These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 39154701)

  • 1. A novel stoploss mutation CYB5R3 c.906A>G(p.*302Trpext*42) involved in the pathogenesis of hereditary methemoglobinemia.
    He KY; Yu HP; Zou J; Chen X; Chen L; Ruan DD; Chen T; Chen Q; Zhang L; Gao MZ; Lin XF; Li H; Fang ZT; Wu J; Luo JW; Liao LS
    Clin Chim Acta; 2025 Jan; 564():119930. PubMed ID: 39154701
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular Dynamic Simulation Analysis of a Novel Missense Variant in
    Ullah A; Shah AA; Syed F; Mahmood A; Ur Rehman H; Khurshid B; Samad A; Ahmad W; Basit S
    Medicina (Kaunas); 2023 Feb; 59(2):. PubMed ID: 36837579
    [No Abstract]   [Full Text] [Related]  

  • 3. Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia.
    Deorukhkar A; Kulkarni A; Kedar P
    Mol Biol Rep; 2022 Mar; 49(3):2141-2147. PubMed ID: 35064402
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial Congenital Methemoglobinemia in Pomeranian Dogs Caused by a Missense Variant in the NADH-Cytochrome B5 Reductase Gene.
    Shino H; Otsuka-Yamasaki Y; Sato T; Ooi K; Inanami O; Sato R; Yamasaki M
    J Vet Intern Med; 2018 Jan; 32(1):165-171. PubMed ID: 29356095
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.
    Kedar PS; Gupta V; Warang P; Chiddarwar A; Madkaikar M
    Hematology; 2018 Sep; 23(8):567-573. PubMed ID: 29482478
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel L218P mutation in NADH-cytochrome b5 reductase associated with type I recessive congenital methemoglobinemia.
    Arikoglu T; Yarali N; Kara A; Bay A; Bozkaya IO; Tunc B; Percy MJ
    Pediatr Hematol Oncol; 2009; 26(5):381-5. PubMed ID: 19579085
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation update: Variants of the CYB5R3 gene in recessive congenital methemoglobinemia.
    Gupta V; Kulkarni A; Warang P; Devendra R; Chiddarwar A; Kedar P
    Hum Mutat; 2020 Apr; 41(4):737-748. PubMed ID: 31898843
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.
    Warang PP; Kedar PS; Shanmukaiah C; Ghosh K; Colah RB
    Clin Genet; 2015; 87(1):62-7. PubMed ID: 24266649
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel Compound Heterogeneous Mutations in CYB5R3 Gene Leading to Methemoglobinemia (Type I) in a Chinese Boy: Case Report and Relevant Comprehensive Analysis.
    Yang Y; Yang Y; Meng Y; Huang L; Yang Z
    Acta Haematol; 2024 May; ():1-7. PubMed ID: 38781945
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular basis of two novel mutations found in type I methemoglobinemia.
    Lorenzo FR; Phillips JD; Nussenzveig R; Lingam B; Koul PA; Schrier SL; Prchal JT
    Blood Cells Mol Dis; 2011 Apr; 46(4):277-81. PubMed ID: 21349748
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical, metabolic, and molecular genetic characterization of hereditary methemoglobinemia caused by cytochrome b
    Jaffey JA; Reading NS; Abdulmalik O; Kreisler R; Bullock G; Wiest A; Villani NA; Mhlanga-Mutangadura T; Johnson GS; Cohn LA; Isaza N; Harvey JW; Giger U
    Sci Rep; 2020 Dec; 10(1):21399. PubMed ID: 33293645
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Congenital Recessive Methemoglobinemia Revealed in Adulthood: Description of a New Mutation in Cytochrome b5 Reductase Gene.
    Forestier A; Pissard S; Cretet J; Mambie A; Pascal L; Cliquennois M; Cambier N; Rose C
    Hemoglobin; 2015; 39(6):438-41. PubMed ID: 26291966
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene.
    Fermo E; Bianchi P; Vercellati C; Marcello AP; Garatti M; Marangoni O; Barcellini W; Zanella A
    Blood Cells Mol Dis; 2008; 41(1):50-5. PubMed ID: 18343696
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of a novel nicotinamide adenine dinucleotide-cytochrome b5 reductase mutation associated with canine hereditary methemoglobinemia.
    Otsuka-Yamasaki Y; Inanami O; Shino H; Sato R; Yamasaki M
    J Vet Med Sci; 2021 Mar; 83(2):315-321. PubMed ID: 33342963
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Novel large deletion c.22-1320_633+1224del in the CYB5R3 gene from patients with hereditary methemoglobinemia].
    Galeeva NM; Nenasheva SA; Kleĭmenova IS; Poliakov AV
    Genetika; 2012 Nov; 48(11):1336-46. PubMed ID: 23297489
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CYB5R3 homozygous pathogenic variant as a rare cause of cyanosis in the newborn.
    Molina Herranz D; García Escudero C; Rite Gracia S; Aguilar de la Red Y; Martínez Nieto J; Izquierdo Álvarez S; Montañés Gracia MA; Recasens V; Hernández Mata CF
    Clin Biochem; 2022 Apr; 102():67-70. PubMed ID: 35104462
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Population frequency and age of c.806C > T mutation in CYB5R3 gene as cause of recessive congenital methemoglobinemia in Yakutia].
    Galeeva NM; Voevoda MI; Spiridonova MG; Stepanov VA; Poliakov AV
    Genetika; 2013 Apr; 49(4):523-30. PubMed ID: 23866629
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel G143D mutation in the NADH-cytochrome b5 reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
    Kedar PS; Warang P; Nadkarni AH; Colah RB; Ghosh K
    Blood Cells Mol Dis; 2008; 40(3):323-7. PubMed ID: 17964195
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital Methemoglobinemia Type II-Clinical Improvement with Short-Term Methylene Blue Treatment.
    Cooper MS; Randall M; Rowell M; Charlton M; Greenway A; Barnes C
    Pediatr Blood Cancer; 2016 Mar; 63(3):558-60. PubMed ID: 26574897
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary Congenital Methemoglobinemia Diagnosed at the Age of 79 Years: A Case Report.
    Nakata M; Yokota N; Tabata K; Morikawa T; Shibata H; Kenzaka T
    Medicina (Kaunas); 2023 Mar; 59(3):. PubMed ID: 36984616
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.