94 related articles for article (PubMed ID: 12632327)
1. Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hips.
Hellemans J; Coucke PJ; Giedion A; De Paepe A; Kramer P; Beemer F; Mortier GR
Am J Hum Genet; 2003 Apr; 72(4):1040-6. PubMed ID: 12632327
[TBL] [Abstract][Full Text] [Related]
2. Brachydactyly A-1 mutations restricted to the central region of the N-terminal active fragment of Indian Hedgehog.
Byrnes AM; Racacho L; Grimsey A; Hudgins L; Kwan AC; Sangalli M; Kidd A; Yaron Y; Lau YL; Nikkel SM; Bulman DE
Eur J Hum Genet; 2009 Sep; 17(9):1112-20. PubMed ID: 19277064
[TBL] [Abstract][Full Text] [Related]
3. IHH enhancer variant within neighboring NHEJ1 intron causes microphthalmia anophthalmia and coloboma.
Wormser O; Perez Y; Dolgin V; Kamali B; Tangeman JA; Gradstein L; Yogev Y; Hadar N; Freund O; Drabkin M; Halperin D; Irron I; Grajales-Esquivel E; Del Rio-Tsonis K; Birnbaum RY; Akler G; Birk OS
NPJ Genom Med; 2023 Aug; 8(1):22. PubMed ID: 37580330
[TBL] [Abstract][Full Text] [Related]
4. IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy.
Vasques GA; Funari MFA; Ferreira FM; Aza-Carmona M; Sentchordi-MontanĂ© L; Barraza-GarcĂa J; Lerario AM; Yamamoto GL; Naslavsky MS; Duarte YAO; Bertola DR; Heath KE; Jorge AAL
J Clin Endocrinol Metab; 2018 Feb; 103(2):604-614. PubMed ID: 29155992
[TBL] [Abstract][Full Text] [Related]
5. Suppression of apoptosis impairs phalangeal joint formation in the pathogenesis of brachydactyly type A1.
Leung AOW; Poon ACH; Wang X; Feng C; Chen P; Zheng Z; To MK; Chan WCW; Cheung M; Chan D
Nat Commun; 2024 Mar; 15(1):2229. PubMed ID: 38472182
[TBL] [Abstract][Full Text] [Related]
6. Hedgehog-Related Mutation Causes Bone Malformations with or without Hereditary Gene Mutations.
Onodera S; Azuma T
Int J Mol Sci; 2023 Aug; 24(16):. PubMed ID: 37629084
[TBL] [Abstract][Full Text] [Related]
7. Hedgehog Signaling in Gonadal Development and Function.
Dilower I; Niloy AJ; Kumar V; Kothari A; Lee EB; Rumi MAK
Cells; 2023 Jan; 12(3):. PubMed ID: 36766700
[TBL] [Abstract][Full Text] [Related]
8. From mesenchymal niches to engineered
Ghuloum FI; Johnson CA; Riobo-Del Galdo NA; Amer MH
Mater Today Bio; 2022 Dec; 17():100502. PubMed ID: 36457847
[TBL] [Abstract][Full Text] [Related]
9. Inactivation of Ihh in Sp7-Expressing Cells Inhibits Osteoblast Proliferation, Differentiation, and Bone Formation, Resulting in a Dwarfism Phenotype with Severe Skeletal Dysplasia in Mice.
Wang Y; Dong Z; Yang R; Zong S; Wei X; Wang C; Guo L; Sun J; Li H; Li P
Calcif Tissue Int; 2022 Nov; 111(5):519-534. PubMed ID: 35731246
[TBL] [Abstract][Full Text] [Related]
10. Molecular Bases of Human Malformation Syndromes Involving the SHH Pathway: GLIA/R Balance and Cardinal Phenotypes.
Niida Y; Togi S; Ura H
Int J Mol Sci; 2021 Dec; 22(23):. PubMed ID: 34884862
[TBL] [Abstract][Full Text] [Related]
11. SAG therapy restores bone growth and reduces enchondroma incidence in a model of skeletal chondrodysplasias caused by Ihh deficiency.
Li X; Yang S; Chinipardaz Z; Koyama E; Yang S
Mol Ther Methods Clin Dev; 2021 Dec; 23():461-475. PubMed ID: 34820473
[TBL] [Abstract][Full Text] [Related]
12. The Hedgehog Signaling Pathway is Expressed in the Adult Mouse Hypothalamus and Modulated by Fasting.
Antonellis PJ; Engle SE; Brewer KM; Berbari NF
eNeuro; 2021; 8(5):. PubMed ID: 34535504
[TBL] [Abstract][Full Text] [Related]
13. Highly Conserved
Wang X; Liu H; Liu Y; Han G; Wang Y; Chen H; He L; Ma G
Biomolecules; 2021 May; 11(6):. PubMed ID: 34070546
[TBL] [Abstract][Full Text] [Related]
14. Signaling Pathways in Bone Development and Their Related Skeletal Dysplasia.
Guasto A; Cormier-Daire V
Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33919228
[TBL] [Abstract][Full Text] [Related]
15. Exposure to tert-Butylphenyl Diphenyl Phosphate, an Organophosphate Ester Flame Retardant and Plasticizer, Alters Hedgehog Signaling in Murine Limb Bud Cultures.
Yan H; Hales BF
Toxicol Sci; 2020 Dec; 178(2):251-263. PubMed ID: 32976586
[TBL] [Abstract][Full Text] [Related]
16. Cilia signaling and obesity.
Engle SE; Bansal R; Antonellis PJ; Berbari NF
Semin Cell Dev Biol; 2021 Feb; 110():43-50. PubMed ID: 32466971
[TBL] [Abstract][Full Text] [Related]
17. A novel variant of IHH in a Chinese family with brachydactyly type 1.
Yang Q; Wang J; Tian X; Shen F; Lan J; Zhang Q; Fan X; Yi S; Li M; Shen Y
BMC Med Genet; 2020 Mar; 21(1):60. PubMed ID: 32209048
[TBL] [Abstract][Full Text] [Related]
18. Whole-exome sequencing identified a novel variant in an Iranian patient affected by pycnodysostosis.
Razmara E; Azimi H; Bitaraf A; Daneshmand MA; Galehdari M; Dokhanchi M; Esmaeilzadeh-Gharehdaghi E; Garshasbi M
Mol Genet Genomic Med; 2020 Mar; 8(3):e1118. PubMed ID: 31944631
[TBL] [Abstract][Full Text] [Related]
19. Hedgehog Signal and Genetic Disorders.
Sasai N; Toriyama M; Kondo T
Front Genet; 2019; 10():1103. PubMed ID: 31781166
[TBL] [Abstract][Full Text] [Related]
20. Recent Insights into Long Bone Development: Central Role of Hedgehog Signaling Pathway in Regulating Growth Plate.
Haraguchi R; Kitazawa R; Kohara Y; Ikedo A; Imai Y; Kitazawa S
Int J Mol Sci; 2019 Nov; 20(23):. PubMed ID: 31757091
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]