5 Einträge gefunden

1. Dysfunction of the MDM2/p53 axis is linked to premature aging

   1. Lessel, Davor
   2. Wu, Danyi
   3. Trujillo, Carlos
   4. Ramezani, Thomas
   5. Lessel, Ivana
   6. Alwasiyah, Mohammad K
   7. Saha, Bidisha

   2017 - Forschungsinformationssystem des UKE
2. POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome

   1. Lessel, Davor
   2. Hisama, Fuki M
   3. Szakszon, Katalin
   4. Saha, Bidisha
   5. Sanjuanelo, Alexander Barrios
   6. Salbert, Bonnie A
   7. Steele, Pamela D

   2015 - Forschungsinformationssystem des UKE
3. Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry

   1. Saha, Bidisha
   2. Lessel, Davor
   3. Nampoothiri, Sheela
   4. Rao, Anuradha S
   5. Hisama, Fuki M
   6. Peter, Dincy
   7. Bennett, Chris

   2013 - Forschungsinformationssystem des UKE - frei zugänglich
4. Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.

   1. Hisama, Fuki M
   2. Lessel, Davor
   3. Leistritz, Dru
   4. Friedrich, Katrin
   5. McBride, Kim L
   6. Pastore, Matthew T
   7. Gottesman, Gary S

   2011 - Forschungsinformationssystem des UKE
5. WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.

   1. Friedrich, Katrin
   2. Lee, Lin
   3. Leistritz, Dru F
   4. Nürnberg, Gudrun
   5. Saha, Bidisha
   6. Hisama, Fuki M
   7. Eyman, Daniel K

   2010 - Forschungsinformationssystem des UKE