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Papers authored by Jakobs P

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Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.

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Hemphill AW, Akkari Y, Newell AH, Schultz RA, Grompe M, North PS, Hickson ID, Jakobs PM, Rennie S, Pauw D, Hejna J, Olson SB, and Moses RE

Cytogenetic and genome research 125(3):165-75, 2009 - Who cited this? | PubMed ID: 19738377 | Fulltext

ERCC1 is required for FANCD2 focus formation.

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McCabe KM, Hemphill A, Akkari Y, Jakobs PM, Pauw D, Olson SB, Moses RE, and Grompe M

Molecular genetics and metabolism, 2008 Jul 29 - Who cited this? | PubMed ID: 18672388 | Fulltext

Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy.

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Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Peterson A, Li D, Jakobs P, Litt M, Porter CB, Rahko PS, and Hershberger RE

American heart journal 156(1):161, 2008 Jul - Who cited this? | PubMed ID: 18585512 | Fulltext

Role for DNA Polymerase {kappa} in the Processing of N2-N2-Guanine Interstrand Cross-links.

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Minko IG, Harbut MB, Kozekov ID, Kozekova A, Jakobs PM, Olson SB, Moses RE, Harris TM, Rizzo CJ, and Lloyd RS

The Journal of biological chemistry 283(25):17075, 2008 Jun 20 - Who cited this? | PubMed ID: 18434313 | Fulltext

Tolerability and safety profile of 12- to 28-week treatment with interferon beta-1b 250 and 500 microg QOD in patients with relapsing-remitting multiple sclerosis: A multicenter, randomized, double-blind, parallel-group pilot study.

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Hurwitz BJ, Jeffery D, Arnason B, Bigley K, Coyle P, Goodin D, Kaba S, Kirzinger S, Lynch S, Mandler R, Mikol D, Rammohan K, Sater R, Sriram S, Thrower B, Boateng F,

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Clinical therapeutics 30(6):1102, 2008 Jun - Who cited this? | PubMed ID: 18640466 | Fulltext

Mammalian SNM1 is required for genome stability.

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Hemphill AW, Bruun D, Thrun L, Akkari Y, Torimaru Y, Hejna K, Jakobs PM, Hejna J, Jones S, Olson SB, and Moses RE

Molecular genetics and metabolism 94(1):38-45, 2008 May - Who cited this? | PubMed ID: 18180189 | Fulltext

Mutations of presenilin genes in dilated cardiomyopathy and heart failure.

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Li D, Parks SB, Kushner JD, Nauman D, Burgess D, Ludwigsen S, Partain J, Nixon RR, Allen CN, Irwin RP, Jakobs PM, Litt M, and Hershberger RE

American journal of human genetics 79(6):1030-9, 2006 Dec - Who cited this? | PubMed ID: 17186461 | Fulltext

Blockade of chemokine signaling in patients with multiple sclerosis.

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Zipp F, Hartung HP, Hillert J, Schimrigk S, Trebst C, Stangel M, Infante-Duarte C, Jakobs P, Wolf C, Sandbrink R, Pohl C, Filippi M, and CCR1 Antagonist Study Group

Neurology 67(10):1880-3, 2006 Nov 28 - Who cited this? | PubMed ID: 17130431 | Fulltext

Treatment with interferon beta-1b delays conversion to clinically definite and McDonald MS in patients with clinically isolated syndromes.

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Kappos L, Polman CH, Freedman MS, Edan G, Hartung HP, Miller DH, Montalban X, Barkhof F, Bauer L, Jakobs P, Pohl C, and Sandbrink R

Neurology 67(7):1242-9, 2006 Oct 10 - Who cited this? | PubMed ID: 16914693 | Fulltext

Fifty-four new gene-based canine microsatellite markers.

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Litt M, Bestwick ML, Winther MJ, and Jakobs PM

The Journal of heredity 96(7):843-6, 2005 - Who cited this? | PubMed ID: 15958789 | Fulltext

Oral interferon beta-1a in relapsing-remitting multiple sclerosis: a double-blind randomized study.

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Polman C, Barkhof F, Kappos L, Pozzilli C, Sandbrink R, Dahlke F, Jakobs P, Lorenz A, and European Oral Interferon Beta-1a in Relapsing-Remitting MS Study Group

Multiple sclerosis (Houndmills, Basingstoke, England) 9(4):342-8, 2003 Aug - Who cited this? | PubMed ID: 12926838 | Fulltext

Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia.

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Lensch MW, Tischkowitz M, Christianson TA, Reifsteck CA, Speckhart SA, Jakobs PM, O'Dwyer ME, Olson SB, Le Beau MM, Hodgson SV, Mathew CG, Larson RA, and Bagby GC

Blood 102(1):7-16, 2003 Jul 1 - Who cited this? | PubMed ID: 12637330 | Fulltext

A novel lamin A/C mutation in a family with dilated cardiomyopathy, prominent conduction system disease, and need for permanent pacemaker implantation.

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Hershberger RE, Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, and Litt M

American heart journal 144(6):1081-6, 2002 Dec - Who cited this? | PubMed ID: 12486434 | Fulltext

Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy.

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Hanson EL, Jakobs PM, Keegan H, Coates K, Bousman S, Dienel NH, Litt M, and Hershberger RE

Journal of cardiac failure 8(1):28-32, 2002 Feb - Who cited this? | PubMed ID: 11862580 | Fulltext

Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease.

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Jakobs PM, Hanson EL, Crispell KA, Toy W, Keegan H, Schilling K, Icenogle TB, Litt M, and Hershberger RE

Journal of cardiac failure 7(3):249-56, 2001 Sep - Who cited this? | PubMed ID: 11561226 | Fulltext

Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3.

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Hejna JA, Timmers CD, Reifsteck C, Bruun DA, Lucas LW, Jakobs PM, Toth-Fejel S, Unsworth N, Clemens SL, Garcia DK, Naylor SL, Thayer MJ, Olson SB, Grompe M, and Moses RE

American journal of human genetics 66(5):1540-51, 2000 May - Who cited this? | PubMed ID: 10762542 | Fulltext

Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2.

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Jakobs PM, Hess JF, FitzGerald PG, Kramer P, Weleber RG, and Litt M

American journal of human genetics 66(4):1432-6, 2000 Apr - Who cited this? | PubMed ID: 10739768 | Fulltext

Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome.

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Jakobs PM, Smith L, Thayer M, and Grompe M

Mammalian genome : official journal of the International Mammalian Genome Society 10(4):381-4, 1999 Apr - Who cited this? | PubMed ID: 10087297 | Fulltext

Subtyping analysis of Fanconi anemia by immunoblotting and retroviral gene transfer.

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Pulsipher M, Kupfer GM, Naf D, Suliman A, Lee JS, Jakobs P, Grompe M, Joenje H, Sieff C, Guinan E, Mulligan R, and D'Andrea AD

Molecular medicine (Cambridge, Mass.) 4(7):468-79, 1998 Jul - Who cited this? | PubMed ID: 9713825 | Fulltext

[Total quality management: a big bluff?. Quality procedures: more sham than truth].

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Jakobs P

Krankenpflege. Soins infirmiers 90(1):1-3, 1997 Jan - Who cited this? | PubMed ID: 9069894 | Fulltext

Complementation group assignments in Fanconi anemia fibroblast cell lines from North America.

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Jakobs PM, Fiddler-Odell E, Reifsteck C, Olson S, Moses RE, and Grompe M

Somatic cell and molecular genetics 23(1):1-7, 1997 Jan - Who cited this? | PubMed ID: 9217996 | Fulltext

Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure.

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Jakobs PM, Sahaayaruban P, Saito H, Reifsteck C, Olson S, Joenje H, Moses RE, and Grompe M

Somatic cell and molecular genetics 22(2):151-7, 1996 Mar - Who cited this? | PubMed ID: 8782494 | Fulltext

[Analysis of regional differences in hospitalization rate and length of stay costs].

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Swart E, Böhlert I, Jakobs P, Robra BP, Schneider F, Leber WD, and Dembski U

Gesundheitswesen (Bundesverband der Arzte des Offentlichen Gesundheitsdienstes (Germany)) 58(1):10-5, 1996 Jan - Who cited this? | PubMed ID: 8851126 | Fulltext

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p.

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Whitney M, Thayer M, Reifsteck C, Olson S, Smith L, Jakobs PM, Leach R, Naylor S, Joenje H, and Grompe M

Nature genetics 11(3):341-3, 1995 Nov - Who cited this? | PubMed ID: 7581463 | Fulltext

Cloning and characterization of a human cDNA (INPPL1) sharing homology with inositol polyphosphate phosphatases.

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Hejna JA, Saito H, Merkens LS, Tittle TV, Jakobs PM, Whitney MA, Grompe M, Friedberg AS, and Moses RE

Genomics 29(1):285-7, 1995 Sep 1 - Who cited this? | PubMed ID: 8530088 | Fulltext

Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism.

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Quan F, Grompe M, Jakobs P, and Popovich BW

Human molecular genetics 4(9):1681-4, 1995 Sep - Who cited this? | PubMed ID: 8541863 | Fulltext

Fanconi anemia cells have a normal gene structure for topoisomerase I.

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Saito H, Grompe M, Neeley TL, Jakobs PM, and Moses RE

Human genetics 93(5):583-6, 1994 May - Who cited this? | PubMed ID: 8168839 | Fulltext

The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population.

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Whitney MA, Jakobs P, Kaback M, Moses RE, and Grompe M

Human mutation 3(4):339-41, 1994 - Who cited this? | PubMed ID: 8081385 | Fulltext

Sarcoplasmic reticulum calcium ATPase. Labeling of a putative Mg2+ site by reaction with a carbodiimide and a spin-label.

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Coan C, Jakobs P, Ji JY, and Murphy AJ

FEBS letters 335(1):33-6, 1993 Nov 29 - Who cited this? | PubMed ID: 7902300 | Fulltext

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews.

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Whitney MA, Saito H, Jakobs PM, Gibson RA, Moses RE, and Grompe M

Nature genetics 4(2):202-5, 1993 Jun - Who cited this? | PubMed ID: 8348157 | Fulltext

Binding of ATP to uncoupling protein of brown fat mitochondria as studied by means of spin-labeled ATP derivatives.

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Jakobs P, Braun A, Jezek P, and Trommer WE

FEBS letters 284(2):195-8, 1991 Jun 24 - Who cited this? | PubMed ID: 1647981 | Fulltext

Synthesis of spin-labeled 2-azido-ATP: evidence for distinct nucleotide-binding sites in calcium pump protein from sarcoplasmic reticulum.

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Jakobs P, Sauer HE, McIntyre JO, Fleischer S, and Trommer WE

FEBS letters 254(1-2):8-12, 1989 Aug 28 - Who cited this? | PubMed ID: 2550279 | Fulltext

[The therapy of tinnitus resulting from blast injury (author's transl)].

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Jakobs P and Martin G

HNO 26(3):104-6, 1978 Mar - Who cited this? | PubMed ID: 346541 | Fulltext

[The treatment of acute acoustic trauma (blast injury) with dextran 40 (author's transl)].

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Jakobs P and Martin G

HNO 25(10):349-52, 1977 Oct - Who cited this? | PubMed ID: 914661 | Fulltext

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