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 *

182 related articles for article (PubMed ID: 10844410)

  • 1. Alternative splicing of exon 17 and a missense mutation in exon 20 of the insulin receptor gene in two brothers with a novel syndrome of insulin resistance (congenital fiber-type disproportion myopathy).
    Vorwerk P; Christoffersen CT; Müller J; Vestergaard H; Pedersen O; De Meyts P
    Horm Res; 1999; 52(5):211-20. PubMed ID: 10844410
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Insulin resistance and diabetes due to different mutations in the tyrosine kinase domain of both insulin receptor gene alleles.
    Kusari J; Takata Y; Hatada E; Freidenberg G; Kolterman O; Olefsky JM
    J Biol Chem; 1991 Mar; 266(8):5260-7. PubMed ID: 2002058
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Implications of compound heterozygous insulin receptor mutations in congenital muscle fibre type disproportion myopathy for the receptor kinase activation.
    Klein HH; Müller R; Vestergaard H; Pedersen O
    Diabetologia; 1999 Feb; 42(2):245-9. PubMed ID: 10064106
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Substitution of Leu for Pro-193 in the insulin receptor in a patient with a genetic form of severe insulin resistance.
    Carrera P; Cordera R; Ferrari M; Cremonesi L; Taramelli R; Andraghetti G; Carducci C; Dozio N; Pozza G; Taylor SI
    Hum Mol Genet; 1993 Sep; 2(9):1437-41. PubMed ID: 8242067
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A mutation (Trp1193-->Leu1193) in the tyrosine kinase domain of the insulin receptor associated with type A syndrome of insulin resistance.
    Iwanishi M; Haruta T; Takata Y; Ishibashi O; Sasaoka T; Egawa K; Imamura T; Naitou K; Itazu T; Kobayashi M
    Diabetologia; 1993 May; 36(5):414-22. PubMed ID: 8390949
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An in-frame insertion in exon 3 and a nonsense mutation in exon 2 of the insulin receptor gene associated with severe insulin resistance in a patient with Rabson-Mendenhall syndrome.
    Müller-Wieland D; van der Vorm ER; Streicher R; Krone W; Seemanova E; Dreyer M; Rüdiger HW; Rosipal SR; Maassen JA
    Diabetologia; 1993 Nov; 36(11):1168-74. PubMed ID: 8270132
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Four mutant alleles of the insulin receptor gene associated with genetic syndromes of extreme insulin resistance.
    Kadowaki H; Takahashi Y; Ando A; Momomura K; Kaburagi Y; Quin JD; MacCuish AC; Koda N; Fukushima Y; Taylor SI; Akanuma Y; Yazaki Y; Kadowaki T
    Biochem Biophys Res Commun; 1997 Aug; 237(3):516-20. PubMed ID: 9299395
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical characteristics of adolescent cases with Type A insulin resistance syndrome caused by heterozygous mutations in the β-subunit of the insulin receptor (INSR) gene.
    Takasawa K; Tsuji-Hosokawa A; Takishima S; Wada Y; Nagasaki K; Dateki S; Numakura C; Hijikata A; Shirai T; Kashimada K; Morio T
    J Diabetes; 2019 Jan; 11(1):46-54. PubMed ID: 29877041
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of two novel insulin receptor mutations, Asp59Gly and Leu62Pro, in type A syndrome of extreme insulin resistance.
    Rouard M; Macari F; Bouix O; Lautier C; Brun JF; Lefebvre P; Renard E; Bringer J; Jaffiol C; Grigorescu F
    Biochem Biophys Res Commun; 1997 May; 234(3):764-8. PubMed ID: 9175790
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A naturally occurring mutation of insulin receptor alanine 1134 impairs tyrosine kinase function and is associated with dominantly inherited insulin resistance.
    Moller DE; Yokota A; White MF; Pazianos AG; Flier JS
    J Biol Chem; 1990 Sep; 265(25):14979-85. PubMed ID: 2168397
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Insulin resistance associated with decreased levels of insulin-receptor messenger ribonucleic acid: evidence of a de novo mutation in the maternal allele.
    Suzuki Y; Hatanaka Y; Taira M; Shimada F; Hashimoto N; Takayanagi M; Taylor SI; Makino H; Yoshida S
    J Clin Endocrinol Metab; 1995 Apr; 80(4):1214-20. PubMed ID: 7714091
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Severe resistance to insulin and insulin-like growth factor-I in cells from a patient with leprechaunism as a result of two mutations in the tyrosine kinase domain of the insulin receptor.
    Desbois-Mouthon C; Danan C; Amselem S; Blivet-Van Eggelpoel MJ; Sert-Langeron C; Goossens M; Besmond C; Capeau J; Caron M
    Metabolism; 1996 Dec; 45(12):1493-500. PubMed ID: 8969282
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A glycine-1008 to valine mutation in the insulin receptor in a woman with type A insulin resistance.
    Nozaki O; Suzuki Y; Shimada F; Hashimoto N; Taira M; Hatanaka Y; Notoya Y; Kanashiro O; Makino H; Yoshida S
    J Clin Endocrinol Metab; 1993 Jul; 77(1):169-72. PubMed ID: 8392082
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Ala1048-->Asp mutation in the kinase domain of insulin receptor causes defective kinase activity and insulin resistance.
    Haruta T; Takata Y; Iwanishi M; Maegawa H; Imamura T; Egawa K; Itazu T; Kobayashi M
    Diabetes; 1993 Dec; 42(12):1837-44. PubMed ID: 8243830
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human diabetes associated with a deletion of the tyrosine kinase domain of the insulin receptor.
    Taira M; Taira M; Hashimoto N; Shimada F; Suzuki Y; Kanatsuka A; Nakamura F; Ebina Y; Tatibana M; Makino H
    Science; 1989 Jul; 245(4913):63-6. PubMed ID: 2544997
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of novel C253Y missense and Y864X nonsense mutations in the insulin receptor gene in type A insulin-resistant patients.
    Osawa H; Nishimiya T; Ochi M; Niiya T; Onuma H; Kitamuro F; Kaino Y; Kida K; Makino H
    Clin Genet; 2001 Mar; 59(3):194-7. PubMed ID: 11260230
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of three novel mutations in the insulin receptor gene in type A insulin resistant patients.
    Riqué S; Nogués C; Ibàñez L; Marcos MV; Ferragut J; Carrascosa A; Potau N
    Clin Genet; 2000 Jan; 57(1):67-9. PubMed ID: 10733238
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of mutations in the insulin receptor gene in subjects with features of the type A syndrome of insulin resistance.
    Moller DE; Cohen O; Yamaguchi Y; Assiz R; Grigorescu F; Eberle A; Morrow LA; Moses AC; Flier JS
    Diabetes; 1994 Feb; 43(2):247-55. PubMed ID: 8288049
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A 3-basepair in-frame deletion (delta Leu999) in exon 17 of the insulin receptor gene in a family with insulin resistance.
    Awata T; Matsumoto C; Momomura K; Takahashi Y; Odawara M; Kasuga M; Kadowaki T; Iwamoto Y
    J Clin Endocrinol Metab; 1994 Dec; 79(6):1840-4. PubMed ID: 7989492
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Arg1201Gln mutation of insulin receptor impairs tyrosine kinase activity and causes insulin resistance: a case report.
    Ding Q; Liang M
    Gynecol Endocrinol; 2020 Jun; 36(6):558-560. PubMed ID: 31899992
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.