.4161/cbt.20554

By:

Vainrib, Michael;
Golan, Maya;
Amir, Sharon;
Dang, Duyen T.;
Dang, Long H.;
Bar-Shira, Anat;
Orr-Urtreger, Avi;
Matzkin, Haim;
Mabjeesh, Nicola J.

Publication type:

Article

Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism.

Published in:

2012

By:

van Nuenen BF;
Helmich RC;
Ferraye M;
Thaler A;
Hendler T;
Orr-Urtreger A;
Mirelman A;
Bressman S;
Marder KS;
Giladi N;
van de Warrenburg BP;
Bloem BR;
Toni I;
LRRK2 Ashkenazi Jewish Consortium;
van Nuenen, Bart F L;
Helmich, Rick C;
Ferraye, Murielle;
Thaler, Avner;
Hendler, Talma;
Orr-Urtreger, Avi

Publication type:

journal article

Cerebral pathological and compensatory mechanisms in the premotor phase of leucine-rich repeat kinase 2 parkinsonism.

Published in:

Brain: A Journal of Neurology, 2012, v. 135, n. 12, p. 3687

By:

van Nuenen, Bart F. L.;
Helmich, Rick C.;
Ferraye, Murielle;
Thaler, Avner;
Hendler, Talma;
Orr-Urtreger, Avi;
Mirelman, Anat;
Bressman, Susan;
Marder, Karen S.;
Giladi, Nir;
van de Warrenburg, Bart P. C.;
Bloem, Bastiaan R.;
Toni, Ivan

Publication type:

Article

Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Evidence for a founder effect.

Published in:

2002

By:

Rozen, Paul;
Naiman, Tova;
Strul, Hana;
Taussky, Philipp;
Karminsky, Nataly;
Shomrat, Ruth;
Samuel, Ziona;
Yaron, Yuval;
Orr-Urtreger, Avi

Publication type:

journal article

Maternal serum HCG is higher in the presence of a female fetus as early as week 3 post-fertilization.

Published in:

2002

By:

Yaron, Yuval;
Lehavi, Ofer;
Orr-Urtreger, Avi;
Gull, Ilan;
Lessing, Joseph B.;
Amit, Ami;
Ben-Yosef, Dalit

Publication type:

journal article

The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population.

Published in:

Human Genetics, 2000, v. 106, n. 1, p. 50, doi. 10.1007/s004390051009

By:

Sobe, Tama;
Vreugde, Sarah;
Shahin, Hashem;
Berlin, Mira;
Davis, Noa;
Kanaan, Moien;
Yaron, Yuval;
Orr-Urtreger, Avi;
Frydman, Moshe;
Shohat, Mordechai;
Avraham, Karen B.

Publication type:

Article

Being ‘at-risk’ for developing cancer: cognitive representations and psychological outcomes.

Published in:

Journal of Behavioral Medicine, 2009, v. 32, n. 2, p. 197, doi. 10.1007/s10865-008-9178-z

By:

Shiloh, Shoshana;
Drori, Erga;
Orr-Urtreger, Avi;
Friedman, Eitan

Publication type:

Article

Gait alterations in healthy carriers of the LRRK2 G2019S mutation.

Published in:

Annals of Neurology, 2011, v. 69, n. 1, p. 193, doi. 10.1002/ana.22165

By:

Mirelman, Anat;
Gurevich, Tanya;
Giladi, Nir;
Bar-Shira, Anat;
Orr-Urtreger, Avi;
Hausdorff, Jeffrey M.

Publication type:

Article

Analysis of the Hoxd-3 Gene: Structure and Localization of Its Sense and Natural Antisense Transcripts.

Published in:

DNA & Cell Biology, 1995, v. 14, n. 4, p. 295, doi. 10.1089/dna.1995.14.295

By:

BEDFORD, MARK;
ARMAN, ESTHER;
ORR-URTREGER, AVI;
LONAI, PETER

Publication type:

Article

The role of the nAChR subunits α5, β2, and β4 on synaptic transmission in the mouse superior cervical ganglion.

Published in:

Physiological Reports, 2019, v. 7, n. 6, p. N.PAG, doi. 10.14814/phy2.14023

By:

Simeone, Xenia;
Karch, Rudolf;
Ciuraszkiewicz, Anna;
Orr‐Urtreger, Avi;
Lemmens‐Gruber, Rosa;
Scholze, Petra;
Huck, Sigismund

Publication type:

Article