FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Anat Blumenfeld

Research Profile

Disorders

Anatomy

Living Beings

Jews
Mouse

Chemicals & Drugs

Concepts & Ideas

Procedures

Geographic Areas

Israel

Genes & Molecular Sequences

Amino Acid Sequences

Co-author Network

Publications

TOP 3
Claudia Yahalom; Anat Blumenfeld; Dalia Eli; Sherry Glanzer; Gabriel Greifner; Ada Rosenmann; Veronica Tzur; Irene Anteby
Refractive profile in oculocutaneous albinism and its correlation with final visual outcome.
Dan Deutsch; Philip Lazarovici; Shimon Lecht; Dekel Shilo; Nechama Silverstein; Anat Blumenfeld
Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cells.
Yoav Leiser; Nechama Silverstein; Anat Blumenfeld; Dekel Shilo; Amir Haze; Eli Rosenfeld; Boaz Shay; Rinat Tabakman; Shimon Lecht; Philip Lazarovici; Dan Deutsch
The induction of tuftelin expression in PC12 cell line during hypoxia and NGF-induced differentiation.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Anat Blumenfeld (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2012: Claudia Yahalom; Anat Blumenfeld; Dalia Eli; Sherry Glanzer; Gabriel Greifner; Ada Rosenmann; Veronica Tzur; Irene Anteby
Refractive profile in oculocutaneous albinism and its correlation with final visual outcome.
The British journal of ophthalmology 2012;96(4):537-9.
2011: Dan Deutsch; Philip Lazarovici; Shimon Lecht; Dekel Shilo; Nechama Silverstein; Anat Blumenfeld
Biphasic influence of hypoxia on tuftelin expression in mouse mesenchymal C3H10T1/2 stem cells.
European journal of oral sciences 2011;119 Suppl 1():55-61.
2011: Yoav Leiser; Nechama Silverstein; Anat Blumenfeld; Dekel Shilo; Amir Haze; Eli Rosenfeld; Boaz Shay; Rinat Tabakman; Shimon Lecht; Philip Lazarovici; Dan Deutsch
The induction of tuftelin expression in PC12 cell line during hypoxia and NGF-induced differentiation.
Journal of cellular physiology 2011;226(1):165-72.
2009: Boaz Shay; Yael Gruenbaum-Cohen; A S Tucker; Angela L Taylor; Eli Rosenfeld; Amir Haze; Leah Dafni; Yoav Leiser; Eran Fermon; tsafi danieli; Anat Blumenfeld; Dan Deutsch
High yield expression of biologically active recombinant full length human tuftelin protein in baculovirus-infected insect cells.
Protein expression and purification 2009;68(1):90-8.
2009: Ada Rosenmann; Idit Bejarano-Achache; Dalia Eli; Genia Maftsir; Liliana Mizrahi-Meissonnier; Anat Blumenfeld
Prenatal molecular diagnosis of oculocutaneous albinism (OCA) in a large cohort of Israeli families.
Prenatal diagnosis 2009;29(10):939-46.
2009: Yael Gruenbaum-Cohen; Abigail S Tucker; Amir Haze; Dekel Shilo; Angela L Taylor; Boaz Shay; Paul T Sharpe; Thimios A Mitsiadis; Asher Ornoy; Anat Blumenfeld; Dan Deutsch
Amelogenin in cranio-facial development: the tooth as a model to study the role of amelogenin during embryogenesis.
Journal of experimental zoology. Part B, Molecular and developmental evolution 2009;312B(5):445-57.
2009: Amir Haze; Angela L Taylor; Stefan Haegewald; Yoav Leiser; Boaz Shay; Eli Rosenfeld; Yael Gruenbaum-Cohen; Leah Dafni; Bernd Zimmermann; Kristiina Heikinheimo; Carolyn W Gibson; LW Fisher; Marian F Young; Anat Blumenfeld; Jean-Pierre Bernimoulin; Dan Deutsch
Regeneration of bone and periodontal ligament induced by recombinant amelogenin after periodontitis.
Journal of cellular and molecular medicine 2009;13(6):1110-24.
2008: Dikla Bandah; Ada Rosenmann; Anat Blumenfeld; Edward Averbukh; Eyal Banin; Dror Sharon
A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia.
Molecular vision 2008;14():142-5.
2007: Anat Beit-Ya'acov; Liliana Mizrahi-Meissonnier; Alexey Obolensky; Carmit Landau; Anat Blumenfeld; Ada Rosenmann; Eyal Banin; Dror Sharon
Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease.
Investigative ophthalmology & visual science 2007;48(9):4308-14.
2007: Yoav Leiser; Anat Blumenfeld; Amir Haze; Leah Dafni; Angela L Taylor; Eli Rosenfeld; Eran Fermon; Yael Gruenbaum-Cohen; Boaz Shay; Dan Deutsch
Localization, quantification, and characterization of tuftelin in soft tissues.
Anatomical record (Hoboken, N.J. : 2007) 2007;290(5):449-54.
2007: Amir Haze; Angela L Taylor; Anat Blumenfeld; Eli Rosenfeld; Yoav Leiser; Leah Dafni; Boaz Shay; Yael Gruenbaum-Cohen; Eran Fermon; Stefan Haegewald; Jean-Pierre Bernimoulin; Dan Deutsch
Amelogenin expression in long bone and cartilage cells and in bone marrow progenitor cells.
Anatomical record (Hoboken, N.J. : 2007) 2007;290(5):455-60.
2006: Nira Schreyer-Shafir; Marjan Huizing; Yair Anikster; Ziva Nusinker; Idit Bejarano-Achache; Genia Maftzir; Luba Resnik; Amanda Helip-Wooley; Wendy Westbroek; Libe Gradstein; Ada Rosenmann; Anat Blumenfeld
A new genetic isolate with a unique phenotype of syndromic oculocutaneous albinism: clinical, molecular, and cellular characteristics.
Human mutation 2006;27(11):1158.
2006: Dan Deutsch; Amir Haze-Filderman; Anat Blumenfeld; Leah Dafni; Yoav Leiser; Boaz Shay; Yael Gruenbaum-Cohen; Eli Rosenfeld; Eran Fermon; Bernard Zimmermann; Stefan Haegewald; Jean-Pierre Bernimoulin; Angela L Taylor
Amelogenin, a major structural protein in mineralizing enamel, is also expressed in soft tissues: brain and cells of the hematopoietic system.
European journal of oral sciences 2006;114 Suppl 1():183-9; discussion 201-2, 381.
2006: Angela L Taylor; Amir Haze-Filderman; Anat Blumenfeld; Boaz Shay; Leah Dafni; Eli Rosenfeld; Yoav Leiser; Eran Fermon; Yael Gruenbaum-Cohen; Dan Deutsch
High yield of biologically active recombinant human amelogenin using the baculovirus expression system.
Protein expression and purification 2006;45(1):43-53.
2005: Ariel Rokach; Arthur Pollak; Laura Rosen; Yechiel Friedlander; Anat Blumenfeld; Luba Reznik; Rivka Dresner Pollak
Estrogen receptor alpha gene polymorphisms are associated with the angiographic extent of coronary artery disease.
The Journal of clinical endocrinology and metabolism 2005;90(12):6556-60.
2004: Eyal Y Anteby; Banan Musalam; Ariel Milwidsky; Anat Blumenfeld; Shmuel Gilis; Dan V Valsky; Yaron Hamani
Fetal inherited thrombophilias influence the severity of preeclampsia, IUGR and placental abruption.
European journal of obstetrics, gynecology, and reproductive biology 2004;113(1):31-5.
2004: Arthur Pollak; Ariel Rokach; Anat Blumenfeld; Laura J Rosen; Luba Resnik; Rivka Dresner Pollak
Association of oestrogen receptor alpha gene polymorphism with the angiographic extent of coronary artery disease.
European heart journal 2004;25(3):240-5.
2003: Maire Leyne; James Mull; Sandra P Gill; Math P Cuajungco; Carole Oddoux; Anat Blumenfeld; Channa Maayan; James Gusella; Felicia B Axelrod; Susan A Slaugenhaupt
Identification of the first non-Jewish mutation in familial Dysautonomia.
American journal of medical genetics. Part A 2003;118A(4):305-8.
2001: Rivka Dresner Pollak; Anat Blumenfeld; Idit Bejarano-Achache; Maria Idelson; D Celinke Hochner
The BsmI vitamin D receptor gene polymorphism in Israeli populations and in perimenopausal and osteoporotic Ashkenazi women.
American journal of nephrology 2001;21(3):185-8.
2001: Susan A Slaugenhaupt; Anat Blumenfeld; Sandra P Gill; Maire Leyne; James Mull; Math P Cuajungco; CB Liebert; BP Chadwick; Maria Idelson; Luba Reznik; Christiane Robbins; Izabela Makalowska; Michael J Brownstein; Daniel Krappmann; Claus Scheidereit; Channa Maayan; Felicia B Axelrod; James Gusella
Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia.
American journal of human genetics 2001;68(3):598-605.
2000: R Dresner Pollack; Eliezer A Rachmilewitz; Anat Blumenfeld; Maria Idelson; A W Goldfarb
Bone mineral metabolism in adults with beta-thalassaemia major and intermedia.
British journal of haematology 2000;111(3):902-7.
2000: Rivka Dresner Pollak; Arthur Pollak; Maria Idelson; Idit Bejarano-Achache; Dafna Doron; Anat Blumenfeld
The C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene and vascular dementia.
Journal of the American Geriatrics Society 2000;48(6):664-8.
2000: Rivka Dresner Pollak; Yechiel Friedlander; Arthur Pollak; Maria Idelson; Anat Blumenfeld
Ethnic differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in healthy Israeli populations.
Genetic testing 2000;4(3):309-11.
2000: BP Chadwick; Maire Leyne; Sandra Gill; CB Liebert; James Mull; Eva Mezey; Christiane M Robbins; Heather Pinkett; Izabela Makalowska; Channa Maayan; Anat Blumenfeld; Felicia B Axelrod; Michael J Brownstein; James Gusella; Susan A Slaugenhaupt
Cloning, mapping, and expression of a novel brain-specific transcript in the familial dysautonomia candidate region on chromosome 9q31.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(1):81-3.
1999: BP Chadwick; Sandra Gill; Maire Leyne; James Mull; CB Liebert; Christiane M Robbins; Heather Pinkett; Izabela Makalowska; Channa Maayan; Anat Blumenfeld; Felicia B Axelrod; Michael J Brownstein; Susan A Slaugenhaupt
Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene.
Gene 1999;240(1):67-73.
1999: Eliezer Rosenmann; Ada Rosenmann; Zvi Ne'eman; A Lewin; Idit Bejarano-Achache; Anat Blumenfeld
Prenatal diagnosis of oculocutaneous albinism type I: review and personal experience.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 1999;2(5):404-14.
1999: BP Chadwick; James Mull; LA Helbling; Sandra Gill; Maire Leyne; Christiane M Robbins; Heather Pinkett; Izabela Makalowska; Channa Maayan; Anat Blumenfeld; Felicia B Axelrod; Michael J Brownstein; James Gusella; Susan A Slaugenhaupt
Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familial dysautonomia candidate region on 9q31.
Genomics 1999;58(3):302-9.
1999: Anat Blumenfeld; Susan A Slaugenhaupt; CB Liebert; V Temper; Channa Maayan; Sandra Gill; D E Lucente; Maria Idelson; K MacCormack; M A Monahan; James Mull; Maire Leyne; M Mendillo; Taryn A Schiripo; E Mishori; X Breakefield; Felicia B Axelrod; James Gusella
Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31.
American journal of human genetics 1999;64(4):1110-8.
1997: Diana Prus; Andrew E Rosenberg; Anat Blumenfeld; R Udassin; Zvi Ne'eman; R H Young; Ilana Ariel
Infantile hemangioendothelioma of the ovary: a monodermal teratoma or a neoplasm of ovarian somatic cells?
The American journal of surgical pathology 1997;21(10):1231-5.
1996: G Davar; Christo Shalish; Anat Blumenfeld; X O Breakfield
Exclusion of p75NGFR and other candidate genes in a family with hereditary sensory neuropathy type II.
Pain 1996;67(1):135-9.
1995: Christine M Eng; Susan A Slaugenhaupt; Anat Blumenfeld; Felicia B Axelrod; James Gusella; Robert J Desnick
Prenatal diagnosis of familial dysautonomia by analysis of linked CA-repeat polymorphisms on chromosome 9q31-q33.
American journal of medical genetics 1995;59(3):349-55.
1995: Carole Oddoux; E Reich; Felicia B Axelrod; Anat Blumenfeld; Channa Maayan; Susan A Slaugenhaupt; James Gusella; Harry Ostrer
Prenatal diagnostic testing for familial dysautonomia using linked genetic markers.
Prenatal diagnosis 1995;15(9):817-26.
1995: Susan A Slaugenhaupt; Anat Blumenfeld; CB Liebert; James Mull; D E Lucente; M Monahan; Xandra O Breakefield; Channa Maayan; L Parada; Felicia B Axelrod
The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene.
Genomics 1995;25(3):730-2.
1995: Anat Blumenfeld; Felicia B Axelrod; V Tamper; Channa Maayan
[Localization of the familial dysautonomia gene to chromosome 9q31-33 and the development of a genetic test for the disease].
Harefuah 1995;128(2):97-100.
1995: Anat Blumenfeld; D E Lucente; J A Trofatter; Terry J Lerner; Susan A Slaugenhaupt; CB Liebert; M Monahan; Jonathan L Haines; James Gusella; Xandra O Breakefield; L M Parysek
Peripherin gene is linked to keratin 18 gene on human chromosome 12.
Somatic cell and molecular genetics 1995;21(1):83-8.
1993: Anat Blumenfeld; Susan A Slaugenhaupt; Felicia B Axelrod; D E Lucente; Channa Maayan; CB Liebert; Laurie J Ozelius; J A Trofatter; Jonathan L Haines; Xandra O Breakefield
Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis.
Nature genetics 1993;4(2):160-4.
1993: Anat Blumenfeld; Felicia B Axelrod; J A Trofatter; Channa Maayan; D E Lucente; Susan A Slaugenhaupt; CB Liebert; Laurie J Ozelius; Jonathan L Haines; Xandra O Breakefield
Exclusion of familial dysautonomia from more than 60% of the genome.
Journal of medical genetics 1993;30(1):47-52.