158 related articles for article (PubMed ID: 38265673)
1. Role of Skewed X-Chromosome Inactivation in Common Variable Immunodeficiency.
Garcia-Prat M; Batlle-Masó L; Parra-Martínez A; Franco-Jarava C; Martinez-Gallo M; Aguiló-Cucurull A; Perurena-Prieto J; Castells N; Urban B; Dieli-Crimi R; Soler-Palacín P; Colobran R
J Clin Immunol; 2024 Jan; 44(2):54. PubMed ID: 38265673
[TBL] [Abstract][Full Text] [Related]
2. Improved HUMARA for the Detection of X-Linked Agammaglobulinemia Carriers.
Carrillo-Tapia E; Espinosa-Padilla SE; Perez-Perez D; Gonzalez-Serrano ME; Berron-Ruiz L; Espinosa-Rosales FJ; Rodriguez-Alba JC; Mújica-Guzman F; Yokoyama-Rebollar E; García-Flores JR; Herrera-González NE; Scheffler-Mendoza S; Yamazaki-Nakashimada MA; Staines-Boone AT; Lopez-Herrera G
Genet Test Mol Biomarkers; 2022 Apr; 26(4):220-227. PubMed ID: 35394812
[No Abstract] [Full Text] [Related]
3. Molecular Mechanisms of Skewed X-Chromosome Inactivation in Female Hemophilia Patients-Lessons from Wide Genome Analyses.
Dardik R; Avishai E; Lalezari S; Barg AA; Levy-Mendelovich S; Budnik I; Barel O; Khavkin Y; Kenet G; Livnat T
Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445777
[TBL] [Abstract][Full Text] [Related]
4. Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort.
Yazdani R; Abolhassani H; Kiaee F; Habibi S; Azizi G; Tavakol M; Chavoshzadeh Z; Mahdaviani SA; Momen T; Gharagozlou M; Movahedi M; Hamidieh AA; Behniafard N; Nabavi M; Bemanian MH; Arshi S; Molatefi R; Sherkat R; Shirkani A; Amin R; Aleyasin S; Faridhosseini R; Jabbari-Azad F; Mohammadzadeh I; Ghaffari J; Shafiei A; Kalantari A; Mansouri M; Mesdaghi M; Babaie D; Ahanchian H; Khoshkhui M; Soheili H; Eslamian MH; Cheraghi T; Dabbaghzadeh A; Tavassoli M; Kalmarzi RN; Mortazavi SH; Kashef S; Esmaeilzadeh H; Tafaroji J; Khalili A; Zandieh F; Sadeghi-Shabestari M; Darougar S; Behmanesh F; Akbari H; Zandkarimi M; Abolnezhadian F; Fayezi A; Moghtaderi M; Ahmadiafshar A; Shakerian B; Sajedi V; Taghvaei B; Safari M; Heidarzadeh M; Ghalebaghi B; Fathi SM; Darabi B; Bazregari S; Bazargan N; Fallahpour M; Khayatzadeh A; Javahertrash N; Bashardoust B; Zamani M; Mohsenzadeh A; Ebrahimi S; Sharafian S; Vosughimotlagh A; Tafakoridelbari M; Rahim M; Ashournia P; Razaghian A; Rezaei A; Samavat A; Mamishi S; Khazaei HA; Mohammadi J; Negahdari B; Parvaneh N; Rezaei N; Lougaris V; Giliani S; Plebani A; Ochs HD; Hammarström L; Aghamohammadi A
J Allergy Clin Immunol Pract; 2019 Mar; 7(3):864-878.e9. PubMed ID: 30240888
[TBL] [Abstract][Full Text] [Related]
5. Evaluating the Genetics of Common Variable Immunodeficiency: Monogenetic Model and Beyond.
de Valles-Ibáñez G; Esteve-Solé A; Piquer M; González-Navarro EA; Hernandez-Rodriguez J; Laayouni H; González-Roca E; Plaza-Martin AM; Deyà-Martínez Á; Martín-Nalda A; Martínez-Gallo M; García-Prat M; Del Pino-Molina L; Cuscó I; Codina-Solà M; Batlle-Masó L; Solís-Moruno M; Marquès-Bonet T; Bosch E; López-Granados E; Aróstegui JI; Soler-Palacín P; Colobran R; Yagüe J; Alsina L; Juan M; Casals F
Front Immunol; 2018; 9():636. PubMed ID: 29867916
[TBL] [Abstract][Full Text] [Related]
6. Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes.
Giovenino C; Trajkova S; Pavinato L; Cardaropoli S; Pullano V; Ferrero E; Sukarova-Angelovska E; Carestiato S; Salmin P; Rinninella A; Battaglia A; Bertoli L; Fadda A; Palermo F; Carli D; Mussa A; Dimartino P; Bruselles A; Froukh T; Mandrile G; Pasini B; De Rubeis S; Buxbaum JD; Pippucci T; Tartaglia M; Rossato M; Delledonne M; Ferrero GB; Brusco A
Eur J Hum Genet; 2023 Nov; 31(11):1228-1236. PubMed ID: 36879111
[TBL] [Abstract][Full Text] [Related]
7. Functional Evaluation of an IKBKG Variant Suspected to Cause Immunodeficiency Without Ectodermal Dysplasia.
Frans G; van der Werff Ten Bosch J; Moens L; Gijsbers R; Changi-Ashtiani M; Rokni-Zadeh H; Shahrooei M; Wuyts G; Meyts I; Bossuyt X
J Clin Immunol; 2017 Nov; 37(8):801-810. PubMed ID: 28993958
[TBL] [Abstract][Full Text] [Related]
8. Case Report:
Sun Y; Qian Y; Sun HX; Chen M; Luo Y; Xu X; Yan K; Wang L; Hu J; Dong M
Front Genet; 2022; 13():999442. PubMed ID: 36299587
[TBL] [Abstract][Full Text] [Related]
9. Histocompatibility Complex Status and Mendelian Randomization Analysis in Unsolved Antibody Deficiency.
Abolhassani H; Lim CK; Aghamohammadi A; Hammarström L
Front Immunol; 2020; 11():14. PubMed ID: 32038658
[TBL] [Abstract][Full Text] [Related]
10. Heterozygous Deletion of the
Sun Y; Luo Y; Qian Y; Chen M; Wang L; Li H; Zou Y; Dong M
Front Genet; 2019; 10():1086. PubMed ID: 31781162
[TBL] [Abstract][Full Text] [Related]
11. The Rapidly Expanding Genetic Spectrum of Common Variable Immunodeficiency-Like Disorders.
Ameratunga R; Edwards ESJ; Lehnert K; Leung E; Woon ST; Lea E; Allan C; Chan L; Steele R; Longhurst H; Bryant VL
J Allergy Clin Immunol Pract; 2023 Jun; 11(6):1646-1664. PubMed ID: 36796510
[TBL] [Abstract][Full Text] [Related]
12. Skewed X chromosome inactivation in diploid and triploid female human embryonic stem cells.
Liu W; Sun X
Hum Reprod; 2009 Aug; 24(8):1834-43. PubMed ID: 19429659
[TBL] [Abstract][Full Text] [Related]
13. A Novel Targeted Amplicon Next-Generation Sequencing Gene Panel for the Diagnosis of Common Variable Immunodeficiency Has a High Diagnostic Yield: Results from the Perth CVID Cohort Study.
Kermode W; De Santis D; Truong L; Della Mina E; Salman S; Thompson G; Nolan D; Loh R; Mallon D; Mclean-Tooke A; John M; Tangye SG; O'Sullivan M; D'Orsogna LJ
J Mol Diagn; 2022 Jun; 24(6):586-599. PubMed ID: 35570134
[TBL] [Abstract][Full Text] [Related]
14. Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease.
Minamikawa S; Nozu K; Nozu Y; Yamamura T; Taniguchi-Ikeda M; Nakanishi K; Fujimura J; Horinouchi T; Shima Y; Nakanishi K; Hattori M; Kanda K; Tanaka R; Morisada N; Nagano C; Sakakibara N; Nagase H; Morioka I; Kaito H; Iijima K
J Hum Genet; 2018 May; 63(5):589-595. PubMed ID: 29459630
[TBL] [Abstract][Full Text] [Related]
15. A new sex-specific underlying mechanism for female schizophrenia: accelerated skewed X chromosome inactivation.
Zhang X; Li Y; Ma L; Zhang G; Liu M; Wang C; Zheng Y; Li R
Biol Sex Differ; 2020 Jul; 11(1):39. PubMed ID: 32680558
[TBL] [Abstract][Full Text] [Related]
16. Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8.
Waldrep ML; Zhuang Y; Schroeder HW
BMC Med Genet; 2009 Sep; 10():100. PubMed ID: 19775471
[TBL] [Abstract][Full Text] [Related]
17. Genes associated with common variable immunodeficiency: one diagnosis to rule them all?
Bogaert DJ; Dullaers M; Lambrecht BN; Vermaelen KY; De Baere E; Haerynck F
J Med Genet; 2016 Sep; 53(9):575-90. PubMed ID: 27250108
[TBL] [Abstract][Full Text] [Related]
18. X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative Group.
Moschese V; Orlandi P; Plebani A; Arvanitidis K; Fiorini M; Speletas M; Mella P; Ritis K; Sideras P; Finocchi A; Livadiotti S; Rossi P
Mol Med; 2000 Feb; 6(2):104-13. PubMed ID: 10859027
[TBL] [Abstract][Full Text] [Related]
19. Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients.
Bagheri Y; Vosughi A; Azizi G; Yazdani R; Kiaee F; Hafezi N; Alimorad S; Khoshmirsafa M; Seif F; Hassanpour G; Abolhassani H; Aghamohammadi A
Immunol Lett; 2019 Jun; 210():55-62. PubMed ID: 31059734
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]