BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

256 related articles for article (PubMed ID: 27756091)

  • 1. Identification of Novel PROP1 and POU1F1 Mutations in Patients with Combined Pituitary Hormone Deficiency.
    Birla S; Khadgawat R; Jyotsna VP; Jain V; Garg MK; Bhalla AS; Sharma A
    Horm Metab Res; 2016 Dec; 48(12):822-827. PubMed ID: 27756091
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.
    de Graaff LC; Argente J; Veenma DC; Drent ML; Uitterlinden AG; Hokken-Koelega AC
    Horm Res Paediatr; 2010; 73(5):363-71. PubMed ID: 20389107
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Identification of novel GHRHR and GH1 mutations in patients with isolated growth hormone deficiency.
    Birla S; Khadgawat R; Jyotsna VP; Jain V; Garg MK; Bhalla AS; Sharma A
    Growth Horm IGF Res; 2016 Aug; 29():50-56. PubMed ID: 27114065
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.
    Baş F; Uyguner ZO; Darendeliler F; Aycan Z; Çetinkaya E; Berberoğlu M; Şiklar Z; Öcal G; Darcan Ş; Gökşen D; Topaloğlu AK; Yüksel B; Özbek MN; Ercan O; Evliyaoğlu O; Çetinkaya S; Şen Y; Atabek E; Toksoy G; Aydin BK; Bundak R
    Endocrine; 2015 Jun; 49(2):479-91. PubMed ID: 25500790
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic screening of regulatory regions of pituitary transcription factors in patients with idiopathic pituitary hormone deficiencies.
    Elizabeth M; Hokken-Koelega ACS; Schuilwerve J; Peeters RP; Visser TJ; de Graaff LCG
    Pituitary; 2018 Feb; 21(1):76-83. PubMed ID: 29255988
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.
    Choi JH; Jung CW; Kang E; Kim YM; Heo SH; Lee BH; Kim GH; Yoo HW
    Yonsei Med J; 2017 May; 58(3):527-532. PubMed ID: 28332357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Long-Term Outcomes, Genetics, and Pituitary Morphology in Patients with Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiencies: A Single-Centre Experience of Four Decades of Growth Hormone Replacement.
    Rohayem J; Drechsel H; Tittel B; Hahn G; Pfaeffle R; Huebner A
    Horm Res Paediatr; 2016; 86(2):106-116. PubMed ID: 27487097
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency.
    Vieira TC; Boldarine VT; Abucham J
    Arq Bras Endocrinol Metabol; 2007 Oct; 51(7):1097-103. PubMed ID: 18157385
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism.
    Fritez N; Sobrier ML; Iraqi H; Vié-Luton MP; Netchine I; El Annas A; Pantel J; Collot N; Rose S; Piterboth W; Legendre M; Chraibi A; Amselem S; Kadiri A; Hilal L
    Clin Endocrinol (Oxf); 2015 Jun; 82(6):876-84. PubMed ID: 25557026
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].
    Halász Z
    Orv Hetil; 2011 Feb; 152(6):221-32. PubMed ID: 21278027
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic spectrum and predictors of mutations in four known genes in Asian Indian patients with growth hormone deficiency and orthotopic posterior pituitary: an emphasis on regional genetic diversity.
    Kale S; Gada JV; Jadhav S; Lila AR; Sarathi V; Budyal S; Patt H; Goroshi MR; Thadani PM; Arya S; Kamble AA; Patil VA; Acharya S; Sankhe S; Shivane V; Raghavan V; Bandgar TR; Shah NS
    Pituitary; 2020 Dec; 23(6):701-715. PubMed ID: 32894409
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations Within the Transcription Factor
    Bulut FD; Özdemir Dilek S; Kotan D; Mengen E; Gürbüz F; Yüksel B
    J Clin Res Pediatr Endocrinol; 2020 Sep; 12(3):261-268. PubMed ID: 31948187
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two coexisting heterozygous frameshift mutations in PROP1 are responsible for a different phenotype of combined pituitary hormone deficiency.
    Ziemnicka K; Budny B; Drobnik K; Baszko-Błaszyk D; Stajgis M; Katulska K; Waśko R; Wrotkowska E; Słomski R; Ruchała M
    J Appl Genet; 2016 Aug; 57(3):373-81. PubMed ID: 26608600
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Combined pituitary hormone deficiency due to gross deletions in the POU1F1 (PIT-1) and PROP1 genes.
    Bertko E; Klammt J; Dusatkova P; Bahceci M; Gonc N; Ten Have L; Kandemir N; Mansmann G; Obermannova B; Oostdijk W; Pfäffle H; Rockstroh-Lippold D; Schlicke M; Tuzcu AK; Pfäffle R
    J Hum Genet; 2017 Aug; 62(8):755-762. PubMed ID: 28356564
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
    Avbelj Stefanija M; Kotnik P; Bratanič N; Žerjav Tanšek M; Bertok S; Bratina N; Battelino T; Trebušak Podkrajšek K
    Horm Res Paediatr; 2015; 84(3):153-8. PubMed ID: 26111865
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
    Reynaud R; Gueydan M; Saveanu A; Vallette-Kasic S; Enjalbert A; Brue T; Barlier A
    J Clin Endocrinol Metab; 2006 Sep; 91(9):3329-36. PubMed ID: 16735499
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Characterization of a Novel POU1F1 Mutation Identified on Screening 160 Growth Hormone Deficiency Patients.
    Birla S; Vijayakumar P; Sehgal S; Bhatnagar S; Pallavi K; Sharma A
    Horm Metab Res; 2019 Apr; 51(4):248-255. PubMed ID: 31022740
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.
    Rainbow LA; Rees SA; Shaikh MG; Shaw NJ; Cole T; Barrett TG; Kirk JM
    Clin Endocrinol (Oxf); 2005 Feb; 62(2):163-8. PubMed ID: 15670191
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
    Turton JP; Mehta A; Raza J; Woods KS; Tiulpakov A; Cassar J; Chong K; Thomas PQ; Eunice M; Ammini AC; Bouloux PM; Starzyk J; Hindmarsh PC; Dattani MT
    Clin Endocrinol (Oxf); 2005 Jul; 63(1):10-8. PubMed ID: 15963055
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
    Madeira JL; Nishi MY; Nakaguma M; Benedetti AF; Biscotto IP; Fernandes T; Pequeno T; Figueiredo T; Franca MM; Correa FA; Otto AP; Abrão M; Miras MB; Santos S; Jorge AA; Costalonga EF; Mendonca BB; Arnhold IJ; Carvalho LR
    Clin Endocrinol (Oxf); 2017 Dec; 87(6):725-732. PubMed ID: 28734020
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.