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Stella Mitrani-Rosenbaum

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Ilan Sela; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Stella Mitrani-Rosenbaum
Variable phenotypes of knockin mice carrying the M712T Gne mutation.
Stella Mitrani-Rosenbaum; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Avi Harazi; Michal Telem; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Ilan Sela
Sustained expression and safety of human GNE in normal mice after gene transfer based on AAV8 systemic delivery.
Takeshi Yoshimura; Akihiro Ishii; Takako Koike; Stella Mitrani-Rosenbaum; Mai Narumi; Ilan Sela; Gen Yamada; Kazuhiro Ikenaka
Detection of N-glycans on small amounts of glycoproteins in tissue samples and sodium dodecyl sulfate-polyacrylamide gels.

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2013: Ilan Sela; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Stella Mitrani-Rosenbaum
Variable phenotypes of knockin mice carrying the M712T Gne mutation.
Neuromolecular medicine 2013;15(1):180-91.
2012: Stella Mitrani-Rosenbaum; Zohar Argov; Michal Becker Cohen; Uri Ben Shlomo; Moran Elbaz; Yakov Fellig; Avi Harazi; Michal Telem; Lena Yakovlev; Nurit Yanay; Hagit Yotvat; Ilan Sela
Sustained expression and safety of human GNE in normal mice after gene transfer based on AAV8 systemic delivery.
Neuromuscular disorders : NMD 2012;22(11):1015-24.
2012: Takeshi Yoshimura; Akihiro Ishii; Takako Koike; Stella Mitrani-Rosenbaum; Mai Narumi; Ilan Sela; Gen Yamada; Kazuhiro Ikenaka
Detection of N-glycans on small amounts of glycoproteins in tissue samples and sodium dodecyl sulfate-polyacrylamide gels.
Analytical biochemistry 2012;423(2):253-60.
2012: Aviram Nissan; Lloyd John Old; Gerd Ritter; Marina Roistacher; Alexander Stojadinovic; David Halle; Stella Mitrani-Rosenbaum; Musa Akoglu; Andrea Bochem; Erdal Birol Bostanci; Yao-Tseng Chen; Baris Emre Dayanc; Ismail Gomceli; Ronit Grinbaum; Ali Osmay Gure
Colon cancer associated transcript-1: a novel RNA expressed in malignant and pre-malignant human tissues.
International journal of cancer. Journal international du cancer 2012;130(7):1598-606.
2011: Haggi Mazeh; Ido Mizrahi; David Halle; Nadia Ilyayev; Alexander Stojadinovic; Barry Trink; Stella Mitrani-Rosenbaum; Marina Roistacher; Ilana Ariel; Ahmed Eid; Herbert R Freund; Aviram Nissan
Development of a microRNA-based molecular assay for the detection of papillary thyroid carcinoma in aspiration biopsy samples.
Thyroid : official journal of the American Thyroid Association 2011;21(2):111-8.
2011: Irit Milman Krentsis; Ilan Sela; Michal Becker Cohen; Markus Berger; Véronique Blanchard; Rachel Eiges; Stella Mitrani-Rosenbaum
GNE is involved in the early development of skeletal and cardiac muscle.
PloS one 2011;6(6):e21389.
2011: Ilan Sela; Irit Milman Krentsis; Zipora Shlomai; Menachem Sadeh; Ron Dabby; Zohar Argov; Hannah Ben-Bassat; Stella Mitrani-Rosenbaum
The proteomic profile of hereditary inclusion body myopathy.
PloS one 2011;6(1):e16334.
2009: Nigel G Laing; Danielle E Dye; Carina Wallgren-Pettersson; Gabriele Richard; Nicole Monnier; Suzanne Lillis; Thomas L Winder; Hanns Lochmüller; Claudio Graziano; Stella Mitrani-Rosenbaum; Darren Twomey; John C Sparrow; Alan H Beggs; Kristen J Nowak
Mutations and polymorphisms of the skeletal muscle alpha-actin gene (ACTA1).
Human mutation 2009;30(9):1267-77.
2008: Anat Agranat-Meged; Yoad Ghanadri; Iris Eisenberg; Ziva Ben-Neriah; Eva Kieselstein-Gross; Stella Mitrani-Rosenbaum
Attention deficit hyperactivity disorder in obese melanocortin-4-receptor (MC4R) deficient subjects: a newly described expression of MC4R deficiency.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(8):1547-53.
2008: Iris Eisenberg; Noa Novershtern; Zohar Itzhaki; Michal Becker-Cohen; Menachem Sadeh; Peter H G M Willems; Nir Friedman; Werner J H Koopman; Stella Mitrani-Rosenbaum
Mitochondrial processes are impaired in hereditary inclusion body myopathy.
Human molecular genetics 2008;17(23):3663-74.
2008: Zohar Argov; Stella Mitrani-Rosenbaum
The hereditary inclusion body myopathy enigma and its future therapy.
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 2008;5(4):633-7.
2008: Shira Amsili; Hagit Zer; Stephan Hinderlich; Sabine Krause; Michal Becker-Cohen; Daniel G MacArthur; Kathryn N North; Stella Mitrani-Rosenbaum
UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) binds to alpha-actinin 1: novel pathways in skeletal muscle?
PloS one 2008;3(6):e2477.
2007: S Amsili; Zipora Shlomai; Rubina Levitzki; S Krause; Hanns Lochmuller; Hannah Ben-Bassat; Stella Mitrani-Rosenbaum
Characterization of hereditary inclusion body myopathy myoblasts: possible primary impairment of apoptotic events.
Cell death and differentiation 2007;14(11):1916-24.
2007: Iris Eisenberg; Alal Eran; Ichizo Nishino; Maurizio Moggio; Costanza Lamperti; Anthony A Amato; Hart G W Lidov; Peter B Kang; Kathryn N North; Stella Mitrani-Rosenbaum; Kevin M Flanigan; Lori A Neely; Duncan Whitney; Alan H Beggs; Isaac S Kohane; Louis Kunkel
Distinctive patterns of microRNA expression in primary muscular disorders.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(43):17016-21.
2007: Sabine Krause; A Aleo; Stephan Hinderlich; Luciano Merlini; I Tournev; Maggie C Walter; Zohar Argov; Stella Mitrani-Rosenbaum; Hanns Lochmüller
GNE protein expression and subcellular distribution are unaltered in HIBM.
Neurology 2007;69(7):655-9.
2007: Zohar Argov; Stella Mitrani-Rosenbaum
Hereditary inclusion body myopathy and other rimmed vacuolar myopathies.
Handbook of clinical neurology 2007;86():243-53.
2006: Aviram Nissan; D Jager; M Roystacher; Diana Prus; Tamar Peretz; Iris Eisenberg; Herbert R Freund; M Scanlan; G Ritter; Lloyd J Old; Stella Mitrani-Rosenbaum
Multimarker RT-PCR assay for the detection of minimal residual disease in sentinel lymph nodes of breast cancer patients.
British journal of cancer 2006;94(5):681-5.
2006: Juliane Penner; Lars R Mantey; Sharona Elgavish; Darius Ghaderi; Sebahattin Cirak; Markus Berger; Sabine Krause; Lothar Lucka; Thomas Voit; Stella Mitrani-Rosenbaum; Stephan Hinderlich
Influence of UDP-GlcNAc 2-epimerase/ManNAc kinase mutant proteins on hereditary inclusion body myopathy.
Biochemistry 2006;45(9):2968-77.
2005: Sabine Krause; Stephan Hinderlich; Shira Amsili; Rüdiger Horstkorte; Heinz Wiendl; Zohar Argov; Stella Mitrani-Rosenbaum; Hanns Lochmüller
Localization of UDP-GlcNAc 2-epimerase/ManAc kinase (GNE) in the Golgi complex and the nucleus of mammalian cells.
Experimental cell research 2005;304(2):365-79.
2005: Ilan Salama; Stephan Hinderlich; Zipora Shlomai; Iris Eisenberg; Sabine Krause; Kevin J Yarema; Zohar Argov; Hanns Lochmuller; Werner Reutter; Ron Dabby; Menachem Sadeh; Hannah Ben-Bassat; Stella Mitrani-Rosenbaum
No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation.
Biochemical and biophysical research communications 2005;328(1):221-6.
2004: Stephan Hinderlich; Ilan Salama; Iris Eisenberg; Tamara Potikha; Lars R Mantey; Kevin J Yarema; Rüdiger Horstkorte; Zohar Argov; Menachem Sadeh; Werner Reutter; Stella Mitrani-Rosenbaum
The homozygous M712T mutation of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase results in reduced enzyme activities but not in altered overall cellular sialylation in hereditary inclusion body myopathy.
FEBS letters 2004;566(1-3):105-9.
2004: Boaz Avidor; Gabi Efrat; Mark Weinberg; Zipi Kra-Oz; Judith Satinger; Stella Mitrani-Rosenbaum; Yuval Yaron; Lester Shulman; Michal Tepperberg-Oikawa; Dana Wolf; Stephen A Berger; Shlomo Lipitz; Ella Mendelson; Michael Giladi
Insight into the intrinsic sensitivity of the PCR assay used to detect CMV infection in amniotic fluid specimens.
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology 2004;29(4):260-70.
2003: Stephan Hinderlich; Ilan Salama; Iris Eisenberg; Stella Mitrani-Rosenbaum
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.
Neurology 2003;61(1):145; author reply 145.
2003: Zohar Argov; Iris Eisenberg; Gil Grabov-Nardini; Menachem Sadeh; Itzhak Wirguin; Dov Soffer; Stella Mitrani-Rosenbaum
Hereditary inclusion body myopathy: the Middle Eastern genetic cluster.
Neurology 2003;60(9):1519-23.
2003: Iris Eisenberg; Gil Grabov-Nardini; Hagit Hochner; Mira Korner; Menachem Sadeh; Tulio Bertorini; Kate Bushby; Claudio Castellan; Kevin Felice; Jerry Mendell; Luciano Merlini; Christopher Shilling; Itzhak Wirguin; Zohar Argov; Stella Mitrani-Rosenbaum
Mutations spectrum of GNE in hereditary inclusion body myopathy sparing the quadriceps.
Human mutation 2003;21(1):99.
2002: Iris Eisenberg; Hagit Hochner; Tatjana Levi; Ronit Yelin; Tamar Kahan; Stella Mitrani-Rosenbaum
Cloning and characterization of a novel human gene RNF38 encoding a conserved putative protein with a RING finger domain.
Biochemical and biophysical research communications 2002;294(5):1169-76.
2002: Iris Eisenberg; Mark Barash; Tamar Kahan; Stella Mitrani-Rosenbaum
Cloning and characterization of a human novel gene C9orf19 encoding a conserved putative protein with an SCP-like extracellular protein domain.
Gene 2002;293(1-2):141-8.
2002: Iris Eisenberg; Hagit Hochner; Menachem Sadeh; Zohar Argov; Stella Mitrani-Rosenbaum
Establishment of the genomic structure and identification of thirteen single-nucleotide polymorphisms in the human RECK gene.
Cytogenetic and genome research 2002;97(1-2):58-61.
2001: Hagai Amsalem; R Tsvieli; BS Zentner; Simcha Yagel; Stella Mitrani-Rosenbaum; Arye Hurwitz
Monopaternal superfecundation of quintuplets after transfer of two embryos in an in vitro fertilization cycle.
Fertility and sterility 2001;76(3):621-3.
2001: Iris Eisenberg; Nili Avidan; Tamara Potikha; Hagit Hochner; M Chen; Tsviya Olender; M Barash; Mordechai Shemesh; Menachem Sadeh; Gil Grabov-Nardini; I Shmilevich; A Friedmann; George Karpati; Walter G Bradley; Lisa Baumbach; Doron Lancet; E B Asher; Jacques Beckmann; Zohar Argov; Stella Mitrani-Rosenbaum
The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy.
Nature genetics 2001;29(1):83-7.
2001: Iris Eisenberg; Hagit Hochner; Mordechai Shemesh; Tatjana Levi; Tamara Potikha; Menachem Sadeh; Zohar Argov; C L Jackson; Stella Mitrani-Rosenbaum
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13.
European journal of human genetics : EJHG 2001;9(7):501-9.
2000: R Avner; Jacob Wahrman; Carmelit Richler; N Ayoub; A Friedmann; N Laufer; Stella Mitrani-Rosenbaum
X inactivation-specific transcript expression in mouse oocytes and zygotes.
Molecular human reproduction 2000;6(7):591-4.
2000: Zohar Argov; Menachem Sadeh; K Mazor; Dov Soffer; Esther Kahana; Iris Eisenberg; Stella Mitrani-Rosenbaum; Isabelle Richard; Jacques Beckmann; Sharon M Keers; Rumaisa Bashir; Kate Bushby; Hanna Rosenmann
Muscular dystrophy due to dysferlin deficiency in Libyan Jews. Clinical and genetic features.
Brain : a journal of neurology 2000;123 ( Pt 6)():1229-37.
2000: Elizabeth McNally; CT Ly; Hanna Rosenmann; Stella Mitrani-Rosenbaum; W Jiang; Louise V B Anderson; Dov Soffer; Zohar Argov
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.
American journal of medical genetics 2000;91(4):305-12.
1999: Iris Eisenberg; C Thiel; Tatjana Levi; Efrat Tiram; Zohar Argov; Menachem Sadeh; C L Jackson; Ludwig Thierfelder; Stella Mitrani-Rosenbaum
Fine-structure mapping of the hereditary inclusion body myopathy locus.
Genomics 1999;55(1):43-8.
1998: Zohar Argov; Iris Eisenberg; Stella Mitrani-Rosenbaum
Genetics of inclusion body myopathies.
Current opinion in rheumatology 1998;10(6):543-7.
1998: Shlomo Lipitz; Ariel Many; Stella Mitrani-Rosenbaum; Howard Carp; Yair Frenkel; Reuven Achiron
Obstetric outcome after RhD and Kell testing.
Human reproduction (Oxford, England) 1998;13(6):1472-5.
1998: Zohar Argov; Menachem Sadeh; Iris Eisenberg; George Karpati; Stella Mitrani-Rosenbaum
Facial weakness in hereditary inclusion body myopathies.
Neurology 1998;50(6):1925-6.
1997: Emmilia Hodak; Akiva Trattner; Hana Feuerman; Meora Feinmesser; R Tsvieli; Stella Mitrani-Rosenbaum; Michael David
Lupus miliaris disseminatus faciei--the DNA of Mycobacterium tuberculosis is not detectable in active lesions by polymerase chain reaction.
The British journal of dermatology 1997;137(4):614-9.
1997: Zohar Argov; Efrat Tiram; Iris Eisenberg; Menachem Sadeh; C E Seidman; J G Seidman; George Karpati; Stella Mitrani-Rosenbaum
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1.
Annals of neurology 1997;41(4):548-51.
1996: Benjamin E Reubinoff; R Avner; Nathan Rojansky; N Manny; A Friedmann; Neri Laufer; Stella Mitrani-Rosenbaum
RhD genotype determination by single sperm cell analysis.
American journal of obstetrics and gynecology 1996;174(4):1300-5.
1996: R Avner; Benjamin E Reubinoff; Alex Simon; BS Zentner; A Friedmann; Stella Mitrani-Rosenbaum; Neri Laufer
Management of rhesus isoimmunization by preimplantation genetic diagnosis.
Molecular human reproduction 1996;2(1):60-2.
1996: Stella Mitrani-Rosenbaum; Zohar Argov; A Blumenfeld; Christine E Seidman; Jonathan G Seidman
Hereditary inclusion body myopathy maps to chromosome 9p1-q1.
Human molecular genetics 1996;5(1):159-163.
1994: Z Landau; R Gross; A Sanilevich; A Friedmann; Stella Mitrani-Rosenbaum
Presence of infective Epstein-Barr virus in the urine of patients with infectious mononucleosis.
Journal of medical virology 1994;44(3):229-33.
1994: Stella Mitrani-Rosenbaum; R Tsvieli; Ofer Lavie; R Boldes; E Anteby; S Shimonovitch; T Lazarovitch; A Friedmann
Simultaneous detection of three common sexually transmitted agents by polymerase chain reaction.
American journal of obstetrics and gynecology 1994;171(3):784-90.
1994: R Avner; Neri Laufer; Anat Safran; B S Kerem; A Friedmann; Stella Mitrani-Rosenbaum
Preimplantation diagnosis of cystic fibrosis by simultaneous detection of the W1282X and delta F508 mutations.
Human reproduction (Oxford, England) 1994;9(9):1676-80.
1994: Stella Mitrani-Rosenbaum
Human papillomaviruses and the diagnosis of genital microorganisms.
Israel journal of medical sciences 1994;30(5-6):443-7.
1992: Stella Mitrani-Rosenbaum; R Tsvieli
Differential cooperation of a carcinogen with human papillomavirus type 6 and 16 DNAs in in vitro oncogenic transformation.
Intervirology 1992;33(2):76-85.
1989: Stella Mitrani-Rosenbaum; R Tsvieli; R Tur-Kaspa
Oestrogen stimulates differential transcription of human papillomavirus type 16 in SiHa cervical carcinoma cells.
The Journal of general virology 1989;70 ( Pt 8)():2227-32.
1989: D Gal; M Friedman; Stella Mitrani-Rosenbaum
Transmissibility and treatment failures of different types of human papillomavirus.
Obstetrics and gynecology 1989;73(3 Pt 1):308-11.
1988: Stella Mitrani-Rosenbaum; D Gal; M Friedman; N Kitron; R Tsvieli; N Mordel; Shaoul O Anteby
Papillomaviruses in lesions of the lower genital tract in Israeli patients.
European journal of cancer & clinical oncology 1988;24(4):725-31.
1988: Stella Mitrani-Rosenbaum
Use of a stable bovine papillomavirus vector to study inducible genes.
Intervirology 1988;29(2):108-14.
1987: Stella Mitrani-Rosenbaum; N Kitron
Integration and transcription of human papillomavirus type 6 recombinant DNA in mouse cells.
Virus research 1987;8(4):335-47.