A population-based audit of ethnicity and breast cancer risk in one general practice catchment area in North London, UK: implications for practice von Ferris, Michelle, Easton, Douglas F, Doherty, Rebecca J, Briggs, Brian Hj, Newman, Michelle, Saraf, Ifthikhar M, Scambler, Sarah, Wagman, Lyndon, Wyndham, Michael T, Ward, Ann, Eeles, Rosalind A

Volltext

Implications for cancer genetics practice of pro-actively assessing family history in a General Practice cohort in North West London von Kohut, Kelly, D’Mello, Lucia, Bancroft, Elizabeth K., Thomas, Sarah, Young, Mary-Anne, Myhill, Kathryn, Shanley, Susan, Briggs, Brian H. J., Newman, Michelle, Saraf, Ifthikhar M., Cox, Penny, Scambler, Sarah, Wagman, Lyndon, Wyndham, Michael T., Eeles, Rosalind A., Ferris, Michelle

Volltext

The CXCL12/CXCR4 Axis Plays a Critical Role in Coronary Artery Development von Ivins, Sarah, Chappell, Joel, Vernay, Bertrand, Suntharalingham, Jenifer, Martineau, Alexandrine, Mohun, Timothy J., Scambler, Peter J.

Volltext

Loss of CXCL12/CXCR4 signalling impacts several aspects of cardiovascular development but does not exacerbate Tbx1 haploinsufficiency von Page, Mahalia, Ridge, Liam, Gold Diaz, Diana, Tsogbayar, Tsolmon, Scambler, Peter J, Ivins, Sarah

Volltext

HIRA Is Required for Heart Development and Directly Regulates Tnni2 and Tnnt3 von Dilg, Daniel, Saleh, Rasha Noureldin M, Phelps, Sarah Elizabeth Lee, Rose, Yoann, Dupays, Laurent, Murphy, Cian, Mohun, Timothy, Anderson, Robert H, Scambler, Peter J, Chapgier, Ariane L A

Volltext

Dual role for CXCL12 signaling in semilunar valve development von Ridge, Liam A., Kewbank, Dania, Schütz, Dagmar, Stumm, Ralf, Scambler, Peter J., Ivins, Sarah

Volltext

Family functioning and preschool children's oral health‐related quality of life von Almutairi, Sarah, Scambler, Sasha, Bernabé, Eduardo

Volltext

Hearing loss in a mouse model of 22q11.2 Deletion Syndrome von Fuchs, Jennifer C, Zinnamon, Fhatarah A, Taylor, Ruth R, Ivins, Sarah, Scambler, Peter J, Forge, Andrew, Tucker, Abigail S, Linden, Jennifer F

Volltext

Family functioning and dental caries among preschool children von Almutairi, Sarah, Scambler, Sasha, Bernabé, Eduardo

Volltext

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome von Paylor, Richard, Glaser, Beate, Mupo, Annalisa, Ataliotis, Paris, Spencer, Corinne, Sobotka, Angela, Sparks, Chelsey, Choi, Chul-Hee, Oghalai, John, Curran, Sarah, Murphy, Kieran C, Monks, Stephen, Williams, Nigel, O'Donovan, Michael C, Owen, Michael J, Scambler, Peter J, Lindsay, Elizabeth

Volltext

The mouth and oral health in the field of dementia von Scambler, Sasha, Curtis, Sarah, Manthorpe, Jill, Samsi, Kritika, Rooney, Yvonne M, Gallagher, Jennifer E

Volltext

An expression and function analysis of the CXCR4/SDF-1 signalling axis during pituitary gland development von Gonzalez-Meljem, Jose Mario, Ivins, Sarah, Andoniadou, Cynthia Lilian, Le Tissier, Paul, Scambler, Peter, Martinez-Barbera, Juan Pedro

Volltext

Tbx1 controls cardiac neural crest cell migration during arch artery development by regulating Gbx2 expression in the pharyngeal ectoderm von Calmont, Amélie, Ivins, Sarah, Van Bueren, Kelly Lammerts, Papangeli, Irinna, Kyriakopoulou, Vanessa, Andrews, William D, Martin, James F, Moon, Anne M, Illingworth, Elizabeth A, Basson, M Albert, Scambler, Peter J

Volltext

Contextualising disability and dentistry: challenging perceptions and removing barriers von Scambler, Sasha, Curtis, Sarah A.

Volltext

Retinoic acid down‐regulates Tbx1 expression in vivo and in vitro von Roberts, Catherine, Ivins, Sarah M., James, Chela T., Scambler, Peter J.

Volltext

Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1 von Ivins, Sarah, Lammerts van Beuren, Kelly, Roberts, Catherine, James, Chela, Lindsay, Elizabeth, Baldini, Antonio, Ataliotis, Paris, Scambler, Peter J.

Volltext

Cyp26 genes a1, b1 and c1 are down-regulated in Tbx1 null mice and inhibition of Cyp26 enzyme function produces a phenocopy of DiGeorge Syndrome in the chick von Roberts, Catherine, Ivins, Sarah, Cook, Andrew C., Baldini, Antonio, Scambler, Peter J.

Volltext

Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome von Bassett, Anne S., MD, McDonald-McGinn, Donna M., MS, CGC, Devriendt, Koen, MD, Digilio, Maria Cristina, MD, Goldenberg, Paula, MD, MSW, Habel, Alex, MD, Marino, Bruno, MD, Oskarsdottir, Solveig, MD, PhD, Philip, Nicole, MD, Sullivan, Kathleen, MD, PhD, Swillen, Ann, PhD, Vorstman, Jacob, MD, PhD

Volltext

Combined exome and whole-genome sequencing identifies mutations in ARMC4 as a cause of primary ciliary dyskinesia with defects in the outer dynein arm von Onoufriadis, Alexandros, Shoemark, Amelia, Munye, Mustafa M, James, Chela T, Schmidts, Miriam, Patel, Mitali, Rosser, Elisabeth M, Bacchelli, Chiara, Beales, Philip L, Scambler, Peter J, Hart, Stephen L, Danke-Roelse, Jeannette E, Sloper, John J, Hull, Sarah, Hogg, Claire, Emes, Richard D, Pals, Gerard, Moore, Anthony T, Chung, Eddie M K, Mitchison, Hannah M

Volltext

Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice von Randall, Victoria, McCue, Karen, Roberts, Catherine, Kyriakopoulou, Vanessa, Beddow, Sarah, Barrett, Angela N, Vitelli, Francesca, Prescott, Katrina, Shaw-Smith, Charles, Devriendt, Koen, Bosman, Erika, Steffes, Georg, Steel, Karen P, Simrick, Subreena, Basson, M Albert, Illingworth, Elizabeth, Scambler, Peter J

Volltext