Report for Baas F

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References (13)

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 : Conlon_2018_Elife_7_
ESTHER : Conlon_2018_Elife_7_
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 : Piet_2011_J.Bacteriol_193_2371
ESTHER : Piet_2011_J.Bacteriol_193_2371
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 : van Es_2008_Nat.Genet_40_29
ESTHER : van Es_2008_Nat.Genet_40_29
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 : Kalaydjieva_2000_Am.J.Hum.Genet_67_47
ESTHER : Kalaydjieva_2000_Am.J.Hum.Genet_67_47
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 : Chandler_2000_Neuromuscul.Disord_10_584
ESTHER : Chandler_2000_Neuromuscul.Disord_10_584
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 : Van Ommen_1989_Biochimie_71_211
ESTHER : Van Ommen_1989_Biochimie_71_211
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 : Kok_1987_J.Hered_78_298
ESTHER : Kok_1987_J.Hered_78_298
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 : Baas_1986_Nucleic.Acids.Res_14_5171
ESTHER : Baas_1986_Nucleic.Acids.Res_14_5171
PubMedSearch : Baas_1986_Nucleic.Acids.Res_14_5171
PubMedID: 3016640

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 : Landegent_1985_Nature_317_175
ESTHER : Landegent_1985_Nature_317_175
PubMedSearch : Landegent_1985_Nature_317_175
PubMedID: 3839907

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 : Baas_1985_Hum.Genet_69_138
ESTHER : Baas_1985_Hum.Genet_69_138
PubMedSearch : Baas_1985_Hum.Genet_69_138
PubMedID: 2982724

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 : Baas_1984_Hum.Genet_67_301
ESTHER : Baas_1984_Hum.Genet_67_301
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: