Coletto, Erika, Latousakis, Dimitrios, Pontifex, Matthew G. ORCID: https://orcid.org/0000-0003-2174-2313, Crost, Emmanuelle H., Vaux, Laura, Perez Santamarina, Estella, Goldson, Andrew, Brion, Arlaine, Hajihosseini, Mohammad K., Vauzour, David ORCID: https://orcid.org/0000-0001-5952-8756, Savva, George M. and Juge, Nathalie (2022) The role of the mucin-glycan foraging Ruminococcus gnavus in the communication between the gut and the brain. Gut Microbes, 14 (1). ISSN 1949-0976
Mauduit, Olivier, Aure, Marit H., Delcroix, Vanessa, Basova, Liana, Srivastava, Amrita, Umazume, Takeshi, Mays, Jacqueline W., Bellusci, Saverio, Tucker, Abigail S., Hajihosseini, Mohammad K., Hoffman, Matthew P. and Makarenkova, Helen P. (2022) A mesenchymal to epithelial switch in Fgf10 expression specifies an evolutionary-conserved population of ionocytes in salivary glands. Cell Reports, 39 (2). ISSN 2211-1247
Leomnia, Chatzeli, Teshima, Tathyane H. N., Hajihosseini, Mohammad K., Gaete, Marcia, Proctor, Gordon B. and Tucker, Abigail S. (2021) Comparing development and regeneration in the submandibular gland highlights distinct mechanisms. Journal of Anatomy, 238 (6). pp. 1371-1385. ISSN 0021-8782
Zhang, Yang, Fons, Juan M., Hajihosseini, Mohammad K., Zhang, Tianyu and Tucker, Abigail S. (2020) An essential requirement for Fgf10 in pinna extension sheds light on auricle defects in LADD syndrome. Frontiers in Cell and Developmental Biology, 8. ISSN 2296-634X
Goodman, Timothy, Nayar, Stuart G., Clare, Shaun, Mikolajczak, Marta, Rice, Ritva, Mansour, Suzanne, Bellusci, Saverio and Hajihosseini, Mohammad K. (2020) Fibroblast growth factor 10 is a negative regulator of postnatal neurogenesis in the mouse hypothalamus. Development, 147 (13). ISSN 0950-1991
Hagan, Andrew, Boylan, Michael, Smith, Craig, Perez Santamarina, Estela, Kowalska, Karolina, Huang, Irene, Lewis, Renate M., Hajihosseini, Mohammad K., Lewandoski, Mark and Ornitz, David M. (2019) Generation and validation of novel conditional flox and inducible Cre alleles targeting fibroblast growth factor 18 (Fgf18). Developmental Dynamics, 248 (9). pp. 882-893. ISSN 1058-8388
Kaminskas, Benediktas, Goodman, Timothy, Hagan, Andrew, Bellusci, Saverio, Ornitz, David M. and Hajihosseini, Mohammad K. (2019) Characterization of endogenous players in Fibroblast Growth Factor‐regulated functions of hypothalamic tanycytes and energy‐balance nuclei. Journal of Neuroendocrinology, 31 (8). ISSN 0953-8194
Pla-Navarro, Irene, Bevan, Damon, Hajihosseini, Mohammad K., Lee, Martin and Gavrilovic, Jelena ORCID: https://orcid.org/0000-0002-5312-1784 (2018) Interplay between metalloproteinases and cell signalling in blood brain barrier integrity. Histology and Histopathology, 33. pp. 1253-1270. ISSN 0213-3911
Mikolajczak, Marta, Goodman, Timothy and Hajihosseini, Mohammad K. (2016) Interrogation of a lacrimo-auriculo-dento-digital syndrome protein reveals novel modes of fibroblast growth factor 10 (FGF10) function. Biochemical Journal, 473 (24). pp. 4593-4607. ISSN 0264-6021
Goodman, Timothy and Hajihosseini, Mohammad K. (2015) Hypothalamic tanycytes—masters and servants of metabolic, neuroendocrine, and neurogenic functions. Frontiers in Neuroscience, 9. ISSN 1662-4548
Siggers, Pam, Carré, Gwenn-Aël, Bogani, Debora, Warr, Nick, Wells, Sara, Hilton, Helen, Esapa, Chris, Hajihosseini, Mohammad K. and Greenfield, Andy (2014) A novel mouse Fgfr2 mutant, hobbyhorse (hob), exhibits complete XY gonadal sex reversal. PLoS One, 9 (6). ISSN 1932-6203
Danopoulos, Soula, Parsa, Sara, Al Alam, Denise, Tabatabai, Reza, Baptista, Sheryl, Tiozzo, Caterina, Carraro, Gianni, Wheeler, Matthew, Barreto, Guillermo, Braun, Thomas, Li, Xiaokun, Hajihosseini, Mohammad K. and Bellusci, Saverio (2013) Transient inhibition of FGFR2b-ligands signaling leads to irreversible loss of cellular β-catenin organization and signaling in AER during mouse limb development. PLoS One, 8 (10). ISSN 1932-6203
Haan, Niels, Goodman, Timothy, Najdi-Samiei, Alaleh, Stratford, Christina M., Rice, Ritva, El Agha, Elie, Bellusci, Saverio and Hajihosseini, Mohammad K. (2013) Fgf10-expressing tanycytes add new neurons to the appetite/energy-balance regulating centers of the postnatal and adult hypothalamus. The Journal of Neuroscience, 33 (14). pp. 6170-6180. ISSN 0270-6474
El Agha, Elie, Al Alam, Denise, Carraro, Gianni, MacKenzie, BreAnne, Goth, Kerstin, De Langhe, Stijn P., Voswinckel, Robert, Hajihosseini, Mohammad K., Rehan, Virender K. and Bellusci, Saverio (2012) Characterization of a novel fibroblast growth factor 10 (Fgf10) knock-in mouse line to target mesenchymal progenitors during embryonic development. PLoS One, 7 (6). ISSN 1932-6203
Swingler, Tracey E., Wheeler, Guy, Carmont, Virginia, Elliott, Hannah R., Barter, Matthew J., Abu-Elmagd, Muhammad, Donell, Simon T., Boot-Handford, Raymond P., Hajihosseini, Mohammad K., Munsterberg, Andrea ORCID: https://orcid.org/0000-0002-4577-4240, Dalmay, Tamas ORCID: https://orcid.org/0000-0003-1492-5429, Young, David A. and Clark, Ian M. (2012) The expression and function of microRNAs in chondrogenesis and osteoarthritis. Arthritis & Rheumatism, 64 (6). pp. 1909-1919. ISSN 1529-0131
Wheldon, Lee M., Khodabukus, Naila, Patey, Susannah J., Smith, Terence G., Heath, John K. and Hajihosseini, Mohammad K. (2011) Identification and characterization of an inhibitory fibroblast growth factor receptor 2 (FGFR2) molecule, up-regulated in an Apert Syndrome mouse model. Biochemical Journal, 436 (1). pp. 71-81. ISSN 0264-6021
Swingler, TE, Culley, KL, Nicolas, F, Soond, S, Abu-Elmagd, M, Boot-Handford, RP, Young, DA, Chantry, A, Munsterberg, A ORCID: https://orcid.org/0000-0002-4577-4240 and Hajihosseini, M (2010) 066 Identification and Characterisation of Micrornas Involved in Chondrocyte Differentiation and Osteoarthritis. Working Paper. UNSPECIFIED.
Tiozzo, Caterina, De Langhe, Stijn, Carraro, Gianni, Alam, Denise Al, Nagy, Andre, Wigfall, Clarence, Hajihosseini, Mohammad, Warburton, David, Minoo, Parviz and Bellusci, Saverio (2009) Fibroblast growth factor 10 plays a causative role in the tracheal cartilage defects in a mouse model of Apert syndrome. Pediatric Research, 66 (4). pp. 386-390. ISSN 0031-3998
Garcia-Morales, Carla, Liu, Chiung-Hui, Abu-Elmagd, Muhammad, Hajihosseini, Mohammad K. and Wheeler, Grant N. ORCID: https://orcid.org/0000-0002-4335-8577 (2009) Frizzled-10 promotes sensory neuron development in Xenopus embryos. Developmental Biology, 335 (1). pp. 143-155. ISSN 1095-564X
Hajihosseini, Mohammad K., Duarte, Raquel, Pegrum, Jean, Donjacour, Anne, Lana-Elola, Eva, Rice, David P., Sharpe, James and Dickson, Clive (2009) Evidence that Fgf10 contributes to the skeletal and visceral defects of an Apert syndrome mouse model. Developmental Dynamics, 238. pp. 376-385. ISSN 1097-0177
Redshaw, Nicholas, Wheeler, Guy, Hajihosseini, Mohammad K. and Dalmay, Tamas ORCID: https://orcid.org/0000-0003-1492-5429 (2009) microRNA-449 is a putative regulator of choroid plexus development and function. Brain Research, 1250. pp. 20-26. ISSN 1872-6240
Hajihosseini, Mohammad K., De Langhe, Stijn P., Lana-Elola, Eva, Morrison, Harris, Sparshott, Neil, Kelly, Robert, Sharpe, James, Rice, David and Bellusci, Saverio (2008) Localization and fate of Fgf10-expressing cells in the adult mouse brain implicate Fgf10 in control of neurogenesis. Molecular and Cellular Neuroscience, 37 (4). pp. 857-868.
De Langhe, Stijn P., Carraro, Gianni, Tefft, Denise, Li, Changgong, Xu, Xin, Chai, Yang, Minoo, Parviz, Hajihosseini, Mohammad K., Drouin, Jacques, Kaartinen, Vesa and Bellusci, Savério (2008) Formation and differentiation of multiple mesenchymal lineages during lung development is regulated by beta-catenin signaling. PLoS One, 3 (1). ISSN 1932-6203
Hajihosseini, MK (2008) FGF Signalling in cranial suture development and pathogenesis. In: Craniofacial sutures: Development, Disease and Treatment. S. Karger AG, pp. 160-177.
De Langhe, Stijn P., Carraro, Gianni, Warburton, David, Hajihosseini, Mohammad K. and Bellusci, Saverio (2006) Levels of mesenchymal FGFR2 signalling modulate smooth muscle progenitor cell commitment in the lung. Developmental Biology, 299 (1). pp. 52-62. ISSN 1095-564X
Tuddenham, Lee, Wheeler, Guy, Ntouniafousara, Sofia, Waters, Jasmine, Hajihosseini, Mohammad, Clark, Ian and Dalmay, Tamas ORCID: https://orcid.org/0000-0003-1492-5429 (2006) The cartilage specific microRNA-140 targets histone deacetylase 4 in mouse cells. FEBS Letters, 580 (17). pp. 4214-4217. ISSN 1873-3468
Jaskoll, Tina, Abichaker, George, Witcher, Daniel, Sala, Frederic G., Bellusci, Saverio, Hajihosseini, Mohammad K. and Melnick, Michael (2005) FGF10/FGFR2b signaling plays essential roles during in vivo embryonic submandibular salivary gland morphogenesis. BMC Developmental Biology, 5. ISSN 1471-213X
Hajihosseini, Mohammad K., Lalioti, Maria D., Arthaud, Sandrine, Burgar, Helen R., Brown, Jill M., Twigg, Stephen R., Wilkie, Andrew O. M. and Heath, John K. (2004) Skeletal development is regulated by fibroblast growth factor receptor 1 signalling. Development, 113 (2). pp. 325-335. ISSN 0950-1991
Satoh, Yoshihiko, Haraguchi, Ryuma, Wright, Tracy J., Mansour, Suzanne L., Partanen, Juha, Hajihosseini, Mohammad K., Eswarakumar, Veraragavan P., Lonai, Peter and Yamada, Gen (2004) Regulation of external genitalia development by concerted action of FGF ligands and FGF receptors. Anatomy and Embryology, 208 (6). pp. 479-486. ISSN 1432-0568
Hajihosseini, Mohammad K. and Heath, John K. (2002) Expression patterns of fibroblast growth factors-18 and -20 in mouse embryos is suggestive of novel roles in calvarial and limb development. Mechanisms of Development, 113 (1). pp. 79-83. ISSN 0925-4773
Jaskoll, T., Zhou, Y.M., Chai, Y., Makarenkova, H.P., Collinson, J.M., West, J.D., Hajihosseini, M.K., Lee, J. and Melnick, M. (2002) Embryonic submandibular gland morphogenesis: stage-specific protein localization of FGFs, BMPs, Pax6 and Pax9 in normal mice and abnormal SMG phenotypes in FgfR2-IIIc(+/*), BMP7(-/-) and Pax6(-/-) mice. Cells Tissues Organs, 170. pp. 83-98. ISSN 1422-6421
Hajihosseini, Mohammad K., Wilson, Stephen, De Moerlooze, Laurence and Dickson, Clive (2001) A splicing switch and gain-of-function mutation in FgfR2-IIIc hemizygotes causes Apert/Pfeiffer-syndrome-like phenotypes. Proceedings of the National Academy of Sciences, 98 (7). pp. 3855-3860. ISSN 0027-8424