Title : Unexpected similarities between C9ORF72 and sporadic forms of ALS\/FTD suggest a common disease mechanism - Conlon_2018_Elife_7_ |
Author(s) : Conlon EG , Fagegaltier D , Agius P , Davis-Porada J , Gregory J , Hubbard I , Kang K , Kim D , Phatnani H , Kwan J , Sareen D , Broach JR , Simmons Z , Arcila-Londono X , Lee EB , Van Deerlin VM , Shneider NA , Fraenkel E , Ostrow LW , Baas F , Zaitlen N , Berry JD , Malaspina A , Fratta P , Cox GA , Thompson LM , Finkbeiner S , Dardiotis E , Miller TM , Chandran S , Pal S , Hornstein E , MacGowan DJ , Heiman-Patterson T , Hammell MG , Patsopoulos NA , Dubnau J , Nath A , Manley JL |
Ref : Elife , 7 : , 2018 |
Abstract : |
PubMedSearch : Conlon_2018_Elife_7_ |
PubMedID: 30003873 |
Title : Genome sequence of Neisseria meningitidis serogroup B strain H44\/76 - Piet_2011_J.Bacteriol_193_2371 |
Author(s) : Piet JR , Huis in 't Veld RA , van Schaik BD , van Kampen AH , Baas F , van de Beek D , Pannekoek Y , van der Ende A |
Ref : Journal of Bacteriology , 193 :2371 , 2011 |
Abstract : |
PubMedSearch : Piet_2011_J.Bacteriol_193_2371 |
PubMedID: 21378179 |
Gene_locus related to this paper: neigo-pip , neima-metx , neime-ESD , neime-NMA2216 , neime-NMB0276 , neime-NMB1877 |
Title : Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis - van Es_2008_Nat.Genet_40_29 |
Author(s) : van Es MA , van Vught PW , Blauw HM , Franke L , Saris CG , Van den Bosch L , de Jong SW , de Jong V , Baas F , van't Slot R , Lemmens R , Schelhaas HJ , Birve A , Sleegers K , Van Broeckhoven C , Schymick JC , Traynor BJ , Wokke JH , Wijmenga C , Robberecht W , Andersen PM , Veldink JH , Ophoff RA , van den Berg LH |
Ref : Nat Genet , 40 :29 , 2008 |
Abstract : |
PubMedSearch : van Es_2008_Nat.Genet_40_29 |
PubMedID: 18084291 |
Title : N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom - Kalaydjieva_2000_Am.J.Hum.Genet_67_47 |
Author(s) : Kalaydjieva L , Gresham D , Gooding R , Heather L , Baas F , de Jonge R , Blechschmidt K , Angelicheva D , Chandler D , Worsley P , Rosenthal A , King RH , Thomas PK |
Ref : American Journal of Human Genetics , 67 :47 , 2000 |
Abstract : |
PubMedSearch : Kalaydjieva_2000_Am.J.Hum.Genet_67_47 |
PubMedID: 10831399 |
Gene_locus related to this paper: human-NDRG1 |
Title : Hereditary motor and sensory neuropathy--Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries - Chandler_2000_Neuromuscul.Disord_10_584 |
Author(s) : Chandler D , Angelicheva D , Heather L , Gooding R , Gresham D , Yanakiev P , de Jonge R , Baas F , Dye D , Karagyozov L , Savov A , Blechschmidt K , Keats B , Thomas PK , King RH , Starr A , Nikolova A , Colomer J , Ishpekova B , Tournev I , Urtizberea JA , Merlini L , Butinar D , Chabrol B , Voit T , Baethmann M , Nedkova V , Corches A , Kalaydjieva L |
Ref : Neuromuscular Disorders , 10 :584 , 2000 |
Abstract : |
PubMedSearch : Chandler_2000_Neuromuscul.Disord_10_584 |
PubMedID: 11053686 |
Title : Studies on the structures of the normal and abnormal goat thyroglobulin genes - Van Ommen_1989_Biochimie_71_211 |
Author(s) : van Ommen GJ , Sterk A , Mercken LO , Arnberg AC , Baas F , de Vijlder JJ |
Ref : Biochimie , 71 :211 , 1989 |
Abstract : |
PubMedSearch : Van Ommen_1989_Biochimie_71_211 |
PubMedID: 2495821 |
Title : Autosomal recessive inheritance of goiter in Dutch goats - Kok_1987_J.Hered_78_298 |
Author(s) : Kok K , van Dijk JE , Sterk A , Baas F , van Ommen GJ , de Vijlder JJ |
Ref : Journal of Heredity , 78 :298 , 1987 |
Abstract : |
PubMedSearch : Kok_1987_J.Hered_78_298 |
PubMedID: 3680925 |
Title : The human thyroglobulin gene is over 300 kb long and contains introns of up to 64 kb - Baas_1986_Nucleic.Acids.Res_14_5171 |
Author(s) : Baas F , van Ommen GJ , Bikker H , Arnberg AC , de Vijlder JJ |
Ref : Nucleic Acids Research , 14 :5171 , 1986 |
Abstract : |
PubMedSearch : Baas_1986_Nucleic.Acids.Res_14_5171 |
PubMedID: 3016640 |
Title : The human thyroglobulin gene: a polymorphic marker localized distal to C-MYC on chromosome 8 band q24 - Baas_1985_Hum.Genet_69_138 |
Author(s) : Baas F , Bikker H , Geurts van Kessel A , Melsert R , Pearson PL , de Vijlder JJ , van Ommen GJ |
Ref : Hum Genet , 69 :138 , 1985 |
Abstract : |
PubMedSearch : Baas_1985_Hum.Genet_69_138 |
PubMedID: 2982724 |
Title : Chromosomal localization of a unique gene by non-autoradiographic in situ hybridization - Landegent_1985_Nature_317_175 |
Author(s) : Landegent JE , Jansen in de Wal N , van Ommen GJ , Baas F , de Vijlder JJ , van Duijn P , Van der Ploeg M |
Ref : Nature , 317 :175 , 1985 |
Abstract : |
PubMedSearch : Landegent_1985_Nature_317_175 |
PubMedID: 3839907 |
Title : Unusual scarcity of restriction site polymorphism in the human thyroglobulin gene. A linkage study suggesting autosomal dominance of a defective thyroglobulin allele - Baas_1984_Hum.Genet_67_301 |
Author(s) : Baas F , Bikker H , van Ommen GJ , de Vijlder JJ |
Ref : Hum Genet , 67 :301 , 1984 |
Abstract : |
PubMedSearch : Baas_1984_Hum.Genet_67_301 |
PubMedID: 6088387 |
Title : Chromosome mapping and polymorphism study of the human thyroglobulin gene. (Abstract) - |
Author(s) : Van Ommen G-JB , Baas F , Arnberg AC , Pearson PL , De Vijlder JJM |
Ref : Cytogenet Cell Genet , 37 :562 , 1984 |
PubMedID: |
Title : Autosomal dominant inheritance of a thyroglobulin abnormality suggests cooperation of sub-units in hormone formation - |
Author(s) : De Vijlder JJM , Baas F , Koch CAM , Kok K , Gons M |
Ref : Ann Endocrinol (Paris) , 44 :36 , 1983 |
PubMedID: |