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Richard Swank

Research Profile

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Xuemei Guo; Liyu Tu; Iwona Gumper; Heide Plesken; Edward K Novak; Sreenivasulu Chintala; Richard T Swank; Gregory Pastores; Paola Torres; Tetsuro Izumi; Tung-Tien Sun; David D Sabatini; Gert Kreibich
Involvement of vps33a in the fusion of uroplakin-degrading multivesicular bodies with lysosomes.
Sreenivasulu Chintala; Edward K Novak; Joseph A Spernyak; richard mazurchuk; German Torres; Suchith Patel; Kristie Busch; Beth A Meeder; Judith M Horowitz; Mary M Vaughan; Richard T Swank
The Vps33a gene regulates behavior and cerebellar Purkinje cell number.
Sreenivasulu Chintala; Jian Tan; Rashi Gautam; Michael E Rusiniak; Xiaoli Guo; Wei Li; William A Gahl; Marjan Huizing; Richard A Spritz; Saunie Hutton; Edward K Novak; Richard T Swank
The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules.

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All Publications

2009: Xuemei Guo; Liyu Tu; Iwona Gumper; Heide Plesken; Edward K Novak; Sreenivasulu Chintala; Richard T Swank; Gregory Pastores; Paola Torres; Tetsuro Izumi; Tung-Tien Sun; David D Sabatini; Gert Kreibich
Involvement of vps33a in the fusion of uroplakin-degrading multivesicular bodies with lysosomes.
Traffic (Copenhagen, Denmark) 2009;10(9):1350-61.
2009: Sreenivasulu Chintala; Edward K Novak; Joseph A Spernyak; richard mazurchuk; German Torres; Suchith Patel; Kristie Busch; Beth A Meeder; Judith M Horowitz; Mary M Vaughan; Richard T Swank
The Vps33a gene regulates behavior and cerebellar Purkinje cell number.
Brain research 2009;1266():18-28.
2007: Sreenivasulu Chintala; Jian Tan; Rashi Gautam; Michael E Rusiniak; Xiaoli Guo; Wei Li; William A Gahl; Marjan Huizing; Richard A Spritz; Saunie Hutton; Edward K Novak; Richard T Swank
The Slc35d3 gene, encoding an orphan nucleotide sugar transporter, regulates platelet-dense granules.
Blood 2007;109(4):1533-40.
2006: Rashi Gautam; Edward K Novak; Jian Tan; Kazumasa Wakamatsu; Shosuke Ito; Richard T Swank
Interaction of Hermansky-Pudlak Syndrome genes in the regulation of lysosome-related organelles.
Traffic (Copenhagen, Denmark) 2006;7(7):779-92.
2005: Sreenivasulu Chintala; Wei Li; M Lynn Lamoreux; Shosuke Ito; Kazumasa Wakamatsu; Elena V Sviderskaya; Dorothy C Bennett; Young-Mee Park; William A Gahl; Marjan Huizing; Richard A Spritz; Songtao Ben; Edward K Novak; Jian Tan; Richard T Swank
Slc7a11 gene controls production of pheomelanin pigment and proliferation of cultured cells.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(31):10964-9.
2005: Susan H Guttentag; Amana Akhtar; Jian-Qin Tao; Elena N Atochina; Michael E Rusiniak; Richard T Swank; Sandra R Bates
Defective surfactant secretion in a mouse model of Hermansky-Pudlak syndrome.
American journal of respiratory cell and molecular biology 2005;33(1):14-21.
2004: Wei Li; Michael E Rusiniak; Sreenivasulu Chintala; Rashi Gautam; Edward K Novak; Richard T Swank
Murine Hermansky-Pudlak syndrome genes: regulators of lysosome-related organelles.
BioEssays : news and reviews in molecular, cellular and developmental biology 2004;26(6):616-28.
2004: Rashi Gautam; Sreenivasulu Chintala; Wei Li; Qing Zhang; Jian Tan; Edward K Novak; Santiago M Di Pietro; Esteban C Dell'Angelica; Richard T Swank
The Hermansky-Pudlak syndrome 3 (cocoa) protein is a component of the biogenesis of lysosome-related organelles complex-2 (BLOC-2).
The Journal of biological chemistry 2004;279(13):12935-42.
2003: Sanjay Tiwari; Joseph E Italiano; Duarte C Barral; Emilie H Mules; Edward K Novak; Richard T Swank; Miguel C Seabra; Ramesh A Shivdasani
A role for Rab27b in NF-E2-dependent pathways of platelet formation.
Blood 2003;102(12):3970-9.
2003: Wei Li; Qing Zhang; Naoki Oiso; Edward K Novak; Rashi Gautam; Edward P O'Brien; Caroline L Tinsley; Derek J Blake; Richard A Spritz; Neal G Copeland; Nancy A Jenkins; Dominick Amato; Bruce A Roe; Marta Starcevic; Esteban C Dell'Angelica; Rosemary W Elliott; Vishnu Mishra; Stephen Kingsmore; Richard Paylor; Richard T Swank
Hermansky-Pudlak syndrome type 7 (HPS-7) results from mutant dysbindin, a member of the biogenesis of lysosome-related organelles complex 1 (BLOC-1).
Nature genetics 2003;35(1):84-9.
2003: Timothy A Lyerla; Michael E Rusiniak; Michael T Borchers; Gerald Jahreis; Jian Tan; Patricia Ohtake; Edward K Novak; Richard T Swank
Aberrant lung structure, composition, and function in a murine model of Hermansky-Pudlak syndrome.
American journal of physiology. Lung cellular and molecular physiology 2003;285(3):L643-53.
2003: Pei-Wen Chiang; Naoki Oiso; Rashi Gautam; Tamio Suzuki; Richard T Swank; Richard A Spritz
The Hermansky-Pudlak syndrome 1 (HPS1) and HPS4 proteins are components of two complexes, BLOC-3 and BLOC-4, involved in the biogenesis of lysosome-related organelles.
The Journal of biological chemistry 2003;278(22):20332-7.
2003: Tamio Suzuki; Naoki Oiso; Rashi Gautam; Edward K Novak; Jean-Jacques Panthier; P G Suprabha; Thomas Vida; Richard T Swank; Richard A Spritz
The mouse organellar biogenesis mutant buff results from a mutation in Vps33a, a homologue of yeast vps33 and Drosophila carnation.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(3):1146-50.
2003: Qing Zhang; Baohui Zhao; Wei Li; Naoki Oiso; Edward K Novak; Michael E Rusiniak; Rashi Gautam; Sreenivasulu Chintala; Edward P O'Brien; Yuke Zhang; Bruce A Roe; Rosemary W Elliott; Eva M Eicher; Ping Liang; Christian Kratz; Eric Legius; Richard A Spritz; T Norene O'Sullivan; Neal G Copeland; Nancy A Jenkins; Richard T Swank
Ru2 and Ru encode mouse orthologs of the genes mutated in human Hermansky-Pudlak syndrome types 5 and 6.
Nature genetics 2003;33(2):145-53.
2002: Thuyen Nguyen; Edward K Novak; Maryam Kermani; Joachim W Fluhr; Luanne L Peters; Richard T Swank; Maria L Wei
Melanosome morphologies in murine models of hermansky-pudlak syndrome reflect blocks in organelle development.
The Journal of investigative dermatology 2002;119(5):1156-64.
2002: Edward K Novak; Rashi Gautam; Madonna Reddington; Lucy M Collinson; Neal G Copeland; Nancy A Jenkins; Michael P McGarry; Richard T Swank
The regulation of platelet-dense granules by Rab27a in the ashen mouse, a model of Hermansky-Pudlak and Griscelli syndromes, is granule-specific and dependent on genetic background.
Blood 2002;100(1):128-35.
2002: Michael P McGarry; Michael T Borchers; Edward K Novak; Nancy A Lee; Patricia J Ohtake; James J Lee; Richard T Swank
Pulmonary pathologies in pallid mice result from nonhematopoietic defects.
Experimental and molecular pathology 2002;72(3):213-20.
2002: Qing Zhang; Lijie Zhen; Wei Li; Edward K Novak; Lucy M Collinson; Elliott K Jang; Richard J Haslam; Rosemary W Elliott; Richard T Swank
Cell-specific abnormal prenylation of Rab proteins in platelets and melanocytes of the gunmetal mouse.
British journal of haematology 2002;117(2):414-23.
2002: Qing Zhang; Wei Li; Edward K Novak; Amna Karim; Vishnu S Mishra; Stephen Kingsmore; Bruce A Roe; Tamio Suzuki; Richard T Swank
The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking.
Human molecular genetics 2002;11(6):697-706.
2002: Lijun Feng; Edward K Novak; Lisa M Hartnell; Juan Bonifacino; Lucy M Collinson; Richard T Swank
The Hermansky-Pudlak syndrome 1 (HPS1) and HPS2 genes independently contribute to the production and function of platelet dense granules, melanosomes, and lysosomes.
Blood 2002;99(5):1651-8.
2002: Tamio Suzuki; Wei Li; Qing Zhang; Amna Karim; Edward K Novak; Elena V Sviderskaya; Simon P Hill; Dorothy C Bennett; Alex V Levin; H Karel Nieuwenhuis; Chin-To Fong; Claudio Castellan; Bianca Miterski; Richard T Swank; Richard A Spritz
Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene.
Nature genetics 2002;30(3):321-4.
2001: Tamio Suzuki; W Li; Q Zhang; Edward K Novak; Elena V Sviderskaya; A Wilson; Dorothy C Bennett; B A Roe; Richard T Swank; Richard A Spritz
The gene mutated in cocoa mice, carrying a defect of organelle biogenesis, is a homologue of the human Hermansky-Pudlak syndrome-3 gene.
Genomics 2001;78(1-2):30-7.
2001: Yair Anikster; Marjan Huizing; J White; Yuriy Shevchenko; Diana L Fitzpatrick; Jeffrey W Touchman; John G Compton; Sherri J Bale; Richard T Swank; William A Gahl; JR Toro
Mutation of a new gene causes a unique form of Hermansky-Pudlak syndrome in a genetic isolate of central Puerto Rico.
Nature genetics 2001;28(4):376-80.
2000: Babette Gwynn; Steven L Ciciotte; S J Hunter; Linda L Washburn; Richard S Smith; Sabra G Andersen; Richard T Swank; Esteban C Dell'Angelica; Juan Bonifacino; Eva M Eicher; Luanne L Peters
Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky-Pudlak syndrome by an AP-3-independent mechanism.
Blood 2000;96(13):4227-35.
2000: Ashu Sharma; Edward K Novak; Hakimuddin T Sojar; Richard T Swank; Howard K Kuramitsu; Robert J Genco
Porphyromonas gingivalis platelet aggregation activity: outer membrane vesicles are potent activators of murine platelets.
Oral microbiology and immunology 2000;15(6):393-6.
2000: Wei Li; John C Detter; HJ Weiss; Elisabeth M Cramer; Qing Zhang; Edward K Novak; R Favier; Stephen Kingsmore; Richard T Swank
5'-UTR structural organization, transcript expression, and mutational analysis of the human Rab geranylgeranyl transferase alpha-subunit (RABGGTA) gene.
Molecular genetics and metabolism 2000;71(4):599-608.
2000: L Feng; Brian W Rigatti; Edward K Novak; Michael B Gorin; Richard T Swank
Genomic structure of the mouse Ap3b1 gene in normal and pearl mice.
Genomics 2000;69(3):370-9.
2000: Scott Michael Wilson; R Yip; Deborah A Swing; T Norene O'Sullivan; Y Zhang; Edward K Novak; Richard T Swank; L B Russell; Neal G Copeland; Nancy A Jenkins
A mutation in Rab27a causes the vesicle transport defects observed in ashen mice.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(14):7933-8.
2000: John C Detter; Qing Zhang; Emilie H Mules; Edward K Novak; Vishnu S Mishra; Wei Li; EB McMurtrie; Velizar T Tchernev; Margaret R Wallace; Miguel C Seabra; Richard T Swank; Stephen Kingsmore
Rab geranylgeranyl transferase alpha mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesis.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(8):4144-9.
2000: Richard T Swank; Edward K Novak; Michael P McGarry; Y Zhang; Wei Li; Qing Zhang; L Feng
Abnormal vesicular trafficking in mouse models of Hermansky-Pudlak syndrome.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 2000;13 Suppl 8():59-67.
1999: B Richards-Smith; Edward K Novak; Elliott K Jang; P He; Richard J Haslam; D Castle; S W Whiteheart; Richard T Swank
Analyses of proteins involved in vesicular trafficking in platelets of mouse models of Hermansky Pudlak syndrome.
Molecular genetics and metabolism 1999;68(1):14-23.
1999: Michael P McGarry; Madonna Reddington; C W Jackson; Lijie Zhen; Edward K Novak; Richard T Swank
Increased incidence and analysis of emperipolesis in megakaryocytes of the mouse mutant gunmetal.
Experimental and molecular pathology 1999;66(3):191-200.
1999: Lijie Zhen; S Jiang; L Feng; Nicholas A Bright; Andrew A Peden; A B Seymour; Edward K Novak; R Elliott; Michael B Gorin; Margaret S Robinson; Richard T Swank
Abnormal expression and subcellular distribution of subunit proteins of the AP-3 adaptor complex lead to platelet storage pool deficiency in the pearl mouse.
Blood 1999;94(1):146-55.
1999: W LI; Rosemary W Elliott; Edward K Novak; Richard T Swank
cDNA sequence and mapping of the mouse Copb gene encoding the beta subunit of the COPI coatomer complex.
Somatic cell and molecular genetics 1999;25(3):177-83.
1999: Michael P McGarry; Madonna Reddington; Edward K Novak; Richard T Swank
Survival and lung pathology of mouse models of Hermansky-Pudlak syndrome and Chediak-Higashi syndrome.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.) 1999;220(3):162-8.
1999: L Feng; A B Seymour; S Jiang; A To; Andrew A Peden; Edward K Novak; Lijie Zhen; Michael E Rusiniak; Eva M Eicher; Margaret S Robinson; Michael B Gorin; Richard T Swank
The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness.
Human molecular genetics 1999;8(2):323-30.
1998: M Faiyaz ul Haque; Lily M King; Deborah Krakow; R M Cantor; Michael E Rusiniak; Richard T Swank; andrea superti-furga; S Haque; H Abbas; Wasim Ahmad; M Ahmad; Daniel H Cohn
Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia and the brachymorphic mouse.
Nature genetics 1998;20(2):157-62.
1998: Richard T Swank; Edward K Novak; Michael P McGarry; Michael E Rusiniak; L Feng
Mouse models of Hermansky Pudlak syndrome: a review.
Pigment cell research / sponsored by the European Society for Pigment Cell Research and the International Pigment Cell Society 1998;11(2):60-80.
1998: Elena V Sviderskaya; Edward K Novak; Richard T Swank; Dorothy C Bennett
The murine misty mutation: phenotypic effects on melanocytes, platelets and brown fat.
Genetics 1998;148(1):381-90.
1997: JM Gardner; Scott C Wildenberg; N M Keiper; Edward K Novak; Michael E Rusiniak; Richard T Swank; N Puri; J N Finger; Nobuko Hagiwara; AL Lehman; TL Gales; M E Bayer; Richard A King; Murray H Brilliant
The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(17):9238-43.
1997: Craig A Jones; N Petrovic; Edward K Novak; Richard T Swank; Curt D Sigmund; Kenneth W Gross
Biosynthesis of renin in mouse kidney tumor As4.1 cells.
European journal of biochemistry / FEBS 1997;243(1-2):181-90.
1996: Karen L Mohlke; William C Nichols; Randal J Westrick; Edward K Novak; Kathleen Cooney; Richard T Swank; David Ginsburg
A novel modifier gene for plasma von Willebrand factor level maps to distal mouse chromosome 11.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(26):15352-7.
1996: Christophe Poirier; E P O'Brien; A L Bueno Brunialti; J Chambard; Richard T Swank; Jean-Louis Guénet
The gene encoding the thrombin receptor (Cf2r) maps to mouse chromosome 13.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(4):322.
1996: E P O'Brien; Lijie Zhen; S Y Jiang; Edward K Novak; Richard T Swank
High-resolution genetic mapping of the gunmetal gene which regulates platelet production.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(3):206-8.
1996: Michael E Rusiniak; E P O'Brien; Edward K Novak; S M Barone; Michael P McGarry; M Reddington; Richard T Swank
Molecular markers near the mouse brachymorphic (bm) gene, which affects connective tissues and bleeding time.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(2):98-102.
1996: Richard T Swank; M Reddington; Edward K Novak
Inherited prolonged bleeding time and platelet storage pool deficiency in the subtle gray (sut) mouse.
Laboratory animal science 1996;46(1):56-60.
1995: William C Nichols; Kathleen Cooney; Karen L Mohlke; J D Ballew; A Yang; M E Bruck; M Reddington; Edward K Novak; Richard T Swank; David Ginsburg
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene.
Blood 1995;86(6):2461.
1995: Lijie Zhen; Michael E Rusiniak; Richard T Swank
The beta-glucuronidase propeptide contains a serpin-related octamer necessary for complex formation with egasyn esterase and for retention within the endoplasmic reticulum.
The Journal of biological chemistry 1995;270(20):11912-20.
1995: Edward K Novak; M Reddington; Lijie Zhen; P E Stenberg; C W Jackson; Michael P McGarry; Richard T Swank
Inherited thrombocytopenia caused by reduced platelet production in mice with the gunmetal pigment gene mutation.
Blood 1995;85(7):1781-9.
1995: E P O'Brien; Edward K Novak; Lijie Zhen; K F Manly; D Stephenson; Richard T Swank
Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD).
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(1):19-24.
1994: S A Keller; Julie M Jones; A Boyle; L L Barrow; Paul D Killen; Daniel G Green; N V Kapousta; Peter F Hitchcock; Richard T Swank; Miriam H Meisler
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.
Genomics 1994;23(2):309-20.
1994: William C Nichols; Kathleen Cooney; Karen L Mohlke; J D Ballew; A Yang; M E Bruck; M Reddington; Edward K Novak; Richard T Swank; David Ginsburg
von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene.
Blood 1994;83(11):3225-31.
1994: E P O'Brien; Edward K Novak; S A Keller; Christophe Poirier; Jean-Louis Guénet; Richard T Swank
Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(6):356-60.
1993: Lijie Zhen; Heinz Baumann; Edward K Novak; Richard T Swank
The signal for retention of the egasyn-glucuronidase complex within the endoplasmic reticulum.
Archives of biochemistry and biophysics 1993;304(2):402-14.
1993: Richard T Swank; S Y Jiang; M Reddington; J Conway; D Stephenson; Michael P McGarry; Edward K Novak
Inherited abnormalities in platelet organelles and platelet formation and associated altered expression of low molecular weight guanosine triphosphate-binding proteins in the mouse pigment mutant gunmetal.
Blood 1993;81(10):2626-35.
1991: M Ovnic; Richard T Swank; C Fletcher; Lijie Zhen; Edward K Novak; Heinz Baumann; N Heintz; R E Ganschow
Characterization and functional expression of a cDNA encoding egasyn (esterase-22): the endoplasmic reticulum-targeting protein of beta-glucuronidase.
Genomics 1991;11(4):956-67.
1991: Richard T Swank; M Reddington; O Howlett; Edward K Novak
Platelet storage pool deficiency associated with inherited abnormalities of the inner ear in the mouse pigment mutants muted and mocha.
Blood 1991;78(8):2036-44.
1991: Richard T Swank; H O Sweet; M T Davisson; M Reddington; Edward K Novak
Sandy: a new mouse model for platelet storage pool deficiency.
Genetical research 1991;58(1):51-62.
1991: Edward K Novak; Heinz Baumann; M Ovnic; Richard T Swank
Expression of egasyn-esterase in mammalian cells. Sequestration in the endoplasmic reticulum and complexation with beta-glucuronidase.
The Journal of biological chemistry 1991;266(10):6377-80.
1990: Michael P McGarry; Edward K Novak; M Reddington; Richard T Swank
Effects of mixed chimeric bone marrow repopulation on platelet storage pool-associated bleeding defects in mouse mutants.
Experimental hematology 1990;18(11):1174-9.
1990: J D Sweeney; Edward K Novak; M Reddington; K H Takeuchi; Richard T Swank
The RIIIS/J inbred mouse strain as a model for von Willebrand disease.
Blood 1990;76(11):2258-65.
1990: H Li; K H Takeuchi; K Manly; Verne M Chapman; Richard T Swank
The propeptide of beta-glucuronidase. Further evidence of its involvement in compartmentalization of beta-glucuronidase and sequence similarity with portions of the reactive site region of the serpin superfamily.
The Journal of biological chemistry 1990;265(25):14732-5.
1989: S Medda; R M Chemelli; Jackie L Martin; L R Pohl; Richard T Swank
Involvement of the carboxyl-terminal propeptide of beta-glucuronidase in its compartmentalization within the endoplasmic reticulum as determined by a synthetic peptide approach.
The Journal of biological chemistry 1989;264(27):15824-8.
1989: K H Takeuchi; Richard T Swank
Inhibitors of elastase and cathepsin G in Chédiak-Higashi (beige) neutrophils.
The Journal of biological chemistry 1989;264(13):7431-6.
1988: Edward K Novak; H O Sweet; M Prochazka; M Parentis; R Soble; M Reddington; A Cairo; Richard T Swank
Cocoa: a new mouse model for platelet storage pool deficiency.
British journal of haematology 1988;69(3):371-8.
1987: K H Takeuchi; Michael P McGarry; Richard T Swank
Elastase and cathepsin G activities are present in immature bone marrow neutrophils and absent in late marrow and circulating neutrophils of beige (Chediak-Higashi) mice.
The Journal of experimental medicine 1987;166(5):1362-76.
1987: J Brown; E K Novak; K Takeuchi; K Moore; S Medda; Richard T Swank
Lumenal location of the microsomal beta-glucuronidase-egasyn complex.
The Journal of cell biology 1987;105(4):1571-8.
1987: S Medda; A M Stevens; Richard T Swank
Involvement of the esterase active site of egasyn in compartmentalization of beta-glucuronidase within the endoplasmic reticulum.
Cell 1987;50(2):301-10.
1987: S Medda; K Takeuchi; D Devore-Carter; O von Deimling; E Heymann; Richard T Swank
An accessory protein identical to mouse egasyn is complexed with rat microsomal beta-glucuronidase and is identical to rat esterase-3.
The Journal of biological chemistry 1987;262(15):7248-53.
1987: M Reddington; Edward K Novak; E Hurley; C Medda; Michael P McGarry; Richard T Swank
Immature dense granules in platelets from mice with platelet storage pool disease.
Blood 1987;69(5):1300-6.
1986: Michael P McGarry; Edward K Novak; Richard T Swank
Progenitor cell defect correctable by bone marrow transplantation in five independent mouse models of platelet storage pool deficiency.
Experimental hematology 1986;14(4):261-5.
1986: S Medda; O von Deimling; Richard T Swank
Identity of esterase-22 and egasyn, the protein which complexes with microsomal beta-glucuronidase.
Biochemical genetics 1986;24(3-4):229-43.
1985: S Medda; Richard T Swank
Egasyn, a protein which determines the subcellular distribution of beta-glucuronidase, has esterase activity.
The Journal of biological chemistry 1985;260(29):15802-8.
1985: Edward K Novak; Michael P McGarry; Richard T Swank
Correction of symptoms of platelet storage pool deficiency in animal models for Chediak-Higashi syndrome and Hermansky-Pudlak syndrome.
Blood 1985;66(5):1196-201.
1985: J A Brown; E K Novak; Richard T Swank
Effects of ammonia on processing and secretion of precursor and mature lysosomal enzyme from macrophages of normal and pale ear mice: evidence for two distinct pathways.
The Journal of cell biology 1985;100(6):1894-904.
1984: E K Novak; S W Hui; Richard T Swank
Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic loci.
Blood 1984;63(3):536-44.
1981: J A Brown; G P Jahreis; Richard T Swank
The synthesis and processing of beta-glucuronidase in normal and egasyn deficient mouse kidney.
Biochemical and biophysical research communications 1981;99(2):691-9.
1981: E K Novak; S W Hui; Richard T Swank
The mouse pale ear pigment mutant as a possible animal model for human platelet storage pool deficiency.
Blood 1981;57(1):38-43.
1980: A E Piccini; G P Jahreis; E K Novak; Richard T Swank
Intracellular distribution of lysosomal enzymes in the mouse pigment mutants pale ear and pallid.
Molecular and cellular biochemistry 1980;31(2):89-95.
1980: E K Novak; F Wieland; G P Jahreis; Richard T Swank
Altered secretion of kidney lysosomal enzymes in the mouse pigment mutants ruby-eye, ruby-eye-2-J, and maroon.
Biochemical genetics 1980;18(5-6):549-61.
1980: E K Novak; Richard T Swank; Miriam H Meisler
Pigmentation and lysosome function in mice homozygous for both pale ear and beige-J pigment genes.
Genetical research 1980;35(2):195-204.