We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

Search results

From Proteopedia

You searched for Lissencephaly

Jump to: navigation, search

There is no page with the exact title "Lissencephaly". The search results for "Lissencephaly" are displayed below. You can create a page titled Lissencephaly (by clicking on the red link).

For more information about searching Proteopedia, see Help.

To exclude pages titled with 4-character PDB codes, use the checkbox "only Human created pages" at the bottom of this page.

Showing below up to 20 results starting with #1.


View (previous 20) (next 20) (20 | 50 | 100 | 250 | 500)

Article title matches

  1. Category:Lissencephaly (44 bytes)
    1: List of pages with the keyword Lissencephaly

Page text matches

  1. 1uuj (6,370 bytes)
    2: ==N-terminal domain of Lissencephaly-1 protein (Lis-1)==
    24: ...ins the molecular basis of a low severity form of lissencephaly.
    26: ...re of the N-terminal domain of the product of the lissencephaly gene Lis1 and its functional implications.,Kim MH...
  2. 9e0w (4,164 bytes)
    11: ...://www.uniprot.org/uniprot/LIS1_HUMAN LIS1_HUMAN] Lissencephaly due to LIS1 mutation;17p13.3 microduplication syn...
  3. 1mfw (4,428 bytes)
    24: ...Mutations in the gene encoding doublecortin cause lissencephaly in males and the 'double-cortex syndrome' in fema...
  4. 1mjd (6,000 bytes)
    10: ... chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1).
    25: ...Mutations in the gene encoding doublecortin cause lissencephaly in males and the 'double-cortex syndrome' in fema...
  5. 1vyh (4,181 bytes)
    23: ...rface of LIS1 contains sites of mutations causing lissencephaly and overlaps with a putative dynein binding surfa...
  6. 2bqq (6,217 bytes)
    10: ... chromosomal aberration involving DCX is found in lissencephaly. Translocation t(X;2)(q22.3;p25.1).
  7. 9qfw (2,986 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  8. 9qfb (2,996 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  9. 9qfd (2,990 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  10. 9e0t (4,164 bytes)
    11: ...://www.uniprot.org/uniprot/LIS1_HUMAN LIS1_HUMAN] Lissencephaly due to LIS1 mutation;17p13.3 microduplication syn...
  11. 9p1i (3,132 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  12. 8ru2 (3,078 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  13. 9qfk (3,018 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  14. 9qey (3,044 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  15. 9qf2 (2,996 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  16. 9fjm (2,982 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  17. 2v66 (5,272 bytes)
    24: ...ed lissencephaly sequence (ILS) and Miller-Dieker lissencephaly. The molecular basis of the interactions of Ndel1...
    26: ...on with Lis1, the causal protein of Miller-Dieker lissencephaly.,Derewenda U, Tarricone C, Choi WC, Cooper DR, Lu...
  18. 2v71 (3,977 bytes)
    22: ...ed lissencephaly sequence (ILS) and Miller-Dieker lissencephaly. The molecular basis of the interactions of Ndel1...
    24: ...on with Lis1, the causal protein of Miller-Dieker lissencephaly.,Derewenda U, Tarricone C, Choi WC, Cooper DR, Lu...
  19. 9qew (3,038 bytes)
    11: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...
  20. 3byh (3,441 bytes)
    10: ...n malformation consisting of anterior-predominant lissencephaly. Other typical features include postnatal short s...

View (previous 20) (next 20) (20 | 50 | 100 | 250 | 500)



Search in namespaces:

Include only Seeded (Automatic) pages - only Human created pages
List redirects
Search for

You may also try
Views
Personal tools