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Alfred Nobel
www.bibalex.org/bioalex2004conf The BioVisionAlexandria 2004 Conference Newsletter November 2003 Volume 1, Issue 2 BioVisionAlexandria ALFRED NOBEL 2004 aims to celebrate the The inventor, the industrialist outstanding scientists and scholars, in a he Nobel Prize is one of the highest distinctions recognized, granting its winner century dominated by instant fame. However, many do not know the interesting history and background technological and T that led to this award. scientific revolutions, through its It all began with a chemist, known as Alfred Nobel, born in Stockholm, Sweden in 1833. Nobel Day on 3 April Alfred Nobel moved to Russia when he was eight, where his father, Immanuel Nobel, 2004! started a successful mechanical workshop. He provided equipment for the Russian Army and designed naval mines, which effectively prevented the British Royal Navy from moving within firing range of St. Petersburg during the Crimean War. Immanuel Nobel was also a pioneer in the manufacture of arms, and in designing steam engines. INSIDE Scientific awards .........3 Immanuel’s success enabled him to Alfred met Ascanio Sobrero, the Italian Confirmed laureates ....4 Lady laureates ............7 provide his four sons with an excellent chemist who had invented Nitroglycerine education in natural sciences, languages three years earlier. Nitroglycerine, a and literature. Alfred, at an early age, highly explosive liquid, was produced by acquired extensive literary knowledge, mixing glycerine with sulfuric and nitric mastering many foreign languages. His acid. It was an invention that triggered a Nobel Day is interest in science, especially chemistry, fascination in the young scientist for many dedicated to many of was also apparent. -
Female Fellows of the Royal Society
Female Fellows of the Royal Society Professor Jan Anderson FRS [1996] Professor Ruth Lynden-Bell FRS [2006] Professor Judith Armitage FRS [2013] Dr Mary Lyon FRS [1973] Professor Frances Ashcroft FMedSci FRS [1999] Professor Georgina Mace CBE FRS [2002] Professor Gillian Bates FMedSci FRS [2007] Professor Trudy Mackay FRS [2006] Professor Jean Beggs CBE FRS [1998] Professor Enid MacRobbie FRS [1991] Dame Jocelyn Bell Burnell DBE FRS [2003] Dr Philippa Marrack FMedSci FRS [1997] Dame Valerie Beral DBE FMedSci FRS [2006] Professor Dusa McDuff FRS [1994] Dr Mariann Bienz FMedSci FRS [2003] Professor Angela McLean FRS [2009] Professor Elizabeth Blackburn AC FRS [1992] Professor Anne Mills FMedSci FRS [2013] Professor Andrea Brand FMedSci FRS [2010] Professor Brenda Milner CC FRS [1979] Professor Eleanor Burbidge FRS [1964] Dr Anne O'Garra FMedSci FRS [2008] Professor Eleanor Campbell FRS [2010] Dame Bridget Ogilvie AC DBE FMedSci FRS [2003] Professor Doreen Cantrell FMedSci FRS [2011] Baroness Onora O'Neill * CBE FBA FMedSci FRS [2007] Professor Lorna Casselton CBE FRS [1999] Dame Linda Partridge DBE FMedSci FRS [1996] Professor Deborah Charlesworth FRS [2005] Dr Barbara Pearse FRS [1988] Professor Jennifer Clack FRS [2009] Professor Fiona Powrie FRS [2011] Professor Nicola Clayton FRS [2010] Professor Susan Rees FRS [2002] Professor Suzanne Cory AC FRS [1992] Professor Daniela Rhodes FRS [2007] Dame Kay Davies DBE FMedSci FRS [2003] Professor Elizabeth Robertson FRS [2003] Professor Caroline Dean OBE FRS [2004] Dame Carol Robinson DBE FMedSci -
FORMATO PDF Ranking Instituciones No Acadã©Micas Por Sub Ã
Ranking Instituciones No Académicas por sub área OCDE 2020 3. Ciencias Médicas y de la Salud > 3.02 Medicina Clínica PAÍS INSTITUCIÓN RANKING PUNTAJE USA VA Boston Healthcare System 1 5,000 FRANCE Assistance Publique Hopitaux Paris (APHP) 2 5,000 USA UTMD Anderson Cancer Center 3 5,000 USA Mayo Clinic 4 5,000 USA Memorial Sloan Kettering Cancer Center 5 5,000 USA Dana-Farber Cancer Institute 6 5,000 USA Massachusetts General Hospital 7 5,000 FRANCE Institut National de la Sante et de la Recherche Medicale (Inserm) 8 5,000 USA National Institutes of Health (NIH) - USA 9 5,000 FRANCE UNICANCER 10 5,000 USA Harvard School of Dental Medicine 11 5,000 CANADA University Health Network Toronto 12 5,000 USA Cleveland Clinic Foundation 13 5,000 USA Johns Hopkins Medicine 14 5,000 FRANCE Gustave Roussy 15 5,000 NETHERLANDS Erasmus University Medical Center 16 5,000 GERMANY Helmholtz Association 17 5,000 NETHERLANDS Academic Medical Center Amsterdam 18 5,000 SPAIN CIBER - Centro de Investigacion Biomedica en Red 19 5,000 USA Beth Israel Deaconess Medical Center 20 5,000 SWITZERLAND Roche Holding 21 5,000 CANADA Princess Margaret Cancer Centre 22 5,000 USA H Lee Moffitt Cancer Center & Research Institute 23 5,000 SPAIN Hospital Universitari Vall d'Hebron 24 5,000 BELGIUM University Hospital Leuven 25 5,000 USA NIH National Cancer Institute (NCI) 26 5,000 SPAIN Hospital Clinic de Barcelona 27 5,000 USA Bristol-Myers Squibb 28 5,000 USA Merck & Company 29 5,000 UNITED KINGDOM Royal Marsden NHS Foundation Trust 30 5,000 SOUTH KOREA Seoul National University -
2004 Albert Lasker Nomination Form
albert and mary lasker foundation 110 East 42nd Street Suite 1300 New York, ny 10017 November 3, 2003 tel 212 286-0222 fax 212 286-0924 Greetings: www.laskerfoundation.org james w. fordyce On behalf of the Albert and Mary Lasker Foundation, I invite you to submit a nomination Chairman neen hunt, ed.d. for the 2004 Albert Lasker Medical Research Awards. President mrs. anne b. fordyce The Awards will be offered in three categories: Basic Medical Research, Clinical Medical Vice President Research, and Special Achievement in Medical Science. This is the 59th year of these christopher w. brody Treasurer awards. Since the program was first established in 1944, 68 Lasker Laureates have later w. michael brown Secretary won Nobel Prizes. Additional information on previous Lasker Laureates can be found jordan u. gutterman, m.d. online at our web site http://www.laskerfoundation.org. Representative Albert Lasker Medical Research Awards Program Nominations that have been made in previous years may be updated and resubmitted in purnell w. choppin, m.d. accordance with the instructions on page 2 of this nomination booklet. daniel e. koshland, jr., ph.d. mrs. william mccormick blair, jr. the honorable mark o. hatfied Nominations should be received by the Foundation no later than February 2, 2004. Directors Emeritus A distinguished panel of jurors will select the scientists to be honored. The 2004 Albert Lasker Medical Research Awards will be presented at a luncheon ceremony given by the Foundation in New York City on Friday, October 1, 2004. Sincerely, Joseph L. Goldstein, M.D. Chairman, Awards Jury Albert Lasker Medical Research Awards ALBERT LASKER MEDICAL2004 RESEARCH AWARDS PURPOSE AND DESCRIPTION OF THE AWARDS The major purpose of these Awards is to recognize and honor individuals who have made signifi- cant contributions in basic or clinical research in diseases that are the main cause of death and disability. -
NIH Public Access Author Manuscript Nat Genet
NIH Public Access Author Manuscript Nat Genet. Author manuscript; available in PMC 2013 October 01. NIH-PA Author ManuscriptPublished NIH-PA Author Manuscript in final edited NIH-PA Author Manuscript form as: Nat Genet. 2013 April ; 45(4): 371–384e2. doi:10.1038/ng.2566. Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer Stig E Bojesen1,2,*, Karen A Pooley3,*, Sharon E Johnatty4,*, Jonathan Beesley4,*, Kyriaki Michailidou3,*, Jonathan P Tyrer5,*, Stacey L Edwards6, Hilda A Pickett7,8, Howard C Shen9, Chanel E Smart10, Kristine M Hillman6, Phuong L Mai11, Kate Lawrenson9, Michael D Stutz7,8, Yi Lu4, Rod Karevan9, Nicholas Woods12, Rebecca L Johnston10, Juliet D French6, Xiaoqing Chen4, Maren Weischer1,2, Sune F Nielsen1,2, Melanie J Maranian5, Maya Ghoussaini5, Shahana Ahmed5, Caroline Baynes5, Manjeet K Bolla3, Qin Wang3, Joe Dennis3, Lesley McGuffog3, Daniel Barrowdale3, Andrew Lee3, Sue Healey4, Michael Lush3, Daniel C Tessier13,14, Daniel Vincent13,14, Françis Bacot13,14, Study Group members15, Ignace Vergote16,17, Sandrina Lambrechts16,17, Evelyn Despierre16,17, Harvey A Risch18, Anna González-Neira19, Mary Anne Rossing20,21, Guillermo Pita19, Jennifer A Doherty22, Nuria Álvarez19, Melissa C Larson23, Brooke L Fridley23, Nils Schoof24, Jenny Chang- Claude25, Mine S Cicek26, Julian Peto27, Kimberly R Kalli28, Annegien Broeks29, Sebastian M Armasu23, Marjanka K Schmidt29,30, Linde M Braaf29, Boris Winterhoff31, Heli Nevanlinna32, Gottfried E Konecny33, Diether Lambrechts34,35, -
KIF1A-Related Autosomal Dominant Spastic Paraplegias (SPG30) in Russian Families G
Rudenskaya et al. BMC Neurology (2020) 20:290 https://doi.org/10.1186/s12883-020-01872-4 RESEARCH ARTICLE Open Access KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian families G. E. Rudenskaya1 , V. A. Kadnikova1* , O. P. Ryzhkova1 , L. A. Bessonova1, E. L. Dadali1 , D. S. Guseva1 , T. V. Markova1 , D. N. Khmelkova2 and A. V. Polyakov1 Abstract Background: Spastic paraplegia type 30 (SPG30) caused by KIF1A mutations was first reported in 2011 and was initially considered a very rare autosomal recessive (AR) form. In the last years, thanks to the development of massive parallel sequencing, SPG30 proved to be a rather common autosomal dominant (AD) form of familial or sporadic spastic paraplegia (SPG),, with a wide range of phenotypes: pure and complicated. The aim of our study is to detect AD SPG30 cases and to examine their molecular and clinical characteristics for the first time in the Russian population. Methods: Clinical, genealogical and molecular methods were used. Molecular methods included massive parallel sequencing (MPS) of custom panel ‘spastic paraplegias’ with 62 target genes complemented by familial Sanger sequencing. One case was detected by the whole -exome sequencing. Results: AD SPG30 was detected in 10 unrelated families, making it the 3rd (8.4%) most common SPG form in the cohort of 118 families. No AR SPG30 cases were detected. In total, 9 heterozygous KIF1A mutations were detected, with 4 novel and 5 known mutations. All the mutations were located within KIF1A motor domain. Six cases had pure phenotypes, of which 5 were familial, where 2 familial cases demonstrated incomplete penetrance, early onset and slow relatively benign SPG course. -
Dimerization of Mammalian Kinesin-3 Motors Results in Superprocessive Motion
Dimerization of mammalian kinesin-3 motors results in superprocessive motion Virupakshi Soppinaa,1, Stephen R. Norrisa,b, Aslan S. Dizajia, Matt Kortusa, Sarah Veatchb, Michelle Peckhamc, and Kristen J. Verheya,1 aDepartment of Cell and Developmental Biology, University of Michigan Medical School, Ann Arbor, MI 48109; bDepartment of Biophysics, University of Michigan, Ann Arbor, MI 48109; and cSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, United Kingdom Edited by J. Richard McIntosh, University of Colorado, Boulder, CO, and approved March 7, 2014 (received for review January 15, 2014) The kinesin-3 family is one of the largest among the kinesin Defects in kinesin-3 transport have been implicated in a wide superfamily and its members play important roles in a wide range variety of neurodegenerative, developmental, and cancer dis- of cellular transport activities, yet the molecular mechanisms of eases (22). However, a mechanistic understanding of this im- kinesin-3 regulation and cargo transport are largely unknown. portant class of cellular transporters is currently limited. We performed a comprehensive analysis of mammalian kinesin-3 To date, mechanistic studies have focused on truncated ver- motors from three different subfamilies (KIF1, KIF13, and KIF16). sions of mammalian KIF1A and its homolog CeUNC-104, and Using Forster resonance energy transfer microscopy in live cells, these studies have yielded contradictory results (23). For exam- we show for the first time to our knowledge that KIF16B motors ple, murine KIF1A has been proposed to function as a monomer undergo cargo-mediated dimerization. The molecular mechanisms that diffuses along the microtubule surface or as a processive dimer. -
A Conversation with Caroline Dean
A Conversation with Caroline Dean INTERVIEWER:JAN WITKOWSKI Cold Spring Harbor Laboratory Dame Caroline Dean, DBE, FRS is a Group Leader and Royal Society Professor in the Department of Cell and Developmental Biology at the John Innes Centre. Jan Witkowski: Can you give me an overview of your scripts are made constitutively at a low level but are work and how you came to do this? strongly induced by low temperature. We’ve looked at how they’re cold-induced, and it involves a promoter Dr. Dean: My lab works on how plants know when region that aligns with the end of the sense transcript. to flower, so I got into this wonderful world of chroma- This promoter is stimulated by cold temperature in a tin and RNA through quite an unintentional route. process involving a chromatin structure called an R- Many years ago I went back to the U.K., having been loop, where the antisense RNA invades the chromatin. a postdoc in the U.S., and decided seasonal timing was How that is regulated by temperature, we still don’t really interesting. The place I live in—Norwich—has know. fairly distinct winters and in spring we have this won- derful bloom. The question is, how is flowering so Jan Witkowski: Are there parallels with regulation in synchronized? other organisms? My lab decided to study the molecular control of flow- ering, focusing on how plants decide whether to overwin- Dr. Dean: ter before flowering, and how they perceive winter. The The parallel that I like to follow is the RNA- many genetic routes we used to study these questions led mediated chromatin silencing mechanism from Rob Mar- ’ ’ us into the study of one gene. -
EMBO Facts & Figures
excellence in life sciences Reykjavik Helsinki Oslo Stockholm Tallinn EMBO facts & figures & EMBO facts Copenhagen Dublin Amsterdam Berlin Warsaw London Brussels Prague Luxembourg Paris Vienna Bratislava Budapest Bern Ljubljana Zagreb Rome Madrid Ankara Lisbon Athens Jerusalem EMBO facts & figures HIGHLIGHTS CONTACT EMBO & EMBC EMBO Long-Term Fellowships Five Advanced Fellows are selected (page ). Long-Term and Short-Term Fellowships are awarded. The Fellows’ EMBO Young Investigators Meeting is held in Heidelberg in June . EMBO Installation Grants New EMBO Members & EMBO elects new members (page ), selects Young EMBO Women in Science Young Investigators Investigators (page ) and eight Installation Grantees Gerlind Wallon EMBO Scientific Publications (page ). Programme Manager Bernd Pulverer S Maria Leptin Deputy Director Head A EMBO Science Policy Issues report on quotas in academia to assure gender balance. R EMBO Director + + A Conducts workshops on emerging biotechnologies and on H T cognitive genomics. Gives invited talks at US National Academy E IC of Sciences, International Summit on Human Genome Editing, I H 5 D MAN 201 O N Washington, DC.; World Congress on Research Integrity, Rio de A M Janeiro; International Scienti c Advisory Board for the Centre for Eilish Craddock IT 2 015 Mammalian Synthetic Biology, Edinburgh. Personal Assistant to EMBO Fellowships EMBO Scientific Publications EMBO Gold Medal Sarah Teichmann and Ido Amit receive the EMBO Gold the EMBO Director David del Álamo Thomas Lemberger Medal (page ). + Programme Manager Deputy Head EMBO Global Activities India and Singapore sign agreements to become EMBC Associate + + Member States. EMBO Courses & Workshops More than , participants from countries attend 6th scienti c events (page ); participants attend EMBO Laboratory Management Courses (page ); rst online course EMBO Courses & Workshops recorded in collaboration with iBiology. -
Supplementary Table S4. FGA Co-Expressed Gene List in LUAD
Supplementary Table S4. FGA co-expressed gene list in LUAD tumors Symbol R Locus Description FGG 0.919 4q28 fibrinogen gamma chain FGL1 0.635 8p22 fibrinogen-like 1 SLC7A2 0.536 8p22 solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 DUSP4 0.521 8p12-p11 dual specificity phosphatase 4 HAL 0.51 12q22-q24.1histidine ammonia-lyase PDE4D 0.499 5q12 phosphodiesterase 4D, cAMP-specific FURIN 0.497 15q26.1 furin (paired basic amino acid cleaving enzyme) CPS1 0.49 2q35 carbamoyl-phosphate synthase 1, mitochondrial TESC 0.478 12q24.22 tescalcin INHA 0.465 2q35 inhibin, alpha S100P 0.461 4p16 S100 calcium binding protein P VPS37A 0.447 8p22 vacuolar protein sorting 37 homolog A (S. cerevisiae) SLC16A14 0.447 2q36.3 solute carrier family 16, member 14 PPARGC1A 0.443 4p15.1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha SIK1 0.435 21q22.3 salt-inducible kinase 1 IRS2 0.434 13q34 insulin receptor substrate 2 RND1 0.433 12q12 Rho family GTPase 1 HGD 0.433 3q13.33 homogentisate 1,2-dioxygenase PTP4A1 0.432 6q12 protein tyrosine phosphatase type IVA, member 1 C8orf4 0.428 8p11.2 chromosome 8 open reading frame 4 DDC 0.427 7p12.2 dopa decarboxylase (aromatic L-amino acid decarboxylase) TACC2 0.427 10q26 transforming, acidic coiled-coil containing protein 2 MUC13 0.422 3q21.2 mucin 13, cell surface associated C5 0.412 9q33-q34 complement component 5 NR4A2 0.412 2q22-q23 nuclear receptor subfamily 4, group A, member 2 EYS 0.411 6q12 eyes shut homolog (Drosophila) GPX2 0.406 14q24.1 glutathione peroxidase -
Summary Publication and Bibliometric Information: Total Number of Peer-Reviewed Publications: 15
CV Andreas Sebastian Marquardt Education: 16/7/2010 Ph. D. in Biological Sciences, University of East Anglia, Norwich, UK. 2005 Diplom (M. Sc.) in Biochemistry, Free University Berlin, Berlin, Germany. 2002-2005 Undergraduate studies in Biochemistry at Free University Berlin, Berlin, Germany. 1999-2002 Undergraduate studies in Biochemistry at University of Tübingen, Tübingen, Germany. Employment: Jan. 2018 – Tenured Associate Professor, University of Copenhagen, Copenhagen Plant Science Centre (CPSC), Denmark. Leader of non-coding transcription group. 2015 - 2017 Assistant Professor, University of Copenhagen, Copenhagen Plant Science Centre (CPSC), Denmark. Leader of non-coding transcription group. 2012 - 2014 Visiting Scientist at Whitehead Institute for Biomedical Research, MIT, Cambridge, USA. Topic: Arabidopsis epigenetics & Pol II kinetics, with Prof. Mary Gehring. 2010 - 2014 Postdoc at the Harvard Medical School (HMS), Boston, USA. Topic: chromatin-based lncRNA repression in budding yeast with Prof. Steve Buratowski. 2006 - 2009 Ph. D. thesis research with Prof. Caroline Dean at John Innes Centre (JIC), Norwich, UK. Topic: lncRNA-mediated chromatin regulation of Arabidopsis flowering. 2005-2006 Ph. D. rotation projects with: Prof. David Baulcombe, Dr. Sean Walsh and Prof. Caroline Dean. 2004-2005 Diplom thesis research with Prof. Arp Schnittger at Max-Planck Institute (MPI) for Plant Breeding Research, Cologne, Germany. Summary publication and bibliometric information: Total number of peer-reviewed publications: 15. First author publications: 6 (e.g. Science, Cell, Mol. Cell). Corresponding author publications: 5 (e.g. Nat. Commun, eLife, PLoS Gen). Last author publications: 5 (e.g. Nat. Commun, eLife, PLoS Gen). Citations: 1309 source, H-index: 21: https://scholar.google.com/citations?user=_miZw7oAAAAJ&hl=en ). -
Natural Variants in C. Elegans Atg-5 3'UTR Uncover Divergent Effects of Autophagy on Polyglutamine Aggregation in Different Tissues
bioRxiv preprint doi: https://doi.org/10.1101/670042; this version posted June 13, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Natural variants in C. elegans atg-5 3'UTR uncover divergent effects of autophagy on polyglutamine aggregation in different tissues Alexander-Floyd J1, Haroon S2, Ying M1, Entezari AA1,3, Jaeger C1,4, Vermulst M2,5, Gidalevitz T1,#. 1 Biology Department, Drexel University, Philadelphia, PA 19104 2 Department of Pathology and Laboratory Medicine, Children’s Hospital of Philadelphia, Philadelphia, PA 19104 3Current address: Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA 19107 4Current address: Department of Neuroradiology, Technical University of Munich, Munich, Germany TUM-Neuroimaging Center, Technical University of Munich, Munich, Germany 5Current address: Leonard Davis School of Gerontology, University of Southern California, Los Angeles, CA 90089 # Corresponding author. Address correspondence to T.G. ([email protected]) Short title: Divergent effects of autophagy on polyglutamine aggregation in different tissues bioRxiv preprint doi: https://doi.org/10.1101/670042; this version posted June 13, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Abstract Diseases caused by protein misfolding and aggregation, in addition to cell selectivity, often exhibit variation among individuals in the age of onset, progression, and severity of disease.