Tom M Glaser

Title(s)Professor, MED: Cell Biology & Human Anat
SchoolSchool of Medicine
Phone530-752-9575
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Novel CRB1 pathogenic variant in Chuuk families with Leber congenital amaurosis. Am J Med Genet A. 2023 04; 191(4):1007-1012. Albakri A, Pisuchpen P, Capasso JE, Schneider A, Kopinsky S, Glaser T, Chiang JP, Yomai AA, McNear D, Levin AV. PMID: 36595661; PMCID: PMC10262898.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    2. Axenfeld-Rieger syndrome: more than meets the eye. J Med Genet. 2023 04; 60(4):368-379. Reis LM, Maheshwari M, Capasso J, Atilla H, Dudakova L, Thompson S, Zitano L, Lay-Son G, Lowry RB, Black J, Lee J, Shue A, Kremlikova Pourova R, Vaneckova M, Skalicka P, Jedlickova J, Trkova M, Williams B, Richard G, Bachman K, Seeley AH, Costakos D, Glaser TM, Levin AV, Liskova P, Murray JC, Semina EV. PMID: 35882526; PMCID: PMC9912354.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    3. Arap1 loss causes retinal pigment epithelium phagocytic dysfunction and subsequent photoreceptor death. Dis Model Mech. 2022 07 01; 15(7). Shao A, Lopez AJ, Chen J, Tham A, Javier S, Quiroz A, Frick S, Levine EM, Lloyd KCK, Leonard BC, Murphy CJ, Glaser TM, Moshiri A. PMID: 35758026; PMCID: PMC9346516.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    4. Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders. Hum Mol Genet. 2021 08 12; 30(17):1591-1606. Reis LM, Sorokina EA, Dudakova L, Moravikova J, Skalicka P, Malinka F, Seese SE, Thompson S, Bardakjian T, Capasso J, Allen W, Glaser T, Levin AV, Schneider A, Khan A, Liskova P, Semina EV. PMID: 34046667; PMCID: PMC8369840.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    5. Atoh7-independent specification of retinal ganglion cell identity. Sci Adv. 2021 03; 7(11). Brodie-Kommit J, Clark BS, Shi Q, Shiau F, Kim DW, Langel J, Sheely C, Ruzycki PA, Fries M, Javed A, Cayouette M, Schmidt T, Badea T, Glaser T, Zhao H, Singer J, Blackshaw S, Hattar S. PMID: 33712461; PMCID: PMC7954457.
      View in: PubMed   Mentions: 33     Fields:    
    6. The rax homeobox gene is mutated in the eyeless axolotl, Ambystoma mexicanum. Dev Dyn. 2021 06; 250(6):807-821. Davis ES, Voss G, Miesfeld JB, Zarate-Sanchez J, Voss SR, Glaser T. PMID: 32864847; PMCID: PMC8907009.
      View in: PubMed   Mentions: 3     Fields:    Translation:Animals
    7. The Atoh7 remote enhancer provides transcriptional robustness during retinal ganglion cell development. Proc Natl Acad Sci U S A. 2020 09 01; 117(35):21690-21700. Miesfeld JB, Ghiasvand NM, Marsh-Armstrong B, Marsh-Armstrong N, Miller EB, Zhang P, Manna SK, Zawadzki RJ, Brown NL, Glaser T. PMID: 32817515; PMCID: PMC7474671.
      View in: PubMed   Mentions: 25     Fields:    Translation:AnimalsCells
    8. Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice. Dev Biol. 2020 02 15; 458(2):141-152. Kwon YS, Tham A, Lopez AJ, Edwards S, Woods S, Chen J, Wong-Fortunato J, Quiroz Alonso A, Javier S, Au I, Clarke M, Humpal D, Lloyd KCK, Thomasy S, Murphy C, Glaser TM, Moshiri A. PMID: 31634437; PMCID: PMC6995765.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    9. NAA10 polyadenylation signal variants cause syndromic microphthalmia. J Med Genet. 2019 07; 56(7):444-452. Johnston JJ, Williamson KA, Chou CM, Sapp JC, Ansari M, Chapman HM, Cooper DN, Dabir T, Dudley JN, Holt RJ, Ragge NK, Schäffer AA, Sen SK, Slavotinek AM, FitzPatrick DR, Glaser TM, Stewart F, Black GC, Biesecker LG. PMID: 30842225; PMCID: PMC7032957.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    10. Considerations for the use of Cre recombinase for conditional gene deletion in the mouse lens. Hum Genomics. 2019 02 15; 13(1):10. Lam PT, Padula SL, Hoang TV, Poth JE, Liu L, Liang C, LeFever AS, Wallace LM, Ashery-Padan R, Riggs PK, Shields JE, Shaham O, Rowan S, Brown NL, Glaser T, Robinson ML. PMID: 30770771; PMCID: PMC6377743.
      View in: PubMed   Mentions: 15     Fields:    Translation:Animals
    11. Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease. Cell Rep. 2018 05 29; 23(9):2643-2652. Kaukonen M, Woods S, Ahonen S, Lemberg S, Hellman M, Hytönen MK, Permi P, Glaser T, Lohi H. PMID: 29847795; PMCID: PMC6546432.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    12. The dynamics of native Atoh7 protein expression during mouse retinal histogenesis, revealed with a new antibody. Gene Expr Patterns. 2018 01; 27:114-121. Miesfeld JB, Glaser T, Brown NL. PMID: 29225067; PMCID: PMC5835195.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimalsCells
    13. Astrocytes follow ganglion cell axons to establish an angiogenic template during retinal development. Glia. 2017 10; 65(10):1697-1716. O'Sullivan ML, Puñal VM, Kerstein PC, Brzezinski JA, Glaser T, Wright KM, Kay JN. PMID: 28722174; PMCID: PMC5561467.
      View in: PubMed   Mentions: 51     Fields:    Translation:HumansAnimalsCells
    14. Arap1 Deficiency Causes Photoreceptor Degeneration in Mice. Invest Ophthalmol Vis Sci. 2017 03 01; 58(3):1709-1718. Moshiri A, Humpal D, Leonard BC, Imai DM, Tham A, Bower L, Clary D, Glaser TM, Lloyd KC, Murphy CJ. PMID: 28324111; PMCID: PMC5361582.
      View in: PubMed   Mentions: 6     Fields:    Translation:AnimalsCells
    15. Biochemical Basis for Dominant Inheritance, Variable Penetrance, and Maternal Effects in RBP4 Congenital Eye Disease. Cell. 2015 Apr 23; 161(3):634-646. Chou CM, Nelson C, Tarlé SA, Pribila JT, Bardakjian T, Woods S, Schneider A, Glaser T. PMID: 25910211; PMCID: PMC4409664.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansAnimalsCells
    16. Heterochronic misexpression of Ascl1 in the Atoh7 retinal cell lineage blocks cell cycle exit. Mol Cell Neurosci. 2013 May; 54:108-20. Hufnagel RB, Riesenberg AN, Quinn M, Brzezinski JA, Glaser T, Brown NL. PMID: 23481413; PMCID: PMC3622171.
      View in: PubMed   Mentions: 11     Fields:    Translation:AnimalsCells
    17. Focal facial dermal dysplasia, type IV, is caused by mutations in CYP26C1. Hum Mol Genet. 2013 Feb 15; 22(4):696-703. Slavotinek AM, Mehrotra P, Nazarenko I, Tang PL, Lao R, Cameron D, Li B, Chu C, Chou C, Marqueling AL, Yahyavi M, Cordoro K, Frieden I, Glaser T, Prescott T, Morren MA, Devriendt K, Kwok PY, Petkovich M, Desnick RJ. PMID: 23161670; PMCID: PMC3554199.
      View in: PubMed   Mentions: 20     Fields:    Translation:HumansAnimalsCells
    18. Math5 (Atoh7) gene dosage limits retinal ganglion cell genesis. Neuroreport. 2012 Jul 11; 23(10):631-4. Prasov L, Nagy M, Rudolph DD, Glaser T. PMID: 22660169; PMCID: PMC3733793.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    19. Analysis of FOXD3 sequence variation in human ocular disease. Mol Vis. 2012; 18:1740-9. Kloss BA, Reis LM, Brémond-Gignac D, Glaser T, Semina EV. PMID: 22815627; PMCID: PMC3398501.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansAnimalsCells
    20. ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous. Hum Mol Genet. 2012 Aug 15; 21(16):3681-94. Prasov L, Masud T, Khaliq S, Mehdi SQ, Abid A, Oliver ER, Silva ED, Lewanda A, Brodsky MC, Borchert M, Kelberman D, Sowden JC, Dattani MT, Glaser T. PMID: 22645276; PMCID: PMC3406761.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansAnimalsCells
    21. Pushing the envelope of retinal ganglion cell genesis: context dependent function of Math5 (Atoh7). Dev Biol. 2012 Aug 15; 368(2):214-30. Prasov L, Glaser T. PMID: 22609278; PMCID: PMC3402631.
      View in: PubMed   Mentions: 29     Fields:    Translation:AnimalsCells
    22. Dynamic expression of ganglion cell markers in retinal progenitors during the terminal cell cycle. Mol Cell Neurosci. 2012 Jun; 50(2):160-8. Prasov L, Glaser T. PMID: 22579728; PMCID: PMC3383354.
      View in: PubMed   Mentions: 20     Fields:    Translation:AnimalsCells
    23. Math5 defines the ganglion cell competence state in a subpopulation of retinal progenitor cells exiting the cell cycle. Dev Biol. 2012 May 15; 365(2):395-413. Brzezinski JA, Prasov L, Glaser T. PMID: 22445509; PMCID: PMC3337348.
      View in: PubMed   Mentions: 87     Fields:    Translation:AnimalsCells
    24. Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease. Nat Neurosci. 2011 May; 14(5):578-86. Ghiasvand NM, Rudolph DD, Mashayekhi M, Brzezinski JA, Goldman D, Glaser T. PMID: 21441919; PMCID: PMC3083485.
      View in: PubMed   Mentions: 92     Fields:    Translation:HumansAnimalsCells
    25. A critical analysis of Atoh7 (Math5) mRNA splicing in the developing mouse retina. PLoS One. 2010 Aug 24; 5(8):e12315. Prasov L, Brown NL, Glaser T. PMID: 20808762; PMCID: PMC2927423.
      View in: PubMed   Mentions: 13     Fields:    Translation:AnimalsCells
    26. Generating somatic mosaicism with a Cre recombinase-microsatellite sequence transgene. Nat Methods. 2008 Mar; 5(3):231-3. Akyol A, Hinoi T, Feng Y, Bommer GT, Glaser TM, Fearon ER. PMID: 18264107; PMCID: PMC2279183.
      View in: PubMed   Mentions: 29     Fields:    Translation:AnimalsCells
    27. Math5 expression and function in the central auditory system. Mol Cell Neurosci. 2008 Jan; 37(1):153-69. Saul SM, Brzezinski JA, Altschuler RA, Shore SE, Rudolph DD, Kabara LL, Halsey KE, Hufnagel RB, Zhou J, Dolan DF, Glaser T. PMID: 17977745; PMCID: PMC2266824.
      View in: PubMed   Mentions: 38     Fields:    Translation:AnimalsCells
    28. Further support of the role of CYP1B1 in patients with Peters anomaly. Mol Vis. 2006 May 16; 12:506-10. Vincent A, Billingsley G, Priston M, Glaser T, Oliver E, Walter M, Ritch R, Levin A, Heon E. PMID: 16735991.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    29. Targeting of GFP to newborn rods by Nrl promoter and temporal expression profiling of flow-sorted photoreceptors. Proc Natl Acad Sci U S A. 2006 Mar 07; 103(10):3890-5. Akimoto M, Cheng H, Zhu D, Brzezinski JA, Khanna R, Filippova E, Oh EC, Jing Y, Linares JL, Brooks M, Zareparsi S, Mears AJ, Hero A, Glaser T, Swaroop A. PMID: 16505381; PMCID: PMC1383502.
      View in: PubMed   Mentions: 183     Fields:    Translation:HumansAnimalsCells
    30. Loss of circadian photoentrainment and abnormal retinal electrophysiology in Math5 mutant mice. Invest Ophthalmol Vis Sci. 2005 Jul; 46(7):2540-51. Brzezinski JA, Brown NL, Tanikawa A, Bush RA, Sieving PA, Vitaterna MH, Takahashi JS, Glaser T. PMID: 15980246; PMCID: PMC1570190.
      View in: PubMed   Mentions: 33     Fields:    Translation:AnimalsCells
    31. Ribosomal protein L24 defect in belly spot and tail (Bst), a mouse Minute. Development. 2004 Aug; 131(16):3907-20. Oliver ER, Saunders TL, Tarlé SA, Glaser T. PMID: 15289434; PMCID: PMC2262800.
      View in: PubMed   Mentions: 143     Fields:    Translation:AnimalsCells
    32. Conserved and divergent functions of Drosophila atonal, amphibian, and mammalian Ath5 genes. Evol Dev. 2003 Sep-Oct; 5(5):532-41. Sun Y, Kanekar SL, Vetter ML, Gorski S, Jan YN, Glaser T, Brown NL. PMID: 12950631; PMCID: PMC2262842.
      View in: PubMed   Mentions: 10     Fields:    Translation:AnimalsCells
    33. Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development. Mamm Genome. 2002 Feb; 13(2):95-101. Brown NL, Dagenais SL, Chen CM, Glaser T. PMID: 11889557; PMCID: PMC2262845.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimalsCells
    34. Mouse eye gene microarrays for investigating ocular development and disease. Vision Res. 2002 Feb; 42(4):463-70. Farjo R, Yu J, Othman MI, Yoshida S, Sheth S, Glaser T, Baehr W, Swaroop A. PMID: 11853762.
      View in: PubMed   Mentions: 14     Fields:    Translation:Animals
    35. The eyeless mouse mutation (ey1) removes an alternative start codon from the Rx/rax homeobox gene. Genesis. 2001 Sep; 31(1):43-53. Tucker P, Laemle L, Munson A, Kanekar S, Oliver ER, Brown N, Schlecht H, Vetter M, Glaser T. PMID: 11668677.
      View in: PubMed   Mentions: 27     Fields:    Translation:AnimalsCells
    36. Math5 is required for retinal ganglion cell and optic nerve formation. Development. 2001 Jul; 128(13):2497-508. Brown NL, Patel S, Brzezinski J, Glaser T. PMID: 11493566; PMCID: PMC1480839.
      View in: PubMed   Mentions: 241     Fields:    Translation:AnimalsCells
    37. Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly. J Med Genet. 2001 May; 38(5):324-6. Vincent A, Billingsley G, Priston M, Williams-Lyn D, Sutherland J, Glaser T, Oliver E, Walter MA, Heathcote G, Levin A, Héon E. PMID: 11403040; PMCID: PMC1734880.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    38. 3' deletions cause aniridia by preventing PAX6 gene expression. Proc Natl Acad Sci U S A. 2000 Dec 05; 97(25):13755-9. Lauderdale JD, Wilensky JS, Oliver ER, Walton DS, Glaser T. PMID: 11087823; PMCID: PMC17648.
      View in: PubMed   Mentions: 65     Fields:    Translation:HumansAnimalsCells
    39. Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus. Genetics. 2000 May; 155(1):291-300. Hallsson JH, Favor J, Hodgkinson C, Glaser T, Lamoreux ML, Magnúsdóttir R, Gunnarsson GJ, Sweet HO, Copeland NG, Jenkins NA, Steingrímsson E. PMID: 10790403; PMCID: PMC1461060.
      View in: PubMed   Mentions: 31     Fields:    Translation:AnimalsCells
    40. Math5 encodes a murine basic helix-loop-helix transcription factor expressed during early stages of retinal neurogenesis. Development. 1998 Dec; 125(23):4821-33. Brown NL, Kanekar S, Vetter ML, Tucker PK, Gemza DL, Glaser T. PMID: 9806930.
      View in: PubMed   Mentions: 155     Fields:    Translation:AnimalsCells
    41. Mutation at the anophthalmic white locus in Syrian hamsters: haploinsufficiency in the Mitf gene mimics human Waardenburg syndrome type 2. Hum Mol Genet. 1998 Apr; 7(4):703-8. Hodgkinson CA, Nakayama A, Li H, Swenson LB, Opdecamp K, Asher JH, Arnheiter H, Glaser T. PMID: 9499424.
      View in: PubMed   Mentions: 12     Fields:    Translation:AnimalsCells
    42. Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing. Genes Dev. 1994 Sep 01; 8(17):2022-34. Epstein JA, Glaser T, Cai J, Jepeal L, Walton DS, Maas RL. PMID: 7958875.
      View in: PubMed   Mentions: 131     Fields:    Translation:HumansAnimalsCells
    43. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. Nat Genet. 1994 Aug; 7(4):463-71. Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, Maas RL. PMID: 7951315.
      View in: PubMed   Mentions: 245     Fields:    Translation:HumansAnimalsCells
    44. Identification of a Pax paired domain recognition sequence and evidence for DNA-dependent conformational changes. J Biol Chem. 1994 Mar 18; 269(11):8355-61. Epstein J, Cai J, Glaser T, Jepeal L, Maas R. PMID: 8132558.
      View in: PubMed   Mentions: 140     Fields:    Translation:HumansAnimalsCells
    45. Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutation. Dev Dyn. 1994 Mar; 199(3):214-28. Maas R, Elfering S, Glaser T, Jepeal L. PMID: 7517224.
      View in: PubMed   Mentions: 12     Fields:    Translation:AnimalsCells
    46. Absence of PAX6 gene mutations in Gillespie syndrome (partial aniridia, cerebellar ataxia, and mental retardation). Genomics. 1994 Jan 01; 19(1):145-8. Glaser T, Ton CC, Mueller R, Petzl-Erler ML, Oliver C, Nevin NC, Housman DE, Maas RL. PMID: 8188215.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansCells
    47. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene. Nat Genet. 1992 Nov; 2(3):232-9. Glaser T, Walton DS, Maas RL. PMID: 1345175.
      View in: PubMed   Mentions: 195     Fields:    Translation:HumansAnimalsCells
    48. Mapping and characterization of 129 cosmids on human chromosome 11p. Somat Cell Mol Genet. 1992 Sep; 18(5):463-75. Call KM, Ito CY, Lindberg C, Memisoglu A, Petrou C, Glaser T, Jones C, Housman DE. PMID: 1475712.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    49. Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus. Hum Genet. 1992 May; 89(2):187-93. Larsson C, Weber G, Kvanta E, Lewis K, Janson M, Jones C, Glaser T, Evans G, Nordenskjöld M. PMID: 1350263.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    50. The recombination activating genes, RAG 1 and RAG 2, are on chromosome 11p in humans and chromosome 2p in mice. Immunogenetics. 1992; 35(2):97-101. Oettinger MA, Stanger B, Schatz DG, Glaser T, Call K, Housman D, Baltimore D. PMID: 1735560.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    51. Mapping of 262 DNA markers into 24 intervals on human chromosome 11. Am J Hum Genet. 1992 Jan; 50(1):56-64. Tanigami A, Tokino T, Takiguchi S, Mori M, Glaser T, Park JW, Jones C, Nakamura Y. PMID: 1346079; PMCID: PMC1682531.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    52. Detailed physical map of human chromosomal region 11q12-13 shows high meiotic recombination rate around the MEN1 locus. Proc Natl Acad Sci U S A. 1991 Dec 01; 88(23):10609-13. Janson M, Larsson C, Werelius B, Jones C, Glaser T, Nakamura Y, Jones CP, Nordenskjöld M. PMID: 1683706; PMCID: PMC52979.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimalsCells
    53. WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour. Nature. 1991 Oct 03; 353(6343):431-4. Pelletier J, Bruening W, Li FP, Haber DA, Glaser T, Housman DE. PMID: 1654525.
      View in: PubMed   Mentions: 102     Fields:    Translation:HumansCells
    54. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare. Genes Chromosomes Cancer. 1991 Mar; 3(2):89-100. Royer-Pokora B, Ragg S, Heckl-Ostreicher B, Held M, Loos U, Call K, Glaser T, Housman D, Saunders G, Zabel B, et al. PMID: 1648959.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    55. Isolation, characterization, and expression of the murine Wilms' tumor gene (WT1) during kidney development. Mol Cell Biol. 1991 Mar; 11(3):1707-12. Buckler AJ, Pelletier J, Haber DA, Glaser T, Housman DE. PMID: 1671709; PMCID: PMC369476.
      View in: PubMed   Mentions: 61     Fields:    Translation:HumansAnimalsCells
    56. Isolation and mapping of 62 new RFLP markers on human chromosome 11. Am J Hum Genet. 1991 Feb; 48(2):258-68. Tokino T, Takahashi E, Mori M, Tanigami A, Glaser T, Park JW, Jones C, Hori T, Nakamura Y. PMID: 1671318; PMCID: PMC1683017.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansAnimalsCells
    57. A mouse model of the aniridia-Wilms tumor deletion syndrome. Science. 1990 Nov 09; 250(4982):823-7. Glaser T, Lane J, Housman D. PMID: 2173141.
      View in: PubMed   Mentions: 33     Fields:    Translation:Animals
    58. Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor. Genomics. 1990 Jul; 7(3):434-8. Jeanpierre C, Antignac C, Beroud C, Lavedan C, Henry I, Saunders G, Williams B, Glaser T, Junien C. PMID: 1973142.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    59. An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor. Cell. 1990 Jun 29; 61(7):1257-69. Haber DA, Buckler AJ, Glaser T, Call KM, Pelletier J, Sohn RL, Douglass EC, Housman DE. PMID: 2163761.
      View in: PubMed   Mentions: 154     Fields:    Translation:HumansCells
    60. Complete physical map of the WAGR region of 11p13 localizes a candidate Wilms' tumor gene. Cell. 1990 Feb 09; 60(3):495-508. Rose EA, Glaser T, Jones C, Smith CL, Lewis WH, Call KM, Minden M, Champagne E, Bonetta L, Yeger H, et al. PMID: 2154334.
      View in: PubMed   Mentions: 55     Fields:    Translation:HumansCells
    61. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus. Cell. 1990 Feb 09; 60(3):509-20. Call KM, Glaser T, Ito CY, Buckler AJ, Pelletier J, Haber DA, Rose EA, Kral A, Yeger H, Lewis WH, et al. PMID: 2154335.
      View in: PubMed   Mentions: 463     Fields:    Translation:HumansCells
    62. Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10. Genomics. 1990 Jan; 6(1):115-22. Brilliant MH, Szabo G, Katarova Z, Kozak CA, Glaser TM, Greenspan RJ, Housman DE. PMID: 1968040.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimalsCells
    63. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex. Genomics. 1990 Jan; 6(1):48-64. Glaser T, Rose E, Morse H, Housman D, Jones C. PMID: 2154397.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    64. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids. Somat Cell Mol Genet. 1989 Nov; 15(6):477-501. Glaser T, Housman D, Lewis WH, Gerhard D, Jones C. PMID: 2595451.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansAnimalsCells
    65. A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome. Genomics. 1989 Nov; 5(4):880-93. Glaser T, Driscoll DJ, Antonarakis S, Valle D, Housman D. PMID: 2574149.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    66. Localization of the muscle, liver, and brain glycogen phosphorylase genes on linkage maps of mouse chromosomes 19, 12, and 2, respectively. Genomics. 1989 Oct; 5(3):510-21. Glaser T, Matthews KE, Hudson JW, Seth P, Housman DE, Crerar MM. PMID: 2575583.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimalsCells
    67. Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma. Proc Natl Acad Sci U S A. 1989 May; 86(9):3247-51. Henry I, Grandjouan S, Couillin P, Barichard F, Huerre-Jeanpierre C, Glaser T, Philip T, Lenoir G, Chaussain JL, Junien C. PMID: 2566168; PMCID: PMC287107.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    68. Linkage analysis of multiple endocrine neoplasia type 1 with INT2 and other markers on chromosome 11. Genomics. 1989 Apr; 4(3):320-2. Bale SJ, Bale AE, Stewart K, Dachowski L, McBride OW, Glaser T, Green JE, Mulvihill JJ, Brandi ML, Sakaguchi K, et al. PMID: 2565877.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
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